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首页> 外文期刊>Journal of Medical Virology >Genotype 3b of Human Parvovirus B19 Detected From Hospitalized Children With Solid Malignancies in a North Indian Tertiary Care Hospital
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Genotype 3b of Human Parvovirus B19 Detected From Hospitalized Children With Solid Malignancies in a North Indian Tertiary Care Hospital

机译:在北印度三级护理医院从住院的患有实体恶性肿瘤的儿童中检测到人类细小病毒B19的基因型3b

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Human parvovirus B19 (B19V) infection is known to cause serious consequences in immuno-compromized individuals. The present cross sectional study was designed to estimate the prevalence and genotype distribution of B19V in children receiving chemotherapy for solid malignancies at a tertiary care hospital in North India during October 2013 to May 2015. Serum samples from all the patients were tested for anti-B19V IgM and IgG antibodies and for B19V-DNA as soon as received. Samples testing positive for B19V-DNA were subjected to viral load estimation and to genotype determination by sequencing. Total 96 children were enrolled of which 9 (9.3%), 32 (33.3%), and 25 (26%) tested positive for anti-B19V IgM, anti-B19V IgG, and B19V-DNA, respectively. The viral load of B19V-DNA positive children ranged from 5.5 x 10(2) to 3.5 x 10(12) copies/ml. Accordingly children were divided into three groups: group I, with acute infection (n = 25); group II, previously exposed (n = 27), and group III, negative for B19V infection or with inappropriate antibody response (n = 44). B19V positivity was significantly associated (P-value < 0.0001) with a history of blood transfusion in the past 6 months, severe anemia (hemoglobin levels < 6 gm%) and thrombocytopenia (platelets < 150,000/cu. mm.). Sequence analysis of 21 of 25 DNA positive samples showed that all of them were Genotype 3b that clustered into three groups. All the sequences within each cluster were identical. The nucleotide identity of the sequences suggests a nosocomial outbreak of B19V during the study period. Children on chemotherapy for solid tumors should be routinely screened for B19V infection by both serology and PCR. (C) 2016 Wiley Periodicals, Inc.
机译:已知人类细小病毒B19(B19V)感染会对免疫受损的个体造成严重后果。本横断面研究旨在评估2013年10月至2015年5月在印度北部三级医院接受实体恶性肿瘤化疗的儿童中B19V的患病率和基因型分布。对所有患者的血清样本进行了抗B19V检测收到IgM和IgG抗体以及B19V-DNA。对B19V-DNA检测呈阳性的样品进行病毒载量估计并通过测序确定基因型。共有96名儿童入选,其中9名(9.3%),32名(33.3%)和25名(26%)分别检测出抗B19V IgM,抗B19V IgG和B19V-DNA阳性。 B19V-DNA阳性儿童的病毒载量范围为5.5 x 10(2)至3.5 x 10(12)拷贝/ ml。因此,将儿童分为三组:第一组为急性感染(n = 25);第二组为急性感染。第二组是先前暴露的(n = 27),第三组是B19V感染阴性或抗体反应不良(n = 44)。 B19V阳性与过去6个月的输血史,严重贫血(血红蛋白水平<6 gm%)和血小板减少症(血小板<150,000 / mm2)显着相关(P值<0.0001)。对25个DNA阳性样品中的21个进行序列分析,结果显示它们都是基因型3b,并分为三组。每个簇内的所有序列都是相同的。序列的核苷酸同一性表明在研究期间医院内爆发了B19V。对于接受实体瘤化疗的儿童,应通过血清学和PCR常规筛查B19V感染。 (C)2016威利期刊公司

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