Evaluating rodent experimental models for studies of Blastocystis ST1
Language English Country United States Media print-electronic
Document type Comparative Study, Evaluation Study, Journal Article
PubMed
29959915
DOI
10.1016/j.exppara.2018.06.009
PII: S0014-4894(18)30178-4
Knihovny.cz E-resources
- Keywords
- Blastocystis ST1, Colonization longevity, Experimental colonization, In vivo model, Rat, Susceptibility to colonization,
- MeSH
- Blastocystis growth & development pathogenicity MeSH
- Blastocystis Infections diagnosis parasitology MeSH
- Centrifugation, Density Gradient MeSH
- Feces parasitology MeSH
- Gerbillinae MeSH
- Rats MeSH
- Humans MeSH
- Disease Models, Animal * MeSH
- Murinae MeSH
- Mice MeSH
- Disease Susceptibility MeSH
- Specific Pathogen-Free Organisms MeSH
- Rats, Wistar MeSH
- Health Status MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Humans MeSH
- Male MeSH
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Evaluation Study MeSH
- Comparative Study MeSH
Blastocystis is a common inhabitant of the human gut, colonizing at least one billion people at a prevalence ranging from <10% to 100% in healthy human populations globally. The majority of carriers remain asymptomatic, suggesting that Blastocystis is largely a commensal, though Blastocystis has also been implicated in disease in some people. However, there are no in vivo model systems in which to experimentally test the impact of Blastocystis on mammalian hosts and the gut ecosystem and determine which factors underlie these variable clinical outcomes. We evaluated a rat model for sustaining of a human-derived Blastocystis ST1 and assess colonization success and longevity. Because of the broad host range of Blastocystis, we compared the rat with three other rodent species to establish the reproducibility of our method. Blastocystis was introduced by esophageal gavage and colonization success evaluated by Blastocystis culture. Culture was also used to determine that all animals were negative prior to colonization and negative controls remain Blastocystis-free. In this study, Blastocystis ST1 established in 100% of the outbred rats (Rattus norvegicus) and gerbils (Meriones unguiculatus) challenged. Rats were colonized asymptomatically for more than one year, but Blastocystis ST1 was not transmitted between rats. Mus musculus strain CD1 and Mastomys coucha were not susceptible to Blastocystis ST1. Thus, rats appear to be a suitable in vivo model for studies of Blastocystis ST1, as do gerbils though testing was less extensive. This work lays the foundation for experimental work on the role of Blastocystis in health and disease.
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