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印度源鸡贫血病毒分离株的生物学和分子特征

Biological and molecular characterization of chicken anaemia virus isolates of Indian origin.

作者信息

Natesan Senthilkumar, Kataria J M, Dhama K, Rahul S, Bhardwaj N

机构信息

Molecular Biology Laboratory, Division of Avian Diseases, Indian Veterinary Research Institute, Izatnagar, Bareilly, UP 243122, India.

出版信息

Virus Res. 2006 Jun;118(1-2):78-86. doi: 10.1016/j.virusres.2005.11.017. Epub 2005 Dec 27.

Abstract

In the present study, four chicken anaemia virus (CAV) isolates (CAV-A, -B, -E and -P) recovered from different geographical regions of India were characterized. CAV genome of 1,766 bp nucleotide region containing the complete coding region of VP2 and VP3 proteins, and partial coding region of VP1 protein were sequenced. The nucleotide and deduced amino acid sequence of the Indian CAV isolates were aligned and compared with CAV isolates of European, Asian, American and Australian origin. Phylogenetic analysis of the Indian CAV isolates were also carried out based on the nucleotide and deduced amino acid sequences. The results indicated that Indian isolates were genetically evolved from different parts of the world. Indian isolate, CAV-A was found closely related to European Cux-1 strain, CAV-B and -P were closely related to Bangladesh BD-3 strain and CAV-E was closely related to Australian 704 strain. The pathogenicity of the four CAV isolates was studied in day-old specific pathogen free (SPF) chicks. Day-old SPF chicks (n=50) were divided into five groups comprised of 10 chicks in each group. Group 1 was kept as control and groups 2-5 were infected with each CAV isolate separately. The chicks were infected at a dose rate of 1 ml cell culture fluid (10(4.5)TCID(50)/0.1 ml) per bird intramuscularly. The clinical signs, mortality and packed cell volume (PCV) and body weight gain were recorded on 5, 10 and 15 days post-infection. At 15th day, all the birds were sacrificed and various organs, viz., thymus, bone marrow, spleen, liver and bursa were examined for gross and microscopic changes. The pathogenicity study indicated that all the CAVs except CAV-B were able to produce clinical disease and immunosuppression in young chicks whereas the isolate CAV-B produced no clinical disease but only induced immunosuppression, which was revealed by microscopic examination of the lymphoid organs. The study showed valuable information on molecular epidemiological status of CAV isolates prevalent in India for the first time.

摘要

在本研究中,对从印度不同地理区域分离得到的4株鸡贫血病毒(CAV)(CAV-A、-B、-E和-P)进行了特性分析。对包含VP2和VP3蛋白完整编码区以及VP1蛋白部分编码区的1766 bp核苷酸区域的CAV基因组进行了测序。将印度CAV分离株的核苷酸和推导氨基酸序列与欧洲、亚洲、美洲和澳大利亚来源的CAV分离株进行比对和比较。还基于核苷酸和推导氨基酸序列对印度CAV分离株进行了系统发育分析。结果表明,印度分离株在遗传上源自世界不同地区。发现印度分离株CAV-A与欧洲Cux-1株密切相关,CAV-B和-P与孟加拉国BD-3株密切相关,CAV-E与澳大利亚704株密切相关。在1日龄无特定病原体(SPF)雏鸡中研究了这4株CAV分离株的致病性。1日龄SPF雏鸡(n = 50)分为5组,每组10只雏鸡。第1组作为对照,第2 - 5组分别用每株CAV分离株感染。雏鸡以每只1 ml细胞培养液(10(4.5)TCID(50)/0.1 ml)的剂量率进行肌肉注射感染。在感染后第5、10和15天记录临床症状、死亡率、红细胞压积(PCV)和体重增加情况。在第15天,处死所有鸡,检查各种器官,即胸腺、骨髓、脾脏、肝脏和法氏囊的大体和微观变化。致病性研究表明,除CAV-B外,所有CAV均能在幼雏中引起临床疾病和免疫抑制,而分离株CAV-B未引起临床疾病,但仅诱导了免疫抑制,这通过对淋巴器官的微观检查得以揭示。该研究首次展示了印度流行的CAV分离株的分子流行病学状况的宝贵信息。

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