Dagnaes-Hansen F, Horsman M R
Institute of Medical Microbiology and Immunology, Bartholin Building, University of Aarhus, Denmark.
Lab Anim. 2005 Oct;39(4):394-9. doi: 10.1258/002367705774286358.
Transmission of viral infection by tumour lines or other biological materials may have confounding effects on research. Many research organizations require screening for viral agents of all cell lines, tumours, sera and other biologicals before implantation or inoculation into animal models. Screening for viral contamination is done by the mouse antibody production (MAP) test, by cell culture, or alternatively by direct detection of the viral agents by polymerase chain reaction (PCR). The description of procedures for sanitation of infected cell lines or tumours is sparse. The present report describes the procedures used for sanitation of three transplantable murine tumour lines, which were transplanted in vivo in a mouse hepatitis virus (MHV)-infected colony of mice at the Department of Experimental Clinical Oncology (DECO). The tumours were frozen and serially transplanted three times in a quarantine colony of syngenic mice. Serological examination of the mice transplanted with tumours as well as their cage mates in the quarantine colony did not detect any antibodies against MHV. After repeated serial transplantation in seronegative animals, tumour material was frozen and thawed tumours were later used for transplantation into the newly established virus-free colony of mice at DECO. PCR-based detection of MHV did not reveal any contamination of the tumour examined by this technique, indicating that this murine tumour apparently did not transmit MHV or that MHV was eliminated from the tissue so fast after the infection that it could not be transmitted by the tumour tissue. It is concluded that MHV infection of mice with transplantable murine tumours does not necessarily cause the tumours to be contaminated.
肿瘤细胞系或其他生物材料导致的病毒感染传播可能会对研究产生混淆效应。许多研究机构要求在将所有细胞系、肿瘤、血清及其他生物制品植入或接种到动物模型之前,对其进行病毒因子筛查。病毒污染的筛查通过小鼠抗体产生(MAP)试验、细胞培养,或者通过聚合酶链反应(PCR)直接检测病毒因子来进行。关于感染细胞系或肿瘤的净化程序的描述很少。本报告描述了用于三种可移植小鼠肿瘤细胞系净化的程序,这些细胞系在实验临床肿瘤学系(DECO)的感染小鼠肝炎病毒(MHV)的小鼠群体中进行了体内移植。将肿瘤冷冻,并在同基因小鼠的隔离群体中连续传代移植三次。对移植了肿瘤的小鼠及其在隔离群体中的同笼伙伴进行血清学检查,未检测到任何针对MHV的抗体。在血清阴性动物中反复连续移植后,将肿瘤材料冷冻,解冻后的肿瘤随后用于移植到DECO新建立的无病毒小鼠群体中。基于PCR的MHV检测未显示该技术检测的肿瘤有任何污染,这表明这种小鼠肿瘤显然未传播MHV,或者感染后MHV从组织中消除得如此之快,以至于无法通过肿瘤组织传播。结论是,可移植小鼠肿瘤的小鼠感染MHV不一定会导致肿瘤被污染。