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Establishing Caenorhabditis elegans as a model for Mycobacterium avium subspecies hominissuis infection and intestinal colonization

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https://ir.library.oregonstate.edu/concern/articles/h989r4900

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  • The nematode Caenorhabditis elegans has become a model system for studying the disease interaction between pathogens and the host. To determine whether the transparent nematode could serve as a useful model for Mycobacterium avium subspecies hominissuis (MAH) infection of the intestinal tract, worms were fed MAH and assayed for the effects of the bacterial infection on the worm. It was observed during feeding that viable MAH increases in the intestinal lumen in a time dependent manner. Ingestion of MAH was deemed non-toxic to worms as MAH-fed populations have similar survival curves to those fed E. coli strain OP50. Pulse-chase analysis using E. coli strain OP50 revealed that MAH colonize the intestinal tract, as viable MAH remain within the intestine after the assay. Visualization of intestinal MAH using histology and transmission electron microscopy demonstrates that MAH localizes to the intestinal lumen, as well as establishes direct contact with intestinal epithelium. Bacterial colonization appears to have a detrimental effect on the microvilli of the intestinal epithelial cells. The MAH ΔGPL/4B2 strain with a mutation in glycopeptidolipid production is deficient in binding to human epithelial cells (HEp-2), as well as deficient in its ability to bind to and colonize the intestinal tract of C. elegans as efficiently as wild-type MAH. These data indicate the C. elegans may serve as a useful model system for MAH pathogenesis and in determining the mechanisms used by MAH during infection and colonization of the intestinal epithelium.
  • Keywords: C. elegans, Colonization, Mycobacterium avium, Intestines, Host
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  • Everman, J. L., Ziaie, N. R., Bechler, J., & Bermudez, L. E. (2015). Establishing Caenorhabditis elegans as a model for Mycobacterium avium subspecies hominissuis infection and intestinal colonization. Biology Open, 4(10), 1330-1335. doi:10.1242/bio.012260
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  • 4
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  • 10
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  • We acknowledge that this TEM material is based upon work supported by the National Science Foundation via the Major Research Instrumentation (MRI) Program under Grant No. [1040588]. We gratefully acknowledge financial support for acquisition of the TEM instrument from the Murdock Charitable Trust and the Oregon Nanoscience and Microtechnologies Institute (ONAMI).
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