Secretion of Virulence Proteins from <i>Campylobacter jejuni</i> Is Dependent on a Functional Flagellar Export Apparatus

Michael E. Konkel, John D. Klena, Vanessa Rivera‐Amill, Marshall R. Monteville, Debabrata Biswas, Brian H. Raphael, Joey Mickelson

Journal of Bacteriology · 2004 · 360 citations · 38 references

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TL;DR

Campylobacter jejuni secretes a set of virulence proteins called Campylobacter invasion antigens (Cia proteins). The study aimed to test whether the flagellar apparatus functions as the export system for Cia proteins. Researchers introduced mutations into genes encoding flagellar basal body (flgB, flgC), hook (flgE2), filament (flaA, flaB), and export components (flhB, fliI) to assess their impact on Cia secretion. Mutants lacking filament assembly were nonmotile and failed to secrete Cia proteins, whereas a flaA (flaB+) mutant remained nonmotile but secreted Cia proteins; complementation with flaA or flaB restored secretion, and invasion of human intestinal cells required motile, secretion‑competent bacteria, indicating that Cia proteins are exported via the flagellar apparatus.

Abstract

Campylobacter jejuni, a gram-negative motile bacterium, secretes a set of proteins termed the Campylobacter invasion antigens (Cia proteins). The purpose of this study was to determine whether the flagellar apparatus serves as the export apparatus for the Cia proteins. Mutations were generated in five genes encoding three structural components of the flagella, the flagellar basal body (flgB and flgC), hook (flgE2), and filament (flaA and flaB) genes, as well as in genes whose products are essential for flagellar protein export (flhB and fliI). While mutations that affected filament assembly were found to be nonmotile (Mot-) and did not secrete Cia proteins (S-), a flaA (flaB+) filament mutant was found to be nonmotile but Cia protein secretion competent (Mot-, S+). Complementation of a flaA flaB double mutant with a shuttle plasmid harboring either the flaA or flaB gene restored Cia protein secretion, suggesting that Cia export requires at least one of the two filament proteins. Infection of INT 407 human intestinal cells with the C. jejuni mutants revealed that maximal invasion of the epithelial cells required motile bacteria that are secretion competent. Collectively, these data suggest that the C. jejuni Cia proteins are secreted from the flagellar export apparatus.

References

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