Literature DB >> 19836820

Detection of Toxoplasma gondii oocysts and surrogate microspheres in water using ultrafiltration and capsule filtration.

Karen Shapiro1, Jonna A K Mazet, Alexander Schriewer, Stefan Wuertz, Heather Fritz, Woutrina A Miller, John Largier, Patricia A Conrad.   

Abstract

While reports on waterborne infections with Toxoplasma gondii are emerging worldwide, detection of this zoonotic parasite in water remains challenging. Lack of standardized and quantitative methods for detection of T. gondii oocysts in water also limits research on the transport and fate of this pathogen through aquatic habitats. Here, we compare the ability of hollow-fiber ultrafiltration and capsule filtration to concentrate oocysts in spiked tap water, fresh surface water, and seawater samples. Detection of T. gondii oocysts in concentrated samples was achieved using molecular methods, as well as visually via epifluorescent microscopy. In addition to oocysts, water samples were spiked with T. gondii surrogate microspheres, and detection of microspheres was performed using flow cytometry and epifluorescent microscopy. Results demonstrate that both water concentration methods followed by microscopy allowed for quantitative detection of T. gondii oocysts and surrogate microspheres. For T. gondii oocysts, microscopy was more sensitive than TaqMan and conventional PCR, and allowed for detection of oocysts in all water samples tested. Compared with flow cytometry, microscopy was also a more cost-efficient and precise method for detection of fluorescent surrogate microspheres in tap, fresh and seawater samples. This study describes a novel approach for quantitative detection of T. gondii oocysts in drinking and environmental water samples. The techniques described for concentrating and detecting surrogate microspheres have broad application for evaluating the transport and fate of oocysts, as well as the efficiency of water treatment methods for removal of T. gondii from water supplies. (c) 2009 Elsevier Ltd. All rights reserved.

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Year:  2009        PMID: 19836820     DOI: 10.1016/j.watres.2009.09.061

Source DB:  PubMed          Journal:  Water Res        ISSN: 0043-1354            Impact factor:   11.236


  15 in total

1.  Methods to produce and safely work with large numbers of Toxoplasma gondii oocysts and bradyzoite cysts.

Authors:  H Fritz; B Barr; A Packham; A Melli; P A Conrad
Journal:  J Microbiol Methods       Date:  2011-10-20       Impact factor: 2.363

2.  Comparison of PCR assays to detect Toxoplasma gondii oocysts in green-lipped mussels (Perna canaliculus).

Authors:  Alicia Coupe; Laryssa Howe; Karen Shapiro; Wendi D Roe
Journal:  Parasitol Res       Date:  2019-06-14       Impact factor: 2.289

Review 3.  The impact of the waterborne transmission of Toxoplasma gondii and analysis efforts for water detection: an overview and update.

Authors:  Panagiotis Karanis; Hebatalla M Aldeyarbi; Marzieh E Mirhashemi; Khalil M Khalil
Journal:  Environ Sci Pollut Res Int       Date:  2012-09-19       Impact factor: 4.223

4.  Effect of estuarine wetland degradation on transport of Toxoplasma gondii surrogates from land to sea.

Authors:  Karen Shapiro; Patricia A Conrad; Jonna A K Mazet; Wesley W Wallender; Woutrina A Miller; John L Largier
Journal:  Appl Environ Microbiol       Date:  2010-08-27       Impact factor: 4.792

Review 5.  Epidemiology of and diagnostic strategies for toxoplasmosis.

Authors:  Florence Robert-Gangneux; Marie-Laure Dardé
Journal:  Clin Microbiol Rev       Date:  2012-04       Impact factor: 26.132

6.  Assessment of Toxoplasma gondii levels in zebra mussel (Dreissena polymorpha) by real-time PCR: an organotropism study.

Authors:  M Palos Ladeiro; A Bigot-Clivot; D Aubert; I Villena; A Geffard
Journal:  Environ Sci Pollut Res Int       Date:  2015-03-14       Impact factor: 4.223

7.  Recovery of diverse microbes in high turbidity surface water samples using dead-end ultrafiltration.

Authors:  Bonnie Mull; Vincent R Hill
Journal:  J Microbiol Methods       Date:  2012-10-12       Impact factor: 2.363

8.  Hydrologic and vegetative removal of Cryptosporidium parvum, Giardia lamblia, and Toxoplasma gondii Surrogate microspheres in coastal wetlands.

Authors:  Jennifer N Hogan; Miles E Daniels; Fred G Watson; Stori C Oates; Melissa A Miller; Patricia A Conrad; Karen Shapiro; Dane Hardin; Clare Dominik; Ann Melli; David A Jessup; Woutrina A Miller
Journal:  Appl Environ Microbiol       Date:  2013-01-11       Impact factor: 4.792

Review 9.  Molecules to modeling: Toxoplasma gondii oocysts at the human-animal-environment interface.

Authors:  Elizabeth VanWormer; Heather Fritz; Karen Shapiro; Jonna A K Mazet; Patricia A Conrad
Journal:  Comp Immunol Microbiol Infect Dis       Date:  2012-12-04       Impact factor: 2.268

10.  Attempted detection of Toxoplasma gondii oocysts in environmental waters using a simple approach to evaluate the potential for waterborne transmission in the Galápagos Islands, Ecuador.

Authors:  Michelle L Verant; Noemi d'Ozouville; Patricia G Parker; Karen Shapiro; Elizabeth VanWormer; Sharon L Deem
Journal:  Ecohealth       Date:  2013-12-05       Impact factor: 3.184

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