Department of Microbiology and Immunology, Jefferson Medical College, Kimmel Cancer Center, Thomas Jefferson University, 233 S, 10th St BLSB, rm 526, Philadelphia, PA 19107, USA.
Virol J. 2014 Apr 18;11:71. doi: 10.1186/1743-422X-11-71.
Murine cytomegalovirus (MCMV) is increasingly used as an infectious model to investigate host-pathogen interactions in mice. Detailed methods have been published for using primary murine embryonic fibroblasts (MEFs) for preparing stocks and determining viral titers of MCMV. For determining the titer of MCMV by plaque assay, these methods rely on a high viscosity media that restricts viral spreading through the supernatant of the culture, but is also usually too viscous to pipet. Moreover, MEFs must be repeatedly generated and can vary widely from batch-to-batch in purity, proliferation rates, and the development of senescence. In contrast, the M2-10B4 bone marrow stromal cell line (ATCC # CRL-1972), which is also permissive for MCMV, has been reported to produce high-titer stocks of MCMV and has the considerable advantages of growing rapidly and consistently. However, detailed methods using these cells have not been published.
We modified existing protocols to use M2-10B4 cells for measuring MCMV titers by plaque assay.
We found that MCMV plaques could be easily resolved on monolayers of M2-10B4 cells. Moreover, plaques formed normally even when cultures of M2-10B4 cells were less than 50% confluent on the day of infection, as long as we also used a reduced viscosity overlay.
Overall, our protocol enabled us to use a consistent cell line to assess viral titers, rather than repeatedly producing primary MEFs. It also allowed us to start the assay with 4-fold fewer cells than would be required to generate a confluent monolayer, reducing the lead-time prior to the start of the assay. Finally, the reduced viscosity CMC could be handled by pipet and did not need to be pre-mixed with media, thus increasing its shelf-life and ease-of-use. We describe our results here, along with detailed protocols for the use of the M2-10B4 cell lines to determine the titer and grow stocks of MCMV.
鼠巨细胞病毒(MCMV)越来越多地被用作一种感染模型,用于研究小鼠中的宿主-病原体相互作用。已经发表了详细的方法,用于使用原代鼠胚胎成纤维细胞(MEFs)来制备病毒储备液并确定 MCMV 的病毒滴度。对于通过噬斑测定来确定 MCMV 的滴度,这些方法依赖于高粘度的培养基,该培养基限制了病毒通过培养物上清液的扩散,但通常也过于粘稠而无法用移液器吸取。此外,MEFs 必须反复生成,并且批次间的纯度、增殖率和衰老的发展差异很大。相比之下,也允许 MCMV 感染的 M2-10B4 骨髓基质细胞系(ATCC # CRL-1972)已被报道能够产生高滴度的 MCMV 储备液,并且具有快速且一致地生长的显著优势。然而,尚未发表使用这些细胞的详细方法。
我们修改了现有的方案,使用 M2-10B4 细胞通过噬斑测定来测量 MCMV 滴度。
我们发现 MCMV 噬斑可以在 M2-10B4 细胞单层上轻松分辨。此外,即使在感染当天 M2-10B4 细胞培养物不到 50%汇合的情况下,只要我们还使用低粘度覆盖物,噬斑也能正常形成。
总的来说,我们的方案使我们能够使用一致的细胞系来评估病毒滴度,而不是反复生成原代 MEFs。它还使我们能够在开始测定之前使用比生成汇合单层所需的细胞少 4 倍的细胞,从而缩短了测定开始前的时间。最后,低粘度的 CMC 可以用移液器吸取,并且不需要与培养基预先混合,从而增加了其保质期和易用性。我们在这里描述了我们的结果,以及使用 M2-10B4 细胞系确定 MCMV 滴度和生长储备液的详细方案。