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Páginas 136-144 (Febrero 2001)
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Vol. 54. Núm. 2.
Páginas 136-144 (Febrero 2001)
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Ribovirus emergentes implicados en las gastroenteritis
Emergent riboviruses implicated in gastroenteritis
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J.M.a Eiros Bouzaa,
Autor para correspondencia
eiros@med.uva.es

Correspondencia: Dr. J.M.a Eiros Bouza. Departamento de Microbiología. 6.a pl. Facultad de Medicina. Avda. Ramón y Cajal, 7. 47005 Valladolid.
, M.aR. Bachiller Luqueb, R. Ortiz de Lejarazua
a Departamentos de Microbiología Facultad de Medicina. Universidad de Valladolid
b Departamentos de Pediatría. Facultad de Medicina. Universidad de Valladolid
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Los virus se sitúan en un lugar preferente entre los agentes causales de diarrea aguda, en particular en la infancia. En este contexto el papel de los astrovirus, coronavirus, torovirus y picobirnavirus es emergente. Los astrovirus se han detectado en las heces entre el 1,2 y el 20 % de niños con diarrea que requieren atención médica en una gran variedad de localizaciones geográficas. Se han descrito brotes epidémicos en escuelas, guarderías y salas pediátricas, y son más frecuentes entre niños de menos de 3 años. En climas templados se ha demostrado una mayor incidencia invernal, y en climas tropicales ésta es similar en todo el año, siendo su transmisión preferente por vía orofecal. Se han reconocido siete serotipos de astrovirus humanos, de los cuales el más común es el uno. Los viriones pueden eliminarse durante amplios períodos y detectarse mediante microscopia electrónica. En estudios epidemiológicos se emplean técnicas de enzimoinmunoanálisis para detectar el antígeno común de grupo y se han desarrollado también técnicas basadas en la detección de ácidos nucleicos mediante hibridación y amplificación (reacción en cadena de la polimerasa).

Los coronavirus entéricos se han asociado con frecuencia con enfermedad gastrointestinal en recién nacidos y niños menores de 12 años. El papel de los torovirus y picobirnavirus como causa de gastroenteritis es también emergente. Se necesitan estudios epidemiológicos para determinar su verdadera frecuencia en la comunidad, identificar sus mecanismos de transmisión y explicar la fisiopatología de los cuadros provocados por estos agentes.

Palabras clave:
Gastroenteritis
Astrovirus
Coronavirus
Torovirus
Picobirnavirus

Viral agents are one of the main causes of acute diarrhea, particularly in infants and young children. Astrovirus, coronavirus, torovirus, and picobirnavirus are increasingly being identified as causative agents of gastroenteritis. Astroviruses have been detected in the stools of between 1.2 % and 20 % of children with diarrhea requiring medical care in a variety of geographical areas. Outbreaks have been described in schools, day care settings and pediatric wards. Children younger than 3 years old are the most frequently affected. In temperate climates incidence is greater in winter whereas in tropical areas infection occurs throughout the year. Transmission is mainly through the fecal-oral route. At least seven serotypes of human astroviruses have been recognized and serotype 1 is more common than the other serotypes. Astroviruses are often shed in stools during long periods and can be detected by electron microscopy. An enzyme-immunoassay technique that detects the astrovirus group antigen has been widely used in epidemiological studies. Nucleic acid hybridization and polymerase chain reaction-based techniques have also been used. Enteric coronaviruses have most frequently been associated with gastrointestinal disease in neonates and children younger than 12 years old. The role of toroviruses and picobirnaviruses as causative agents of gastroenteritis is still emerging.

Further epidemiological studies to determine the frequency of these viruses in the community and to identify their mechanisms of transmission are needed, as are further studies to elucidate the pathophysiology of diseases due to these agents.

Key words:
Gastroenteritis
Astrovirus
Coronavirus
Torovirus
Picobirnavirus
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Bibliografía
[1.]
N.R. Blacklow, H.B. Greenberg.
Viral gastroenteritis.
N Engl J Med, 325 (1991), pp. 252-264
[2.]
P.M. Sherman, M. Petric, M.B. Cohen.
Infectious gastroenterocolitides in children: an update on emerging pathogens.
Pediatr Clin North Am, 43 (1996), pp. 391-407
[3.]
S.R. Framm, R. Soave.
Agents of diarrhea.
Med Clin North Am, 81 (1997), pp. 427-447
[4.]
J.J. Treanor, R. Dolin.
Astrovirus, Toroviruses and Picobirnaviruses.
Mandell, Douglas and Bennett's. Principles and practice of infectious diseases, 5.a, pp. 1956-1958
[5.]
K.Y. Green.
Summary of the first international workshop on human caliciviruses.
J Infect Dis, 181 (2000), pp. 252-253
[6.]
R. Ortiz de Lejarazu Leonardo, J.I. Reguera Useros, J.M. Eiros Bouza, A. Rodriguez Torres.
Detección de adenovirus en heces mediante látex y comprobación por microscopia electrónica.
Enferm Infecc Microbiol Clin, 8 (1990), pp. 468-469
[7.]
R. Ortiz de Lejarazu Leonardo, J.I. Reguera Useros, J.M. Eiros Bouza, A. Rodriguez Torres.
Evaluacion de un enzimoinmunoanalisis rapido de rotavirus.
Enferm Infecc Microbiol Clin, 10 (1992), pp. 240-242
[8.]
J.I. Reguera, R. Ortiz de Lejarazu, J.M. Eiros, M.A. Bratos, M.P. Gonzalo, P. Pérez-Pascual, A. Rodríguez Torres.
Estudio de 3 años de los patrones de electroforesis de ARN de rotavirus en Valladolid.
Enferm Infecc Microbiol Clin, 11 (1993), pp. 309-313
[9.]
S.M. Matsui, H.B. Greenberg.
Astroviruses.
Fields Virology, 3.a, pp. 811-824
[10.]
D.M. Bass.
Rotavirus ans other agents of viral gastroenteritis.
Nelson texbook of pediatrics, 16.a, pp. 997-999
[11.]
F. Denis, E. Barriere, C. Venot, S. Ranger-Rogez, N. Durepaire, C. Martin, et al.
Virus et infections gastro-intestinales.
Ann Biol Clin (Paris), 55 (1997), pp. 275-287
[12.]
C.R. Ashley, E.O. Caul, W.K. Paver.
Astrovirus-associated gastroenteritis in children.
J Clin Pathol, 31 (1978), pp. 939-943
[13.]
C. Risco, J.L. Carrascosa, A.M. Pedregosa, C.D. Humphrey, A. Sanchez-Fauquier.
Ultraestructure of human astrovirus serotype 2.
J Gen Virol, 76 (1995), pp. 2075-2080
[14.]
M.M. Willcocks, T.D. Brown, C.R. Madeley, M.J. Carter.
The complete sequence of a human astrovirus.
J Gen Virol, 75 (1994), pp. 1785-1788
[15.]
M.J. Carter, M.M. Willcocks.
The molecular biology of astroviruses.
Arch Virol, 12 (1996), pp. 277-285
[16.]
K. Midthun, H.B. Greenberg, J.B. Kurtz, G.W. Gary, F.Y. Lin, A.Z. Kapikian.
Characterization and seroepidemiology of a type 5 astrovirus associated with an outbreak of gastroenteritis in Marin Country, California.
J Clin Microbiol, 31 (1993), pp. 955-962
[17.]
E.A. Palombo, R.F. Bishop.
Annual incidence, serotype distribution, and generic diversity of human astrovirus isolates from hospitalized children in Melbourne, Australia.
J Clin Microbiol, 34 (1996), pp. 1750-1753
[18.]
D.K. Mitchell, D.O. Matson, X. Jiang, T. Berke, S.S. Monroe, M.J. Carter, et al.
Molecular epidemiology of childhood astrovirus in child care centers.
J Infect Dis, 180 (1999), pp. 514-517
[19.]
U. Geigenmuller, N.H. Ginzton, S.M. Matsui.
Construction of a genome-length cDNA clone for human astrovirus serotype 1 and synthesis of infectious RNA transcripts.
J Virol, 7 (1997), pp. 1713-1717
[20.]
D.M. Bass, S. Qiu.
Proteolytic processing of the astrovirus capsid.
J Virol, 74 (2000), pp. 1810-1814
[21.]
D.R. Snodgrass, K.W. Angus, E.W. Gray, J.D. Menzies, G. Paul.
Pathogenesis of diarrhoea caused by astrovirus infecions in lambs.
Arch Virol, 60 (1979), pp. 217-226
[22.]
M.L. Thouvenelle, J.S. Haynes, J.L. Sell, D.L. Reynolds.
Astrovirus infection in hatchling turkeys: alterations in intestinal maltase activity.
Avian Dis, 39 (1995), pp. 343-348
[23.]
J.E. Herrmann, D.N. Taylor, P. Echeverria, N.R. Blacklow.
Astroviruses as a cause of gastroenteritis in children.
N Engl J Med, 324 (1991), pp. 1757-1760
[24.]
J.F. Lew, C.L. Moe, S.S. Monroe, J.R. Allen, B.M. Harrison, B.D. Forrester, et al.
Astrovirus and adenovirus associated with diarrhea in children in day care settings.
J Infect Dis, 164 (1991), pp. 673-678
[25.]
K.L. Kotloff, J.E. Herrmann, N.R. Blacklow, R.W. Hudson, S.S. Wasserman, J.G. Morris Jr..
The frequency of astrovirus as a causa of diarrhea in Baltimore children.
Pediatr Infect Dis J, 11 (1992), pp. 587-589
[26.]
I. Oishi, K. Yamazaki, T. Kimoto, Y. Minekawa, E. Utagawa, S. Yamazaki, et al.
A large outbreak of acute gastroenteritis associated with astrovirus among students ans teachers in Osaka, Japan.
J Infect Dis, 170 (1994), pp. 439-443
[27.]
L.E. Unicomb, N.N. Banu, T. Azim, A. Islam, P.K. Bardhan, A.S. Faruque, et al.
Astrovirus infection in association with acute, persistent asn nosocomial diarrhea in Bangladesh.
Pediatr Infect Dis J, 17 (1998), pp. 611-614
[28.]
X.L. Pang, T. Vesikari.
Human astrovirus-associated gastroenteritis in children under 2 years of age followed prospectively during a rotavirus vaccine trial.
Acta Paediatr, 88 (1999), pp. 532-536
[29.]
S. Shastri, A.M. Doane, J. Gonzales, U. Upadhyayula, D.M. Bass.
Prevalence of astrovirus in a children's hospital.
J Clin Microbiol, 36 (1998), pp. 2571-2574
[30.]
M. Putzker, H. Sauer, G. Kirchner, O. Keksel, A. Marlic.
Community acquired diarrhea-the incidence of astrovirus infections in Germany.
Clin Lab, 46 (2000), pp. 269-273
[31.]
M.L. Guerrero, J.S. Noel, D.K. Mitchell, J.J. Calva, A.L. Morrow, J. Martinez, et al.
A prospective study of astrovirus diarrhea of infancy in Mexico City.
Pediatr Infect Dis J, 17 (1998), pp. 723-727
[32.]
D.K. Mitchell, S.S. Monroe, X. Jiamg, D.O. Matson, R.I. Glass, L.K. Pickering.
Virologic features of an antrovirus diarrhea outbreak in a day care center revealed by reverse transcriptase-polymerase chain reaction.
J Infect Dis, 172 (1995), pp. 1437-1444
[33.]
J.F. Lew, R.I. Glass, M. Petric, C.W. Lebaron, G.W. Hammond, S.E. Miller, et al.
Six-year retrospective surveillance of gastroenteritis viruses identified at ten electron microscopy centres in the United States and Canada.
Pediatr Infect Dis, 9 (1990), pp. 709-714
[34.]
S.S. Monroe, R.I. Glass, N. Noah, T.H. Flewett, E.O. Caul, C.I. Ashton, et al.
Electro microscopic reporting of gastrointestinal viruses in the United Kingdom, 1985-1987.
J Med Virol, 33 (1991), pp. 193-198
[35.]
M.P. Koopmans, M.H. Bijen, S.S. Monroe, J. Vinje.
Age-stratified seroprevalence of neutralizing antibodies to astrovirus types 1 to 7 in humans in The Netherlands.
Clin Diag Lab Immunol, 5 (1998), pp. 33-37
[36.]
J.E. Herrmann, R.W. Hudson, D.M. Perron-Henry, J.B. Kurtz, N.R. Blacklow.
Antigenic characterization of cell-cultivated astrovirus serotypes ans development of astrovirus-specific monoclonal antibodies.
J Infec Dis, 158 (1988), pp. 182-185
[37.]
M.M. Willcocks, M.J. Carter, F.R. Laidler, C.R. Madeley.
Growth and characterisation of human faecal astrovirus in a continuous cell line.
Arch Virol, 113 (1990), pp. 73-81
[38.]
H. Mustafa, E.A. Palombo, R.F. Bishop.
Epidemiology of astrovirus in young children hospitalizad with acute gastroenteritis in Melbourne, Australia, over a period of four consecutive years, 1995 to 1998.
J Clin Microbiol, 38 (2000), pp. 1058-1062
[39.]
R.I. Glass, J. Noel, D. Mitchell, J.E. Herrmann, N.R. Blacklow, L.K. Pickering, et al.
The changing epidemiology of astrovirus-associated gastroenteritis: a review.
Arch Virol, 12 (1996), pp. 287-300
[40.]
J.E. Herrmann, N.A. Nowak, D.M. Perron-Henry, R.W. Hudson, W.D. Cubitt, N.R. Blacklow.
Diagnosis of astrovirus gastroenteritis by antigen detection with monoclonal antibodies.
J Infect Dis, 161 (1990), pp. 226-229
[41.]
C.J. McIver, E.A. Palombo, J.C. Doultree, H. Mustafa, J.A. Marshall, W.D. Rawlinson.
Detection of astrovirus gastroenteritis in children.
J Virol Methods, 84 (2000), pp. 99-105
[42.]
W.D. Cubitt, D.K. Mitchell, M.J. Carter, M.M. Willcocks, H. Holzel.
Application of electronmicroscopy, enzyme immunoassay, and RT-PCR to monitor an outbreak of astrovirus type 1 in a paediatric bone marrow transplant unit.
J Med Virol, 57 (1999), pp. 313-321
[43.]
M.B. Taylor, F.E. Marx, W.O. Grabow.
Rotavirus, astrovirus and adenovirus associated with an outbreak of gastroenteritis in a South African child care centre.
Epidemiol Infect, 119 (1997), pp. 227-230
[44.]
A.D. Steele, H.R. Basetse, N.R. Blacklow, J.E. Herrmann.
Astrovirus infection in South Africa: a pilot study.
Ann Trop Paediatr, 18 (1998), pp. 315-319
[45.]
A. Gaggero, M. O'Ryan, J.S. Noel, R.I. Glass, S.S. Monroe, N. Mamani, et al.
Prevalence of astrovirus infection among Chilean children with acute gastroenteritis.
J Clin Microbiol, 36 (1998), pp. 3691-3693
[46.]
Y. Maldonado, M. Cantwell, M. Old, D. Hill, M.L. Sanchez, L. Logan, et al.
Population-based prevalence of symptomatic and asymptomatic astrovirus infection in rural mayan infants.
J Infect Dis, 178 (1998), pp. 334-339
[47.]
F. Bon, P. Fascia, M. Dauvergne, D. Tenenbaum, H. Planson, A.M. Petion, et al.
Prevalence of group A rotavirus, human calicivirus, astrovirus, and adenovirus type 40 and 41 infections among children with acute gastroenteritis in Dijon, France.
J Clin Microbiol, 37 (1999), pp. 3055-3058
[48.]
J.M. Eiros, R. Ortiz de Lejarazu, R. Bachiller, B. Hernández, M. Ortega, A. Rodríguez Torres.
Diagnosis of Astrovirus associated gastroenteritis in children. Presentado en el Europaediatrics 2000. The UNEPSA and CESP European Congress of Paediatrics, 18-21.
pp. 161
[49.]
T. Konno, H. Suzuki, N. Ishida, R. Chiba, K. Mochizuki, A. Tsunoda.
Astrovirus-associated epidemic gastroenteritis in Japan.
J Med Virol, 9 (1982), pp. 11-17
[50.]
H. Esahli, K. Breback, R. Bennet, A. Ehrnst, M. Eriksson, K.O. Hedlund.
Astroviruses as a cause of nosocomial outbreaks of infant diarrhea.
Pediatr Infect Dis J, 10 (1991), pp. 511-515
[51.]
M.B. Liste, I. Natera, J.A. Suarez, F.H. Pujol, F. Liprandi, J.E. Ludert.
Enteric virus infections and diarrhea in healthy and human immunodeficiency virus-infected children.
J Clin Microbiol, 38 (2000), pp. 2873-2877
[52.]
T.W. Lee, J.B. Kurtz.
Prevalence of human astrovirus serotypes in the Oxford region 1976-1992, with evidence for two new serotypes.
Epidemiol Infect, 112 (1994), pp. 187-193
[53.]
J.S. Noel, T.W. Lee, J.B. Kurtz, R.I. Glass, S.S. Monroe.
Typing of human astroviruses from clinical isolates by enzyme immunoassay and nucleotide sequencing.
J Clin Microbiol, 33 (1995), pp. 797-801
[54.]
R.W. Hudson, J.E. Herrmann, N.R. Blacklow.
Plaque cuantitation and virus neutralization assays for human astroviruses.
Arch Virol, 108 (1989), pp. 33-38
[55.]
J. Kurtz, T. Lee.
Astrovirus gastroenteritis age distribution of antibody.
Med Microbiol Immunol (Berl), 166 (1978), pp. 227-230
[56.]
S. Kriston, M.M. Willcocks, M.J. Carter, W.D. Cubitt.
Seroprevalence of astrovirus types 1 and 6 in London, determined using recombinant virus antigen.
Epidemiol Infect, 117 (1996), pp. 159-164
[57.]
D.K. Mitchell, D.O. Matson, W.D. Cubitt, L.J. Jackson, M.M. Willcocks, L.K. Pickering, et al.
Prevalence of antibodies to astrovirus types 1 and 3 in children and adolescents in Norfolk, Virginia.
Pediatr Infect Dis J, 18 (1999), pp. 249-254
[58.]
K. McIntosh.
Coronaviruses.
Mandell, Douglas and Bennett's. Principles and practice of infectious diseases, 5.a, pp. 1767-1770
[59.]
C. Chany, O. Moscovici, P. Lebon, S. Rousset.
Association of coronavirus infection with neonatal necroziting enterocolitis.
Pediatrics, 69 (1982), pp. 209-214
[60.]
Y.E. Vaucher, C.G. Ray, L.L. Minnich, C.M. Payne, D. Beck, P. Lowe.
Pleomorphic, enveloped, virus-like particles associated with gastrointestinal illness in neonates.
J Infect Dis, 145 (1982), pp. 27-36
[61.]
G. Gerna, N. Passarani, M. Battaglia, E.G. Rondanello.
Human enteric coronaviruses: antigenic relatedness to human coronavirus OC43 and possible etiologic role in viral gastroenteritis.
J Infect Dis, 151 (1985), pp. 796-803
[62.]
P. González, A. Sanches, P. Rivera, C. Jiménez, F. Hernández.
Rotavirus ans coronavirus outbreak: etiology of annual diarrhea in Costa Rican children.
Rev Biol Trop, 45 (1997), pp. 898-991
[63.]
C.M. Sánchez, A. Izeta, J.M. Sánchez-Morgado, S. Alonso, I. Sola, M. Balasch, et al.
Targeted recombination demonstrates that the spike gene of trnasmissible gastroenteritis coronaviru is a determinant of its enteric tropism and virulence.
J Virol, 73 (1999), pp. 7607-7618
[64.]
F. Almazán, J.M. González, Z. Penzes, A. Izeta, E. Calvo, J. Plana-Durán, et al.
Engineering the laargest RNA virus genome as an infectious bacterial artificial chromosome.
Proc Natl Acad Sci USA, 97 (2000), pp. 5516-5521
[65.]
K.V. Holmes, D.B. Tresnan, B.D. Zelus.
Virus-receptor interactions in the enteric tract. Virus-receptor interactions.
Adv Exp Med Biol, 412 (1997), pp. 125-133
[66.]
A.R. Collins.
HLA class I antigen serves as a receptor for human coronavirus OC43.
Immunol Invest, 22 (1993), pp. 95-103
[67.]
C.M. Payne, C.G. Ray, V. Borduin, L.L. Minnich, M.D. Lebowitz.
An eight-year study of the viral agents of acute gastroenteritis in humans: ultrastructural observations and seasonal distribution with a major emphasis on coronavirus-like particles.
Diagn Microbiol Infect Dis, 5 (1996), pp. 39-54
[68.]
M.L. Mortensen, C.G. Ray, C.M. Payne, A.D. Friedman, L.L. Minnich, C. Rousseau.
Coronaviruslike particles in human gastrointestinal disease. Epidemiologic, clinical, and laboratory observations.
Am J Dis Child, 139 (1985), pp. 928-934
[69.]
J.A. Marshall, C.J. Birch, H.G. Williamson, D.K. Bowden, C.M. Boveington, T. Kuberski, et al.
Coronavirus-like particles and other agents in the faeces of children in Efate, Vanuatu.
J Trop Med Hyg, 85 (1982), pp. 213-215
[70.]
J.P. Luby, R. Clinton, S. Kurtz.
Adaptation of human enteric coronavirus to growth in cell lines.
J Clin Virol, 12 (1999), pp. 43-51
[71.]
C.A. De Haan, H. Vennema, P.J. Rottier.
Coronavirus envelope assembly in sensitive to changes in the terminal regions of the viral M protein.
Adv Exp Med Biol, 440 (1998), pp. 367-375
[72.]
A. Cristallo, G. Biamonti, M. Battaglia, P.M. Cereda.
DNA probe for the human coronavirus OC43 also detects neonatal calf diarrhea coronavirus (NCDCV).
New Microbiol, 19 (1996), pp. 251-256
[73.]
A. McGoldrick, J.P. Lowings, D.J. Paton.
Characterisation of a recent virulent transmissible gastroenteritis virus from Britain with a deleted ORF 3a.
Arch Virol, 144 (1999), pp. 763-770
[74.]
D. Cavanagh, M.C. Horzinek.
Genus Torovirus assigned to the Coronaviridae.
Arch Virol, 128 (1993), pp. 395-396
[75.]
M.C. Horzinek.
Molecular evolution of corona-and toroviruses.
Adv Exp Med Biol, 473 (1999), pp. 61-72
[76.]
G.M. Beards, C. Hall, J. Green, T.H. Flewett, F. Lamouliatte, P. Du Pasquier.
An enveloped virus in stools of children and adults with gastroenteritis that resembles the Breda virus of calves.
Lancet, 1 (1984), pp. 1050-1052
[77.]
M. Koopmans, A. Herrewegh, M.C. Horzinek.
Diagnosis of torovirus infection.
Lancet, 337 (1991), pp. 859
[78.]
M. Koopmans, M. Petric, R. Glass, S.S. Monroe.
Enzyme-linked immunosorbent assay reactivity of torovirus-like particles in fecal specimens from humans wuth diarrhea.
J Clin Microbiol, 31 (1993), pp. 2738-2744
[79.]
T. Krishnan, T.N. Naik.
Electronmicroscopic evidence of totovirus like particles in children with diarrhoea.
Indian J Med Res, 105 (1997), pp. 108-110
[80.]
F.B. Jamieson, E.E. Wang, C. Bain, J. Good, L. Duckmanton, M. Petric.
Human torovirus: a new nosocomial gastrointestinal pathogen.
J Infect Dis, 178 (1998), pp. 1263-1269
[81.]
L. Duckmanton, B. Luan, J. Devenish, R. Tellier, M. Petric.
Characterizarion of torovirus from human fecal specimens.
Virology, 239 (1997), pp. 158-168
[82.]
M.P. Koopmans, E.S. Goosen, A.A. Lima, I.T. McAuliffe, J.P. Nataro, L.J. Barrett, et al.
Association of torovirus with acute and persistent diarrhea in children.
Pediatr Infect Dis J, 16 (1997), pp. 504-507
[83.]
E.J. Snijder, M.C. Horzinek.
Toroviruses: replication, evolution and comparison with other members of the coronavirus-like superfamily.
J Gen Virol, 74 (1993), pp. 2305-2316
[84.]
H.G. Pereira, A.M. Fialho, T.H. Flewett, J.M. Teixeira, Z.P. Andrade.
Novel viruses in human faeces.
Lancet, 2 (1988), pp. 103-104
[85.]
R. Chandra.
Picobirnavirus, a novel group of undescribed viruses of mammals and birds: a minireview.
Acta Virol, 41 (1997), pp. 59-62
[86.]
G.S. Grohmann, R.I. Glass, H.G. Pereira, S.S. Monroe, A.W. Hightower, R. Weber, et al.
Enteric viruses and diarrhea in HIV-infected patients. Enteric oportunistic Infectoins Working Group.
N Engl J Med, 329 (1993), pp. 14-20
[87.]
M.O. Giordano, L.C. Martinez, D. Rinaldi, C. Espul, N. Martinez, M.B. Isa, et al.
Diarrhea and enteric emerging viruses in HIV-infected patients.
AIDS Res Hum Retroviruses, 15 (1999), pp. 1427-1432
[88.]
G.G. Gonzalez, F.H. Pujol, F. Liprandi, L. Deibis, J.E. Ludert.
Prevalence of enteric viruses in human immunodeficiency virus seropositive patients in Venezuela.
J Med Virol, 55 (1998), pp. 288-292
[89.]
C.I. Gallimore, H. Appleton, D. Lewis, J. Green, D.W. Brown.
Detection and characterization of bisegmented double-stranded RNA viruses (picobirnaviruses in human faecal specimens).
J Med Virol, 45 (1995), pp. 135-140
[90.]
A. Cascio, M. Bosco, E. Vizzi, A. Giammanco, D. Ferraro, S. Arista.
Identification of picobirnavirus from faeces of Italian children suffering from acute diarrhea.
Eur J Epidemiol, 12 (1996), pp. 545-547
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