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光杆状菌属和异小杆线虫属分离株的分子鉴定及遗传多样性

Molecular identification and genetic diversity among Photorhabdus and Xenorhabdus isolates.

作者信息

Moghaieb Reda E A, Abdelhadi Abdelhadi A, El-Sadawy Hanan A, Allam Nesreen A T, Baiome Baiome Abdelmaguid, Soliman Mohamed H

机构信息

Department of Genetics and Genetic Engineering Research Center (GERC), Faculty of Agriculture Cairo University, Giza, 12613, Egypt.

College of Biotechnology, University of Modern Science, UAE, 232816, Dubai, United Arab Emirates.

出版信息

3 Biotech. 2017 May;7(1):6. doi: 10.1007/s13205-016-0594-4. Epub 2017 Apr 8.

Abstract

Five bacterial strains were isolated from the hemocoel of the greater wax moth larvae (Galleria mellonella) infected with the entomopathogenic nematodes: Heterorhabditis bacteriophora HP88, Heterorhabditis indicus RM1 and Heterorhabditis sp (S1), Steinernema abbasi and Steinernema sp. (S II). Strains were identified as Photorhabdus luminescens HRM1, P. luminescens HS1, P. luminescens HP88, Xenorhabdus indica and X. nematophila ATTC19061 using 16S rDNA sequence analysis. To reveal the genetic diversity among these strains, three molecular markers (RAPD, ISSR and SRAP) were employed. RAPD analysis showed 73.8 and 54.5 polymorphism percentages for the Photorhabdus and Xenorhabdus strains, respectively. ISSR analysis resulted in 70.1 and 75.2 polymorphism percentages among the Photorhabdus and Xenorhabdus strains, respectively. The SRAP analysis indicated that 75.6 and 61.2% genetic polymorphism was detected among Photorhabdus and Xenorhabdus strains, respectively. The cluster analysis grouped the three Photorhabdus strains together in one cluster and the two Xenorhabdus strains together in another cluster indicating the phylogenetic relationships among them. The genotype-specific markers detected from the three molecular markers (RAPD, ISSR and SRAP) were sufficient to distinguish between the different bacterial strains tested and can be used in the future IBM program that could be built on the use of these strains.

摘要

从感染了昆虫病原线虫的大蜡螟幼虫(大蜡螟)血腔中分离出五株细菌菌株,分别为:嗜菌异小杆线虫HP88、印度异小杆线虫RM1和异小杆线虫属(S1)、阿巴斯斯氏线虫和斯氏线虫属(S II)。通过16S rDNA序列分析,这些菌株被鉴定为发光光杆状菌HRM1、发光光杆状菌HS1、发光光杆状菌HP88、嗜线虫致病杆菌和嗜线虫致病杆菌ATTC19061。为揭示这些菌株之间的遗传多样性,采用了三种分子标记(随机扩增多态性DNA、简单序列重复区间扩增和相关序列扩增多态性)。随机扩增多态性DNA分析显示,发光光杆状菌和嗜线虫致病杆菌菌株的多态性百分比分别为73.8%和54.5%。简单序列重复区间扩增分析分别在发光光杆状菌和嗜线虫致病杆菌菌株中产生了70.1%和75.2%的多态性百分比。相关序列扩增多态性分析表明,发光光杆状菌和嗜线虫致病杆菌菌株中分别检测到75.6%和61.2%的遗传多态性。聚类分析将三株发光光杆状菌菌株聚为一个簇,两株嗜线虫致病杆菌菌株聚为另一个簇,表明了它们之间的系统发育关系。从三种分子标记(随机扩增多态性DNA、简单序列重复区间扩增和相关序列扩增多态性)中检测到的基因型特异性标记足以区分所测试的不同细菌菌株,并且可用于未来基于这些菌株使用构建的IBM程序。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb77/5385175/c8313f24d5a6/13205_2016_594_Fig1_HTML.jpg

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