Literature DB >> 10473398

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

T R Slifko1, D E Huffman, J B Rose.   

Abstract

Cryptosporidium is globally established as a contaminant of drinking and recreational waters. A previously described cell culture infectivity assay capable of detecting infectious oocysts was adapted to quantify viable oocysts through sporozoite invasion and clustering of foci. Eight experiments were performed by using oocysts less than 4 months of age to inoculate host HCT-8 cell monolayers. Oocysts were diluted in a standard 5- or 10-fold multiple dilution format, levels of infection and clustering were determined, and the most probable number (MPN) of infectious oocysts in the stock suspension was calculated. The MPN was compared to the initial oocyst inoculum to determine the level of correlation. For oocysts less than 30 days of age, the correlation coefficient (r) was 0.9726 (0.9306 to 0.9893; n = 20). A two-tailed P value (alpha = 0.05) indicated that P was less than 0.0001. This strong correlation suggests that the MPN can be used to effectively enumerate infectious oocysts in a cell culture system. Age affected the degree of oocyst infectivity. Oocyst infectivity was tested by the focus detection method (FDM)-MPN assay and in BALB/c mice before and after treatment with pulsed white light (PureBrite). The FDM-MPN assay and animal infectivity assays both demonstrated more than a 4 log(10) inactivation. Municipal water systems and a host of other water testing organizations could utilize the FDM-MPN assay for routine survival and disinfection studies.

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Year:  1999        PMID: 10473398      PMCID: PMC99723     

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


  22 in total

1.  Survival of Cryptosporidium parvum oocysts under various environmental pressures.

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

2.  Application of Statistics to Problems in Bacteriology: I. A Means of Determining Bacterial Population by the Dilution Method.

Authors:  H O Halvorson; N R Ziegler
Journal:  J Bacteriol       Date:  1933-02       Impact factor: 3.490

3.  PCR detection of cryptosporidium: the way forward?

Authors:  U M Morgan; R C Thompson
Journal:  Parasitol Today       Date:  1998-12

4.  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

5.  A new method for evaluating experimental cryptosporidial parasite loads using immunofluorescent flow cytometry.

Authors:  M J Arrowood; M R Hurd; J R Mead
Journal:  J Parasitol       Date:  1995-06       Impact factor: 1.276

6.  Comparative development of Cryptosporidium parvum (Apicomplexa) in 11 continuous host cell lines.

Authors:  S J Upton; M Tilley; D B Brillhart
Journal:  FEMS Microbiol Lett       Date:  1994-05-15       Impact factor: 2.742

7.  Cryptosporidium parvum oocysts recovered from water by the membrane filter dissolution method retain their infectivity.

Authors:  T K Graczyk; R Fayer; M R Cranfield; R Owens
Journal:  J Parasitol       Date:  1997-02       Impact factor: 1.276

8.  Effects of low temperatures on viability of Cryptosporidium parvum oocysts.

Authors:  R Fayer; T Nerad
Journal:  Appl Environ Microbiol       Date:  1996-04       Impact factor: 4.792

9.  Cryptosporidium parvum infection of Caco-2 cell monolayers induces an apical monolayer defect, selectively increases transmonolayer permeability, and causes epithelial cell death.

Authors:  J K Griffiths; R Moore; S Dooley; G T Keusch; S Tzipori
Journal:  Infect Immun       Date:  1994-10       Impact factor: 3.441

10.  Dose response of Cryptosporidium parvum in outbred neonatal CD-1 mice.

Authors:  G R Finch; C W Daniels; E K Black; F W Schaefer; M Belosevic
Journal:  Appl Environ Microbiol       Date:  1993-11       Impact factor: 4.792

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  26 in total

1.  Decrease in Cryptosporidium parvum oocyst infectivity in vitro by using the membrane filter dissolution method for recovering oocysts from water samples.

Authors:  R A Carreno; N J Pokorny; S C Weir; H Lee; J T Trevors
Journal:  Appl Environ Microbiol       Date:  2001-07       Impact factor: 4.792

Review 2.  In vitro cultivation of cryptosporidium species.

Authors:  Michael J Arrowood
Journal:  Clin Microbiol Rev       Date:  2002-07       Impact factor: 26.132

3.  Effects of the Norwegian winter environment on Giardia cysts and Cryptosporidium oocysts.

Authors:  L J Robertson; B K Gjerde
Journal:  Microb Ecol       Date:  2004-02-02       Impact factor: 4.552

4.  Assessment of methods for detection of infectious Cryptosporidium oocysts and Giardia cysts in reclaimed effluents.

Authors:  W Quintero-Betancourt; A L Gennaccaro; T M Scott; J B Rose
Journal:  Appl Environ Microbiol       Date:  2003-09       Impact factor: 4.792

5.  In vitro determination of anticryptosporidial activity of phytogenic extracts and compounds.

Authors:  Klaus Teichmann; Maxime Kuliberda; Gerd Schatzmayr; Franz Hadacek; Anja Joachim
Journal:  Parasitol Res       Date:  2012-01-26       Impact factor: 2.289

6.  Use of cell culture to assess Cryptosporidium parvum survival rates in natural groundwaters and surface waters.

Authors:  Rebecca L Ives; Amy M Kamarainen; David E John; Joan B Rose
Journal:  Appl Environ Microbiol       Date:  2007-08-03       Impact factor: 4.792

7.  Interactions of Cryptosporidium parvum, Giardia lamblia, vaccinal poliovirus type 1, and bacteriophages phiX174 and MS2 with a drinking water biofilm and a wastewater biofilm.

Authors:  Karim Helmi; Sylvain Skraber; Christophe Gantzer; Raphaël Willame; Lucien Hoffmann; Henry-Michel Cauchie
Journal:  Appl Environ Microbiol       Date:  2008-02-15       Impact factor: 4.792

8.  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

9.  Impact of zooplankton grazing on the excystation, viability, and infectivity of the protozoan pathogens Cryptosporidium parvum and Giardia lamblia.

Authors:  S J Connelly; E A Wolyniak; K L Dieter; C E Williamson; K L Jellison
Journal:  Appl Environ Microbiol       Date:  2007-09-14       Impact factor: 4.792

10.  Comparison of method 1623 and cell culture-PCR for detection of Cryptosporidium spp. in source waters.

Authors:  Mark W LeChevallier; George D Di Giovanni; Jennifer L Clancy; Zia Bukhari; Shan Bukhari; Jeffrey S Rosen; Jose Sobrinho; Michelle M Frey
Journal:  Appl Environ Microbiol       Date:  2003-02       Impact factor: 4.792

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