Lack of MSMEG_6281, a peptidoglycan amidase, affects cell wall integrity and virulence of Mycobacterium smegmatis.
Amidohydrolases
/ genetics
Animals
Bacterial Proteins
/ genetics
Cell Division
Cell Wall
/ genetics
Cytokines
/ metabolism
Disease Models, Animal
Gene Expression Profiling
Gene Expression Regulation
Gene Knockout Techniques
Genes, Bacterial
/ genetics
Homologous Recombination
Interleukin-1beta
/ metabolism
Lung
/ microbiology
Male
Mice
Mice, Inbred C57BL
Mycobacterium Infections, Nontuberculous
/ immunology
Mycobacterium smegmatis
/ enzymology
Nitric Oxide Synthase Type II
/ metabolism
Peptide Fragments
/ metabolism
Peptidoglycan
/ metabolism
Toll-Like Receptor 2
/ metabolism
Virulence
beta-Defensins
/ metabolism
Cell wall integrity
MSMEG_6281
Mycobacterial virulence
Peptidoglycan amidase
Journal
Microbial pathogenesis
ISSN: 1096-1208
Titre abrégé: Microb Pathog
Pays: England
ID NLM: 8606191
Informations de publication
Date de publication:
Mar 2019
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
405-413Informations de copyright
Copyright © 2019. Published by Elsevier Ltd.