Literature DB >> 8721298

Assessment of the conventional detection of fecal Cryptosporidium serpentis oocysts in subclinically infected captive snakes.

T K Graczyk1, M R Cranfield.   

Abstract

Fecal specimens of seven captive snakes naturally subclinically infected with Cryptosporidium serpentis were monitored for 131 days for the presence and concentration of oocysts. Thirty-three of 81 (41%) of the monoclonal antibody positive stools were read as negative (sensitivity 59%) by the acid-fast-stained (AFS) fecal smears. Oocyst concentrations in the false-negative stools ranged between 6.0 x 10(3)/g to 2.5 x 10(4)/g. The experimentally determined concentration-threshold of oocyst detection by AFS fecal smear was 3.0 x 10(4)/g. The stool weights did not conform to a normal distribution; the oocyst concentration was significantly correlated with the stool weight (P < 0.01). Due to this correlation, stools which constituted less than 0.41% of the snake weight were classified as negative by the AFS fecal smears. The AFS fecal smear technique should be used exclusively for the determination of Cryptosporidium-positive snakes, but not for diagnosis of snake negativity for Cryptosporidium; it should be applied only for larger fecal specimens, such as those which constitute more than 0.41% of snake weight. At least five to seven stool samples should be examined by fecal smear in order to determine snake positivity for Cryptosporidium in subclinical infection.

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Year:  1996        PMID: 8721298

Source DB:  PubMed          Journal:  Vet Res        ISSN: 0928-4249            Impact factor:   3.683


  7 in total

1.  Cryptosporidium sp. Infections in Green Turtles, Chelonia mydas, as a Potential Source of Marine Waterborne Oocysts in the Hawaiian Islands.

Authors:  T K Graczyk; G H Balazs; T Work; A A Aguirre; D M Ellis; S Murakawa; R Morris
Journal:  Appl Environ Microbiol       Date:  1997-07       Impact factor: 4.792

2.  Physical, epidemiological, and molecular evaluation of infection by Cryptosporidium galli in Passeriformes.

Authors:  Deuvânia C da Silva; Camila G Homem; Alex A Nakamura; Weslen Fabrício P Teixeira; Sílvia Helena V Perri; Marcelo V Meireles
Journal:  Parasitol Res       Date:  2010-04-21       Impact factor: 2.289

3.  Biomonitoring of surface and coastal water for Cryptosporidium, Giardia, and human-virulent microsporidia using molluscan shellfish.

Authors:  Frances E Lucy; Thaddeus K Graczyk; Leena Tamang; Allen Miraflor; Dan Minchin
Journal:  Parasitol Res       Date:  2008-08-14       Impact factor: 2.289

4.  Giardia sp. cysts and infectious Cryptosporidium parvum oocysts in the feces of migratory Canada geese (Branta canadensis).

Authors:  T K Graczyk; R Fayer; J M Trout; E J Lewis; C A Farley; I Sulaiman; A A Lal
Journal:  Appl Environ Microbiol       Date:  1998-07       Impact factor: 4.792

5.  Viability and infectivity of Cryptosporidium parvum oocysts are retained upon intestinal passage through a refractory avian host.

Authors:  T K Graczyk; M R Cranfield; R Fayer; M S Anderson
Journal:  Appl Environ Microbiol       Date:  1996-09       Impact factor: 4.792

6.  Molecular Identification of Cryptosporidium Species from Pet Snakes in Thailand.

Authors:  Benjarat Yimming; Khampee Pattanatanang; Pornchai Sanyathitiseree; Tawin Inpankaew; Ketsarin Kamyingkird; Nongnuch Pinyopanuwat; Wissanuwat Chimnoi; Jumnongjit Phasuk
Journal:  Korean J Parasitol       Date:  2016-08-31       Impact factor: 1.341

7.  Infectivity of Cryptosporidium parvum oocysts is retained upon intestinal passage through a migratory water-fowl species (Canada goose, Branta canadensis).

Authors:  T K Graczyk; M R Cranfield; R Fayer; J Trout; H J Goodale
Journal:  Trop Med Int Health       Date:  1997-04       Impact factor: 2.622

  7 in total

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