Mycobacterium abscessus is a non-tuberculous mycobacteria that is an important cause of progressive human pulmonary infection. While it is a bona fide cause of lung and extra-pulmonary disease, its potential to do so is relatively low. Indeed, M. abscessus pulmonary infection does not typically occur in immunocompetent individuals with normal lung airways. On the other hand, individuals with abnormal lung airways who are otherwise immunocompetent can develop progressive, severe, intractable pulmonary infection. As further evidence of its low pathogenicity, significant experimental modifications in the study design are often required in order to establish a productive infection in mice; i.e., use of various types of immunodeficient mice is typically needed to create an established infection. The lack of suitable mouse models that reproduce abnormal lung airways seen in humans further hampers these efforts. One important aspect of M. abscessus pathogenesis is colonization of abnormal lung airways with glycopeptidolipid (GPL)—expressing smooth colony variants that are able to form biofilms. Spontaneous emergence of virulent rough colony variants lacking GPL leads to invasive lung infection and resultant increased lung inflammation (Byrd and Lyons, 1999; Howard et al., 2006; Catherinot et al., 2007, 2009; Nessar et al., 2011).
The articles in this Research Topic describing M. abscessus biofilm formation in synthetic medium (Belardinelli et al.) and increased virulence of outer membrane porin mutants of M. abscessus (de Moura et al.) provide evidence for modulation of M. abscessus pathogenicity by selective pressure within the lung airways of cystic fibrosis patients. These studies focus on the evolving pathogenic sequence of M. abscessus lung infection when the low pathogenic colonizing lung airway phenotype is transitioning to its more virulent, proinflammatory phenotype. The biofilm study elucidates the genetic and biochemical differences between M. abscessus subsp. abscessus grown as biofilm in minimal synthetic medium to the same organism grown in an enriched medium designed to mimic the conditions M. abscessus may encounter in the lung airways of cystic fibrosis patients (synthetic cystic fibrosis medium—SCFM). Among the differences noted was the significant presence of GPLs in the extracellular matrix of biofilms formed by M. abscessus in SCFM, highlighting the important role that these cell wall components play in M. abscessus biofilm formation. Extracellular DNA was also present in relative abundance in the biofilms matrix formed in SCFM and provides support for the established use of recombinant human DNase treatment in patients with cystic fibrosis. These results indicate that growth of M. abscessus biofilm in SCFM is a useful method for identifying potential virulence determinants upregulated under conditions that mimic the airways of cystic fibrosis patients. Similarly the porin paper provides evidence that deletions and rearrangements in porin genes of serially collected M. abscessus isolates from cystic fibrosis patients occur in response to host selection pressure. Specifically, deletion of two of these porin genes, mmpA and mmpB leads to enhanced replication of the knock out mutants in bone-marrow derived mouse macrophages from SCID and GM-CSF knock-out mice, as well as in a SCID mouse model of infection. Findings from both these studies support the concept that host selection pressures enhance M. abscessus virulence once colonization of lung airways occurs.
One hypothesis for the establishment of M. abscessus lung infection is that chronic inflammation results in suppression of the Th1 immune response needed for clearance (Orme and Ordway, 2014). If this is the case, the paper describing the effects of Rufomycin directly on M. abscessus and the host immune response (Park et al.) suggests a dual mechanistic strategy for treatment of M. abscessus lung infection using this drug. By both directly inhibiting the organism and blunting the proinflammatory response elicited by rough invasive variants, this drug may act in a novel way to prevent this bacterium from achieving its full virulence potential. The paper describing an interferon-gamma release assay (IGRA) (Steindor et al.) demonstrates the potential use of an M. abscessus specific antigen in an IGRA designed to diagnose M. abscessus infection. The question of what is the correlate of an effective immune response to M. abscessus lung infection remains open. In this study, the majority of patients were cystic fibrosis patients with only a small number of non-CF bronchiectasis patients. Additional studies using the assay would be informative in distinguishing the IGRA response in patients with chronic lung airway colonization compared to those with invasive parenchymal lung disease as well as in those patients colonized/infected with smooth GPL expressing isolates compared to rough isolates lacking GPL.
Together these articles are important contributions to the M. abscessus field, and provide evidence that supports the concept that M. abscessus has low pathogenicity until it is able to colonize its preferred niche in abnormal lung airways leading to enhanced virulence, invasive lung infection and avoidance of host immune defense mechanisms.
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Statements
Author contributions
TB and EC contributed to the development of the idea for this Research Topic, solicited manuscripts, and contributed to the final version of the Editorial.
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.
References
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ByrdT. F.LyonsC. R. (1999). Preliminary characterization of a Mycobacterium abscessus mutant in human and murine models of infection. Infect. Immun. 67, 4700–4707. 10.1128/IAI.67.9.4700-4707.1999
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CatherinotE.ClarissouJ.EtienneG.RipollF.EmileJ. F.DaffeM.et al. (2007). Hypervirulence of a rough variant of the Mycobacterium abscessus type strain. Infect. Immun. 75, 1055–1058. 10.1128/IAI.00835-06
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CatherinotE.RouxA. L.MacherasE.HubertD.MatmarM.DannhofferL.et al. (2009). Acute respiratory failure involving an R variant of Mycobacterium abscessus. J. Clin. Microbiol. 47, 271–274. 10.1128/JCM.01478-08
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HowardS. T.RhoadesE.RechtJ.PangX.AlsupA.KolterR.et al. (2006). Spontaneous reversion of Mycobacterium abscessus from a smooth to a rough morphotype is associated with reduced xpression of glycopeptidolipid and reacquisition of an invasive phenotype. Microbiology.152, 1581–1590. 10.1099/mic.0.28625-0
5
NessarR.ReyratJ. M.DavidsonL. B.ByrdT. F. (2011). Deletion of the mmpL4b gene in the Mycobacterium abscessus glycopeptidolipid biosynthetic pathway results in loss of surface colonization capability, but enhanced ability to replicate in human macrophages and stimulate their innate immune response. Microbiology157, 1187–1195. 10.1099/mic.0.046557-0
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OrmeI. M.OrdwayD. J. (2014). Host response to nontuberculous mycobacterial infections of current clinical importance. Infect. Immun. 82, 3516–3522. 10.1128/IAI.01606-13
Summary
Keywords
Mycobacterium abscessus, cystic fibrosis, porin, biofilm, glycopeptidolipid
Citation
Byrd TF and Chan ED (2022) Editorial: Mycobacterium abscessus; The Paradox of Low Pathogenicity and High Virulence. Front. Microbiol. 13:943694. doi: 10.3389/fmicb.2022.943694
Received
14 May 2022
Accepted
24 May 2022
Published
10 June 2022
Volume
13 - 2022
Edited and reviewed by
Axel Cloeckaert, Institut National de recherche pour l'agriculture, l'alimentation et l'environnement (INRAE), France
Updates
Copyright
© 2022 Byrd and Chan.
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: Thomas F. Byrd tbyrd@salud.unm.edu
This article was submitted to Infectious Agents and Disease, a section of the journal Frontiers in Microbiology
Disclaimer
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.