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传染性法氏囊病病毒在无特定病原体肉鸡和商品肉鸡中的检测与持续存在情况。

Detection and persistence of infectious bursal disease virus in specific-pathogen-free and commercial broiler chickens.

作者信息

Abdel-Alim G A, Saif Y M

机构信息

Food Animal Health Research Program, Ohio Agricultural Research and Development Center, The Ohio State University, Wooster 44691, USA.

出版信息

Avian Dis. 2001 Jul-Sep;45(3):646-54.

Abstract

In an earlier study, specific-pathogen-free (SPF) chickens were inoculated with infectious bursal disease virus (IBDV) at 3 wk of age. Their bursas were examined for virus at different intervals postinoculation (PI) by reverse transcriptase (RT)/polymerase chain reaction (PCR) and by virus isolation in chicken embryos up to 21 days PI. The RT/PCR was positive, but attempts to isolate infectious virus from bursal homogenates failed. This prompted us to investigate the persistence of IBDV or its RNA in the bursa of Fabricius (BF) of inoculated and vaccinated SPF chicks and of inoculated and vaccinated commercial broiler chicks that have maternally derived antibodies. Four trials were conducted in SPF and commercial broiler chickens. Infectious virus was detected by embryo inoculation up to 7 days PI in the BF of SPF chickens inoculated at 2 or 3 wk of age and up to 21 days PI by RT/PCR, whereas the viral RNA was detected by RT/PCR for up to 28 days PI. In SPF chicks inoculated at 1 day of age, the bursa-derived virus or its RNA was detected at 7 and 14 days PI when inoculated at a high dose (10(4) mean embryo infective dose [EID50]/bird) or at a low dose (10(2.5) EID50/bird). In commercial 1-day-old broiler chicks, the bursa-derived virus was detected at 7 and 14 days PI when inoculated at a high dose (10(4) EID50/bird), whereas the virus was detected only at 14 days PI when inoculated at a low dose (10(2.5) EID50/bird). In SPF and commercial chicks vaccinated with a modified live IBDV vaccine, the virus or its RNA was detected at 7 and 14 days postvaccination in SPF chicks, but neither the live vaccine virus nor its RNA was detected in commercial broilers vaccinated at 1 day or 2 wk of age.

摘要

在一项早期研究中,对无特定病原体(SPF)鸡在3周龄时接种传染性法氏囊病病毒(IBDV)。在接种后(PI)的不同时间间隔,通过逆转录酶(RT)/聚合酶链反应(PCR)以及在鸡胚中进行病毒分离,直至接种后21天,对其法氏囊进行病毒检测。RT/PCR呈阳性,但从法氏囊匀浆中分离传染性病毒的尝试失败。这促使我们研究IBDV或其RNA在接种和接种疫苗的SPF雏鸡以及具有母源抗体的接种和接种疫苗的商品肉鸡雏鸡的法氏囊中持续存在的情况。在SPF鸡和商品肉鸡中进行了四项试验。通过鸡胚接种,在2或3周龄接种的SPF鸡的法氏囊中,直至接种后7天可检测到传染性病毒,通过RT/PCR直至接种后21天可检测到;而通过RT/PCR,直至接种后28天可检测到病毒RNA。在1日龄接种的SPF雏鸡中,当以高剂量(10⁴平均鸡胚感染剂量[EID50]/只)或低剂量(10².⁵EID50/只)接种时,在接种后7天和14天可检测到法氏囊来源的病毒或其RNA。在1日龄商品肉鸡雏鸡中,当以高剂量(10⁴EID50/只)接种时,在接种后7天和14天可检测到法氏囊来源的病毒,而当以低剂量(10².⁵EID50/只)接种时,仅在接种后14天可检测到病毒。在用改良活IBDV疫苗接种的SPF和商品雏鸡中,在接种后7天和14天在SPF雏鸡中可检测到病毒或其RNA,但在1日龄或2周龄接种的商品肉鸡中,既未检测到活疫苗病毒也未检测到其RNA。

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