Candida albicans Isolates 529L and CHN1 Exhibit Stable Colonization of the Murine Gastrointestinal Tract.
Candida albicans Isolates 529L and CHN1 Exhibit Stable Colonization of the Murine Gastrointestinal Tract.
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DOI:
10.1128/mbio.02878-21
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发表时间:
2021-12-21
期刊:
影响因子:
6.4
通讯作者:
Ene IV
中科院分区:
文献类型:
--
作者:
McDonough LD;Mishra AA;Tosini N;Kakade P;Penumutchu S;Liang SH;Maufrais C;Zhai B;Taur Y;Belenky P;Bennett RJ;Hohl TM;Koh AY;Ene IV
Candida albicans is a pathobiont that colonizes multiple niches in the body including the gastrointestinal (GI) tract but is also responsible for both mucosal and systemic infections. Despite its prevalence as a human commensal, the murine GI tract is generally refractory to colonization with the C. albicans reference isolate SC5314. Here, we identify two C. albicans isolates, 529L and CHN1, that stably colonize the murine GI tract in three different animal facilities under conditions where SC5314 is lost from this niche. Analysis of the bacterial microbiota did not show notable differences among mice colonized with the three C. albicans strains. We compared the genotypes and phenotypes of these three strains and identified thousands of single nucleotide polymorphisms (SNPs) and multiple phenotypic differences, including their ability to grow and filament in response to nutritional cues. Despite striking filamentation differences under laboratory conditions, however, analysis of cell morphology in the GI tract revealed that the three isolates exhibited similar filamentation properties in this in vivo niche. Notably, we found that SC5314 is more sensitive to the antimicrobial peptide CRAMP, and the use of CRAMP-deficient mice modestly increased the ability of SC5314 to colonize the GI tract relative to CHN1 and 529L. These studies provide new insights into how strain-specific differences impact C. albicans traits in the host and advance CHN1 and 529L as relevant strains to study C. albicans pathobiology in its natural host niche.
DOI:
10.1093/g3journal/jkab110
发表时间:
2021-07-14
期刊:
G3 (Bethesda, Md.)
影响因子:
--
作者:
Thomson GJ;Kakade P;Hirakawa MP;Ene IV;Bennett RJ
通讯作者:
Bennett RJ