Literature DB >> 9279581

Nucleic acid stains as indicators of Cryptosporidium parvum oocyst viability.

M Belosevic1, R A Guy, R Taghi-Kilani, N F Neumann, L L Gyürék, L R Liyanage, P J Millard, G R Finch.   

Abstract

We developed nucleic acid dye staining methodology for untreated, heat-treated and chemically inactivated C. parvum oocysts. The nucleic acid staining was compared to in vitro excystation and animal infectivity using split samples of oocysts. Among the nucleic acid stains tested, SYTO-9, hexidium and SYTO-59 stained the oocysts consistently, and the staining was related to the infectivity of the oocysts to neonatal CD-1 mice but not to in vitro excystation. The nucleic acid viability assay was used to determine log-inactivations of the oocysts after treatment with ozone, chlorine, chlorine dioxide and combinations of different chemical disinfectants, and was found to indicate log-inactivation levels similar to that of animal infectivity. A combined immunofluorescence-nucleic acid staining assay was developed for the oocysts of C. parvum and this assay will be invaluable for the detection and viability of oocysts in the laboratory and in environmental samples.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9279581     DOI: 10.1016/s0020-7519(97)00033-7

Source DB:  PubMed          Journal:  Int J Parasitol        ISSN: 0020-7519            Impact factor:   3.981


  11 in total

1.  Comparison of animal infectivity and nucleic acid staining for assessment of Cryptosporidium parvum viability in water.

Authors:  N F Neumann; L L Gyürek; L Gammie; G R Finch; M Belosevic
Journal:  Appl Environ Microbiol       Date:  2000-01       Impact factor: 4.792

2.  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

3.  Chlorine dioxide inactivation of Cryptosporidium parvum oocysts and bacterial spore indicators.

Authors:  C P Chauret; C Z Radziminski; M Lepuil; R Creason; R C Andrews
Journal:  Appl Environ Microbiol       Date:  2001-07       Impact factor: 4.792

4.  A most-probable-number assay for enumeration of infectious Cryptosporidium parvum oocysts.

Authors:  T R Slifko; D E Huffman; J B Rose
Journal:  Appl Environ Microbiol       Date:  1999-09       Impact factor: 4.792

5.  Quantitative flow cytometric evaluation of maximal Cryptosporidium parvum oocyst infectivity in a neonate mouse model.

Authors:  A Delaunay; G Gargala; X Li; L Favennec; J J Ballet
Journal:  Appl Environ Microbiol       Date:  2000-10       Impact factor: 4.792

6.  Discrimination between viable and dead Encephalitozoon cuniculi (Microsporidian) spores by dual staining with sytox green and calcofluor white M2R.

Authors:  L C Green; P J LeBlanc; E S Didier
Journal:  J Clin Microbiol       Date:  2000-10       Impact factor: 5.948

7.  Quantitative-PCR assessment of Cryptosporidium parvum cell culture infection.

Authors:  George D Di Giovanni; Mark W LeChevallier
Journal:  Appl Environ Microbiol       Date:  2005-03       Impact factor: 4.792

8.  CP2 gene as a useful viability marker for Cryptosporidium parvum.

Authors:  Soo-Ung Lee; Migyo Joung; Myoung-Hee Ahn; Sun Huh; Hyunje Song; Woo-Yoon Park; Jae-Ran Yu
Journal:  Parasitol Res       Date:  2007-12-01       Impact factor: 2.289

9.  Viability of preserved Cryptosporidium baileyi oocysts.

Authors:  Chan-Gu Surl; Se-Min Kim; Hyeon-Cheol Kim
Journal:  Korean J Parasitol       Date:  2003-12       Impact factor: 1.341

10.  Molecular evidence of Sarcocystis nesbitti in water samples of Tioman Island, Malaysia.

Authors:  Shahhaziq Shahari; Tengku Idzzan Nadzirah Tengku-Idris; Mun Yik Fong; Yee Ling Lau
Journal:  Parasit Vectors       Date:  2016-11-23       Impact factor: 3.876

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.