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.
{"title":"Donor Screening Failure for Strongyloides stercoralis in Solid Organ Transplantation.","authors":"Rocio Kohan,Helena Gil-Campesino,Inés O García Rodríguez,Magdalena Lara","doi":"10.3201/eid3201.251483","DOIUrl":"https://doi.org/10.3201/eid3201.251483","url":null,"abstract":"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.","PeriodicalId":11595,"journal":{"name":"Emerging Infectious Diseases","volume":"20 1","pages":""},"PeriodicalIF":11.8,"publicationDate":"2026-01-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145986283","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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.
{"title":"Genomic Insights into Marburg Virus Strains from 2023 and 2025 Outbreaks in Kagera, Tanzania.","authors":"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","doi":"10.3201/eid3201.251314","DOIUrl":"https://doi.org/10.3201/eid3201.251314","url":null,"abstract":"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.","PeriodicalId":11595,"journal":{"name":"Emerging Infectious Diseases","volume":"10 1","pages":""},"PeriodicalIF":11.8,"publicationDate":"2026-01-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145971881","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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.
{"title":"Evidence of Rat Hepatitis E Virus Circulation through Wastewater Surveillance, Central Argentina.","authors":"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","doi":"10.3201/eid3201.251218","DOIUrl":"10.3201/eid3201.251218","url":null,"abstract":"<p><p>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.</p>","PeriodicalId":11595,"journal":{"name":"Emerging Infectious Diseases","volume":"32 1","pages":"133-136"},"PeriodicalIF":6.6,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12870092/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146084937","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}
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.
{"title":"Enhanced Isolation and Detection of COVID-19 in Hospitalized Patients Undergoing Antiviral Therapy.","authors":"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","doi":"10.3201/eid3201.251011","DOIUrl":"10.3201/eid3201.251011","url":null,"abstract":"<p><p>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.</p>","PeriodicalId":11595,"journal":{"name":"Emerging Infectious Diseases","volume":"32 1","pages":"103-113"},"PeriodicalIF":6.6,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12870042/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146084964","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}
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.
{"title":"Molecular Analysis of Emerging MT27 Macrolide-Resistant Bordetella pertussis, Kobe, Japan, 2025.","authors":"Shoko Komatsu, Noriko Nakanishi, Kousaku Matsubara, Yuui Inenaga, Masayuki Hori, Kiyo Shiotani, Rumi Morimoto, Chie Nantani, Yuki Muneta, Nobuya Kusunoki","doi":"10.3201/eid3201.250890","DOIUrl":"10.3201/eid3201.250890","url":null,"abstract":"<p><p>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.</p>","PeriodicalId":11595,"journal":{"name":"Emerging Infectious Diseases","volume":"32 1","pages":"150-153"},"PeriodicalIF":6.6,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12872074/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146084889","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}
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.
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.
{"title":"Emergence of New Delhi Metallo-β-Lactamase 14-Producing Klebsiella pneumoniae Sequence Type 147 Clone in Spain and Outbreak in the Canary Islands.","authors":"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","doi":"10.3201/eid3201.251504","DOIUrl":"10.3201/eid3201.251504","url":null,"abstract":"<p><p>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.</p>","PeriodicalId":11595,"journal":{"name":"Emerging Infectious Diseases","volume":"32 1","pages":"63-73"},"PeriodicalIF":6.6,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12870054/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146084971","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}
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.
{"title":"Mycobacterium decipiens Infection in Patient Receiving Anti-TNF-α Therapy, France, 2024.","authors":"Justin Charles-Antoine Destoop, Corentin Poignon, William Danjou, Alexandre Bleibtreu, Valerie Pourcher, Gentiane Monsel","doi":"10.3201/eid3201.250518","DOIUrl":"10.3201/eid3201.250518","url":null,"abstract":"<p><p>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.</p>","PeriodicalId":11595,"journal":{"name":"Emerging Infectious Diseases","volume":"32 1","pages":"146-148"},"PeriodicalIF":6.6,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12870094/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146084896","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}
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.
{"title":"Integrating Prevention and Response at the Crossroads of Henipavirus Preparedness, Hendra@30 Conference, 2024.","authors":"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","doi":"10.3201/eid3201.250979","DOIUrl":"10.3201/eid3201.250979","url":null,"abstract":"<p><p>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.</p>","PeriodicalId":11595,"journal":{"name":"Emerging Infectious Diseases","volume":"32 1","pages":"1-7"},"PeriodicalIF":6.6,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12870148/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146084910","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}
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.
{"title":"Group A Streptococcus Meningitis, United States, 1997-2022.","authors":"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","doi":"10.3201/eid3201.250871","DOIUrl":"10.3201/eid3201.250871","url":null,"abstract":"<p><p>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.</p>","PeriodicalId":11595,"journal":{"name":"Emerging Infectious Diseases","volume":"32 1","pages":""},"PeriodicalIF":6.6,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12870060/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146084921","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}