Identification of MrtAB, an ABC transporter specifically required for Yersinia pseudotuberculosis to colonize the

Gregory T Crimmins1, Sina Mohammadi, Erin R Green

  • 1Department of Molecular Biology and Microbiology, Tufts University School of Medicine, Boston, Massachusetts, USA.

Plos Pathogens
|August 10, 2012
PubMed

Insights

A novel ABC transporter, MrtAB, is crucial for Yersinia pseudotuberculosis survival in mouse lymph nodes, even without its virulence plasmid. This discovery highlights chromosomal factors enabling bacterial systemic infection.

Area of Science:

  • Microbiology
  • Bacterial Pathogenesis
  • Molecular Biology

Background:

  • The primary Yersinia virulence plasmid, encoding a type III secretion system, is vital for mammalian infection.
  • However, plasmid loss doesn't abolish Yersinia growth in host organs, suggesting chromosomal factors contribute to virulence.

Purpose of the Study:

  • To identify chromosomal virulence factors enabling plasmid-independent survival of Yersinia pseudotuberculosis during systemic mouse infection.

Main Methods:

  • Generated and screened over 20,000 transposon insertion mutants in plasmid-deficient Yersinia pseudotuberculosis.
  • Assessed bacterial colonization in mouse organs (mesenteric lymph nodes, liver, spleen).
  • Investigated the function of the identified mrtAB operon, including ATPase activity and substrate resistance.

Main Results:

  • Insertions in the previously uncharacterized mrtAB operon, encoding an ABC transporter, caused the most significant defect in plasmid-deficient Yersinia pseudotuberculosis.
  • MrtAB deficiency severely impaired mesenteric lymph node colonization but not liver or spleen growth in plasmid-deficient strains.
  • MrtAB ATPase activity was essential for virulence, suggesting an efflux pump mechanism involved in inner membrane transport.

Conclusions:

  • The MrtAB ABC transporter is a critical chromosomal virulence factor for Yersinia pseudotuberculosis, particularly in mesenteric lymph nodes.
  • MrtAB functions as an efflux pump, contributing to bacterial survival and colonization during systemic infection independently of the main virulence plasmid.
  • This finding expands our understanding of Yersinia pathogenesis beyond plasmid-encoded factors.

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