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Updated: May 11, 2026

Analysis of Yersinia enterocolitica Effector Translocation into Host Cells Using Beta-lactamase Effector Fusions
Published on: October 13, 2015
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.
Abstract:
A highly conserved virulence plasmid encoding a type III secretion system is shared by the three Yersinia species most pathogenic for mammals. Although factors encoded on this plasmid enhance the ability of Yersinia to thrive in their mammalian hosts, the loss of this virulence plasmid does not eliminate growth or survival in host organs. Most notably, yields of viable plasmid-deficient Yersinia pseudotuberculosis (Yptb) are indistinguishable from wild-type Yptb within mesenteric lymph nodes. To identify chromosomal virulence factors that allow for plasmid-independent survival during systemic infection of mice, we generated transposon insertions in plasmid-deficient Yptb, and screened a library having over 20,000 sequence-identified insertions. Among the previously uncharacterized loci, insertions in mrtAB, an operon encoding an ABC family transporter, had the most profound phenotype in a plasmid-deficient background. The absence of MrtAB, however, had no effect on growth in the liver and spleen of a wild type strain having an intact virulence plasmid, but caused a severe defect in colonization of the mesenteric lymph nodes. Although this result is consistent with lack of expression of the type III secretion system by Wt Yptb in the mesenteric lymph nodes, a reporter for YopE indicated that expression of the system was robust. We demonstrate that the ATPase activity of MrtB is required for growth in mice, indicating that transport activity is required for virulence. Indeed, MrtAB appears to function as an efflux pump, as the ATPase activity enhances resistance to ethidium bromide while increasing sensitivity to pyocyanin, consistent with export across the inner membrane.
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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