Chapter 5 Virus Occurrence and Survival in the Environmental Waters

Perspectives in Medical Virology

Volumn 17, Issue , 2007, Pages 91-108

  Gerba, Charles P ^a  

^a UNIVERSITY OF ARIZONA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 34548398871     PISSN: 01687069     EISSN: None     Source Type: Book Series    
DOI: 10.1016/S0168-7069(07)17005-1     Document Type: Review

References (100)

1. Abbaszadegan M., LeChevallier M., and Gerba C.P. Occurrence of viruses in U.S. groundwaters. J Am Water Works Assoc 95 9 (2003) 107-120
2. Abbaszadegan M., Stewart P., and LeChevallier M. A strategy for detection of viruses in groundwater by PCR. Appl Environ Microbiol 65 (1999) 444-449
3. Ansari S.A., Farrah S.R., and Chaudhry G.R. Presence of human immunodeficiency virus nucleic acids in wastewater and their detection by polymerase chain reaction. Appl Environ Microbiol 58 (1992) 3984-3990
4. Benton W.H., and Hurst C.J. Evaluation of mixed cell types and 5-iodo-2′-deoxyuridine treatment upon plaque assay titers of human enteric viruses. Appl Environ Microbiol 51 (1986) 1036-1040
5. Betancourt W.Q., and Rose J.B. Microbiological assessment of ambient waters and proposed water sources for restoration of a Florida wetland. J Water Health 3 (2005) 89-100
6. Bofill-Mass S., Pina S., and Girones R. Documenting the epidemiologic patterns of polymaviruses in human populations by studying their presence in urban sewage. Appl Environ Microbiol 66 (2000) 238-245
7. Borchardt M.A., Bertz P.D., Spencer S.K., and Battigelli D.A. Incidence of enteric viruses in groundwater from household wells in Wisconsin. Appl Environ Microbiol 69 (2003) 1172-1180
8. Borchardt M.A., Haas N.L., and Hunt R.J. Vulnerability of drinking-water wells in La Crosse, Wisconsin, to enteric-virus contamination from surface water contributions. Appl Environ Microbiol 70 (2004) 5937-5946
9. Bosch A., Lucena F., Girones R., and Cofre J. Survey of viral pollution in Besos River. J Water Pollut Control Fed 58 (1986) 87-91
10. Bosch A., Pinto R.M., and Abad F.X. Survival and transport of enteric viruses in the environment. In: Goyal S.M. (Ed). Viruses in Foods (2006), Springer, New York, NY 151-187
11. Bruniger S., Peters J., Borchers U., and Kao M. Further studies on the thermal resistance of bovine parvovirus against moist and dry heat. Int J Hyg Environ Health 203 (2000) 71-75
12. Carducci A., Casni B., Bani A., Rovini E., Verani M., Masón F., and Giuntin A. Virological control of groundwater quality using bimolecular tests. Water Sci Technol 47 (2003) 261-266
13. Chan-Yeung M., and Xu R.H. SARS: epidemiology. Respirology 8 Suppl. (2003) S9-S14
14. Chang S.L. Interactions between animal viruses and higher forms of microbes. J Sanit. Eng Div Am Soc Civil Eng 96 (1971) 151-161
15. Chapron C.D., Ballester N.A., Fontaine J.H., Frades C.N., and Margolin A.B. Detection of astroviruses, enteroviruses, and adenovirus types 40 and 41 in surface water collected and evaluated by the information collection rule and an integrated cell culture-nested PCR procedure. Appl Environ Microbiol 66 (2000) 2525-2529
16. Cliver D.O., and Hermann J.E. Proteolytic and microbial inactivation of enteroviruses. Water Res 6 (1972) 797-805
17. Crance J.M., Gantzer C., Schwartzbrod, and Deloince R. Effect of temperature on the survival of hepatitis A virus and its capsidal antigen in synthetic seawater. Environ Toxicol Water Qual 13 (1998) 89-92
18. Curriero F.C., Patz J.A., Rose J.B., and Leile S. The association between extreme precipitation and waterborne disease outbreaks in the United States, 1948-1994. Am J Public Health 91 (2001) 1194-1199
19. De Flora S., De Renzi G., and Badolati G. Detection of animal viruses in coastal seawater and sediments. Appl Environ Microbiol 30 (1975) 472-475
20. Dimmock N.J. Differences between the thermal inactivation of picornaviruses at "high" and "low" temperatures. Virology 31 (1967) 338-353
21. Divizia M., De Filippi P., Di Napoli A., Venuti A., Perez-Bercoff R., and Pana A. Isolation of wild-type hepatitis A virus from the environment. Water Res 23 (1989) 1155-1160
22. Donaldson K.A., Griffin D.W., and Paul J.H. Detection, quantitation and identification of enteroviruses from surface waters and sponge tissue from the Florida Keys using real time PCR. Water Res 36 (2002) 2414-2505
23. Estes M.K., Graham D.Y., Smith E.M., and Gerba C.P. Rotavirus stability and inactivation. J Gen Virol 43 (1979) 403-409
24. Fattal B., Vasl R.J., Katzenelson E., and Shuval H.I. Survival of bacterial indicator organisms and enteric viruses in the Mediterranean coastal waters of Tel Aviv. Water Res 17 (1983) 397-402
25. Finance C., Briguad M., Lucena F., Aymard M., Bosch A., and Schwartzbrod L. Viral pollution of seawater of Barcelona. Zentralbl Bakteriol Mikrobiol Hyg B176 (1982) 530-536
26. Fout G.S., Martinson B.C., Moyer M.W.N., and Dahling D.R. A multiplex reverse transcription-PCR method for detection of human enteric viruses in groundwater. Appl Environ Microbiol 69 (2003) 3158-3164
27. Fujioka R.S., Loh P.C., and Lau L.S. Survival of human enteroviruses in the Hawaiian ocean environment: evidence for virus-inactivating microorganisms. Appl Environ Microbiol 39 (1980) 1105-1110
28. Fujioka R.S., and Yoneyama B.S. Sunlight inactivation of human enteric viruses and fecal bacteria. Water Sci Technol 46 (2002) 291-295
29. Fujsaki M., Uchida S., Kojima M., Hota S., Kuroda H., and Hamada K. Studies inhibiting substances of bacterial origin. III. Antiviral substances extractable from Streptococcus faecalis: its in vitro activities and some biological characteristics. Kobe J Med Sci 24 (1978) 99-114
30. Gajardo R., Diez J.M., Cofre J., and Bosch A. Adsorption-elution with negatively and positively-charged glass powder for the concentration of hepatitis A virus from water. J Virol Methods 31 (1991) 345-351
31. Genthe B., Gericke M., Bateman B., Mjoli N., and Kfir R. Detection of enteric adenoviruses in South African water using gene probes. Water Sci Tech 31 (1995) 345-350
32. Gerba C.P. Assessment of the enteric pathogens shedding by bathers during recreational activity and its impact on water quality. Quant Microbiol 2 (2000) 55-68
33. Gerba C.P. Survival of viruses in the marine environment. In: Belkin S., and Colwell R.R. (Eds). Ocean and Health (2006), Springer, New York, NY 133-142
34. Gerba C.P., Farrah S.R., Goyal S.M., Wallis C., and Melnick J.L. Concentration of enteroviruses from large volumes of tap water, treated sewage, and sweater. Appl Environ Microbiol 35 (1978) 540-548
35. Gerba C.P., and Goyal S.M. Methods in Environmental Virology (1982), Marcel Dekker, New York, NY
36. Gerba C.P., Gramos D.M., and Nwachuku. Comparative inactivation of enteroviruses and adenovirus 2 by UV Light. Appl Environ Microbiol 68 (2002) 5167-5169
37. Girones R., Puig M., Allard A., Lucena F., Wadekk G., and Jofre J. Detection of adenoviruses and enteroviruses by amplification in polluted waters. Waer Sci Technol 31 (1995) 351-357
38. Goyal S.M., Gerba C.P., and Melnick J.L. Human enteroviruses in oysters and their overlaying waters. Appl Environ Microbiol 37 (1978) 572-581
39. Goyal S.M. Viral pollution of the marine environment. Crit Rev Environ Contr 14 (1984) 1-32
40. Grabow W.O., Puttergill D.L., and Bosch A. Propagation of adenovirus types 40 and 41 in the PLC/PLF/5 primary liver cacinonma cell line. J Virol Meth 37 (1992) 201-207
41. Griffin D., Gibson III C.J., Lipp E.K., Riley K., Paul J.H., and Rose J.B. Detection of viral pathogens by reverse transcriptase PCR and of microbial indicators by standard methods in the canals of the Florida Keys. Appl Environ Microbiol 65 (1999) 4118-4125
42. Griffin D.W., Donaldson K.A., Paul J.H., and Rose J.B. Pathogenic human viruses in coastal waters. Clin Microbiol Rev 16 (2003) 129-143
43. Haas C.N., Rose J.B., and Gerba C.P. Quantitative Microbial Risk Assessment (1999), Wiley, New York, NY
44. Hejkal T.W., Smith E.M., and Gerba C.P. Seasonal occurrence of rotavirus in sewage. Appl Environ Microbiol 47 (1984) 588-590
45. Hot D., Legeay D., Jacques J., Gantzer C., Caudrelier Y., Guyard K., Lange M., and Andreoletti L. Detection of somatic phages, infectious enteroviruses and enterovirus genomes as indicators of human enteric viral pollution in surface water. Water Res 37 (2003) 4703-4710
46. Hugues B., Cini A., Plissier M., and Lefebre J.R. Resherche des virus dans le marina a parit'echantilons de volumes differents. Eau Ouectc 13 (1980) 199-203
47. Jiang S., and Chu W. PCR detection of pathogenic viruses in southern California urban rivers. J Appl Microbiol 97 (2004) 17-28
48. Jiang S., Noble R., and Chu W. Human adenoviruses and coliphages in urban runoff-impacted coastal waters of Southern California. Appl Environ Microbiol 67 (2001) 179-184
49. John D.E., and Rose J.B. A review of factors affecting microbial survival in ground water. Environ Sci Technol 39 (2005) 7345-7356
50. Kapuscinski R.B., and Mitchell R. Processes controlling virus inactivation in coastal waters. Water Res 14 (1980) 363-371
51. Katayama H., Okuma K., Furumai H., and Ohgaki S. Series of surveys for enteric viruses and indicator organisms in Tokyo Bay after an event of combined sewer over flows. Water Sci Technol 50 (2004) 259-362
52. Kingsley R., Hoover D.G., Papafragjou W., and Richards G.P. Inactivation of hepatitis A virus and a calicivirus. J Food Protect 65 (2002) 1605-1609
53. Kittigul L., Raengsakulrach B., Sirtanikorn S., Kanyok R., Utraachkij F., Diraphat P., Thirawuth V., Sirpanichgon K., Pungchitton S., Chitpirom K., Chaichantanakit N., and Vethanophas K. Detection of poliovirus, hepatitis A virus and rotavirus from sewage and water samples. Southeast Asian J Trop Med Public Health 31 (2000) 41-46
54. Kutz S.M., and Gerba C.P. Comparison of virus survival in freshwater sources. Water Sci Technol 20 (1988) 467-471
55. Lee S.H., Lee C., Lee K.W., Cho H.B., and Kim S.J. The simultaneous detection of both enteroviruses and adenoviruses in environmental water samples including tap water with an integrated cell culture- multiplex-nested PCR procedure. J Appl Microbiol 98 (2005) 1020-1029
56. Liew P.F., and Gerba C.P. Thermostabilization of enteroviruses by estuarine sediment. Appl Environ Microbiol 40 (1980) 249-305
57. Lipp E.K., Farrah S.R., and Rose J.B. Assessment and impact of microbial fecal contamination and human enteric pathogens in a coastal community. Mar Pollut Bull 42 (2001) 258-286
58. Lipp E.K., Jarrell J.L., Griffin D.W., Lukasik J., Jacukiewicz J., and Rose J.B. Preliminary evidence for human fecal contamination in corals of the Florida Keys. Mar Pollut Bull 44 (2001) 666-670
59. Lipp E.K., Kurz R., Vincent R., Rodiguez-Palacios C., Farrah S.R., and Rose J.B. The effects of seasonal variability and weather on microbial fecal pollution and enteric pathogens in a subtropical estuary. Estuaries 24 (2001) 238-258
60. Lodder W.J., and de Roda Husman A.M. Presence of noroviruses and other enteric viruses in sewage and surface waters in the Netherlands. Appl Environ Microbiol 71 (2005) 1453-1461
61. Lucena F., Schwartzbrod L., and Bosch A. The effect of mass poliomyelitis vaccination program on the occurrence of enterovirus in seawater. Zentralbl Bakteriol Mikrobiol Hyg B183 (1986) 67-69
62. Marzouk Y., Goyal S.M., and Gerba C.P. Prevalence of enteroviruses in ground water of Israel 17 (1979) 487-491
63. Mathur A.K., Nivedita K., Rejesh S.C., Maitra, and Chaturvedi U.C. Viruria during acute Japanese encephalitis virus infection. Int J Exp Path 76 (1995) 103-109
64. Melnick J.L., and Gerba C.P. The ecology of enteroviruses in natural waters. Crit Rev Environ Contr 10 (1980) 65-93
65. Morris R., and Waite W.M. Evaluation of procedures for recovery of viruses from water-II detection systems. Water Res 14 (1980) 795-798
66. Murray J.P., and Laband J.J. Degradation of poliovirus adsorption on inorganic surfaces. Appl Environ Microbiol 37 (1979) 480-486
67. Noble R.T., and Fuhrman J.A. Enteroviruses detected by reverse transcripase polymerase chain reaction from coastal waters of Santa Monica Bay, California: low correlation to bacterial indicator levels. Hydrobiologia 460 (2001) 175-184
68. Payment P., Berte A., Prevost M., Menard B., and Barbeau B. Occurrence of pathogenic microorganisms in the Saint-Lawrence River (Canada) and comparison of health risks for populations using it as their source of drinking water. Can J Microbiol 46 (2000) 565-576
69. Pianetti A., Baffone B., Citterio A., Casaroli F., Bruscolini F., and Salvaggio L. Presence of enteroviruses and reoviruses in waters of the Italian coast of the Adriatic Sea. Epidemiol Infect 125 (2000) 455-462
70. Pina S., Puig M., Lucena F., Cofre J., and Girones R. Viral pollution in the environment and in shellfish: human adenovirus detection by PCR as an index of human viruses. Appl Environ Microbiol 64 (1998) 3376-3382
71. Pinto R.M., Diez J.M., and Bosch A. Use of the colonia carcinoma cell line CaCo-2 for in vivo amplification and detection of enteric viruses. J Med Virol 44 (1994) 310-315
72. Pohjanpelto P. Response of enteroviruses to cystine. Virology 15 (1961) 225-230
73. Powell K.L., Taylor R.G., Cronin A.A., Barrett M.H., Pedley S., Sellwood J., Trowsdale S.A., and Lerner D.N. Microbial contamination of two urban sandstone aquifers in the UK. Water Res 37 (2003) 339-352
74. Pusch D., Oh D.Y., Wolf S., Dumke R., Schroter-Bobsin U., Hohne M., Roske I., and Schreier E. Detection of enteric viruses and bacterial indicators in German environmental waters. Arch Virol 150 (2005) 929-947
75. Rao V.C., Metcalf T.C., and Melnick J.L. Development of a method for concentration of rotavirus and its application to recovery of rotaviruses in estuarine waters. Appl Environ Microbiol 52 (1986) 484-488
76. Rao V.C., Seidel K.N., Goyal S.M., Metcalf T.C., and Melnick J.L. Isolation of enteroviruses from water, suspended solids and sediments from Galveston bay; survival of poliovirus and rotavirus adsorbed to sediments. Appl Environ Microbiol 48 (1984) 404-409
77. Reynolds K.A., Gerba C.P., and Pepper I.L. Detection of infectious enteroviruses by an integrated cell culture-PCR procedure. Appl Environ Microbiol 62 (1996) 1424-1427
78. Reynolds K.A., Roll K., Fujioka R.S., Gerba C.P., and Pepper I.L. Incidence of enteroviruses in Mamala Bay, Hawaii using cell culture and direct polymerase chain reaction methodologies. Can J Microbiol 44 (1998) 598-604
79. Rose J.B., Mullinax R.L., Singh S.N., Yates M.V., and Gerba C.P. Occurrence of rotaviruses and enteroviruses in recreational waters of Oak Creek, Arizona. Water Res 21 (1987) 1375-1381
80. Rose M.A., Dhar A.K., Brooks H.A., Zecchini F., and Gersberg R.M. Quanitation of hepatitis A virus and enterovirus levels in the lagoon canals and Lido beach of Venice, Italy, using real-time RT-PCR. Water Res 40 (2006) 2387-2396
81. Salo R.J., and Cliver D.O. Effect of acid, salts, and temperature on the infectivity and physical integrity of enteroviruses. Arch Virol 52 (1976) 269-282
82. Sarker J.K., Mitra A.C., Mukherjee M.K., and De S.K. Virus excretion in smallpox. Bull World Organ 48 (1973) 523-527
83. Schaiberger G.E., Edmond T.D., and Gerba C.P. Distribution of enteroviruses in sediments contiguous with a deep marine sewage outfall. Water Res 16 (1982) 1425-1428
84. Singer B., and Fraenkel-Conrat H. Effects of benonite and stability of TMV-RNA. Virology 14 (1961) 59-65
85. Smith E.M., Gerba C.P., and Melnick J.L. Role of sediment in the persistence of enteroviruses in the estuarine environment. Appl Environ Microbiol 35 (1978) 685-689
86. Tani N., Dohi Y., Kurumatani N., and Yonemasu K. Seasonal distribution of adenoviruses, enteroviruses and reoviruses in urban river water. Microbiol Immunol 39 (1995) 577-580
87. Taylor M.B., Cox N., Very M.A., and Grabow W.O. The occurrence of hepatitis A and astroviruses in selected river and dam waters in South Africa. Water Res 35 (2001) 2653-2660
88. Thompson S.S., and Yates M.V. Bacteriophages inactivation at the air-water-solid interface in dynamic batch systems. Appl Environ Microbiol 65 (1999) 1186-1190
89. Thurman R.B., and Gerba C.P. Molecular mechanisms of viral inactivation by water disinfectants. Adv Appl Microbiol 33 (1988) 75-105
90. Vaidya S.R., Chitambar S.D., and Arankalle V.A. Polymerase chain reaction-based prevalence of hepatitis A, hepatitis E and TT viruses in sewage from an endemic area. J Hepatol 37 (2002) 131-136
91. Van Heerden J., Ehlers M.M., Hiem A., and Grabow W.O.K. Prevalence, quantification and typing of adenoviruses detected in river and treated drinking water in South Africa 99 (2005) 234-242
92. Van Heerden J., Ehlers M.M., van Zyl W.V., and Grabow W.O.K. Incidence of adenoviruses in raw and treated water. Water Res 37 (2003) 3704-3708
93. Van Zyl W.B., Williams P.J., Grabow W.O., and Taylor M.B. Application of a molecular method for the detection of group A rotavirus in raw and treated water. Water Sci Technol 50 (2004) 223-228
94. Vantarakis A.C., and Papapetropoulou M. Detection of enteroviruses and adenoviruses in coastal waters in SW Greece by nested polymerase chain reaction. Water Res 32 (1998) 2356-2372
95. Vaughn J.M., Landry E.F., Thomas M.Z., Vicale T.J., and Penello W.F. Survey of human enterovirus occurrence in fresh and marine waters on Long-Island. Appl Environ Microbiol 38 (1979) 290-296
96. Wallis C., and Melnick J.L. Photodynamic inactivation of animal viruses: a review. Photochem Photobiol 4 (1965) 159-170
97. 4 on the thermostability of viruses. Virology 26 (1965) 694-695
98. Walter R., Macht W., Durkrop J., Hecht R., Hornig U., and Schulze P. Virus levels in river water. Water Res 23 (1989) 133-138
99. Wetz J.J., Lipp E.K., Griffin D.W., Lukasik J., Wait D., Sobsey M.D., Scott T.M., and Rose J.B. Presence, infectivity and stability of enteric viruses in seawater: relationship to marine water quality in the Florida Keys. Mar Pollut Bull 48 (2004) 698-704
100. Yates M.V., Gerba C.P., and Kelly L.M. Virus persistence in groundwater. Appl Environ Microbiol 49 (1985) 778-781