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用于定量污水中呼肠孤病毒的细胞系、免疫荧光和蚀斑测定程序的评估。

Evaluation of cell lines and immunofluorescence and plaque assay procedures for quantifying reoviruses in sewage.

作者信息

Ridinger D N, Spendlove R S, Barnett B B, George D B, Roth J C

出版信息

Appl Environ Microbiol. 1982 Apr;43(4):740-6. doi: 10.1128/aem.43.4.740-746.1982.

DOI:10.1128/aem.43.4.740-746.1982
PMID:7044308
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC241911/
Abstract

Twelve continuous cell lines were tested to determine their sensitivity to reovirus types 1, 2, and 3 isolated from sewage. Madin-Darby bovine kidney (MDBK), rhesus monkey kidney (LLC-MK2), and human embryonic intestinal (intestinal 407) cells were most sensitive, respectively. In a similar study, MDBK cells were more sensitive than LLC-MK2 and Buffalo green monkey kidney (BGM) cells to sewage-isolated, protamine-precipitated reoviruses which had not been serotyped and had no previous cell contact. Sewage-isolated, protamine-precipitated reoviruses were also used in conjunction with MDBK cells in a comparative evaluation of immunofluorescent cell count and plaque assay procedures. The immunofluorescence assay is more sensitive and more rapid than the plaque assay. Reoviruses in excess of 10(4)/liter of raw sewage were detected by the immunofluorescent cell count assay.

摘要

对12种连续传代细胞系进行了检测,以确定它们对从污水中分离出的1型、2型和3型呼肠孤病毒的敏感性。结果发现,马迪-达比牛肾(MDBK)细胞、恒河猴肾(LLC-MK2)细胞和人胚胎肠(肠407)细胞分别最为敏感。在一项类似研究中,对于未经血清分型且此前未接触过细胞的污水分离、鱼精蛋白沉淀的呼肠孤病毒,MDBK细胞比LLC-MK2细胞和布法罗绿猴肾(BGM)细胞更敏感。污水分离、鱼精蛋白沉淀的呼肠孤病毒还与MDBK细胞一起用于免疫荧光细胞计数和蚀斑测定程序的比较评估。免疫荧光测定比蚀斑测定更灵敏、更快速。通过免疫荧光细胞计数测定法可检测出每升原污水中超过10⁴个的呼肠孤病毒。

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本文引用的文献

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EFFECT OF ANTIMITOTIC AGENTS ON INTRACELLULAR REOVIRUS ANTIGEN.抗有丝分裂剂对细胞内呼肠孤病毒抗原的作用。
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BGM, a continuous cell line more sensitive than primary rhesus and African green kidney cells for the recovery of viruses from water.BGM是一种连续细胞系,在从水中分离病毒方面比恒河猴原代肾细胞和非洲绿猴肾细胞更敏感。
Health Lab Sci. 1974 Oct;11(4):275-82.
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Concentration of reovirus and adenovirus from sewage and effluents by protamine sulfate (salmine) treatment.通过硫酸鱼精蛋白(精胺)处理从污水和废水中浓缩呼肠孤病毒和腺病毒。
Appl Microbiol. 1972 Sep;24(3):510-2. doi: 10.1128/am.24.3.510-512.1972.
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