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不同引物检测 Anastrepha(双翅目:瘿蚊科)中 Wolbachia 的灵敏度变化。

Variations in the sensitivity of different primers for detecting Wolbachia in Anastrepha (diptera: tephritidae).

机构信息

Departamento de Genética, Instituto de Biociências, Universidade Estadual Paulista Júlio de Mesquita Filho , Botucatu, SP , Brasil.

出版信息

Braz J Microbiol. 2011 Apr;42(2):778-85. doi: 10.1590/S1517-838220110002000046. Epub 2011 Jun 1.

Abstract

Wolbachia are endosymbiont bacteria of the family Rickettsiacea that are widespread in invertebrates and occur between 20% and 60% of Neotropical insects. These bacteria are responsible for reproductive phenomena such as cytoplasmic incompatibility, male killing, feminization and parthenogenesis. Supergroups A and B of Wolbachia are common in insects and can be identified using primers for 16S rDNA, ftsZ and wsp; these primers vary in their ability to detect Wolbachia. The ftsZ primer was the first primer used to detect Wolbachia in Anastrepha fruit flies. The primers for 16S rDNA, ftsZ and wsp and the corresponding PCR conditions have been optimized to study the distribution of Wolbachia and their effect on the biology of Anastrepha in Brazil. In this work, we examined the ability of these primers to detect Wolbachia in Anastrepha populations from three regions in the State of São Paulo, southeastern Brazil. All of the samples were positive for Wolbachia supergroup A when screened with primers for 16S A rDNA and wsp A; the wsp B primer also gave a positive result, indicating cross-reactivity. The ftsZ primer showed a poor ability to detect Wolbachia in Anastrepha and generated false negatives in 44.9% of the samples. These findings indicate that reliable PCR detection of Wolbachia requires the use of primers for 16S rDNA and wsp to avoid cross-reactions and false negatives, and that the ftsZ primer needs to be redesigned to improve its selectivity.

摘要

沃尔巴克氏体是立克次体科的内共生细菌,广泛存在于无脊椎动物中,在 20%至 60%的新热带昆虫中出现。这些细菌负责细胞质不亲和、雄性致死、雌性化和孤雌生殖等生殖现象。沃尔巴克氏体的 A 组和 B 组超群在昆虫中很常见,可以使用 16S rDNA、ftsZ 和 wsp 的引物来识别;这些引物在检测沃尔巴克氏体的能力上有所不同。ftsZ 引物是第一个用于检测番石榴实蝇中沃尔巴克氏体的引物。用于 16S rDNA、ftsZ 和 wsp 的引物和相应的 PCR 条件已被优化,以研究沃尔巴克氏体在巴西的分布及其对番石榴生物学的影响。在这项工作中,我们研究了这些引物在巴西圣保罗州三个地区的番石榴种群中检测沃尔巴克氏体的能力。当用 16S rDNA 和 wsp A 的引物进行筛选时,所有的样本都对沃尔巴克氏体 A 超群呈阳性;wsp B 引物也产生了阳性结果,表明存在交叉反应。ftsZ 引物检测番石榴中的沃尔巴克氏体的能力较差,在 44.9%的样本中产生了假阴性。这些发现表明,为了避免交叉反应和假阴性,可靠的 PCR 检测沃尔巴克氏体需要使用 16S rDNA 和 wsp 的引物,并且需要重新设计 ftsZ 引物以提高其选择性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f59/3769819/a79c924c2ab3/bjm-42-778-g001.jpg

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