Abstract
Recent studies have provided a greater understanding of the movement of viruses in the environment by their attachment to solids. These studies have focused on solids-associated viruses present in wastewater discharged into the ocean and on viruses in sludge and wastewater that may be retained in soil following their land disposal. Such ocean or land disposal of wastewater and sludge may result in a discharge of one or more of 120 human enteric virus pathogens including those causing poliomyelitis, viral hepatitis A and acute gastroenteritis.
Solids-associated viruses in effluents discharged into coastal waters accumulate in bottom sediments, which may contain 10 to 10 000 more virus per unit volume than the overlying seawater. Solids-associated viruses resuspended by water turbulence may be transported from polluted to distant non-polluted recreational or shellfish-growing water. Transmission of viruses causing hepatitis or gastroenteritis may result from contact by bathers or swimmers with these viruses in recreational waters, or from ingestion of raw or improperly cooked shellfish in which the solids-associated virus had been bioaccumulated.
The land disposal of sludge and wastewater has a potential of causing infections in farm workers, contamination of crops, pollution of raw potable water sources or infiltration of ground water. Viruses retained on soils can be released by rain water and may contaminate ground water through lateral and vertical movements.
Full text
PDF













Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Berg G., Berman D. Destruction by anaerobic mesophilic and thermophilic digestion of viruses and indicator bacteria indigenous to domestic sludges. Appl Environ Microbiol. 1980 Feb;39(2):361–368. doi: 10.1128/aem.39.2.361-368.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Berg G., Berman D. Destruction by anaerobic mesophilic and thermophilic digestion of viruses and indicator bacteria indigenous to domestic sludges. Appl Environ Microbiol. 1980 Feb;39(2):361–368. doi: 10.1128/aem.39.2.361-368.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Frösner G. G. Züchtung des Hepatitis-A-Virus in Gewebekultur: Möglichkeit zur Virusproduktion für Impfstoffe und Testzwecke, zur Untersuchung von Patienten auf Infektiosität und zur Prüfung von Desinfektionsmitteln. Offentl Gesundheitswes. 1982 Jun;44(6):370–373. [PubMed] [Google Scholar]
- Goyal S. M., Schaub S. A., Wellings F. M., Berman D., Glass J. S., Hurst C. J., Brashear D. A., Sorber C. A., Moore B. E., Bitton G. Round robin investigation of methods for recovering human enteric viruses from sludge. Appl Environ Microbiol. 1984 Sep;48(3):531–538. doi: 10.1128/aem.48.3.531-538.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Melnick J. L., Gerba C. P. Viruses in water and soil. Public Health Rev. 1980 Jul-Dec;9(3-4):185–213. [PubMed] [Google Scholar]
- Melnick J. L., Gerba C. P. Viruses in water and soil. Public Health Rev. 1980 Jul-Dec;9(3-4):185–213. [PubMed] [Google Scholar]
- Siegl G., Weitz M., Kronauer G. Stability of hepatitis A virus. Intervirology. 1984;22(4):218–226. doi: 10.1159/000149554. [DOI] [PubMed] [Google Scholar]
- Wait D. A., Sobsey M. D. Method for recovery of enteric viruses from estuarine sediments with chaotropic agents. Appl Environ Microbiol. 1983 Aug;46(2):379–385. doi: 10.1128/aem.46.2.379-385.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ward R. L., Ashley C. S. Heat inactivation of enteric viruses in dewatered wastewater sludge. Appl Environ Microbiol. 1978 Dec;36(6):898–905. doi: 10.1128/aem.36.6.898-905.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]