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本文引用的文献

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MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods.MEGA5:用于最大似然法、进化距离法和最大简约法的分子进化遗传学分析。
Mol Biol Evol. 2011 Oct;28(10):2731-9. doi: 10.1093/molbev/msr121. Epub 2011 May 4.
2
Human parechoviruses in infants with systemic infection.人类肠道病毒在伴有全身感染的婴儿中的情况。
J Med Virol. 2010 Oct;82(10):1790-6. doi: 10.1002/jmv.21878.
3
Recombination dynamics of human parechoviruses: investigation of type-specific differences in frequency and epidemiological correlates.人类肠道孤儿病毒的重组动力学:频率和流行病学相关性的型特异性差异研究。
J Gen Virol. 2010 May;91(Pt 5):1229-38. doi: 10.1099/vir.0.018747-0. Epub 2010 Jan 20.
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Infant deaths associated with human parechovirus infection in Wisconsin.威斯康星州与人类副肠孤病毒感染相关的婴儿死亡。
Clin Infect Dis. 2010 Feb 1;50(3):357-61. doi: 10.1086/649863.
5
Novel human parechovirus, Sri Lanka.新型人类肠道病毒,斯里兰卡。
Emerg Infect Dis. 2010 Jan;16(1):130-2. doi: 10.3201/eid1601.091105.
6
Human parechovirus-3 infection: emerging pathogen in neonatal sepsis.人细小病毒B3感染:新生儿败血症中的新兴病原体
Pediatr Infect Dis J. 2009 Jun;28(6):545-7. doi: 10.1097/INF.0b013e318194596a.
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Clinical severity and molecular typing of human rhinovirus C strains during a fall outbreak affecting hospitalized patients.秋季影响住院患者的疫情期间人鼻病毒C株的临床严重程度及分子分型
J Clin Virol. 2009 Aug;45(4):311-7. doi: 10.1016/j.jcv.2009.04.016. Epub 2009 May 26.
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Human parechoviruses: biology, epidemiology and clinical significance.人细小病毒:生物学、流行病学及临床意义
J Clin Virol. 2009 May;45(1):1-9. doi: 10.1016/j.jcv.2009.03.009. Epub 2009 Apr 15.
9
Novel human parechovirus from Brazil.来自巴西的新型人细小病毒。
Emerg Infect Dis. 2009 Feb;15(2):310-3. doi: 10.3201/eid1502.081028.
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Genomic characterization of novel human parechovirus type.新型人副肠道病毒的基因组特征
Emerg Infect Dis. 2009 Feb;15(2):288-91. doi: 10.3201/eid1502.080341.

2008-2010 年意大利北部住院患者中人类副肠孤病毒感染。

Human parechovirus infections in patients admitted to hospital in Northern Italy, 2008-2010.

机构信息

Virology and Microbiology Department, Molecular Virology Unit, Foundation IRCCS Policlinico San Matteo, Pavia, Italy.

出版信息

J Med Virol. 2012 Apr;84(4):686-90. doi: 10.1002/jmv.23197.

DOI:10.1002/jmv.23197
PMID:22337310
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7166678/
Abstract

Human parechoviruses (HPeVs) infection is associated with a wide range of clinical syndromes such as respiratory, gastrointestinal, neurologic diseases, and neonatal sepsis-like illness. The main objective of this study was to investigate the epidemiology of HPeVs infection in hospitalized patients in a period of 2 years. Respiratory samples from 3,525 patients with respiratory syndrome, cerebrospinal fluid (CSF) from 340 patients with neurologic syndrome as well as CSF and plasma samples from five neonatal patients with sepsis-like illness collected from October 2008 to 2010 were tested retrospectively using HPeV-specific real-time RT-PCR. Phylogenetic analysis of VP3/VP1 region was performed on the positive samples. Fourteen out of 3,525 (0.4%) patients with respiratory syndrome and five out of five patients with sepsis-like illness were positive for HPeV. In 3/5 patients with sepsis-like illness multiple samples (e.g., stool, plasma, CSF, or respiratory samples) were available, and HPeV was found in all specimens. In contrast, no positive CSF was detected among the 340 patients with neurologic syndromes. Eleven patients (57.9%) were infected with HPeV1 strain, 7 (36.8%) with HPeV3, and 1 (5.3%) with HPeV6 strains. Ten of the 14 HPeV patients with respiratory syndrome were co-infected with other respiratory viruses (eight with rhinovirus and two with coronavirus OC43). All five patients with sepsis-like illness were less than 1 month of age and were infected with HPeV3. Although not circulating at high frequency and unlikely to cause respiratory syndrome, HPeV was associated with severe clinical syndromes in a minority of newborns.

摘要

人肠道病毒(HPeV)感染与广泛的临床综合征有关,如呼吸道、胃肠道、神经疾病和新生儿类似败血症的疾病。本研究的主要目的是调查 2 年内住院患者中 HPeV 感染的流行病学情况。2008 年 10 月至 2010 年,回顾性检测了 3525 例呼吸道综合征患者的呼吸道样本、340 例神经综合征患者的脑脊液(CSF)以及 5 例类似败血症新生儿患者的 CSF 和血浆样本,采用 HPeV 特异性实时 RT-PCR 进行检测。对阳性样本进行 VP3/VP1 区的系统进化分析。在 3525 例呼吸道综合征患者中有 14 例(0.4%)和 5 例(100%)类似败血症的患者 HPeV 检测阳性。在 5 例类似败血症的患者中,有 3 例(60%)患者有多个样本(如粪便、血浆、CSF 或呼吸道样本),且 HPeV 存在于所有样本中。相比之下,340 例神经综合征患者中未检测到阳性 CSF。11 例(57.9%)患者感染 HPeV1 株,7 例(36.8%)感染 HPeV3 株,1 例(5.3%)感染 HPeV6 株。14 例呼吸道综合征 HPeV 患者中有 10 例合并其他呼吸道病毒感染(8 例感染鼻病毒,2 例感染冠状病毒 OC43)。5 例类似败血症的患者均小于 1 个月龄,且感染 HPeV3。尽管 HPeV 频率不高且不太可能引起呼吸道综合征,但在少数新生儿中,它与严重的临床综合征有关。