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重组病毒蛋白对强毒禽副粘病毒呼吸道攻击的保护作用。

Protection by recombinant viral proteins against a respiratory challenge with virulent avian metapneumovirus.

作者信息

Chary Parag, Njenga M Kariuki, Sharma Jagdev M

机构信息

Department of Veterinary and Biomedical Sciences, College of Veterinary Medicine, University of Minnesota, St. Paul, MN 55108, USA.

出版信息

Vet Immunol Immunopathol. 2005 Dec 15;108(3-4):427-32. doi: 10.1016/j.vetimm.2005.06.012. Epub 2005 Aug 19.

DOI:10.1016/j.vetimm.2005.06.012
PMID:16112741
Abstract

Protection by recombinant avian metapneumovirus (aMPV) N or M proteins against a respiratory challenge with virulent aMPV was examined. N, M or N+M proteins were administered intramuscularly (IM) with incomplete Freund's adjuvant (IFA) or by the oculonasal (ON) route with cholera toxin-B (CTB). Each turkey received 40 or 80 microg of each recombinant protein. Birds were considered protected against challenge if the challenge virus was not detectable in the choanal swabs by RT-PCR. At a dose of 40 microg/bird, N protein given with IFA by the IM route protected eight out of nine birds. M protein at the same dose protected three out of seven birds, while a combination of N+M proteins (40 microg each) protected three out of four birds. At a dose of 80 microg of each of N and M proteins per bird given with IFA by the IM route, 100% protection was achieved. ON immunization with a mixture of N and M proteins induced partial protection when the proteins were given with CTB; no detectable protection was noted without CTB. N and M proteins induced anti-aMPV antibodies, although protection against virulent virus challenge did not appear to be associated with the level or presence of antibodies.

摘要

研究了重组禽偏肺病毒(aMPV)N或M蛋白对强毒aMPV呼吸道攻击的保护作用。N、M或N+M蛋白通过不完全弗氏佐剂(IFA)肌肉注射(IM)或通过霍乱毒素B(CTB)经眼鼻(ON)途径给药。每只火鸡接受40或80微克的每种重组蛋白。如果通过RT-PCR在鼻后孔拭子中未检测到攻击病毒,则认为鸟类受到保护而免受攻击。以每只鸟40微克的剂量,通过IM途径与IFA一起给予的N蛋白保护了9只鸟中的8只。相同剂量的M蛋白保护了7只鸟中的3只,而N+M蛋白组合(各40微克)保护了4只鸟中的3只。以每只鸟80微克的剂量,通过IM途径与IFA一起给予N和M蛋白,可实现100%的保护。当N和M蛋白与CTB一起给予时,通过ON免疫诱导了部分保护;没有CTB时未观察到可检测到的保护。N和M蛋白诱导了抗aMPV抗体,尽管对强毒病毒攻击的保护似乎与抗体水平或存在无关。

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