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Full genomic analyses of human rotavirus G4P[4], G4P[6], G9P[19] and G10P[6] strains from North-eastern India: evidence for interspecies transmission and complex reassortment events.对来自印度东北部的人类轮状病毒 G4P[4]、G4P[6]、G9P[19]和 G10P[6]株的全基因组分析:种间传播和复杂重组事件的证据。
Clin Microbiol Infect. 2011 Sep;17(9):1343-6. doi: 10.1111/j.1469-0691.2010.03383.x. Epub 2010 Nov 12.
2
Projected impact and cost-effectiveness of a rotavirus vaccination program in India, 2008.2008 年印度轮状病毒疫苗接种计划的预期影响和成本效益。
Clin Infect Dis. 2011 Jan 15;52(2):171-7. doi: 10.1093/cid/ciq094.
3
Instability of human rotavirus G genotypes circulating in a rural area of Bangladesh.孟加拉国农村地区流行的人类轮状病毒G基因型的不稳定性
Mymensingh Med J. 2011 Jan;20(1):1-8.
4
Infantile diarrhoea: An Analysis of 216 Cases with Special Reference to Institutional Outbreaks.婴儿腹泻:216例分析,特别提及机构内暴发情况
Arch Dis Child. 1945 Mar;20(101):22-7. doi: 10.1136/adc.20.101.22.
5
Identification of a G2-like porcine rotavirus bearing a novel VP4 type, P[32].鉴定一种具有新型 VP4 型(P[32])的 G2 样猪轮状病毒。
Vet Res. 2010 Sep-Oct;41(5):73. doi: 10.1051/vetres/2010045. Epub 2010 Jul 29.
6
Performance of rotavirus vaccines in developed and developing countries.轮状病毒疫苗在发达国家和发展中国家的性能。
Hum Vaccin. 2010 Jul;6(7):532-42. doi: 10.4161/hv.6.7.11278.
7
Effect of human rotavirus vaccine on severe diarrhea in African infants.人轮状病毒疫苗对非洲婴幼儿严重腹泻的影响。
N Engl J Med. 2010 Jan 28;362(4):289-98. doi: 10.1056/NEJMoa0904797.
8
Surveillance and molecular characterization of rotavirus strains circulating in Manipur, north-eastern India: increasing prevalence of emerging G12 strains.印度东北部曼尼普尔邦轮状病毒流行株的监测和分子特征:新兴 G12 株的流行率上升。
Infect Genet Evol. 2010 Mar;10(2):311-20. doi: 10.1016/j.meegid.2010.01.002. Epub 2010 Jan 18.
9
A long-term survey on the distribution of the human rotavirus G type in Thailand.泰国人类轮状病毒 G 型分布的长期调查。
J Med Virol. 2010 Jan;82(1):157-63. doi: 10.1002/jmv.21596.
10
Disease and economic burden of rotavirus diarrhoea in India.印度轮状病毒腹泻的疾病负担和经济负担。
Vaccine. 2009 Nov 20;27 Suppl 5:F18-24. doi: 10.1016/j.vaccine.2009.08.098.

轮状病毒感染:关于流行病学、基因组多样性及疫苗策略的观点

Rotavirus infection: a perspective on epidemiology, genomic diversity and vaccine strategies.

作者信息

Mukherjee Anupam, Chawla-Sarkar Mamta

机构信息

Division of Virology, National Institute of Cholera and Enteric Diseases, P-33, C.I.T. Road, Scheme-XM, Beliaghata, Kolkata, 700010 West Bengal India.

出版信息

Indian J Virol. 2011 Jun;22(1):11-23. doi: 10.1007/s13337-011-0039-y. Epub 2011 Jun 14.

DOI:10.1007/s13337-011-0039-y
PMID:23637497
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3550723/
Abstract

For centuries, acute diarrhea has been a major cause of death in young children worldwide, and until 1973, before rotavirus was discovered; no infectious agents could be identified in about 80% of patients admitted to hospital with severe dehydrating diarrhea. Rotaviruses have now been shown to cause 40-50% of severe acute diarrhea in young children worldwide in both developing and developed countries. More than 600,000 young children die and approximately 2.4 million hospitalize annually from rotavirus disease, especially in South-East Asia and sub-Saharan Africa. Two safe and effective vaccines are now licensed in 100 countries but used in 17 countries. Rotarix (GSK) vaccine is derived from single attenuated human rotavirus G1P[8], representative of the most common serotype identified worldwide. RotaTeq (Merck) is a pentavalent mixture of naturally attenuated bovine/human rotavirus reassortants representing G1, G2, G3, G4, and P[8] serotypes. Though these vaccines have already dramatically decreased the morbidity associated with rotavirus in countries where they are widely used, the third generation of vaccines, based on inactivated viruses or recombinant virus like particle are already in pipeline. Continuous surveillance and the genetic and antigenic analysis of the various strains of rotavirus circulating worldwide will aid significantly in assessing the effectiveness of these vaccines and monitor emergence of new strains. Introduction of rotavirus vaccines in national vaccine policy along with other childhood vaccines may result in significant reduction in mortality in children in poor socioeconomic countries.

摘要

几个世纪以来,急性腹泻一直是全球幼儿死亡的主要原因。直到1973年轮状病毒被发现之前,在因严重脱水腹泻住院的患者中,约80%无法确定感染源。现已证明,在全球范围内,无论发展中国家还是发达国家,轮状病毒都是导致40%-50%幼儿严重急性腹泻的病因。每年有超过60万幼儿死于轮状病毒疾病,约240万幼儿因该疾病住院,尤其是在东南亚和撒哈拉以南非洲地区。目前,两种安全有效的疫苗已在100个国家获得许可,但仅在17个国家使用。Rotarix(葛兰素史克公司)疫苗源自单一减毒人轮状病毒G1P[8],这是全球最常见的血清型代表。RotaTeq(默克公司)是一种五价疫苗,由天然减毒的牛/人轮状病毒重配株混合而成,代表G1、G2、G3、G4和P[8]血清型。尽管这些疫苗在广泛使用的国家已显著降低了与轮状病毒相关的发病率,但基于灭活病毒或重组病毒样颗粒的第三代疫苗已在研发中。对全球范围内传播的各种轮状病毒株进行持续监测以及基因和抗原分析,将有助于评估这些疫苗的有效性,并监测新毒株的出现。将轮状病毒疫苗纳入国家疫苗政策以及其他儿童疫苗,可能会使社会经济贫困国家的儿童死亡率大幅降低。