期刊论文详细信息
BMC Infectious Diseases
Examining strain diversity and phylogeography in relation to an unusual epidemic pattern of respiratory syncytial virus (RSV) in a long-term refugee camp in Kenya
D James Nokes2  Robert F Breiman3  Joel M Montgomery3  Wagacha Burton3  Nina Marano1  Rachel B Eidex1  Raymond Nyoka1  Lilian W Waiboci1  Barry S Fields1  Jamal A Ahmed1  James R Otieno4  Lillian M Mayieka1  Charles N Agoti4 
[1] United States Centers for Disease Control and Prevention, Nairobi, Kenya;School of Life Sciences and WIDER, Warwick University, Coventry, UK;Division of Global Health Protection, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, USA;Kenya Medical Research Institute (KEMRI)–Wellcome Trust Research Programme, Kilifi, Kenya
关键词: RSV;    Refugee;    Genotype;    Genetic diversity;    Epidemics;    Displaced population;    Attachment (G) protein;   
Others  :  1134217
DOI  :  10.1186/1471-2334-14-178
 received in 2014-01-05, accepted in 2014-03-24,  发布年份 2014
PDF
【 摘 要 】

Background

A recent longitudinal study in the Dadaab refugee camp near the Kenya-Somalia border identified unusual biannual respiratory syncytial virus (RSV) epidemics. We characterized the genetic variability of the associated RSV strains to determine if viral diversity contributed to this unusual epidemic pattern.

Methods

For 336 RSV positive specimens identified from 2007 through 2011 through facility-based surveillance of respiratory illnesses in the camp, 324 (96.4%) were sub-typed by PCR methods, into 201 (62.0%) group A, 118 (36.4%) group B and 5 (1.5%) group A-B co-infections. Partial sequencing of the G gene (coding for the attachment protein) was completed for 290 (89.5%) specimens. These specimens were phylogenetically analyzed together with 1154 contemporaneous strains from 22 countries.

Results

Of the 6 epidemic peaks recorded in the camp over the period, the first and last were predominantly made up of group B strains, while the 4 in between were largely composed of group A strains in a consecutive series of minor followed by major epidemics. The Dadaab group A strains belonged to either genotype GA2 (180, 98.9%) or GA5 (2, < 1%) while all group B strains (108, 100%) belonged to BA genotype. In sequential epidemics, strains within these genotypes appeared to be of two types: those continuing from the preceding epidemics and those newly introduced. Genotype diversity was similar in minor and major epidemics.

Conclusion

RSV strain diversity in Dadaab was similar to contemporaneous diversity worldwide, suggested both between-epidemic persistence and new introductions, and was unrelated to the unusual epidemic pattern.

【 授权许可】

   
2014 Agoti et al.; licensee BioMed Central Ltd.

【 预 览 】
附件列表
Files Size Format View
20150305115220517.pdf 1016KB PDF download
Figure 6. 106KB Image download
Figure 5. 110KB Image download
Figure 4. 95KB Image download
Figure 3. 106KB Image download
Figure 2. 40KB Image download
Figure 1. 40KB Image download
【 图 表 】

Figure 1.

Figure 2.

Figure 3.

Figure 4.

Figure 5.

Figure 6.

【 参考文献 】
  • [1]Toole MJ: Mass population displacement. A global public health challenge. Infect Dis Clin North Am 1995, 9:353-366.
  • [2]Toole MJ, Waldman RJ: Refugees and displaced persons. War, hunger, and public health. JAMA 1993, 270:600-605.
  • [3]Ahmed JA, Katz MA, Auko E, Njenga MK, Weinberg M, Kapella BK, Burke H, Nyoka R, Gichangi A, Waiboci LW, Mahamud A, Qassim M, Swai B, Wagacha B, Mutonga D, Nguhi M, Breiman RF, Eidex RB: Epidemiology of respiratory viral infections in two long-term refugee camps in Kenya, 2007–2010. BMC Infect Dis 2012, 12:7. BioMed Central Full Text
  • [4]Polonsky JA, Ronsse A, Ciglenecki I, Rull M, Porten K: High levels of mortality, malnutrition, and measles, among recently-displaced somali refugees in dagahaley camp, dadaab refugee camp complex, Kenya, 2011. Confl Health 2013, 7:1. BioMed Central Full Text
  • [5]Thomas SL, Thomas SD: Displacement and health. Br Med Bull 2004, 69:115-127.
  • [6]Toole MJ, Waldman RJ: Prevention of excess mortality in refugee and displaced populations in developing countries. JAMA 1990, 263:3296-3302.
  • [7]White LJ, Mandl JN, Gomes MG, Bodley-Tickell AT, Cane PA, Perez-Brena P, Aguilar JC, Siqueira MM, Portes SA, Straliotto SM, Waris M, Nokes DJ, Medley GF: Understanding the transmission dynamics of respiratory syncytial virus using multiple time series and nested models. Math Biosci 2006, 209:222-239.
  • [8]Cane P: Molecular Epidemiology and Evolution of RSV. In Respiratory Syncytial Virus. Volume 1 edition. Edited by Cane P. Elsevier; 2007:89-113. A.J. Zuckerman IKM (Series Editor): PERSPECTIVES IN MEDICAL VIROLOGY
  • [9]Zlateva KT, Vijgen L, Dekeersmaeker N, Naranjo C, Van Ranst M: Subgroup prevalence and genotype circulation patterns of human respiratory syncytial virus in Belgium during ten successive epidemic seasons. J Clin Microbiol 2007, 45:3022-3030.
  • [10]White LJ, Waris M, Cane PA, Nokes DJ, Medley GF: The transmission dynamics of groups A and B human respiratory syncytial virus (hRSV) in England & Wales and Finland: seasonality and cross-protection. Epidemiol Infect 2005, 133:279-289.
  • [11]Botosso VF, Zanotto PM, Ueda M, Arruda E, Gilio AE, Vieira SE, Stewien KE, Peret TC, Jamal LF, Pardini MI, Pinho JR, Massad E, Sant'anna OA, Holmes EC, Durigon EL: Positive selection results in frequent reversible amino acid replacements in the G protein gene of human respiratory syncytial virus. PLoS Pathog 2009, 5:e1000254.
  • [12]Cane PA, Pringle CR: Evolution of subgroup A respiratory syncytial virus: evidence for progressive accumulation of amino acid changes in the attachment protein. J Virol 1995, 69:2918-2925.
  • [13]Kim C, Ahmed JA, Eidex RB, Nyoka R, Waiboci LW, Erdman D, Tepo A, Mahamud AS, Kabura W, Nguhi M, Muthoka P, Burton W, Breiman RF, Njenga MK, Katz MA: Comparison of nasopharyngeal and oropharyngeal swabs for the diagnosis of eight respiratory viruses by real-time reverse transcription-PCR assays. PLoS One 2011, 6:e21610.
  • [14]Gunson RN, Collins TC, Carman WF: Real-time RT-PCR detection of 12 respiratory viral infections in four triplex reactions. J Clin Virol 2005, 33:341-344.
  • [15]Agoti CN, Mwihuri AG, Sande CJ, Onyango CO, Medley GF, Cane PA, Nokes DJ: Genetic relatedness of infecting and reinfecting respiratory syncytial virus strains identified in a birth cohort from rural kenya. J Infect Dis 2012, 206:1532-1541.
  • [16]Katoh K, Toh H: Recent developments in the MAFFT multiple sequence alignment program. Brief Bioinform 2008, 9:286-298.
  • [17]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 Evol 2011, 28:2731-2739.
  • [18]Anonymous: Toward a unified nomenclature system for highly pathogenic avian influenza virus (H5N1). Emerg Infect Dis 2008, 14:e1.
  • [19]Shobugawa Y, Saito R, Sano Y, Zaraket H, Suzuki Y, Kumaki A, Dapat I, Oguma T, Yamaguchi M, Suzuki H: Emerging genotypes of human respiratory syncytial virus subgroup A among patients in Japan. J Clin Microbiol 2009, 47:2475-2482.
  • [20]Baek YH, Choi EH, Song MS, Pascua PN, Kwon HI, Park SJ, Lee JH, Woo SI, Ahn BH, Han HS, Hahn YS, Shin KS, Jang HL, Kim SY, Choi YK: Prevalence and genetic characterization of respiratory syncytial virus (RSV) in hospitalized children in Korea. Arch Virol 2012, 157:1039-1050.
  • [21]Dapat IC, Shobugawa Y, Sano Y, Saito R, Sasaki A, Suzuki Y, Kumaki A, Zaraket H, Dapat C, Oguma T, Yamaguchi M, Suzuki H: New genotypes within respiratory syncytial virus group B genotype BA in Niigata, Japan. J Clin Microbiol 2010, 48:3423-3427.
  • [22]Trento A, Viegas M, Galiano M, Videla C, Carballal G, Mistchenko AS, Melero JA: Natural history of human respiratory syncytial virus inferred from phylogenetic analysis of the attachment (G) glycoprotein with a 60-nucleotide duplication. J Virol 2006, 80:975-984.
  • [23]Eshaghi A, Duvvuri VR, Lai R, Nadarajah JT, Li A, Patel SN, Low DE, Gubbay JB: Genetic variability of human respiratory syncytial virus A strains circulating in Ontario: a novel genotype with a 72 nucleotide G gene duplication. PLoS One 2012, 7:e32807.
  • [24]Khor CS, Sam IC, Hooi PS, Chan YF: Displacement of predominant respiratory syncytial virus genotypes in Malaysia between 1989 and 2011. Infect Genet Evol 2013, 14:357-360.
  • [25]Agoti CN, Mbisa JL, Bett A, Medley GF, Nokes DJ, Cane PA: Intrapatient variation of the respiratory syncytial virus attachment protein gene. J Virol 2010, 84:10425-10428.
  • [26]Scott PD, Ochola R, Ngama M, Okiro EA, Nokes DJ, Medley GF, Cane PA: Molecular epidemiology of respiratory syncytial virus in Kilifi district, Kenya. J Med Virol 2004, 74:344-354.
  • [27]Agoti CN, Gitahi CW, Medley GF, Cane PA, Nokes DJ: Identification of group B respiratory syncytial viruses that lack the 60-nucleotide duplication after six consecutive epidemics of total BA dominance at coastal Kenya. Influenza Respi Viruses 2013, 7:1008-1012.
  • [28]Waris M: Pattern of respiratory syncytial virus epidemics in Finland: two-year cycles with alternating prevalence of groups A and B. J Infect Dis 1991, 163:464-469.
  • [29]Mlinaric-Galinovic G, Welliver RC, Vilibic-Cavlek T, Ljubin-Sternak S, Drazenovic V, Galinovic I, Tomic V: The biennial cycle of respiratory syncytial virus outbreaks in Croatia. Virol J 2008, 5:18. BioMed Central Full Text
  • [30]Duppenthaler A, Gorgievski-Hrisoho M, Frey U, Aebi C: Two-year periodicity of respiratory syncytial virus epidemics in Switzerland. Infection 2003, 31:75-80.
  • [31]Weigl JA, Puppe W, Schmitt HJ: Seasonality of respiratory syncytial virus-positive hospitalizations in children in Kiel, Germany, over a 7-year period. Infection 2002, 30:186-192.
  • [32]Mlinaric-Galinovic G, Tabain I, Kukovec T, Vojnovic G, Bozikov J, Bogovic-Cepin J, Ivkovic-Jurekovic I, Knezovic I, Tesovic G, Welliver RC: Analysis of biennial outbreak pattern of respiratory syncytial virus according to subtype (A and B) in the Zagreb region. Pediatr Int 2012, 54:331-335.
  • [33]Mlinaric-Galinovic G, Vojnovic G, Cepin-Bogovic J, Bace A, Bozikov J, Welliver RC, Wahn U, Cebalo L: Does the viral subtype influence the biennial cycle of respiratory syncytial virus? Virol J 2009, 6:133. BioMed Central Full Text
  • [34]Wangui J, Nokes DJ, Nyaigoti CA, Achilla R, Onyango CO, Wurapa E, Bulimo W: Prevalence of acute respiratory infections caused by RSV and Adeno viruses in Kenya in 2007–2009. Int J Infect Dis 2012., 16(Suppl 1):e118-e119
  • [35]Arnott A, Vong S, Mardy S, Chu S, Naughtin M, Sovann L, Buecher C, Beaute J, Rith S, Borand L, Asgari N, Frutos R, Guillard B, Touch S, Deubel V, Buchy P: A study of the genetic variability of human respiratory syncytial virus (HRSV) in Cambodia reveals the existence of a new HRSV group B genotype. J Clin Microbiol 2011, 49:3504-3513.
  • [36]Zhang RF, Jin Y, Xie ZP, Liu N, Yan KL, Gao HC, Song JR, Yuan XH, Xiao NG, Guo MW, Zhou QH, Hou YD, Duan Z: Human respiratory syncytial virus in children with acute respiratory tract infections in China. J Clin Microbiol 2010, 48:4193-4199.
  • [37]Zhang ZY, Du LN, Chen X, Zhao Y, Liu EM, Yang XQ, Zhao XD: Genetic variability of respiratory syncytial viruses (RSV) prevalent in Southwestern China from 2006 to 2009: emergence of subgroup B and A RSV as dominant strains. J Clin Microbiol 2010, 48:1201-1207.
  • [38]Nokes DJ, Ngama M, Bett A, Abwao J, Munywoki P, English M, Scott JA, Cane PA, Medley GF: Incidence and severity of respiratory syncytial virus pneumonia in rural Kenyan children identified through hospital surveillance. Clin Infect Dis 2009, 49:1341-1349.
  • [39]Peret TC, Hall CB, Hammond GW, Piedra PA, Storch GA, Sullender WM, Tsou C, Anderson LJ: Circulation patterns of group A and B human respiratory syncytial virus genotypes in 5 communities in North America. J Infect Dis 2000, 181:1891-1896.
  • [40]Katzov-Eckert H, Botosso VF, Neto EA, Zanotto PM: Phylodynamics and dispersal of HRSV entails its permanence in the general population in between yearly outbreaks in children. PLoS One 2012, 7:e41953.
  文献评价指标  
  下载次数:77次 浏览次数:17次