Impact Factor 4.235 | CiteScore 6.4
More on impact ›

Frontiers in Microbiology

Fungi and Their Interactions

Original Research ARTICLE

Front. Microbiol., 20 August 2020 | https://doi.org/10.3389/fmicb.2020.01955

Phagolysosomal Survival Enables Non-lytic Hyphal Escape and Ramification Through Lung Epithelium During Aspergillus fumigatus Infection

Constanze Seidel, Sergio D. Moreno-Velásquez†‡, Nagwa Ben-Ghazzi, Sara Gago, Nick D. Read and Paul Bowyer*
  • Manchester Fungal Infection Group, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester Academic Health Science Centre, Core Technology Facility, Manchester, United Kingdom

Aspergillus fumigatus is the most important mould pathogen in immunosuppressed patients. Suboptimal clearance of inhaled spores results in the colonisation of the lung airways by invasive hyphae. The first point of contact between A. fumigatus and the host is the lung epithelium. In vitro and ex vivo studies have characterised critical aspects of the interaction of invasive hyphae on the surface of epithelial cells. However, the cellular interplay between internalised A. fumigatus and the lung epithelium remains largely unexplored. Here, we use high-resolution live-cell confocal microscopy, 3D rendered imaging and transmission electron microscopy to define the development of A. fumigatus after lung epithelium internalisation in vitro. Germination, morphology and growth of A. fumigatus were significantly impaired upon internalisation by alveolar (A549) and bronchial (16HBE) lung epithelial cells compared to those growing on the host surface. Internalised spores and germlings were surrounded by the host phagolysosome membrane. Sixty per cent of the phagosomes containing germlings were not acidified at 24 h post infection allowing hyphal development. During escape, the phagolysosomal membrane was not ruptured but likely fused to host plasma membrane allowing hyphal exit from the intact host cell in an non-lytic Manner. Subsequently, escaping hyphae elongated between or through adjacent epithelial lung cells without penetration of the host cytoplasm. Hyphal tips penetrating new epithelial cells were surrounded by the recipient cell plasma membrane. Altogether, our results suggest cells of lung epithelium survive fungal penetration because the phagolysosomal and plasma membranes are never breached and that conversely, fungal spores survive due to phagosome maturation failure. Consequently, fungal hyphae can grow through the epithelial cell layer without directly damaging the host. These processes likely prevent the activation of downstream immune responses alongside limiting the access of professional phagocytes to the invading fungal hypha. Further research is needed to investigate if these events also occur during penetration of fungi in endothelial cells, fibroblasts and other cell types.

Introduction

Invasive fungal infections are a major cause of mortality, with more people dying from the ten main invasive fungal diseases than from tuberculosis or malaria (Brown et al., 2012). Despite the development of new antifungal drugs and medical procedures, mortality rates for these diseases remain extremely high (Bongomin et al., 2017). This is the case of fungal lung infections caused by the opportunistic mould Aspergillus fumigatus for which mortality can reach 90% despite treatment. A. fumigatus is a saprophytic mould which produces millions of small conidia (2–3 μm) that are released into nearly all human accessible habitats (Bennett, 2010; O’Gorman, 2011; Kwon-Chung and Sugui, 2013; Knox et al., 2016). Typically, humans inhale up to several hundred A. fumigatus conidia per day, which are efficiently eliminated by the innate lung defences (Mullins and Seaton, 1978; Latgé, 1999; Balloy and Chignard, 2009). However, in some immunocompromised patients or those with a prior respiratory condition such as a past history of tuberculosis infection, COPD, asthma or cystic fibrosis, conidia can evade the host response, germinate and colonise the lung epithelium leading to the development fungal disease (Wasylnka et al., 2005; Mccormick et al., 2010; Kosmidis and Denning, 2015; van de Veerdonk et al., 2017; Gago et al., 2018).

The respiratory epithelium is the initial point of contact of inhaled conidia with the host (Filler and Sheppard, 2006). Although professional phagocytes, like alveolar macrophages, have been traditionally described as the main host effectors in the anti-Aspergillus response, an increasing body of evidence suggests the airway epithelium is an extension of the innate immune system and plays a critical role in fungal clearance (Herzog et al., 2008; Osherov, 2012; Bertuzzi et al., 2019; Amich et al., 2020). Additionally, uptake of A. fumigatus by epithelial cells triggers the activation of signalling pathways leading to the release of cytokines and antimicrobial peptides facilitating a coordinated immune response (Wasylnka and Moore, 2002; Bellanger et al., 2009; Sharon et al., 2011; Escobar et al., 2016; Richard et al., 2018).

During its contact with the airway epithelium, conidia have been shown to adhere to the epithelial cells and extracellular matrix (Bromley and Donaldson, 1996; DeHart et al., 1997; Latgé, 1999; Bertuzzi et al., 2019). Invasion of the lung epithelia is a common pathogenic strategy used by microorganisms to entry into the vascular endothelium and cause a systemic infection (DeHart et al., 1997; Paris et al., 1997; Han et al., 2011; Sun et al., 2012; Bertuzzi et al., 2019). Several in vitro and ex vivo infection studies have shown that bronchial and alveolar epithelial cells can internalise adherent fungal conidia in a time-dependent manner (Wasylnka and Moore, 2002; Han et al., 2011; Xu et al., 2012; Bertuzzi et al., 2014; Gago et al., 2018; Richard et al., 2018; Clark et al., 2019). In vitro analyses of the interaction between lung epithelial cells and A. fumigatus have shown that epithelial cells are able to form pseudopods to facilitate conidia engulfment on an actin, cofilin-1, phospholipase-D-dependent manner (Paris et al., 1997; Wasylnka and Moore, 2002; Han et al., 2011; Bertuzzi et al., 2014; Bao et al., 2015). Subsequently, internalised conidia are trafficked into acidic phagosomes, where class III PI3P kinases are critical for processing (Clark et al., 2019). This process strongly limits viability of internalised conidia and only 3% survive after 24 h (Wasylnka and Moore, 2003). This small proportion of conidia can germinate and escape the epithelial cells without clear evidence of host death (Amin et al., 2014; Bertuzzi et al., 2014). However, the spatial and temporal interplay between the host and internalised A. fumigatus spores upon escape have not been explored.

Here, we studied the dynamics involved in the early stages of the growth of A. fumigatus during infection of alveolar and bronchial epithelial cells on a time-dependent manner. Our data demonstrate that survival of the lung epithelium upon infection relies on the phagolysosomal and plasma membrane compartmentalisation of internalised A. fumigatus thus limiting direct fungus-host contact.

Materials and Methods

A. fumigatus Strains and Growth Conditions

Aspergillus fumigatus A1163 expressing cytosolic GFP and RFP under the control of the B-tubulin gene were kindly provided by Dr. Michael Bromley (Macdonald et al., 2019). A. fumigatus ATCC 46645 expressing cytosolic YFP [PgpdA::yfp(ptrA)] constructed as previously described (Lother et al., 2014) was a kind gift from Prof. Sven Krappmann, and used for hyphal extension imaging. Strains were maintained at 37°C for 5 days in Aspergillus minimal media (AMM) containing 2% sucrose, 1.5% agar (w/v). Conidia were harvested with 0.05% PBS Tween 20 and concentration was determined by using a haemocytometer.

Cell Lines

The type II alveolar epithelial cell line A549 (Lieber et al., 1976; American Type Culture Collection CCL-18) and the cytosolic-GFP stable A549 cell line (SC043-Bsd, Amsbio, United States) were maintained by serial passage in Dulbecco’s Modified Eagle Medium (DMEM) supplemented with 10% foetal bovine serum (FBS), streptomycin (100 μg/ml) and penicillin (16 μg/ml). 16HBE bronchial epithelial cells (Cozens et al., 1994) were a kind gift from Dr. Sarah Herrick (The University of Manchester). 16HBE cells were maintained in Eagle Minimal Essential Media (MEM) supplemented with L-glutamine (1%), FBS (10%), streptomycin (100 μg/ml) and penicillin (16 μg/ml). All cell lines were grown at 37°C, 5% CO2 and used after the second or third passage. All reagents were purchased from Sigma unless otherwise stated.

Exposure of Epithelial Cells to A. fumigatus Conidia

For all experiments, 105 epithelial cells/ml were seeded in 2- or 8-well chambers (Nunc LabTek chamber slide system, Life Technologies) and incubated at 37°C, 5% CO2 for 24 h to approximately 90% confluency. Monolayers were then challenged with 106 A. fumigatus spores/ml (1:10 multiplicity of infection) from 6 to 24 h depending on the experiment’s readout. Epithelial cells were washed 3 times with pre-warmed PBS and cells were incubated with pre-warmed DMEM/F12 medium (without phenol red) for live-cell imaging.

Characterisation of A. fumigatus Development Within Lung Epithelial Cells

To track the cell biology of internalised A. fumigatus spores, the cytoplasmic membrane of the 16HBE and A549 epithelial monolayers was either stained using CellMask Deep Red Membrane dye (Life Technologies, Eugene, OR, United States) or transiently transfected using the CellLight Plasma Membrane-GFP BacMam 2.0 system (GFP-myristolyation/palmitoylation sequence from LcK tyrosine kinase) (Life Technologies, United States) (Celik et al., 2013). For CellMask Deep Red staining (excitation = 649 nm, emission = 666 nm), epithelial cells were stained after infection for 10 min at 37°C and 5% CO2 using a final concentration of 5 μg/ml of the dye. To induce transient expression of GFP in the host plasma membrane, epithelial cell monolayers at a confluency not higher than 70% were transfected using the CellLight Plasma Membrane-GFP system (excitation = 488 nm, emission = 510 nm) according to manufacturer’s instructions; cells were then incubated until confluence and further challenged with A. fumigatus spores as described above. Transfection efficiency was below 100%.

For the detection of acidic intracellular compartments, infected monolayers were stained with 10 nM of LysoTracker DND 99 red (excitation = 577 nm, emission = 590 nm; Life Technologies, Waltham, MA, United States). Additionally, phagolysosomal membranes were labelled by transient expression of the lysosomal associated membrane protein (LAMP-1) using the CellLight Lysosome-GFP or RFP BacMam 2.0 system (Life Technologies, United States) on uninfected and subconfluent monolayers as described above. After staining with any of the dyes, monolayers were washed twice with pre-warmed PBS and maintained in supplemented DMEM.

All the experiments aiming to characterise the intracellular events of A. fumigatus interaction with the lung epithelium were done using A549 alveolar epithelial cells. Experiments aiming to characterise the mechanistic of A. fumigatus fate and escape during the infection of the lung epithelia and phagosome maturation were also performed using 16HBE bronchial epithelial cells.

Nystatin Protection and Cell Viability Assays

The nystatin protection assay was performed as previously described (Wasylnka and Moore, 2002). Briefly, confluent epithelial monolayers were challenged with 106 spores of A. fumigatus either expressing GFP or RFP cytosolic proteins for 4 h. Monolayers were then washed twice with pre-warmed PBS and incubated with 50 μg/ml of nystatin in cell culture media (DMEM or MEM for A549 or 16HBE, respectively), at 37°C, 5% CO2 for 3 h. Samples were washed twice with pre-warmed PBS and further incubated for 1 h in supplemented DMEM/MEM until analysis. Susceptibility of the strains to nystatin was verified as previously reported (Bertuzzi et al., 2014). Live-cell imaging was performed using phenol red-free DMEM/F12 Medium (Thermo Fisher Scientific) supplemented with 10% FBS, 15 mM HEPES (pH 7).

Confocal Microscopy

Live-cell imaging at high resolution was performed using a laser scanning confocal microscope (Leica, TCS SP8 X), which was mounted on an inverted microscope and equipped with photo multiplier tubes (PMT), hybrid GaAsP (HyD) detectors and a 63× water immersion objective. A Leica turntable white light laser (WLL, 450-750 nm), argon laser (458, 476, 488, and 496 nm) and UV laser (405 nm) were used for fluorescence excitation. Simultaneous brightfield images were captured with a transmitted light detector. The laser intensity and exposure of the cells were kept to a minimum to reduce photobleaching and phototoxic effects. A 40x/0.85 NA dry and a 63x/1.4 NA water objective lens were used. Live-cell imaging was carried out at 37°C and 5% CO2 in a microscope-controlled chamber (Cube & Box, Switzerland). Confocal images were captured using Leica microsystem CMS software (v. 3.3, LAS AF). To visualize the GFP or RFP targeted to the cytoplasm of A. fumigatus, excitation of fluorescent proteins was performed at 488 and 555 nm, respectively. The fluorescent signal emitted was detected over the range of 505 to 550 nm for GFP, and 570 to 700 nm for RFP. To image the host plasma membrane and acidic compartments, the dyes CellMask deep red (Excitation/Emission 649/660-750 nm), LysoTracker red DND-99 (Excitation/Emission 577/590-700 nm), CellLight Lysosomes-RFP BacMam 2.0 (Excitation/Emission 555-560/570-590 nm) and CellLight Plasma membrane-GFP BacMam 2.0 (Excitation/Emission 485-488/500-550 nm) were used. 3D images and 4D videos of vertical cross sections through infected monolayers were generated using the IMARIS software package (Bitplane AG, Zurich, Switzerland). IMARIS images were then processed using ImageJ (v. 1.44, MacBiophotonics) and Adobe Photoshop (v. 13, Adobe). Live-cell imaging videos generated in this study were exported from LAS AF software and processed in FIJI1.

For quantitative data analysis of the conidia area, confocal images were segmented and the surface area was measured in IMARIS; length of the main hyphae was estimated using the NeuronJ plugin in FIJI as previously reported (Shen et al., 2016). The percentage of A. fumigatus spore germination and hyphal length inside or outside the epithelial monolayer were determined in a minimum of 500 events from experiments run in biological and technical triplicates using ImageJ. The percentage of conidia internalisation was estimated as described in Bleichrodt et al. (2020). The fluorescence intensity within acidified phagolysosomes or non-acidified phagolysosomes was determined in arbitrary fluorescence units using IMARIS.

Electron Microscopy

Correlative live-cell imaging (confocal microscopy) and Transmission Electron Microscopy (TEM) was performed to secure imaging of cells in the desired stage of infection. For that, A549 alveolar epithelial cells were seeded on 35 mm glass bottom petri dishes with a grid (MatTek, Ashland, MA, United States) until 40% confluence and consequently infected with GFP-expressing A. fumigatus strain for 12 h. Cells were treated with nystatin at 4 h post-infection as described above. To establish the coordinates of the areas of interest for comparative confocal-electron microscopy analyses, live-cell 3D datasets were generated using confocal laser microscopy. Samples were then fixed with 4% formaldehyde and 2.5% glutaraldehyde in 0.1 M HEPES buffer (pH 7.2). Subsequently, fixed samples were treated with 1% osmium tetroxide and 1.5% potassium ferrocynaide in 0.1 M cacodylate buffer (pH 7.2) for 1 h and then, treated with 1% uranyl acetate in water for an extra hour. Samples were dehydrated in increasing ethanol series, infiltrated with TAAB 812 resin and polymerized for 24 h at 60°C. The coordinates of the areas of interest in resin blocks were identified using the replica of etched location grid from MatTek coverslips. Serial ultrathin sections were cut with Reichert Ultracut ultramicrotome and observed with FEI Tecnai 12 Biotwin microscope at 100 kV accelerating voltage. Images were taken with Gatan Orius SC1000 CCD camera in the Electron Microscopy Core Facility at the University of Manchester.

Statistical Analyses

Statistical analysis was performed using IBM SPSS software (version 20.0) and GraphPad Prism v8.1 (La Jolla, CA, United States). Statistical analysis included two-tailed Student’s t-tests for comparing pairs of normally distributed data, one-way ANOVA with Tukey’s post hoc test for comparing datasets containing multiple treatment groups and two-way ANOVA for comparing differences in germination time across treatments. Differences in proportions were analysed using Fisher’s exact test. Comparisons were deemed significant with a P-value of ≤0.05. All experiments were performed in biological and technical triplicates. Data is represented as mean and standard deviation, unless other stated.

Results

Morphogenesis of Aspergillus fumigatus During Early Stages of the Lung Epithelia Infection

The adhesion and internalisation of A. fumigatus conidia by alveolar epithelial cells has previously been described (Wasylnka and Moore, 2002, 2003; Bertuzzi et al., 2014). However, little is known about fungal development and host cell dynamics of internalised A. fumigatus spores during lung epithelia infection. To address this question, the isotropic growth (increment on the spore area overtime after breaking dormancy) and germination (emergence of a germ tube with polarised growth) of fluorescent labelled A. fumigatus spores within and on the lung epithelia surface was comparatively analysed in a 12 h infection experiment. This time point was chosen as spore uptake was gradually increased on a time-dependent manner (Figure 1A). Isotropic growth rates in culture media were used as control.

FIGURE 1
www.frontiersin.org

Figure 1. Germination and morphology of internalised A. fumigatus is impaired during infection of type II alveolar cells. (A) A. fumigatus spore uptake by A549 epithelial cells. (B) Live-cell imaging of hyphae of A. fumigatus expressing cytoplasmic GFP in DMEM, on the alveolar host surface or within the host cells at 37°C, 5% CO2 for 18 h in the absence of nystatin. Arrows indicate vacuoles. Asterisks highlight sites of second germ tube initiation. A. fumigatus (C) germination rate (%), (D) swelling rate (%), (E) hyphal extension rate and (F) degree of branching in the presence or absence of A549 alveolar cells (G) Live-cell imaging of the different strategies of A. fumigatus infections of A549 alveolar cells. Magenta = host’s plasma membrane stained with CellMask deep red. Green = A. fumigatus expressing cytosolic GFP. Measurements were performed in three biological and technical replicates (average ± standard deviation [SD]). P < 0.05; ∗∗P < 0.01; ∗∗∗P < 0.001; ****P < 0.0001.

Germination and the rate of area increment for swelling spores were significantly higher in culture media (12 h percentage of germination = 98%; swelling rate = 20.66 μm/h) compared to spores growing on (12 h percentage of germination = 57.8%; swelling rate = 17.8 μm/h) or even inside the host cells (12 h percentage of germination = 11.5%; swelling rate = 10.28 μm/h) (Figures 1B–D). Interestingly, A. fumigatus germlings growing on the epithelia surface showed a significant decrease in hyphal length, decreased spore swelling and increased hyphal tip branching when compared to those incubated the absence of host cells (P < 0.05) (Figures 1D–F). After 20 h of A. fumigatus-A549 co-culture, hyphae on the epithelial surface developed into an extensive fungal network that covered the monolayer’s surface (Figure 1G). This A. fumigatus growth pattern was similar to that shown by A. fumigatus spores growing in the absence of epithelial cells (Figure 1A).

In order to monitor the growth and germination of exclusively internalised A. fumigatus spores during early infection stages, A549 epithelial cells were treated with nystatin. Spore swelling and growth was significantly reduced in those germinating internalised spores (Figures 1C,D and Supplementary Video 1). The formation of a second germ tube opposite to the first germ tube was frequently observed after germination of internalised spores (Figure 1B). Branching of internalised germlings (2.64 ± 0.21 hyphal tips/spore) and in those attached to the host surface (2.18 ± 0.42 hyphal tips/spore) was significantly lower than for germlings growing in the absence of cells (4.58 ± 0.30 hyphal tips/spore), (P < 0.05) (Figure 1F). This branching pattern occurred rarely in A. fumigatus germlings growing in cell culture media. Furthermore, an increased number of vacuoles was observed in internalised A. fumigatus germlings than those growing on the surface of the lung epithelia (Figure 1B). Maximal-3D Z-stack projections revealed that during early infection with A. fumigatus, the cellular integrity of the epithelial monolayer remained apparently unaffected (Supplementary Video 2).

In order to confirm these observations in a different cellular system, A. fumigatus fate was analysed during its interaction with 16HBE bronchial epithelial cells. A different cellular morphology and growth pattern of A. fumigatus during infection characterised by increased extracellular and decreased intracellular swelling and impaired intracellular branching was observed compared to alveolar epithelial cells (Supplementary Figure 1). Overall, internalised A. fumigatus conidia showed delayed germination (Supplementary Figure 1F), impaired growth and morphogenesis in both, alveolar and bronchial epithelial cell lines.

Internalised A. fumigatus Can Grow Between Adjacent Epithelial Cells

Live-cell confocal imaging demonstrated that A. fumigatus conidia germinate on the host surface or intracellularly during its interaction with the lung epithelia. Continuous hyphal extension of internalised spores resulted in the formation of mature hyphae which either extended into the adjacent or through many host cells. Additionally, young germlings growing within the host cells also displayed an abnormal morphology, produced more than one germ tube, extended extracellularly and subsequently invaded the adjacent cells (Figures 2A–C). Interestingly, the growing fraction of A. fumigatus escaping from the respiratory epithelium exhibited similar leading hyphae morphology to those growing only in cultured media.

FIGURE 2
www.frontiersin.org

Figure 2. Internalised A. fumigatus can expand between adjacent epithelial cells. (A) Live-cell imaging of hyphae of A. fumigatus cytoplasmically labelled with GFP infecting a monolayer of A549 alveolar cells cultured in DMEM at 37°C, 5% CO2 for 18 h. 1- 3-D rendered image of an infected alveolar monolayer stained with Cell Mask Deep Red. 2- Internalised A. fumigatus hyphae 3- Merge of 1 and 2. Scale bars: 5 μm. (B) Lateral view of the 3-D confocal stack displayed in (A) Arrowheads indicate hyphal tips escaping the host monolayer Scale bar: 5 μm. (C) A. fumigatus hyphal (red) invasion of the epithelial cells (green) 18 h post-inoculation, a magnification of the part indicated with dashed white rectangle with surface rendering, and with 60% transparency demonstrating the internal invading hypha. White arrows indicate hypha that have emerged or growth through unlabelled (asterisks) cells and yellow arrows indicate intracellular parts of the hypha. Scale bars: 40 μm.

Hyphal length was comparatively assessed on the surface and within alveolar and bronchial epithelial cells using cell culture media as control. Hyphae growing within alveolar or bronchial epithelial monolayers displayed a filament length of 23.66 and 22.08 μm, respectively. This length of the hypha was significantly lower than that observed for simultaneously inoculated conidia growing on the cell surface (Figure 1D and Supplementary Figure 1C). Notably, neither A. fumigatus filaments growing within nor those hyphal fractions escaping the host cell, exhibited obvious subcellular damage during early infection as shown by transmission electron microscopy imaging (Supplementary Figures 2, 3). Once hyphae escape toward the extracellular milieu, subsequent hyphal penetration to a new epithelial host cell was also observed (Figure 2C). These observations highlight the ability of A. fumigatus to disseminate during early stages of the colonisation of respiratory epithelia without causing significant host damage.

FIGURE 3
www.frontiersin.org

Figure 3. A. fumigatus conidia are surrounded by a phagolysosomal membrane upon internalisation, germination and during A549 escape. (A) Single internalised conidia surrounded by a phagolysosomal membrane. A large number of individual lysosomes are accumulated in proximity to the host cell membrane (arrows). (B) Multiple internalised conidia surrounded by a single phagolysosomal compartment. (C) Time course of escaping of an extending hyphae from the phagolysosome demonstrates this process to involve (a) stretching of the phagosome; (b) escape from the host cell and (c) escape from the phagolysosome. Yellow arrows and dashes indicate the host cytoplasmic membrane; white arrows indicate the distal part of the tip escaping from the phagolysosome (Scale bars = 5 μm). Red = A. fumigatus expressing cytoplasmic RFP; Green = phagolysosomal compartment stained with LAMP-1 GFP. Magenta = A549 cell plasma membrane stained with CellMask deep red.

Internalised A. fumigatus Germlings Are Surrounded by a Phagolysosomal Membrane Upon A549-Host Escape

Early during the infection of the respiratory epithelium in vitro, internalised A. fumigatus spores are fused to lysosomes and acidic vesicles that inhibit the germination of the majority of the A. fumigatus spores (Wasylnka and Moore, 2002; Ibrahim-Granet et al., 2003; Botterel et al., 2008). Live-cell confocal imaging demonstrated that the percentage of A. fumigatus conidia which germinate is 5-fold decreased from 12 to 48 h in both cell lines. This reduced viability indicates that most of the internalised conidia by epithelial cells are killed at 48 h post infection and the surviving ones are able to outgrowth by hyphal extension with no obvious host cell injury (Figure 1C, Supplementary Figures 4A,B, 5). To further characterise the mechanistic of this process, internalisation, intracellular extension and escape of A. fumigatus germlings from the phagosome was investigated in a time-dependent manner.

After A. fumigatus uptake by the lung epithelium, conidia were surrounded by a single LAMP-1 expressing host membrane suggesting phagosome maturation to phagolysosome (Figure 3A). In rare occasions (<1%), a single large phagolysosome compartment surrounding several conidia was observed (Figure 3B). Persistent spores contained within phagolysosomes were able to germinate (6–9 h post-infection), and the host phagolysosomal membrane was continuously extended while surrounding the intracellular growing young germling (Figure 3C). The aforementioned phagolysosome was extended until the tip of the growing germling contacted the host plasma membrane. While the hyphae fraction that remains inside of the host cell was covered by the phagolysosomal membrane, the apical fraction of A. fumigatus that escaped the host cells was not further covered. This phagolysosome-plasma membrane interaction likely resulted in the migration of the host cytoplasmic membrane into the phagolysosomal membrane surrounding the intracellular growing germlings (Figure 3). This suggests that the phagolysosome and the host plasma membrane likely fuse at the point of hyphal exit in the same manner as observed during escape of other pathogens from the host (Hissa et al., 2012; Pereira et al., 2019).

Transmission electron microscopy (TEM) was performed upon A549 alveolar epithelial cells during A. fumigatus challenge to confirm the results from confocal imaging. 3-D datasets (Figure 4A) of A549 epithelial cells containing internalised A. fumigatus germlings were created followed by TEM analysis (Figure 4B). On an ultrastructural level, A. fumigatus germlings were tightly surrounded by a host’s lipid-bilayer membrane prior to escape (Figures 4C,D), which confirmed our initial live-cell confocal imaging observations (Figure 3). Notably, this presumably LAMP-1 phagolysosomal-associated membrane was intact during its interaction with A. fumigatus. Upon interaction of the extending phagosome covering the growing hyphal tip with the host plasma membrane, a protrusion of plasma membrane covering the apical area of the hyphae was noticed which might play a role in preventing host’s death (Supplementary Figure 3).

FIGURE 4
www.frontiersin.org

Figure 4. Correlative live-cell imaging and transmission electron microscopy (TEM) confirms that internalised A. fumigatus growing germlings are engulfed within the lung epithelium phagosome. (A) Confocal live-cell imaging of an internalised germling by A549 epithelial cells. (B) TEM image of a cross-section of the same infected A549 cell. (C) Magnification of the tip of the internalised germling. (D) Sections of the germling cell wall, PM: A. fumigatus plasma membrane; CW: A. fumigatus cell wall; LM: host phagolysosomal membrane. Note the host’s lipid bilayer that surrounds A. fumigatus within A549 host cells shown in panel (D).

The Alveolar and Bronchial Plasma Membrane Fuses With the Phagosomal Membrane After A. fumigatus Escape

We previously observed that the plasma membrane-specific dye (CellMask Deep Red) was able to stain the epithelial cell plasma membrane but also partially labelled the membrane surrounding the portion of the germling remaining within the host during escape (Figure 3). However, at this stage we were unable to discriminate whether this dye was either staining the plasma membrane of the host or A. fumigatus. To overcome this problem, A549 and 16HBE epithelial cells were transfected with a GFP plasma membrane specific marker for mammalian cells (GFP-myristolyation/palmitoylation sequence from Lck tyrosine kinase) and monitored during A. fumigatus infection as previously described. Uninfected epithelial cells showed a homogeneous GFP signal throughout the epithelial cell plasma membrane with no evidence of transfection toxicity (data not shown). During A. fumigatus challenge experiments, the lck-GFP marker did not label the fungal plasma membrane (Figure 5), despite germlings being enclosed within phagolysosomes (Figure 3). Interestingly, an accumulation of lck-GFP surrounding extending A. fumigatus hyphal tips was evident in both alveolar and bronchial epithelial cells prior to hyphal escape (Figures 5B–H; Supplementary Video 3). As hyphal escape progressed, the lck-GFP plasma membrane signal slowly migrated into the host lipid bilayer membrane surrounding both growing germlings and basal conidia with no obvious fungal cytological damage (Figure 5C). Remarkably, an accumulation of strained host plasma membrane signal was observed around the points of fungal escape in agreement with the TEM experiments described above (Figures 5D, 4 and Supplementary Figure 3). Maximal projections of the same infected epithelial cells and ultrastructural analysis showed that the host’s plasma membrane was sealed upon hyphal escape with no loss of cell contents (Figure 5F, Supplementary Figure 5) presumably by fusion with the phagolysosomal membrane (Figures 3D,E).

FIGURE 5
www.frontiersin.org

Figure 5. Internalised A. fumigatus cells are surrounded by the host’s plasma membrane upon escape of alveolar and bronchial epithelial cells. Confocal live-cell imaging shows A. fumigatus expressing cytoplasmic RFP within A549 and 16HBE epithelial cells expressing GFP in the plasma membrane. (A) Internalised germling before reaching the host plasma membrane. (B) The tip (arrow) of the internalised germlings is surrounded by host plasma membrane during early interaction. (C) After late interaction of the internalised germling tip, the host plasma membrane surrounds the basal part of the germling (arrowhead). (D) Host plasma membrane is accumulated in the regions of hyphal escape (arrows). (E) Host plasma membrane surrounds an extension of the escaping germling. (F) Maximal projection shown in panel (E). (G–I) 16HBE plasma membrane (arrows) surrounds internalised A. fumigatus germlings upon escape. Scale bars = 5 μm.

A. fumigatus Mature Germlings Are Surrounded by a Non-acidic Compartment

One of the early features of phagosome maturation is acidification. Low pH directly affects many pathogens and provides optimal pH for maximal activity of many hydrolytic enzymes (Uribe-Querol and Rosales, 2017). To determine whether the observed fungal germination and hyphal growth within the host epithelium was linked to reduced A. fumigatus-containing phagosome acidification, confluent alveolar (A549) and bronchial (16HBE) epithelia monolayers were labelled with the pH sensor LysoTracker Red DND-99. The progress of acidification within conidium-containing phagosomes was tracked for 2 h.

After engulfment of A. fumigatus, spores were co-localised within phagosomes which were acidified on a time-dependent manner by the addition of small acidic vesicles at discrete sites around the conidium (Figures 6A,B). This acidification process was observed to commence 5 min after engulfment. Overall, the increase in acidification rate was significantly higher in A. fumigatus containing phagosomes of 16HBE bronchial epithelial cells compared to A549 alveolar epithelial cells, which suggest improved fungal clearance capability of the bronchial epithelium (Figure 6C). Only one third of the germlings were surrounded by acidic phagosome after 24 h of infection while spores which were mainly contained within acidified phagosomes (Figures 6D–F). Overall, phagosomes containing spores displayed ∼4-fold higher fluorescence intensity compared to phagosomes containing germlings (Figure 6G, Supplementary Figure 6). Remarkably, phagosome acidification was not observed in the recipient cell after escape (Supplementary Figure 5).

FIGURE 6
www.frontiersin.org

Figure 6. Escaping A. fumigatus germlings are surrounded by a non-acidic phagosomal compartment. Alveolar monolayers were challenged with A. fumigatus (green) for 18 h at 37°C, 5% CO2. Following incubation times, cells were stained with Cell Mask Deep Red (magenta) and LysoTracker (red). (A) Time lapse (min) of an internalised spore surrounded by an acidic phagosome. (B) LysoTracker channel shown in A. Arrowheads highlight the site of lysosome fusion with the phagosome. (C) Acidification rate of spores internalised by either alveolar or bronchial cells. r.a.u estates for relative abundance units. (D) Time-lapse quantification of the percentage of germlings surrounded by acidified and non-acidified phagosomes. (E) Merged images of an internalised young germling. The arrow highlights the acidic compartment that surrounds A. fumigatus. The arrowhead highlights the fusion site of the acidic compartments. (F) Merged images of an internalised mature germling. The asterisk highlights the initial interaction between the mature germling tip and the protrusion of the host plasma membrane. Note there is no fusion of acidic compartments surrounding A. fumigatus. (G) Relative fluorescence of LysoTracker in internalised spores and germlings. Measurements were performed three times on three biological samples (average ± standard deviation [SD]) (**P < 0.01 and ****P < 0.0001). Scale bars: 5 μm.

These results suggest that successful phagosome acidification prevents spore germination within the phagosome. Although a potential alternative would be that the phagosomal membrane loses integrity and reduces phagosome efficacy, loss of integrity or leakage of acidic contents into the cytoplasm were not observed in this study.

Host Plasma Compartmentalisation of A. fumigatus Hyphae Occurs During Invasion of Neighbouring Naive Host Cells

Based on our previous observation of the capability of A. fumigatus hyphae to grow through an epithelial cell layer without causing cell injury (Figure 2), we hypothesised that lack of host cell injury could be explained by failure of the hypha to rupture the host plasma membrane. To test this, A549 expressing a GFP labelled plasma membrane were challenged with A. fumigatus spores and visualised over 24 h.

Escaping hyphae were able to either grow on the upper surface of the host cells, or toward neighbouring uninfected lung epithelial cells. The portion of hyphae extending into uninfected neighbouring cells was surrounded by the plasma membrane of the recipient cell (Figure 7). Epithelial cell injury or death in the fungal recipient epithelial cells was not observed. Interestingly, the apical segment of A. fumigatus hyphae growing in neighbouring uninfected epithelial cells was also morphologically unaffected. These results show that A. fumigatus hyphae that grow through adjacent epithelial cells are also surrounded by plasma membrane of the new host cell (Fernandes et al., 2018).

FIGURE 7
www.frontiersin.org

Figure 7. Host plasma membrane compartmentalisation of A. fumigatus hyphae occurs upon invasion of naïve lung epithelial neighbouring cells. Confocal live-cell imaging of A. fumigatus expressing cytoplasmic RFP within a GFP-plasma membrane transfected A549 epithelial cell line at 37°C, 5% CO2. (A) Germ-tubes of internalised spores extend toward adjacent cells. (B) Maximal projection of the same cells shown in A. (C) Upon escape of an epithelial host the apical zone of an invading leading hyphae is surrounded by the plasma membrane of a naïve host cell. (D) Zoom in of the apical region of the hypha shown in (A). White arrows indicate the plasma membrane of the new host. Asterisks highlight epithelial cells that were not transfected. Scale bars: 5 μm.

Altogether, our results suggest that phagosome maturation failure facilitates Aspergillus germination and escape in a non-lytic manner. Upon hyphal escape, the phagosome membrane which can be at different maturation stages and cytoplasmic membrane are likely fused, sealing the host intracellular environment and avoiding the host cell death (Figure 8). Neighbouring cell-penetrating hyphae were also surrounded by recipient host cell plasma membrane.

FIGURE 8
www.frontiersin.org

Figure 8. Phagolysosome–Plasma membrane dynamics during A. fumigatus escape. (1) Most A. fumigatus conidia are killed by acidification of phagosomes and lysosomal fusion, (2) In some circumstances lysosome recruitment to the phagosome containing A. fumigatus conidia does not inhibit fungal growth and acidification does not occur allowing conidial germination. (3) The PLm continuously extends while surrounding the intracellular growing germling until the PLm contacts the plasma membrane. (4) The PLm and Pm fuse and (5) the host plasma membrane migrates into the phagolysosome membrane facilitating hyphal escape. (6) Hyphae then proceed to penetrate further host cells without rupture of the plasma membrane. LY: lysosome, PL: phagolysosome, PLm; phagolysosome membrane, Pm: plasma membrane.

Discussion

The efficiency of alveolar macrophages in ingesting and killing A. fumigatus spores early after infection has hidden the potential role of the most abundant host cells in the lung, the airway epithelium (Crapo et al., 1982; Latgé, 1999; Luther et al., 2008; Croft et al., 2016). However, the relevance of uptake by epithelial cells of metabolically active germinating A. fumigatus early after infection remains unclear.

The development of mature hyphae requires A. fumigatus spore germination. This process depends on several factors including pH, temperature and the presence of stressors such as antifungal agents (Araujo and Rodrigues, 2004; Moreno-Velásquez et al., 2017). In previous studies (Escobar et al., 2016; Richard et al., 2018), impaired germination of A. fumigatus spores has been reported on alveolar, bronchial and primary lung epithelial cells in agreement with our results. However, our data further show that germination of internalised A. fumigatus conidia is one hour delayed compared to those growing on the surface of the respiratory epithelia (Wasylnka and Moore, 2002; Escobar et al., 2016) in the same manner as it is after phagocytosis by macrophages (Schaffner et al., 1983; Van Waeyenberghe et al., 2012). This delay in spore germination within epithelial cells is not surprising considering the stressful conditions within phagosomes and phagolysosomes (Heinekamp et al., 2015). Furthermore, we observed that the cellular environment of human host induced an aberrant morphology and growth of internalised A. fumigatus young germlings, such as reduced hyphal extension, increased branching, and a large number of vacuoles. Changes in fungal morphology within host cells characterised by the generation of new hyphal branches have been previously described as a fungal mechanism to facilitate invasive growth (Ellett et al., 2017). No host cell injury was noticed after germination and growth of internalised A. fumigatus, even when individual epithelial cells were infected with several germlings, as reported for both, professional and non-professional phagocytes (Paris et al., 1997; Rosowski et al., 2018).

Here, we observed that acidification was four-fold reduced in phagosomes containing growing germlings compared to those containing spores. Inability of macrophages to sustain acidification has been reported as a mechanism for bacteria replication and escape from the host environment (Jubrail et al., 2015). Additionally, increased fungal size leads to reduced phagosome and phagolysosome acidification of engulfed Candida albicans and Cryptococcus neoformans cells by macrophages while promoting fungal escape and host integrity (DeLeon-Rodriguez and Casadevall, 2016; Westman et al., 2018). A similar escaping mechanism has been described for A. fumigatus during epithelial cell infection and confirmed by us in this study (Wasylnka and Moore, 2002; Filler and Sheppard, 2006; Croft et al., 2016; Escobar et al., 2016). In some circumstances we observed the capacity of lung epithelial cells to form large phagolysosomes, which contained several ingested conidia as previously observed in macrophages (Alpuche-Aranda et al., 1994; Luther et al., 2008).

Several pathogenic fungi are able to invade mammalian host cells by a species-specific lytic and non-lytic egress mechanisms (Káposzta et al., 1999; Filler and Sheppard, 2006; Escobar et al., 2016). For example, C. albicans can form germ tubes within phagolysosomes facilitating fungal escape and macrophage killing (Káposzta et al., 1999). Similarly, phagocytosis of C. neoformans by macrophages results in aberrant lysosomal trafficking, pathogen release and death (Feldmesser et al., 2001). In A. fumigatus, internalised conidia are trafficked via the late endosomes/lysosomes route (Botterel et al., 2008). Some studies have shown that a small population of conidia can germinate and escape the host cells with no obvious evidence of host cell death (Wasylnka and Moore, 2002; Escobar et al., 2016). To further characterise this process using live-cell imaging we showed that hyphal tips of A. fumigatus are able to emerge either to the extracellular milieu or towards neighbouring epithelial cells. These escaping filaments displayed unaffected apical morphology compared to the internalised fragments and only a small proportion of host cells were detached or killed.

With a view to further identifying the mechanism underlying A. fumigatus escape, a combinatorial approach using live-cell confocal imaging and TEM was performed. Our data demonstrated a transient interaction between the mature phagosome and plasma membrane of the host upon A. fumigatus escape which reduces host injury (DeHart et al., 1997; Zhang et al., 2005). In order to escape from the host antimicrobial response, A. fumigatus conidia within mature phagosomes dysregulate several cellular processes such as Lamp1 and vATPase-driven acidification, Rab5 and Vamp8-dependent endocytic trafficking or cathepsin Z expression (Schmidt et al., 2018). Additionally, A. fumigatus is able to control some host cellular responses by impairing phagosome-lysosome fusion, inhibiting apoptosis or preventing the oxidative stress responses of lung epithelial cells (Jahn et al., 2002; Berkova et al., 2006; Féménia et al., 2009; Gomez et al., 2010; Oosthuizen et al., 2011; Thywißen et al., 2011). Therefore, a process combining reduction of phagosome maturation, resistance to digestion and hyphal escape via a non-lytic mechanism would allow A. fumigatus to survive and escape without causing significant cellular damage to the human host cell (Figure 8). Given that only a fraction of spores survive, we suggest that some spore subpopulations are able to adapt to conditions within the phagolysosome and successfully germinate leading to ramification of hyphae through the living epithelium, thus facilitating the development of invasive or chronic conditions (Grant and Hung, 2013; Ballard et al., 2018).

In this work, we highlighted that internalised A. fumigatus does not directly interact with the cytosol of lung epithelial cells. Additionally, penetration of intracellular hyphae growing out of phagolysosomal compartments in neighboring cells does not break the host plasma membrane. It is possible that A. fumigatus hyphae ramifying through epithelial cells in this manner are able to actively acquire nutrients from the host in the same manner as that displayed by haustoria in biotrophic plant-fungal interactions. Host plasma membrane coating of fungi allows host receptors to be triggered but limits the ability of immune responses particularly macrophages and neutrophils to reach the fungus (Berkova et al., 2006). Further molecular studies are required to determine whether this is a defense mechanism governed by the host or controlled by the fungus.

Data Availability Statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Author Contributions

CS, SM-V, and NB-G performed the experiments and analysed the data. CS, SM-V, SG, NR, and PB conceived, drafted and edited the manuscript. All authors have given approval to the final version of the manuscript.

Funding

CS was funded by the German Science Foundation (DFG, SE2405/1-1). SM-V was funded by the CONACyT (Consejo Nacional de Ciencia y Tecnología) grant 359173. SG was co-funded by the NIHR Manchester Biomedical Research Centre and a NC3Rs Training Fellowship (NC/P002390/1). NB-G was supported by the Libyan Ministry of Higher Education and Scientific Research. Financial support was also provided by the European Union (grant PITN-GA-2013-607963) to NR and NC3Rs (NC/P002390/1) to PB and SG.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

We thank Dr. Mike Bromley and Prof. Sven Krappmann for the A. fumigatus fluorescent strain. We thank the personal in the EM facility in the Core Facility in the Faculty of Biology, Medicine and Health for their assistance, and the Wellcome Trust for equipment grant support to the EM Core facility. We also acknowledge the Phenotyping Centre at Manchester (PCaM) for assistance with the provision of cell culture, generation of imaging data and automated image analysis support. The work was initially conceived, funded and planned by NR who sadly died early in 2020 and to whom this paper is dedicated.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmicb.2020.01955/full#supplementary-material

Footnotes

  1. ^ https://fiji.sc/

References

Alpuche-Aranda, C. M., Racoosin, E. L., Swanson, J. A., and Miller, S. I. (1994). Salmonella stimulate macrophage macropinocytosis and persist within spacious phagosomes. J. Exp. Med. 179, 601–608. doi: 10.1084/jem.179.2.601

PubMed Abstract | CrossRef Full Text | Google Scholar

Amich, J., Mokhtari, Z., Strobel, M., Vialetto, E., Sheta, D., Yu, Y., et al. (2020). Three-dimensional light sheet fluorescence microscopy of lungs to dissect local host immune-Aspergillus fumigatus interactions. mBio 11:e02752-9. doi: 10.1128/mBio.02752-19

PubMed Abstract | CrossRef Full Text | Google Scholar

Amin, S., Thywissen, A., Heinekamp, T., Saluz, H. P., and Brakhage, A. A. (2014). Melanin dependent survival of Apergillus fumigatus conidia in lung epithelial cells. Int. J. Med. Microbiol. 304, 626–636. doi: 10.1016/j.ijmm.2014.04.009

PubMed Abstract | CrossRef Full Text | Google Scholar

Araujo, R., and Rodrigues, A. G. (2004). Variability of germinative potential among pathogenic species of Aspergillus. J. Clin. Microbiol. 42, 4335–4337. doi: 10.1128/JCM.42.9.4335-4337.2004

PubMed Abstract | CrossRef Full Text | Google Scholar

Ballard, E., Melchers, W. J. G., Zoll, J., Brown, A. J. P., Verweij, P. E., and Warris, A. (2018). In-host microevolution of Aspergillus fumigatus: a phenotypic and genotypic analysis. Fungal Genet. Biol. 113, 1–13. doi: 10.1016/j.fgb.2018.02.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Balloy, V., and Chignard, M. (2009). The innate immune response to Aspergillus fumigatus. Microbes Infect. 11, 919–927. doi: 10.1016/j.micinf.2009.07.002

PubMed Abstract | CrossRef Full Text | Google Scholar

Bao, Z., Han, X., Chen, F., Jia, X., Zhao, J., Zhang, C., et al. (2015). Evidence for the involvement of cofilin in Aspergillus fumigatus internalization into type II alveolar epithelial cells. BMC Microbiol. 15:161. doi: 10.1186/s12866-015-0500-y

PubMed Abstract | CrossRef Full Text | Google Scholar

Bellanger, A.-P., Millon, L., Khoufache, K., Rivollet, D., Bièche, I., Laurendeau, I., et al. (2009). Aspergillus fumigatus germ tube growth and not conidia ingestion induces expression of inflammatory mediator genes in the human lung epithelial cell line A549. J. Med. Microbiol. 58, 174–179. doi: 10.1099/jmm.0.005488-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Bennett, W. J. (2010). An overview of the genus Aspergillus. Mol. Biol. Genomics 1–17. doi: 10.1201/9781420008517.sec1

CrossRef Full Text | Google Scholar

Berkova, N., Lair-Fulleringer, S., Féménia, F., Huet, D., Wagner, M. C., Gorna, K., et al. (2006). Aspergillus fumigatus conidia inhibit tumour necrosis factor- or staurosporine-induced apoptosis in epithelial cells. Int. Immunol. 18, 139–150. doi: 10.1093/intimm/dxh356

PubMed Abstract | CrossRef Full Text | Google Scholar

Bertuzzi, M., Hayes, G. E., and Bignell, E. M. (2019). Microbial uptake by the respiratory epithelium: outcomes for host and pathogen. FEMS Microbiol. Rev. 43, 145–161. doi: 10.1093/femsre/fuy045

PubMed Abstract | CrossRef Full Text | Google Scholar

Bertuzzi, M., Schrettl, M., Alcazar-Fuoli, L., Cairns, T. C., Munoz, A., Walker, L. A., et al. (2014). The pH-responsive PacC transcription factor of Aspergillus fumigatus governs epithelial entry and tissue invasion during pulmonary aspergillosis. PLoS Pathog. 10:e1004413. doi: 10.1371/journal.ppat.1004413

PubMed Abstract | CrossRef Full Text | Google Scholar

Bleichrodt, R. J., Foster, P., Howell, G., Latgé, J. P., and Read, N. D. (2020). Cell wall composition heterogeneity between single cells in Aspergillus fumigatus leads to heterogeneous behaviour during antifungal treatment and phagocytosis. mBio 11:e03015-19. doi: 10.1128/mBio.03015-19

PubMed Abstract | CrossRef Full Text | Google Scholar

Bongomin, F., Gago, S., Oladele, R. O., and Denning, D. W. (2017). Global and multi-national prevalence of fungal diseases-estimate precision. J. Fungi. 3:57. doi: 10.3390/jof3040057

PubMed Abstract | CrossRef Full Text | Google Scholar

Botterel, F., Gross, K., Ibrahim-Granet, O., Khoufache, K., Escabasse, V., Coste, A., et al. (2008). Phagocytosis of Aspergillus fumigatus conidia by primary nasal epithelial cells in vitro. BMC Microbiol. 8:97. doi: 10.1186/1471-2180-8-97

PubMed Abstract | CrossRef Full Text | Google Scholar

Bromley, I. M., and Donaldson, K. (1996). Binding of Aspergillus fumigatus spores to lung epithelial cells and basement membrane proteins: relevance to the asthmatic lung. Thorax 51, 1203–1209. doi: 10.1136/thx.51.12.1203

PubMed Abstract | CrossRef Full Text | Google Scholar

Brown, G. D., Denning, D. W., Gow, N. A. R., Levitz, S. M., Netea, M. G., and White, T. C. (2012). Hidden killers: human fungal infections. Sci. Transl. Med. 4, 1–9. doi: 10.1126/scitranslmed.3004404

PubMed Abstract | CrossRef Full Text | Google Scholar

Celik, E., Faridi, M. H., Kumar, V., Deep, S., Moy, V. T., and Gupta, V. (2013). Agonist leukadherin-1 increases CD11b/CD18-dependent adhesion via membrane tethers. Biophys. J. 105, 2517–2527. doi: 10.1016/j.bpj.2013.10.020

PubMed Abstract | CrossRef Full Text | Google Scholar

Clark, H. R., Powell, A. B., Simmons, K. A., Ayubi, T., and Kale, S. D. (2019). Endocytic markers associated with the internalization and processing of Aspergillus fumigatus conidia by BEAS-2B cells. mSphere 4:e00663-18. doi: 10.1128/mSphere.00663-18

PubMed Abstract | CrossRef Full Text | Google Scholar

Cozens, A. L., Yezzi, M. J., Kunzelmann, K., Ohrui, T., Chin, L., Eng, K., et al. (1994). CFTR expression and chloride secretion in polarized immortal human bronchial epithelial cells. Am. J. Respir. Cell Mol. Biol. 10, 38–47. doi: 10.1165/ajrcmb.10.1.7507342

PubMed Abstract | CrossRef Full Text | Google Scholar

Crapo, J. D., Barry, B. E., Gehr, P., Bachofen, M., and Weibel, E. R. (1982). Cell number and cell characteristics of the normal human lung. Am. Rev. Respir. Dis. 125, 740–745. doi: 10.1164/arrd.1982.125.6.740

PubMed Abstract | CrossRef Full Text | Google Scholar

Croft, C. A., Culibrk, L., Moore, M. M., and Tebbutt, S. J. (2016). Interactions of Aspergillus fumigatus conidia with airway epithelial cells: a critical review. Front. Microbiol. 7:472. doi: 10.3389/fmicb.2016.00472

PubMed Abstract | CrossRef Full Text | Google Scholar

DeHart, D. J., Agwu, D. E., Julian, N. C., and Washburn, R. G. (1997). Binding and germination of Aspergillus fumigatus conidia on cultured A549 pneumocytes. J. Infect. Dis. 175, 146–150. doi: 10.1093/infdis/175.1.146

PubMed Abstract | CrossRef Full Text | Google Scholar

DeLeon-Rodriguez, C. M., and Casadevall, A. (2016). Cryptococcus neoformans: tripping on acid in the phagolysosome. Front. Microbiol. 7:164. doi: 10.3389/fmicb.2016.00164

PubMed Abstract | CrossRef Full Text | Google Scholar

Ellett, F., Jorgensen, J., Frydman, G. H., Jones, C. N., and Irimia, D. (2017). Neutrophil interactions stimulate evasive hyphal branching by Aspergillus fumigatus. PLoS Pathog. 13:e6154. doi: 10.1371/journal.ppat.1006154

PubMed Abstract | CrossRef Full Text | Google Scholar

Escobar, N., Ordonez, S. R., Wösten, H. A. B., Haas, P. J. A., de Cock, H., and Haagsman, H. P. (2016). Hide, keep quiet, and keep low: properties that make Aspergillus fumigatus a successful lung pathogen. Front. Microbiol. 7:438. doi: 10.3389/fmicb.2016.00438

PubMed Abstract | CrossRef Full Text | Google Scholar

Feldmesser, M., Tucker, S., and Casadevall, A. (2001). Intracellular parasitism of macrophages by Cryptococcus neoformans. Trends Microbiol. 9, 273–278. doi: 10.1016/S0966-842X(01)02035-2

CrossRef Full Text | Google Scholar

Féménia, F., Huet, D., Lair-Fulleringer, S., Wagner, M. C., Sarfati, J., Shingarova, L., et al. (2009). Effects of conidia of various Aspergillus species on apoptosis of human pneumocytes and bronchial epithelial cells. Mycopathologia 167, 249–262. doi: 10.1007/s11046-008-9175-3

PubMed Abstract | CrossRef Full Text | Google Scholar

Fernandes, J., Hamidi, F., Leborgne, R., Beau, R., Castier, Y., Mordant, P., et al. (2018). Penetration of the humanpulmonary epithelium by Aspergillus fumigatus hyphae. J. Infect. Dis. 218, 1306–1313. doi: 10.1093/infdis/jiy298

PubMed Abstract | CrossRef Full Text | Google Scholar

Filler, S. G., and Sheppard, D. C. (2006). Fungal invasion of normally non-phagocytic host cells. PLoS Pathog. 2:e0020129. doi: 10.1371/journal.ppat.0020129

PubMed Abstract | CrossRef Full Text | Google Scholar

Gago, S., Denning, D. W., and Bowyer, P. (2018). Pathophysiological aspects of Aspergillus colonization in disease. Med. Mycol. 57, S219–S227. doi: 10.1093/mmy/myy076

PubMed Abstract | CrossRef Full Text | Google Scholar

Gomez, P., Hackett, T. L., Moore, M. M., Knight, D. A., and Tebbutt, S. J. (2010). Functional genomics of human bronchial epithelial cells directly interacting with conidia of Aspergillus fumigatus. BMC Genomics 11:358. doi: 10.1186/1471-2164-11-358

PubMed Abstract | CrossRef Full Text | Google Scholar

Grant, S. S., and Hung, D. T. (2013). Persistent bacterial infections, antibiotic tolerance, and the oxidative stress response. Virulence 4, 273–283. doi: 10.4161/viru.23987

PubMed Abstract | CrossRef Full Text | Google Scholar

Han, X., Yu, R., Zhen, D., Tao, S., Schmidt, M., and Han, L. (2011). β-1,3-glucan-induced host phospholipase D activation is involved in Aspergillus fumigatus internalization into type II human pneumocyte A549 Cells. PLoS One 6:e0021468. doi: 10.1371/journal.pone.0021468

PubMed Abstract | CrossRef Full Text | Google Scholar

Heinekamp, T., Schmidt, H., Lapp, K., Pähtz, V., Shopova, I., Köster-Eiserfunke, N., et al. (2015). Interference of Aspergillus fumigatus with the immune response. Semin. Immunopathol. 37, 141–152. doi: 10.1007/s00281-014-0465-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Herzog, E. L., Brody, A. R., Colby, T. V., Mason, R., and Williams, M. C. (2008). Knowns and unknowns of the alveolus. Proc. Am. Thorac. Soc. 5, 778–782. doi: 10.1513/pats.200803-028HR

PubMed Abstract | CrossRef Full Text | Google Scholar

Hissa, B., Duarte, J. G., Kelles, L. F., Santos, F. P., del Puerto, H. L., Gazzinelli-Guimarães, P. H., et al. (2012). Membrane cholesterol regulates lysosome-plasma membrane fusion events and modulates Trypanosoma cruzi invasion of host cells. PLoS Negl. Trop. Dis. 6:e1583. doi: 10.1371/journal.pntd.0001583

PubMed Abstract | CrossRef Full Text | Google Scholar

Ibrahim-Granet, O., Philippe, B., Boleti, H., Boisvieux-Ulrich, E., Grenet, D., Stern, M., et al. (2003). Phagocytosis and intracellular fate of Aspergillus fumigatus conidia in alveolar macrophages. Infect. Immun. 71, 891–903. doi: 10.1128/IAI.71.2.891-903.2003

PubMed Abstract | CrossRef Full Text | Google Scholar

Jahn, B., Langfelder, K., Schneider, U., Schindel, C., and Brakhage, A. A. (2002). PKSP-dependent reduction of phagolysosome fusion and intracellular kill of Aspergillus fumigatus conidia by human monocyte-derived macrophages. Cell. Microbiol. 4, 793–803. doi: 10.1046/j.1462-5822.2002.00228.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Jubrail, J., Morris, P., Bewley, M. A., Stoneham, S., Johnson, S. A., Foster, S. J., et al. (2015). Inability to sutain intraphagolysosomal killing of Staphylococcus aureus predisposes to bacterial persistence in macrophages. Cell Microbiol. 18, 80–96. doi: 10.1111/cmi.12485

PubMed Abstract | CrossRef Full Text | Google Scholar

Káposzta, R., Maródi, L., Hollinshead, M., Gordon, S., da Silva, R. P. P., Kaposzta, R., et al. (1999). Rapid recruitment of late endosomes and lysosomes in mouse macrophages ingesting Candida albicans. J. Cell Sci. 112, 3237–3248.

Google Scholar

Knox, B. P., Blachowicz, A., Palmer, J. M., Romsdahl, J., Huttenlocher, A., Wang, C. C. C., et al. (2016). Characterization of Aspergillus fumigatus isolates from air and surfaces of the international space station. mSphere 1:e00227-16. doi: 10.1128/mSphere.00227-16

PubMed Abstract | CrossRef Full Text | Google Scholar

Kosmidis, C., and Denning, D. W. (2015). The clinical spectrum of pulmonary aspergillosis. Thorax 70, 270–277. doi: 10.1136/thoraxjnl-2014-206291

PubMed Abstract | CrossRef Full Text | Google Scholar

Kwon-Chung, K. J., and Sugui, J. A. (2013). Aspergillus fumigatus-What makes the species a ubiquitous human fungal pathogen? PLoS Pathog. 9:e3743. doi: 10.1371/journal.ppat.1003743

PubMed Abstract | CrossRef Full Text | Google Scholar

Latgé, J. P. (1999). Aspergillus fumigatus and Aspergillosis. Clin. Microbiol. Rev. 12, 310–350. doi: 10.1128/JCM.01704-14

PubMed Abstract | CrossRef Full Text | Google Scholar

Lieber, M., Smith, B., Szakal, A., Nelson-Rees, W., and Todaro, G. (1976). A continuous tumor-cell line from a human lung carcinoma with properties of type II alveolar epithelial cells. Int. J. Cancer 17, 62–70. doi: 10.1002/ijc.2910170110

PubMed Abstract | CrossRef Full Text | Google Scholar

Lother, J., Breitschopf, T., Krappmann, S., Morton, C. O., Bouzani, M., Kurzai, O., et al. (2014). Human dendritic cell subsets display distinct interactions with the pathongeic mould Aspergillus fumigatus. Int. J. Med. Microbiol. 304, 1160–1168. doi: 10.1016/j.ijmm.2014.08.009

PubMed Abstract | CrossRef Full Text | Google Scholar

Luther, K., Rohde, M., Sturm, K., Kotz, A., Heesemann, J., and Ebel, F. (2008). Characterisation of the phagocytic uptake of Aspergillus fumigatus conidia by macrophages. Microbes Infect. 10, 175–184. doi: 10.1016/j.micinf.2007.11.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Macdonald, D., Thomson, D. D., Johns, A., Contreras-Valenzuela, A., Gilsenan, J. M., Lord, K. M., et al. (2019). Inducibe cell fusion permits use of competitive fitness profiling in the human phatogenic fungus Aspergillus fumigatus. Antimicrob. Agents Chemother. 63:e01615-18. doi: 10.1128/AAC.01615-18

PubMed Abstract | CrossRef Full Text | Google Scholar

Mccormick, A., Loeffler, J., and Ebel, F. (2010). Aspergillus fumigatus: contours of an opportunistic human pathogen. Cell. Microbiol. 12, 1535–1543. doi: 10.1111/j.1462-5822.2010.01517.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Moreno-Velásquez, S. D., Seidel, C., Juvvadi, P. R., Steinbach, W. J., and Read, N. D. (2017). Caspofungin-mediated growth inhibition and paradoxical growth in Aspergillus fumigatus involve fungicidal hyphal tip lysis coupled with regenerative intrahyphal growth and dynamic changes in β-1,3-glucan synthase localization. Antimicrob. Agents Chemother. 61, 710–717. doi: 10.1128/AAC.00710-17

PubMed Abstract | CrossRef Full Text | Google Scholar

Mullins, J., and Seaton, A. (1978). Fungal spores in lung and sputum. Clin. Exp. Allergy 8, 525–533. doi: 10.1111/j.1365-2222.1978.tb01506.x

PubMed Abstract | CrossRef Full Text | Google Scholar

O’Gorman, C. M. (2011). Aiborne Aspergillus fumigatus conidia: a risk factor for aspergillosis. Fungal Biol. Rev. 25, 151–157. doi: 10.1016/j.fbr.2011.07.002

CrossRef Full Text | Google Scholar

Oosthuizen, J. L., Gomez, P., Ruan, J., Hackett, T. L., Moore, M. M., Knight, D. A., et al. (2011). Dual organism transcriptomics of airway epithelial cells interacting with conidia of Aspergillus fumigatus. PLoS One 6:e20527. doi: 10.1371/journal.pone.0020527

PubMed Abstract | CrossRef Full Text | Google Scholar

Osherov, N. (2012). Interaction of the pathogenic mold Aspergillus fumigatus with lung epithelial cells. Front. Microbiol. 8:346. doi: 10.3389/fmicb.2012.00346

PubMed Abstract | CrossRef Full Text | Google Scholar

Paris, S., Boisvieux-Ulrich, E., Crestani, B., Houcine, O., Taramelli, D., Lombardi, L., et al. (1997). Internalization of Aspergillus fumigatus conidia by epithelial and endothelial cells. Infect. Immun. 65, 1510–1514. doi: 10.1128/iai.65.4.1510-1514.1997

PubMed Abstract | CrossRef Full Text | Google Scholar

Pereira, P. M., Albrecht, D., Culley, S., Jacobs, C., Marsh, M., Mercer, J., et al. (2019). Fix your membrane receptor imaging: actin cytoskeleton and CD4 membrane organization disruption by chemical fixation. Front. Immunol. 5:675. doi: 10.3389/fimmu.2019.00675

PubMed Abstract | CrossRef Full Text | Google Scholar

Richard, N., Marti, L., Varrot, A., Guillot, L., Guitard, J., Hennequin, C., et al. (2018). Human bronchial epithelial cells inhibit Aspergillus fumigatus germination of extracellular conidia via FleA recognition. Sci. Rep. 8:15699. doi: 10.1038/s41598-018-33902-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Rosowski, E. E., Raffa, N., Knox, B. P., Golenberg, N., Keller, N. P., and Huttenlocher, A. (2018). Macrophages inhibit Aspergillus fumigatus germination and neutrophil-mediated fungal killing. PLoS Pathog. 14:e7229. doi: 10.1371/journal.ppat.1007229

PubMed Abstract | CrossRef Full Text | Google Scholar

Schaffner, A., Douglas, H., Braude, A. I., and Davis, C. E. (1983). Killing of Aspergillus spores depends on the anatomical source of the macrophage. Infect. Immun. 42, 1109–1115. doi: 10.1128/iai.42.3.1109-1115.1983

PubMed Abstract | CrossRef Full Text | Google Scholar

Schmidt, H., Vlaic, S., Krüger, T., Schmidt, F., Balkenhol, J., Dandekar, T., et al. (2018). Proteomics of Aspergillus fumigatus conidia-containing phagolysosomes identifies processes governing immune evasion. Mol. Cell. Proteomics 17, 1084–1096. doi: 10.1074/mcp.RA117.000069

PubMed Abstract | CrossRef Full Text | Google Scholar

Sharon, H., Amar, D., Levdansky, E., Mircus, G., Shadkchan, Y., Shamir, R., et al. (2011). PrtT-regulated proteins secreted by Aspergillus fumigatus activate MAPK signaling in exposed A549 lung cells leading to necrotic cell death. PLoS One 6:e17509. doi: 10.1371/journal.pone.0017509

PubMed Abstract | CrossRef Full Text | Google Scholar

Shen, Q., Kirschbaum, M. U. F., Hedley, M. J., and Camps Arbestain, M. (2016). Testing an alternative method for estimating the length of fungal hyphae using photomicrography and image processing. PLoS One 11:e0157017. doi: 10.1371/journal.pone.0157017

PubMed Abstract | CrossRef Full Text | Google Scholar

Sun, W.-K., Lu, X., Li, X., Sun, Q.-Y., Su, X., Song, Y., et al. (2012). Dectin-1 is inducible and plays a crucial role in Aspergillus-induced innate immune responses in human bronchial epithelial cells. Eur. J. Clin. Microbiol. Infect. Dis. 31, 2755–2764. doi: 10.1007/s10096-012-1624-8

PubMed Abstract | CrossRef Full Text | Google Scholar

Thywißen, A., Heinekamp, T., Dahse, H. M., Schmaler-Ripcke, J., Nietzsche, S., Zipfel, P. F., et al. (2011). Conidial dihydroxynaphthalene melanin of the human pathogenic fungus Aspergillus fumigatus interferes with the host endocytosis pathway. Front. Microbiol. 2:96. doi: 10.3389/fmicb.2011.00096

PubMed Abstract | CrossRef Full Text | Google Scholar

Uribe-Querol, E., and Rosales, C. (2017). Control of phagocytosis by microbial pathogens. Front. Immunol. 8:1368. doi: 10.3389/fimmu.2017.01368

PubMed Abstract | CrossRef Full Text | Google Scholar

van de Veerdonk, F. L., Gresnigt, M. S., Romani, L., Netea, M. G., and Latgé, J.-P. (2017). Aspergillus fumigatus morphology and dynamic host interactions. Nat. Rev. Microbiol. 15, 661–674. doi: 10.1038/nrmicro.2017.90

PubMed Abstract | CrossRef Full Text | Google Scholar

Van Waeyenberghe, L., Pasmans, F., Dherde, K., Ducatelle, R., Favoreel, H., Li, S. J., et al. (2012). Germination of Aspergillus fumigatus inside avian respiratory macrophages is associated with cytotoxicity. Vet. Res. 43:32. doi: 10.1186/1297-9716-43-32

PubMed Abstract | CrossRef Full Text | Google Scholar

Wasylnka, J. A., Hissen, A. H. T., Wan, A. N. C., and Moore, M. M. (2005). Intracellular and extracellular growth of Aspergillus fumigatus. Med. Mycol. 43, S27–S30. doi: 10.1080/13693780400029247

PubMed Abstract | CrossRef Full Text | Google Scholar

Wasylnka, J. A., and Moore, M. M. (2002). Uptake of Aspergillus fumigatus conidia by phagocytic and nonphagocytic cells in vitro: quantitation using strains expressing green fluorescent protein. Infect. Immun. 70, 3156–3163. doi: 10.1128/IAI.70.6.3156-3163.2002

PubMed Abstract | CrossRef Full Text | Google Scholar

Wasylnka, J. A., and Moore, M. M. (2003). Aspergillus fumigatus conidia survive and germinate in acidic organelles of A549 epithelial cells. J. Cell Sci. 116, 1579–1587. doi: 10.1242/jcs.00329

PubMed Abstract | CrossRef Full Text | Google Scholar

Westman, J., Moran, G., Mogavero, S., Hube, B., and Grinstein, S. (2018). Candida albicans hyphal expansion causes phagosomal membrane damage and luminal alkalinization. mBio 9:e01226-18. doi: 10.1128/mBio.01226-18

PubMed Abstract | CrossRef Full Text | Google Scholar

Xu, X., Shi, Y., Zhang, P., Zhang, F., Shen, Y., Su, X., et al. (2012). E-cadherin mediates adhesion and endocytosis of Aspergillus fumigatus blastospores in human epithelial cells. Chin. Med. J. 125, 617–621. doi: 10.3760/cma.j.isnn.0366-6999.2012.04.011

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, Z., Liu, R., Noordhoek, J. A., and Kauffman, H. F. (2005). Interaction of airway epithelial cells (A549) with spores and mycelium of Aspergillus fumigatus. J. Infect. 51, 375–382. doi: 10.1016/j.jinf.2004.12.012

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: Aspergillus fumigatus, epithelial cell infection, membrane compartmentalisation, aspergillosis, phagolysosome, airway epithelium, microscopy

Citation: Seidel C, Moreno-Velásquez SD, Ben-Ghazzi N, Gago S, Read ND and Bowyer P (2020) Phagolysosomal Survival Enables Non-lytic Hyphal Escape and Ramification Through Lung Epithelium During Aspergillus fumigatus Infection. Front. Microbiol. 11:1955. doi: 10.3389/fmicb.2020.01955

Received: 18 May 2020; Accepted: 24 July 2020;
Published: 20 August 2020.

Edited by:

Agostinho Carvalho, University of Minho, Portugal

Reviewed by:

Thorsten Heinekamp, Leibniz Institute for Natural Product Research and Infection Biology, Germany
Falk Hillmann, Leibniz Institute for Natural Product Research and Infection Biology, Germany

Copyright © 2020 Seidel, Moreno-Velásquez, Ben-Ghazzi, Gago, Read and Bowyer. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Paul Bowyer, paul.bowyer@manchester.ac.uk

These authors have contributed equally to this work

Present address: Sergio D. Moreno-Velásquez, Interdisciplinary Center for Clinical Research, Institute for Molecular Infection Biology, University Hospital Würzburg, Würzburg, Germany