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从伊朗西北部分离出的内共生菌(立克次氏体目:无形体科)的分子检测与系统发育分析

Molecular Detection and Phylogenetic Analysis of Endosymbiont (Rickettsiales: Anaplasmataceae) Isolated from in Northwest of Iran.

作者信息

Khanmohammadi Majid, Falak Reza, Meamar Ahmad Reza, Arshadi Mehdi, Akhlaghi Lame, Razmjou Elham

机构信息

Department of Parasitology and Mycology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.

Department of Laboratory Science, Marand Branch, Islamic Azad University, Marand, Iran.

出版信息

J Arthropod Borne Dis. 2019 Mar 30;13(1):83-93. eCollection 2019 Mar.

Abstract

BACKGROUND

The purpose of this study was molecular detection and phylogenetic analysis of species of .

METHODS

Adult filarial nematodes were collected from the cardiovascular and pulmonary arterial systems of naturally infected dogs, which caught in different geographical areas of Meshkin Shahr in Ardabil Province, Iran, during 2017. genomic DNA were extracted. Phylogenetic analysis for proofing of was carried out using cytochrome oxidase I () gene. Afterward, the purified DNA was used to determine the molecular pattern of the surface protein () gene sequence by PCR.

RESULTS

Phylogeny and homology studies showed high consistency of the gene with the previously-registered sequences for . Comparison of DNA sequences revealed no nucleotide variation between them. PCR showed that all of the collected parasites were infected with . The sequence of the gene in species from was significantly different from other species of as well as other filarial species. The maximum homology was observed with the isolated from . The greatest distance between nucleotides of species found between and those isolated from .

CONCLUSION

PCR could be a simple but suitable method for detection of species. There is a pattern of host specificity between and that can be related to ancestral evolutions. The results of this phylogenetic analysis and molecular characterization may help us for better identification of species and understanding of their coevolution.

摘要

背景

本研究的目的是对[具体物种名称]进行分子检测和系统发育分析。

方法

2017年期间,从伊朗阿尔达比勒省梅什金沙尔不同地理区域捕获的自然感染犬的心血管和肺动脉系统中收集成年丝虫线虫。提取基因组DNA。使用细胞色素氧化酶I(COI)基因进行系统发育分析以验证[具体物种名称]。之后,将纯化的DNA用于通过PCR确定[具体物种名称]表面蛋白(SP)基因序列的分子模式。

结果

系统发育和同源性研究表明,COI基因与先前登记的[具体物种名称]序列高度一致。DNA序列比较显示它们之间没有核苷酸变异。PCR表明所有收集的寄生虫均感染了[具体物种名称]。来自[具体地区]的[具体物种名称]的SP基因序列与[具体物种名称]的其他物种以及其他丝虫物种有显著差异。与从[具体地区]分离的[具体物种名称]观察到最大同源性。在[具体地区]发现的[具体物种名称]的核苷酸与从[其他地区]分离的那些之间的距离最大。

结论

PCR可能是检测[具体物种名称]的一种简单但合适的方法。[具体物种名称]与[宿主名称]之间存在宿主特异性模式,这可能与祖先进化有关。这种系统发育分析和分子特征的结果可能有助于我们更好地鉴定[具体物种名称]并了解它们的共同进化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/365b/6643019/a8fc9d12f011/JAD-13-83-g001.jpg

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