2006, Número 4
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Enf Infec Microbiol 2006; 26 (4)
Aspectos moleculares de coinfecciones de virus respiratorios con bacterias
Arrevillaga BG, Gómez GB
Idioma: Español
Referencias bibliográficas: 48
Paginas: 115-122
Archivo PDF: 86.74 Kb.
RESUMEN
Estudios epidemiológicos, así como modelos experimentales, sugieren que cuadros clínicos por infecciones virales respiratorias, frecuentemente se complican por infecciones bacterianas secundarias. Los mecanismos moleculares y bioquímicos responsables de la coinfección no están aclarados del todo, a pesar de que estudios sobre la interacción entre virus respiratorios y bacterias datan desde los años veinte del siglo pasado. Las alteraciones por el virus en las células infectadas modifican directa y/o indirectamente las actividades microbicidas de la célula. Los procesos bactericidas de la célula son iniciados en respuesta al reconocimiento del hospedero de patrones moleculares asociados a patógenos (PAMPs), a través de sensores membranales o intracelulares como los receptores tipo toll (TLR). La interacción del receptor con PAMPs activa vías de transducción de señales que inducen la expresión de genes involucrados en el control de la respuesta celular contra la bacteria. El control de la infección primaria viral y secundaria bacteriana depende de un balance fino y multifactorial entre célula, bacteria y virus, el cual es seriamente perturbado por la coinfección. En esta revisión se analizan los cambios en la célula hospedera originados por virus respiratorios y bacterias que favorecen la coinfección.
REFERENCIAS (EN ESTE ARTÍCULO)
Abas AK y Lichtman AH. Inmunología celular y molecular. Elsevier, Madrid, 2004, pp. 241-345.
Aktan F. iNOS-mediated nitric oxide production and its regulation. Life Sci 2004; 75: 639-653.
Avadhanula V, Rodríguez CA, Devincenzo JP, Wang Y, Webby RJ, Ulett GC, Adderson EE. Respiratory viruses augment the adhesion of bacterial pathogens to respiratory epithelium in a viral species- and cell type-dependent manner. J. Virol 2006; 80: 1629-1636.
Avadhanula V, Rodríguez CA, Klett GC, Bakaletz LO, Adderson EE. Nontypeable Haemophilus influenzae adheres to intercellular adhesion molecule 1 (ICAM-1) on respiratory epithelial cells and upregulates ICAM-1 expression. J. Virol 2006; 74: 830-838.
Beadling C, Cundell DR, Sandros J, Pearce BJ, Idanpaan- Heikkila I, Rosenow C, Masure HR. Pyruvate oxidase, as a determinant of virulence in Streptococcus pneumoniae. Spellerberg. Mol. Microbiol 1996; 19: 803-813.
Beadling C, Slifka MK. How do viral infections predispose patients to bacterial infections? Curr Opin Infect Dis. 2004, 17: 185-191.
Bernard M y Babior JM. NADPH oxidase: An Update. Blood 1999; 93: 1464-1476.
Bogdan C. Nitric oxide and the immune response. Nat Immunol 2001; 2: 907-916.
Bulut Y, Guven M, Otlu B, Yenisehirli G, Aladag I, Eyibilen A, Dogru S. Acute otitis media and respiratory viruses. Eur. J. Pediatr 2006 (en prensa).
Chi B et al. Alpha and lambda interferon together mediate suppression of CD4 T cells induced by respiratory syncytial virus. Virology 2006; 80: 5032-5040.
Conron M, Andreakos E, Pantelidis P, Smith C, Beynon HL, Dubois RM, Foxwel BM. Nuclear factor-kappaB activation in alveolar macrophages requires IkappaB kinase-beta, but not nuclear factor-kappaB inducing kinase. Am. J. Respir. Crit. Care. Med 2002; 165: 996-1000.
Fang FC. Antimicrobial reactive oxygen and nitrogen species: concepts and controversies. Nat. Rev. Microbiol 2004; 10: 820-832.
Fritz JH y Girardin SE. How Toll-like receptors and Nodlike receptors contribute to innate immunity in mammals. J. Endotoxin Res 2005; 11: 390-394
Haller O, Kochs G, Weber F. The interferon response circuit: induction and suppression by pathogenic viruses. Virology 2006; 344: 119-130.
Hament JM, Aerts PC, Fleer A, van Dijk H, Harmsen T, Kimpen JL, Wolfs TF. Direct binding of respiratory syncytial virus to pneumococci: a phenomenon that enhances both pneumococcal adherence to human epithelial cells and pneumococcal invasiveness in a murine model. Pediatr. Res 2005; 58: 1198-1203.
Hament JM, Kimpen JL, Fleer A, Wolfs TF. Respiratory viral infection predisposing for bacterial disease: a concise review.FEMS. Immunol. Med. Microbiol 1999; 26: 189-195.
Heikkinen T, Ruuskanen O, Waris M, Ziegler T, Arola M, Halonen P. Influenza vaccination in the prevention of acute otitis media in children. Am. J. Dis. Child 1991; 146: 1018-1019.
Higashimoto Y et al. Effect of the adenovirus E1A gene on nitric oxide production in alveolar epithelial cells. Clin. Microbiol. Infect 2005; 11: 644-650.
Hilleman MR. Realities and enigmas of human viral influenza: pathogenesis, epidemiology and control. Vaccine 2002; 20: 3068-3087.
Janew WL, Dietlein F, Low G, Burch and W Mogabgab. Bronchotracheal response in human influenza. Arch. Intern. Med 1960; 108: 376-388.
Janeway CA Jr. How the immune system protects the host from infection. Microbes Infect 2001; 13: 1167-1171.
Jansen HM, Lutter R, van der Poll T. Involvement of the platelet-activating factor receptor in host defense against Streptococcus pneumoniae during postinfluenza pneumonia. Am. J. Physiol. Lung. Cell. Mol. Physiol 2005; 290: L194-199
Jiang Z, Nagata N, Molina E, Bakaletz LO, Hawkins H, Patel JA. Fimbria-mediated enhanced attachment of nontypeable Haemophilus influenzae to respiratory syncytial virus-infected respiratory epithelial cells. Infect. Immun 1999; 67:187-192.
Lehtinen P, Jartti T, Virkki R, Vuorinen T, Leinonen M, Peltola V, Ruohola A, Ruuskanen O. Bacterial coinfections in children with viral wheezing. Eur. J. Clin. Microbiol. Infect. Dis. 2006; 25: 463-469.
Loosli CG. Influenza and the interaction of viruses and bacteria in respiratory infections. Medicine (Baltimore) 1973; 52: 369-384.
McCullers JA, Bartmess KC. Role of neuraminidase in lethal synergism between influenza virus and Streptococcus pneumoniae. J. Infect. Dis. 2003; 187: 1000-1009.
McCullers JA, Tuomanen EI. Molecular pathogenesis of pneumococcal pneumonia. Front. Biosci 2001; 6: D877-889.
McCullers. JA. Insights into the interaction between influenza virus and pneumococcus. Clin. Microbiol. Rev 2006; 19: 571-582.
Medzhitov R y Janeway CA Jr. Innate immunity: impact on the adaptive immune response. Curr. Opin. Immunol 1997; 9: 4- 9.
Monobe H, Ishibashi T, Nombra Y, Shinogami M, Yano J. Role of respiratory viruses in children with acute otitis media Int J Pediatr Otorhinolaryngol 2003; 67: 8016.
Netea MG, van der Graaf C, Van der Meer JW, Kullberg BJ. Toll-like receptors and the host defense against microbial pathogens: bringing specificity to the innate-immune system. J. Leukoc. Biol 2004; 75: 749-755.
Pizarro-Cerda J, Cossart P. Bacterial adhesion and entry into host cells. Cell. 2006; 124: 715-727.
Plotkowski MC, Bajolet-Laudinat O y Puchelle E. Cellular mechanisms of bacterial adhesion to respiratory mucosa. Eur. Respir. J. 1993 ; 6: 903-916.
Ramphal R, Small P, Shands J, Fischschweiger W y Small P. Adherence of Pseudomonas aeruginosa to tracheal cells injured by influenza infection or endotracheal intubation. Infect. Immun 1980; 27: 614-619.
Raza MW, Blackwell CC, Elton RA, Weir DM. Bactericidal activity of a monocytic cell line (THP-1) against common respiratory tract bacterial pathogens is depressed after infection with respiratory syncytial virus. J. Med. Microbiol 2000; 49: 227-233.
Raza MW, El Ahmer OR, Ogilvie MM, Blackwell CC, Saadi AT, Elton RA, Weir DM. Infection with respiratory syncytial virus enhances expression of native receptors for non-pilate Neisseria meningitidis on HEp-2 cells. FEMS Immunol. Med. Microbiol 1999; 23: 115-124.
Reddy MS, Bernstein JM, Murphy TF, Faden HS. Binding between outer membrane proteins of nontypeable Haemophilus influenzae and human nasopharyngeal mucin. Infect. Immun 1996; 64: 1477-1479.
Ricciardolo FL, Di Stefano A, Sabatini F, Folkerts G. Reactive nitrogen species in the respiratory tract. Eur. J. Pharmacol 2006; 533: 240-252.
Sagai S et al. Relationship between respiratory syncytial virus infection and acute otitis media in children. Auris. Nasus. Larynx 2004; 31: 341-345.
Selinger DS, Reed WP, McLaren LC. Model for studying bacterial adherence to epithelial cells infected with viruses. Infect. Immun 1981; 32: 941-944.
Sinaniotis CA. Viral pneumonia in children: incidence and etiology. Paediatr. Respir. Rev 2004; 5 Suppl A: S197-200.
Slifka MK, Homann D, Tishon A, Pagarigan R, Oldstone MB. Measles virus infection results in suppression of both innate and adaptive immune responses to secondary bacterial infection. J. Clin. Invest 2003; 111: 805-810.
Spann KM, Tran KC, Chi B, Rabin RL, Collins PL. Suppression of the induction of alpha, beta, and lambda interferons by the NS1 and NS2 proteins of human respiratory syncytial virus in human epithelial cells and macrophages [corrected]. J. Virol 2004; 78: 4363-4369. Erratum in: J. Virol 2005; 78: 6705.
Suzuki K, Bakaletz LO. Synergistic effect of adenovirus type 1 and nontypeable Haemophilus influenzae in a chinchilla model of experimental otitis media. Infect. Immun 1994; 62: 1710-1718.
Uematsu S, Akira S. Toll-like receptors and innate immunity. Mol. Med 2006; Aug 10 (en prensa).
Van der Sluijs KF et al. Involvement of the platelet-activating factor receptor in host defense against Streptococcus pneumoniae during postinfluenza pneumonia. Am. J. Physiol. Lung Cell Mol. Physiol 2006; 290: L194-199.
Weber F, Kochs G, Haller O. Inverse interference: how viruses fight the interferon system. Viral. Immunol 2004; 17: 498-515.
Wright PF, Thompson J and Karzon DT. Differing virulence of H1N1 and H3N2 influenza strains. Am. J. Epidemiol 1980; 112: 814-819.