Multidrug Efflux Pumps in the Genus Erwinia: Physiology and Regulation of Efflux Pump Gene Expression

J. Thekkiniath, R. Ravirala, M. San Francisco

Research output: Chapter in Book/Report/Conference proceedingChapter

2 Scopus citations

Abstract

Plant pathogens belonging to the genus Erwinia cause diseases in several economically important plants. Plants respond to bacterial infection with a powerful chemical arsenal and signaling molecules to rid themselves of the microbes. Although our understanding of how Erwinia initiate infections in plants has become clear, a comprehensive understanding of how these bacteria rid themselves of noxious antimicrobial agents during the infection is important. Multidrug efflux pumps are key factors in bacterial resistance toward antibiotics by reducing the level of antimicrobial compounds in the bacterial cell. Erwinia induce the expression of efflux pump genes in response to plant-derived antimicrobials. The capability of Erwinia to co-opt plant defense signaling molecules such as salicylic acid to trigger multidrug efflux pumps might have developed to ensure bacterial survival in susceptible host plants. In this review, we discuss the developments in Erwinia efflux pumps, focusing in particular on efflux pump function and the regulation of efflux pump gene expression.

Original languageEnglish
Title of host publicationHost-Microbe Interactions, 2016
EditorsBrian San Francisco, Michael San Francisco
PublisherElsevier B.V.
Pages131-149
Number of pages19
ISBN (Print)9780128093856
DOIs
StatePublished - 2016

Publication series

NameProgress in Molecular Biology and Translational Science
Volume142
ISSN (Print)1877-1173
ISSN (Electronic)1878-0814

Keywords

  • bacterial efflux
  • efflux pump
  • gene expression
  • plant–pathogen interaction

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    Thekkiniath, J., Ravirala, R., & San Francisco, M. (2016). Multidrug Efflux Pumps in the Genus Erwinia: Physiology and Regulation of Efflux Pump Gene Expression. In B. San Francisco, & M. San Francisco (Eds.), Host-Microbe Interactions, 2016 (pp. 131-149). (Progress in Molecular Biology and Translational Science; Vol. 142). Elsevier B.V.. https://doi.org/10.1016/bs.pmbts.2016.05.011