Mycobacterium abscessus Opsonization Allows an Escape from the Defensin Bactericidal Action in Drosophila

ABSTRACT Mycobacterium abscessus, an intracellular nontuberculous mycobacterium, is considered the most pathogenic species among the group of rapidly growing mycobacteria. The resistance of M. abscessus to the host innate response contributes to its pathogenicity in addition to several virulence fac...

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Main Authors: Hamadoun Touré, Nicolas Durand, Isabelle Guénal, Jean-Louis Herrmann, Fabienne Girard-Misguich, Sébastien Szuplewski
Format: Article
Language:English
Published: American Society for Microbiology 2023-08-01
Series:Microbiology Spectrum
Subjects:
Online Access:https://journals.asm.org/doi/10.1128/spectrum.00777-23
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author Hamadoun Touré
Nicolas Durand
Isabelle Guénal
Jean-Louis Herrmann
Fabienne Girard-Misguich
Sébastien Szuplewski
author_facet Hamadoun Touré
Nicolas Durand
Isabelle Guénal
Jean-Louis Herrmann
Fabienne Girard-Misguich
Sébastien Szuplewski
author_sort Hamadoun Touré
collection DOAJ
description ABSTRACT Mycobacterium abscessus, an intracellular nontuberculous mycobacterium, is considered the most pathogenic species among the group of rapidly growing mycobacteria. The resistance of M. abscessus to the host innate response contributes to its pathogenicity in addition to several virulence factors. We have recently shown in Drosophila that antimicrobial peptides (AMPs), whose production is induced by M. abscessus, are unable to control mycobacterial infection. This could be due to their inability to kill mycobacteria and/or the hidden location of the pathogen in phagocytic cells. Here, we demonstrate that the rapid internalization of M. abscessus by Drosophila macrophages allows it to escape the AMP-mediated humoral response. By depleting phagocytes in AMP-deficient flies, we found that several AMPs were required for the control of extracellular M. abscessus. This was confirmed in the Tep4 opsonin-deficient flies, which we show can better control M. abscessus growth and have increased survival through overproduction of some AMPs, including Defensin. Furthermore, Defensin alone was sufficient to kill extracellular M. abscessus both in vitro and in vivo and control its infection. Collectively, our data support that Tep4-mediated opsonization of M. abscessus allows its escape and resistance toward the Defensin bactericidal action in Drosophila. IMPORTANCE Mycobacterium abscessus, an opportunistic pathogen in cystic fibrosis patients, is the most pathogenic species among the fast-growing mycobacteria. How M. abscessus resists the host innate response before establishing an infection remains unclear. Using Drosophila, we have recently demonstrated that M. abscessus resists the host innate response by surviving the cytotoxic lysis of the infected phagocytes and the induced antimicrobial peptides (AMPs), including Defensin. In this work, we demonstrate that M. abscessus resists the latter response by being rapidly internalized by Drosophila phagocytes. Indeed, by combining in vivo and in vitro approaches, we show that Defensin is able to control extracellular M. abscessus infection through a direct bactericidal action. In conclusion, we report that M. abscessus escapes the host AMP-mediated humoral response by taking advantage of its internalization by the phagocytes.
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spelling doaj.art-5ed4f8f7305747ae95e9ac6b765b2b572023-08-17T13:04:15ZengAmerican Society for MicrobiologyMicrobiology Spectrum2165-04972023-08-0111410.1128/spectrum.00777-23Mycobacterium abscessus Opsonization Allows an Escape from the Defensin Bactericidal Action in DrosophilaHamadoun Touré0Nicolas Durand1Isabelle Guénal2Jean-Louis Herrmann3Fabienne Girard-Misguich4Sébastien Szuplewski5Université Paris-Saclay, UVSQ, INSERM, Infection et Inflammation, Montigny-Le-Bretonneux, FranceUniversité Paris-Saclay, UVSQ, INSERM, Infection et Inflammation, Montigny-Le-Bretonneux, FranceUniversité Paris-Saclay, UVSQ, LGBC, Versailles, FranceUniversité Paris-Saclay, UVSQ, INSERM, Infection et Inflammation, Montigny-Le-Bretonneux, FranceUniversité Paris-Saclay, UVSQ, INSERM, Infection et Inflammation, Montigny-Le-Bretonneux, FranceUniversité Paris-Saclay, UVSQ, LGBC, Versailles, FranceABSTRACT Mycobacterium abscessus, an intracellular nontuberculous mycobacterium, is considered the most pathogenic species among the group of rapidly growing mycobacteria. The resistance of M. abscessus to the host innate response contributes to its pathogenicity in addition to several virulence factors. We have recently shown in Drosophila that antimicrobial peptides (AMPs), whose production is induced by M. abscessus, are unable to control mycobacterial infection. This could be due to their inability to kill mycobacteria and/or the hidden location of the pathogen in phagocytic cells. Here, we demonstrate that the rapid internalization of M. abscessus by Drosophila macrophages allows it to escape the AMP-mediated humoral response. By depleting phagocytes in AMP-deficient flies, we found that several AMPs were required for the control of extracellular M. abscessus. This was confirmed in the Tep4 opsonin-deficient flies, which we show can better control M. abscessus growth and have increased survival through overproduction of some AMPs, including Defensin. Furthermore, Defensin alone was sufficient to kill extracellular M. abscessus both in vitro and in vivo and control its infection. Collectively, our data support that Tep4-mediated opsonization of M. abscessus allows its escape and resistance toward the Defensin bactericidal action in Drosophila. IMPORTANCE Mycobacterium abscessus, an opportunistic pathogen in cystic fibrosis patients, is the most pathogenic species among the fast-growing mycobacteria. How M. abscessus resists the host innate response before establishing an infection remains unclear. Using Drosophila, we have recently demonstrated that M. abscessus resists the host innate response by surviving the cytotoxic lysis of the infected phagocytes and the induced antimicrobial peptides (AMPs), including Defensin. In this work, we demonstrate that M. abscessus resists the latter response by being rapidly internalized by Drosophila phagocytes. Indeed, by combining in vivo and in vitro approaches, we show that Defensin is able to control extracellular M. abscessus infection through a direct bactericidal action. In conclusion, we report that M. abscessus escapes the host AMP-mediated humoral response by taking advantage of its internalization by the phagocytes.https://journals.asm.org/doi/10.1128/spectrum.00777-23Mycobacterium abscessusphagocytesopsonizationDefensinDrosophila
spellingShingle Hamadoun Touré
Nicolas Durand
Isabelle Guénal
Jean-Louis Herrmann
Fabienne Girard-Misguich
Sébastien Szuplewski
Mycobacterium abscessus Opsonization Allows an Escape from the Defensin Bactericidal Action in Drosophila
Microbiology Spectrum
Mycobacterium abscessus
phagocytes
opsonization
Defensin
Drosophila
title Mycobacterium abscessus Opsonization Allows an Escape from the Defensin Bactericidal Action in Drosophila
title_full Mycobacterium abscessus Opsonization Allows an Escape from the Defensin Bactericidal Action in Drosophila
title_fullStr Mycobacterium abscessus Opsonization Allows an Escape from the Defensin Bactericidal Action in Drosophila
title_full_unstemmed Mycobacterium abscessus Opsonization Allows an Escape from the Defensin Bactericidal Action in Drosophila
title_short Mycobacterium abscessus Opsonization Allows an Escape from the Defensin Bactericidal Action in Drosophila
title_sort mycobacterium abscessus opsonization allows an escape from the defensin bactericidal action in drosophila
topic Mycobacterium abscessus
phagocytes
opsonization
Defensin
Drosophila
url https://journals.asm.org/doi/10.1128/spectrum.00777-23
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