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基于16S rRNA基因序列的系统发育分析揭示了牦牛(Bos grunniens)瘤胃细菌的多样性。

Phylogenetic analysis of 16S rRNA gene sequences reveals rumen bacterial diversity in Yaks (Bos grunniens).

作者信息

Yang L Y, Chen J, Cheng X L, Xi D M, Yang S L, Deng W D, Mao H M

机构信息

Faculty of Animal Science and Technology, Yunnan Agricultural University, Kunming, China.

出版信息

Mol Biol Rep. 2010 Jan;37(1):553-62. doi: 10.1007/s11033-009-9794-x.

Abstract

Six matured male Yaks (Bos grunniens) with a mean live weight of 450 +/- 23 kg (mean +/- SD), were housed indoors in metabolism cages and fed pelleted lucerne (Medicago sativum). After an adjustment period of 24 days of feeding the diet, samples of rumen content were obtained for analysis of the bacteria in the liquor. The diversity of rumen bacteria was investigated by constructing a 16S rRNA gene clone library using the general bacterial primers F27 and R1492. A total of 130 clones, comprising nearly full length sequences (approx. 1.5 kb) were sequenced and submitted to BLAST and phylogenetic analysis. Using the criterion that similarity of 97% or greater with the sequences of cultivated bacteria, 16 clones were identified as Butyrivibrio fibrisolvens, Pseudobutyrivibrio ruminis, Ruminococcus flavefaciens, Succiniclasticum ruminis, Selenomonas ruminantium and Prevotella ruminicola, respectively. A further 10 clones shared similarity ranging from 90 to 97% with cultivated bacteria but the similarity in sequences for the remaining 104 clones were less than 90% of those of cultivated bacteria. Using a phylogenetic analysis it was found that the majority of the clones identified (63.8%) were located in the Low G + C Subdivision, with most of the remainder (35.4% of clones) located in the Cytophaga-Flexibacter-Bacteroides phylum and one clone (0.8%) was identified as a Proteobacteria. It was apparent that Yaks have a large and diverse range of bacteria in the rumen content which differ from those of cattle and other ruminants.

摘要

选用6头成熟雄性牦牛(牦牛属),平均体重450±23千克(平均值±标准差),将其圈养在室内代谢笼中,投喂紫花苜蓿颗粒饲料(紫花苜蓿)。在投喂该日粮24天的适应期后,采集瘤胃液样本以分析其中的细菌。使用通用细菌引物F27和R1492构建16S rRNA基因克隆文库,研究瘤胃细菌的多样性。共对130个包含近全长序列(约1.5 kb)的克隆进行测序,并提交至BLAST进行系统发育分析。根据与已培养细菌序列相似度达97%或更高的标准,分别鉴定出16个克隆为溶纤维丁酸弧菌、瘤胃假丁酸弧菌、黄化瘤胃球菌、瘤胃琥珀酸分解菌、反刍月形单胞菌和瘤胃普雷沃氏菌。另有10个克隆与已培养细菌的相似度在90%至97%之间,但其余104个克隆的序列相似度低于已培养细菌的90%。通过系统发育分析发现,鉴定出的大多数克隆(63.8%)位于低G + C分类群,其余大部分克隆(占克隆总数的35.4%)位于噬纤维菌-屈挠杆菌-拟杆菌门,1个克隆(0.8%)被鉴定为变形菌门。显然,牦牛瘤胃液中的细菌种类繁多且多样,与牛和其他反刍动物不同。

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