Large scale survey of enteric viruses in river and waste water underlines the health status of the local population

Environment International

Volumn 79, Issue , 2015, Pages 42-50

  Prevost, B ^a   Lucas, F S ^a   Goncalves, A ^b   Richard, F ^b   Moulin, L ^c   Wurtzer, S ^c  

^a AGROPARISTECH   (France)

^b SIAAP   (France)

^c R and D biologie   (France)

Author keywords

Enteric viruses; PCR; River water; Viral load; Wastewater effluent; Water contamination

Indexed keywords

CONTAMINATION; EFFLUENTS; RIVER POLLUTION; VIRUSES;

ENTERIC VIRUS; RIVER WATER; VIRAL LOAD; WASTEWATER EFFLUENTS; WATER CONTAMINATION;

RIVERS;

SURFACE WATER; VIRUS RNA; WASTE WATER;

EFFLUENT; GASTROENTERITIS; HEALTH STATUS; POLYMERASE CHAIN REACTION; RIVER WATER; VIRUS; WASTEWATER; WATER POLLUTION; WATER QUALITY; WATERBORNE DISEASE;

ADENOVIRIDAE; AICHIVIRUS; ARTICLE; ASTROVIRUS; AUTUMN; COSAVIRUS; ENTERIC VIRUS; ENTEROVIRUS; ENVIRONMENTAL IMPACT ASSESSMENT; ENVIRONMENTAL MONITORING; FRANCE; HEALTH STATUS; HEPATITIS A VIRUS; HEPATITIS E VIRUS; NONHUMAN; NOROVIRUS; POPULATION RESEARCH; PREVALENCE; PRIORITY JOURNAL; RIVER; SEASONAL VARIATION; SUMMER; URBAN AREA; VIRUS LOAD; WASTE WATER; WATER CONTAMINATION; WATER POLLUTION; WATER SAMPLING; WINTER; ANALYSIS; GENETICS; HUMAN; ISOLATION AND PURIFICATION; POLYMERASE CHAIN REACTION; PROCEDURES; VIROLOGY;

FRANCE; ILE DE FRANCE; PARIS; SEINE RIVER; VILLE DE PARIS;

ADENOVIRIDAE; ASTROVIRIDAE; ENTEROVIRUS; NOROVIRUS; ROTAVIRUS A;

ENTEROVIRUS; ENVIRONMENTAL MONITORING; FRANCE; HEALTH STATUS; HUMANS; POLYMERASE CHAIN REACTION; RIVERS; RNA, VIRAL; VIRAL LOAD; WASTE WATER; WATER POLLUTION;

EID: 84924939658     PISSN: 01604120     EISSN: 18736750     Source Type: Journal    
DOI: 10.1016/j.envint.2015.03.004     Document Type: Article

References (37)

1. Albinana-Gimenez N., Miagostovich M.P., Calgua B., Huguet J.M., Matia L., Girones R. Analysis of adenoviruses and polyomaviruses quantified by qPCR as indicators of water quality in source and drinking-water treatment plants. Water Res. 2009, 43:2011-2019.
2. Alcala A., Vizzi E., Rodriguez-Diaz J., Zambrano J.L., Betancourt W., Liprandi F. Molecular detection and characterization of Aichi viruses in sewage-polluted waters of Venezuela. Appl. Environ. Microbiol. 2010, 76:4113-4115.
3. Blacklow N.R., Greenberg H.B. Viral gastroenteritis. N. Engl. J. Med. 1991, 325:252-264.
4. Blinkova O., Rosario K., Li L., Kapoor A., Slikas B., Bernardin F., Breitbart M., Delwart E. Frequent detection of highly diverse variants of cardiovirus, cosavirus, bocavirus, and circovirus in sewage samples collected in the United States. J. Clin. Microbiol. 2009, 47:3507-3513.
5. Bucardo F., Nordgren J., Carlsson B., Kindberg E., Paniagua M., Mollby R., Svensson L. Asymptomatic norovirus infections in Nicaraguan children and its association with viral properties and histo-blood group antigens. Pediatr. Infect. Dis. J. 2010, 29:934-939.
6. Cadilhac P., Roudot-Thoraval F. Seroprevalence of hepatitis A virus infection among sewage workers in the Parisian area, France. Eur. J. Epidemiol. 1996, 12:237-240.
7. Cantalupo P.G., Calgua B., Zhao G., Hundesa A., Wier A.D., Katz J.P., Grabe M., Hendrix R.W., Girones R., Wang D., Pipas J.M. Raw sewage harbors diverse viral populations. mBio 2011, 2.
8. Cheong S., Lee C., Song S.W., Choi W.C., Lee C.H., Kim S.J. Enteric viruses in raw vegetables and groundwater used for irrigation in South Korea. Appl. Environ. Microbiol. 2009, 75:7745-7751.
9. Contreras-Coll N., Lucena F., Mooijman K., Havelaar A., Pierz V., Boque M., Gawler A., Holler C., Lambiri M., Mirolo G., Moreno B., Niemi M., Sommer R., Valentin B., Wiedenmann A., Young V., Jofre J. Occurrence and levels of indicator bacteriophages in bathing waters throughout Europe. Water Res. 2002, 36:4963-4974.
10. Dorevitch S., Dworkin M.S., Deflorio S.A., Janda W.M., Wuellner J., Hershow R.C. Enteric pathogens in stool samples of Chicago-area water recreators with new-onset gastrointestinal symptoms. Water Res. 2012, 46:4961-4972.
11. Enserink R., van den Wijngaard C., Bruijning-Verhagen P., van Asten L., Mughini-Gras L., Duizer E., Kortbeek T., Scholts R., Nagelkerke N., Smit H.A., Kooistra-Smid M., van Pelt W. Gastroenteritis attributable to 16 Enteropathogens in children attending day care. Significant effects of Rotavirus, Norovirus, Astrovirus, Cryptosporidium and Giardia. Pediatr. Infect. Dis. J. 2015, 34(1):5-10.
12. Gerba C.P., Rose J.B., Haas C.N. Sensitive populations: who is at the greatest risk?. Int. J. Food Microbiol. 1996, 30:113-123.
13. Grøndahl-Rosado R., Yarovitsyna E., Trettenes E., Myrmel M., Robertson L. A one year study on the concentrations of norovirus and enteric adenoviruses in wastewater and a surface drinking water source in Norway. Food Environ. Virol. 2014, 6:232-245.
14. Hamza I.A., Jurzik L., Stang A., Sure K., Uberla K., Wilhelm M. Detection of human viruses in rivers of a densely-populated area in Germany using a virus adsorption elution method optimized for PCR analyses. Water Res. 2009, 43:2657-2668.
15. Haramoto E., Kitajima M., Otagiri M. Development of a reverse transcription-quantitative PCR assay for detection of salivirus/klassevirus. Appl. Environ. Microbiol. 2013, 79:3529-3532.
16. Hewitt J., Greening G.E., Leonard M., Lewis G.D. Evaluation of human adenovirus and human polyomavirus as indicators of human sewage contamination in the aquatic environment. Water Res. 2013, 47:6750-6761.
17. Huang Z.-M., Hsu B.-M., Kao P.-M., Chang T.-Y., Hsu T.-K., Ho Y.-N., Yang Y.-C., Huang Y.-L. Prevalence, quantification, and typing of human adenoviruses detected in river water in Taiwan. Environ. Sci. Pollut. Res. 2014, 1-8.
18. Iritani N., Kaida A., Abe N., Kubo H., Sekiguchi J., Yamamoto S.P., Goto K., Tanaka T., Noda M. Detection and genetic characterization of human enteric viruses in oyster-associated gastroenteritis outbreaks between 2001 and 2012 in Osaka City, Japan. J. Med. Virol. 2014, 86:2019-2025.
19. Jothikumar N., Cromeans T.L., Robertson B.H., Meng X.J., Hill V.R. A broadly reactive one-step real-time RT-PCR assay for rapid and sensitive detection of hepatitis E virus. J. Virol. Methods 2006, 131:65-71.
20. Jung J.H., Yoo C.H., Koo E.S., Kim H.M., Na Y., Jheong W.H., Jeong Y.S. Occurrence of norovirus and other enteric viruses in untreated groundwaters of Korea. J. Water Health 2011, 9:544-555.
21. Kishida N., Noda N., Haramoto E., Kawaharasaki M., Akiba M., Sekiguchi Y. Quantitative detection of human enteric adenoviruses in river water by microfluidic digital polymerase chain reaction. Water Sci. Technol. 2014, 70:555-560.
22. Kitajima M., Haramoto E., Phanuwan C., Katayama H., Furumai H. Molecular detection and genotyping of human noroviruses in influent and effluent water at a wastewater treatment plant in Japan. J. Appl. Microbiol. 2012, 112:605-613.
23. Kundu A., McBride G., Wuertz S. Adenovirus-associated health risks for recreational activities in a multi-use coastal watershed based on site-specific quantitative microbial risk assessment. Water Res. 2013, 47:6309-6325.
24. Lodder W.J., de Roda Husman A.M. Presence of noroviruses and other enteric viruses in sewage and surface waters in the Netherlands. Appl. Environ. Microbiol. 2005, 71:1453-1461.
25. Lodder W.J., Rutjes S.A., Takumi K., de Roda Husman A.M. Aichi virus in sewage and surface water, the Netherlands. Emerg. Infect. Dis. 2013, 19:1222-1230.
26. Lorrot M., Bon F., El Hajje M.J., Aho S., Wolfer M., Giraudon H., Kaplon J., Marc E., Raymond J., Lebon P., Pothier P., Gendrel D. Epidemiology and clinical features of gastroenteritis in hospitalised children: prospective survey during a 2-year period in a Parisian hospital, France. Eur. J. Clin. Microbiol. Infect. Dis. 2011, 30:361-368.
27. Lucas F.S., Therial C., Goncalves A., Servais P., Rocher V., Mouchel J.M. Variation of raw wastewater microbiological quality in dry and wet weather conditions. Environ. Sci. Pollut. Res. Int. 2014, 21:5318-5328.
28. Maunula L., Miettinen I.T., von Bonsdorff C.H. Norovirus outbreaks from drinking water. Emerg. Infect. Dis. 2005, 11:1716-1721.
29. Maylin S., Stephan R., Molina J.M., Peraldi M.N., Scieux C., Nicand E., Simon F., Delaugerre C. Prevalence of antibodies and RNA genome of hepatitis E virus in a cohort of French immunocompromised. J. Clin. Virol. 2012, 53:346-349.
30. Nielsen A.C., Gyhrs M.L., Nielsen L.P., Pedersen C., Bottiger B. Gastroenteritis and the novel picornaviruses aichi virus, cosavirus, saffold virus, and salivirus in young children. J. Clin. Virol. 2013, 57:239-242.
31. Patil P.R., Chitambar S.D., Gopalkrishna V. Molecular surveillance of non-polio enterovirus infections in patients with acute gastroenteritis in Western India: 2004-2009. J. Med. Virol. 2015, 87:154-161.
32. Prado T., Silva D.M., Guilayn W.C., Rose T.L., Gaspar A.M., Miagostovich M.P. Quantification and molecular characterization of enteric viruses detected in effluents from two hospital wastewater treatment plants. Water Res. 2011, 45:1287-1297.
33. Rajko-Nenow P., Waters A., Keaveney S., Flannery J., Tuite G., Coughlan S., O'Flaherty V., Dore W. Norovirus genotypes present in oysters and in effluent from a wastewater treatment plant during the seasonal peak of infections in Ireland in 2010. Appl. Environ. Microbiol. 2013, 79:2578-2587.
34. Tree J.A., Adams M.R., Lees D.N. Chlorination of indicator bacteria and viruses in primary sewage effluent. Appl. Environ. Microbiol. 2003, 69:2038-2043.
35. WHO Guidelines for Drinking-water Quality 2011, World Health Organization. fourth edition.
36. Wurtzer S., Prevost B., Lucas F.S., Moulin L. Detection of enterovirus in environmental waters: a new optimized method compared to commercial real-time RT-qPCR kits. J. Virol. Methods 2014, 209:47-54.
37. Yezli S., Otter J. Minimum infective dose of the major human respiratory and enteric viruses transmitted through food and the environment. Food Environ. Virol. 2011, 3:1-30.