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光滑双脐螺作为曼氏血吸虫中间宿主时,对其潜伏期感染的分子检测

Molecular detection of prepatent Schistosoma mansoni infection in Biomphalaria glabrata snail vectors.

作者信息

Casotti Márcia Oliveira, Gryschek Ronaldo Cesar Borges, Paula Fabiana Martins de, Gomes-Gouvêa Michele, Pinho João Renato Rebello, Tuan Roseli, Dias-Neto Emmanuel, Luna Expedito José de Albuquerque, Espírito-Santo Maria Cristina Carvalho do

机构信息

Universidade de São Paulo, Faculdade de Medicina, Departamento de Moléstias Infecciosas e Parasitárias, Laboratório de Imunopatologia da Esquistossomose (LIM-06), São Paulo, São Paulo, Brazil.

Universidade de São Paulo, Instituto de Medicina Tropical da São Paulo, Laboratório de Helmintologia, São Paulo, São Paulo, Brazil.

出版信息

Rev Inst Med Trop Sao Paulo. 2020 Mar 2;62:e17. doi: 10.1590/S1678-9946202062017. eCollection 2020.

Abstract

Approximately 240 million people worldwide are infected by Schistosoma. In Brazil, one of the main intermediate hosts of this parasite is Biomphalaria glabrata snails. The early detection of larval stages in intermediate hosts is an important challenge to public health, but it also represents an opportunity as a new alternative to indicate earlier natural infections before cercariae differentiation and emergence. In this context, we demonstrated that PCR amplification of a 28S gene fragment from the parasite does demonstrate S. mansoni infection in snails 14 days post infection. This conventional polymerase chain reaction amplified clear bands and was able to detect parasitic infection in the intermediate host B. glabrata under experimental conditions. However, we reinforce that this approach requires deeper investigations and further comparisons to confirm its specificity and sensitivity in earlier time points after miracidia infection. This approach has relevant potential as an effective molecular-based strategy for the monitoring of schistosomiasis transmission.

摘要

全球约有2.4亿人感染血吸虫。在巴西,这种寄生虫的主要中间宿主之一是光滑双脐螺。在中间宿主中早期检测幼虫阶段对公共卫生来说是一项重大挑战,但这也代表了一个机会,可作为一种新的替代方法,在尾蚴分化和出现之前更早地指示自然感染。在此背景下,我们证明,从寄生虫中扩增28S基因片段的PCR确实能在感染后14天检测到光滑双脐螺感染曼氏血吸虫。这种传统的聚合酶链反应扩增出了清晰的条带,并且能够在实验条件下检测中间宿主光滑双脐螺中的寄生虫感染。然而,我们强调,这种方法需要更深入的研究和进一步比较,以确认其在毛蚴感染后更早时间点的特异性和敏感性。作为一种基于分子的有效策略,这种方法在监测血吸虫病传播方面具有重要潜力。

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