Lungs of CF patients constitute a stressful environment for colonizing microorganisms, especially due to toxic, osmotic, or oxidative stresses induced by the host immune system and recurring antibiotic treatments. Anoxia or micro-anaerobia, acidity and the nutritional characteristics of the CF environment can also hamper bacterial growth and persistence (Yang et al., 2011; La Rosa et al., 2019). Nevertheless, P. aeruginosa was shown to adapt in response to these different selective pressures. Numerous sequencing studies of longitudinal isolates of P. aeruginosa revealed that the bacterium accumulates a significant number of small mutations (SNP and small insertions and deletions) during its evolution in CF lungs. So, some genomic modification were found to be positively selected due to their beneficial impacts on P. aeruginosa fitness in the stressful CF environment (Smith et al., 2006; Marvig et al.,2015b,c; Klockgether et al., 2018; Khademi et al., 2019). There were called pathoadaptive modifications as they promote the pathogen survival and persistence at the infectious site. As a result, CF-adapted isolates of P. aeruginosa present convergent expression profiles and phenotypes, conferring advantageous features (Folkesson et al., 2012; Winstanley et al., 2016; La Rosa et al., 2019). Table 1 gathers the main pathoadaptive genomic regions of P. aeruginosa, as well as the associated phenotypes (Table 1).

Firstly, CF-adapted strains of P. aeruginosa adjust their energetic metabolism to the particular nutritional composition of the CF environment (Palmer et al., 2007; La Rosa et al., 2018, 2019). This is mainly reflected by a restriction of the catabolic repertory and the slowed growth of clinical isolates in comparison to non-adapted strains (Marvig et al., 2015a; La Rosa et al., 2018, 2019). In response to iron sequestration by the host, P. aeruginosa also adapts its iron uptake mechanisms for the benefit of heme-based assimilation. Alteration of pvd genes in CF isolates was indeed shown to decrease the production of the pyoverdine siderophore and thus ferric iron acquisition. In contrast, mutations in the phuS//phuR intergenic region increase the expression of the heme receptor PhuR and thus acquisition of host-sequestered iron (Table 1; Marvig et al., 2014; Minandri et al., 2016). Iron and nutrient acquisition nonetheless remains difficult in CF lung, hampering the costly production of many iron-dependent virulence factors. P. aeruginosa virulence is also reduced by genetic alterations and/or transcriptomic dysregulations of genomic regions involved in motility (pilJ and chpA), secretion (phz and Hcp genes) and regulation of virulence (lasR, retS, exsA, and rpoN) (Marvig et al., 2015a; Winstanley et al., 2016). Most of these factors being immunogenic, the down-regulation of their production allows a better escape of P. aeruginosa from the host immune system. Such escape and resistance to immune responses is also promoted by the increased biofilm production of CF-adapted P. aeruginosa. In particular, mutations in mucA and alg genes induce the overproduction of alginate, an exopolysaccharide composing the biofilm matrix and responsible for the frequent mucoid phenotype (Marvig et al., 2015b; Winstanley et al., 2016). Finally, adapted strains of P. aeruginosa exhibit increased antibiotic resistance related to genic alterations of antibiotic targets (for instance the gyrases gyrA, gyrB), efflux pumps (mex genes), lactamases (amp genes), as well as lipopolysaccharide (LPS) and porin synthesis (pagL, pmrB, and opr genes) (Table 1; Folkesson et al., 2012; Marvig et al., 2015b; Winstanley et al., 2016). Altogether, these adaptations induce a weakly virulent but highly resistant state of P. aeruginosa, promoting its persistence within CF lungs.

In addition to limiting the effectiveness of the immune response and antibiotic treatments, adaptations of P. aeruginosa can also modify its interactions with other microbial species, in particular with S. aureus. The anti-staphylococcal behavior of P. aeruginosa relies on mechanisms of bacterial lysis and growth suppression, as well as metabolic alterations, virulence and biofilm formation (Figure 1A; Hotterbeekx et al., 2017). However, several studies demonstrated that such behavior was not conserved in CF-adapted strains of P. aeruginosa, allowing the establishment of a coexisting interaction with S. aureus (Baldan et al., 2014; Michelsen et al., 2014, 2016; Limoli et al., 2017; Briaud et al., 2019). It thus appears that the relationship between P. aeruginosa and S. aureus evolves from competition to coexistence, a process resulting from the adaptation of P. aeruginosa.

Although bacterial features play an important role in shaping inter-species interaction, environmental factors can have an even more decisive impact on them. Environmental conditions such as antibiotic and oxidant stresses are known to shape the CF ecosystem and promote a biofilm-based lifestyle of microorganisms within lungs (Feraco et al., 2016; Riquelme et al., 2020). Biofilm conditions reducing the competitive relationship between P. aeruginosa and S. aureus, the CF environment may favor a coexistence interaction between the two pathogens independently of P. aeruginosa’s genetic adaptation. Indeed, several environmental factors inherent to CF lungs were shown to decrease the anti-staphylococcal behavior of P. aeruginosa. Pallett et al. (2019) recently observed that oxygen limitation decreased the production of P. aeruginosa virulence factors such as proteases and pyocyanin. In these conditions, not only the reference strain PAO1 but also clinical isolates thus coexisted with S. aureus despite competitive behavior under normoxia (Pallett et al., 2019). Within mixed-species biofilm formed with the PA14 reference strain, S. aureus survival was improved thanks to bacterial stratification as a function of oxygen levels (Cendra et al., 2019). In addition to oxygen, nutrient availability can also modify interaction within biofilm (Mashburn et al., 2005; Filkins et al., 2015; Nguyen et al., 2015; Hotterbeekx et al., 2017; Miller et al., 2017; Cendra et al., 2019). Miller et al. (2017) observed that S. aureus was even able to strongly outcompete P. aeruginosa within mixed-species biofilm grown under rich conditions, but not in the same diluted and thus impoverished medium. Besides nutritive richness, limited alkalization of the co-culture medium was also shown to improve S. aureus survival during interaction with the PA14 reference strain (Cendra et al., 2019). Finally, the depletion of zinc and manganese, notably observed on the edge of the biofilm architecture, represses the expression of P. aeruginosa’s virulence genes and thus S. aureus inhibition (Wakeman et al., 2016; Figure 1C).

Interestingly, all these conditions promoting coexistence interaction between the two pathogens seem to be combined in the CF environment. CF sputum is indeed considered a rich medium but it contains limited oxygen concentrations, favoring anaerobic and micro-anaerobic metabolisms (La Rosa et al., 2019). Sputa from CF patients were also shown to be relatively acidic (Bhagirath et al., 2016). Moreover, host-pathogen interfaces are known to be depleted in zinc and manganese, especially through sequestration by the host protein calprotectin (Kehl-Fie and Skaar, 2010; Hood et al., 2012; Wakeman et al., 2016). Altogether, this suggests that in vivo conditions, and especially the CF environment, may promote non-competitive interaction between P. aeruginosa and S. aureus (Figure 1C). This hypothesis is supported by several studies showing the improved survival of S. aureus during non-human in vivo co-infections with P. aeruginosa, in comparison to in vitro co-cultures. Yadav and colleagues demonstrated a higher proportion of S. aureus within an in vivo mixed-species biofilm in the presence of P. aeruginosa (Yadav et al., 2017; Millette et al., 2019). In addition, P. aeruginosa strains such as PA14 were shown to promote S. aureus colonization and maintenance in a murine lung infection model (Yadav et al., 2017; Millette et al., 2019). Similar results were obtained in the context of chronic wound co-infections (Pastar et al., 2013; DeLeon et al., 2014). Since these co-infections were maintained for a limited duration (24 h to 1 week), it is unlikely that genetic adaptation drove the establishment of a coexistence interaction between P. aeruginosa and S. aureus. This phenomenon seems to be more related to non-fixed acclimatization reducing P. aeruginosa virulence, or spatial compartmentalization isolating the two species from each other in vivo. In all cases, it appears that besides promoting P. aeruginosa genetic adaptation and then reducing anti-staphylococcal behavior, in vivo conditions are themselves favorable to non-competitive interactions with S. aureus (Figure 1C).

A 21-month longitudinal study performed on 183 CF patients depicted that the clonal diversity of S. aureus strains decreased as patient aged, pointing out that some isolates tended to adapt more efficiently and dominate the airway sphere during infection history (Westphal et al., 2020). Several studies indeed highlighted that S. aureus isolates evolve in the CF lung environment and acquire features leading to better-fitted isolates (Figure 2; Chatterjee et al., 2008; Treffon et al., 2018, 2020; Herzog et al., 2019; Lennartz et al., 2019; Tan et al., 2019; Westphal et al., 2020).

Genomic, transcriptomic, and proteomic comparisons between early and late strains of S. aureus highlighted adaptations in the transport and the metabolism of carbohydrates and amino acids (Treffon et al., 2018; Tan et al., 2019). Late isolates thus often presented auxotrophies toward thymidine (TD), menadione or hemin (Kahl et al., 1998). These auxotrophies promote the formation of SCV (Chatterjee et al., 2008; Tan et al., 2019), a frequent S. aureus phenotype isolated from 4 to 50% of CF patients depending on the studies (Kahl et al., 2016). S. aureus SCVs are associated with worse lung function and patient age, in relation with their increased antibiotic resistance and persistence (Besier et al., 2007). Indeed, mutations in the thyA gene hindering TD biosynthesis were shown to facilitate resistance to trimethoprim-sulfamethoxazole (SXT) and the presence of TD-auxotrophic SCV is associated with previous antibiotic treatment with SXT (Kahl et al., 1998; Chatterjee et al., 2008; Yagci et al., 2013; Figure 2). Late isolates from antibiotic-treated patients showed other mutations in gyrB and rpsJ, that are not associated with the SCV phenotype but can explain antibiotic resistance to fluoroquinolones and cyclines (Kriegeskorte et al., 2015; Tan et al., 2019; Figure 2). Besides antibiotic resistance, SCVs are specialized for extracellular and intracellular persistence. This phenomenon is related to: (i) decreased expression of the α-toxin involved in lysis of eukaryotic cells by S. aureus, and (ii) increased expression of cell wall-associated genes which facilitate colonization to extracellular matrix proteins and internalization in eukaryotic cells (Figure 2). In line with this, S. aureus SCVs were shown to survive better intracellularly in eukaryotic cells than their isogenic parental strain (Kahl et al., 2016). CF-adapted S. aureus strains also tend to be better intracellular survivors than the corresponding early isolates (Treffon et al., 2020).

Another feature promoting the persistence of S. aureus CF isolates is the improvement of defense mechanisms against killing by polymorphonuclear leukocytes. Neutrophils usually eradicate invading pathogens by releasing reactive oxygen species (ROS) or forming Neutrophil Extracellular Trap (NETs). In comparison to their early counterparts, CF-adapted S. aureus presented an increased genic expression of the superoxide dismutase SodM involved in ROS detoxification (Treffon et al., 2018, 2020). Moreover, Herzog et al. (2019) showed that late isolates were more resistant to NETs mediated-killing through the over-expression of the nuc1 gene encoding the nuclease protein. Given the high pro-inflammatory territory in patient lungs overwhelmed by the neutrophilic attacks, the over-production of SodM and Nuc1 could be a major step in the adaptation of S. aureus in CF lungs (Figure 2).

Interestingly, S. aureus isolates overexpressing the nuc1 gene also presented a down-expression of the RNA regulator RNAIII. RNAIII is the major effector of the agr QS-system of S. aureus that positively controls the expression of many virulence factors. A decrease of RNAIII expression thus reflects reduced production of virulence factors. nuc1-overexpressing S. aureus were also shown to overexpress protein A (SpA), permease, coagulase, and adhesins (Jenul and Horswill, 2018), involved in colonization. Similarly, transcriptional analysis revealed that S. aureus SCVs have a less virulent phenotype in comparison to normal isolates (Kahl et al., 2005; Moisan et al., 2006; Seggewiss et al., 2006). Altogether, these results suggest that adaptation to the CF environment could lead toward a low-virulence but highly invasive state of S. aureus.

Finally, biofilm production appears to be increased in late S. aureus isolates. In the study of Tan et al. (2019), two out of three CF-late isolates over-produced biofilm and the same pattern was observed within late isolates of non-CF lung infections, suggesting that this characteristic was independent of the CF-lung environment. Such increased biofilm production by late isolates can be related to the development of mucoidy in S. aureus. This phenotype arises from a 5 bp deletion within the intergenic region of icaR/icaA genes, inducing an overproduction of S. aureus exopolysaccharide poly-N-acetylglucosamine (Schwartbeck et al., 2016; Figure 2). Mucoid S. aureus isolates are thus found in 2.5% of CF airways and tend to be more frequently isolated from older patients than non-mucoid isolates (Lennartz et al., 2019). These data suggest that mucoidy and strong biofilm production play a role in S. aureus adaptation to the CF environment.

Some of the S. aureus adaptations to the CF environment can impact its relationship with P. aeruginosa. Among them, the SCV phenotype appears to be crucial for S. aureus survival during competitive interaction, as SCV present increased resistance to P. aeruginosa mediated-killing (Hotterbeekx et al., 2017). Once P. aeruginosa has evolved to a non-aggressive status toward S. aureus, the staphylococcus can then switch to a non-defective growth mode and coexist with its partner. The increased biofilm production of CF-adapted S. aureus isolates could also promote the formation of mixed-species biofilm with P. aeruginosa, although no direct correlation has yet been established. These hypotheses could explain (i) the high proportion of co-infected patients with S. aureus and P. aeruginosa in international cohorts (Hubert et al., 2013; Limoli et al., 2016; Briaud et al., 2020), and (ii) the high proportion of isolates presenting a non-competitive interaction (Briaud et al., 2020). Further investigations need to be conducted to confirm this model and fully understand the effects of S. aureus adaptation on its relationship with P. aeruginosa.

However, several studies suggested that S. aureus can influence the establishment of a coexisting interaction through alterations of the adaptive process of P. aeruginosa. Using an in vitro evolution assay, the adaptation of P. aeruginosa was studied in the presence or absence of S. aureus over 150 generations (Tognon et al., 2017). Mutations in the LPS biosynthesis pathway occurred only in the presence of S. aureus and increased P. aeruginosa’s fitness and resistance toward β-lactams antibiotics (Tognon et al., 2017). Repeated in vitro co-cultures with S. aureus also induced a decrease of P. aeruginosa QS regulation and may provide a departure point for a coexisting interaction (Zhao et al., 2018). It is worth recalling that modifications of LPS production, increased antibiotic resistance and down-regulation of QS are also frequently depicted in CF-adapted P. aeruginosa isolates (Folkesson et al., 2012; Marvig et al., 2015b; Winstanley et al., 2016). These results indicate that the presence of S. aureus influences P. aeruginosa’s adaptation, and that a co-evolution phenomenon could even promote a non-competitive relationship between the two pathogens. Several results obtained from CF clinical strains support these hypotheses. First, Martha et al. (2010) observed that P. aeruginosa presented a higher probability to develop a mucoid phenotype in the absence of S. aureus. Secondly, coexisting strains of S. aureus and P. aeruginosa were shown to better produce and catabolize acetoin, respectively, in comparison to competitive strains. The authors concluded that strains co-evolved to promote trophic cooperation (Camus et al., 2020). Finally, the genetic alterations of LasR that reduce P. aeruginosa anti-staphylococcal behavior are frequently observed in longitudinal studies (Marvig et al.,2015b,c). One might wonder if the presence of S. aureus in CF lungs could contribute to the selection of lasR mutants and thus non-competitive P. aeruginosa. Indeed, promoting a coexisting and even a cooperative behavior with other co-colonizing microorganisms can be a strategy to improve fitness in a stressful environment such as CF lungs. However, most of longitudinal studies focused on P. aeruginosa and no data are available concerning potential co-infections with S. aureus. It thus remains difficult to determine if S. aureus can effectively influence the fixation of lasR mutations in P. aeruginosa genome. It would be interesting to study the long-term evolution of both S. aureus and P. aeruginosa in several co-infected CF patients to reveal the bacterial adaptations leading to the establishment of coexistence.

Co-existence interaction leads to increased S. aureus survival in comparison to a common competitive interaction with P. aeruginosa. Bacterial enumerations performed during co-culture kinetics can thus easily reveal and quantify this phenomenon (Miller et al., 2017; Cendra et al., 2019; Pallett et al., 2019; Figure 3A). Less cumbersome procedures were nonetheless developed to assess interaction status between clinical CF isolates in large set of strains (Figure 3B; Baldan et al., 2014; Michelsen et al., 2014, 2016; Limoli et al., 2017; Briaud et al., 2019, 2020; Camus et al., 2020). Baldan and colleagues thus performed competition tests on plates during which a spot of P. aeruginosa culture is deposited on a lawn of S. aureus. Four categories of interaction status were established (no, weak, strong, and very strong inhibition) according to the size of the inhibition halo of S. aureus induced by the 24 P. aeruginosa strains tested (Baldan et al., 2014). In other studies, growth inhibition of S. aureus was observed through cross-streak assays and visual evaluation of each bacterium population after the streak intersection (Michelsen et al., 2014, 2016; Limoli et al., 2017; Figure 3C).

Despite the different methods and media employed, several studies highlighted that the interaction pattern with S. aureus was related to the adaptation of P. aeruginosa to the CF environment. Reduced anti-staphylococcal behavior was indeed observed for late isolates of P. aeruginosa, which were recovered several years after their clonal ancestor and presented common pathoadaptive traits. This evolution was thus shown in the DK2 lineage as well as in mucoid isolates (Michelsen et al., 2014, 2016; Limoli et al., 2017). However, it is noteworthy that the adaptation of P. aeruginosa in the CF lung is driven by adaptive radiation and spatial isolation mechanisms, inducing a high genotypic and phenotypic heterogeneity in the evolving population (Winstanley et al., 2016). It is therefore likely that clonally related isolates simultaneously recovered from the same patient can present different interaction statuses with S. aureus due to such diversification processes. On the other hand, it is also conceivable that the interaction statuses of competition and coexistence are dynamic and transitional within a single P. aeruginosa population. Assessing the interaction status of numerous P. aeruginosa isolates, collected longitudinally or recovered from different pulmonary niches, would lead to better understanding of this phenomenon.

In all cases, coexistence could be defined as a neutral interaction during which both bacteria are not affected by each other. However, increasing evidence shows that cooperative behaviors can positively affect P. aeruginosa and S. aureus during coexistence (Figure 4).

Several in vitro studies focusing on CF isolates highlighted that coexistence between P. aeruginosa and S. aureus can improve the antibiotic resistance of both pathogens (Figure 4A). S. aureus was recently shown to overexpress genes coding efflux pumps from the Nor family during coexisting interaction with P. aeruginosa. As a result, clinical S. aureus isolates presented significantly increased resistance to tetracycline and ciprofloxacin in the presence of P. aeruginosa, in comparison to monocultures (Briaud et al., 2019). While direct contact between bacterial cells was presumed to mediate this effect, other studies identified P. aeruginosa secreted products affecting the resistance of S. aureus to antimicrobial compounds. In particular, secondary metabolites from the 4-hydroxy-2-alkylquinolines (HAQ) family such as HQNO increase the resistance of S. aureus to aminoglycosides notably through the induction of the SCV phenotype i (Hoffman et al., 2006; Mitchell et al., 2010; DeLeon et al., 2014; Orazi and O’Toole, 2017; Orazi et al., 2019, 2020). Interestingly, late P. aeruginosa isolates from CF infections often lack HQNO production but are still able to protect S. aureus from tobramycin. The implication of other molecules than HQNO was confirmed by an atypical HAQ profile developed during adaptation to the CF environment (Michelsen et al., 2016). It thus appears that both competitive (i.e., HQNO-producing) and coexisting P. aeruginosa can protect S. aureus from antibiotic effects but through different mechanisms. Alginate produced by CF-adapted P. aeruginosa may also protect S. aureus from antimicrobial compounds since this exopolysaccharide can impact HAQ synthesis and mixed-species biofilm formation (Limoli et al., 2017; Price et al., 2020).

Conversely, interaction with S. aureus can also trigger resistance mechanisms in P. aeruginosa (Figure 4A). Co-evolution with S. aureus was shown to promote the alteration of genes from the LPS biosynthesis pathway in PAO1, leading to greater resistance to β-lactam antibiotics (Tognon et al., 2017). Michelsen and colleagues demonstrated that S. aureus cells and their supernatant can also induce the SCV phenotype and antibiotic tolerance in CF-adapted strains of P. aeruginosa (Fugère et al., 2014; Michelsen et al., 2014). Similar results were obtained using persistent CF isolates of P. aeruginosa grown in biofilm, as they presented improved tobramycin resistance upon exposure to S. aureus supernatant. In this case, the phenomenon was attributed to the formation of P. aeruginosa aggregates within the biofilm architecture (Beaudoin et al., 2017).

Recent transcriptomic studies suggested that trophic cooperation could establish between S. aureus and P. aeruginosa (Figure 4B). The four-carbon molecule acetoin, produced by S. aureus, was shown to induce the overexpression of the aco system in CF P. aeruginosa strains during coexistence interaction (Camus et al., 2020). In line with this, P. aeruginosa presented an enhanced ability to catabolize acetoin produced by S. aureus as an alternative carbon source, resulting in increased survival during co-culture. Acetoin catabolism was also shown to benefit S. aureus and improve its survival in co-culture. Acetoin thus appears to be the keystone of trophic cooperation between P. aeruginosa and S. aureus during which both partners are beneficiaries. Interestingly, this cooperative behavior seems to be selected during bacterial evolution in the CF environment. Acetoin production by S. aureus and catabolism by P. aeruginosa were indeed more efficient for coexisting isolates in comparison to competitive ones (Camus et al., 2020). As acetoin could be detected in CF sputa, these results go along with the trophic adaptation of P. aeruginosa strains to resources present in the CF environment (Španěl et al., 2016; La Rosa et al., 2018, 2019; Camus et al., 2020). Other studies suggest that lactate, also detected in CF sputa, may also play a role in metabolic interactions between P. aeruginosa and S. aureus (Filkins et al., 2015; Tognon et al., 2017; La Rosa et al., 2019). Co-culture with P. aeruginosa was shown to induce the overexpression of genes involved in glucose fermentation and lactate production in S. aureus, leading to lactate accumulation in the medium. In turn, P. aeruginosa overexpressed genes responsible for lactate utilization and was able to use the molecule as a carbon source (Filkins et al., 2015; Tognon et al., 2017). However, this phenomenon was observed during a competitive interaction (using PAO1 or PA14 strains) and the impacts of lactate catabolism on both pathogens remain unknown.

Cooperative behaviors such as protection against antimicrobials and trophic cooperation probably contribute to the establishment and maintenance of P. aeruginosa and S. aureus co-infections. In addition, interactions between the two pathogens were shown to affect their abilities to colonize host and settle as chronic infections (Figure 4C). Adhesion to host components is an important feature for colonization, and S. aureus can attach more efficiently to abiotic surfaces during co-culture with P. aeruginosa (Kumar and Ting, 2015). In these conditions, S. aureus presented an up-regulation of several proteins involved in adhesion to platelets or to the extracellular matrixes of various hosts, such as serine rich glycoproteins and the Ebh protein. These results suggest that co-culture may increase S. aureus’s adhesion to host cells (Kumar and Ting, 2015). In line with this, co-culture with P. aeruginosa CF strains was shown to induce the overexpression of nine virulence factors of S. aureus. Among them, the Tet38 transporter promoted the internalization of S. aureus within epithelial pulmonary cells during coexistence with P. aeruginosa (Briaud et al., 2019). Finally, HQNO-mediated induction of the SCV phenotype can increase the intracellular survival of S. aureus (Mitchell et al., 2010). Cell internalization and the SCV phenotype, both promoted by P. aeruginosa, could thus contribute to the success of S. aureus infection.

Limiting the induction and efficiency of immune responses is a strategy already developed by P. aeruginosa during its genetic adaptation to the CF environment. Interestingly, P. aeruginosa-S. aureus co-infection induces a specific host response different from mono-infections in a rat otitis model (Yadav et al., 2017). Using bacterial supernatants, Chekabab et al. (2015) observed that molecules secreted by S. aureus decreased the hosts’ immune response induced by P. aeruginosa supernatant. Thus, the protein SpA produced by S. aureus was shown to bind either to P. aeruginosa Psl exopolysaccharide or to anti-Psl IgG antibodies, protecting P. aeruginosa from Psl recognition by neutrophils and thus phagocytosis (Armbruster et al., 2016; Figure 4C). In addition, S. aureus presence induces transcriptomic down-regulation of several antigenic factors in P. aeruginosa, such as genes involved in secretion and flagellum synthesis (Miller et al., 2017).

Consequently, several studies suggest that P. aeruginosa and S. aureus co-infection favors chronic infections. Cigana et al. (2018) indeed observed that preliminary colonization by S. aureus increased the ability of PA14 and CF-adapted strains to establish a chronic infection in a murine model. Interestingly, such infection kinetics are frequent in CF patients as S. aureus is one of the first colonizers in the lungs of young children, whereas P. aeruginosa infection occurs upon adolescence (French Cystic Fibrosis Register, 2017). On another note, S. aureus-P. aeruginosa co-infections were shown to delay chronic wound healing and thus bacterial clearing (Pastar et al., 2013). Finally, Zhao et al. (2018) observed that mice presented an improved survival when their lungs were infected by a mix of P. aeruginosa, S. aureus and Klebsiella pneumoniae, in comparison to mice infected only with P. aeruginosa. Although this effect cannot be specifically attributed to the presence of S. aureus and/or K. pneumoniae, co-infection appears to reduce the host mortality of P. aeruginosa infections and thus promote longer infections. Altogether, these studies suggest that co-infection favors the establishment of chronicity, since the concomitant presence of pathogens will improve their persistence within the infection site (Limoli and Hoffman, 2019).