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鸭源和鹅源细小病毒对北京鸭雏的致病性。

Pathogenicity of Pekin duck- and goose-origin parvoviruses in Pekin ducklings.

机构信息

Key Laboratory of Animal Epidemiology of the Ministry of Agriculture, College of Veterinary Medicine, China Agricultural University, Beijing, China.

Key Laboratory of Animal Epidemiology of the Ministry of Agriculture, College of Veterinary Medicine, China Agricultural University, Beijing, China.

出版信息

Vet Microbiol. 2017 Oct;210:17-23. doi: 10.1016/j.vetmic.2017.08.020. Epub 2017 Aug 31.

Abstract

Goose parvovirus (GPV) usually affects goslings and Muscovy ducks but not Pekin ducks. Earlier works showed that a variant GPV can cause short beak and dwarfism syndrome (SBDS) in Pekin ducks. Here, we investigated the pathogenicity of a variant GPV of Pekin duck-origin (JS1) and a classical GPV of goose-origin (H) in Pekin ducklings. Following intramuscular infection at two days of age, both JS1 and H strains influenced weight gain and development of beaks and bones of wings and legs, and caused microscopic lesions of internal organs of ducks. However, the clinical signs typical of SBDS could only be replicated with the JS1 isolate. The findings suggest that both variant and classical GPVs are pathogenic for Pekin ducklings, while the former is more virulent than the latter. Using a quantitative real-time PCR assay, high levels of viral load were detected from bloods, internal organs, leg muscles, and ileac contents in JS1- and H-infected ducks from 6h to 35days postinfection (DPI). Using a GPV VP3-based ELISA, antibodies in sera of JS1- and H-infected ducks were detectable at 1 DPI and then persistently rose during the subsequent five weeks. These results suggest that both variant and classical GPVs can infect Pekin ducklings. The present work contributes to the understanding of pathogenicity of GPV to Pekin ducks and may provide clues to pathogenesis of GPV-related SBDS.

摘要

鹅细小病毒(GPV)通常感染鹅和麝香鸭,但不感染北京鸭。早期的研究表明,一种变异的 GPV 可导致北京鸭发生短喙矮小型综合征(SBDS)。本研究中,我们调查了一株源自北京鸭的变异型 GPV(JS1)和一株源自鹅的经典型 GPV(H)在雏鸭中的致病性。在雏鸭 2 日龄时肌肉注射感染后,JS1 和 H 株均影响了雏鸭的体重增长和喙与翅膀、腿部骨骼的发育,并引起了鸭内脏器官的显微镜下病变。然而,只有 JS1 分离株才能复制出典型的 SBDS 临床症状。这些结果表明,变异型和经典型 GPV 均对北京鸭易感,而前者比后者的毒力更强。使用实时定量 PCR 检测,在感染 JS1 和 H 的鸭的血液、内脏器官、腿部肌肉和回肠内容物中,从感染后 6 小时到 35 天(DPI)均可检测到高水平的病毒载量。使用基于 GPV VP3 的 ELISA 检测,在感染 JS1 和 H 的鸭的血清中,1 DPI 时即可检测到抗体,随后在接下来的 5 周内持续升高。这些结果表明,变异型和经典型 GPV 均可感染北京鸭。本研究有助于了解 GPV 对北京鸭的致病性,也可能为 GPV 相关 SBDS 的发病机制提供线索。

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