genetic analysis of anti-amoebae and anti-bacterial activities of the type vi secretion system in vibrio cholerae遗传分析anti-amoebae和抗菌活动vi型分泌系统的霍乱弧菌.pdfVIP
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genetic analysis of anti-amoebae and anti-bacterial activities of the type vi secretion system in vibrio cholerae遗传分析anti-amoebae和抗菌活动vi型分泌系统的霍乱弧菌
Genetic Analysis of Anti-Amoebae and Anti-Bacterial
Activities of the Type VI Secretion System in Vibrio
cholerae
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Jun Zheng , Brian Ho, John J. Mekalanos*
Department of Microbiology and Molecular Genetics, Harvard Medical School, Boston, Massachusetts, United States of America
Abstract
A type VI secretion system (T6SS) was recently shown to be required for full virulence of Vibrio cholerae O37 serogroup
strain V52. In this study, we systematically mutagenized each individual gene in T6SS locus and characterized their functions
based on expression and secretion of the hemolysin co-regulated protein (Hcp), virulence towards amoebae of
Dictyostelium discoideum and killing of Escherichia coli bacterial cells. We group the 17 proteins characterized in the T6SS
locus into four categories: twelve (VipA, VipB, VCA0109–VCA0115, ClpV, VCA0119, and VasK) are essential for Hcp secretion
and bacterial virulence, and thus likely function as structural components of the apparatus; two (VasH and VCA0122) are
regulators that are required for T6SS gene expression and virulence; another two, VCA0121 and valine-glycine repeat
protein G 3 (VgrG-3), are not essential for Hcp expression, secretion or bacterial virulence, and their functions are unknown;
the last group is represented by VCA0118, which is not required for Hcp expression or secretion but still plays a role in both
amoebae and bacterial killing and may therefore be an effector protein. We also showed that the clpV gene product is
required for Dictyostelium virulence but is less important for killing E. coli. In addition, one vgrG gene (vgrG-2) outside of the
T6SS gene cluster was required for bacterial killing but another (vgrG-1) was not. However, a bacterial killing defect was
observed when vgrG-1 and vgrG-3 were both deleted. Several gene
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