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Frontiers in Molecular Biosciences / Small Things Matter: The 11.6-kDa TraB Protein is Crucial for Antibiotic Resistance Transfer Among Enterococci

Authors :
Berger, Tamara M.I.
Berger, Tamara M.I.
Michaelis, Claudia
Probst, Ines
Sagmeister, Theo
Petrowitsc, Lukas
Puchner, Sandra
Pavkov-Keller, Tea
Gesslbauer, Bernd
Grohmann, Elisabeth
Keller, Walter
Berger, Tamara M.I.
Berger, Tamara M.I.
Michaelis, Claudia
Probst, Ines
Sagmeister, Theo
Petrowitsc, Lukas
Puchner, Sandra
Pavkov-Keller, Tea
Gesslbauer, Bernd
Grohmann, Elisabeth
Keller, Walter
Publication Year :
2022

Abstract

Conjugative transfer is the most important means for spreading antibiotic resistance genes. It is used by Gram-positive and Gram-negative bacteria, and archaea as well. Conjugative transfer is mediated by molecular membrane-spanning nanomachines, so called Type 4 Secretion Systems (T4SS). The T4SS of the broad-host-range inc18-plasmid pIP501 is organized in a single operon encoding 15 putative transfer proteins. pIP501 was originally isolated from a clinical Streptococcus agalactiae strain but is mainly found in Enterococci. In this study, we demonstrate that the small transmembrane protein TraB is essential for pIP501 transfer. Complementation of a markerless pIP501∆traB knockout by traB lacking its secretion signal sequence did not fully restore conjugative transfer. Pull-downs with Strep-tagged TraB demonstrated interactions of TraB with the putative mating pair formation proteins, TraF, TraH, TraK, TraM, and with the lytic transglycosylase TraG. As TraB is the only putative mating pair formation complex protein containing a secretion signal sequence, we speculate on its role as T4SS recruitment factor. Moreover, structural features of TraB and TraB orthologs are presented, making an essential role of TraB-like proteins in antibiotic resistance transfer among Firmicutes likely.<br />Version of record

Details

Database :
OAIster
Notes :
text/html, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1366940661
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.3389.fmolb.2022.867136