Whole genome detection of rotavirus mixed infections in human, porcine and bovine samples co-infected with various rotavirus strains collected from sub-Saharan Africa

被引:37
|
作者
Nyaga, Martin M. [1 ]
Jere, Khuzwayo C. [1 ,2 ]
Esona, Mathew D. [1 ,3 ]
Seheri, Mapaseka L. [1 ]
Stucker, Karla M. [4 ]
Halpin, Rebecca A. [4 ]
Akopov, Asmik [4 ]
Stockwell, Timothy B. [4 ]
Peenze, Ina [1 ]
Diop, Amadou [5 ]
Ndiaye, Kader [6 ]
Boula, Angeline [7 ]
Maphalala, Gugu [8 ]
Berejena, Chipo [9 ]
Mwenda, Jason M. [10 ]
Steele, A. Duncan [1 ,11 ]
Wentworth, David E. [4 ]
Mphahlele, M. Jeffrey [1 ]
机构
[1] Sefako Makgatho Hlth Sci Univ, Fac Hlth Sci, South African Med Res Council, Diarrhoeal Pathogens Res Unit, Pretoria, South Africa
[2] Univ Liverpool, Dept Clin Infect Microbiol & Immunol, Inst Infect & Global Hlth, Liverpool L69 3BX, Merseyside, England
[3] CDC, Gastroenteritis & Resp Viruses Lab Branch, Div Viral Dis, NCIRD, Atlanta, GA 30333 USA
[4] J Craig Venter Inst, Rockville, MD USA
[5] Albert Royer Natl Paediat Hosp Lab, Dakar, Senegal
[6] Inst Pasteur, Unite Virol Med, Dakar, Senegal
[7] Chantal Biya Fdn, Mother & Child Ctr, Yaounde, Cameroon
[8] Natl Clin Lab Serv, Mbabane, Eswatini
[9] Univ Zimbabwe, Dept Med Microbiol, Virol Sect, Harare, Zimbabwe
[10] WHO, Reg Off Africa, Brazzaville, Rep Congo
[11] Bill & Melinda Gates Fdn, Enter & Diarrhoeal Dis Programme, Global Hlth Program, Seattle, WA USA
基金
新加坡国家研究基金会; 美国国家卫生研究院; 英国医学研究理事会;
关键词
Rotavirus; Mixed infections; Reassortants; Whole genome; Africa; GROUP-A ROTAVIRUS; SEQUENCE-INDEPENDENT AMPLIFICATION; THAN; 5; YEARS; MOLECULAR EPIDEMIOLOGY; CHILDREN YOUNGER; NUCLEIC-ACID; P TYPES; VACCINE; SURVEILLANCE; GASTROENTERITIS;
D O I
10.1016/j.meegid.2015.02.011
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Group A rotaviruses (RVA) are among the main global causes of severe diarrhea in children under the age of 5 years. Strain diversity, mixed infections and untypeable RVA strains are frequently reported in Africa. We analysed rotavirus-positive human stool samples (n = 13) obtained from hospitalised children under the age of 5 years who presented with acute gastroenteritis at sentinel hospital sites in six African countries, as well as bovine and porcine stool samples (n = 1 each), to gain insights into rotavirus diversity and evolution. Polyacrylamide gel electrophoresis (PAGE) analysis and genotyping with G-(VP7) and P-specific (VP4) typing primers suggested that 13 of the 15 samples contained more than 11 segments and/or mixed G/P genotypes. Full-length amplicons for each segment were generated using RVA-specific primers and sequenced using the Ion Torrent and/or Illumina MiSeq next-generation sequencing platforms. Sequencing detected at least one segment in each sample for which duplicate sequences, often having distinct genotypes, existed. This supported and extended the PAGE and RT-PCR genotyping findings that suggested these samples were collected from individuals that had mixed rotavirus infections. The study reports the first porcine (MRC-DPRU1567) and bovine (MRC-DPRU3010) mixed infections. We also report a unique genome segment 9 (VP7), whose G9 genotype belongs to lineage VI and clusters with porcine reference strains. Previously, African G9 strains have all been in lineage III. Furthermore, additional RVA segments isolated from humans have a clear evolutionary relationship with porcine, bovine and ovine rotavirus sequences, indicating relatively recent interspecies transmission and reassortment. Thus, multiple RVA strains from sub-Saharan Africa are infecting mammalian hosts with unpredictable variations in their gene segment combinations. Whole-genome sequence analyses of mixed RVA strains underscore the considerable diversity of rotavirus sequences and genome segment combinations that result from a complex evolutionary history involving multiple host species. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:321 / 334
页数:14
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