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首页> 外文期刊>Memorias do Instituto Oswaldo Cruz >Detection of Leishmania infantum in naturally infected Lutzomyia longipalpis (Diptera: Psychodidae: Phlebotominae) and Canis familiaris in Misiones, Argentina: the first report of a PCR-RFLP and sequencing-based confirmation assay
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Detection of Leishmania infantum in naturally infected Lutzomyia longipalpis (Diptera: Psychodidae: Phlebotominae) and Canis familiaris in Misiones, Argentina: the first report of a PCR-RFLP and sequencing-based confirmation assay

机译:在阿根廷米西奥内斯(Misiones)的自然感染的长足Lutzomyia longipalpis(双翅目:Psychodidae:Phlebotominae)和Canisaffariis中检测婴儿利什曼原虫:PCR-RFLP和基于测序的确证测定法的首次报道

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In this study, a genotypification of Leishmania was performed using polimerase chain reaction-restriction fragment length polymorfism (PCR-RFLP) and sequencing techniques to identify species of Leishmania parasites in phlebotomine sand flies and dogs naturally infected. Between January-February of 2009, CDC light traps were used to collect insect samples from 13 capture sites in the municipality of Posadas, which is located in the province of Misiones of Argentina. Sand flies identified as Lutzomyia longipalpis were grouped into 28 separate pools for molecular biological analysis. Canine samples were taken from lymph node aspirates of two symptomatic stray animals that had been positively diagnosed with canine visceral leishmaniasis. One vector pool of 10 sand flies (1 out of the 28 pools tested) and both of the canine samples tested positively for Leishmania infantum by PCR and RFLP analysis. PCR products were confirmed by sequencing and showed a maximum identity with L. infantum. Given that infection was detected in one out of the 28 pools and that at least one infected insect was infected, it was possible to infer an infection rate at least of 0.47% for Lu. longipalpis among the analyzed samples. These results contribute to incriminate Lu. longipalpis as the vector of L. infantumin the municipality of Posadas, where cases of the disease in humans and dogs have been reported since 2005.
机译:在这项研究中,利什曼原虫的基因分型是通过使用polimerase链反应限制片段长度多态性(PCR-RFLP)和测序技术进行的,以鉴定静脉毒沙蝇和自然感染的狗中的利什曼原虫的种类。在2009年1月至2月之间,疾病预防控制中心的光阱被用于收集位于阿根廷米西奥内斯省Posadas市13个捕获点的昆虫样本。被鉴定为长鳍金枪鱼的沙蝇被分成28个单独的池,用于分子生物学分析。犬样本取自两只有症状的流浪动物的淋巴结抽吸物,这些动物已被确诊为犬内脏利什曼病。一个载体池,由10个沙蝇组成(测试的28个池中有1个),并且通过PCR和RFLP分析对两种犬样品的婴儿利什曼原虫进行了阳性测试。通过测序确认PCR产物,并显示出与婴儿乳杆菌的最大同一性。假设在28个池中有一个检测到感染,并且至少感染了一只昆虫,则可以推断出Lu的感染率至少为0.47%。被分析样品中的longipalpis。这些结果助长了陆某的罪名。 longipalpis是波萨达斯市婴儿肺炎克雷伯氏菌的媒介,自2005年以来已有人和狗患此病的报道。

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