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建立无特定逆转录病毒的猕猴繁殖群体:一种初步筛选和监测方法

Establishing specific retrovirus-free breeding colonies of macaques: an approach to primary screening and surveillance.

作者信息

Lerche N W, Yee J L, Jennings M B

机构信息

Simian Retrovirus Reference Laboratory, University of California, Davis 95616.

出版信息

Lab Anim Sci. 1994 Jun;44(3):217-21.

PMID:7933966
Abstract

For reasons of occupational safety and animal health, as well as to improve the quality of nonhuman primates used in biomedical research, the establishment and maintenance of specific retrovirus-free breeding colonies of macaques (genus Macaca) are now high priorities. Sensitive and specific screening tests are now available for use in identifying macaques infected with the exogenous simian retroviruses simian immunodeficiency virus (SIV), simian T-lymphotropic virus (STLV), and simian type D retrovirus (SRV/D). A testing algorithm of repeated antibody screening by enzyme immunoassay with confirmatory testing of enzyme immunoassay-reactive sera by Western blot (immunoblot) has proved adequate for identification and exclusion of SIV- and STLV-infected animals in five facilities. In follow-up testing of animals seronegative on primary screening, seroconversions to these two viruses have been rare (0% and < 0.01%, respectively). The testing algorithm for SRV/D must include virus isolation in addition to antibody screening, as some SRV/D-infected animals lack detectable antibody or exhibit a prolonged interval between infection and seroconversion. This parallel testing for SRV/D antibody and virus is critical, especially during primary screening of potential specific pathogen-free stock obtained from external sources. "Indeterminate" immunoblot results, particularly for SRV/D, continue to pose a problem of interpretation. However, preliminary results indicate that newer diagnostic test methods, such as polymerase chain reaction for amplification of proviral DNA, will be useful in resolving SRV/D infection status and will contribute substantially to specific pathogen-free colony development and maintenance.

摘要

出于职业安全和动物健康的考虑,以及为了提高生物医学研究中使用的非人灵长类动物的质量,建立和维持特定的无逆转录病毒猕猴(猕猴属)繁殖群体现在已成为高度优先事项。现在有灵敏且特异的筛查试验可用于识别感染外源性猿猴逆转录病毒的猕猴,这些病毒包括猿猴免疫缺陷病毒(SIV)、猿猴嗜T淋巴细胞病毒(STLV)和猿猴D型逆转录病毒(SRV/D)。通过酶免疫测定进行重复抗体筛查,并通过蛋白质印迹法(免疫印迹)对酶免疫测定反应性血清进行确证检测的检测算法,已被证明足以在五个机构中识别和排除感染SIV和STLV的动物。在对初次筛查血清阴性的动物进行后续检测中,这两种病毒的血清转化很少见(分别为0%和<0.01%)。SRV/D的检测算法除了抗体筛查外还必须包括病毒分离,因为一些感染SRV/D的动物缺乏可检测到的抗体,或者在感染和血清转化之间表现出较长的间隔。对SRV/D抗体和病毒进行这种平行检测至关重要,尤其是在对从外部来源获得的潜在无特定病原体种群进行初次筛查期间。“不确定”的免疫印迹结果,特别是对于SRV/D,仍然存在解释问题。然而,初步结果表明,更新的诊断测试方法,如用于扩增前病毒DNA的聚合酶链反应,将有助于解决SRV/D感染状态,并将对无特定病原体群体的发展和维持做出重大贡献。

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