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淋巴细胞性脉络丛脑膜炎病毒糖蛋白中的单个氨基酸变化与导致生长激素缺乏综合征的能力有关。

A single amino acid change in the glycoprotein of lymphocytic choriomeningitis virus is associated with the ability to cause growth hormone deficiency syndrome.

作者信息

Teng M N, Borrow P, Oldstone M B, de la Torre J C

机构信息

Department of Neuropharmacology, The Scripps Research Institute, La Jolla, California 92037, USA.

出版信息

J Virol. 1996 Dec;70(12):8438-43. doi: 10.1128/JVI.70.12.8438-8443.1996.

Abstract

Persistent infection of C3H/St mice with certain strains of lymphocytic choriomeningitis virus (LCMV) causes a growth hormone (GH) deficiency syndrome (GHDS) manifested as growth retardation and hypoglycemia. Infected mice show high levels of viral replication in the GH-producing cells in the anterior pituitary leading to decreased synthesis of GH mRNA and protein despite the absence of detectable virus-induced cell structural damage. Virus clones isolated from the GHDS-negative LCMV WE strain can cause the disease, while others cannot. The genetic basis of this phenotypic difference is a nucleotide substitution resulting in a single amino acid difference in the viral glycoprotein. Reassortant studies indicate that the single amino acid substitution (Ser-153 to Phe) is sufficient to allow infection of the GH-producing cells and cause GHDS. These results show that a single change in the genome can affect viral pathogenicity by altering the tropism of the virus.

摘要

某些淋巴细胞性脉络丛脑膜炎病毒(LCMV)株持续感染C3H/St小鼠会导致生长激素(GH)缺乏综合征(GHDS),表现为生长迟缓与低血糖。受感染小鼠的垂体前叶产生生长激素的细胞中存在高水平的病毒复制,尽管未检测到病毒诱导的细胞结构损伤,但这导致了GH mRNA和蛋白质的合成减少。从GHDS阴性的LCMV WE株分离出的病毒克隆可引发该疾病,而其他克隆则不能。这种表型差异的遗传基础是一个核苷酸替换,导致病毒糖蛋白中出现一个氨基酸差异。重配研究表明,单一氨基酸替换(丝氨酸153变为苯丙氨酸)足以使产生生长激素的细胞受到感染并导致GHDS。这些结果表明,基因组中的单一变化可通过改变病毒的嗜性来影响病毒致病性。

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