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基于线粒体DNA细胞色素氧化酶亚基II区域的物种特异性检测法对库氏按蚊复合种成员的鉴定评估

Evaluation of the mtDNA-COII Region Based Species Specific Assay for Identifying Members of the Anopheles culicifacies Species Complex.

作者信息

Manonmani Arulsamy Mary, Mathivanan Ashok Kumar, Sadanandane Candassamy, Jambulingam Purushothaman

机构信息

Vector Control Research Centre, Medical Complex, Indira Nagar, Puducherry, India.

出版信息

J Arthropod Borne Dis. 2013 Aug 31;7(2):154-63. eCollection 2013.

Abstract

BACKGROUND

Anopheles culicifacies, a major malarial vector has been recognized as a complex of five sibling species, A, B, C, D and E. These sibling species exhibit varied vectorial capacity, host specificity and susceptibility to malarial parasites/ insecticides. In this study, a PCR assay developed earlier for distinguishing the five individual species was validated on samples of An. culicifacies collected from various parts of India.

METHODS

The samples were initially screened using the rDNA-ITS2 region based primers which categorised the samples into either A/D group or B/C/E group. A proportion of samples belonging to each group were subjected to the mtDNA-COII PCR assay for identifying individual species.

RESULTS

Among the 615 samples analysed by rDNA-ITS2 PCR assay, 303 were found to belong to A/D group and 299 to B/C/E group while 13 turned negative. Among 163 samples belonging to A/D group, only one sample displayed the profile characteristic of species A and among the 176 samples falling in the B/C/E group, 51 were identified as species B, 14 as species C and 41 as species E respectively by the mtDNA-COII PCR assay. Samples exhibiting products diagnostic of B/C/E, when subjected to PCR-RFLP assay identified 15 samples as species E.

CONCLUSION

Validation of the mtDNA-COII PCR assay on large number of samples showed that this technique cannot be used universally to distinguish the 5 members of this species complex, as it has been designed based on minor/single base differences observed in the COII region.

摘要

背景

嗜人按蚊是主要的疟疾传播媒介,已被确认为由五个姐妹种A、B、C、D和E组成的复合体。这些姐妹种表现出不同的传病能力、宿主特异性以及对疟原虫/杀虫剂的易感性。在本研究中,对先前开发的用于区分这五个单独物种的PCR检测方法在从印度各地收集的嗜人按蚊样本上进行了验证。

方法

最初使用基于核糖体DNA内转录间隔区2(rDNA-ITS2)区域的引物对样本进行筛选,将样本分为A/D组或B/C/E组。对每组中的一部分样本进行线粒体DNA细胞色素氧化酶亚基II(mtDNA-COII)PCR检测以鉴定单个物种。

结果

在通过rDNA-ITS2 PCR检测分析的615个样本中,303个属于A/D组,299个属于B/C/E组,13个呈阴性。在属于A/D组的163个样本中,只有一个样本显示出物种A的特征图谱;在属于B/C/E组的176个样本中,通过mtDNA-COII PCR检测分别鉴定出51个为物种B,14个为物种C,41个为物种E。表现出诊断B/C/E特征产物的样本,经PCR限制性片段长度多态性(PCR-RFLP)检测鉴定出15个样本为物种E。

结论

对大量样本进行mtDNA-COII PCR检测的验证表明,由于该技术是基于在细胞色素氧化酶亚基II区域观察到的微小/单碱基差异设计的,因此不能普遍用于区分该物种复合体的5个成员。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed5/3875882/846daecf1334/jad-7-154f1.jpg

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