Literature DB >> 10675606

Intact Cryptosporidium parvum oocysts isolated after in vitro excystation are infectious to neonatal mice.

N F Neumann1, L L Gyürék, G R Finch, M Belosevic.   

Abstract

In vitro excystation is often used as a measure of viability of encysted protozoan parasites. Parasites that do not excyst in vitro are assumed to be non-viable and non-infectious, whereas those that do excyst are assumed viable. To test the validity of these assumptions, Cryptosporidium parvum oocysts were excysted in vitro using two different excystation protocols, and the non-excysted intact oocysts were isolated using flow cytometry. Non-excysted sorted oocysts readily infected neonatal CD-1 mice. Increasing the duration of the excystation assays from 1 h to 3 h resulted in a higher percent of excysted oocysts, but the remaining non-excysted parasites were still capable of infecting neonatal CD-1 mice. Our results suggest that in vitro excystation is not an accurate measure of the viability or infectious potential of C. parvum oocysts.

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Year:  2000        PMID: 10675606     DOI: 10.1111/j.1574-6968.2000.tb08980.x

Source DB:  PubMed          Journal:  FEMS Microbiol Lett        ISSN: 0378-1097            Impact factor:   2.742


  10 in total

Review 1.  Evaluation of the effect of temperature on the die-off rate for Cryptosporidium parvum oocysts in water, soils, and feces.

Authors:  X Peng; T Murphy; N M Holden
Journal:  Appl Environ Microbiol       Date:  2008-10-10       Impact factor: 4.792

2.  Cryptosporidium parvum oocyst viability and behaviour of the residual body during the excystation process.

Authors:  Sirri Kar; Arwid Daugschies; Ayse Cakmak; Nadim Yilmazer; Katja Dittmar; Berit Bangoura
Journal:  Parasitol Res       Date:  2011-05-21       Impact factor: 2.289

3.  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

4.  Detection of infectious Cryptosporidium oocysts by cell culture immunofluorescence assay: applicability to environmental samples.

Authors:  F M Schets; G B Engels; M During; A M de Roda Husman
Journal:  Appl Environ Microbiol       Date:  2005-11       Impact factor: 4.792

5.  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

6.  Neonatal-mouse infectivity of intact Cryptosporidium parvum oocysts isolated after optimized in vitro excystation.

Authors:  L Hou; X Li; L Dunbar; R Moeller; B Palermo; E R Atwill
Journal:  Appl Environ Microbiol       Date:  2004-01       Impact factor: 4.792

7.  In vitro excystation of Cryptosporidium muris oocysts and viability of released sporozoites in different incubation media.

Authors:  Janka Melicherová; Veronika Mazourová; Andrea Valigurová
Journal:  Parasitol Res       Date:  2015-12-18       Impact factor: 2.289

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

Authors:  Cristin C Brescia; Shannon M Griffin; Michael W Ware; Eunice A Varughese; Andrey I Egorov; Eric N Villegas
Journal:  Appl Environ Microbiol       Date:  2009-09-11       Impact factor: 4.792

9.  Aged HCT-8 cell monolayers support Cryptosporidium parvum infection.

Authors:  Laura Y Sifuentes; George D Di Giovanni
Journal:  Appl Environ Microbiol       Date:  2007-10-12       Impact factor: 4.792

10.  Cryptosporidium rubeyi n. sp. (Apicomplexa: Cryptosporidiidae) in multiple Spermophilus ground squirrel species.

Authors:  Xunde Li; Maria das Graças Cabral Pereira; Royce Larsen; Chengling Xiao; Ralph Phillips; Karl Striby; Brenda McCowan; Edward R Atwill
Journal:  Int J Parasitol Parasites Wildl       Date:  2015-08-24       Impact factor: 2.674

  10 in total

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