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聚合酶链式反应-变性梯度凝胶电泳分析蚯蚓体内、肠道和粪便中的细菌群落结构。

Polymerase chain reaction-denaturing gradient gel electrophoresis analysis of bacterial community structure in the food, intestines, and feces of earthworms.

机构信息

Division of Biological Science and Technology, Yonsei University, Wonju 220-710, Republic of Korea.

出版信息

J Microbiol. 2011 Aug;49(4):544-50. doi: 10.1007/s12275-011-0423-8. Epub 2011 Sep 2.

DOI:10.1007/s12275-011-0423-8
PMID:21887635
Abstract

The bacterial communities in the food, intestines, and feces of earthworms were investigated by PCR-denaturing Gradient gel electrophoresis (DGGE). In this study, PCR-DGGE was optimized by testing 6 universal primer sets for microbial 16S rRNA in 6 pure culture strains of intestinal microbes in earthworms. One primer set effectively amplified 16S rRNA from bacterial populations that were found in the food, intestines, and feces of earthworms. Compared with the reference markers from the pure culture strains, the resulting DGGE profiles contained 28 unique DNA fragments. The dominant microorganisms in the food, intestines, and feces of earthworms included Rhodobacterales bacterium, Fusobacteria, Ferrimonas marina, Aeromonas popoffii, and soil bacteria. Other straisn, such as Acinetobacter, Clostridium, and Veillonella, as well as rumen bacteria and uncultured bacteria also were present. These results demonstrated that PCR-DGGE analysis can be used to elucidate bacterial diversity and identify unculturable microorganisms.

摘要

采用 PCR-变性梯度凝胶电泳(DGGE)技术研究了蚯蚓体内、肠道和粪便中的细菌群落。本研究通过对 6 株蚯蚓肠道微生物纯培养物的 6 种通用引物进行测试,优化了 PCR-DGGE。其中一组引物能够有效地从蚯蚓体内、肠道和粪便中的细菌种群中扩增出 16S rRNA。与纯培养菌株的参考标记相比,得到的 DGGE 图谱含有 28 个独特的 DNA 片段。蚯蚓体内、肠道和粪便中的优势微生物包括红杆菌目(Rhodobacterales bacterium)、梭菌纲(Fusobacteria)、海栖费氏菌(Ferrimonas marina)、波弗特氏菌(Aeromonas popoffii)和土壤细菌。其他菌株,如不动杆菌(Acinetobacter)、梭菌(Clostridium)和韦荣球菌(Veillonella)以及瘤胃细菌和未培养细菌也存在。这些结果表明,PCR-DGGE 分析可用于阐明细菌多样性并鉴定不可培养的微生物。

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