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采用新型实时聚合酶链反应策略检测登革热、西尼罗河病毒、立克次体病和钩端螺旋体病。

Detection of dengue, west Nile virus, rickettsiosis and leptospirosis by a new real-time PCR strategy.

作者信息

García-Ruíz Daniel, Martínez-Guzmán Marco A, Cárdenas-Vargas Albertina, Marino-Marmolejo Erika, Gutiérrez-Ortega Abel, González-Díaz Esteban, Morfin-Otero Rayo, Rodríguez-Noriega Eduardo, Pérez-Gómez Hector, Elizondo-Quiroga Darwin

机构信息

Dirección de Biotecnología Médica y Farmacéutica, Centro de Investigación y Asistencia en Tecnología y Diseño del Estado de Jalisco (CIATEJ), Avenida Normalistas No. 800, Colinas de la Normal, C.P. 44270 Guadalajara, Jalisco Mexico.

Departamento de Infectología, Hospital Civil Fray Antonio Alcalde, Calle Hospital No. 270, El Retiro, 44200 Guadalajara, Jalisco Mexico.

出版信息

Springerplus. 2016 May 20;5(1):671. doi: 10.1186/s40064-016-2318-y. eCollection 2016.

Abstract

Dengue virus (DENV) infection causes sudden fever along with several nonspecific signs and symptoms and in severe cases, death. DENV is transmitted to people by Aedes aegypti and Ae. albopictus mosquitoes, whose populations increase during rainy season. West Nile Virus (WNV), Rickettsia spp. and Leptospira spp. are fever-causing pathogens that share many of the initial symptoms of DENV infection and also thrive in the rainy season. Outbreaks in some regions may be due to any of these pathogens that can co-circulate. Plus, they are clinically indistinguishable until severe symptoms appear, even though these diseases should be treated differently. An effective differential diagnosis would help clinicians and vector control departments to make right decisions for control and treatment of these diseases. Therefore, we developed four different SYBR green (®) -based reverse transcription quantitative PCR (RT-qPCR) assays for simultaneous detection of DENV, WNV, Rickettsia spp. and Leptospira spp. The assay has been optimized to yield results in less than 1 h; and in order to reduce contamination risk, all reagents were premixed and lyophilized on 96 well plates and thus only requires the addition of water and total nucleic acids from the sample. Sensitivities of the assays were less than 100 copies of nucleic acid targeted for these four pathogens. Assays did not show cross reactivity with any of the four pathogens nor to human nucleic acids. We are presenting a sensitive and selective kit that detects four relevant pathogens from tropical regions, that is quick, cost-effective and easy to use.

摘要

登革病毒(DENV)感染会引发突发发热以及多种非特异性体征和症状,严重时可导致死亡。DENV通过埃及伊蚊和白纹伊蚊传播给人类,这些蚊子的数量在雨季会增加。西尼罗河病毒(WNV)、立克次氏体属和钩端螺旋体属是引发发热的病原体,它们与DENV感染有许多初始症状相同,且在雨季也大量繁殖。某些地区的疫情可能是由这些能够共同传播的病原体中的任何一种引起的。此外,在严重症状出现之前,它们在临床上难以区分,尽管这些疾病的治疗方法不同。有效的鉴别诊断将有助于临床医生和病媒控制部门对这些疾病的控制和治疗做出正确决策。因此,我们开发了四种基于SYBR green(®)的逆转录定量PCR(RT-qPCR)检测方法,用于同时检测DENV、WNV、立克次氏体属和钩端螺旋体属。该检测方法已优化,可在不到1小时内得出结果;为降低污染风险,所有试剂预先混合并冻干在96孔板上,因此只需加入水和样品中的总核酸。这些检测方法对这四种病原体的核酸敏感性均低于100拷贝。检测方法对这四种病原体中的任何一种以及人类核酸均未显示交叉反应性。我们展示了一种灵敏且具选择性的试剂盒,可检测来自热带地区的四种相关病原体,该试剂盒快速、经济高效且易于使用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a55/4899400/8637dc648c2c/40064_2016_2318_Fig3_HTML.jpg

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