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Molecular Epidemiology and Disease Severity of Human Respiratory Syncytial Virus in Vietnam
被引:48
|作者:
Dinh Nguyen Tran
[1
,2
,3
]
Thi Minh Hong Pham
[2
]
Manh Tuan Ha
[3
]
Thi Thu Loan Tran
[3
]
Thi Kim Huyen Dang
[3
]
Yoshida, Lay-Myint
[4
]
Okitsu, Shoko
[1
,5
]
Hayakawa, Satoshi
[5
]
Mizuguchi, Masashi
[1
]
Ushijima, Hiroshi
[1
,5
]
机构:
[1] Univ Tokyo, Grad Sch Med, Sch Int Hlth, Dept Dev Med Sci, Tokyo, Japan
[2] Univ Med & Pharm Ho Chi Minh City, Dept Pediat, Ho Chi Minh City, Vietnam
[3] Childrens Hosp 2, Ho Chi Minh City, Vietnam
[4] Nagasaki Univ, Inst Trop Med, Nagasaki 852, Japan
[5] Nihon Univ, Sch Med, Div Microbiol, Dept Pathol & Microbiol, Tokyo, Japan
来源:
PLOS ONE
|
2013年
/
8卷
/
01期
关键词:
GROUP-A;
SUBGROUP-A;
GROUP-B;
GENETIC-VARIABILITY;
G-PROTEIN;
CLINICAL CHARACTERISTICS;
VIRAL PATHOGENS;
INFECTION;
INFANTS;
CHILDREN;
D O I:
10.1371/journal.pone.0045436
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Respiratory syncytial virus (RSV) is a major cause of acute respiratory infections (ARIs) in children worldwide and can cause high mortality, especially in developing countries. However, information on the clinical and molecular characteristics of RSV infection in developing countries is limited. From April 2010 to May 2011, 1,082 nasopharyngeal swabs were collected from children with ARI admitted to the Children's Hospital 2, Ho Chi Minh City, Vietnam. Samples were screened for RSV and genotyped by reverse transcription-PCR and sequencing. Demographic and clinical data was also recorded. RSV was found in 23.8% (257/1,082) of samples. RSV A was the dominant subgroup, accounting for 91.4% (235/257), followed by RSV B, 5.1% (13/257), and 9 cases (3.5%) were mixed infection of these subgroups. The phylogenetic analysis revealed that all group A strains belonged to the GA2 genotype. All group B strains belonged to the recently identified BA genotype, and further clustered into 2 recently described subgenotypes BA9 and BA10. One GA2 genotype strain had a premature stop codon which shortened the G protein length. RSV infection was significantly associated with younger age and higher severity score than those without. Co-infection with other viruses did not affect disease severity. RSV A caused more severe disease than RSV B. The results from this study will not only contribute to the growing database on the molecular diversity of RSV circulating worldwide but may be also useful in clinical management and vaccine development.
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