Literature DB >> 20107835

Comparative efficacy of conventional primer sets in detection of Cryptosporidium parvum for diagnostic use.

Sirri Kar1, Arwid Daugschies, Berit Bangoura.   

Abstract

In this study, the sensitivity and specificity of different previously described primer sets for Cryptosporidium parvum detection by polymerase chain reaction (PCR) was evaluated. For this purpose, the primer sets defined by Cacciò et al. (FEMS Microbiol Lett 170(1):173-179, 1999) (tub), Widmer et al. (Appl Environ Microbiol 64(11):4477-4481, 1998) (btub) and Rochelle et al. (Appl Environ Microbiol 63:2029-2037, 1997) (cphsp), respectively, were used. Deoxyribonucleic acid (DNA) was isolated from three different sample materials: (1) from the faeces of an experimentally C. parvum-infected calf, (2) from purified C. parvum oocysts, and (3) from C. parvum-infected HCT-8 cell cultures. The DNA samples were subjected to PCR reactions with each of the three given primer sets to investigate sensitivity and suitability for routine use. The primers described by Cacciò et al. (FEMS Microbiol Lett 170(1):173-179, 1999) (TUB) were superior regarding sensitivity and specificity in terms of detection of C. parvum in faeces, in purified oocysts and also in cell culture, and may thus be applied for routine diagnostic use in common sample materials.

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Year:  2010        PMID: 20107835     DOI: 10.1007/s00436-010-1737-x

Source DB:  PubMed          Journal:  Parasitol Res        ISSN: 0932-0113            Impact factor:   2.289


  29 in total

1.  Phylogenetic relationships of Cryptosporidium parasites based on the 70-kilodalton heat shock protein (HSP70) gene.

Authors:  I M Sulaiman; U M Morgan; R C Thompson; A A Lal; L Xiao
Journal:  Appl Environ Microbiol       Date:  2000-06       Impact factor: 4.792

2.  PCR detection of cryptosporidium: the way forward?

Authors:  U M Morgan; R C Thompson
Journal:  Parasitol Today       Date:  1998-12

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Authors:  J R Harris; F Petry
Journal:  J Parasitol       Date:  1999-10       Impact factor: 1.276

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5.  Threshold of detection of Cryptosporidium oocysts in human stool specimens: evidence for low sensitivity of current diagnostic methods.

Authors:  R Weber; R T Bryan; H S Bishop; S P Wahlquist; J J Sullivan; D D Juranek
Journal:  J Clin Microbiol       Date:  1991-07       Impact factor: 5.948

6.  Sequence polymorphism in the beta-tubulin gene reveals heterogeneous and variable population structures in Cryptosporidium parvum.

Authors:  G Widmer; L Tchack; C L Chappell; S Tzipori
Journal:  Appl Environ Microbiol       Date:  1998-11       Impact factor: 4.792

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Authors:  V F Del Coco; M A Córdoba; J A Basualdo
Journal:  Rev Argent Microbiol       Date:  2009 Jun-Sep       Impact factor: 1.852

8.  Comparison of fluorescence, antigen and PCR assays to detect Cryptosporidium parvum in fecal specimens.

Authors:  Ralf Bialek; Nicole Binder; Klaus Dietz; Anja Joachim; Jürgen Knobloch; Ulrike E Zelck
Journal:  Diagn Microbiol Infect Dis       Date:  2002-08       Impact factor: 2.803

9.  Studies of in vitro excystation of Cryptosporidium parvum from calves.

Authors:  D B Woodmansee
Journal:  J Protozool       Date:  1987-11

10.  Genetic polymorphism at the beta-tubulin locus among human and animal isolates of Cryptosporidium parvum.

Authors:  S Cacciò; W Homan; K van Dijk; E Pozio
Journal:  FEMS Microbiol Lett       Date:  1999-01-01       Impact factor: 2.742

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  1 in total

1.  Cryptosporidium parvum oocyst viability and behaviour of the residual body during the excystation process.

Authors:  Sirri Kar; Arwid Daugschies; Ayse Cakmak; Nadim Yilmazer; Katja Dittmar; Berit Bangoura
Journal:  Parasitol Res       Date:  2011-05-21       Impact factor: 2.289

  1 in total

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