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Articles from Emerging Infectious Diseases

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Corynebacterium diphtheriae Infections, South Africa, 2015–2023 [PDF - 931 KB - 10 pages]
M. du Plessis et al.

We reviewed Corynebacterium spp. infection cases reported in South Africa during 2015–2023. We analyzed 84 isolates from 83 patients with C. diphtheriae, as well as 1 C. belfantii and 3 C. ulcerans isolates. Among C. diphtheriae cases, we observed respiratory diphtheria (26/83 patients [31%]), endocarditis (14/83 [17%]), cutaneous diphtheria (22/83 [27%]), nonspecific respiratory illnesses (5/83 [6%]), and asymptomatic carriage (16/83 [19%]). The median patient age was 19 (range 0–88) years. Diphtheria-tetanus-pertussis vaccination was incomplete for 26% (5/19) or unknown for 68% (13/19) of children 0–9 years of age. C. diphtheriae was intermediately resistant to penicillin (82/84 [98%] isolates; MIC90 0.5 μg/mL) but susceptible to erythromycin (83/84 [99%] isolates; MIC90 0.25 μg/mL). Eighteen unique sequence types were identified, corroborating C. diphtheriae heterogeneity. Toxin-producing strains were detected among cutaneous and respiratory diphtheria cases, indicating all forms of disease require monitoring and prompt public health action to curb transmission.

EID du Plessis M, Mikhari R, de Gouveia L, Duma N, Lovelock T, Lawrence C, et al. Corynebacterium diphtheriae Infections, South Africa, 2015–2023. Emerg Infect Dis. 2025;31(3):417-426. https://doi.org/10.3201/eid3103.241211
AMA du Plessis M, Mikhari R, de Gouveia L, et al. Corynebacterium diphtheriae Infections, South Africa, 2015–2023. Emerging Infectious Diseases. 2025;31(3):417-426. doi:10.3201/eid3103.241211.
APA du Plessis, M., Mikhari, R., de Gouveia, L., Duma, N., Lovelock, T., Lawrence, C....von Gottberg, A. (2025). Corynebacterium diphtheriae Infections, South Africa, 2015–2023. Emerging Infectious Diseases, 31(3), 417-426. https://doi.org/10.3201/eid3103.241211.

Genetic Diversity and Geographic Spread of Henipaviruses [PDF - 2.04 MB - 11 pages]
Y. Kane et al.

Henipaviruses, such as Hendra and Nipah viruses, are major zoonotic pathogens that cause encephalitis and respiratory infections in humans and animals. The recent emergence of Langya virus in China highlights the need to understand henipavirus host diversity and geographic spread to prevent future outbreaks. Our analysis of the National Center for Biotechnology Information Virus and VIRION databases revealed ≈1,117 henipavirus sequences and 142 complete genomes. Bats (64.7%) and shrews (11.7%) dominated the host species record, and the genera Pteropus and Crocidura contained key henipavirus hosts in Asia, Australia, and Africa. Henipaviruses found in the Eidolon bat genus exhibited the highest within-host genetic distance. Phylogenetic analysis revealed batborne and rodent- or shrew-derived henipaviruses diverged ≈11,000 years ago and the first known lineage originating in Eidolon genus bats ≈9,900 years ago. Pathogenic henipaviruses diverged from their ancestors 2,800–1,200 years ago. Including atypical hosts and regions in future investigations is necessary to control future outbreaks.

EID Kane Y, Nalikka B, Tendu A, Omondi V, Bienes K, Padane A, et al. Genetic Diversity and Geographic Spread of Henipaviruses. Emerg Infect Dis. 2025;31(3):427-437. https://doi.org/10.3201/eid3103.241134
AMA Kane Y, Nalikka B, Tendu A, et al. Genetic Diversity and Geographic Spread of Henipaviruses. Emerging Infectious Diseases. 2025;31(3):427-437. doi:10.3201/eid3103.241134.
APA Kane, Y., Nalikka, B., Tendu, A., Omondi, V., Bienes, K., Padane, A....Wong, G. (2025). Genetic Diversity and Geographic Spread of Henipaviruses. Emerging Infectious Diseases, 31(3), 427-437. https://doi.org/10.3201/eid3103.241134.

Candida auris Outbreak and Epidemiologic Response in Burn Intensive Care Unit, Illinois, USA, 2021–2023 [PDF - 1.11 MB - 10 pages]
H. J. Barbian et al.

Candida auris is an emerging fungal pathogen associated with outbreaks in healthcare settings. We report a multiyear outbreak of C. auris in a burn intensive care unit in Illinois, USA, during 2021–2023. We identified 28 C. auris cases in the unit over a 2-year period, despite outbreak response and multimodal mitigation measures. Of the 28 case-patients, 15 (53.6%) were considered colonized and 13 (46.4%) had clinical infections. Phylogenetic analysis of whole-genome sequences revealed 4 distinct clusters of closely related (0–6 SNP differences) genomes containing 3–6 cases. Clusters generally contained temporally related isolates from patients with epidemiologic links; this finding suggests that multiple introductions and within-unit spread over a limited time were responsible for the outbreak, rather than transmission from a long-term source (e.g., persistent environmental contamination or staff carriage). Here, integrated traditional and genomic epidemiology supported C. auris outbreak investigation and response and informed targeted interventions.

EID Barbian HJ, Lie L, Kittner A, Harrington A, Carson J, Frias M, et al. Candida auris Outbreak and Epidemiologic Response in Burn Intensive Care Unit, Illinois, USA, 2021–2023. Emerg Infect Dis. 2025;31(3):438-447. https://doi.org/10.3201/eid3103.241195
AMA Barbian HJ, Lie L, Kittner A, et al. Candida auris Outbreak and Epidemiologic Response in Burn Intensive Care Unit, Illinois, USA, 2021–2023. Emerging Infectious Diseases. 2025;31(3):438-447. doi:10.3201/eid3103.241195.
APA Barbian, H. J., Lie, L., Kittner, A., Harrington, A., Carson, J., Frias, M....Hayden, M. K. (2025). Candida auris Outbreak and Epidemiologic Response in Burn Intensive Care Unit, Illinois, USA, 2021–2023. Emerging Infectious Diseases, 31(3), 438-447. https://doi.org/10.3201/eid3103.241195.

Epidemiology of Buruli Ulcer in Victoria, Australia, 2017–2022 [PDF - 1.40 MB - 10 pages]
B. Ravindran et al.

Buruli ulcer (BU) is a rare, neglected tropical disease caused by Mycobacterium ulcerans that can lead to severe skin ulcers. To determine the epidemiology of BU in Victoria, Australia, during 2017–2022 we analyzed surveillance data. A total of 1,751 cases of BU were notified; 968 (55%) patients were male and 781 (45%) female (2 were missing sex data), and 984 (56%) resided in established BU-endemic areas, although an increasing number were in new BU-endemic areas. Most cases (83%, 1,301) were classified as category I. Multivariate modeling demonstrated that factors for severe BU included being male, being older, and living in a new BU-endemic or non–BU-endemic area. A relatively shorter interval between first visit to a clinician and receipt of diagnosis was protective against severe disease. The expansion of BU-endemic areas throughout Victoria remains a public health concern and calls for targeted action, particularly for patients and clinicians in new BU-endemic areas.

EID Ravindran B, Hennessy D, O’Hara M, Tay E, Banuve R, McVernon J, et al. Epidemiology of Buruli Ulcer in Victoria, Australia, 2017–2022. Emerg Infect Dis. 2025;31(3):448-457. https://doi.org/10.3201/eid3103.240938
AMA Ravindran B, Hennessy D, O’Hara M, et al. Epidemiology of Buruli Ulcer in Victoria, Australia, 2017–2022. Emerging Infectious Diseases. 2025;31(3):448-457. doi:10.3201/eid3103.240938.
APA Ravindran, B., Hennessy, D., O’Hara, M., Tay, E., Banuve, R., McVernon, J....Carville, K. (2025). Epidemiology of Buruli Ulcer in Victoria, Australia, 2017–2022. Emerging Infectious Diseases, 31(3), 448-457. https://doi.org/10.3201/eid3103.240938.
Research

Effect of Prior Influenza A(H1N1)pdm09 Virus Infection on Pathogenesis and Transmission of Human Influenza A(H5N1) Clade 2.3.4.4b Virus in Ferret Model [PDF - 1.26 MB - 9 pages]
X. Sun et al.

Reports of human infections with influenza A(H5N1) clade 2.3.4.4b viruses associated with outbreaks in dairy cows in the United States underscore the need to assess the potential cross-protection conferred by existing influenza immunity. We serologically evaluated ferrets previously infected with an influenza A(H1N1)pdm09 virus for cross-reactive antibodies and then challenged 3 months later with either highly pathogenic H5N1 clade 2.3.4.4b or low pathogenicity H7N9 virus. Our results showed that prior influenza A(H1N1)pdm09 virus infection more effectively reduced the replication and transmission of the H5N1 virus than did the H7N9 virus, a finding supported by the presence of group 1 hemagglutinin stalk and N1 neuraminidase antibodies in preimmune ferrets. Our findings suggest that prior influenza A(H1N1)pdm09 virus infection may confer some level of protection against influenza A(H5N1) clade 2.3.4.4.b virus.

EID Sun X, Belser JA, Li Z, Brock N, Pulit-Penaloza JA, Kieran TJ, et al. Effect of Prior Influenza A(H1N1)pdm09 Virus Infection on Pathogenesis and Transmission of Human Influenza A(H5N1) Clade 2.3.4.4b Virus in Ferret Model. Emerg Infect Dis. 2025;31(3):458-466. https://doi.org/10.3201/eid3103.241489
AMA Sun X, Belser JA, Li Z, et al. Effect of Prior Influenza A(H1N1)pdm09 Virus Infection on Pathogenesis and Transmission of Human Influenza A(H5N1) Clade 2.3.4.4b Virus in Ferret Model. Emerging Infectious Diseases. 2025;31(3):458-466. doi:10.3201/eid3103.241489.
APA Sun, X., Belser, J. A., Li, Z., Brock, N., Pulit-Penaloza, J. A., Kieran, T. J....Maines, T. R. (2025). Effect of Prior Influenza A(H1N1)pdm09 Virus Infection on Pathogenesis and Transmission of Human Influenza A(H5N1) Clade 2.3.4.4b Virus in Ferret Model. Emerging Infectious Diseases, 31(3), 458-466. https://doi.org/10.3201/eid3103.241489.

Medscape CME Activity
Efficacy and Safety of 4-Month Rifapentine-Based Tuberculosis Treatments in Persons with Diabetes [PDF - 985 KB - 10 pages]
E. V. Kurbatova et al.

A previous study demonstrated noninferior efficacy of 4-month rifapentine/moxifloxacin regimen for tuberculosis (TB) treatment compared with the standard regimen. We explored results among study participants with diabetes. Among 2,516 randomized participants, 181 (7.2%) had diabetes. Of 166 participants with diabetes in the microbiologically eligible analysis group, 26.3% (15/57) had unfavorable outcomes in the control regimen, 13.8% (8/58) in the rifapentine/moxifloxacin regimen, and 29.4% (15/51) in the rifapentine regimen. The difference in proportion of unfavorable outcomes between the control and rifapentine/moxifloxacin arms in the microbiologically eligible analysis group was –12.5% (95% CI –27.0% to 1.9%); the difference between the control and rifapentine arms was 3.1% (95% CI –13.8% to 20.0%). Safety outcomes were similar in the rifapentine/moxifloxacin regimen and control arms. Among participants with TB and diabetes, the rifapentine/moxifloxacin arm had fewest unfavorable outcomes and was safe. Our findings indicate that the rifapentine/moxifloxacin regimen can be used in persons with TB and diabetes.

EID Kurbatova EV, Whitworth WC, Peddareddy L, Phillips P, Scott NA, Bryant KE, et al. Efficacy and Safety of 4-Month Rifapentine-Based Tuberculosis Treatments in Persons with Diabetes. Emerg Infect Dis. 2025;31(3):467-476. https://doi.org/10.3201/eid3103.241634
AMA Kurbatova EV, Whitworth WC, Peddareddy L, et al. Efficacy and Safety of 4-Month Rifapentine-Based Tuberculosis Treatments in Persons with Diabetes. Emerging Infectious Diseases. 2025;31(3):467-476. doi:10.3201/eid3103.241634.
APA Kurbatova, E. V., Whitworth, W. C., Peddareddy, L., Phillips, P., Scott, N. A., Bryant, K. E....Nguyen, N. V. (2025). Efficacy and Safety of 4-Month Rifapentine-Based Tuberculosis Treatments in Persons with Diabetes. Emerging Infectious Diseases, 31(3), 467-476. https://doi.org/10.3201/eid3103.241634.

Influenza A(H5N1) Immune Response among Ferrets with Influenza A(H1N1)pdm09 Immunity [PDF - 1.90 MB - 11 pages]
V. Le Sage et al.

The emergence of highly pathogenic avian influenza A(H5N1) virus in dairy cattle herds across the United States in 2024 caused several human infections. Understanding the risk for spillover infections into humans is crucial for protecting public health. We investigated whether immunity from influenza A(H1N1)pdm09 (pH1N1) virus would provide protection from death and severe clinical disease among ferrets intranasally infected with H5N1 virus from dairy cows from the 2024 outbreak. We observed differential tissue tropism among pH1N1-immune ferrets. pH1N1-immune ferrets also had little H5N1 viral dissemination to organs outside the respiratory tract and much less H5N1 virus in nasal secretions and the respiratory tract than naive ferrets. In addition, ferrets with pH1N1 immunity produced antibodies that cross-reacted with H5N1 neuraminidase protein. Taken together, our results suggest that humans with immunity to human seasonal influenza viruses may experience milder disease from the 2024 influenza A(H5N1) virus strain.

EID Le Sage V, Werner BD, Merrbach GA, Petnuch SE, O’Connell AK, Simmons HC, et al. Influenza A(H5N1) Immune Response among Ferrets with Influenza A(H1N1)pdm09 Immunity. Emerg Infect Dis. 2025;31(3):477-487. https://doi.org/10.3201/eid3103.241485
AMA Le Sage V, Werner BD, Merrbach GA, et al. Influenza A(H5N1) Immune Response among Ferrets with Influenza A(H1N1)pdm09 Immunity. Emerging Infectious Diseases. 2025;31(3):477-487. doi:10.3201/eid3103.241485.
APA Le Sage, V., Werner, B. D., Merrbach, G. A., Petnuch, S. E., O’Connell, A. K., Simmons, H. C....Lakdawala, S. S. (2025). Influenza A(H5N1) Immune Response among Ferrets with Influenza A(H1N1)pdm09 Immunity. Emerging Infectious Diseases, 31(3), 477-487. https://doi.org/10.3201/eid3103.241485.

Postelimination Cluster of Lymphatic Filariasis, Futuna, 2024 [PDF - 1.24 MB - 9 pages]
C. Couteaux et al.

After detection of 2 clinical lymphatic filariasis (LF) cases in a postelimination context in 2023 on the island of Futuna (Wallis and Futuna archipelago), the Wallis and Futuna Health Agency conducted a LF prevalence survey in Futuna in May 2024. This cross-sectional study, carried out among schoolchildren <18 years of age, identified 5 children with antigenemia, indicating an estimated antigenemia prevalence in Futuna children nearing 2%. The study also confirmed a spatial cluster of cases in the village of Taoa, where the child antigenemia prevalence reached 7.5% (95% CI 2.1%–18.2%), and demonstrated a link between infection and traditional housing. We observed microfilariae in contact cases during secondary investigations. These findings suggest resurgence of LF in a postelimination context, in which the expected child antigenemia prevalence should not exceed 1%. This situation should prompt a new mass drug administration campaign using triple therapy and the reinforcement of epidemiologic and entomologic surveillance.

EID Couteaux C, Demaneuf T, Bien L, Munoz M, Worms B, Chésimar S, et al. Postelimination Cluster of Lymphatic Filariasis, Futuna, 2024. Emerg Infect Dis. 2025;31(3):488-496. https://doi.org/10.3201/eid3103.241317
AMA Couteaux C, Demaneuf T, Bien L, et al. Postelimination Cluster of Lymphatic Filariasis, Futuna, 2024. Emerging Infectious Diseases. 2025;31(3):488-496. doi:10.3201/eid3103.241317.
APA Couteaux, C., Demaneuf, T., Bien, L., Munoz, M., Worms, B., Chésimar, S....Goarant, C. (2025). Postelimination Cluster of Lymphatic Filariasis, Futuna, 2024. Emerging Infectious Diseases, 31(3), 488-496. https://doi.org/10.3201/eid3103.241317.

Model-Based Analysis of Impact, Costs, and Cost-effectiveness of Tuberculosis Outbreak Investigations, United States [PDF - 1.32 MB - 10 pages]
S. Shrestha et al.

Outbreak investigation is an essential component of tuberculosis (TB) control in the United States, but its epidemiologic impact and cost-effectiveness have not been quantified. We modeled outbreak investigation activities in the United States during 2023–2032 and estimated corresponding epidemiologic impact, economic costs (in 2022 US$), and incremental cost-effectiveness ratios from the healthcare system perspective (cost per additional quality-adjusted life-year gained). We projected that outbreak investigations would result in 1,030,000 (95% uncertainty interval [UI] 376,000–1,740,000) contacts investigated, leading to 4,130 (95% UI 1,420–7,640) TB diagnoses and 104,000 (95% UI 37,600–181,000) latent TB infection diagnoses, at a total cost of US $219 million (95% UI $80–$387 million). We estimated that 5,560 (95% UI 1,720–11,400) TB cases would be averted through early detection and treatment, and the incremental cost-effectiveness of outbreak investigations, compared with no outbreak investigations, was $27,800 per quality-adjusted life-year gained (95% UI $4,580–$68,700).

EID Shrestha S, Cilloni L, Asay G, Kammerer J, Raz K, Shaw T, et al. Model-Based Analysis of Impact, Costs, and Cost-effectiveness of Tuberculosis Outbreak Investigations, United States. Emerg Infect Dis. 2025;31(3):497-506. https://doi.org/10.3201/eid3103.240633
AMA Shrestha S, Cilloni L, Asay G, et al. Model-Based Analysis of Impact, Costs, and Cost-effectiveness of Tuberculosis Outbreak Investigations, United States. Emerging Infectious Diseases. 2025;31(3):497-506. doi:10.3201/eid3103.240633.
APA Shrestha, S., Cilloni, L., Asay, G., Kammerer, J., Raz, K., Shaw, T....Dowdy, D. (2025). Model-Based Analysis of Impact, Costs, and Cost-effectiveness of Tuberculosis Outbreak Investigations, United States. Emerging Infectious Diseases, 31(3), 497-506. https://doi.org/10.3201/eid3103.240633.

Mycobacterium nebraskense Isolated from Patients in Connecticut and Oregon, USA [PDF - 2.36 MB - 9 pages]
M. L. Metersky et al.

Mycobacterium nebraskense infection is rarely encountered; only 7 human cases have been reported worldwide since the initial report of 5 cases in Nebraska, USA, in 2004. We report 9 patients from Connecticut and 2 from Oregon, USA, who had M. nebraskense isolated from respiratory secretions; 7 patients met the American Thoracic Society/Infectious Diseases Society of America criteria for nontuberculous mycobacterial pulmonary disease. In 4 cases, the organism was isolated 1 time and caused brief or no symptoms. Most cases in Connecticut were reported after 2017. Antimicrobial drug susceptibility testing of 6 isolates showed clarithromycin susceptibility. In 2 cases, infection was refractory to treatment. The 9 Connecticut patients lived in 8 different towns; thus, a common water supply did not explain the high frequency of M. nebraskense isolation. M. nebraskense is a clinically significant cause of nontuberculous mycobacterial pulmonary disease in Connecticut; continued surveillance will be needed to determine its frequency and optimum treatment.

EID Metersky ML, Losier AJ, Fraulino DA, Warnock TA, Varley CD, Le AM, et al. Mycobacterium nebraskense Isolated from Patients in Connecticut and Oregon, USA. Emerg Infect Dis. 2025;31(3):507-515. https://doi.org/10.3201/eid3103.240608
AMA Metersky ML, Losier AJ, Fraulino DA, et al. Mycobacterium nebraskense Isolated from Patients in Connecticut and Oregon, USA. Emerging Infectious Diseases. 2025;31(3):507-515. doi:10.3201/eid3103.240608.
APA Metersky, M. L., Losier, A. J., Fraulino, D. A., Warnock, T. A., Varley, C. D., Le, A. M....Khare, R. (2025). Mycobacterium nebraskense Isolated from Patients in Connecticut and Oregon, USA. Emerging Infectious Diseases, 31(3), 507-515. https://doi.org/10.3201/eid3103.240608.

Genomic Characterization of Circulating Dengue Virus, Ethiopia, 2022–2023 [PDF - 1.30 MB - 10 pages]
A. Abera et al.

In Ethiopia, dengue virus (DENV) infections have been reported in several regions; however, little is known about the genetic diversity of circulating viruses. We conducted clinical surveillance of DENV during the 2023 nationwide outbreak in Ethiopia. We enrolled patients at 3 sentinel hospital sites. Using reverse transcription PCR, we screened serum samples for 3 arboviruses and then serotyped and whole-genome sequenced DENV-positive samples. We detected DENV-1 and DENV-3 serotypes. Phylogenetic analysis identified 1 transmission cluster for DENV-1 (genotype III major lineage A) and 2 clusters for DENV-3 (genotype III major lineage B). The first DENV-3 cluster was closely related to an isolate from a 2023 dengue outbreak in Italy; the second cluster was related to isolates from India. Co-circulation of DENV-1 and DENV-3 in Ethiopia highlights the potential for severe dengue. Intensified surveillance and coordinated public health responses are needed to address the threat of severe dengue outbreaks.

EID Abera A, Tegally H, Tasew G, Wilkinson E, Ali A, Regasa F, et al. Genomic Characterization of Circulating Dengue Virus, Ethiopia, 2022–2023. Emerg Infect Dis. 2025;31(3):516-525. https://doi.org/10.3201/eid3103.240996
AMA Abera A, Tegally H, Tasew G, et al. Genomic Characterization of Circulating Dengue Virus, Ethiopia, 2022–2023. Emerging Infectious Diseases. 2025;31(3):516-525. doi:10.3201/eid3103.240996.
APA Abera, A., Tegally, H., Tasew, G., Wilkinson, E., Ali, A., Regasa, F....de Oliveira, T. (2025). Genomic Characterization of Circulating Dengue Virus, Ethiopia, 2022–2023. Emerging Infectious Diseases, 31(3), 516-525. https://doi.org/10.3201/eid3103.240996.

High Prevalence of atpE Mutations in Bedaquiline-Resistant Mycobacterium tuberculosis Isolates, Russia [PDF - 1.22 MB - 10 pages]
D. Zimenkov et al.

Bedaquiline is a cornerstone drug for treating drug-resistant tuberculosis. We analyzed 11 isolates from 9 patients who were treated with a bedaquiline-based regimen and remained culture-positive long after treatment start. In 4 of 8 resistant isolates, we found substitutions in AtpE, which encodes subunit c of the Mycobacterium tuberculosis ATP synthase and is rarely identified in clinical isolates. We found Ile66Met and Glu61Asp substitutions in 2 cases each. Additional mutations in mmpL5, mmpL4, and atpB genes could affect the susceptibility to bedaquiline. MmpL5(Asn772Thr) emerged during bedaquiline treatment, whereas AtpB(Val165Leu) was found in 1 case simultaneously with the loss-of-function mmpR5 mutation in a susceptible strain. The loss-of-function mutation in the mmpL4 efflux gene was identified in the mixed state, pointing to ongoing selection in a bedaquiline-resistant isolate. Another case of the emergence of the mmpL4 mutation, accompanied by a proportional increase in bedaquiline MIC, was identified by retrospective analysis of genomes from bedaquiline-resistant isolates.

EID Zimenkov D, Ushtanit A, Gordeeva E, Guselnikova E, Schwartz Y, Stavitskaya N. High Prevalence of atpE Mutations in Bedaquiline-Resistant Mycobacterium tuberculosis Isolates, Russia. Emerg Infect Dis. 2025;31(3):525-536. https://doi.org/10.3201/eid3103.241488
AMA Zimenkov D, Ushtanit A, Gordeeva E, et al. High Prevalence of atpE Mutations in Bedaquiline-Resistant Mycobacterium tuberculosis Isolates, Russia. Emerging Infectious Diseases. 2025;31(3):525-536. doi:10.3201/eid3103.241488.
APA Zimenkov, D., Ushtanit, A., Gordeeva, E., Guselnikova, E., Schwartz, Y., & Stavitskaya, N. (2025). High Prevalence of atpE Mutations in Bedaquiline-Resistant Mycobacterium tuberculosis Isolates, Russia. Emerging Infectious Diseases, 31(3), 525-536. https://doi.org/10.3201/eid3103.241488.

A 28-Year Multicenter Cohort Study of Nontuberculous Mycobacterial Lymphadenitis in Children, Spain [PDF - 1.33 MB - 11 pages]
A. Martínez-Planas et al.

We describe the epidemiology, diagnosis, and management of nontuberculous mycobacterial lymphadenitis cases detailed in a 28-year (1996–2023) multicenter cohort from Spain. The case numbers remained stable during the initial prospective phase (2013–2020), but a sharp decline was observed during 2021–2022. Disease onset occurred during spring or June in 45.9% of cases. Mycobacterium avium complex (43.1%) and M. lentiflavum (39.9%) were the most common species detected. M. lentiflavum affected mostly younger children from central Spain. The most common treatment strategy was complete surgical resection with (n = 80) or without (n = 88) antimicrobial drug treatment, followed by antimicrobial drugs alone (n = 76). Facial palsy developed in 10.4% of surgical cases. Adverse events because of antimicrobial drugs were uncommon. New fistula formation during follow-up occurred more in children managed with observation alone than in those treated with antimicrobial drugs alone (relative risk 2.7 [95% CI 1.3–5.3]; p = 0.014).

EID Martínez-Planas A, Baquero-Artigao F, Méndez-Echevarría A, Del Rosal T, Rodríguez-Molino P, Toro-Rueda C, et al. A 28-Year Multicenter Cohort Study of Nontuberculous Mycobacterial Lymphadenitis in Children, Spain. Emerg Infect Dis. 2025;31(3):536-546. https://doi.org/10.3201/eid3103.241254
AMA Martínez-Planas A, Baquero-Artigao F, Méndez-Echevarría A, et al. A 28-Year Multicenter Cohort Study of Nontuberculous Mycobacterial Lymphadenitis in Children, Spain. Emerging Infectious Diseases. 2025;31(3):536-546. doi:10.3201/eid3103.241254.
APA Martínez-Planas, A., Baquero-Artigao, F., Méndez-Echevarría, A., Del Rosal, T., Rodríguez-Molino, P., Toro-Rueda, C....Noguera-Julian, A. (2025). A 28-Year Multicenter Cohort Study of Nontuberculous Mycobacterial Lymphadenitis in Children, Spain. Emerging Infectious Diseases, 31(3), 536-546. https://doi.org/10.3201/eid3103.241254.

Diphtheria Outbreak among Persons Experiencing Homelessness, 2023, Linked to 2022 Diphtheria Outbreak, Frankfurt am Main, Germany [PDF - 805 KB - 8 pages]
J. Haller et al.

After 3 cases of Corynebacterium diphtheriae infection associated with intravenous drug use among persons experiencing homelessness (PEH) were reported to the Health Protection Authority in Frankfurt am Main, Germany, in 2023, we examined pathogen spread among PEH. Furthermore, we investigated a possible link with the 2022 outbreak of diphtheria in Europe. From swab samples collected during August–November 2023 from 36 PEH and cutaneous lesions, we detected 3 additional cases of cutaneous toxigenic C. diphtheriae. Sequence type 574 was identified in 5 case-isolates and is genetically associated with 1 of the predominant clusters in identified in the 2022 outbreak. Our findings demonstrate the need for increased detection and monitoring of cutaneous diphtheria and boosting immunity against diphtheria in groups with increased risk for infection. Genomic analyses are valuable for identifying genetic relationships between outbreaks, even when epidemiologic data are scarce.

EID Haller J, Berger A, Dangel A, Bengs K, Friedrichs I, Kleine C, et al. Diphtheria Outbreak among Persons Experiencing Homelessness, 2023, Linked to 2022 Diphtheria Outbreak, Frankfurt am Main, Germany. Emerg Infect Dis. 2025;31(3):547-554. https://doi.org/10.3201/eid3103.241217
AMA Haller J, Berger A, Dangel A, et al. Diphtheria Outbreak among Persons Experiencing Homelessness, 2023, Linked to 2022 Diphtheria Outbreak, Frankfurt am Main, Germany. Emerging Infectious Diseases. 2025;31(3):547-554. doi:10.3201/eid3103.241217.
APA Haller, J., Berger, A., Dangel, A., Bengs, K., Friedrichs, I., Kleine, C....Sing, A. (2025). Diphtheria Outbreak among Persons Experiencing Homelessness, 2023, Linked to 2022 Diphtheria Outbreak, Frankfurt am Main, Germany. Emerging Infectious Diseases, 31(3), 547-554. https://doi.org/10.3201/eid3103.241217.
Dispatches

Macrolide-Resistant Mycoplasma pneumoniae Infections among Children after COVID-19 Pandemic, Ohio, USA [PDF - 479 KB - 4 pages]
A. L. Leber et al.

Mycoplasma pneumoniae infections decreased in Ohio, USA, during the COVID-19 pandemic but reemerged in 2023; >2,000 cases were reported during September 2023­–September 2024. Of 995 M. pneumoniae–positive samples, 24 (2.4%) had mutations for macrolide-resistant M. pneumoniae (MRMp). MRMp rates are low but increasing. MRMp surveillance is crucial for monitoring antimicrobial resistance.

EID Leber AL, Embry T, Everhart K, Taveras J, Oyeniran SJ, Wang H. Macrolide-Resistant Mycoplasma pneumoniae Infections among Children after COVID-19 Pandemic, Ohio, USA. Emerg Infect Dis. 2025;31(3):555-558. https://doi.org/10.3201/eid3103.241570
AMA Leber AL, Embry T, Everhart K, et al. Macrolide-Resistant Mycoplasma pneumoniae Infections among Children after COVID-19 Pandemic, Ohio, USA. Emerging Infectious Diseases. 2025;31(3):555-558. doi:10.3201/eid3103.241570.
APA Leber, A. L., Embry, T., Everhart, K., Taveras, J., Oyeniran, S. J., & Wang, H. (2025). Macrolide-Resistant Mycoplasma pneumoniae Infections among Children after COVID-19 Pandemic, Ohio, USA. Emerging Infectious Diseases, 31(3), 555-558. https://doi.org/10.3201/eid3103.241570.

Simultaneous Detection of Sarcocystis hominis, S. heydorni, and S. sigmoideus in Human Intestinal Sarcocystosis, France, 2021–2024 [PDF - 762 KB - 5 pages]
M. Moniot et al.

To elucidate the epidemiology of Sarcocystis spp. parasites in human intestinal infections, we used high-throughput sequencing to investigate human intestinal sarcocystosis cases identified by microscopy in France during 2021–2024. Our results indicate that humans are a definitive host of S. sigmoideus parasites and that occurrence of multiple species in 1 patient is common.

EID Moniot M, Combes P, Costa D, Argy N, Durieux M, Nicol T, et al. Simultaneous Detection of Sarcocystis hominis, S. heydorni, and S. sigmoideus in Human Intestinal Sarcocystosis, France, 2021–2024. Emerg Infect Dis. 2025;31(3):559-563. https://doi.org/10.3201/eid3103.241640
AMA Moniot M, Combes P, Costa D, et al. Simultaneous Detection of Sarcocystis hominis, S. heydorni, and S. sigmoideus in Human Intestinal Sarcocystosis, France, 2021–2024. Emerging Infectious Diseases. 2025;31(3):559-563. doi:10.3201/eid3103.241640.
APA Moniot, M., Combes, P., Costa, D., Argy, N., Durieux, M., Nicol, T....Poirier, P. (2025). Simultaneous Detection of Sarcocystis hominis, S. heydorni, and S. sigmoideus in Human Intestinal Sarcocystosis, France, 2021–2024. Emerging Infectious Diseases, 31(3), 559-563. https://doi.org/10.3201/eid3103.241640.

National Active Case-Finding Program for Tuberculosis in Prisons, Peru, 2024 [PDF - 1.01 MB - 5 pages]
E. Jung et al.

During January–September 2024, a national active case-finding program in Peru’s prisons screened >38,000 persons for tuberculosis (TB) using chest radiography with automated interpretation and rapid molecular tests. The program found high percentages of TB, rifampin-resistant TB, and asymptomatic infections, demonstrating the urgent need for systematic screening among incarcerated populations.

EID Jung E, Alarcón VA, Solís Tupes W, Avalos-Cruz T, Tovar M, Abregu E, et al. National Active Case-Finding Program for Tuberculosis in Prisons, Peru, 2024. Emerg Infect Dis. 2025;31(3):564-568. https://doi.org/10.3201/eid3103.241727
AMA Jung E, Alarcón VA, Solís Tupes W, et al. National Active Case-Finding Program for Tuberculosis in Prisons, Peru, 2024. Emerging Infectious Diseases. 2025;31(3):564-568. doi:10.3201/eid3103.241727.
APA Jung, E., Alarcón, V. A., Solís Tupes, W., Avalos-Cruz, T., Tovar, M., Abregu, E....Huaman, M. A. (2025). National Active Case-Finding Program for Tuberculosis in Prisons, Peru, 2024. Emerging Infectious Diseases, 31(3), 564-568. https://doi.org/10.3201/eid3103.241727.

Mycobacterium ulcerans in Possum Feces before Emergence in Humans, Australia [PDF - 1.99 MB - 5 pages]
B. J. McNamara et al.

We describe emergence of Buruli ulcer in urban Geelong, Victoria, Australia, and examine timing and proximity of human cases to detection of Mycobacterium ulcerans DNA in possum feces. M. ulcerans–positive feces preceded human cases by up to 39 months, constituting an early warning of impending risk for Buruli ulcer.

EID McNamara BJ, Cornish J, Blasdell KR, Athan E, Clarke NE, Pe T, et al. Mycobacterium ulcerans in Possum Feces before Emergence in Humans, Australia. Emerg Infect Dis. 2025;31(3):569-573. https://doi.org/10.3201/eid3103.240657
AMA McNamara BJ, Cornish J, Blasdell KR, et al. Mycobacterium ulcerans in Possum Feces before Emergence in Humans, Australia. Emerging Infectious Diseases. 2025;31(3):569-573. doi:10.3201/eid3103.240657.
APA McNamara, B. J., Cornish, J., Blasdell, K. R., Athan, E., Clarke, N. E., Pe, T....O’Brien, D. P. (2025). Mycobacterium ulcerans in Possum Feces before Emergence in Humans, Australia. Emerging Infectious Diseases, 31(3), 569-573. https://doi.org/10.3201/eid3103.240657.

Extended-Spectrum β-Lactamase–Producing Enterobacterales in Municipal Wastewater Collections, Switzerland, 2019–2023 [PDF - 1.25 MB - 5 pages]
L. Aguilar-Bultet et al.

We quantified presumptive extended-spectrum β-lactamase–producing Escherichia coli and Klebsiella, Enterobacter, Serratia, and Citrobacter group colonies from wastewater in Basel, Switzerland, across 3 years to represent before, during, and after the COVID-19 pandemic. Wastewater surveillance might be a noninvasive, sensitive, rapid, and cost-effective instrument for early detection and monitoring local epidemiology.

EID Aguilar-Bultet L, Gómez-Sanz E, García-Martín AB, Hug M, Furger R, Eichenberger L, et al. Extended-Spectrum β-Lactamase–Producing Enterobacterales in Municipal Wastewater Collections, Switzerland, 2019–2023. Emerg Infect Dis. 2025;31(3):574-578. https://doi.org/10.3201/eid3103.240099
AMA Aguilar-Bultet L, Gómez-Sanz E, García-Martín AB, et al. Extended-Spectrum β-Lactamase–Producing Enterobacterales in Municipal Wastewater Collections, Switzerland, 2019–2023. Emerging Infectious Diseases. 2025;31(3):574-578. doi:10.3201/eid3103.240099.
APA Aguilar-Bultet, L., Gómez-Sanz, E., García-Martín, A. B., Hug, M., Furger, R., Eichenberger, L....Tschudin-Sutter, S. (2025). Extended-Spectrum β-Lactamase–Producing Enterobacterales in Municipal Wastewater Collections, Switzerland, 2019–2023. Emerging Infectious Diseases, 31(3), 574-578. https://doi.org/10.3201/eid3103.240099.

Haemophilus influenzae Type b Meningitis in Infants, New York, New York, USA, 2022–2023 [PDF - 1.03 MB - 4 pages]
A. Ewing et al.

Two unvaccinated infants residing in the same borough of New York, New York, USA, had Haemophilus influenzae type b meningitis develop 1 year apart. Whole-genome sequencing and phylogenetic analysis revealed the isolates shared a previously undescribed multilocus sequence type and were more closely related to each other than to other sequenced strains.

EID Ewing A, Haldeman S, Job MJ, Otto C, Ratner AJ. Haemophilus influenzae Type b Meningitis in Infants, New York, New York, USA, 2022–2023. Emerg Infect Dis. 2025;31(3):579-582. https://doi.org/10.3201/eid3103.240946
AMA Ewing A, Haldeman S, Job MJ, et al. Haemophilus influenzae Type b Meningitis in Infants, New York, New York, USA, 2022–2023. Emerging Infectious Diseases. 2025;31(3):579-582. doi:10.3201/eid3103.240946.
APA Ewing, A., Haldeman, S., Job, M. J., Otto, C., & Ratner, A. J. (2025). Haemophilus influenzae Type b Meningitis in Infants, New York, New York, USA, 2022–2023. Emerging Infectious Diseases, 31(3), 579-582. https://doi.org/10.3201/eid3103.240946.

Meningococcal Sepsis in Patient with Paroxysmal Nocturnal Hemoglobinuria during Pegcetacoplan Therapy [PDF - 623 KB - 4 pages]
L. Starck et al.

Complement C5 inhibitors bring an increased risk for Neisseria infections. A novel complement C3 inhibitor, pegcetacoplan, was recently approved to treat paroxysmal nocturnal hemoglobinuria, a condition commonly treated with complement C5 inhibitors. We present a case of meningococcal sepsis in a pegcetacoplan-treated patient with aplastic anemia and paroxysmal nocturnal hemoglobinuria.

EID Starck L, Nummi V, Poikonen E, Lehtinen A, Kivelä P, Friberg N, et al. Meningococcal Sepsis in Patient with Paroxysmal Nocturnal Hemoglobinuria during Pegcetacoplan Therapy. Emerg Infect Dis. 2025;31(3):583-586. https://doi.org/10.3201/eid3103.241182
AMA Starck L, Nummi V, Poikonen E, et al. Meningococcal Sepsis in Patient with Paroxysmal Nocturnal Hemoglobinuria during Pegcetacoplan Therapy. Emerging Infectious Diseases. 2025;31(3):583-586. doi:10.3201/eid3103.241182.
APA Starck, L., Nummi, V., Poikonen, E., Lehtinen, A., Kivelä, P., Friberg, N....Meri, S. (2025). Meningococcal Sepsis in Patient with Paroxysmal Nocturnal Hemoglobinuria during Pegcetacoplan Therapy. Emerging Infectious Diseases, 31(3), 583-586. https://doi.org/10.3201/eid3103.241182.

Donor-Derived Ehrlichiosis Caused by Ehrlichia chaffeensis from Living Donor Kidney Transplant [PDF - 1.22 MB - 4 pages]
M. J. Scolarici et al.

Tickborne infections are challenging to diagnose, particularly among solid organ transplant recipients. We report a US case of donor-derived ehrlichiosis from a living kidney donation that highlights how screening for living donors may miss tickborne infections. Clinicians should consider the epidemiology of the donor when screening donations and evaluating recipients for donor-derived infection.

EID Scolarici MJ, Kuehler D, Osborn R, Doyle A, Schiffman EK, Garvin A, et al. Donor-Derived Ehrlichiosis Caused by Ehrlichia chaffeensis from Living Donor Kidney Transplant. Emerg Infect Dis. 2025;31(3):587-590. https://doi.org/10.3201/eid3103.241723
AMA Scolarici MJ, Kuehler D, Osborn R, et al. Donor-Derived Ehrlichiosis Caused by Ehrlichia chaffeensis from Living Donor Kidney Transplant. Emerging Infectious Diseases. 2025;31(3):587-590. doi:10.3201/eid3103.241723.
APA Scolarici, M. J., Kuehler, D., Osborn, R., Doyle, A., Schiffman, E. K., Garvin, A....Odorico, J. (2025). Donor-Derived Ehrlichiosis Caused by Ehrlichia chaffeensis from Living Donor Kidney Transplant. Emerging Infectious Diseases, 31(3), 587-590. https://doi.org/10.3201/eid3103.241723.

Cefotaxime-Resistant Neisseria meningitidis Sequence Type 4821 Causing Fulminant Meningitis [PDF - 1.50 MB - 5 pages]
Y. Shao et al.

We explored the role of commensal Neisseria in the emergence of third-generation cephalosporin-resistant N. meningitidis. Cefotaxime resistance–conferring penA795 was prevalent among commensal Neisseria isolates in Shanghai, China, and was acquired by a serogroup C quinolone-resistant sequence type 4821 N. meningitidis, Nm507, causing fulminant meningitis in an unvaccinated 2-year-old child.

EID Shao Y, Chen M, Cai J, Doi Y, Chen M, Wang M, et al. Cefotaxime-Resistant Neisseria meningitidis Sequence Type 4821 Causing Fulminant Meningitis. Emerg Infect Dis. 2025;31(3):591-595. https://doi.org/10.3201/eid3103.241493
AMA Shao Y, Chen M, Cai J, et al. Cefotaxime-Resistant Neisseria meningitidis Sequence Type 4821 Causing Fulminant Meningitis. Emerging Infectious Diseases. 2025;31(3):591-595. doi:10.3201/eid3103.241493.
APA Shao, Y., Chen, M., Cai, J., Doi, Y., Chen, M., Wang, M....Guo, Q. (2025). Cefotaxime-Resistant Neisseria meningitidis Sequence Type 4821 Causing Fulminant Meningitis. Emerging Infectious Diseases, 31(3), 591-595. https://doi.org/10.3201/eid3103.241493.

Tsukamurella tyrosinosolvens Respiratory Infection in Immunocompetent Man [PDF - 753 KB - 4 pages]
A. Clifford et al.

Tsukamurella spp. are an infrequent and underdiagnosed cause of bacterial respiratory infection, usually occurring in patients with structural lung disease or immune compromise. We describe T. tyrosinosolvens respiratory infection in a patient in Australia without structural lung disease or known immune deficiency. The patient was successfully treated with oral ciprofloxacin and clarithromycin.

EID Clifford A, Wong J, Aw-Yeong B, Lea K, Globan M, Smith B. Tsukamurella tyrosinosolvens Respiratory Infection in Immunocompetent Man. Emerg Infect Dis. 2025;31(3):596-599. https://doi.org/10.3201/eid3103.241365
AMA Clifford A, Wong J, Aw-Yeong B, et al. Tsukamurella tyrosinosolvens Respiratory Infection in Immunocompetent Man. Emerging Infectious Diseases. 2025;31(3):596-599. doi:10.3201/eid3103.241365.
APA Clifford, A., Wong, J., Aw-Yeong, B., Lea, K., Globan, M., & Smith, B. (2025). Tsukamurella tyrosinosolvens Respiratory Infection in Immunocompetent Man. Emerging Infectious Diseases, 31(3), 596-599. https://doi.org/10.3201/eid3103.241365.

Outbreak Caused by Multidrug-Resistant Mycobacterium Tuberculosis with Unusual Combination of Resistance Mutations, Northern Argentina, 2006–2022 [PDF - 1.21 MB - 6 pages]
R. Paul et al.

To reconstruct transmission chains of the multidrug-resistant tuberculosis Ch strain, which harbors a unique combination of resistance mutations, we analyzed genomes of 25 isolates from 12 patients with diagnosis during 2006–2022 in Chaco Province, Argentina. Amplification of resistance, high mortality rates, and indications of a wider outbreak raise concerns for surveillance programs.

EID Paul R, Lorenzo F, López B, Alegre M, Couvin D, Rastogi N, et al. Outbreak Caused by Multidrug-Resistant Mycobacterium Tuberculosis with Unusual Combination of Resistance Mutations, Northern Argentina, 2006–2022. Emerg Infect Dis. 2025;31(3):601-606. https://doi.org/10.3201/eid3103.241272
AMA Paul R, Lorenzo F, López B, et al. Outbreak Caused by Multidrug-Resistant Mycobacterium Tuberculosis with Unusual Combination of Resistance Mutations, Northern Argentina, 2006–2022. Emerging Infectious Diseases. 2025;31(3):601-606. doi:10.3201/eid3103.241272.
APA Paul, R., Lorenzo, F., López, B., Alegre, M., Couvin, D., Rastogi, N....Yokobori, N. (2025). Outbreak Caused by Multidrug-Resistant Mycobacterium Tuberculosis with Unusual Combination of Resistance Mutations, Northern Argentina, 2006–2022. Emerging Infectious Diseases, 31(3), 601-606. https://doi.org/10.3201/eid3103.241272.
Research Letters

Fluoroquinolone Resistance in Drug-Resistant Tuberculosis, Kharkiv, Ukraine, 2019–2023 [PDF - 312 KB - 3 pages]
O. Konstantynovska et al.

Rifampin-resistant Mycobacterium tuberculosis was identified by the World Health Organization as a pathogen of public health critical importance. During 2014–2023, an increase in fluoroquinolone resistance in rifampin-resistant M. tuberculosis from Kharkiv, Ukraine, was observed. Efforts to mitigate factors contributing to resistance should be prioritized to prevent further escalation of that threat.

EID Konstantynovska O, Synenko T, Honcharenko A, Volobuieva O, Liadova T, Reimann M, et al. Fluoroquinolone Resistance in Drug-Resistant Tuberculosis, Kharkiv, Ukraine, 2019–2023. Emerg Infect Dis. 2025;31(3):615-617. https://doi.org/10.3201/eid3103.241675
AMA Konstantynovska O, Synenko T, Honcharenko A, et al. Fluoroquinolone Resistance in Drug-Resistant Tuberculosis, Kharkiv, Ukraine, 2019–2023. Emerging Infectious Diseases. 2025;31(3):615-617. doi:10.3201/eid3103.241675.
APA Konstantynovska, O., Synenko, T., Honcharenko, A., Volobuieva, O., Liadova, T., Reimann, M....Chesov, D. (2025). Fluoroquinolone Resistance in Drug-Resistant Tuberculosis, Kharkiv, Ukraine, 2019–2023. Emerging Infectious Diseases, 31(3), 615-617. https://doi.org/10.3201/eid3103.241675.

Neurosarcocystosis in Patient with HIV-Induced Immunodeficiency [PDF - 638 KB - 3 pages]
T. Skarpengland et al.

Sarcocystis is a genus of protozoan parasites that can infect various vertebrates. In humans, Sarcocystis infection usually is asymptomatic but might manifest as a mild gastroenteritis or extraintestinal myositis. We report a case of human central nervous system infection in Norway caused by S. nesbitti parasites.

EID Skarpengland T, Tveita AA, Berntsen CF, Christensen EE, Macpherson ME, Stiksrud B, et al. Neurosarcocystosis in Patient with HIV-Induced Immunodeficiency. Emerg Infect Dis. 2025;31(3):617-619. https://doi.org/10.3201/eid3103.241361
AMA Skarpengland T, Tveita AA, Berntsen CF, et al. Neurosarcocystosis in Patient with HIV-Induced Immunodeficiency. Emerging Infectious Diseases. 2025;31(3):617-619. doi:10.3201/eid3103.241361.
APA Skarpengland, T., Tveita, A. A., Berntsen, C. F., Christensen, E. E., Macpherson, M. E., Stiksrud, B....Pettersen, F. (2025). Neurosarcocystosis in Patient with HIV-Induced Immunodeficiency. Emerging Infectious Diseases, 31(3), 617-619. https://doi.org/10.3201/eid3103.241361.

Lack of Competence of US Mosquito Species for Circulating Oropouche Virus [PDF - 303 KB - 3 pages]
A. F. Payne et al.

Given recent outbreaks of Oropouche virus in Latin America and >100 confirmed travel-associated cases in the United States, we evaluated the competence of US vectors, including Aedes albopictus, Culex quinquefasciatus, Culex pipiens, and Anopheles quadrimaculatus mosquitoes. Results with historic and recent isolates suggest transmission potential for those species is low.

EID Payne AF, Stout J, Dumoulin P, Locksmith T, Heberlein LA, Mitchell M, et al. Lack of Competence of US Mosquito Species for Circulating Oropouche Virus. Emerg Infect Dis. 2025;31(3):619-621. https://doi.org/10.3201/eid3103.241886
AMA Payne AF, Stout J, Dumoulin P, et al. Lack of Competence of US Mosquito Species for Circulating Oropouche Virus. Emerging Infectious Diseases. 2025;31(3):619-621. doi:10.3201/eid3103.241886.
APA Payne, A. F., Stout, J., Dumoulin, P., Locksmith, T., Heberlein, L. A., Mitchell, M....Ciota, A. T. (2025). Lack of Competence of US Mosquito Species for Circulating Oropouche Virus. Emerging Infectious Diseases, 31(3), 619-621. https://doi.org/10.3201/eid3103.241886.

Urban Coatis (Nasua nasua) Exposure to Alphainfluenzavirus influenzae [PDF - 1.04 MB - 4 pages]
B. de Campos et al.

We detected neutralizing antibodies, viral RNA, and sialic acid receptors for Alphainfluenzavirus influenzae in urban coatis (Nasua nasua) in Brazil, suggesting exposure and susceptibility. We used hemagglutination inhibition, reverse transcription quantitative PCR, and histochemistry for detection. Increased epidemiologic wildlife surveillance would improve influenza A emergency event response.

EID de Campos B, de Souza Joaquim J, Hemetrio N, de Almeida L, Lima P, Galinari G, et al. Urban Coatis (Nasua nasua) Exposure to Alphainfluenzavirus influenzae. Emerg Infect Dis. 2025;31(3):621-624. https://doi.org/10.3201/eid3103.231640
AMA de Campos B, de Souza Joaquim J, Hemetrio N, et al. Urban Coatis (Nasua nasua) Exposure to Alphainfluenzavirus influenzae. Emerging Infectious Diseases. 2025;31(3):621-624. doi:10.3201/eid3103.231640.
APA de Campos, B., de Souza Joaquim, J., Hemetrio, N., de Almeida, L., Lima, P., Galinari, G....de Carvalho, M. (2025). Urban Coatis (Nasua nasua) Exposure to Alphainfluenzavirus influenzae. Emerging Infectious Diseases, 31(3), 621-624. https://doi.org/10.3201/eid3103.231640.

Identification of 2 Novel Species, Mycobacterium novusgordonae and M. shingordonae [PDF - 1.09 MB - 4 pages]
K. Hashimoto et al.

We identified 2 novel species, Mycobacterium novusgordonae and M. shingordonae, from sputum specimens of pulmonary disease patients in Japan. Genetic and biochemical analyses revealed a close relationship with M. paragordonae. One M. shingordonae case-patient experienced severe progressive infection, highlighting the variation in pathogenicity of the M. gordonae clade species.

EID Hashimoto K, Abe Y, Fukushima K, Matsumoto Y, Saito H, Akamine Y, et al. Identification of 2 Novel Species, Mycobacterium novusgordonae and M. shingordonae. Emerg Infect Dis. 2025;31(3):624-627. https://doi.org/10.3201/eid3103.240174
AMA Hashimoto K, Abe Y, Fukushima K, et al. Identification of 2 Novel Species, Mycobacterium novusgordonae and M. shingordonae. Emerging Infectious Diseases. 2025;31(3):624-627. doi:10.3201/eid3103.240174.
APA Hashimoto, K., Abe, Y., Fukushima, K., Matsumoto, Y., Saito, H., Akamine, Y....Kida, H. (2025). Identification of 2 Novel Species, Mycobacterium novusgordonae and M. shingordonae. Emerging Infectious Diseases, 31(3), 624-627. https://doi.org/10.3201/eid3103.240174.

Multidrug-Resistant Mycobacterium tuberculosis in a Community Hospital, Luanda, Angola [PDF - 297 KB - 3 pages]
N. M. Francisco et al.

In a longitudinal study in a first-level hospital in Luanda, Angola, we found rifampin-resistant and multidrug-resistant tuberculosis (TB) in 38 (8%, 95% CI 5.7–10.8) of 474 patients with no previous history of TB. Of note, 2 patients (0.4%, 95% CI 0.1–1.5) demonstrated pre–extensively drug-resistant TB.

EID Francisco NM, Gaviraghi A, Alladio F, Huits R, Carnielli B, Salvador E, et al. Multidrug-Resistant Mycobacterium tuberculosis in a Community Hospital, Luanda, Angola. Emerg Infect Dis. 2025;31(3):627-629. https://doi.org/10.3201/eid3103.241831
AMA Francisco NM, Gaviraghi A, Alladio F, et al. Multidrug-Resistant Mycobacterium tuberculosis in a Community Hospital, Luanda, Angola. Emerging Infectious Diseases. 2025;31(3):627-629. doi:10.3201/eid3103.241831.
APA Francisco, N. M., Gaviraghi, A., Alladio, F., Huits, R., Carnielli, B., Salvador, E....Gobbi, F. G. (2025). Multidrug-Resistant Mycobacterium tuberculosis in a Community Hospital, Luanda, Angola. Emerging Infectious Diseases, 31(3), 627-629. https://doi.org/10.3201/eid3103.241831.

Community-Acquired Pneumonia Caused by Avian Chlamydia abortus, the Netherlands [PDF - 1.08 MB - 4 pages]
J. Gooskens et al.

We report avian Chlamydia abortus pneumonia in an immunocompetent elderly patient in the Netherlands after environmental exposure to wild aquatic birds, including seabirds. New molecular surveillance studies are needed in wild and captive birds, as well as increased awareness to establish occurrence, clinical manifestations, and geographic distribution of this rare zoonotic disease.

EID Gooskens J, van Essen E, Kraakman M, Wörz P, Heddema ER, Boers SA. Community-Acquired Pneumonia Caused by Avian Chlamydia abortus, the Netherlands. Emerg Infect Dis. 2025;31(3):630-633. https://doi.org/10.3201/eid3103.241406
AMA Gooskens J, van Essen E, Kraakman M, et al. Community-Acquired Pneumonia Caused by Avian Chlamydia abortus, the Netherlands. Emerging Infectious Diseases. 2025;31(3):630-633. doi:10.3201/eid3103.241406.
APA Gooskens, J., van Essen, E., Kraakman, M., Wörz, P., Heddema, E. R., & Boers, S. A. (2025). Community-Acquired Pneumonia Caused by Avian Chlamydia abortus, the Netherlands. Emerging Infectious Diseases, 31(3), 630-633. https://doi.org/10.3201/eid3103.241406.

Evaluation of High-Dose Isoniazid in Multidrug-Resistant Tuberculosis Treatment [PDF - 407 KB - 3 pages]
V. Gerussi et al.

High-dose isoniazid is recommended to treat multidrug-resistant tuberculosis (MDR TB). Among 958 MDR TB isolates identified in France during 2008–2022, 93.1% exhibited high-level isoniazid resistance, and molecular testing showed limited diagnostic accuracy in predicting resistance. Clinicians should reconsider using high-dose isoniazid in MDR TB treatment because of suboptimal effect and toxicity concerns.

EID Gerussi V, Petersen T, Bonnet I, Aubry A, Bachir M, Gyde E, et al. Evaluation of High-Dose Isoniazid in Multidrug-Resistant Tuberculosis Treatment. Emerg Infect Dis. 2025;31(3):633-636. https://doi.org/10.3201/eid3103.241473
AMA Gerussi V, Petersen T, Bonnet I, et al. Evaluation of High-Dose Isoniazid in Multidrug-Resistant Tuberculosis Treatment. Emerging Infectious Diseases. 2025;31(3):633-636. doi:10.3201/eid3103.241473.
APA Gerussi, V., Petersen, T., Bonnet, I., Aubry, A., Bachir, M., Gyde, E....Guglielmetti, L. (2025). Evaluation of High-Dose Isoniazid in Multidrug-Resistant Tuberculosis Treatment. Emerging Infectious Diseases, 31(3), 633-636. https://doi.org/10.3201/eid3103.241473.

Annual Hospitalizations for COVID-19, Influenza, and Respiratory Syncytial Virus, United States, 2023–2024 [PDF - 591 KB - 3 pages]
K. Bi et al.

Projections for the US 2023–24 respiratory virus season indicated a 31% decrease to a 55% increase in hospitalizations for respiratory syncytial virus, influenza, and COVID-19 compared with 2022–23, depending on circulating variants and vaccination uptake. The projections captured the tripledemic peak but missed the multiwave seasonality of COVID-19.

EID Bi K, Bandekar S, Bouchnita A, Fox SJ, Meyers L. Annual Hospitalizations for COVID-19, Influenza, and Respiratory Syncytial Virus, United States, 2023–2024. Emerg Infect Dis. 2025;31(3):636-638. https://doi.org/10.3201/eid3103.240594
AMA Bi K, Bandekar S, Bouchnita A, et al. Annual Hospitalizations for COVID-19, Influenza, and Respiratory Syncytial Virus, United States, 2023–2024. Emerging Infectious Diseases. 2025;31(3):636-638. doi:10.3201/eid3103.240594.
APA Bi, K., Bandekar, S., Bouchnita, A., Fox, S. J., & Meyers, L. (2025). Annual Hospitalizations for COVID-19, Influenza, and Respiratory Syncytial Virus, United States, 2023–2024. Emerging Infectious Diseases, 31(3), 636-638. https://doi.org/10.3201/eid3103.240594.
Another Dimension

Portraying Tuberculosis through Western Art, 1000–2000 CE [PDF - 5.16 MB - 8 pages]
Y. Kherabi and P. Charlier
EID Kherabi Y, Charlier P. Portraying Tuberculosis through Western Art, 1000–2000 CE. Emerg Infect Dis. 2025;31(3):607-614. https://doi.org/10.3201/eid3103.231581
AMA Kherabi Y, Charlier P. Portraying Tuberculosis through Western Art, 1000–2000 CE. Emerging Infectious Diseases. 2025;31(3):607-614. doi:10.3201/eid3103.231581.
APA Kherabi, Y., & Charlier, P. (2025). Portraying Tuberculosis through Western Art, 1000–2000 CE. Emerging Infectious Diseases, 31(3), 607-614. https://doi.org/10.3201/eid3103.231581.
Etymologia

Tsukamurella tyrosinosolvens (tsū-kə-mə-rel′lə tī′-rǝ-sē-nō-sol′vins) [PDF - 309 KB - 1 page]
C. Partin
EID Partin C. Tsukamurella tyrosinosolvens (tsū-kə-mə-rel′lə tī′-rǝ-sē-nō-sol′vins). Emerg Infect Dis. 2025;31(3):600. https://doi.org/10.3201/eid3103.242004
AMA Partin C. Tsukamurella tyrosinosolvens (tsū-kə-mə-rel′lə tī′-rǝ-sē-nō-sol′vins). Emerging Infectious Diseases. 2025;31(3):600. doi:10.3201/eid3103.242004.
APA Partin, C. (2025). Tsukamurella tyrosinosolvens (tsū-kə-mə-rel′lə tī′-rǝ-sē-nō-sol′vins). Emerging Infectious Diseases, 31(3), 600. https://doi.org/10.3201/eid3103.242004.
Online Reports

Lessons Learned from Early Implementation and Scale-up of Stool-Based Xpert Testing to Diagnose Tuberculosis in Children [PDF - 733 KB - 9 pages]
E. Klinkenberg et al.

In 2020, fecal (stool) testing was recommended for diagnosing Mycobacterium tuberculosis complex (MTBC) infection in children by using the Cepheid Xpert MTB/RIF assay; since then, countries have begun implementing stool-based testing, often as part of a comprehensive strategy to enhance TB case finding among children. On the basis of an experience-sharing workshop in November 2023, we determined insights of 9 early-adopter countries. Across those countries, 71,757 children underwent stool testing over a combined period of 121 months, October 2020–September 2023. A total of 2,892 children were positive for MTBC, and rifampin resistance was confirmed for 43 stool samples. The overall yield of MTBC detection across the countries was 4.1% (range 1.1%–17.3%). Stool collection for Xpert testing was considered noninvasive and as easy as sputum testing. Stool-based testing can be integrated into peripheral healthcare levels as a routine test to increase bacteriologic confirmation among children with presumptive TB.

EID Klinkenberg E, de Haas P, Manyonge C, Namutebi J, Mujangi B, Mutunzi H, et al. Lessons Learned from Early Implementation and Scale-up of Stool-Based Xpert Testing to Diagnose Tuberculosis in Children. Emerg Infect Dis. 2025;31(3):1-9. https://doi.org/10.3201/eid3103.241580
AMA Klinkenberg E, de Haas P, Manyonge C, et al. Lessons Learned from Early Implementation and Scale-up of Stool-Based Xpert Testing to Diagnose Tuberculosis in Children. Emerging Infectious Diseases. 2025;31(3):1-9. doi:10.3201/eid3103.241580.
APA Klinkenberg, E., de Haas, P., Manyonge, C., Namutebi, J., Mujangi, B., Mutunzi, H....Colvin, C. (2025). Lessons Learned from Early Implementation and Scale-up of Stool-Based Xpert Testing to Diagnose Tuberculosis in Children. Emerging Infectious Diseases, 31(3), 1-9. https://doi.org/10.3201/eid3103.241580.
About the Cover

Themes of Holism and Reductionism in the Quest for the Cause of Tuberculosis [PDF - 1.44 MB - 3 pages]
T. Chorba
EID Chorba T. Themes of Holism and Reductionism in the Quest for the Cause of Tuberculosis. Emerg Infect Dis. 2025;31(3):639-641. https://doi.org/10.3201/eid3103.ac3103
AMA Chorba T. Themes of Holism and Reductionism in the Quest for the Cause of Tuberculosis. Emerging Infectious Diseases. 2025;31(3):639-641. doi:10.3201/eid3103.ac3103.
APA Chorba, T. (2025). Themes of Holism and Reductionism in the Quest for the Cause of Tuberculosis. Emerging Infectious Diseases, 31(3), 639-641. https://doi.org/10.3201/eid3103.ac3103.
Page created: February 24, 2025
Page updated: March 04, 2025
Page reviewed: March 04, 2025
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
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