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犬细小病毒——流行病学和诊断方面的综述,重点介绍 2c 型。

Canine parvovirus--a review of epidemiological and diagnostic aspects, with emphasis on type 2c.

机构信息

Department of Veterinary Public Health, Faculty of Veterinary Medicine of Bari, Strada per Casamassima Km 3, 70010 Valenzano, Bari, Italy.

出版信息

Vet Microbiol. 2012 Feb 24;155(1):1-12. doi: 10.1016/j.vetmic.2011.09.007. Epub 2011 Sep 12.

Abstract

Canine parvovirus type 2 (CPV-2) emerged in late 1970s causing severe epizootics in kennels and dog shelters worldwide. Soon after its emergence, CPV-2 underwent genetic evolution giving rise consecutively to two antigenic variants, CPV-2a and CPV-2b that replaced progressively the original type. In 2000, a new antigenic variant, CPV-2c, was detected in Italy and rapidly spread to several countries. In comparison to the original type CPV-2, the antigenic variants display increased pathogenicity in dogs and extended host range, being able to infect and cause disease in cats. Epidemiological survey indicate that the newest type CPV-2c is becoming prevalent in different geographic regions and is often associated to severe disease in adult dogs and also in dogs that have completed the vaccination protocols. However, the primary cause of failure of CPV vaccination is interference by maternally derived immunity. Diagnosis of CPV infection by traditional methods has been shown to be poorly sensitive, especially in the late stages of infections. New diagnostic approaches based on molecular methods have been developed for sensitive detection of CPV in clinical samples and rapid characterisation of the viral type. Continuous surveillance will help assess whether there is a real need to update currently available vaccines and diagnostic tests.

摘要

犬细小病毒 2 型(CPV-2)于 20 世纪 70 年代末出现,导致全球犬舍和收容所爆发严重疫情。出现后不久,CPV-2 发生了遗传进化,相继产生了两种抗原变体 CPV-2a 和 CPV-2b,逐渐取代了原始类型。2000 年,意大利检测到一种新的抗原变体 CPV-2c,迅速传播到多个国家。与原始类型 CPV-2 相比,抗原变体在犬中的致病性增加,宿主范围扩大,能够感染并引起猫的疾病。流行病学调查表明,最新类型 CPV-2c 在不同地理区域流行,并常与成年犬的严重疾病以及已完成疫苗接种方案的犬的疾病有关。然而,CPV 疫苗接种失败的主要原因是母源抗体的干扰。传统方法诊断 CPV 感染的敏感性较差,尤其是在感染后期。已经开发出基于分子方法的新诊断方法,用于在临床样本中敏感检测 CPV 并快速确定病毒类型。持续监测将有助于评估是否有实际需要更新当前可用的疫苗和诊断测试。

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