Literature DB >> 19749067

Cryptosporidium propidium monoazide-PCR, a molecular biology-based technique for genotyping of viable Cryptosporidium oocysts.

Cristin C Brescia1, Shannon M Griffin, Michael W Ware, Eunice A Varughese, Andrey I Egorov, Eric N Villegas.   

Abstract

Cryptosporidium is an important waterborne protozoan parasite that can cause severe diarrhea and death in the immunocompromised. The current methods used to monitor for Cryptosporidium oocysts in water are the microscopy-based USEPA methods 1622 and 1623. These methods assess total levels of oocysts in source waters, but do not determine oocyst viability or genotype. Recently, propidium monoazide (PMA) has been used in conjunction with molecular diagnostic tools to identify species and assess the viability of bacteria. The goal of this study was the development of a Cryptosporidium PMA-PCR (CryptoPMA-PCR) assay that includes PMA treatment prior to PCR analysis in order to prevent the amplification of DNA from dead oocysts. The results demonstrated that PMA penetrates only dead oocysts and blocks amplification of their DNA. The CryptoPMA-PCR assay can also specifically detect live oocysts within a mixed population of live and dead oocysts. More importantly, live oocysts, not dead oocysts, were detected in raw waste or surface water samples spiked with Cryptosporidium oocysts. This proof-of-concept study is the first to demonstrate the use of PMA for pre-PCR treatment of Cryptosporidium oocysts. The CryptoPMA-PCR assay is an attractive approach to specifically detect and genotype viable Cryptosporidium oocysts in the water, which is critical for human health risk assessment.

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Year:  2009        PMID: 19749067      PMCID: PMC2772443          DOI: 10.1128/AEM.00540-09

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


  47 in total

1.  Assessment of a dye permeability assay for determination of inactivation rates of Cryptosporidium parvum oocysts.

Authors:  M B Jenkins; L J Anguish; D D Bowman; M J Walker; W C Ghiorse
Journal:  Appl Environ Microbiol       Date:  1997-10       Impact factor: 4.792

2.  Disinfection of Cryptosporidium parvum oocysts by pulsed light treatment evaluated in an in vitro cultivation model.

Authors:  M J Arrowood; L T Xie; K Rieger; J Dunn
Journal:  J Eukaryot Microbiol       Date:  1996 Sep-Oct       Impact factor: 3.346

3.  An in vitro method for detecting infectious Cryptosporidium oocysts with cell culture.

Authors:  T R Slifko; D Friedman; J B Rose; W Jakubowski
Journal:  Appl Environ Microbiol       Date:  1997-09       Impact factor: 4.792

4.  Visible light generates oxidative DNA base modifications in high excess of strand breaks in mammalian cells.

Authors:  M Pflaum; S Boiteux; B Epe
Journal:  Carcinogenesis       Date:  1994-02       Impact factor: 4.944

5.  A massive outbreak in Milwaukee of cryptosporidium infection transmitted through the public water supply.

Authors:  W R Mac Kenzie; N J Hoxie; M E Proctor; M S Gradus; K A Blair; D E Peterson; J J Kazmierczak; D G Addiss; K R Fox; J B Rose
Journal:  N Engl J Med       Date:  1994-07-21       Impact factor: 91.245

6.  Comparison of assays for Cryptosporidium parvum oocysts viability after chemical disinfection.

Authors:  E K Black; G R Finch; R Taghi-Kilani; M Belosevic
Journal:  FEMS Microbiol Lett       Date:  1996-01-15       Impact factor: 2.742

7.  Viability of Cryptosporidium parvum oocysts: correlation of in vitro excystation with inclusion or exclusion of fluorogenic vital dyes.

Authors:  A T Campbell; L J Robertson; H V Smith
Journal:  Appl Environ Microbiol       Date:  1992-11       Impact factor: 4.792

8.  Surveillance for waterborne-disease outbreaks--United States, 1993-1994.

Authors:  M H Kramer; B L Herwaldt; G F Craun; R L Calderon; D D Juranek
Journal:  MMWR CDC Surveill Summ       Date:  1996-04-12

9.  Use of propidium monoazide for live/dead distinction in microbial ecology.

Authors:  Andreas Nocker; Priscilla Sossa-Fernandez; Mark D Burr; Anne K Camper
Journal:  Appl Environ Microbiol       Date:  2007-06-22       Impact factor: 4.792

10.  The use of a ribosomal RNA targeted oligonucleotide probe for fluorescent labelling of viable Cryptosporidium parvum oocysts.

Authors:  G Vesey; N Ashbolt; E J Fricker; D Deere; K L Williams; D A Veal; M Dorsch
Journal:  J Appl Microbiol       Date:  1998-09       Impact factor: 3.772

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  30 in total

1.  Determining UV inactivation of Toxoplasma gondii oocysts by using cell culture and a mouse bioassay.

Authors:  Michael W Ware; Swinburne A J Augustine; David O Erisman; Mary Jean See; Larry Wymer; Samuel L Hayes; J P Dubey; Eric N Villegas
Journal:  Appl Environ Microbiol       Date:  2010-06-11       Impact factor: 4.792

2.  Use of propidium monoazide in reverse transcriptase PCR to distinguish between infectious and noninfectious enteric viruses in water samples.

Authors:  Sandhya Parshionikar; Ian Laseke; G Shay Fout
Journal:  Appl Environ Microbiol       Date:  2010-05-14       Impact factor: 4.792

Review 3.  Inactivation of exogenous endoparasite stages by chemical disinfectants: current state and perspectives.

Authors:  Arwid Daugschies; Berit Bangoura; Matthias Lendner
Journal:  Parasitol Res       Date:  2013-02-08       Impact factor: 2.289

Review 4.  Dead or alive: molecular assessment of microbial viability.

Authors:  Gerard A Cangelosi; John S Meschke
Journal:  Appl Environ Microbiol       Date:  2014-07-18       Impact factor: 4.792

5.  New perspectives on viable microbial communities in low-biomass cleanroom environments.

Authors:  Parag Vaishampayan; Alexander J Probst; Myron T La Duc; Emilee Bargoma; James N Benardini; Gary L Andersen; Kasthuri Venkateswaran
Journal:  ISME J       Date:  2012-10-11       Impact factor: 10.302

6.  Most probable number - loop mediated isothermal amplification (MPN-LAMP) for quantifying waterborne pathogens in <25min.

Authors:  Farhan Ahmad; Robert D Stedtfeld; Hassan Waseem; Maggie R Williams; Alison M Cupples; James M Tiedje; Syed A Hashsham
Journal:  J Microbiol Methods       Date:  2016-11-14       Impact factor: 2.363

7.  Survival of host-associated bacteroidales cells and their relationship with Enterococcus spp., Campylobacter jejuni, Salmonella enterica serovar Typhimurium, and adenovirus in freshwater microcosms as measured by propidium monoazide-quantitative PCR.

Authors:  Sungwoo Bae; Stefan Wuertz
Journal:  Appl Environ Microbiol       Date:  2011-12-02       Impact factor: 4.792

8.  Quantification of viable Giardia cysts and Cryptosporidium oocysts in wastewater using propidium monoazide quantitative real-time PCR.

Authors:  José L Alonso; Inmaculada Amorós; Rebecca A Guy
Journal:  Parasitol Res       Date:  2014-04-30       Impact factor: 2.289

9.  Quantitative detection of viable helminth ova from raw wastewater, human feces, and environmental soil samples using novel PMA-qPCR methods.

Authors:  P Gyawali; W Ahmed; J P S Sidhu; S V Nery; A C Clements; R Traub; J S McCarthy; S Llewellyn; P Jagals; S Toze
Journal:  Environ Sci Pollut Res Int       Date:  2016-06-15       Impact factor: 4.223

10.  Detection and Quantification of Viable and Nonviable Trypanosoma cruzi Parasites by a Propidium Monoazide Real-Time Polymerase Chain Reaction Assay.

Authors:  Beatriz Cancino-Faure; Roser Fisa; M Magdalena Alcover; Teresa Jimenez-Marco; Cristina Riera
Journal:  Am J Trop Med Hyg       Date:  2016-05-02       Impact factor: 2.345

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