Prospective study on Norovirus infection among allogeneic stem cell transplant recipients: Prolonged viral excretion and viral RNA in the blood

Journal of Clinical Virology

Volumn 61, Issue 3, 2014, Pages 329-333

  Lemes, Lucianna Gonçalves Nepomuceno ^a   Corrêa, Thais Santos ^a   Fiaccadori, Fabíola Souza ^a   Cardoso, Divina das DÔres de Paula ^a   Arantes, Adriano de Moraes ^b   Souza, Keili Maria Cardoso ^a   Souza, Menira ^a  

^a FEDERAL UNIVERSITY OF GOIÁS   (Brazil)

^b Araújo Jorge Hospital   (Brazil)

Author keywords

Calicivirus; Norovirus excretion; Norovirus infection; Stem cell transplant; Viremia

Indexed keywords

ULEX EUROPAEUS AGGLUTININ; VIRUS RNA;

ADULT; ALLOGENEIC STEM CELL TRANSPLANTATION; ARTICLE; CLINICAL ARTICLE; DIARRHEA; ENZYME IMMUNOASSAY; FEMALE; FEVER; GENE SEQUENCE; GENOTYPE; GRAFT RECIPIENT; HUMAN; MALE; MIDDLE AGED; NONHUMAN; NOROVIRUS INFECTION; NUCLEOTIDE SEQUENCE; PHYLOGENY; PROSPECTIVE STUDY; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SAPOVIRUS; VIRUS CAPSID; VIRUS DETECTION; VIRUS EXCRETION; VOMITING; YOUNG ADULT; ALLOTRANSPLANTATION; BLOOD; CALICIVIRIDAE INFECTIONS; CLUSTER ANALYSIS; DNA SEQUENCE; GENETICS; ISOLATION AND PURIFICATION; MULTIPLEX POLYMERASE CHAIN REACTION; NOROVIRUS; STEM CELL; STEM CELL TRANSPLANTATION; VIROLOGY; VIRUS SHEDDING;

ADULT; CALICIVIRIDAE INFECTIONS; CLUSTER ANALYSIS; FEMALE; GENOTYPE; HUMANS; IMMUNOENZYME TECHNIQUES; MALE; MIDDLE AGED; MULTIPLEX POLYMERASE CHAIN REACTION; NOROVIRUS; PHYLOGENY; PROSPECTIVE STUDIES; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; RNA, VIRAL; SAPOVIRUS; SEQUENCE ANALYSIS, DNA; STEM CELL TRANSPLANTATION; STEM CELLS; TRANSPLANT RECIPIENTS; TRANSPLANTATION, HOMOLOGOUS; VIRUS SHEDDING; YOUNG ADULT;

EID: 84908507592     PISSN: 13866532     EISSN: 18735967     Source Type: Journal    
DOI: 10.1016/j.jcv.2014.08.004     Document Type: Article

References (37)

1. Clark I.N., Estes M.K., Green K.Y., Hansman G.S., Knowle N.J., Koopmans M.K., et al. Family Caliciviridae. Virus taxonomy: ninth report of the international committee on taxonomy of viruses 2012, 977-986. Elsevier/Academic Press, London. A.M.Q. King, M.L. Adams, E.B. Carstens, E.J. Lefkowitz (Eds.).
2. Zheng D.P., Ando T., Fankhauser R.L., Beard R.S., Glass R.I., Monroe S.S. Norovirus classification and proposed strain nomenclature. Virology 2006, 346:312-323.
3. Green K.Y. Caliciviridae: the noroviruses. Fields virology 2007, 949-979. Lippincott Williams & Wilkins, Philadelphia. D.M. Knipe, P.M. Howley (Eds.).
4. Koopmans M., Duizer E. Foodborne viruses: an emerging problem. Int J Food Microbiol 2004, 90:23-41.
5. Marks P.J., Vipond I.B., Regan F.M., Wedgwood K., Fey R.E., Caul E.O. A school outbreak of Norwalk-like virus: evidence for airborne transmission. Epidemiol Infect 2003, 131:727-736.
6. Teunis P.F., Moe C.L., Liu P., Miller S.E., Lindesmith L., Baric R.S., et al. Norwalk virus: how infectious is it?. J Med Virol 2008, 80:1469-1476.
7. Lopman B.A., Reacher M.H., Vipond I.B., Sarangi J., Brown D.W. Clinical manifestation of Norovirus gastroenteritis in health care settings. Clin Infect Dis 2004, 39:318-324.
8. Rockx B., Wit M., Vennema H., Vinjé J., Bruin E., van Duynhoven Y., et al. Natural history of human Calicivirus infection: a prospective cohort study. Clin Infect Dis 2002, 35:246-253.
9. Bok K., Green K.Y. Norovirus gastroenteritis in immunocompromised patients. N Engl J Med 2012, 367:2126-2132.
10. Siebenga J.J., Beersma M.F.C., Vennema H., van Biezen P., Hartwig N.J., Koopmans M. High prevalence of prolonged Norovirus shedding and illness among hospitalized patients: a model for in vivo molecular evolution. J Infect Dis 2008, 198:994-1001.
11. Roos-Weil D., Ambert-Balay K., Lanternier F., Mamzer-Bruneel M.F., Nochy D., Pothier P., et al. Impact of norovirus/sapovirus-related diarrhea in renal transplant recipients hospitalized for diarrhea. Transplantation 2011, 92:61-69.
12. Roddie C., Paul J.P.V., Benjamin R., Gallimore C.I., Xerry J., Gray J.J., et al. Allogeneic hematopoietic stem cell transplantation and norovirus gastroenteritis: a previously unrecognized cause of morbidity. Clin Infect Dis 2009, 49:1061-1068.
13. Schwartz S., Vergoulidou M., Schreier E., Loddenkemper C., Reinwald M., Scmidt-Hieber M., et al. Norovirus gastroenteritis causes severe and lethal complications after chemotherapy and hematopoietic stem cell transplantation. Blood 2011, 117:5850-5856.
14. Nordgren J., Nitiema L.W., Ouermi D., Simpore J., Svensson L. Host genetic factors affect susceptibility to Norovirus infections in Burkina Faso. PLoS ONE 2013, 8:1-10.
15. Cardoso D.D.P., Fiaccadori F.S., Souza M.B.D.L., Martins R.M.B., Leite J.P.G. Detection and genotyping of astroviruses from children with acute gastroenteritis from Goiânia, Goiás, Brazil. Med Sci Monit 2002, 8:624-628.
16. Boom R., Sol C.J.A., Salimans M.M.M., Jansen C.L., Wertheim-Van D.P.M.E., Van der Noorda A.J. Rapid and simple method for purification of nucleic acids. J Clin Microbiol 1990, 28:495-503.
17. Yan H., Yagyu F., Okitsu S., Nishio O., Ushijima H. Detection of Norovirus [GI, GII], Sapovirus and astrovirus in fecal samples using reverse transcription single-round multiplex PCR. J Virol Methods 2003, 114:37-44.
18. Kojima S.T., Kageyama S., Fukushi F.B., Hoshino M., Shinohara K., Uchida K., et al. Genogroup-specific PCR primers for detection of Norwalk-like viruses. J Virol Methods 2002, 100:107-114.
19. De Oliveira D.M.M., Souza M., Fiaccadori F.S., Santos H.C.P., das DÔres D.P.C. Monitoring of Calicivirus among day-care children: evidence of asymptomatic viral excretion and first report of GI.7 norovirus and GI.3 sapovirus in Brazil. J Med Virol 2013.
20. Ewing B., Green P. Base-caling of automated sequencer traces using phred II. Error probabilities. Genome Res 1998, 8:186-194.
21. Tompson J.D., Gibson T.J., Plewniak F., Jeanmougin F., Higgins D.G. The CLUSTAL X Windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res 1997, 25:4876-4882.
22. Tamura K., Peterson D., Peterson N., Stecher G., Nei M., Kumar S. MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol Biol Evolut 2011, 28:2731-2739.
23. Doshi M., Woodwell S., Kellerher K., Mangan K., Axelrod P. An outbreak of norovirus infection in a bone marrow transplant unit. Am J Infect Control 2013, 41:820-823.
24. Saif M.A., Bonney D.K., Bigger B., Forsythe L., Williams N., Page J., et al. Chronic norovirus infection in pediatric hematopoietic stem cell transplant recipients: a cause of prolonged intestinal failure requiring intensive nutritional support. Pediatr Transplant 2011, 15:505-509.
25. Robles J.D.F., Cheuk D.K.L., Ha S.Y.Chiang A.K.S., Chan G.C.F. Norovirus infection in pediatric hematopoietic stem cell transplantation recipients: incidence, risk, factors, and outcome. Biol Blood Marrow Transplant 2012, 18:1883-1889.
26. Mattner F., Sohr D., Heim A., Gastmeier P., Vennema H., Koopmans M. Risk groups for clinical complications of norovirus infections: an outbreak investigation. Clin Microbiol Infect 2006, 12:69-74.
27. Chadwick P.R., McCann R. Transmission of a small round structured virus by vomiting during a hospital outbreak of gastroenteritis. J Hosp Infect 1994, 26:251-259.
28. Thorven M., Grahn A., Hedlund K.O., Johansson H., Wahlfrid C., Larson G., et al. A homozygous nonsense mutation (428G→A) in the human secretor (FUT2) gene provides resistance to symptomatic Norovirus (GGII) infections. J Virol 2005, 79:15351-15355.
29. Lindesmith L., Moe C., Marionneau S., Ruvoen N., Jiang X., Lindblad L., et al. Human susceptibility and resistance to Norwalk virus infection. Nat Med 2003, 9:548-553.
30. Schorn R., Höhne M., Meerbach A., Bossart W., Wüthrich R.P., Schreier E., et al. Chronic norovirus infection after kidney transplantation: molecular evidence for immune-driven viral evolution. Clin Infect Dis 2010, 51:307-314.
31. Wingfield T., Gallimore C.I., Xerry J., Gray J.J., Klapper P., Guiver M., et al. Chronic norovirus infection in an HIV-positive patient with persistent diarrhoea: a novel cause. J Clin Virol 2010, 49:219-222.
32. Fumian T.M., Justino M.C., D'Arc J.P.M., Reymão T.K., Abreu E., Soares L., et al. Quantitative and molecular analysis of noroviruses RNA in blood from children hospitalized for acute gastroenteritis in Belém, Brazil. J Clin Virol 2013, 58:31-35.
33. Takanashi S., Hashira S., Matsunaga T., Yoshida A., Shiota T., Tung P.G., et al. Detection, genetic characterization, and quantification of norovirus RNA from sera of children with gastroenteritis. J Clin Virol 2009, 44:161-163.
34. Wobus C.E., Thackray L.B., Virgin 4th H.W. Murine norovirus: a model system to study norovirus biology and pathogenesis. J Virol 2006, 80:5104-5112.
35. Vicentini F., Denadai W., Gomes Y.M., Rose T.L., Ferreira M.S.R., Le Moullac V., et al. Molecular characterization of Noroviruses and HBGA from infected Quilombola children in Espirito Santo State, Brazil. PLoS ONE 2013, 8:e69348.
36. Nenonem N.P., Hannoun C., Larsson C.U., Bergstrom T. Marked genomic diversity of norovirus genogroup I strains in a waterborne outbreak. Appl Environ Microbiol 2012, 78:1846-1852.
37. Morter S., Bennet G., Fish J., Richards J., Allen D.J., Nawazb S., et al. Norovirus in the hospital setting: virus introduction and spread within the hospital environment. J Hosp Infect 2011, 77:106-112.