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Donor Screening Failure for Strongyloides stercoralis in Solid Organ Transplantation. 实体器官移植中粪圆线虫供体筛选失败。
IF 11.8 2区 医学 Q1 IMMUNOLOGY Pub Date : 2026-01-16 DOI: 10.3201/eid3201.251483
Rocio Kohan,Helena Gil-Campesino,Inés O García Rodríguez,Magdalena Lara
We report 2 cases of donor-derived Strongyloides stercoralis infection in renal transplant recipients. Despite initial negative serologic testing in donor samples, retrospective testing confirmed transmission. This report underscores the limitations of serologic screening, the need for targeted protocols in endemic-risk populations, and the importance of close posttransplant surveillance.
我们报告2例肾移植受者供体源性粪圆形线虫感染。尽管供体样本最初的血清学检测呈阴性,但回顾性检测证实了传播。该报告强调了血清学筛查的局限性,在流行危险人群中需要有针对性的方案,以及密切移植后监测的重要性。
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引用次数: 0
Genomic Insights into Marburg Virus Strains from 2023 and 2025 Outbreaks in Kagera, Tanzania. 对2023年和2025年坦桑尼亚卡盖拉暴发的马尔堡病毒株的基因组分析。
IF 11.8 2区 医学 Q1 IMMUNOLOGY Pub Date : 2026-01-14 DOI: 10.3201/eid3201.251314
Lawrence A Mapunda,Medard Beyanga,Nyambura Moremi,Jean N Hakizimana,Doreen Kamori,Alfred Chacha,Edna Mgimba,Dennis Mrosso,Ambele E Mwafulango,Jackson Mushumbusi,Ferdinand Ndunguru,Seif Abdul,Emmanuel Mkumbo,Maria E Kelly,Céline Barnadas,Vida Mmbaga,Rogath Kishimba,Samwel Laizer,Ntuli Kapologwe,Michael Kiremeji,Erasto Sylvanus,Angela Samwel,Saumu Nungu,Emmanuel Achol,Julien Nguinkal,Hakimu Idris Lagu,Muna Affara,Florian Gehre,Calvin Sindato,Chacha Mangu,Elias Nyanda Ntinginya,Saida Murugwa,Pawan Angra,Shannon Whitmer,George Mgomella,Mahesh Swaminathan,Wangeci Gatei,Dorcas Wanjohi,Sofonias Tessema,Yenew Kebede,Said Aboud,Charles Sagoe-Moses,Alex Magesa,Gerald Misinzo,Tumaini Nagu,Grace Magembe
Marburg virus (MARV) is the primary cause of Marburg virus disease (MVD), a severe hemorrhagic fever with a high case-fatality rate. The first reported MVD outbreak in Tanzania occurred in 2023, followed by a second outbreak in 2025, both within the Kagera region. During those MVD outbreaks, 174 suspected cases were identified; of those, 10 were laboratory confirmed. After complete genome assembly and bioinformatic analyses, we found the MARV strains of the 2023 and 2025 outbreaks to be closely related and clustered with MARV strains that caused outbreaks in Rwanda (2024) and Uganda (2014). The sequences from both MVD outbreaks in Tanzania showed >99.71% nucleotide identity, suggesting a possible single spillover event followed by limited human-to-human virus transmission. Further ecologic studies are essential to identify potential spillover events, but our findings indicate that closely related MARV strains circulate in Kagera, Tanzania, posing a risk for future outbreak recurrence.
马尔堡病毒(MARV)是马尔堡病毒病(MVD)的主要病因,马尔堡病毒病是一种病死率很高的严重出血热。坦桑尼亚第一次报告的MVD暴发发生在2023年,随后在2025年发生了第二次暴发,均发生在卡格拉地区。在这些MVD暴发期间,确定了174例疑似病例;其中10例经实验室确认。经过全基因组组装和生物信息学分析,我们发现2023年和2025年爆发的MARV菌株与导致卢旺达(2024年)和乌干达(2014年)爆发的MARV菌株密切相关并聚集在一起。来自坦桑尼亚两次MVD暴发的序列显示>99.71%核苷酸同源,表明可能发生单一溢出事件,随后发生有限的人传人病毒传播。进一步的生态学研究对于确定潜在的外溢事件至关重要,但我们的研究结果表明,密切相关的MARV毒株在坦桑尼亚Kagera流行,构成了未来疫情复发的风险。
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引用次数: 0
Evidence of Rat Hepatitis E Virus Circulation through Wastewater Surveillance, Central Argentina. 阿根廷中部通过废水监测发现戊型肝炎大鼠病毒传播的证据。
IF 6.6 2区 医学 Q1 IMMUNOLOGY Pub Date : 2026-01-01 DOI: 10.3201/eid3201.251218
Bianca Filoni, María Emilia Lucero, Guadalupe Di Cola, Anabella Fantilli, Alfonsina Roccia, Paola Sicilia, Liliana Luque, Ariana Cachi, María de Los Ángeles Marinzalda, Gonzalo Castro, Gisela Masachessi, Viviana Ré, María Belén Pisano

During 2023-2024, we detected rat hepatitis E virus in 67.7% of wastewater samples from central Argentina. This high level of detection opens new inquiries in the region, highlighting the need to investigate the virus in both animal reservoirs and humans, with a focus on hepatitis cases of unknown etiology.

在2023-2024年期间,我们在阿根廷中部67.7%的废水样本中检测到戊型肝炎病毒。这种高水平的发现开启了该区域的新调查,突出表明需要调查动物宿主和人类中的病毒,重点是病因不明的肝炎病例。
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引用次数: 0
Enhanced Isolation and Detection of COVID-19 in Hospitalized Patients Undergoing Antiviral Therapy. 在接受抗病毒治疗的住院患者中加强COVID-19的分离和检测。
IF 6.6 2区 医学 Q1 IMMUNOLOGY Pub Date : 2026-01-01 DOI: 10.3201/eid3201.251011
Ranawaka A P M Perera, Andrew Marques, Jevon Graham-Wooten, Li Hui Tan, Noam Cohen, Kyle Rodino, Ronald G Collman, Frederic D Bushman, Susan R Weiss

We evaluated the efficiency of SARS-CoV-2 detection from patient respiratory specimens by comparing 3 cell lines: Vero E6, Vero E6 expressing transmembrane protease serine 2 (Vero E6 T2), and Vero E6 expressing angiotensin-converting enzyme 2 and transmembrane protease serine 2 (Vero E6 A2T2). We compared a range of sample types, clinical conditions, and real-time reverse transcription PCR cycle threshold values. Vero E6 A2T2 exhibited enhanced sensitivity by supporting efficient virus entry and replication with faster cytopathic effect. Vero E6 culture isolated infectious virus only up to 3 days after PCR confirmation but with Vero E6 A2T2 cells, culture occurred up to 7 days after confirmation. Whole-genome sequencing showed no evidence of adaptive mutations when Vero E6 A2T2 was used for viral culture, supporting use for downstream analyses. Optimized infectious virus detection systems are needed for research and clinical settings, particularly for high-risk, immunocompromised populations that produce virus longer and contribute to variant emergence.

我们通过比较表达跨膜蛋白酶丝氨酸2 (Vero E6 T2)的Vero E6细胞系和表达血管紧张素转换酶2和跨膜蛋白酶丝氨酸2 (Vero E6 A2T2)的Vero E6细胞系,评估了从患者呼吸道标本中检测SARS-CoV-2的效率。我们比较了一系列样品类型、临床条件和实时逆转录PCR周期阈值。Vero E6 A2T2通过支持有效的病毒进入和复制以及更快的细胞病变效应,表现出增强的敏感性。Vero E6培养物在PCR确认后仅分离感染性病毒3天,而Vero E6 A2T2细胞在确认后的7天内进行培养。当使用Vero E6 A2T2进行病毒培养时,全基因组测序显示没有适应性突变的证据,支持下游分析的使用。研究和临床环境需要优化的传染性病毒检测系统,特别是对于产生病毒时间较长并导致变异出现的高风险、免疫功能低下人群。
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引用次数: 0
Molecular Analysis of Emerging MT27 Macrolide-Resistant Bordetella pertussis, Kobe, Japan, 2025. 新兴MT27耐大环内酯百日咳杆菌分子分析,神户,日本,2025。
IF 6.6 2区 医学 Q1 IMMUNOLOGY Pub Date : 2026-01-01 DOI: 10.3201/eid3201.250890
Shoko Komatsu, Noriko Nakanishi, Kousaku Matsubara, Yuui Inenaga, Masayuki Hori, Kiyo Shiotani, Rumi Morimoto, Chie Nantani, Yuki Muneta, Nobuya Kusunoki

We report the emergence and spread of multilocus variable-number tandem-repeat analysis type 27 (MT-27) macrolide-resistant Bordetella pertussis (MRBP) in Kobe, Japan, in 2025. Whole-genome sequencing revealed that MT27-MRBP did not originate from the widely circulating MT27 macrolide-sensitive B. pertussis in Japan but was closely related to MRBP in China.

我们报告了2025年日本神户多位点可变数串联重复分析27型(MT-27)大环内酯耐药百日咳(MRBP)的出现和传播。全基因组测序显示,MT27-MRBP并非起源于日本广泛流行的MT27大环内酯敏感百日咳,但与中国的MRBP密切相关。
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引用次数: 0
Detection of Oropouche and Punta Toro Virus Infections by Enhanced Surveillance, Panama, 2023-2024. 加强监测检测Oropouche和Punta Toro病毒感染,巴拿马,2023-2024。
IF 6.6 2区 医学 Q1 IMMUNOLOGY Pub Date : 2026-01-01 DOI: 10.3201/eid3201.251224
Maria Chen-Germán, Claudia González, Dimelza Araúz, Celestino Aguilar, Melanie Vega, Oris Chavarria, Ambar Moreno, Erika Santiago, Danilo Franco, Elimelec Valdespino, Jessica Gondola, Mayla Pinedo, Domicio Espino, Tamara Salcedo, Leticia Franco, Nicanor Obaldía, Blas Armien, Alexander A Martínez, Brechla Moreno

Enhanced arboviral surveillance in Panama revealed an Oropouche virus case, 5 months before the 2025 national outbreak, in samples that tested negative for routinely screened arboviruses. Subsequent contact tracing identified an additional case of Punta Toro virus. Our findings highlight the importance of expanding diagnostic efforts to identify circulating arboviruses.

在巴拿马加强虫媒病毒监测后,在常规虫媒病毒筛查呈阴性的样本中发现了一例Oropouche病毒病例,这是在2025年全国疫情爆发前5个月。随后的接触者追踪发现了另一例蓬塔托罗病毒病例。我们的发现强调了扩大诊断工作以识别循环虫媒病毒的重要性。
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引用次数: 0
Emergence of New Delhi Metallo-β-Lactamase 14-Producing Klebsiella pneumoniae Sequence Type 147 Clone in Spain and Outbreak in the Canary Islands. 产新德里金属β-内酰胺酶14肺炎克雷伯菌序列147型克隆在西班牙的出现和加那利群岛的爆发。
IF 6.6 2区 医学 Q1 IMMUNOLOGY Pub Date : 2026-01-01 DOI: 10.3201/eid3201.251504
Pablo Aja-Macaya, Tania Blanco-Martín, Cristian Mateo-León, Cristóbal Del Rosario-Quintana, Carmen Piña, Enrique de la Cruz-Tabares, Salud Rodríguez-Pallares, Lucía González-Pinto, Alejandro Beceiro, Marina Oviaño, Germán Bou, Diego García-Martínez de Artola, Jorge Arca-Suárez

The emergence of a high-risk New Delhi metallo-β-lactamase 14-producing Klebsiella pneumoniae sequence type 147 clone is of public health concern because of its rapid international spread. We report cross-border emergence and rapid dissemination of that clone in the Canary Islands, Spain, during 2023-2025. We analyzed 30 isolates recovered during 2023 in detail by reviewing clinical and epidemiologic data, conducting whole-genome sequencing to assess clonal relatedness and analyze resistomes, and performing antimicrobial susceptibility testing of novel therapeutic options through reference broth microdilution. The isolates formed a well-defined cluster, with minimal genomic distance and identical resistomes, confirming the local outbreak. Those clones were also closely related to other international New Delhi metallo-β-lactamase 14-producing K. pneumoniae sequence type 147 isolates, supporting the ongoing cross-border expansion of that clone. Aztreonam/avibactam was the most active therapeutic option (MICs <0.125 mg/L). Our findings highlight the need for close monitoring to prevent further dissemination of this clone.

高风险新德里产金属β-内酰胺酶14肺炎克雷伯菌序列147型克隆的出现由于其在国际上的迅速传播而引起公共卫生关注。我们报告了2023-2025年间该克隆体在西班牙加那利群岛的跨界出现和快速传播。我们通过回顾临床和流行病学数据,进行全基因组测序以评估克隆相关性和分析抗性组,并通过参考肉汤微量稀释对新型治疗方案进行抗生素敏感性测试,详细分析了2023年回收的30株分离株。分离株形成了一个明确的集群,具有最小的基因组距离和相同的抗性组,证实了当地的暴发。这些克隆也与其他国际新德里产金属β-内酰胺酶14肺炎克雷伯菌序列147型分离株密切相关,支持该克隆正在进行的跨境扩展。阿曲南/阿维巴坦是最有效的治疗选择(MICs)
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引用次数: 0
Mycobacterium decipiens Infection in Patient Receiving Anti-TNF-α Therapy, France, 2024. 接受抗肿瘤坏死因子-α治疗的患者的蜕膜分枝杆菌感染,法国,2024。
IF 6.6 2区 医学 Q1 IMMUNOLOGY Pub Date : 2026-01-01 DOI: 10.3201/eid3201.250518
Justin Charles-Antoine Destoop, Corentin Poignon, William Danjou, Alexandre Bleibtreu, Valerie Pourcher, Gentiane Monsel

Mycobacterium decipiens is a newly identified species with high genomic similarity to M. tuberculosis. We report a cutaneous M. decipiens infection in a patient in France who had inflammatory bowel disease being treated with anti-tumor necrosis factor-α therapy. The infection was successfully treated with an oral antimicrobial regimen.

脱毛分枝杆菌是一种与结核分枝杆菌具有高度基因组相似性的新发现物种。我们报告一例皮肤脱皮分枝杆菌感染的患者在法国谁患有炎症性肠病正在治疗抗肿瘤坏死因子-α治疗。通过口服抗菌素方案成功地治疗了感染。
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引用次数: 0
Integrating Prevention and Response at the Crossroads of Henipavirus Preparedness, Hendra@30 Conference, 2024. 在预防的十字路口整合预防和应对亨尼帕病毒,Hendra@30会议,2024。
IF 6.6 2区 医学 Q1 IMMUNOLOGY Pub Date : 2026-01-01 DOI: 10.3201/eid3201.250979
Kim Halpin, Raúl Gómez Román, Emmie de Wit, Alison J Peel, Jonathan H Epstein, Jennifer Barr, Sarah J Edwards, Melanie N Tripp, Berta Blanch-Lázaro, Belinda Linnegar, Gervais Habarugira, Glenn A Marsh, Danielle Anderson, Li-Yen Chang, Wanda Markotter

Diseases caused by henipaviruses, exemplified by Hendra virus and Nipah virus, pose a serious risk to public health because of their epidemic potential and high case-fatality rates and the paucity of medical countermeasures to mitigate them. In December 2024, a group of 150 scientists from 16 countries convened in Geelong, Victoria, Australia, to mark the 30th anniversary of the discovery of Hendra virus. The Hendra@30 conference built upon its predecessor conference held in 2019 in Singapore, Nipah@20, by expanding its program across broader disciplines and integrating sessions on human sociology and disease ecology into the main scientific discussions. We describe key highlights from Hendra@30 and reflect on 4 key elements that have advanced henipavirus research and medical countermeasures research and development. We propose that integrating bat ecology into henipavirus research blueprints will enable development of ecologic countermeasures that prevent spillover and will complement existing preparedness and response efforts with evidence-based prevention strategies.

由亨德拉病毒和尼帕病毒等亨尼帕病毒引起的疾病对公众健康构成严重威胁,因为它们具有流行潜力,致死率高,而且缺乏缓解这些疾病的医疗对策。2024年12月,来自16个国家的150名科学家聚集在澳大利亚维多利亚州吉朗,纪念亨德拉病毒发现30周年。Hendra@30会议以2019年在新加坡(Nipah@20)举行的上届会议为基础,将其计划扩展到更广泛的学科,并将人类社会学和疾病生态学会议纳入主要的科学讨论。我们描述了Hendra@30的主要亮点,并反思了推动亨尼帕病毒研究和医学对策研究与开发的4个关键因素。我们建议将蝙蝠生态学整合到亨尼帕病毒研究蓝图中,将有助于制定防止溢出的生态对策,并将与基于证据的预防战略补充现有的准备和应对工作。
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引用次数: 0
Group A Streptococcus Meningitis, United States, 1997-2022. A群链球菌脑膜炎,美国,1997-2022。
IF 6.6 2区 医学 Q1 IMMUNOLOGY Pub Date : 2026-01-01 DOI: 10.3201/eid3201.250871
Paulina A Hawkins, Sopio Chochua, Namrata Prasad, Jennifer O Okaro, Yuan Li, Tasha Martin, Ann Thomas, Bridget J Anderson, Kari E Burzlaff, Lee Harrison, Shannon Seopaul, Nisha Alden, Rachel Herlihy, William Schaffner, H Keipp Talbot, Ruth Lynfield, Kathy Como-Sabetti, Maria Rosales, Shua Chai, Sam Sefton, Jessica R Howard-Anderson, Sarah Khanlian, Jessica Houston, Susan Petit, Adam L Cohen, Christopher J Gregory

Group A Streptococcus (GAS) causes a variety of diseases in humans but is not widely appreciated as a cause of meningitis. During 1997-2022, ten sites participating in the Active Bacterial Core Surveillance network in the United States identified GAS meningitis cases. We calculated annual incidence and case-fatality rates (CFRs) for 320 of those cases and determined antimicrobial resistance by whole-genome sequencing. Annual incidence of GAS meningitis ranged from 0.02 to 0.07 cases/100,000 persons. Children <1 year of age had the highest average annual incidence, 0.23 cases/100,000 children. GAS meningitis had a higher CFR (19.4%) than meningitis caused by group B Streptococcus, Streptococcus pneumoniae, Neisseria meningitidis, or Haemophilus influenzae. Clindamycin resistance among GAS meningitis isolates increased from 3.2% during 1997-2002 to 17.7% during 2018-2022. Clinicians should be aware that meningitis is an uncommon but severe manifestation of invasive GAS and has a higher CFR than more established meningitis etiologies.

A群链球菌(GAS)在人类中引起多种疾病,但尚未被广泛认为是脑膜炎的原因。在1997-2022年期间,参与美国活性细菌核心监测网络的10个站点发现了GAS脑膜炎病例。我们计算了其中320例的年发病率和病死率(CFRs),并通过全基因组测序确定了抗菌素耐药性。气体性脑膜炎的年发病率为0.02至0.07例/10万人。孩子们
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引用次数: 0
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Emerging Infectious Diseases
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