The virulence of Yersinia pestis KIM6+ was compared with multiple isolates of Yersinia pseudotuberculosis and Yersinia enterocolitica toward larvae of the greater wax moth Galleria mellonella. Although Y. pestis and Y. pseudotuberculosis were able to cause lethal infection in G. mellonella, these species appeared less virulent than the majority of Y. enterocolitica strains tested. Y. pestis survived primarily within hemocytes of G. mellonella, and induced a strong antibacterial peptide response that lasted for at least 3 days in surviving larvae. Immunization with dead bacteria to induce an antibacterial response led to increased survival of the larvae following infection. Mutant strains lacking the either phoP or oxyR, which were less resistant to antibacterial peptides and hydrogen peroxide respectively, were attenuated and restoration of the wild-type genes on plasmids restored virulence. Our results indicate that the Y. pseudotuberculosis-Y. pestis lineage is not as virulent toward G. mellonella as are the majority of Y. enterocolitica isolates. Further, we have shown that G. mellonella is a useful infection model for analyzing Y. pestis host-pathogen interactions, and antibacterial peptide resistance mediated by phoP and reactive oxygen defense mediated by oxyR are important for Y. pestis infection of this insect.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.micpath.2011.08.008DOI Listing

Publication Analysis

Top Keywords

phop oxyr
8
yersinia pestis
8
galleria mellonella
8
majority y enterocolitica
8
antibacterial peptide
8
oxyr transcriptional
4
transcriptional regulators
4
regulators contribute
4
yersinia
4
contribute yersinia
4

Similar Publications

The heat shock response (HSR) is a universal cellular response that promotes survival following temperature increase. In filamentous , which accounts for ∼70% of commercial antibiotic production, HSR is regulated by transcriptional repressors; in particular, the widespread MerR-family regulator HspR has been identified as a key repressor. However, functions of HspR in other biological processes are unknown.

View Article and Find Full Text PDF
Article Synopsis
  • Yersinia pestis causes bubonic and pneumonic plague, primarily affecting wild rodents and requiring fleas for transmission through biofilm formation in the flea's proventriculus.
  • The study introduces a Drosophila melanogaster model to explore how Y. pestis colonizes the insect gut and identified key genes (PhoP and GmhA) that help the bacteria resist gut immunity and support colonization.
  • The findings suggest that biofilm formation may protect Y. pestis from antimicrobial peptides, with reactive oxygen species in the gut limiting bacterial infection, making fruit flies a useful model for studying the interactions between Y. pestis and its flea vector.*
View Article and Find Full Text PDF

The virulence of Yersinia pestis KIM6+ was compared with multiple isolates of Yersinia pseudotuberculosis and Yersinia enterocolitica toward larvae of the greater wax moth Galleria mellonella. Although Y. pestis and Y.

View Article and Find Full Text PDF

The lethal effects of inorganic acid on phoE+ Escherichia coli strains, grown at neutral pHo, were enhanced by chloramphenicol, apparently because some organisms acquire acid tolerance (habituate) during challenge and chloramphenicol stops this. Phosphate (and/or polyphosphate) present during challenge prevented killing and damage by acid to outer membranes, DNA and cellular enzymes but did not prevent acid pHo enhancing novobiocin activity. To reverse acid effects, phosphate must interact with or cross the outer membrane but need not enter the cytoplasm; it is probable that it competes with H+ (or protonated anions) for passage through the PhoE pore.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!