Respiratory syncytial virus associated illness in high-risk children and national characterisation of the circulating virus genotype in South Africa

被引:23
作者
Madhi, SA
Venter, M
Alexandra, R
Lewis, H
Kara, Y
Karshagen, WF
Greef, M
Lassen, C
机构
[1] Baragwanath Hosp, Wits Hlth Consortium, Paediat Infect Dis Res Unit, ZA-2013 Bertsham, South Africa
[2] Natl Inst Communicable Dis, ZA-2131 Johannesburg, South Africa
[3] Natl Hlth Lab Serv, ZA-2013 Johannesburg, South Africa
[4] Panorama Medi Clin, ZA-7500 Parrow, South Africa
[5] Pretoria E Hosp, Pretoria, South Africa
[6] St Augustine Heart Care Hosp, Durban, South Africa
[7] Univ Orange Free State, Sch Med, Dept Paediat, Bloemfontein, South Africa
[8] Abbott Labs S Africa Pty Ltd, ZA-2000 Johannesburg, South Africa
关键词
RSV; pneumonia; high risk; genotype; subtype;
D O I
10.1016/S1386-6532(02)00174-9
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: There is limited information about respiratory syncytial virus (RSV) in high-risk children from developing countries or on the genotype characterisation of the circulating virus. Objective: To define the proportion of children with RSV associated lower respiratory tract infections (LRTI) that had risk factors for severe disease and to genotype the circulating RSV strains across the country. Study design: A prospective study was performed in four distinct regions. During April 2000-December 2000 (period 1), all children, with LRTI or without underlying high risk factors for severe RSV disease were enrolled. During January to September 2001 (period 2), only children with LRTI with underlying high risk factors were enrolled. Nasopharyngeal aspirates were evaluated for RSV infection using an ELISA test. RSV isolates were also subtyped and genotyped. Results: Fifty three (24%) of 220 children enrolled during period I had risk factors for severe RSV disease; in addition to which a further 38 high-risk children were enrolled during 2001. RSV was isolated from 16 (30%) of 53 and 37 (22%) of 167 high-risk and non-high risk children, respectively, P = 0.31. High-risk children were more likely to require intensive unit care (25 vs. 2.7%, P = 0.02) and were also more likely to be hospitalised for a longer duration (median 7 vs. 5 days, P = 0.06) than non high-risk infants. Overall (periods I and 2), RSV was isolated from 34 (37.4%) of the 91 high-risk infants enrolled. Among high-risk children, those from whom RSV was isolated were more likely to require hospitalisation (73.5 vs. 54.4%, P = 0.07) and admission to an intensive care unit (14.7 vs. 1.8%, P = 0.03) than those from whom RSV was not isolated. Of 40 isolates subtyped during period one, 92.5% were subtype A. Further, 27 (83.3%) of 30 subtype A isolates genotyped during period I clustered with GA2. Conclusion: RSV is an important cause of LRTI among high-risk infants in a developing country such as South Africa. For the season in question, the genotype that was dominant in Johannesburg was isolated throughout the country, suggesting that successful genotypes may have the ability to spread nationwide. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:180 / 189
页数:10
相关论文
共 27 条
  • [11] KUMAR SK, 2000, MOL EVOLUTIONARY GEN
  • [12] Differing manifestations of respiratory syncytial virus-associated severe lower respiratory tract infections in human immunodeficiency virus type 1-infected and uninfected children
    Madhi, SA
    Venter, M
    Madhi, A
    Petersen, K
    Klugman, KP
    [J]. PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2001, 20 (02) : 164 - 170
  • [13] Increased burden of respiratory viral associated severe lower respiratory tract infections in children infected with human immunodeficiency virus type-1
    Madhi, SA
    Schoub, B
    Simmank, K
    Blackburn, N
    Klugman, KP
    [J]. JOURNAL OF PEDIATRICS, 2000, 137 (01) : 78 - 84
  • [14] Evolutionary pattern of the G glycoprotein of human respiratory syncytial viruses from antigenic group B:: the use of alternative termination codons and lineage diversification
    Martínez, I
    Valdés, O
    Delfraro, A
    Arbiza, J
    Russi, J
    Melero, JA
    [J]. JOURNAL OF GENERAL VIROLOGY, 1999, 80 : 125 - 130
  • [15] Null D, 1998, PEDIATRICS, V102, P531, DOI 10.1542/peds.102.3.531
  • [16] Circulation patterns of genetically distinct group A and B strains of human respiratory syncytial virus in a community
    Peret, TCT
    Hall, CB
    Schnabel, KC
    Golub, JA
    Anderson, LJ
    [J]. JOURNAL OF GENERAL VIROLOGY, 1998, 79 : 2221 - 2229
  • [17] Circulation patterns of group A and B human respiratory syncytial virus genotypes in 5 communities in North America
    Peret, TCT
    Hall, CB
    Hammond, GW
    Piedra, PA
    Storch, GA
    Sullender, WM
    Tsou, C
    Anderson, LJ
    [J]. JOURNAL OF INFECTIOUS DISEASES, 2000, 181 (06) : 1891 - 1896
  • [18] Genetic variability among group A and B respiratory syncytial viruses in Mozambique:: identification of a new cluster of group B isolates
    Roca, A
    Loscertales, MP
    Quintó, L
    Pérez-Breña, P
    Vaz, N
    Alonso, PL
    Saiz, JC
    [J]. JOURNAL OF GENERAL VIROLOGY, 2001, 82 : 103 - 111
  • [19] SELWYN BJ, 1990, REV INFECT DIS, V12, P870
  • [20] Antigenic and genetic diversity among the attachment proteins of group a respiratory syncytial viruses that have caused repeat infections in children
    Sullender, WM
    Mufson, MA
    Prince, GA
    Anderson, LJ
    Wertz, GW
    [J]. JOURNAL OF INFECTIOUS DISEASES, 1998, 178 (04) : 925 - 932