Literature DB >> 14532030

Development of a PCR-enzyme immunoassay oligoprobe detection method for Toxoplasma gondii oocysts, incorporating PCR controls.

Kellogg J Schwab1, James J McDevitt.   

Abstract

Infections caused by Toxoplasma gondii are widely prevalent in animals and humans throughout the world. In the United States, an estimated 23% of adolescents and adults have laboratory evidence of T. gondii infection. T. gondii has been identified as a major opportunistic pathogen in immunocompromised individuals, in whom it can cause life-threatening disease. Water contaminated with feces from domestic cats or other felids may be an important source of human exposure to T. gondii oocysts. Because of the lack of information regarding the prevalence of T. gondii in surface waters, there is a clear need for a rapid, sensitive method to detect T. gondii from water. Currently available animal models and cell culture methods are time-consuming, expensive, and labor-intensive, requiring days or weeks for results to be obtained. Detection of T. gondii nucleic acid by PCR has become the preferred method. We have developed a PCR amplification and detection method for T. gondii oocyst nucleic acid that incorporates the use of hot-start amplification to reduce nonspecific primer annealing, uracil-N-glycosylase to prevent false-positive results due to carryover contamination, an internal standard control to identify false-negative results due to inadequate removal of sample inhibition, and PCR product oligoprobe confirmation using a nonradioactive DNA hybridization immunoassay. This method can provide positive, confirmed results in less than 1 day. Fewer than 50 oocysts can be detected following recovery of oocyst DNA. Development of a T. gondii oocyst PCR detection method will provide a useful technique to estimate the levels of T. gondii oocysts present in surface waters.

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Year:  2003        PMID: 14532030      PMCID: PMC201176          DOI: 10.1128/AEM.69.10.5819-5825.2003

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  32 in total

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Journal:  Infect Immun       Date:  1997-11       Impact factor: 3.441

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Authors:  J P Dubey; D S Lindsay; C A Speer
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3.  Evaluation of a PCR probe capture assay for the detection of Toxoplasma gondii. Incorporation of uracil N-glycosylase for contamination control.

Authors:  T B Martins; D R Hillyard; C M Litwin; E W Taggart; T D Jaskowski; H R Hill
Journal:  Am J Clin Pathol       Date:  2000-05       Impact factor: 2.493

4.  Toxoplasma gondii in Vancouver Island cougars (Felis concolor vancouverensis): serology and oocyst shedding.

Authors:  J J Aramini; C Stephen; J P Dubey
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5.  Oocyst-induced murine toxoplasmosis: life cycle, pathogenicity, and stage conversion in mice fed Toxoplasma gondii oocysts.

Authors:  J P Dubey; C A Speer; S K Shen; O C Kwok; J A Blixt
Journal:  J Parasitol       Date:  1997-10       Impact factor: 1.276

6.  Diagnosis of Neospora caninum and Toxoplasma gondii infection by PCR and DNA hybridization immunoassay.

Authors:  N Müller; V Zimmermann; B Hentrich; B Gottstein
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Authors:  J C Rodríguez; M M Martínez; A R Martínez; G Royo
Journal:  J Med Microbiol       Date:  1997-07       Impact factor: 2.472

8.  Use of heat release and an internal RNA standard control in reverse transcription-PCR detection of Norwalk virus from stool samples.

Authors:  K J Schwab; M K Estes; F H Neill; R L Atmar
Journal:  J Clin Microbiol       Date:  1997-02       Impact factor: 5.948

9.  Detection of Toxoplasma gondii tachyzoites and bradyzoites in blood, urine, and brains of infected mice.

Authors:  T D Nguyen; M de Kesel; G Bigaignon; P Hoet; G Pazzaglia; M Lammens; M Delmee
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Journal:  Appl Environ Microbiol       Date:  1996-09       Impact factor: 4.792

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Journal:  Appl Environ Microbiol       Date:  2010-06-11       Impact factor: 4.792

2.  Detection of Toxoplasma gondii oocysts in water sample concentrates by real-time PCR.

Authors:  Wenli Yang; H D Alan Lindquist; Vitaliano Cama; Frank W Schaefer; Eric Villegas; Ronald Fayer; Earl J Lewis; Yaoyu Feng; Lihua Xiao
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Review 3.  Molecular detection and genotyping of noroviruses.

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Journal:  Food Environ Virol       Date:  2012-11-04       Impact factor: 2.778

Review 4.  The impact of the waterborne transmission of Toxoplasma gondii and analysis efforts for water detection: an overview and update.

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5.  Prevalence and Molecular Characterization of Toxoplasma gondii and Toxocara cati Among Stray and Household Cats and Cat Owners in Tehran, Iran.

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6.  Detection of Toxoplasma gondii oocysts in environmental soil samples using molecular methods.

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7.  Great efficacy of sulfachloropyrazine-sodium against acute murine toxoplasmosis.

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Journal:  Asian Pac J Trop Biomed       Date:  2012-01

8.  Genotyping of Toxoplasma gondii Isolates from Soil Samples in Tehran, Iran.

Authors:  M Tavalla; H Oormazdi; L Akhlaghi; S Shojaee; E Razmjou; R Hadighi; Ar Meamar
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9.  Molecular Detection and Genotyping of Toxoplasma gondii in Chicken, Beef, and Lamb Meat Consumed in Northwestern Iran.

Authors:  Mahmoud Mahami-Oskouei; Mohammad Moradi; Esmaeil Fallah; Faezeh Hamidi; Najibeh Asl Rahnamaye Akbari
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  9 in total

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