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Monkeypox Clade Ib virus introduction into Burundi: first findings, July to mid-August 2024. 将猴痘 Ib 支系病毒引入布隆迪:2024 年 7 月至 8 月中旬的首次发现。
IF 9.9 2区 医学 Q1 INFECTIOUS DISEASES Pub Date : 2024-10-01 DOI: 10.2807/1560-7917.ES.2024.29.42.2400666
Néhémie Nzoyikorera, Cassien Nduwimana, Leonard Schuele, David F Nieuwenhuijse, Marion Koopmans, Saria Otani, Frank M Aarestrup, Théogène Ihorimbere, Denis Niyomwungere, Armstrong Ndihokubwayo, Idrissa Diawara, Alexis Niyomwungere, Dionis Nizigiyimana, Marie Noelle Uwineza, Bas B Oude Munnink, Joseph Nyandwi

We describe cases with monkeypox virus (MPXV) Clade Ib in Burundi from their first detection in July until 20 August 2024. Testing 442 people with vesicular lesions confirmed 170 cases (98 male; 72 female), 82 (48%) being < 15 years old. Differential diagnosis of the first 30 individuals testing MPXV negative revealed chickenpox in 20. Cases occurred in 26 of 49 Burundi health districts, but mostly in Bujumbura Nord (88/170; 67%). Case-derived MPXV genetic sequences from Burundi and South-Kivu (Democratic Republic of the Congo), clustered together in phylogenetic analysis.

我们描述了布隆迪从7月首次发现猴痘病毒(MPXV)Ib支系到2024年8月20日的病例。对 442 名水泡病患者进行了检测,确诊了 170 例病例(98 名男性;72 名女性),其中 82 例(48%)为猴痘病毒 Ib 支系病例。
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引用次数: 0
Integrating indicator-based and event-based surveillance data for risk mapping of West Nile virus, Europe, 2006 to 2021. 整合基于指标和基于事件的监测数据,绘制西尼罗河病毒风险图,欧洲,2006 年至 2021 年。
IF 9.9 2区 医学 Q1 INFECTIOUS DISEASES Pub Date : 2024-10-01 DOI: 10.2807/1560-7917.ES.2024.29.44.2400084
Kyla Serres, Diana Erazo, Garance Despréaux, María F Vincenti-González, Wim Van Bortel, Elena Arsevska, Simon Dellicour

BackgroundWest Nile virus (WNV) has an enzootic cycle between birds and mosquitoes, humans being incidental dead-end hosts. Circulation of WNV is an increasing public health threat in Europe. While detection of WNV is notifiable in humans and animals in the European Union, surveillance based on human case numbers presents some limitations, including reporting delays.AimWe aimed to perform risk mapping of WNV circulation leading to human infections in Europe by integrating two types of surveillance systems: indicator-based and event-based surveillance.MethodsFor indicator-based surveillance, we used data on human case numbers reported to the European Centre for Disease Prevention and Control (ECDC), and for event-based data, we retrieved information from news articles collected through an automated biosurveillance platform. In addition to these data sources, we also used environmental data to train ecological niche models to map the risk of local WNV circulation leading to human infections.ResultsThe ecological niche models based on both types of surveillance data highlighted new areas potentially at risk of WNV infection in humans, particularly in Spain, Italy, France and Greece.ConclusionAlthough event-based surveillance data do not constitute confirmed occurrence records, integrating both indicator-based and event-based surveillance data proved useful. These results underscore the potential for a more proactive and comprehensive strategy in managing the threat of WNV in Europe by combining indicator- and event-based and environmental data for effective surveillance and public health response.

背景西尼罗河病毒(WNV)在鸟类和蚊子之间进行流行循环,人类是附带的死亡宿主。在欧洲,WNV 的传播对公共健康的威胁日益严重。我们的目标是通过整合两种类型的监测系统:基于指标的监测和基于事件的监测,绘制欧洲导致人类感染的 WNV 循环风险图。除这些数据源外,我们还使用环境数据训练生态位模型,以绘制当地 WNV 病毒传播导致人类感染的风险图。结果基于这两种监测数据的生态位模型突出显示了可能存在人类感染 WNV 风险的新地区,尤其是在西班牙、意大利、法国和希腊。这些结果突出表明,通过将指标数据、基于事件的数据和环境数据相结合,采取更加积极主动和全面的策略来管理欧洲的 WNV 威胁,从而实现有效的监测和公共卫生响应是很有潜力的。
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引用次数: 0
Potentially zoonotic pathogens and parasites in opportunistically sourced urban brown rats (Rattus norvegicus) in and around Helsinki, Finland, 2018 to 2023. 2018年至2023年芬兰赫尔辛基及其周边地区机会性来源的城市褐鼠(Rattus norvegicus)中可能存在的人畜共患病病原体和寄生虫。
IF 9.9 2区 医学 Q1 INFECTIOUS DISEASES Pub Date : 2024-10-01 DOI: 10.2807/1560-7917.ES.2024.29.40.2400031
Tuomas Aivelo, Hussein Alburkat, Nina Suomalainen, Rebekka Kukowski, Petra Heikkinen, Antti Oksanen, Otso Huitu, Rauni Kivistö, Tarja Sironen

BackgroundBrown rats (Rattus norvegicus) are synanthropic rodents with worldwide distribution, which are known to harbour many zoonotic pathogens and parasites. No systematic zoonotic surveys targeting multiple pathogens and parasites have previously been conducted in urban rats in Finland.AimIn Helsinki, Finland, we explored the presence and prevalence in brown rats of certain pathogens and parasites (including helminths, viruses and bacteria) across potentially zoonotic taxa.MethodsWe opportunistically received rat carcasses from pest management operators and citizens from 2018 to 2023. We searched for heart- or lungworms, performed rat diaphragm digestion to check for Trichinella and morphologically identified intestinal helminths. We assessed virus exposure by immunofluorescence assay or PCR, and detected bacteria by PCR (Leptospira) or culture (Campylobacter).ResultsAmong the rats investigated for helminths, no heart- or lungworms or Trichinella species were detected and the most common finding was the cestode Hymenolepis nana (in 9.7% of individuals sampled, 28/288). For some of the surveyed virus taxa, several rats were seropositive (orthopoxviruses, 5.2%, 11/211; arenaviruses, 2.8%, 6/211; hantaviruses 5.2%, 11/211) or tested positive by PCR (rat hepatitis E virus, 1.8%, 4/216). Campylobacter jejuni (6.6%, 17/259) and Leptospira interrogans (1.2%, 2/163) bacteria were also present in the rat population examined.ConclusionsPrevalences of potentially zoonotic pathogens and parasites in brown rats in Helsinki appeared low. This may explain low or non-existent diagnosis levels of rat-borne pathogen and parasite infections reported in people there. Nevertheless, further assessment of under-diagnosis, which cannot be excluded, would enhance understanding the risks of zoonoses.

背景褐鼠(Rattus norvegicus)是一种分布于世界各地的同类啮齿类动物,已知其携带多种人畜共患病病原体和寄生虫。在芬兰赫尔辛基,我们探讨了褐鼠体内某些病原体和寄生虫(包括蠕虫、病毒和细菌)在潜在人畜共患病类群中的存在和流行情况。我们搜索了心丝虫或肺丝虫,进行了大鼠膈消化以检查旋毛虫,并对肠道蠕虫进行了形态鉴定。我们通过免疫荧光检测或 PCR 评估了病毒暴露情况,并通过 PCR(钩端螺旋体)或培养(弯曲杆菌)检测了细菌。结果在调查过蠕虫的大鼠中,没有发现心丝虫、肺丝虫或旋毛虫,最常见的是线虫 Hymenolepis nana(占采样个体的 9.7%,28/288)。在调查的一些病毒分类群中,有几只大鼠的血清反应呈阳性(正痘病毒,5.2%,11/211;禽流感病毒,2.8%,6/211;汉坦病毒,5.2%,11/211),或通过 PCR 检测呈阳性(大鼠戊型肝炎病毒,1.8%,4/216)。空肠弯曲菌(6.6%,17/259)和钩端螺旋体(1.2%,2/163)也出现在受检大鼠群体中。这也许可以解释为什么当地人感染鼠传病原体和寄生虫的诊断率很低或根本不存在。尽管如此,进一步评估诊断不足的情况(这一点不能排除)将有助于更好地了解人畜共患病的风险。
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引用次数: 0
Contact behaviour before, during and after the COVID-19 pandemic in the Netherlands: evidence from contact surveys, 2016 to 2017 and 2020 to 2023. 荷兰 COVID-19 大流行之前、期间和之后的接触行为:2016 至 2017 年和 2020 至 2023 年接触调查的证据。
IF 9.9 2区 医学 Q1 INFECTIOUS DISEASES Pub Date : 2024-10-01 DOI: 10.2807/1560-7917.ES.2024.29.43.2400143
Jantien A Backer, Eric R A Vos, Gerco den Hartog, Cheyenne C E van Hagen, Hester E de Melker, Fiona R M van der Klis, Jacco Wallinga

BackgroundThe first wave of the COVID-19 pandemic in 2020 was largely mitigated by limiting contacts in the general population. In early 2022, most contact-reducing measures were lifted.AimTo assess whether the population has reverted to pre-pandemic contact behaviour and how this would affect transmission potential of a newly emerging pathogen.MethodsWe compared two studies on contact behaviour in the Netherlands: the PIENTER Corona study, conducted during and after the pandemic (held every 2-6 months from April 2020) and the PIENTER3 study (2016-17, as pre-pandemic baseline). In both, participants (ages 1-85 years) reported number and age group of all face-to-face persons contacted on the previous day in a survey. Transmission potential was examined using the next-generation matrix approach.ResultsWe found an average of 15.4 (95% CI: 14.3-16.4) community contacts per person per day after the pandemic in May 2023, 13% lower than baseline (17.8; 95% CI: 17.0-18.5). Among all ages, children (5-9 years) had the highest number of contacts, both pre- and post-pandemic. Mainly adults aged 20-59 years had not reverted to pre-pandemic behaviours, possibly because they more often work from home. Although the number of contacts is lower compared to the pre-pandemic period, the effect on transmission potential of a newly emerging respiratory pathogen is limited if all age groups were equally susceptible.ConclusionContinuous monitoring of contacts can signal changes in contact patterns and can define a 'new normal' baseline. Both aspects are needed to prepare for a future pandemic.

背景2020年的第一波COVID-19大流行在很大程度上是通过限制普通人群的接触来缓解的。方法我们比较了荷兰的两项接触行为研究:在大流行期间和之后进行的 PIENTER Corona 研究(自 2020 年 4 月起每 2-6 个月进行一次)和 PIENTER3 研究(2016-17 年,作为大流行前的基线)。在这两项研究中,参与者(1-85 岁)在调查中报告了前一天所有面对面接触者的人数和年龄组。结果我们发现,2023 年 5 月大流行后,平均每人每天的社区接触人数为 15.4(95% CI:14.3-16.4),比基线(17.8;95% CI:17.0-18.5)低 13%。在所有年龄段中,儿童(5-9 岁)在大流行前后的接触人数最多。主要是 20-59 岁的成年人没有恢复到大流行前的行为,这可能是因为他们更经常在家工作。虽然与大流行前相比,接触者人数有所减少,但如果所有年龄段的人都同样易感,那么新出现的呼吸道病原体对传播潜力的影响是有限的。要为未来的大流行做好准备,这两方面都是必需的。
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引用次数: 0
A cluster of Mayaro virus infections in a film team returning from Suriname, February 2024. 2024 年 2 月,从苏里南返回的电影摄制组中出现马雅罗病毒感染病例。
IF 9.9 2区 医学 Q1 INFECTIOUS DISEASES Pub Date : 2024-10-01 DOI: 10.2807/1560-7917.ES.2024.29.44.2400679
Hans Martin Orth, Stefanie Pfau, Martin Gabriel, Stephan Günther, Dennis Tappe, Daniel Hornuss, Irmela Müller-Stöver, Martha Charlotte Holtfreter, Tom Luedde, Jonas Schmidt-Chanasit, Torsten Feldt

Mayaro virus is endemic to the tropical Americas, where the incidence is currently increasing. Like other viruses of the Semliki Forest virus serocomplex, such as Alphavirus chikungunya, symptomatic infections are typically characterised by an acute febrile disease followed by long-lasting arthralgia. Cases in travellers are rarely reported but may be underdiagnosed. We report on four people who diagnosed with Mayaro fever after working in remote areas of Suriname as members of a film team.

玛雅罗病毒是美洲热带地区的地方病,目前发病率正在上升。与塞姆利基森林病毒血清复合体的其他病毒(如阿尔法病毒基孔肯雅)一样,无症状感染的典型特征是急性发热,随后出现长期关节痛。旅行者中的病例很少见报道,但可能诊断不足。我们报告了四名在苏里南偏远地区工作的电影团队成员被诊断为马雅罗热的病例。
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引用次数: 0
Enhanced echovirus 11 genomic surveillance in neonatal infections in Spain following a European alert reveals new recombinant forms linked to severe cases, 2019 to 2023. 欧洲警报发布后,西班牙加强了对新生儿感染的埃可病毒 11 基因组监测,发现了与严重病例有关的新重组形式,2019 年至 2023 年。
IF 9.9 2区 医学 Q1 INFECTIOUS DISEASES Pub Date : 2024-10-01 DOI: 10.2807/1560-7917.ES.2024.29.44.2400221
Maria Dolores Fernandez-Garcia, Nerea Garcia-Ibañez, Juan Camacho, Almudena Gutierrez, Laura Sánchez García, Cristina Calvo, Antonio Moreno-Docón, Ana Isabel Menasalvas, Antonio Medina, Mercedes Perez-Ruiz, Maria Carmen Nieto Toboso, Carmen Muñoz-Almagro, Cristian Launes, Carla Berengua, María Cabrerizo

BackgroundIn 2023, a European alert was issued regarding an increase in severe enterovirus (EV) neonatal infections associated with echovirus 11 (E11) new lineage 1.AimTo analyse E11-positive cases between 2019 and 2023 to investigate whether the new lineage 1 circulated in Spain causing severe neonatal infections.MethodsEV-positive samples from hospitalised cases are sent for typing to the National Reference Enterovirus Laboratory. Available samples from 2022-23 were subjected to metagenomic next-generation sequencing.ResultsOf 1,288 samples genotyped, 103 were E11-positive (98 patients: 6 adults, 33 neonates, 89 children under 6 years; male to female ratio 1.9). E11 detection rate was similar before and after detection of the new lineage 1 in Spain in June 2022 (9.7% in 2019 vs 10.6% in 2023). The proportion of E11-infected ICU-admitted neonates in 2019-2022 (2/7) vs 2022-2023 (5/12) did not significantly differ (p = 0.65). In severe neonatal infections, 4/7 E11 strains were not linked to the new lineage 1. The three novel E11 recombinant genomes were associated with severe (n = 2) and non-severe (n = 1) cases from 2022-2023 and clustered outside the new lineage 1. Coinfecting pathogenic viruses were present in four of 10 E11-positive samples.ConclusionThe emergence of the new lineage 1 is not linked with an increase in incidence or severity of neonatal E11 infections in Spain. The detection of two novel E11 recombinants associated with severe disease warrants enhancing genomic and clinical surveillance.

背景2023年,欧洲发布了与埃可病毒11(E11)新品系1相关的新生儿严重肠道病毒(EV)感染增加的警报。目的分析2019年至2023年E11阳性病例,调查新品系1是否在西班牙流行,导致新生儿严重感染。结果 在 1,288 份基因分型样本中,103 份为 E11 阳性(98 名患者,6 名成人,33 名新生儿,1 名重症新生儿):98名患者:6名成人、33名新生儿、89名6岁以下儿童;男女比例为1.9)。在 2022 年 6 月西班牙检测出新的 1 号血统之前和之后,E11 的检测率相似(2019 年为 9.7%,2023 年为 10.6%)。2019-2022年(2/7)与2022-2023年(5/12)入住ICU的E11感染新生儿比例没有显著差异(p = 0.65)。在严重的新生儿感染中,4/7 株 E11 菌株与新品系 1 无关联。三个新型 E11 重组基因组与 2022-2023 年的重症病例(n = 2)和非重症病例(n = 1)有关,并聚集在新品系 1 之外。在 10 份 E11 阳性样本中,有 4 份存在共感染致病病毒。检测到两种与严重疾病相关的新型 E11 重组子,需要加强基因组和临床监测。
{"title":"Enhanced echovirus 11 genomic surveillance in neonatal infections in Spain following a European alert reveals new recombinant forms linked to severe cases, 2019 to 2023.","authors":"Maria Dolores Fernandez-Garcia, Nerea Garcia-Ibañez, Juan Camacho, Almudena Gutierrez, Laura Sánchez García, Cristina Calvo, Antonio Moreno-Docón, Ana Isabel Menasalvas, Antonio Medina, Mercedes Perez-Ruiz, Maria Carmen Nieto Toboso, Carmen Muñoz-Almagro, Cristian Launes, Carla Berengua, María Cabrerizo","doi":"10.2807/1560-7917.ES.2024.29.44.2400221","DOIUrl":"10.2807/1560-7917.ES.2024.29.44.2400221","url":null,"abstract":"<p><p>BackgroundIn 2023, a European alert was issued regarding an increase in severe enterovirus (EV) neonatal infections associated with echovirus 11 (E11) new lineage 1.AimTo analyse E11-positive cases between 2019 and 2023 to investigate whether the new lineage 1 circulated in Spain causing severe neonatal infections.MethodsEV-positive samples from hospitalised cases are sent for typing to the National Reference Enterovirus Laboratory. Available samples from 2022-23 were subjected to metagenomic next-generation sequencing.ResultsOf 1,288 samples genotyped, 103 were E11-positive (98 patients: 6 adults, 33 neonates, 89 children under 6 years; male to female ratio 1.9). E11 detection rate was similar before and after detection of the new lineage 1 in Spain in June 2022 (9.7% in 2019 vs 10.6% in 2023). The proportion of E11-infected ICU-admitted neonates in 2019-2022 (2/7) vs 2022-2023 (5/12) did not significantly differ (p = 0.65). In severe neonatal infections, 4/7 E11 strains were not linked to the new lineage 1. The three novel E11 recombinant genomes were associated with severe (n = 2) and non-severe (n = 1) cases from 2022-2023 and clustered outside the new lineage 1. Coinfecting pathogenic viruses were present in four of 10 E11-positive samples.ConclusionThe emergence of the new lineage 1 is not linked with an increase in incidence or severity of neonatal E11 infections in Spain. The detection of two novel E11 recombinants associated with severe disease warrants enhancing genomic and clinical surveillance.</p>","PeriodicalId":12161,"journal":{"name":"Eurosurveillance","volume":"29 44","pages":""},"PeriodicalIF":9.9,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11528903/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142557485","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Detection of airborne wild waterbird-derived DNA demonstrates potential for transmission of avian influenza virus via air inlets into poultry houses, the Netherlands, 2021 to 2022. 2021 年至 2022 年,荷兰通过空气传播的野生水鸟 DNA 表明禽流感病毒有可能通过禽舍的进气口传播。
IF 9.9 2区 医学 Q1 INFECTIOUS DISEASES Pub Date : 2024-10-01 DOI: 10.2807/1560-7917.ES.2024.29.40.2400350
Alex Bossers, Myrna Mt de Rooij, Isabella van Schothorst, Francisca C Velkers, Lidwien Am Smit

BackgroundOutbreaks of highly pathogenic avian influenza (HPAI) on poultry farms and in wild birds worldwide persists despite intensified control measures. It causes unprecedented mortality in bird populations and is increasingly affecting mammalian species. Better understanding of HPAI introduction pathways into farms are needed for targeted disease prevention and control. The relevance of airborne transmission has been suggested but research involving air sampling is limited and unequivocal evidence on transmission routes is lacking.AimWe aimed to investigate whether HPAI virus from wild birds can enter poultry houses through air inlets by characterising host materials through eukaryote DNA sequencing.MethodsWe collected particulate matter samples in and around three HPAI-affected poultry farms which were cleared and decontaminated before sampling. Indoor measurements (n = 61) were taken directly in the airflow entering through air inlets, while outdoor air samples (n = 60) were collected around the poultry house. Positive controls were obtained from a bird rehabilitation shelter. We performed metabarcoding on environmental DNA by deep sequencing 18S rRNA gene amplicons.ResultsWe detected waterbird DNA in air inside all three, and outside of two, poultry farms. Sequences annotated at species level included swans and tufted ducks. Waterbird DNA was present in all indoor and outdoor air samples from the bird shelter.ConclusionAirborne matter derived from contaminated wild birds can potentially introduce HPAI virus to poultry houses through air inlets. The eDNA metabarcoding could assess breaches in biosecurity for HPAI virus and other pathogens potentially transmitted through air via detection of their hosts.

背景尽管采取了强化控制措施,但高致病性禽流感(HPAI)仍在世界各地的家禽养殖场和野生鸟类中爆发。高致病性禽流感导致鸟类空前死亡,并越来越多地影响哺乳动物物种。为了有针对性地预防和控制疾病,需要更好地了解高致病性禽流感传入农场的途径。我们的目的是通过真核生物 DNA 测序确定宿主材料的特征,从而研究野鸟的高致病性禽流感病毒是否会通过进气口进入禽舍。方法我们在三个受高致病性禽流感影响的家禽养殖场及其周围收集了颗粒物样本,这些样本在采样前已被清理和净化。室内测量(n = 61)直接在通过进气口进入的气流中进行,室外空气样本(n = 60)在禽舍周围采集。阳性对照组来自鸟类康复中心。通过对 18S rRNA 基因扩增子进行深度测序,我们对环境 DNA 进行了代谢编码。物种级别的序列包括天鹅和绒鸭。所有来自禽舍的室内和室外空气样本中都含有水鸟 DNA。eDNA 代谢编码可通过检测寄主来评估高致病性禽流感病毒和其他可能通过空气传播的病原体的生物安全漏洞。
{"title":"Detection of airborne wild waterbird-derived DNA demonstrates potential for transmission of avian influenza virus via air inlets into poultry houses, the Netherlands, 2021 to 2022.","authors":"Alex Bossers, Myrna Mt de Rooij, Isabella van Schothorst, Francisca C Velkers, Lidwien Am Smit","doi":"10.2807/1560-7917.ES.2024.29.40.2400350","DOIUrl":"10.2807/1560-7917.ES.2024.29.40.2400350","url":null,"abstract":"<p><p>BackgroundOutbreaks of highly pathogenic avian influenza (HPAI) on poultry farms and in wild birds worldwide persists despite intensified control measures. It causes unprecedented mortality in bird populations and is increasingly affecting mammalian species. Better understanding of HPAI introduction pathways into farms are needed for targeted disease prevention and control. The relevance of airborne transmission has been suggested but research involving air sampling is limited and unequivocal evidence on transmission routes is lacking.AimWe aimed to investigate whether HPAI virus from wild birds can enter poultry houses through air inlets by characterising host materials through eukaryote DNA sequencing.MethodsWe collected particulate matter samples in and around three HPAI-affected poultry farms which were cleared and decontaminated before sampling. Indoor measurements (n = 61) were taken directly in the airflow entering through air inlets, while outdoor air samples (n = 60) were collected around the poultry house. Positive controls were obtained from a bird rehabilitation shelter. We performed metabarcoding on environmental DNA by deep sequencing 18S rRNA gene amplicons.ResultsWe detected waterbird DNA in air inside all three, and outside of two, poultry farms. Sequences annotated at species level included swans and tufted ducks. Waterbird DNA was present in all indoor and outdoor air samples from the bird shelter.ConclusionAirborne matter derived from contaminated wild birds can potentially introduce HPAI virus to poultry houses through air inlets. The eDNA metabarcoding could assess breaches in biosecurity for HPAI virus and other pathogens potentially transmitted through air via detection of their hosts.</p>","PeriodicalId":12161,"journal":{"name":"Eurosurveillance","volume":"29 40","pages":""},"PeriodicalIF":9.9,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11451133/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142371393","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Sweden surpasses the UNAIDS 95-95-95 target: estimating HIV-1 incidence, 2003 to 2022. 瑞典超过联合国艾滋病规划署 95-95-95 目标:2003 年至 2022 年 HIV-1 发病率估算。
IF 9.9 2区 医学 Q1 INFECTIOUS DISEASES Pub Date : 2024-10-01 DOI: 10.2807/1560-7917.ES.2024.29.42.2400058
Erik Lundgren, Macauley Locke, Ethan Romero-Severson, Mira Dimitrijevic, Maria Axelsson, Emmi Andersson, Christina Carlander, Johanna Brännström, Hans Norrgren, Fredrik Mansson, Olof Elvstam, Magnus Gisslén, Lisa Fohlin, Anders Sönnerborg, Jan Albert, Thomas Leitner

BackgroundSweden reached the UNAIDS 90-90-90 target in 2015. It is important to reassess the HIV epidemiological situation due to ever-changing migration patterns, the roll-out of PrEP and the impact of the COVID-19 pandemic.AimWe aimed to assess the progress towards the UNAIDS 95-95-95 targets in Sweden by estimating the proportion of undiagnosed people with HIV (PWHIV) and HIV incidence trends.MethodsWe used routine laboratory data to inform a biomarker model of time since infection. When available, we used previous negative test dates, arrival dates for PWHIV from abroad and transmission modes to inform our incidence model. We also used data collected from the Swedish InfCareHIV register on antiretroviral therapy (ART).ResultsThe yearly incidence of HIV in Sweden decreased after 2014. In part, this was because the fraction of undiagnosed PWHIV had decreased almost twofold since 2006. After 2015, three of four PWHIV in Sweden were diagnosed within 1.9 and 3.2 years after infection among men who have sex with men and in heterosexual groups, respectively. While 80% of new PWHIV in Sweden acquired HIV before immigration, they make up 50% of the current PWHIV in Sweden. By 2022, 96% of all PWHIV in Sweden had been diagnosed, and 99% of them were on ART, with 98% virally suppressed.ConclusionsBy 2022, about half of all PWHIV in Sweden acquired HIV abroad. Using our new biomarker model, we assess that Sweden has reached the UNAIDS goal at 96-99-98.

背景瑞典于 2015 年实现了联合国艾滋病规划署的 90-90-90 目标。由于不断变化的移民模式、PrEP 的推出以及 COVID-19 大流行的影响,重新评估 HIV 流行病学状况非常重要。AimWe aimed to assess the progress towards the UNAIDS 95-95-95 targets in Sweden by estimating the proportion of undiagnosed people with HIV (PWHIV) and HIV incidence trends.MethodsWe used conventional laboratory data to inform a biomarker model of time since infection.我们使用常规实验室数据为感染后时间的生物标志物模型提供信息。在有数据的情况下,我们使用了之前的阴性检测日期、PWHIV 从国外抵达的日期以及传播方式,为我们的发病率模型提供信息。我们还使用了瑞典 InfCareHIV 登记册中收集的抗逆转录病毒疗法(ART)数据。部分原因是自 2006 年以来,未确诊的艾滋病毒感染者比例下降了近两倍。2015 年后,在瑞典的男男性行为者和异性恋群体中,每四名感染艾滋病的艾滋病毒携带者中就有三人分别在感染后 1.9 年和 3.2 年内被确诊。虽然瑞典80%的新感染者是在移民前感染艾滋病毒的,但他们却占瑞典目前感染者总数的50%。到2022年,瑞典96%的艾滋病病毒感染者已被确诊,其中99%的人接受了抗逆转录病毒疗法,98%的人病毒得到抑制。利用我们新的生物标志物模型,我们评估瑞典已经达到了联合国艾滋病规划署设定的 96-99-98% 的目标。
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引用次数: 0
Association between delayed outbreak identification and SARS-CoV-2 infection and mortality among long-term care home residents, Ontario, Canada, March to November 2020: a cohort study. 2020 年 3 月至 11 月加拿大安大略省长期护理院居民中疫情识别延迟与 SARS-CoV-2 感染和死亡率之间的关系:一项队列研究。
IF 9.9 2区 医学 Q1 INFECTIOUS DISEASES Pub Date : 2024-10-01 DOI: 10.2807/1560-7917.ES.2024.29.41.2300719
Kevin A Brown, Sarah A Buchan, Adrienne K Chan, Andrew Costa, Nick Daneman, Gary Garber, Michael Hillmer, Aaron Jones, James M Johnson, Dylan Kain, Kamil Malikov, Richard G Mather, Allison McGeer, Kevin L Schwartz, Nathan M Stall, Jennie Johnstone

BackgroundLate outbreak identification is a common risk factor mentioned in case reports of large respiratory infection outbreaks in long-term care (LTC) homes.AimTo systematically measure the association between late SARS-CoV-2 outbreak identification and secondary SARS-CoV-2 infection and mortality in residents of LTC homes.MethodsWe studied SARS-CoV-2 outbreaks across LTC homes in Ontario, Canada from March to November 2020, before the COVID-19 vaccine rollout. Our exposure (late outbreak identification) was based on cumulative infection pressure (the number of infectious resident-days) on the outbreak identification date (early: ≤ 2 infectious resident-days, late: ≥ 3 infectious resident-days), where the infectious window was -2 to +8 days around onset. Our outcome consisted of 30-day incidence of secondary infection and mortality, based on the proportion of at-risk residents with a laboratory-confirmed SARS-CoV-2 infection with onset within 30 days of the outbreak identification date.ResultsWe identified 632 SARS-CoV-2 outbreaks across 623 LTC homes. Of these, 36.4% (230/632) outbreaks were identified late. Outbreaks identified late had more secondary infections (10.3%; 4,437/42,953) and higher mortality (3.2%; 1,374/42,953) compared with outbreaks identified early (infections: 3.3%; 2,015/61,714; p < 0.001, mortality: 0.9%; 579/61,714; p < 0.001). After adjustment for 12 LTC home covariates, the incidence of secondary infections in outbreaks identified late was 2.90-fold larger than that of outbreaks identified early (OR: 2.90; 95% CI: 2.04-4.13).ConclusionsThe timeliness of outbreak identification could be used to predict the trajectory of an outbreak, plan outbreak measures and retrospectively provide feedback for quality improvement, with the objective of reducing the impacts of respiratory infections in LTC home residents.

Aim To systematically measure the association between late SARS-CoV-2 outbreak identification and secondary SARS-CoV-2 infection and mortality in residents of LTC homes.方法 我们研究了 2020 年 3 月至 11 月(COVID-19 疫苗推出之前)加拿大安大略省各家长期护理机构爆发的 SARS-CoV-2 疫情。我们的暴露(晚期疫情识别)基于疫情识别日(早期:≤ 2 个感染居民日,晚期:≥ 3 个感染居民日)的累积感染压力(感染居民日数),其中感染窗口期为发病前后 -2 至 +8 天。我们的研究结果包括 30 天内的继发感染率和死亡率,其依据是在疫情确定日期后 30 天内发病并经实验室确诊感染 SARS-CoV-2 的高危住院患者比例。其中,36.4%(230/632)的疫情发现较晚。与较早发现的疫情相比,较晚发现的疫情有更多的二次感染(10.3%;4437/42953)和更高的死亡率(3.2%;1374/42953)(感染:3.3%; 2,015/61,714; p
{"title":"Association between delayed outbreak identification and SARS-CoV-2 infection and mortality among long-term care home residents, Ontario, Canada, March to November 2020: a cohort study.","authors":"Kevin A Brown, Sarah A Buchan, Adrienne K Chan, Andrew Costa, Nick Daneman, Gary Garber, Michael Hillmer, Aaron Jones, James M Johnson, Dylan Kain, Kamil Malikov, Richard G Mather, Allison McGeer, Kevin L Schwartz, Nathan M Stall, Jennie Johnstone","doi":"10.2807/1560-7917.ES.2024.29.41.2300719","DOIUrl":"10.2807/1560-7917.ES.2024.29.41.2300719","url":null,"abstract":"<p><p>BackgroundLate outbreak identification is a common risk factor mentioned in case reports of large respiratory infection outbreaks in long-term care (LTC) homes.AimTo systematically measure the association between late SARS-CoV-2 outbreak identification and secondary SARS-CoV-2 infection and mortality in residents of LTC homes.MethodsWe studied SARS-CoV-2 outbreaks across LTC homes in Ontario, Canada from March to November 2020, before the COVID-19 vaccine rollout. Our exposure (late outbreak identification) was based on cumulative infection pressure (the number of infectious resident-days) on the outbreak identification date (early: ≤ 2 infectious resident-days, late: ≥ 3 infectious resident-days), where the infectious window was -2 to +8 days around onset. Our outcome consisted of 30-day incidence of secondary infection and mortality, based on the proportion of at-risk residents with a laboratory-confirmed SARS-CoV-2 infection with onset within 30 days of the outbreak identification date.ResultsWe identified 632 SARS-CoV-2 outbreaks across 623 LTC homes. Of these, 36.4% (230/632) outbreaks were identified late. Outbreaks identified late had more secondary infections (10.3%; 4,437/42,953) and higher mortality (3.2%; 1,374/42,953) compared with outbreaks identified early (infections: 3.3%; 2,015/61,714; p < 0.001, mortality: 0.9%; 579/61,714; p < 0.001). After adjustment for 12 LTC home covariates, the incidence of secondary infections in outbreaks identified late was 2.90-fold larger than that of outbreaks identified early (OR: 2.90; 95% CI: 2.04-4.13).ConclusionsThe timeliness of outbreak identification could be used to predict the trajectory of an outbreak, plan outbreak measures and retrospectively provide feedback for quality improvement, with the objective of reducing the impacts of respiratory infections in LTC home residents.</p>","PeriodicalId":12161,"journal":{"name":"Eurosurveillance","volume":"29 41","pages":""},"PeriodicalIF":9.9,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11484918/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142399843","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Diagnostic and surveillance testing capability for mpox in the EU/EEA, September 2024. 2024 年 9 月欧盟/欧洲经济区的麻风病诊断和监测检测能力。
IF 9.9 2区 医学 Q1 INFECTIOUS DISEASES Pub Date : 2024-10-01 DOI: 10.2807/1560-7917.ES.2024.29.42.2400632
Nina Lagerqvist, Jessica Beser, Tamás Bakonyi, Céline M Gossner, Daniel Palm

In response to the increasing number of mpox cases caused by monkeypox virus (MPXV) clade I in the African continent and the first reported travel-related clade Ib case of mpox in EU/EEA, the European Centre for Disease Prevention and Control surveyed national capability for detection and characterisation of MPXV in the EU/EEA. The results showed high level of capability for case confirmation by PCR, alongside molecular typing methods for identification of MPXV clades and/or clade I subclades within the EU/EEA.

鉴于非洲大陆由猴痘病毒(MPXV)I支系引起的痘病例日益增多,以及欧盟/欧洲经济区首次报告与旅行有关的Ib支系痘病例,欧洲疾病预防控制中心对欧盟/欧洲经济区各国检测和鉴定MPXV的能力进行了调查。结果显示,欧盟/欧洲经济区内通过 PCR 和分子分型方法确认病例的能力很强,同时还能识别 MPXV 支系和/或支系 I 亚支系。
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