In vivo transcriptome analysis provides insights into host-dependent expression 
of virulence factors by Yersinia entomophaga MH96, during infection of Galleria 
mellonella

Paulson, Amber R.; O’Callaghan, Maureen; Zhang, Xue-Xian; Rainey, Paul B.; Hurst, Mark R. H.

doi:10.1093/g3journal/jkaa024

Item

ITEM ACTIONSEXPORT

Add to Basket

Local TagsRelease HistoryDetailsSummary

Released

Journal Article

In vivo transcriptome analysis provides insights into host-dependent expression of virulence factors by Yersinia entomophaga MH96, during infection of Galleria mellonella

MPS-Authors

/persons/resource/persons56872

Rainey, Paul B.
Department Microbial Population Biology, Max Planck Institute for Evolutionary Biology, Max Planck Society;

External Resource

No external resources are shared

Fulltext (restricted access)

There are currently no full texts shared for your IP range.

Fulltext (public)

jkaa024.pdf
(Publisher version), 2MB

Supplementary Material (public)

There is no public supplementary material available

Citation

Paulson, A. R., O’Callaghan, M., Zhang, X.-X., Rainey, P. B., & Hurst, M. R. H. (2021). In vivo transcriptome analysis provides insights into host-dependent expression of virulence factors by Yersinia entomophaga MH96, during infection of Galleria mellonella. G3: Genes, Genomes, Genetics, 11(1): jkaa024. doi:10.1093/g3journal/jkaa024.

Cite as: https://hdl.handle.net/21.11116/0000-0009-1FE8-0

Abstract

The function of microbes can be inferred from knowledge of genes specifically expressed in natural environments. Here, we report the in vivo transcriptome of the entomopathogenic bacterium Yersinia entomophaga MH96, captured during initial, septicemic, and pre-cadaveric stages of intrahemocoelic infection in Galleria mellonella. A total of 1285 genes were significantly upregulated by MH96 during infection; 829 genes responded to in vivo conditions during at least one stage of infection, 289 responded during two stages of infection, and 167 transcripts responded throughout all three stages of infection compared to in vitro conditions at equivalent cell densities. Genes upregulated during the earliest infection stage included components of the insecticidal toxin complex Yen-TC (chi1, chi2, and yenC1), genes for rearrangement hotspot element containing protein yenC3, cytolethal distending toxin cdtAB, and vegetative insecticidal toxin vip2. Genes more highly expressed throughout the infection cycle included the putative heat-stable enterotoxin yenT and three adhesins (usher-chaperone fimbria, filamentous hemagglutinin, and an AidA-like secreted adhesin). Clustering and functional enrichment of gene expression data also revealed expression of genes encoding type III and VI secretion system-associated effectors. Together these data provide insight into the pathobiology of MH96 and serve as an important resource supporting efforts to identify novel insecticidal agents.