Aged HCT-8 Cell Monolayers Support Cryptosporidium parvum Infection
- 1 December 2007
- journal article
- Published by American Society for Microbiology in Applied and Environmental Microbiology
- Vol. 73 (23) , 7548-7551
Abstract
Cell culture assays in various formats have been used to study the infectivity of Cryptosporidium spp. as well as to determine the infectivity of naturally occurring oocysts in water. Currently, cell culture assays for infectious Cryptosporidium spp. in water have largely been limited to practice in research laboratories. One obstacle to the routine use of Cryptosporidium cell culture assays for the analysis of water samples is the coordination of water sample collection and processing with readiness of cell culture monolayers. For most Cryptosporidium cell culture assays, monolayers are allowed to develop for 24 to 48 h to reach 80 to 100% confluence prior to inoculation. In this study, we used immunofluorescent assay microscopy to evaluate freshly confluent (2-day-old) and aged (8- to 67-day-old) HCT-8 cell monolayers for their ability to support Cryptosporidium parvum infection. HCT-8 monolayers as old as 67 days were clearly shown to support infection. In two of three experiments, aged monolayers (8- to 11-day-old and 11- to 22-day-old, respectively) developed the same number of C. parvum clusters of infection as freshly confluent monolayers. Results suggest that it may be possible to use cell monolayers from freshly confluent to 3 weeks old on hand for infectivity assays without having to schedule sample processing to coincide with development of freshly confluent monolayers. This would make Cryptosporidium cell culture assays much more feasible for water quality and utility laboratories.Keywords
This publication has 37 references indexed in Scilit:
- In vitro development of Cryptosporidium parvum in serum-free mediaLetters in Applied Microbiology, 2007
- Molecular Fingerprinting of Cryptosporidium Oocysts Isolated during Water MonitoringApplied and Environmental Microbiology, 2006
- Quantification of In Vitro and In Vivo Cryptosporidium parvum Infection by Using Real-Time PCRApplied and Environmental Microbiology, 2006
- Application of Quantitative Real-Time Reverse Transcription-PCR in Assessing Drug Efficacy against the Intracellular Pathogen Cryptosporidium parvum In VitroAntimicrobial Agents and Chemotherapy, 2005
- UV Inactivation of Cryptosporidium hominis as Measured in Cell CultureApplied and Environmental Microbiology, 2005
- Cell Culture-Taqman PCR Assay for Evaluation of Cryptosporidium parvum DisinfectionApplied and Environmental Microbiology, 2003
- IntactCryptosporidium parvumoocysts isolated after in vitro excystation are infectious to neonatal miceFEMS Microbiology Letters, 2000
- In Vitro Evaluation of Anticryptosporidial Agents Using MDCK Cell Culture and Chemiluminescence ImmunoassayJournal of Eukaryotic Microbiology, 1996
- In vitro anticryptosporidial activity of dinitroaniline herbicidesFEMS Microbiology Letters, 1996
- Comparative development ofCryptosporidium parvum(Apicomplexa) in 11 continuous host cell linesFEMS Microbiology Letters, 1994