首页> 外文OA文献 >Identification and determination of the viability of Giardia lamblia cysts and Cryptosporidium parvum and Cryptosporidium hominis oocysts in human fecal and water supply samples by fluorescent in situ hybridization (FISH) and monoclonal antibodies
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Identification and determination of the viability of Giardia lamblia cysts and Cryptosporidium parvum and Cryptosporidium hominis oocysts in human fecal and water supply samples by fluorescent in situ hybridization (FISH) and monoclonal antibodies

机译:通过荧光原位杂交(FIsH)和单克隆抗体鉴定和测定人类粪便和水供应样品中的贾第鞭毛虫囊肿和隐孢子虫以及隐孢子虫卵囊的活力

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摘要

In the present study, fluorescent in situ hybridization (FISH) and monoclonal antibodies (MAbs) were evaluated for species-specific detection and viability determination of Giardia lamblia, Cryptosporidium parvum, and Cryptosporidium hominis in human fecal and water supply samples. A total of 50 fecal human samples positive for G. lamblia cysts, 38 positive for C. parvum, and 23 positive for C. hominis were studied. Also, 18 water supply samples positive for Giardia spp. and Cryptosporidium spp. by the United States Environmental Protection Agency (USEPA) Method 1623 were studied by FISH and fluorescein isothiocyanate (FITC)-conjugated MAbs. Eighteen percent of the fecal samples parasitologically positive for G. lamblia presented viable and nonviable cysts, and 5% of those positive for Cryptosporidium spp. presented viable and nonviable oocysts. Of the 18 water supply samples analyzed, 6 (33%) presented Giardia spp. viable and nonviable cysts and 2 (11%) presented viable and nonviable Cryptosporidium spp. oocysts. G. lamblia identification was confirmed by polymerase chain reaction (PCR) and sequencing of the ß-giardin gene in the fecal and water samples found positive by FISH and FITC-conjugated MAbs. C. parvum and Cryptosporidium muris were identified, by PCR and sequencing of the small subunit of ribosomal RNA gene, in seven and one water samples, respectively. Our results confirm that this technique enables simultaneous visualization, species-specific identification, and viability determination of the organisms present in human fecal and water supply samples.
机译:在本研究中,评估了荧光原位杂交(FISH)和单克隆抗体(MAbs)对人粪便和供水样品中的贾第鞭毛虫,小隐孢子虫和人隐孢子虫的物种特异性检测和活力测定。总共研究了50个粪便人类样品,它们对G. lamblia囊肿呈阳性,对C. parvum呈阳性,对23个对C. hominis呈阳性。另外,对贾第鞭毛虫属阳性的18个供水样品。和隐孢子虫属。 FISH和异硫氰酸荧光素(FITC)偶联的单克隆抗体研究了美国环境保护局(USEPA)方法1623。粪便样本寄生虫阳性的羊乳杆菌有18%表现出有生存力和无生存力的囊肿,而隐孢子虫呈阳性的则占5%。提出了可行和不可行的卵囊。在分析的18个供水样本中,有6个(33%)出现了贾第鞭毛虫。活的和不活的囊肿,其中2个(11%)表现为活的和不活的隐孢子虫。卵囊。通过聚合酶链反应(PCR)以及粪便和水样中的ß-giardin基因的测序,通过FISH和FITC偶联的单克隆抗体发现阳性,可以鉴定出羊羔。通过PCR和核糖体RNA基因小亚基的测序,分别在7个和1个水样中鉴定了小隐孢子虫和隐孢子虫。我们的结果证实了该技术能够同时可视化,物种特异性鉴定和人类粪便和供水样品中存在的生物的生存力测定。

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