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利用粪肥中 hsp70mRNA 产生的诱导率评估微小隐孢子虫卵囊的活力。

Assessment of the viability of Cryptosporidium parvum oocysts with the induction ratio of hsp70 mRNA production in manure.

机构信息

Technische Universität München, Am Coulombwall, 85748 Garching, Germany.

出版信息

J Microbiol Methods. 2013 Sep;94(3):280-9. doi: 10.1016/j.mimet.2013.05.011. Epub 2013 Jun 6.

DOI:10.1016/j.mimet.2013.05.011
PMID:23747597
Abstract

Determining the presence of viable Cryptosporidium parvum oocysts in complex environmental matrices in hygiene control can prevent the contamination of water resources and food with this pathogen. This study assessed the induction ratio of hsp70 mRNA production by heat shock in different oocysts as a marker of viability. Using different procedures for (m)RNA extraction directly from manure and reverse transcription real-time qPCR, this study found slightly increased hsp70 mRNA contents in viable oocysts that were heat shock induced at 45°C for 20 min compared to not induced oocysts (1.6 fold induction in average). Prolonging the heat shock treatment to 2h did not further increase the copy numbers. Heat shock by consecutive stimuli, such as freezing and then heating, did not yield significantly higher copy numbers than the 45°C treatment. There was a certain background level of hsp70 mRNA in viable oocysts that were not exposed to heat shock, indicating a constitutive production of the transcripts in the oocysts. The production of hsp70 mRNA induced by heat shock in oocysts aged for 9 months that exhibited reduced viability was lower than in fresher oocysts (induction ratio<1.2). No production of hsp70 mRNA by heat shock was detected in 12 months old oocysts that were not viable in the excystation test. Oocysts inactivated at 75°C for 30 min were not able to respond to heat shock, and low amount of copies were occasionally measured only in total RNA extracts, but not in mRNA extracts that were purified directly with an oligo (dT)25 based system. The induction ratio of hsp70 mRNA varied according to the viability of the organisms in a sample. Copy numbers of β-tubulin mRNA in viable oocysts were lower than hsp70 mRNA, therefore the latter is more suitable to detect low numbers of oocysts by RT-qPCR.

摘要

在卫生控制中,确定复杂环境基质中是否存在活的微小隐孢子虫卵囊,可以防止水源和食物受到这种病原体的污染。本研究评估了热休克诱导 hsp70 mRNA 产生的诱导率,作为生存力的标志物。使用不同的程序,从粪便中直接提取(m)RNA 并进行反转录实时 qPCR,本研究发现,与未诱导的卵囊相比,在 45°C 下热休克诱导 20 分钟的活卵囊中的 hsp70 mRNA 含量略有增加(平均诱导 1.6 倍)。将热休克处理延长至 2 小时不会进一步增加拷贝数。连续刺激(如冷冻然后加热)的热休克不会产生比 45°C 处理更高的拷贝数。在未暴露于热休克的活卵囊中存在一定水平的 hsp70 mRNA,表明在卵囊中存在转录本的组成型产生。在老化 9 个月且生存力降低的卵囊中,由热休克诱导的 hsp70 mRNA 的产生低于更新鲜的卵囊(诱导率<1.2)。在未在出芽试验中存活的 12 个月大的卵囊中,未检测到热休克诱导的 hsp70 mRNA 的产生。在 75°C 下失活 30 分钟的卵囊无法对热休克作出反应,偶尔仅在总 RNA 提取物中测量到少量拷贝数,但不能在直接用寡聚(dT)25 基系统纯化的 mRNA 提取物中测量到。hsp70 mRNA 的诱导率根据样品中生物的生存力而变化。活卵囊中β-微管蛋白 mRNA 的拷贝数低于 hsp70 mRNA,因此后者更适合通过 RT-qPCR 检测低数量的卵囊。

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