Species-specific identification of human adenoviruses in sewage

• Autorzy: Wieczorek M. , Krzysztoszek A. , Witek A.
• Języki publikacji: EN

Abstrakty

EN

Human adenovirus (HAdV) diversity in sewage was assessed by species-specific molecular methods. Samples of raw sewage were collected in 14 sewage disposal systems from January to December 2011, in Poland. HAdVs were detected in 92.1% of the analysed sewage samples and was significantly higher at cities of over 100 000 inhabitants. HAdV DNA was detected in sewage during all seasons. The most abundant species identified were HAdV-F (average 89.6%) and -A (average 19.6%), which are associated with intestine infections. Adenoviruses from B species were not detected. The result of the present study demonstrate that human adenoviruses are consistently present in sewage in Poland, demonstrating the importance of an adequate treatment before the disposal in the environment. Multiple HAdV species identified in raw sewage provide new information about HAdV circulation in the Polish population.

• Wydawca: -
• Czasopismo: Polish Journal of Microbiology
• Rocznik: 2015
• Tom: 64
• Numer: 1
• Opis fizyczny: p.23-28,fig.,ref.

Twórcy

autor

Wieczorek M.

• Department of Virology, National Institute of Hygiene, National Institute of Public Health, Warsaw, Poland

autor

Krzysztoszek A.

• Department of Virology, National Institute of Hygiene, National Institute of Public Health, Warsaw, Poland

autor

Witek A.

• Department of Virology, National Institute of Hygiene, National Institute of Public Health, Warsaw, Poland

Bibliografia

• Albinana-Gimenez N., M.P. Miagostovich, B. Calgua, J.M. Huguet, L. Matia and R. Girones. 2009. Analysis of adenoviruses and polyomaviruses quantified by qPCR as indicators of water quality in source and drinking-water treatment plants. Water Res. 43: 2011–2019.
• Barrella K.M., P. Garrafa, T.A. Monezi, C.M. Harsi, C. Salvi, P.A. Violante and D.U. Mehnert. 2009. Longitudinal study on occurrence of adenoviruses and hepatitis A virus in raw domestic sewage in the city of Limeira, Sao Paulo. Braz. J. Microbiol. 40: 102–107.
• Bibby K. and J. Peccia. 2013. Prevalence of respiratory adenovirus species B and C in sewage sludge. Environ. Sci. Process Impacts. 15(2): 336–338
• Cantalupo P.G, B. Calgua, G. Zhao, A. Hundesa, A.D. Wier, J.P. Katz, M. Grabe, R.W. Hendrix, R. Girones, D. Wang and others. 2011. Raw sewage harbors diverse viral populations. MBio. 2(5): e00180–11.
• Cruz J.R., P. Caceres, F. Cano, J. Flores, A. Bartlett and B. Torun. 1990. Adenovirus types 40 and 41 and rotaviruses associated with diarrhea in children from Guatemala. J. Clin. Microbiol. 28: 1780–1784.
• Echavarria M. 2008. Adenoviruses in immunocompromised hosts. Clin. Microbiol. Rev. 21: 704–715.
• Enriquez C.E. and C.P. Gerba. 1995. Concentration of enteric adenovirus 40 from tap, sea and waste water. Water Res. 29: 2554–2560.
• Filho E.P., N.R. da Costa Faria, A.M. Fialho, R.S. de Assis, M.M. Almeida, M. Rocha, M. Galvao, F.B. dos Santos, M.L. Barreto and J.P. Leite. 2007. Adenoviruses associated with acute gastroenteritis in hospitalized and community children up to 5 years old in Rio de Janeiro and Salvador, Brazil. J. Med. Microbiol. 56: 313–319.
• Fong T.T., M.S. Phanikumar, I. Xagoraraki and J.B. Rose. 2010. Quantitive detection of human adenoviruses in wastewater and combined sewer overflows influencing a Michigan river. Appl. Environ. Microbiol. 76: 715–723.
• Gunson R.N., A.R. Maclean, S.J. Shepherd and W.F. Carman. 2009. Simultaneous detection and quantitation of cytomegalovirus, Epstein-Barr virus, and adenovirus by use of real-time PCR and pooled standards. J. Clin. Microbiol. 47: 765–770.
• Hewitt J., G.E. Greening, M. Leonard and G.D. Lewis. 2013. Evaluation of human adenovirus and human polyomavirus as indicators of human sewage contamination in the aquatic environment. Water Res. 47: 6750–6761.
• Hundesa A., C. Maluquer, S. Biofill Mas, N.A. Gimenez and R. Girones. 2006 Idendification of human and animal adenoviruses and polyomaviruses for determination of sources of fecal contamination in the environment. Appl. Environ. Microbiol. 72: 7886–7893.
• Jalal H., D.F. Bibby, J.W. Tang, J. Bennett, C. Kyriakou, K. Peggs, D. Cubitt, N.S. Brink, K.N. Ward and R.S. Tedder. 2005. First reported outbreak of diarrhea due to adenovirus infection in a hematology init for adults. J. Clin. Microbiol. 43: 2575–2580.
• Jarecki-Khan K., S.R. Tzipori and L.E. Unicomb. 1993. Enteric adenovirus infection among infants with diarrhea in rural Bangladesh. J. Clin. Microbiol. 31: 484–489.
• Jiang S.C. 2006 Human adenoviruses in water: occurrence and health implications, a critical review. Environmental Science and Technology 40: 7132–7140.
• Jothikumar N, T.L. Cromeans, V.R. Hill, X. Lu, M.D. Sobsev and D.D. Erdman. 2005. Quantitative real-time PCR assays for detection of human adenoviruses and identification of serotypes 40 and 41. Appl. Environ. Microbiol. 71: 3131–3136.
• Katayama H., E. Haramoto, K. Oguma, H. Yamashita, A. Tajima, H. Nakajima and S. Ohgaki. 2008: One-year monthly quantitative survey of noroviruses, enteroviruses, and adenoviruses in wastewater collected from six plants in Japan. Water Res. 42: 1441–1448.
• Kishida N., H. Morita, E. Haramoto, M. Asami and M. Akiba. 2012. One-year weekly survey of noroviruses and enteric adenoviruses in the Tone River water in Tokyo metropolitan area. Japan. Water Res. 46: 2905–2910.
• Magwalivha M., M. Wolfaardt, N.M. Kiulia, W.B. van Zyl, J.M. Mwenda and M.B. Taylor. 2010. High prevalence of species D human adenoviruses in fecal specimens from Urban Kenyan children with diarrhea. J. Med. Virol. 82: 77–84.
• Ng T.F., R. Marine, C. Wang, P. Simmonds, B. Kapusinszky, L. Bodhidatta, B.S. Oderinde, K.E. Wommack and E. Delwart. 2012. High variety of known and new RNA and DNA viruses of diverse origins in untreated sewage. J. Virol. 86: 12161–12175.
• Pina S., M. Puig, F. Lucena, J. Jofre and R. Girones. 1998. Viral pollution in the envir onment and in shellfish: human adenovirus detection by PCR as an index of human viruses. Appl. Environ. Microbiol. 64: 3376–3382.
• Puig M., J. Jofre, F. Lucena, A. Allard, G. Wadell and R. Girones. 1994. Detection of adenoviruses and enteroviruses in polluted waters by nested PCR amplification. Appl. Environ. Microbiol. 60: 2963–2970.
• Pusch D., D.Y. Oh, S. Wolf, R. Dumke, U. Schroter-Bobsin, M. Hohne, I. Roske and E. Schreier. 2005. Detection of enteric viruses and bacterial indicators in German environmemtal waters. Arch. Virol. 150: 929–947.
• Rodríguez R.A., P.M. Polston, M.J. Wu, J. Wu and M.D. Sobsey. 2013. An improved infectivity assay combining cell culture with real-time PCR for rapid quantification of human adenoviruses 41 and semi-quantification of human adenovirus in sewage. Water Res. 47: 3183–3191.
• Santos F.M., M.J. Vieira, P. Garrafa, T.A. Monezi, V.H. Pellizari, C.M. Harsi and D.U. Mehnert. 2004. Discrimination of adenovirus types circulating in urban sewage and surface polluted waters in Sao Paulo city, Brazil. Water Sci. Technol. 4: 79–85.
• Sibanda T. and A.I. Okoh. 2012. Assessment of the incidence of enteric adenovirus species and serotypes in surface waters in the eastern cape province of South Africa: Tyume River as a case study. The Scientific World Journal Article ID 949216
• Shimizu H., T.G. Phan, S. Nishimura, S. Okitsu, N. Maneekarn and H. Ushijima. 2007. An outbreak of adenovirus serotype 41 infection in infants and children with acute gastroenteritis in Maizuru City, Japan. Infect. Genet. Evol. 7: 279–284.
• Van Heerden J., M.M. Ehlers, A. Heim and W.O. Grabow. 2005. Prevalence, quantification and typing of adenoviruses detected in river and treated drinking water in South Africa. J. Appl. Microbiol. 99: 234–242.
• Xu W., M.C. McDonough and D.D. Erdman. 2000. Species-specific identification of human adenoviruses by a multiplex PCR assay. J. Clin. Microbiol. 38: 4114-4120
• Zurbriggen S., K. Tobler, C. Abril, S. Diedrich, M. Ackermann, M.A. Pallansch and A. Metzler. 2008. Isolation of sabin-like polio-viruses from wastewater in a country using inactivated polio vaccine. Appl. Environ. Microbiol. 74: 5608–5614.