{"title":"调查儿童造血干细胞移植受者医院内BKPyV (BK多瘤病毒)感染:挑战和前景","authors":"Aurélien Aubry, Marie-Laure Nere, Sarah Timsit, Charlotte Calvo, Jean-Hugues Dalle, Julien Gras, Clotilde Chaix, Maud Gits-Muselli, Constance Delaugerre, Jérôme LeGoff, Maud Salmona","doi":"10.1093/infdis/jiaf215","DOIUrl":null,"url":null,"abstract":"Introduction The modes of transmission of BK Polyomavirus (BKPyV) remain incompletely understood. BKPyV infections can lead to hemorrhagic cystitis after hematopoietic stem cell transplantation (HSCT). Hospitalization in a pediatric hematology unit may represent initial exposure to BKPyV due to the high rate of viral shedding among hematology patients. This study explores the potential for nosocomial transmission of BKPyV within a hematology department. Materials and Methods Epidemiologic investigation and BKPyV genome phylogenetic analyses were conducted among individuals with BKPyV DNAuria and/or DNAemia over a three-year period in a pediatric hematology unit. Results From November 2019 to December 2022, BKPyV DNA was detected in the urine or plasma of 34 out of 173 HSCT children. An unusually high prevalence of genotype Ia BKPyV was observed in 2021, suggesting possible patient-to-patient transmission. However, despite closely related sequences, they clustered with several GenBank entries, complicating phylogenetic linkage determination. Genetic signature analysis also did not link these sequences to specific patient clinical profiles. Discussion This study highlights the complexity of establishing nosocomial transmission of BKPyV, even with viral sequence analyses. Future prospective studies should include Non-Coding Control Region (NCCR) analysis, serological data, and environmental factors to enhance understanding of BKPyV transmission routes.","PeriodicalId":501010,"journal":{"name":"The Journal of Infectious Diseases","volume":"5 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-04-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Investigating nosocomial BKPyV (BK Polyomavirus) infections in pediatric hematopoietic stem cell transplantation recipients: challenges and prospects\",\"authors\":\"Aurélien Aubry, Marie-Laure Nere, Sarah Timsit, Charlotte Calvo, Jean-Hugues Dalle, Julien Gras, Clotilde Chaix, Maud Gits-Muselli, Constance Delaugerre, Jérôme LeGoff, Maud Salmona\",\"doi\":\"10.1093/infdis/jiaf215\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Introduction The modes of transmission of BK Polyomavirus (BKPyV) remain incompletely understood. BKPyV infections can lead to hemorrhagic cystitis after hematopoietic stem cell transplantation (HSCT). Hospitalization in a pediatric hematology unit may represent initial exposure to BKPyV due to the high rate of viral shedding among hematology patients. This study explores the potential for nosocomial transmission of BKPyV within a hematology department. Materials and Methods Epidemiologic investigation and BKPyV genome phylogenetic analyses were conducted among individuals with BKPyV DNAuria and/or DNAemia over a three-year period in a pediatric hematology unit. Results From November 2019 to December 2022, BKPyV DNA was detected in the urine or plasma of 34 out of 173 HSCT children. An unusually high prevalence of genotype Ia BKPyV was observed in 2021, suggesting possible patient-to-patient transmission. However, despite closely related sequences, they clustered with several GenBank entries, complicating phylogenetic linkage determination. Genetic signature analysis also did not link these sequences to specific patient clinical profiles. Discussion This study highlights the complexity of establishing nosocomial transmission of BKPyV, even with viral sequence analyses. Future prospective studies should include Non-Coding Control Region (NCCR) analysis, serological data, and environmental factors to enhance understanding of BKPyV transmission routes.\",\"PeriodicalId\":501010,\"journal\":{\"name\":\"The Journal of Infectious Diseases\",\"volume\":\"5 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-04-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Journal of Infectious Diseases\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1093/infdis/jiaf215\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Infectious Diseases","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/infdis/jiaf215","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
导言:人们对 BK 多瘤病毒(BKPyV)的传播方式仍然知之甚少。造血干细胞移植(HSCT)后,BKPyV感染可导致出血性膀胱炎。由于血液病患者的病毒脱落率很高,在儿科血液科住院可能是初次接触 BKPyV。本研究探讨了 BKPyV 在血液科内部传播的可能性。材料与方法 对儿科血液科三年内出现 BKPyV DNA 尿和/或 DNA 血症的患者进行流行病学调查和 BKPyV 基因组系统发育分析。结果 从2019年11月到2022年12月,173名造血干细胞移植患儿中有34人的尿液或血浆中检测到BKPyV DNA。2021 年观察到基因型 Ia BKPyV 的异常高流行率,这表明可能存在患者间传播。然而,尽管序列密切相关,但它们与 GenBank 中的几个条目聚类,使得系统发育联系的确定变得复杂。遗传特征分析也没有将这些序列与特定患者的临床特征联系起来。讨论 本研究强调了确定 BKPyV 非医院传播的复杂性,即使是病毒序列分析也是如此。未来的前瞻性研究应包括非编码控制区 (NCCR) 分析、血清学数据和环境因素,以加深对 BKPyV 传播途径的了解。
Investigating nosocomial BKPyV (BK Polyomavirus) infections in pediatric hematopoietic stem cell transplantation recipients: challenges and prospects
Introduction The modes of transmission of BK Polyomavirus (BKPyV) remain incompletely understood. BKPyV infections can lead to hemorrhagic cystitis after hematopoietic stem cell transplantation (HSCT). Hospitalization in a pediatric hematology unit may represent initial exposure to BKPyV due to the high rate of viral shedding among hematology patients. This study explores the potential for nosocomial transmission of BKPyV within a hematology department. Materials and Methods Epidemiologic investigation and BKPyV genome phylogenetic analyses were conducted among individuals with BKPyV DNAuria and/or DNAemia over a three-year period in a pediatric hematology unit. Results From November 2019 to December 2022, BKPyV DNA was detected in the urine or plasma of 34 out of 173 HSCT children. An unusually high prevalence of genotype Ia BKPyV was observed in 2021, suggesting possible patient-to-patient transmission. However, despite closely related sequences, they clustered with several GenBank entries, complicating phylogenetic linkage determination. Genetic signature analysis also did not link these sequences to specific patient clinical profiles. Discussion This study highlights the complexity of establishing nosocomial transmission of BKPyV, even with viral sequence analyses. Future prospective studies should include Non-Coding Control Region (NCCR) analysis, serological data, and environmental factors to enhance understanding of BKPyV transmission routes.