Literature DB >> 15156028

Detection and differentiation of Cryptosporidium oocysts in water by PCR-RFLP.

Lihua Xiao1, Altaf A Lal, Jianlin Jiang.   

Abstract

Consumption of contaminated water has been implicated as a major source of Cryptosporidium infection in various outbreak investigations and case control studies. Surveys conducted in various regions of the United States demonstrated the presence of Cryptosporidium oocysts in 67-100% of wastewaters, 24-100% of surface waters, and 17-26.8% of drinking waters. The identity and human infective potential of these waterborne oocysts are not known, although it is likely that not all oocysts are from human-infecting Cryptosporidium species. Likewise, the source of the oocyst contamination is also not fully clear. Farm animals and human sewage discharge are generally considered to be the major sources of surface water contamination with C. parvum. Because Cryptosporidium infection is common in wildlife, it is conceivable that wildlife can also be a source for Cryptosporidium oocysts in waters. The presence of host-adapted Cryptosporidium spp. and genotypes makes it possible to develop molecular tools to assess the human infection potential and source of Cryptosporidium oocysts in water.Currently, the identification of Cryptosporidium oocysts in environmental samples is largely made by the use of immunofluorescent assay (IFA) after concentration processes (Environmental Protection Agency [EPA] recommended information collection rule [ICR] method or method 1622/1623 or similar techniques). Because IFA detects oocysts from all Cryptosporidium parasites, the species distribution of Cryptosporidium parasites in environmental samples cannot be assessed. Although many surface water samples contain Cryptosporidium oocysts, it is unlikely that all these oocysts are from human-pathogenic species or genotypes, because only five genotypes of Cryptosporidium parasites (the C. parvum human and bovine genotypes, C. meleagridis, C. canis, and C. felis) are responsible for most human infections. Information on the source of C. parvum contamination is necessary for effective evaluation and selection of management practices for reducing C. parvum contamination of surface water and the risk of cryptosporidiosis. Thus, identification of oocysts to species and genotype levels is of public health importance.

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Year:  2004        PMID: 15156028     DOI: 10.1385/1-59259-766-1:163

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  13 in total

1.  Rapid and sensitive detection of single cryptosporidium oocysts from archived glass slides.

Authors:  O Sunnotel; W J Snelling; L Xiao; K Moule; J E Moore; B Cherie Millar; J S G Dooley; C J Lowery
Journal:  J Clin Microbiol       Date:  2006-09       Impact factor: 5.948

2.  Detection of Cryptosporidium oocysts in water: effect of the number of samples and analytic replicates on test results.

Authors:  Lihua Xiao; Kerri A Alderisio; Jianlin Jiang
Journal:  Appl Environ Microbiol       Date:  2006-09       Impact factor: 4.792

3.  Occurrence, source, and human infection potential of cryptosporidium and Giardia spp. in source and tap water in shanghai, china.

Authors:  Yaoyu Feng; Xukun Zhao; Jiaxu Chen; Wei Jin; Xiaonong Zhou; Na Li; Lin Wang; Lihua Xiao
Journal:  Appl Environ Microbiol       Date:  2011-04-15       Impact factor: 4.792

4.  Cryptosporidium genotypes in wildlife from a new york watershed.

Authors:  Yaoyu Feng; Kerri A Alderisio; Wenli Yang; Lisa A Blancero; William G Kuhne; Christopher A Nadareski; Michael Reid; Lihua Xiao
Journal:  Appl Environ Microbiol       Date:  2007-08-24       Impact factor: 4.792

Review 5.  Infections by Intestinal Coccidia and Giardia duodenalis.

Authors:  Vitaliano A Cama; Blaine A Mathison
Journal:  Clin Lab Med       Date:  2015-04-04       Impact factor: 1.935

6.  Cryptosporidium spp. parasitize exotic birds that are commercialized in markets, commercial aviaries, and pet shops.

Authors:  Raquel Saucier Gomes; Franziska Huber; Sidnei da Silva; Teresa Cristina Bergamo do Bomfim
Journal:  Parasitol Res       Date:  2011-09-16       Impact factor: 2.289

7.  Occurrence of Cryptosporidium suis and Cryptosporidium scrofarum on commercial swine farms in the Czech Republic and its associations with age and husbandry practices.

Authors:  Karel Němejc; Bohumil Sak; Dana Květoňová; Naděžda Kernerová; Michael Rost; Vitaliano A Cama; Martin Kváč
Journal:  Parasitol Res       Date:  2012-12-28       Impact factor: 2.289

8.  Identification and characterization of a Chinese isolate of Cryptosporidium serpentis from dairy cattle.

Authors:  Fu Chen; Huiling Qiu
Journal:  Parasitol Res       Date:  2012-07-11       Impact factor: 2.289

9.  Concentrations, viability, and distribution of Cryptosporidium genotypes in lagoons of swine facilities in the Southern Piedmont and in coastal plain watersheds of Georgia.

Authors:  Michael B Jenkins; Janice L Liotta; Araceli Lucio-Forster; Dwight D Bowman
Journal:  Appl Environ Microbiol       Date:  2010-07-16       Impact factor: 4.792

10.  Cryptosporidium source tracking in the Potomac River watershed.

Authors:  Wenli Yang; Plato Chen; Eric N Villegas; Ronald B Landy; Charles Kanetsky; Vitaliano Cama; Theresa Dearen; Cherie L Schultz; Kenneth G Orndorff; Gregory J Prelewicz; Miranda H Brown; Kim Roy Young; Lihua Xiao
Journal:  Appl Environ Microbiol       Date:  2008-09-05       Impact factor: 4.792

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