Detection of enteric viruses in treated wastewater sludge using cell culture and molecular methods

Persistent Link:
http://hdl.handle.net/10150/191353
Title:
Detection of enteric viruses in treated wastewater sludge using cell culture and molecular methods
Author:
Sabalos, Constantine Marc.
Issue Date:
1998
Publisher:
The University of Arizona.
Rights:
Copyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author.
Abstract:
Two continuous cell lines, BGM and CaCo-2 were compared for the detection of viruses in mesophilic treated sludge (MIS) and secondary disinfected wastewater effluent (WWE) samples. Samples were inoculated in both cell lines and examined microscopically for cytopathogenic effect (CPE) for 14 days. Enumeration by the most probable number (MPN) method and statistical analysis revealed significantly greater MPN values for CaCo-2 than in BGM cells for WWE. Statistical analysis of MTS and WWE samples showed that CaCo-2 cells were more sensitive than BGM (p=0.0287). This suggests that CaCo-2 cells are more sensitive for the detection of enteroviruses in environmental samples. M-PCR was developed to detect and differentiate human adenovirus (Ad) from enteric adenovirus (Ead) from seeded environmental samples. Two sets of primers hexAA1885/1913 and K402/403 (308 bp and 152 bp amplicons respectively) were chosen for combination in M-PCR. The optimum MgC12 concentration was 1.25 mM with primer concentration of 100 pmol for hexAA1885/1913 and 50 pmol for K4021403 primers. Optimum primer annealing temperature was 60° C. Sensitivity of M-PCR was 10^2 TC1D50 for Ead and Ad mixed and 10^0 TCID50 for individual viruses per reaction. M-PCR has potential in the rapid and specific identification of these types of viruses in environmental samples.
Type:
Thesis-Reproduction (electronic); text
LCSH Subjects:
Hydrology.; Sewage sludge -- Analysis.; Sewage sludge -- Health aspects.; Enteroviruses -- Analysis.; Cell culture -- Technique.; Effluent quality -- Measurement.
Degree Name:
M.S.
Degree Level:
masters
Degree Program:
Soil, Water, and Environmental Science; Graduate College
Degree Grantor:
University of Arizona
Committee Chair:
Gerba, Charles P.

Full metadata record

DC FieldValue Language
dc.language.isoenen_US
dc.titleDetection of enteric viruses in treated wastewater sludge using cell culture and molecular methodsen_US
dc.creatorSabalos, Constantine Marc.en_US
dc.contributor.authorSabalos, Constantine Marc.en_US
dc.date.issued1998en_US
dc.publisherThe University of Arizona.en_US
dc.rightsCopyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author.en_US
dc.description.abstractTwo continuous cell lines, BGM and CaCo-2 were compared for the detection of viruses in mesophilic treated sludge (MIS) and secondary disinfected wastewater effluent (WWE) samples. Samples were inoculated in both cell lines and examined microscopically for cytopathogenic effect (CPE) for 14 days. Enumeration by the most probable number (MPN) method and statistical analysis revealed significantly greater MPN values for CaCo-2 than in BGM cells for WWE. Statistical analysis of MTS and WWE samples showed that CaCo-2 cells were more sensitive than BGM (p=0.0287). This suggests that CaCo-2 cells are more sensitive for the detection of enteroviruses in environmental samples. M-PCR was developed to detect and differentiate human adenovirus (Ad) from enteric adenovirus (Ead) from seeded environmental samples. Two sets of primers hexAA1885/1913 and K402/403 (308 bp and 152 bp amplicons respectively) were chosen for combination in M-PCR. The optimum MgC12 concentration was 1.25 mM with primer concentration of 100 pmol for hexAA1885/1913 and 50 pmol for K4021403 primers. Optimum primer annealing temperature was 60° C. Sensitivity of M-PCR was 10^2 TC1D50 for Ead and Ad mixed and 10^0 TCID50 for individual viruses per reaction. M-PCR has potential in the rapid and specific identification of these types of viruses in environmental samples.en_US
dc.description.notehydrology collectionen_US
dc.typeThesis-Reproduction (electronic)en_US
dc.typetexten_US
dc.subject.lcshHydrology.en_US
dc.subject.lcshSewage sludge -- Analysis.en_US
dc.subject.lcshSewage sludge -- Health aspects.en_US
dc.subject.lcshEnteroviruses -- Analysis.en_US
dc.subject.lcshCell culture -- Technique.en_US
dc.subject.lcshEffluent quality -- Measurement.en_US
thesis.degree.nameM.S.en_US
thesis.degree.levelmastersen_US
thesis.degree.disciplineSoil, Water, and Environmental Scienceen_US
thesis.degree.disciplineGraduate Collegeen_US
thesis.degree.grantorUniversity of Arizonaen_US
dc.contributor.chairGerba, Charles P.en_US
dc.identifier.oclc226299211en_US
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