DIAGNOSTICO E EPIDEMIOLOGIA MOLECULAR DO VIRUS DA HEPATITE A

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Nesta revisão, o desenvolvimento de métodos de biologia molecular para o estudo desta virose, tanto para fins de diagnóstico como para estudos de epidemiologia molecular são discutidos.
Autor:
Vanessa Salete de paula
Columnista Experto de SIIC

Institución:
Fundação Oswaldo Cruz


Artículos publicados por Vanessa Salete de paula
Recepción del artículo
27 de Julio, 2006
Aprobación
9 de Noviembre, 2006
Primera edición
26 de Abril, 2007
Segunda edición, ampliada y corregida
7 de Junio, 2021

Resumen
Dados epidemiológicos, sorológicos e moleculares permitem um melhor conhecimento da circulação do HAV na população e podem contribuir para o controle desta doença. Nesta revisão, o desenvolvimento de métodos de biologia molecular para o estudo desta virose, tanto para fins de diagnóstico como para estudos de epidemiologia molecular são discutidos. Quatro métodos diferentes de extração do RNA do HAV foram comparados. A partir da padronização do RT-PCR, foi realizada a detecção do RNA do HAV em amostras de soro de casos de hepatite sem o marcador anti-HAV IgM para definir o diagnóstico precoce de hepatite A na fase pré-soroconversão e esclarecer de casos de hepatite sem etiologia conhecida. O seqüenciamento nucleotídico de isolados de HAV mostrou que a maioria das cepas brasileiras é classificada no genotipo I, com co-circulação dos subgenótipos IA e IB, também mostramos um caso de infecção mista descrito pela primeira vez na literatura. Para facilitar a genotipagem de isolados de HAV, padronizamos a técnica de "heteroduplex mobility assay" o que simplificou nosso trabalho com a mesma eficiência. A detecção do RNA do HAV como ferramenta diagnóstica possibilitou também a identificação de casos de co-infecção de hepatite A em pacientes portadores de hepatite C.

Palabras clave
Hepatite A, diagnóstico molecular, PCR, genotipagem


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Especialidades
Principal: Diagnóstico por Laboratorio
Relacionadas: Bioquímica, Epidemiología, Infectología, Medicina Interna, Salud Pública



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Enviar correspondencia a:
Vanessa S. de Paula, Fundação Oswaldo Cruz, Av. Brasil 4365, Manguinhos, FIOCRUZ - IOC Pavilhão Rocha Lima, Departamento de Virologia 5º andar, Río de Janeiro, Brasil
Patrocinio y reconocimiento:
Os procedimentos foram feitos de acordo aos padrões éticos de experimentação em seres humanos da Declaração de Helsinque e aprovados pelo comitê de ética da Fundação Oswaldo Cruz. Agradecimentos: Ao CNPq e a FAPERJ pelo financiamento dos projetos, a Dra. Ana Maria Coimbra Gaspar, ao Dr. Christian Niel e a Dra. Livia Melo Villar pela orientação e colaboração nos projetos de pesquisa.
Bibliografía del artículo
1. Siegl G, Frosner GG. Characterization and classification of virus particles associated with hepatitis A. Size, density, and sedimentation. J Virol 26:40-47, 1978.
2. Feinstone SM, Kapikian MAS, Purcell RH. Hepatitis A: detection by immunoelectronmicroscopy of a virus like anigen associated with acute illness Science 182:1026-1028, 1973.
3. Provost PJ, Bishop RP, Gerety RJ, Hilleman MR, McAleer WJ, Scolnick EM, stevens CE. New findings in live, attenuated hepatitis A vaccine development. J Med Virol 20:165-175, 1986.
4. Bradley DW, MacCaustaland KA, Schreeder MT, et al. Multiple buoyant densities of hepatitis A virus in cesium chloride gradients. J Med Virol 1:219-226, 1977.
5. Siegl G, Frösner GG, Gauss-Mueller, Tratschin JD, Deinhardt F. The physicochemical properties of infection hepatitis A virions. J Gen Virol 57:331-341, 1981.
6. Cohen JI, Ticehurst JR,Purcell RH, Buckler-White A, Baroudy BM. Complete nucleotide sequence of wilde-type hepatitis A virus: comparison with different strains of hepatits A virus and other picornaviruses. J Virol 61:50-9, 1987.
7. Koff RS. Hepatitis A. Lancet 341:1643-1649, 1998.
8. Jansen RW, Siegel G, lemon SM. Molecular epidemiology of human hepatitis A virus defined by antigen-capture polymerase chain reaction method. Proc Natl Acad Sci USA 87:2867-2871, 1990.
9. Hogle JM, Chow M, Filman DJ. Three-dimensional structure of poliovirus at 2.9 A resolution. Science 229(4720):1358-65, 1985.
10. Toyada H, Nickilin MJH, Murray MG, Anderson CW, Dunn JJ, Studier FW, Wimmer E. A second virus-enconded proteinase involvent in proteolytic processing of picornavirus polyprotein. Cell 45:761-770, 1986.
11. Robertson BH, Jansen RW, Khanna B, Totsuka A, Nainan OV, Sieg G, Widell A, Margolis HS, Isomoura S, Ito K, Ishizu T, Moritsuga Y, Lemon SM. Genetic relatedness of hepatitis A virus strains recovered from different geografic regions. J Gen Virol 73:1365-1377, 1992.
12. Costa-Mattioli M, Cristina J, Romero H, Perez-Bercoff R, Casane D, Colina R, Garcia L, Vega I, Glikman G, Romanowsky V, Castello A, Nicand E, Gassin M, Billaudel S, Ferre V. Molecular evolution of hepatitis A virus: a new classification based on the complete VP1 protein. J Virol 76:9516-9525, 2002.
13. Sanchez G, Bosch A, Pinto RM. Genome variability and capsid structural constraints of hepatitis A virus. J Virol 77:452-459, 2003.
14. Costa-Mattioli M, Di Napoli A, Ferre V, Billaudel S, Perez-Bercoff R, Cristina J. Genetic variability of hepatitis A virus. J Gen Virol 84:3191-201, 2003.
15. Lu L, Ching KZ, De Paula VS, Nakano T, Siegl G, Weitz M, Robertson BH. Characterization of the complete genomic sequence of genotype II hepatitis A virus (CF53/Berne isolate). J Gen Virol 85:2943- 2952, 2004.
16. Costa-Mattioli M, Ferre V, Monpoeho S, Garcia L, Colina R, Billaudel S, Vega I, Perez-Bercoff R, Cristina J. Genetic variability of hepatitis A virus in South America reveals heterogeneity and co-circulation during epidemic outbreaks. J Gen Virol 82:2647-2652, 2001.
17. Diaz BI, Sariol CA, Normann A, Rodríguez L, Flehming B. Genetic relateness of Cuban HAV wild-type isolates. J Med Virol 64:96-103, 2001.
18. Mbayed VA, Sookoian S, Alfonso V, Campos RH. Genetic characterization of hepatitis A virus isolates from Buenos Aires, Argentina. J Med Virol 68:168-174, 2002.
19. De Paula VS, Baptista ML, Lampe E, Niel C, Gaspar AMC. Characterization of hepatitis A virus isolates from subgenotypes IA e IB Rio de Janeiro, Brazil. J Med Virol 66(1):22-27, 2002.
20. De Paula VS, Lu L, Niel C, Gaspar AM, Robertson BH. Genetic analysis of hepatitis A virus isolates from Brazil. J Med Virol 378-383, 2004.
21. De Paula VS, Niel C, Teves SC, Villar LM, Virgulino HA, Gaspar AMC. Molecular epidemiology of hepatitis A virus in Brazilian Amazon. Journal of Gastroenterology and Hepatology 2006 (in press).
22. De Paula VS, Villar LM, Coimbra Gaspar AM. Comparison of four extraction methods to detect hepatitis A virus RNA in serum and stool samples. Braz J Infect Dis 7:135-141, 2003.
23. De Paula VS, Villar LM, Morais LM, Lewis-Ximenez LL, Niel C, Gaspar AMC. Detection of hepatitis A vírus RNA in serum during the window period of infection. J Clin Virol 29:254-259, 2004.
24. De Paula VS, Saback FL, Gaspar AM, Niel C. Mixed infection of a child care provider with hepatitis A virus isolates from subgenotypes IA and IB revealed by heteroduplex mobility assay. J Virol Methods 107:223-228, 2003.
25. Villar LM, Lampe E, Meyer A, Gaspar AM. Genetic variability of hepatitis A virus isolates in Rio de Janeiro: implications for the vaccination of school children. Braz J Med Biol Res 37:1779-1787, 2004.
26. Taylor MB. Molecular epidemiology of South African strains of hepatitis A virus: 1982-1996. J Med Virol 273-279, 1997.
27. Pina S, Buti M, Jardi R, Clemente-Casares P, Jofre J, Girones R. genetic analyses of hepatitis A vírus strains recovered from the enviromental and from patients with acute hepatitis. J Gen Virol 82:2955-2963, 2001.
28. Brown EA, Zajac AJ, Lemon SM. In vitro characterization of an internaç ribosomal entry site (IRES) present within the 5'nontranslated region of hepatitis A virus RNA: comparasion with the IRES of encephalomyocarditis virus. J Virol 68:1066-1074, 1994.
29. Jansen RW, Siegl G, Lemon SM. Molecular epidemiology of human hepatitis A virus (HAV). In: BN Hollinger, SM Lemon and HS Margolis (eds.). Viral hepatitis and liver disease. Williams & Wilkins, Baltimore, Md, 1991 pp. 58-62.
30. Khanna B, Spelbring JE, Innis BL, Robertson BH. Characterization of a genetic variant of a human hepatitis A virus. J Med Virol 36:118-124, 1992.
31. Ching KZ, Nakano T, Chapman LE, Demby A, Robertson BH. Genetic characterization of wild-type genotype VII hepatitis A virus. J Gen Virol 83:53-60, 2002.
32. Lemon SM, Jansen RW, Brown EA. Genetic, antigenic and biological differences between strains of hepatitis A virus. Vaccine 10(suppl I):S40-S44, 1992.
33. Muller C. The hepatitis alphabet--hepatitis A-G and TTV. Wien Klin Wochenschr 18(111): 461-468, 1999.
34. Lednar WM, Lemon SM, Kirkpatrick JW, Redfield RR, Fields ML, Kelley PW. Frequency of illness associated with epidemic hepatitis A virus infections in adults. Am J Epidemiol 122:226-233, 1985.
35. Paul JR, Havens WP, Sabin AB, Philip CB. Transmission experiments in serum jaundice and infectious hepatitis. JAMA 128:911-915, 1945.
36. Decker RH Kosakowski SM,Vanderbilt AS, et al. Diagnosis of acute hepatitis A by HAVB-M: A direct radioimmunoassay for IgM anti-HAV. Am J Clin Pathol 76:140-147, 1981.
37. LaBrecque FD, LaBrecque DR, Klinzman D, Perlman S, Cederna JB, Winokur PL, Han JQ, Stapleton JT. Recombinant hepatitis A virus antigen: improved production and utility in diagnostic immunoassays. J Clin Microbiol 36:2014-2018, 1998.
38. Kao HW, Ashcavai M, Redeker AG. The persistence of hepatitis A IgM antibody after acute clinical hepatitis A. Hepatology 4:933-936, 1984.
39. Yoshizawa H, Akahane Y, Itoh Y, Iwakiri S, kitajima K, Morita M, Tanaka A, Nojiri T, Shimizu M, Miyakawa Y, Mayumi M. Gastroenterology 79(3):512-20, 1980.
40. Seelig R, Renz M, Seelig HP. PCR in the diagnosis of viral hepatitis. Ann Intern Med 24:225-230, 1992.
41. Fujiwara K, Yokosuka O, Ehata T. Frequent detection of hepatitis A viral RNA in serum during the early convalescent phase of acute hepatitis A. Hepatology 26:1634-1639, 1997.
42. Arnal C, Ferre-Aubineau V, Besse B, Billaudel S. Simplified reverse transcription ploymerase chain reaction procedure with detection by microplate hybridization for routine screening of hepatitis A virus. Can J Microbiol 44:298-302, 1998.
43. Hutin YP, Pool V, Cramer EH, Nainan OV, weth J, Williams IT, Goldstein ST, Gensheimer KF, Bell BP, Shapiro CN, Alter MJ, Margolis HS. A multistate, foodborne outbreak of hepatitis A. National Hepatitis A Investigation Team. N Engl J Med 340(8):595-602, 1999.
44. Bower WA, Nainan OV, Han X, Margolis HS. Duration of viremia in hepatitis A virus infection. J Infect Dis 18:12-17, 2000.
45. Monteiro L, Bonnemaison D, Vekris A, Petry KG, Bonnet J, Vidal R, Cabrita J, Megraud F. Complex polysaccharides as PCR inhibitors in feces: Helicobacter pylori model. J Clin Microbiol 35:995-998, 1997.
46. Boom R, Sol CJ, Salimans MM. Rapid and simple method for purification of nucleic acids. J Clin Microbiol 28:495-503, 1990.
47. Turkoglu S, Lazizi Y, Meng H, Kordosi A, Dubreuil P, Crescenzo B, Benjelloun S, Nordmann P, Pillot J. Detection of hepatitis E virus RNA in stools and serum by reverse transcription-PCR. J Clin Microbiol 34:1568-1571, 1996.
48. Fanson BG, Osmack P, Di Bisceglie AM. A comparison between the phenol-chloroform method of RNA extraction and the QIAamp viral RNA kit in the extraction of hepatitis C and GB virus-C/hepatitis G viral RNA from serum. J Virol Methods 89:23-27, 2000.
49. Green J, Norcott JP, Lewis D et al. Norwalk-like viruses: demonstration of genomic diversity by polimerase chain reaction. J Clin Microbiol 31:3007-12, 1993.
50. Hale AD, Green J, Brown DW. Comparison of four RNA extraction methods for the detection of small round structured viruses in faecal specimens. J Virol Methods 57:195-201, 1996.
51. Benjamin RJ. Nucleic acid testing: update and applications. Semin Hematol 38(4 Suppl 9):11-16, 2001.
52. Weimer T, Streichert S, Watson C, Groner A. Hepatitis A virus prevalence in plasma donations. J Med Virol 67:469-471, 2002.
53. Apaire-Marchais V, Robertson BH, Aubineau-Ferre V, Le Roux MG, Leveque F, Schwartzbrod L, Billaudel S. Direct sequencing of hepatitis A virus strains isolated during an epidemic in France. Appl Environ Microbiol 61:3977-3980, 1995.
54. Stene-Johansen K, Skaug K, Blystad H, Grinde B, et al. A unique hepatitis A virus strain caused an epidemic in Norway associated with intravenous drug abuse. Scand J Infect Dis 30:35-38, 1998.
55. Arauz-Ruiz P, Sundqvist L, García Z, Taylor L, Visoná K, Norder H, Magnius LO. Presumed common source outbreaks of hepatitis A in an endemic area confirmed by limited sequencing within the VP1 region. J Med Virol 65:449-456, 2001.
56. Grinde B, Stene-Johansen K, Sharma B, Hoel T, Jensenius M, Skaug K. Characterisation of an epidemic of hepatitis A virus involving intravenous drug abusers-infection by needle sharing? J Med Virol 53:69-75, 1997.
57. Delwart EL, Shpaer EG, Louwagie J, McCutchan FE, Grez M, Rubsamen-Waigmann H, Mullins JI. Genetic relationships determined by a DNA heteroduplex mobility assay: analysis of HIV-1 env genes. Science 262:1257-1261, 1993.
58. Kreis S, Whistler T. Rapid identification of measles virus strains by the heteroduplex mobility assay. Virus Res 47:197-203, 1997.
59. Mattick KL, Green J, Punia P, Belda FJ, Gallimore CI, Brown DW. The heteroduplex mobility assay (HMA) as a pre-sequencing screen for Norwalk-like viruses. J Virol Methods 87:161-169, 2000.
60. Trincado DE, Scott GM, White PA, Hunt C, Rasmussen L, Rawlinson WD. Human cytomegalovirus strains associated with congenital and perinatal infections. J Med Virol 61:481-487, 2000.
61. White PA, Li Z, Zhai X, Marinos G, Rawlinson WD. Mixed viral infection identified using heteroduplex mobility analysis (HMA). Virology 271:382-389, 2000.
62. Zou S, Stansfield C, Bridge J. Identification of new influenza B virus variants by multiplex reverse transcription-PCR and the heteroduplex mobility assay. J Clin Microbiol 36:1544-1548, 1998.
63. Devalle S, De Paula VS, De Oliveira JM, Niel C, Gaspar AM. Hepatitis A virus infection in hepatitis C Brazilian patients. J Infect 47:125-128, 2003.
64. Siddiqui F, Mutchnick M, Kinzie J, Peleman R, Naylor P, Ehrinpreis M. Prevalence of hepatitis A virus and hepatitis B virus immunity in patients with polymerase chain reaction-confirmed hepatitis C: implications for vaccination strategy. Am J Gastroenterol 96:858-863, 2001.
65. Pramoolsinsap C, Poovorawan Y, Hirsch P, Busagorn N, Attamasirikul K. Acute, hepatitis-A super-infection in HBV carriers, or chronic liver disease related to HBV or HCV. Ann Trop Med Parasitol 93:745-751, 1999.
66. Vento S, Garofano T, Renzini C, Cainelli F, Casali F, Ghironzi G, Ferraro T, Concia E. Fulminant hepatitis associated with hepatitis A virus superinfection in patients with chronic hepatitis C. N Engl J Med 338:286-290, 1998.
67. Lee DH, Prince AM. Automation of nucleic acid extraction for NAT screening of individual blood units. Transfusion 41:483-487, 2001.

 
 
 
 
 
 
 
 
 
 
 
 
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