Type III Secretion System Translocon Component EseB Forms Filaments on and Mediates Autoaggregation of and Biofilm Formation by Edwardsiella tarda
Author(s) -
Zhipeng Gao,
Pin Nie,
Jin Fang Lu,
Lu Yi Liu,
Tiao Yi Xiao,
Wei Liu,
Jia Shou Liu,
Hai Xia Xie
Publication year - 2015
Publication title -
applied and environmental microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.552
H-Index - 324
eISSN - 1070-6291
pISSN - 0099-2240
DOI - 10.1128/aem.01254-15
Subject(s) - edwardsiella tarda , biofilm , microbiology and biotechnology , secretion , effector , flagellum , biology , protein filament , bacteria , chemistry , biochemistry , genetics
The type III secretion system (T3SS) ofEdwardsiella tarda plays an important role in infection by translocating effector proteins into host cells. EseB, a component required for effector translocation, is reported to mediate autoaggregation ofE. tarda . In this study, we demonstrate that EseB forms filamentous appendages on the surface ofE. tarda and is required for biofilm formation byE. tarda in Dulbecco's modified Eagle's medium (DMEM). Biofilm formation byE. tarda in DMEM does not require FlhB, an essential component for assembling flagella. Dynamic analysis of EseB filament formation, autoaggregation, and biofilm formation shows that the formation of EseB filaments occurs prior to autoaggregation and biofilm formation. The addition of an EseB antibody toE. tarda cultures before bacterial autoaggregation prevents autoaggregation and biofilm formation in a dose-dependent manner, whereas the addition of the EseB antibody toE. tarda cultures in which biofilm is already formed does not destroy the biofilm. Therefore, EseB filament-mediated bacterial cell-cell interaction is a prerequisite for autoaggregation and biofilm formation.
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