Lack of MSMEG_6281, a peptidoglycan amidase, affects cell wall integrity and virulence of Mycobacterium smegmatis.


Journal

Microbial pathogenesis
ISSN: 1096-1208
Titre abrégé: Microb Pathog
Pays: England
ID NLM: 8606191

Informations de publication

Date de publication:
Mar 2019
Historique:
received: 02 07 2018
revised: 04 01 2019
accepted: 07 01 2019
pubmed: 28 1 2019
medline: 20 3 2019
entrez: 28 1 2019
Statut: ppublish

Résumé

Mycolyl-arabinogalactan-peptidoglycan (mAGP) is the major content of the mycobacterium cell wall structure and essential for mycobacterial survival. Peptidoglycan (PG) plays an important role in maintenance of cell division, cell wall integrity and pathogenesis. Mycobacterium smegmatis MSMEG_6281, a peptidoglycan amidase, is vital for mycobacterial cell division. However, the effects of MSMEG_6281on cell wall integrity and mycobacterial virulence remain unknown. In the current study, we demonstrate that MSMEG_6281gene knockout in M.smegmatis alters the microbiological characteristics. Our results revealed that MSMEG_6281gene knockout bacteria (M. sm-ΔM_6281) lost their acid-fastness, increased their sensitivity to lipophilic compounds and presented an abnormal morphology. Our results revealed that MSMEG_6281was related to maintaining the cell wall integrity. Furthermore, we investigated the effects of MSMEG_6281 inactivation on mycobacterial virulence using mice models infected by different M.smegmatis strains. MSMEG_6281 inactivation in the M sm-ΔM_6281 infected group caused less mycobacterial colonization, reduced pathological signs, decreased the anti-microbial enzymes production including iNOS and β-defensins in mouse lungs. Moreover, IL-1β and TLR2 expression were significantly down-regulated, while the production of IFN-γ and TNF-α was up-regulated. These findings indicated the diversity of host immune responses induced by different strains of M.smegmatis, suggesting that MSMEG_6281 inactivation impact mycobacterial virulence. In conclusion, the MSMEG_6281 protein plays important roles in maintaining cell wall integrity and mycobacterial virulence.

Identifiants

pubmed: 30685363
pii: S0882-4010(18)31194-X
doi: 10.1016/j.micpath.2019.01.013
pii:
doi:

Substances chimiques

Bacterial Proteins 0
Cytokines 0
Interleukin-1beta 0
Peptide Fragments 0
Peptidoglycan 0
Tlr2 protein, mouse 0
Toll-Like Receptor 2 0
beta-Defensins 0
interleukin-1beta (163-171) 106021-96-9
Nitric Oxide Synthase Type II EC 1.14.13.39
Nos2 protein, mouse EC 1.14.13.39
Amidohydrolases EC 3.5.-
amidase EC 3.5.1.4

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

405-413

Informations de copyright

Copyright © 2019. Published by Elsevier Ltd.

Auteurs

Jiajia He (J)

Department of Biotechnology, College of Basic Medical Sciences, Dalian Medical University, Dalian, 116044, China.

Weizhe Fu (W)

Department of Biotechnology, College of Basic Medical Sciences, Dalian Medical University, Dalian, 116044, China.

Shijia Zhao (S)

Department of Biotechnology, College of Basic Medical Sciences, Dalian Medical University, Dalian, 116044, China.

Cuili Zhang (C)

Department of Biotechnology, College of Basic Medical Sciences, Dalian Medical University, Dalian, 116044, China.

Tieying Sun (T)

Department of Biotechnology, College of Basic Medical Sciences, Dalian Medical University, Dalian, 116044, China.

Tao Jiang (T)

Department of Biotechnology, College of Basic Medical Sciences, Dalian Medical University, Dalian, 116044, China. Electronic address: jiangtaodl@163.com.

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Classifications MeSH