Vibrio cholerae accessory colonisation factor AcfC: a chemotactic protein with a role in hyperinfectivity
Vibrio cholerae O1 El Tor is an aquatic Gram-negative bacterium responsible for the current seventh pandemic of the diarrheal disease, cholera. A previous whole-genome analysis on V. cholerae O1 El Tor strains from the 2010 epidemic in Pakistan showed that all strains contained the V. cholerae patho...
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Published in | Scientific reports Vol. 8; no. 1; pp. 8390 - 11 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
30.05.2018
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
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Summary: | Vibrio cholerae
O1 El Tor is an aquatic Gram-negative bacterium responsible for the current seventh pandemic of the diarrheal disease, cholera. A previous whole-genome analysis on
V. cholerae
O1 El Tor strains from the 2010 epidemic in Pakistan showed that all strains contained the
V. cholerae
pathogenicity island-1 and the accessory colonisation gene
acfC
(VC_0841). Here we show that
acfC
possess an open reading frame of 770 bp encoding a protein with a predicted size of 28 kDa, which shares high amino acid similarity with two adhesion proteins found in other enteropathogens, including Paa in serotype O45 porcine enteropathogenic
Escherichia coli
and PEB3 in
Campylobacter jejuni
. Using a defined
acfC
deletion mutant, we studied the specific role of AcfC in
V. cholerae
O1 El Tor environmental survival, colonisation and virulence in two infection model systems (
Galleria mellonella
and infant rabbits). Our results indicate that AcfC might be a periplasmic sulfate-binding protein that affects chemotaxis towards mucin and bacterial infectivity in the infant rabbit model of cholera. Overall, our findings suggest that AcfC contributes to the chemotactic response of WT
V. cholerae
and plays an important role in defining the overall distribution of the organism within the intestine. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/s41598-018-26570-7 |