Intestinal Dysbiosis in Young Cystic Fibrosis Rabbits.
Intestinal Dysbiosis in Young Cystic Fibrosis Rabbits.
复制标题
囊性纤维化幼兔肠道生态失调。
DOI:
10.3390/jpm11020132
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发表时间:
2021-02-16
影响因子:
--
通讯作者:
Xu J
中科院分区:
文献类型:
--
作者:
Liang X;Bouhamdan M;Hou X;Zhang K;Song J;Hao K;Jin JP;Zhang Z;Xu J
Individuals with cystic fibrosis (CF) often experience gastrointestinal (GI) abnormalities. In recent years, the intestinal microbiome has been postulated as a contributor to the development of CF-associated GI complications, hence representing a potential therapeutic target for treatment. We recently developed a rabbit model of CF, which is shown to manifest many human patient-like pathological changes, including intestinal obstruction. Here, we investigated the feces microbiome in young CF rabbits in the absence of antibiotics treatment. Stool samples were collected from seven- to nine-week-old CF rabbits (n = 7) and age-matched wild-type (WT) rabbits (n = 6). Microbiomes were investigated by iTag sequencing of 16S rRNA genes, and functional profiles were predicted using PICRUSt. Consistent with reports of those in pediatric CF patients, the fecal microbiomes of CF rabbits are of lower richness and diversity than that of WT rabbits, with a marked taxonomic and inferred functional dysbiosis. Our work identified a new CF animal model with the manifestation of intestinal dysbiosis phenotype. This model system may facilitate the research and development of novel treatments for CF-associated gastrointestinal diseases.
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影响因子:
14.9
作者:
Kanehisa M;Goto S;Sato Y;Furumichi M;Tanabe M
通讯作者:
Tanabe M
影响因子:
15.5
作者:
Fadrosh DW;Ma B;Gajer P;Sengamalay N;Ott S;Brotman RM;Ravel J
通讯作者:
Ravel J
DOI:
10.1111/j.2517-6161.1995.tb02031.x
发表时间:
1995-01-01
影响因子:
5.8
作者:
BENJAMINI, Y;HOCHBERG, Y
通讯作者:
HOCHBERG, Y
影响因子:
3.2
作者:
Antosca, Katherine M.;Chernikova, Diana A.;Madan, Juliette C.
通讯作者:
Madan, Juliette C.
影响因子:
5.5
作者:
Laselva, Onofrio;Stone, Tracy A.;Deber, Charles M.
通讯作者:
Deber, Charles M.