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马来西亚黄病毒重要血清复合物的分布情况。

The distribution of important sero-complexes of flaviviruses in Malaysia.

作者信息

Kumar Kiven, Arshad Siti Suri, Toung Ooi Peck, Abba Yusuf, Selvarajah Gayathri Thevi, Abu Jalila, A R Yasmin, Ong Bee Lee, Bande Faruku

机构信息

Department of Veterinary Pathology and Microbiology, Faculty of Veterinary Medicine, Universiti Putra Malaysia, UPM, 43400, Serdang, Selangor, Malaysia.

Department of Veterinary Clinical Studies, Faculty of Veterinary Medicine, Universiti Putra Malaysia, UPM, 43400, Serdang, Selangor, Malaysia.

出版信息

Trop Anim Health Prod. 2019 Mar;51(3):495-506. doi: 10.1007/s11250-018-01786-x. Epub 2019 Jan 2.

DOI:10.1007/s11250-018-01786-x
PMID:30604332
Abstract

Flaviviruses (FVs) are arthropod-borne viruses of medical and veterinary importance. Numerous species of FVs have been isolated from various host; mainly humans, animals, ticks, and mosquitoes. Certain FVs are extremely host-specific; at the same time, some FVs can infect an extensive range of species. Based on published literatures, 11 species of FVs have been detected from diverse host species in Malaysia. In humans, dengue virus and Japanese encephalitis virus have been reported since 1901 and 1942. In animals, the Batu Cave virus, Sitiawan virus, Carey Island, Tembusu virus, Duck Tembusu virus, and Japanese encephalitis viruses were isolated from various species. In mosquitoes, Japanese encephalitis virus and Kunjin virus were isolated from Culex spp., while Zika virus and Jugra virus were isolated from Aedes spp. In ticks, the Langat virus was isolated from Ixodes spp. One of the major challenges in the diagnosis of FVs is the presence of sero-complexes as a result of cross-reactivity with one or more FV species. Subsequently, the distribution of specific FVs among humans and animals in a specific population is problematic to assess and often require comprehensive and thorough analyses. Molecular assays such as quantitative reverse transcriptase polymerase chain reaction (qRT-PCR) and digital droplet RT-PCR (ddRT-PCR) have been used for the differentiation of flavivirus infections to increase the accuracy of epidemiological data for disease surveillance, monitoring, and control. In situations where sero-complexes are common in FVs, even sensitive assays such as qRT-pCR can produce false positive results. In this write up, an overview of the various FV sero-complexes reported in Malaysia to date and the challenges faced in diagnosis of FV infections are presented.

摘要

黄病毒(FVs)是对医学和兽医领域具有重要意义的节肢动物传播病毒。众多黄病毒物种已从各种宿主中分离出来,主要包括人类、动物、蜱虫和蚊子。某些黄病毒具有极强的宿主特异性;与此同时,一些黄病毒可感染广泛的物种。根据已发表的文献,在马来西亚已从不同宿主物种中检测到11种黄病毒。在人类中,自1901年和1942年以来分别报告了登革热病毒和日本脑炎病毒。在动物中, Batu Cave病毒、实兆远病毒、凯里岛病毒、坦布苏病毒、鸭坦布苏病毒和日本脑炎病毒已从不同物种中分离出来。在蚊子中,日本脑炎病毒和库京病毒从库蚊属中分离出来,而寨卡病毒和朱格拉病毒从伊蚊属中分离出来。在蜱虫中,兰加特病毒从硬蜱属中分离出来。黄病毒诊断的主要挑战之一是由于与一种或多种黄病毒物种发生交叉反应而存在血清复合物。随后,评估特定人群中人类和动物之间特定黄病毒的分布存在问题,通常需要进行全面而深入的分析。诸如定量逆转录聚合酶链反应(qRT-PCR)和数字液滴RT-PCR(ddRT-PCR)等分子检测方法已用于区分黄病毒感染,以提高疾病监测、监测和控制的流行病学数据的准确性。在黄病毒中血清复合物常见的情况下,即使是qRT-pCR等敏感检测方法也可能产生假阳性结果。在本报告中,概述了迄今为止在马来西亚报告的各种黄病毒血清复合物以及黄病毒感染诊断中面临的挑战。

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本文引用的文献

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Shedding of Japanese Encephalitis Virus in Oral Fluid of Infected Swine.感染猪口腔液中乙型脑炎病毒的脱落
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