Literature DB >> 8875309

Nucleic acid stains as indicators of Giardia muris viability following cyst inactivation.

R Taghi-Kilani1, L L Gyürék, P J Millard, G R Finch, M Belosevic.   

Abstract

A reliable viability assay for Giardia is required for the development of disinfection process design criteria and pathogen monitoring by water treatment utilities. Surveys of single-staining nucleic acid dyes (stain dead parasites only), and double-staining vital dye kits from Molecular Probes (stain live and dead parasites) were conducted to assess the viability of untreated, heat-killed, and chemically inactivated Giardia muris cysts. Nucleic acid staining results were compared to those of in vitro excystation and animal infectivity. Nucleic acid stain, designated as SYTO-9, was considered the best among the single-staining dyes for its ability to stain dead cysts brightly and its relatively slow decay rate of visible light emission following DNA binding. SYTO-9 staining was correlated to animal infectivity. A Live/Dead BacLight was found to be the better of 2 double-staining viability kits tested. Logarithmic survival ratios based on SYTO-9 and Live/Dead BacLight were compared to excystation and infectivity results for G. muris cysts exposed to ozone or free chlorine. The results indicate that SYTO-9 and Live/Dead BacLight staining is stable following treatment of cysts with chemical disinfectants.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8875309     DOI: 10.1016/0020-7519(96)00033-1

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


  5 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.  Responses of Escherichia coli, Listeria monocytogenes, and Staphylococcus aureus to simulated food processing treatments, determined using fluorescence-activated cell sorting and plate counting.

Authors:  Deirdre Kennedy; Ultan P Cronin; Martin G Wilkinson
Journal:  Appl Environ Microbiol       Date:  2011-05-20       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

4.  Critical aspects of using bacterial cell viability assays with the fluorophores SYTO9 and propidium iodide.

Authors:  Philipp Stiefel; Sabrina Schmidt-Emrich; Katharina Maniura-Weber; Qun Ren
Journal:  BMC Microbiol       Date:  2015-02-18       Impact factor: 3.605

5.  Efficiency of chlorine and UV in the inactivation of Cryptosporidium and Giardia in wastewater.

Authors:  Folasade Esther Adeyemo; Gulshan Singh; Poovendhree Reddy; Faizal Bux; Thor Axel Stenström
Journal:  PLoS One       Date:  2019-05-13       Impact factor: 3.240

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.