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Use of HL cells for improved isolation and passage of Chlamydia pneumoniae.

机译:HL细胞用于改善肺炎衣原体分离和传代的用途。

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摘要

We compared growth of the recently discovered respiratory pathogen Chlamydia pneumoniae in McCoy, HeLa 229, BHK-21, and HL cells. When cells were not pretreated with DEAE-dextran, HL cells had significantly higher mean numbers of inclusion-forming units (IFUs) on initial inoculation than the other cell lines. When cells were pretreated with DEAE-dextran, HeLa 229 and HL cells had equivalent mean numbers of IFUs on initial inoculation. HL cells had strikingly higher mean numbers of IFUs in passage than HeLa 229, BHK-21, or McCoy cells. In addition, HL cells did not require pretreatment with DEAE-dextran and could be used from 2 to 4 days after seeding. We conclude that HL cells are an excellent cell culture system for laboratory propagation of C. pneumoniae and may be a more sensitive cell line for initial isolation.
机译:我们比较了最近发现的呼吸道病原体肺炎衣原体在McCoy,HeLa 229,BHK-21和HL细胞中的生长。当未用DEAE-葡聚糖预处理细胞时,HL细胞在初次接种时的平均内含物形成单位(IFU)数量明显高于其他细胞系。当用DEAE-葡聚糖预处理细胞时,HeLa 229和HL细胞在初次接种时具有相等的IFU平均数。 HL细胞比HeLa 229,BHK-21或McCoy细胞具有更高的平均IFU传递数量。此外,HL细胞不需要用DEAE-葡聚糖进行预处理,可以在接种后2至4天使用。我们得出的结论是,HL细胞是用于肺炎衣原体实验室繁殖的出色细胞培养系统,并且可能是用于初始分离的更敏感的细胞系。

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