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通过聚合酶链反应检测活的微小隐孢子虫卵囊

Detection of viable Cryptosporidium parvum oocysts by PCR.

作者信息

Wagner-Wiening C, Kimmig P

机构信息

Landesgesundheitsamt Baden-Württemberg, Stuttgart, Germany.

出版信息

Appl Environ Microbiol. 1995 Dec;61(12):4514-6. doi: 10.1128/aem.61.12.4514-4516.1995.

DOI:10.1128/aem.61.12.4514-4516.1995
PMID:8534121
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC167765/
Abstract

PCR was used to detect and specifically identify a gene fragment from Cryptosporidium parvum. An 873-bp region of a 2,359-bp DNA fragment encoding a repetitive oocyst protein of C. parvum was shown to be specifically amplified in C. parvum. An excystation protocol before DNA extraction allowed the differentiation between live and dead Cryptosporidium parvum oocysts.

摘要

采用聚合酶链反应(PCR)检测并特异性鉴定微小隐孢子虫的一个基因片段。微小隐孢子虫编码一种重复卵囊蛋白的2359 bp DNA片段中的一个873 bp区域在微小隐孢子虫中被特异性扩增。在DNA提取前采用的脱囊方案能够区分活的和死的微小隐孢子虫卵囊。

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本文引用的文献

1
The effects of reducing conditions, medium, pH, temperature, and time on in vitro excystation of Cryptosporidium.还原条件、培养基、pH值、温度和时间对隐孢子虫体外脱囊的影响。
J Protozool. 1984 Nov;31(4):567-9. doi: 10.1111/j.1550-7408.1984.tb05504.x.
2
Separation of Cryptosporidium species oocysts from feces by using a percoll discontinuous density gradient.通过使用不连续 Percoll 密度梯度从粪便中分离隐孢子虫属卵囊。
J Clin Microbiol. 1986 Jan;23(1):199-200. doi: 10.1128/jcm.23.1.199-200.1986.
3
Isolation of Cryptosporidium oocysts and sporozoites using discontinuous sucrose and isopycnic Percoll gradients.使用不连续蔗糖和等密度 Percoll 梯度分离隐孢子虫卵囊和子孢子。
J Parasitol. 1987 Apr;73(2):314-9.
4
Identification of Cryptosporidium oocysts in river water.河水中隐孢子虫卵囊的鉴定
Appl Environ Microbiol. 1987 Apr;53(4):672-6. doi: 10.1128/aem.53.4.672-676.1987.
5
The safety of our drinking water: reason for concern but not alarm.
N Engl J Med. 1989 May 25;320(21):1413-4. doi: 10.1056/NEJM198905253202111.
6
Large community outbreak of cryptosporidiosis due to contamination of a filtered public water supply.因过滤后的公共供水系统受污染导致隐孢子虫病在社区大规模爆发。
N Engl J Med. 1989 May 25;320(21):1372-6. doi: 10.1056/NEJM198905253202103.
7
An outbreak of waterborne cryptosporidiosis caused by post-treatment contamination.由处理后污染引起的水源性隐孢子虫病暴发。
Epidemiol Infect. 1989 Dec;103(3):703-15. doi: 10.1017/s0950268800031101.
8
A probable waterborne outbreak of cryptosporidiosis in the Sheffield area.
J Med Microbiol. 1990 Aug;32(4):239-42. doi: 10.1099/00222615-32-4-239.
9
A 2359-base pair DNA fragment from Cryptosporidium parvum encoding a repetitive oocyst protein.
Mol Biochem Parasitol. 1992 Nov;56(1):69-78. doi: 10.1016/0166-6851(92)90155-d.
10
[Cryptosporidium parvum and Giardia lamblia--incidence in surface and drinking water--significance and detection].[微小隐孢子虫和蓝氏贾第鞭毛虫——地表水和饮用水中的发病率——意义及检测]
Gesundheitswesen. 1992 Nov;54(11):662-5.