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Articles from Emerging Infectious Diseases

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Pediatric Meningoencephalitis Cluster Caused by Snowshoe Hare Virus, Whistler, British Columbia, Canada, 2024 [PDF - 790 KB - 7 pages]
F. Ali et al.

Snowshoe hare virus (SSHV) is an arbovirus in the California serogroup known to circulate throughout Canada and northern latitudes of the United States. The clinical spectrum of SSHV infection ranges from asymptomatic or mild febrile illness to neuroinvasive disease; neuroinvasive disease occurs more often in children and young adults. We describe a cluster of confirmed and probable SSHV meningoencephalitis cases in 3 children from Whistler, British Columbia, Canada, in the summer of 2024. We highlight the shared epidemiology, clinical manifestations, serologic diagnostic methods, and outcomes for the cases. All 3 children acquired the infection locally and made a full recovery. This case series suggests underrecognized SSHV infection prevalence that warrants enhanced surveillance and review of existing diagnostic algorithms. California serogroup viruses, including SSHV, should be recognized as a potential cause of neuroinvasive disease in North America during mosquito season, particularly when initial diagnostic testing is inconclusive.

EID Ali F, Imperial M, Morshed M, Goldfarb DM, Gubbay JB, Hogan CA, et al. Pediatric Meningoencephalitis Cluster Caused by Snowshoe Hare Virus, Whistler, British Columbia, Canada, 2024. Emerg Infect Dis. 2026;32(4):477-483. https://doi.org/10.3201/eid3204.251392
AMA Ali F, Imperial M, Morshed M, et al. Pediatric Meningoencephalitis Cluster Caused by Snowshoe Hare Virus, Whistler, British Columbia, Canada, 2024. Emerging Infectious Diseases. 2026;32(4):477-483. doi:10.3201/eid3204.251392.
APA Ali, F., Imperial, M., Morshed, M., Goldfarb, D. M., Gubbay, J. B., Hogan, C. A....Tam, J. (2026). Pediatric Meningoencephalitis Cluster Caused by Snowshoe Hare Virus, Whistler, British Columbia, Canada, 2024. Emerging Infectious Diseases, 32(4), 477-483. https://doi.org/10.3201/eid3204.251392.

Ecologic Investigative Strategies to Determine Human Plague Exposure Sites, United States, 1991–2018 [PDF - 1.00 MB - 7 pages]
R. J. Eisen et al.

Plague is a rare but potentially life-threatening fleaborne zoonotic disease caused by Yersinia pestis. Public health agencies in the United States use multiple concurrent epidemiologic and ecologic strategies to determine Y. pestis exposure sites. We reviewed 196 plague case files from 1991–2018 to describe effort and yield of implemented strategies. All files included an epidemiologic component, and 71% were followed up with environmental investigations. Environmental samples were collected for laboratory testing in 88% of investigations. The percentages of investigations yielding laboratory evidence of local transmission varied from 28% for testing live-trapped rodents to 50% for pet serology. We suggest that collection and laboratory testing of samples should be prioritized when epidemiologic investigations implicate potential exposure in an unusual setting, in areas where many people could be at risk of exposure to Y. pestis, or in situations where prevention activities extend beyond educational outreach and incur greater costs.

EID Eisen RJ, Osikowicz LM, Foster E. Ecologic Investigative Strategies to Determine Human Plague Exposure Sites, United States, 1991–2018. Emerg Infect Dis. 2026;32(4):484-490. https://doi.org/10.3201/eid3204.251357
AMA Eisen RJ, Osikowicz LM, Foster E. Ecologic Investigative Strategies to Determine Human Plague Exposure Sites, United States, 1991–2018. Emerging Infectious Diseases. 2026;32(4):484-490. doi:10.3201/eid3204.251357.
APA Eisen, R. J., Osikowicz, L. M., & Foster, E. (2026). Ecologic Investigative Strategies to Determine Human Plague Exposure Sites, United States, 1991–2018. Emerging Infectious Diseases, 32(4), 484-490. https://doi.org/10.3201/eid3204.251357.

Circulation Patterns, Genetic Diversity, and Public Health Implications of Enterovirus D68, Europe, 2014–2024 [PDF - 1.24 MB - 9 pages]
C. Andrés et al.

Enterovirus D68 (EV-D68) represents a continuing public health concern, given its association with severe respiratory illness and neurologic complications. In this study, we analyzed EV-D68 circulation and genetic evolution during 2014–2024 using data from 18 countries in Europe. Of 61,297 enterovirus-positive specimens, molecular detection and viral protein 1 sequencing identified 3,541 (6%) EV-D68 cases. A biennial circulation pattern was observed; detection rates ranged from 9% in 2014 to 0.9% in 2019. The pattern was disrupted in 2020 because of measures implemented in response to the COVID-19 pandemic, but then notable increases occurred in 2021 (14%), 2022 (10.7%), and 2024 (20.6%). Subgenogroups B3 (59.8%) and A2/D (28.0%) were predominant; A2/D reemerged as dominant in 2024. Mutation analyses revealed changes in antigenic regions. Our findings underscore the persistent adaptation and resurgence of EV-D68 after COVID-19. Continued genomic surveillance is essential to monitor transmission patterns caused by antigenic changes.

EID Andrés C, Prats-Méndez I, Midgley S, Berginc N, González-Sánchez A, Johannesen C, et al. Circulation Patterns, Genetic Diversity, and Public Health Implications of Enterovirus D68, Europe, 2014–2024. Emerg Infect Dis. 2026;32(4):491-499. https://doi.org/10.3201/eid3204.251022
AMA Andrés C, Prats-Méndez I, Midgley S, et al. Circulation Patterns, Genetic Diversity, and Public Health Implications of Enterovirus D68, Europe, 2014–2024. Emerging Infectious Diseases. 2026;32(4):491-499. doi:10.3201/eid3204.251022.
APA Andrés, C., Prats-Méndez, I., Midgley, S., Berginc, N., González-Sánchez, A., Johannesen, C....Benschop, K. (2026). Circulation Patterns, Genetic Diversity, and Public Health Implications of Enterovirus D68, Europe, 2014–2024. Emerging Infectious Diseases, 32(4), 491-499. https://doi.org/10.3201/eid3204.251022.
Research

Enhanced Detection of Coccidioides spp. Fungi from Environmental Samples Using Droplet Digital PCR [PDF - 8.26 MB - 10 pages]
J. Segovia-Mota et al.

Coccidioidomycosis (Valley fever), caused by Coccidioides spp. fungi, is a reemerging, neglected fungal disease endemic to arid and semiarid regions of the Americas. Environmental detection remains challenging because of spatial heterogeneity, seasonal variability, low DNA abundance, PCR inhibitors, and lack of standardized methods. We conducted environmental surveillance in Baja California, Mexico, an understudied region near the US–Mexico border, by collecting 74 soil samples from active rodent burrows across 5 locations. We evaluated droplet digital PCR (ddPCR) for Coccidioides detection and compared ddPCR with nested PCR targeting the internal transcribed spacer 1 region. ddPCR demonstrated greater sensitivity, detecting Coccidioides spp. DNA at all sampling sites, whereas nested PCR detected Coccidioides spp. DNA from only 1 site. Although additional work is required to rigorously quantify sensitivity and specificity, ddPCR could help identify Coccidioides environmental hotspots, thus enabling public health interventions, such as warning communities of areas that pose higher risk for infection.

EID Segovia-Mota J, Eaton-González R, Carrillo-Tripp J, Riquelme M. Enhanced Detection of Coccidioides spp. Fungi from Environmental Samples Using Droplet Digital PCR. Emerg Infect Dis. 2026;32(4):500-509. https://doi.org/10.3201/eid3204.251146
AMA Segovia-Mota J, Eaton-González R, Carrillo-Tripp J, et al. Enhanced Detection of Coccidioides spp. Fungi from Environmental Samples Using Droplet Digital PCR. Emerging Infectious Diseases. 2026;32(4):500-509. doi:10.3201/eid3204.251146.
APA Segovia-Mota, J., Eaton-González, R., Carrillo-Tripp, J., & Riquelme, M. (2026). Enhanced Detection of Coccidioides spp. Fungi from Environmental Samples Using Droplet Digital PCR. Emerging Infectious Diseases, 32(4), 500-509. https://doi.org/10.3201/eid3204.251146.

Evaluation of Effectiveness of Autocidal Gravid Ovitraps for Preventing Zika Virus Infection, Puerto Rico, USA [PDF - 1.75 MB - 11 pages]
Z. J. Madewell et al.

Aedes aegypti mosquitoes drive arboviral outbreaks in tropical regions. Zika virus (ZIKV), linked to congenital and neurologic complications, caused a major outbreak in Puerto Rico, USA, in 2016, infecting ≈26% of the population. Autocidal gravid ovitraps (AGOs), pesticide-free devices targeting gravid Ae. aegypti mosquitoes, have been shown to reduce transmission of another arbovirus, chikungunya. During March–May 2017, we conducted a household-based serosurvey in 4 demographically similar communities in southeastern Puerto Rico, 2 with long-term AGO deployment (≈85% coverage) and 2 without, to assess effects of AGOs on ZIKV transmission. Among 271 participants >5 years of age, ZIKV seroprevalence was much lower in intervention than nonintervention communities (9.6% vs. 20.0%). Protective effects were strongest among older adults, larger households (>4 persons), and persons spending more time at home. Although study design and measurement limitations could limit generalizability of results, our findings support AGOs as sustainable nonchemical tools for reducing ZIKV infections.

EID Madewell ZJ, Kiplagat SJ, Kellum I, Lozier MJ, Lorenzi O, Perez-Padilla J, et al. Evaluation of Effectiveness of Autocidal Gravid Ovitraps for Preventing Zika Virus Infection, Puerto Rico, USA. Emerg Infect Dis. 2026;32(4):510-520. https://doi.org/10.3201/eid3204.251206
AMA Madewell ZJ, Kiplagat SJ, Kellum I, et al. Evaluation of Effectiveness of Autocidal Gravid Ovitraps for Preventing Zika Virus Infection, Puerto Rico, USA. Emerging Infectious Diseases. 2026;32(4):510-520. doi:10.3201/eid3204.251206.
APA Madewell, Z. J., Kiplagat, S. J., Kellum, I., Lozier, M. J., Lorenzi, O., Perez-Padilla, J....Sharp, T. M. (2026). Evaluation of Effectiveness of Autocidal Gravid Ovitraps for Preventing Zika Virus Infection, Puerto Rico, USA. Emerging Infectious Diseases, 32(4), 510-520. https://doi.org/10.3201/eid3204.251206.

Geographically Distinct Circulation of Genotype II and III St. Louis Encephalitis Virus, Texas, USA, 2009–2024 [PDF - 3.12 MB - 12 pages]
A. R. Kneubehl et al.

We conducted a retrospective genomic surveillance study of St. Louis encephalitis virus (SLEV) in Texas, USA, to determine the genotypes circulating in the region. By using a custom tiled-amplicon assay with Oxford Nanopore sequencing, we generated 63 genomes from SLEV-positive mosquito pools and viral isolates collected during 2009–2024. Phylogenomic analysis revealed temporal overlap of genotype II and III circulation, but with distinct geographic segregation. Genotype II was confined to Gulf Coast counties with sustained local transmission, whereas genotype III was only in north and west Texas, but with persistent circulation and repeated introductions. We identified the earliest known US genotype III sequences, although their phylogenetic placement leaves the entry point of genotype III into the United States unresolved. Our findings emphasize the need for clinical vigilance in West Texas, where SLEV and West Nile virus co-circulate, and suggest the Gulf Coast may be buffered against foreign genotype introduction.

EID Kneubehl AR, Rehm DP, Curtis MW, Wimmer BM, Bolling B, Broussard A, et al. Geographically Distinct Circulation of Genotype II and III St. Louis Encephalitis Virus, Texas, USA, 2009–2024. Emerg Infect Dis. 2026;32(4):521-532. https://doi.org/10.3201/eid3204.250934
AMA Kneubehl AR, Rehm DP, Curtis MW, et al. Geographically Distinct Circulation of Genotype II and III St. Louis Encephalitis Virus, Texas, USA, 2009–2024. Emerging Infectious Diseases. 2026;32(4):521-532. doi:10.3201/eid3204.250934.
APA Kneubehl, A. R., Rehm, D. P., Curtis, M. W., Wimmer, B. M., Bolling, B., Broussard, A....Ronca, S. E. (2026). Geographically Distinct Circulation of Genotype II and III St. Louis Encephalitis Virus, Texas, USA, 2009–2024. Emerging Infectious Diseases, 32(4), 521-532. https://doi.org/10.3201/eid3204.250934.

Confirming ERVEBO Vaccination to Support Ebola Virus Surveillance [PDF - 2.17 MB - 10 pages]
E. Karaaslan et al.

Accurate confirmation of Ebola vaccination (ERVEBO) is essential for interpreting serologic data and assessing vaccine coverage during Ebola virus (EBOV) outbreaks. Current GP1,2-based assays cannot reliably distinguish vaccine-induced immunity from responses generated by natural infection. We developed a multiplex Luminex assay incorporating EBOV GP1,2, secreted glycoprotein (sGP), and a modified vesicular stomatitis virus nucleoprotein (VSV-P-N), a vector antigen encoded by ERVEBO but absent from wild-type EBOV. By using samples from US vaccinees and controls and a small comparison set from the Democratic Republic of the Congo, we found sGP and VSV-P-N demonstrated 100% sensitivity and >97.6% specificity for identifying vaccinees. In samples collected after a ring vaccination campaign in Guinea, combined sGP and VSV-P-N positivity confirmed vaccination in 94.8% of persons with written and 90.8% of persons with verbal confirmation of vaccination history. Our findings show that sGP and VSV-P-N provide a reliable signature of ERVEBO vaccination and support improved Ebola surveillance.

EID Karaaslan E, Whitesell A, Malenfant J, Carson WC, Townsend M, Jolie K, et al. Confirming ERVEBO Vaccination to Support Ebola Virus Surveillance. Emerg Infect Dis. 2026;32(4):533-542. https://doi.org/10.3201/eid3204.251906
AMA Karaaslan E, Whitesell A, Malenfant J, et al. Confirming ERVEBO Vaccination to Support Ebola Virus Surveillance. Emerging Infectious Diseases. 2026;32(4):533-542. doi:10.3201/eid3204.251906.
APA Karaaslan, E., Whitesell, A., Malenfant, J., Carson, W. C., Townsend, M., Jolie, K....Bergeron, É. (2026). Confirming ERVEBO Vaccination to Support Ebola Virus Surveillance. Emerging Infectious Diseases, 32(4), 533-542. https://doi.org/10.3201/eid3204.251906.

Seroprevalence of Crimean-Congo Hemorrhagic Fever Virus Infection in Humans and Domestic Ruminants, Democratic Republic of the Congo [PDF - 1.86 MB - 10 pages]
B. Lombe et al.

Crimean-Congo hemorrhagic fever virus (CCHFV) was first isolated in the Democratic Republic of the Congo (DRC) in 1956. To date, only 3 sporadic human cases have been reported in the DRC, and data on CCHFV infection in livestock, which are key players in transmission, are scant. We conducted a cross-sectional seroepidemiological study on archived human and animal serum samples collected from 25 provinces across the DRC. Samples were tested using an ELISA detecting CCHFV nucleoprotein-specific antibodies. The seroprevalence of CCHFV infection in humans was 4.4% (55/1,239) and in domestic ruminants was 28.9% (322/1,114). High seroprevalences tended to correlate with increased age, specific climate conditions (e.g., tropical monsoon) and vegetation (e.g., mountain savanna) types, and higher elevation (>600 m). Our findings suggest that CCHFV actively circulates in animals and sporadically transmits to humans in the DRC, highlighting the need for continued surveillance of CCHFV infection.

EID Lombe B, Munyeku-Bazitama Y, Kashitu-Mujinga G, Mukadi P, Mampasi H, Tshilenge C, et al. Seroprevalence of Crimean-Congo Hemorrhagic Fever Virus Infection in Humans and Domestic Ruminants, Democratic Republic of the Congo. Emerg Infect Dis. 2026;32(4):543-552. https://doi.org/10.3201/eid3204.250969
AMA Lombe B, Munyeku-Bazitama Y, Kashitu-Mujinga G, et al. Seroprevalence of Crimean-Congo Hemorrhagic Fever Virus Infection in Humans and Domestic Ruminants, Democratic Republic of the Congo. Emerging Infectious Diseases. 2026;32(4):543-552. doi:10.3201/eid3204.250969.
APA Lombe, B., Munyeku-Bazitama, Y., Kashitu-Mujinga, G., Mukadi, P., Mampasi, H., Tshilenge, C....Takada, A. (2026). Seroprevalence of Crimean-Congo Hemorrhagic Fever Virus Infection in Humans and Domestic Ruminants, Democratic Republic of the Congo. Emerging Infectious Diseases, 32(4), 543-552. https://doi.org/10.3201/eid3204.250969.

Border Region Surveillance of Malaria Drug Resistance, Northern Burundi, 2023–2024 [PDF - 904 KB - 10 pages]
D. Niyomwungere et al.

To evaluated artemisinin partial resistance (ART-R) in malaria in Burundi, during December 2023–June 2024, we studied 423 children <5 years of age with uncomplicated Plasmodium falciparum malaria in 8 health facilities in the northern part of the country. After artemether/lumefantrine treatment with only the first dose directly observed, 4.5% remained parasitemic on day 3. No pfkelch13 mutations, validated or candidate markers of ART-R, were detected. However, markers of antifolate and 4-aminoquinoline resistance were widespread: the dhfr triple mutant N51I/C59R/S108N was nearly fixed (92%), dhps double and triple mutants were common (41% and 47%), and pfcrt CVIET, associated with chloroquine and amodiaquine resistance, predominated (84%). Geographic differences occurred in day-3 positivity and haplotype frequencies. Although ART-R markers were absent, delayed parasite clearance and near fixation of multidrug-resistant haplotypes serve as a warning. Strengthened efficacy monitoring and regional molecular surveillance are urgently needed to prevent drug-resistant P. falciparum from becoming established in Burundi.

EID Niyomwungere D, Sinarinzi P, Caspar E, Thiebaut L, Strubel P, Tibiri Y, et al. Border Region Surveillance of Malaria Drug Resistance, Northern Burundi, 2023–2024. Emerg Infect Dis. 2026;32(4):553-562. https://doi.org/10.3201/eid3204.251711
AMA Niyomwungere D, Sinarinzi P, Caspar E, et al. Border Region Surveillance of Malaria Drug Resistance, Northern Burundi, 2023–2024. Emerging Infectious Diseases. 2026;32(4):553-562. doi:10.3201/eid3204.251711.
APA Niyomwungere, D., Sinarinzi, P., Caspar, E., Thiebaut, L., Strubel, P., Tibiri, Y....Nyandwi, J. (2026). Border Region Surveillance of Malaria Drug Resistance, Northern Burundi, 2023–2024. Emerging Infectious Diseases, 32(4), 553-562. https://doi.org/10.3201/eid3204.251711.

Accelerated Increase in Candida auris Bloodstream Infections during COVID-19 Pandemic, South Africa [PDF - 4.29 MB - 10 pages]
H. Ismail et al.

The COVID-19 pandemic coincided with rising secondary bloodstream infections (BSIs) from multidrug-resistant organisms, including Candida auris. To assess candidemia trends, we conducted a retrospective analysis of blood culture isolates from public and private laboratories in South Africa taken during January 2019–June 2022. We evaluated weekly aggregated Candida BSI counts and COVID-19 cases using segmented regression within an interrupted time-series framework. In total, 15,393 candidemia cases were identified, 70% from the private sector. C. parapsilosis accounted for 39% of cases, whereas C. auris represented 26%. The proportion of C. auris increased significantly from 17% in 2019 to 31% in 2021 (p<0.01). After the pandemic onset, Candida BSIs rose by 11 cases per week (p = 0.03), largely driven by C. auris (+5 cases/week; p<0.01); peaks coincided with COVID-19 waves. Those results highlight an accelerated shift toward C. auris in Candida BSIs and the urgent need for enhanced surveillance, diagnostics, and infection prevention.

EID Ismail H, Perovic O, Mpembe R, Lowman W, Govind C, Ekermans P, et al. Accelerated Increase in Candida auris Bloodstream Infections during COVID-19 Pandemic, South Africa. Emerg Infect Dis. 2026;32(4):563-572. https://doi.org/10.3201/eid3204.251407
AMA Ismail H, Perovic O, Mpembe R, et al. Accelerated Increase in Candida auris Bloodstream Infections during COVID-19 Pandemic, South Africa. Emerging Infectious Diseases. 2026;32(4):563-572. doi:10.3201/eid3204.251407.
APA Ismail, H., Perovic, O., Mpembe, R., Lowman, W., Govind, C., Ekermans, P....Govender, N. P. (2026). Accelerated Increase in Candida auris Bloodstream Infections during COVID-19 Pandemic, South Africa. Emerging Infectious Diseases, 32(4), 563-572. https://doi.org/10.3201/eid3204.251407.

Dengue Incidence, Seroprevalence, and Expansion Factors from Active Surveillance, Brazil, 2016–2021 [PDF - 1.68 MB - 11 pages]
E. de Barros et al.

Dengue is hyperendemic in Brazil and is underestimated by passive surveillance. To better understand dengue incidence, we conducted epidemiologic analyses among participants, 2–59 years of age, from the placebo arm of a phase 3 dengue vaccine trial. During 2016–2021, a total of 5,947 participants contributed to 22,028 person-years of follow-up. We identified and virologically confirmed dengue (VCD), Zika, and chikungunya infections. We observed VCD and chikungunya incidence heterogeneity by age, geographic location, and study year. Children 2–6 years of age experienced the highest VCD (2.33/100 person-years) and chikungunya (1.02/100 person-years) incidence. VCD peaked in 2019 (n = 148) whereas chikungunya peaked in 2017 (n = 51). VCD incidence rates from active surveillance were generally higher than those reported to the national passive surveillance system; expansion factor range was <1–9.5 by municipality. Active surveillance is critical to better understand and characterize dengue epidemiology.

EID de Barros E, de Almeida Roediger M, Jackson M, Marks MA, Anderson EM, Esteves-Jaramillo A, et al. Dengue Incidence, Seroprevalence, and Expansion Factors from Active Surveillance, Brazil, 2016–2021. Emerg Infect Dis. 2026;32(4):573-583. https://doi.org/10.3201/eid3204.250942
AMA de Barros E, de Almeida Roediger M, Jackson M, et al. Dengue Incidence, Seroprevalence, and Expansion Factors from Active Surveillance, Brazil, 2016–2021. Emerging Infectious Diseases. 2026;32(4):573-583. doi:10.3201/eid3204.250942.
APA de Barros, E., de Almeida Roediger, M., Jackson, M., Marks, M. A., Anderson, E. M., Esteves-Jaramillo, A....Boulos, F. (2026). Dengue Incidence, Seroprevalence, and Expansion Factors from Active Surveillance, Brazil, 2016–2021. Emerging Infectious Diseases, 32(4), 573-583. https://doi.org/10.3201/eid3204.250942.

Transmissibility and Disease Progression of Asymptomatic Mycobacterium tuberculosis Infection, Lima, Peru [PDF - 569 KB - 8 pages]
R. Wang et al.

Estimating the transmissibility of asymptomatic Mycobacterium tuberculosis infection can clarify its contribution to tuberculosis (TB) spread. We conducted a prospective cohort study in Lima, Peru, enrolling index TB patients and their household contacts (HHCs) and classifying patients by the presence of symptoms including cough, night sweats, weight loss, or fever. We followed HHCs with serial tuberculin skin testing and clinical evaluations. Among 4,296 child HHCs, adjusted estimates for baseline infection (prevalence ratio 0.62 [95% CI 0.37–1.03]), incident infection at 6 months (hazard ratio (aHR) 0.63 [95% CI 0.27–1.49]), and TB disease during 1 year of follow-up (aHR 0.74 [95% CI 0.35–1.56]) were all consistent with lower risk for infection and disease progression among HHCs of asymptomatic compared with symptomatic index patients. Although asymptomatic infections may be less transmissible than symptomatic infections, the high prevalence of asymptomatic patients in national surveys suggest that they may contribute substantially to transmission.

EID Wang R, Huang C, Becerra MC, Calderon RI, Contreras CC, Galea JT, et al. Transmissibility and Disease Progression of Asymptomatic Mycobacterium tuberculosis Infection, Lima, Peru. Emerg Infect Dis. 2026;32(4):584-591. https://doi.org/10.3201/eid3204.251947
AMA Wang R, Huang C, Becerra MC, et al. Transmissibility and Disease Progression of Asymptomatic Mycobacterium tuberculosis Infection, Lima, Peru. Emerging Infectious Diseases. 2026;32(4):584-591. doi:10.3201/eid3204.251947.
APA Wang, R., Huang, C., Becerra, M. C., Calderon, R. I., Contreras, C. C., Galea, J. T....Murray, M. B. (2026). Transmissibility and Disease Progression of Asymptomatic Mycobacterium tuberculosis Infection, Lima, Peru. Emerging Infectious Diseases, 32(4), 584-591. https://doi.org/10.3201/eid3204.251947.

Hemolytic Uremic Syndrome Outbreak in Adults and Shiga Toxin–Producing Escherichia coli Negative for Locus of Enterocyte Effacement, France, 2025 [PDF - 4.08 MB - 11 pages]
J. de Larminat et al.

In January 2025, the Escherichia coli National Reference Center of France detected an outbreak of hemolytic uremic syndrome (HUS) in adults, caused by Shiga toxin–producing E. coli negative for locus of enterocyte effacement (LEE). The outbreak included 18 confirmed cases of E. coli infection, 5 probable or possible cases detected by in-house specific PCR, and 2 additional cases from Scotland and Belgium. Whole-genome sequencing identified the outbreak strain as O77 g:K92:H18, belonging to phylogroup D; the strain harbored the Shiga toxin 2 gene variant stx2d-073-C165-02 and a 134-kb plasmid with enterotoxin genes (estb-STb2 and eltAB). Epidemiologic investigation implicated raw-milk cheese as the contamination source. The strain represents a singular hybrid pathotype of Shiga toxin–producing and enterotoxigenic E. coli, expressing a K92 capsule with known cross-immunogenicity to Neisseria meningitidis group C, which could explain the absence of pediatric cases. Related strains have been identified in international databases since 2005, suggesting global emergence.

EID de Larminat J, La K, Bidet P, Birgy A, Liguori S, Phlipaux P, et al. Hemolytic Uremic Syndrome Outbreak in Adults and Shiga Toxin–Producing Escherichia coli Negative for Locus of Enterocyte Effacement, France, 2025. Emerg Infect Dis. 2026;32(4):592-602. https://doi.org/10.3201/eid3204.251417
AMA de Larminat J, La K, Bidet P, et al. Hemolytic Uremic Syndrome Outbreak in Adults and Shiga Toxin–Producing Escherichia coli Negative for Locus of Enterocyte Effacement, France, 2025. Emerging Infectious Diseases. 2026;32(4):592-602. doi:10.3201/eid3204.251417.
APA de Larminat, J., La, K., Bidet, P., Birgy, A., Liguori, S., Phlipaux, P....Bonacorsi, S. (2026). Hemolytic Uremic Syndrome Outbreak in Adults and Shiga Toxin–Producing Escherichia coli Negative for Locus of Enterocyte Effacement, France, 2025. Emerging Infectious Diseases, 32(4), 592-602. https://doi.org/10.3201/eid3204.251417.

Respirable Aerosol Production and Reduction of Avian Influenza Transmission Risk during Chicken Processing, Bangladesh [PDF - 2.52 MB - 11 pages]
N. Rimi et al.

In Bangladesh, influenza A(H5N1) viruses are endemic in poultry. Processing infected chickens can aerosolize viruses, increasing the risk for human infections. We evaluated particulate matter (PM2.5) mass concentration during slaughtering and defeathering methods used in live bird markets in Bangladesh to identify solutions to reduce aerosol exposure. We slaughtered 675 chickens using cones and barrels with 3 lid types and defeathered 45 chickens using a defeathering machine with 5 lid types. We interviewed 3 slaughterers to understand method preference. For slaughtering, barrels with a solid or star-cut lid reduced PM2.5 mass concentrations by 65%–73% compared with uncovered barrels. For defeathering, machines fully covered by a solid lid or lid with a hole and pivot door reduced PM2.5 mass concentrations by 50% compared with machines with no lid. Slaughterers preferred barrels covered with solid lids and defeathering machines covered with solid or hinged lids. Those methods might reduce aerosol exposure during poultry processing.

EID Rimi N, Saifullah M, Fahad M, Hossain K, Sultana R, Shanta I, et al. Respirable Aerosol Production and Reduction of Avian Influenza Transmission Risk during Chicken Processing, Bangladesh. Emerg Infect Dis. 2026;32(4):603-613. https://doi.org/10.3201/eid3204.251878
AMA Rimi N, Saifullah M, Fahad M, et al. Respirable Aerosol Production and Reduction of Avian Influenza Transmission Risk during Chicken Processing, Bangladesh. Emerging Infectious Diseases. 2026;32(4):603-613. doi:10.3201/eid3204.251878.
APA Rimi, N., Saifullah, M., Fahad, M., Hossain, K., Sultana, R., Shanta, I....Lindsley, W. G. (2026). Respirable Aerosol Production and Reduction of Avian Influenza Transmission Risk during Chicken Processing, Bangladesh. Emerging Infectious Diseases, 32(4), 603-613. https://doi.org/10.3201/eid3204.251878.
Dispatches

Chronic Wasting Disease in Farmed Cervids, South Korea, 2001–2024 [PDF - 1.34 MB - 5 pages]
Y. Choi et al.

Chronic wasting disease (CWD) was identified in imported elk in South Korea in 2001 and has spread among cervids nationwide. The country’s surveillance and control policy culls cervids from any CWD-positive farms, and prevalence during 2020–2024 was <0.5%. Maintaining low prevalence in cervids will limit livestock, wildlife, and human CWD exposure.

EID Choi Y, Lee Y, Park H, Lee Y, Mitchell G, Roh I, et al. Chronic Wasting Disease in Farmed Cervids, South Korea, 2001–2024. Emerg Infect Dis. 2026;32(4):614-618. https://doi.org/10.3201/eid3204.251046
AMA Choi Y, Lee Y, Park H, et al. Chronic Wasting Disease in Farmed Cervids, South Korea, 2001–2024. Emerging Infectious Diseases. 2026;32(4):614-618. doi:10.3201/eid3204.251046.
APA Choi, Y., Lee, Y., Park, H., Lee, Y., Mitchell, G., Roh, I....Sohn, H. (2026). Chronic Wasting Disease in Farmed Cervids, South Korea, 2001–2024. Emerging Infectious Diseases, 32(4), 614-618. https://doi.org/10.3201/eid3204.251046.

Outbreak of Dengue Virus Serotype 3, Republic of the Marshall Islands, 2019–2021 [PDF - 569 KB - 4 pages]
T. M. León et al.

During 2019–2021, the Republic of the Marshall Islands experienced a dengue outbreak involving 1,908 cases. Environmental sanitation helped stop transmission on Ebeye island, but transmission continued for >1 year on Majuro atoll. The Pacific region urgently needs to develop vector control capacity to address future dengue outbreaks.

EID León TM, McCready J, Chutaro E, McAllister J, Solomon B, Hapairai LK. Outbreak of Dengue Virus Serotype 3, Republic of the Marshall Islands, 2019–2021. Emerg Infect Dis. 2026;32(4):619-622. https://doi.org/10.3201/eid3204.251135
AMA León TM, McCready J, Chutaro E, et al. Outbreak of Dengue Virus Serotype 3, Republic of the Marshall Islands, 2019–2021. Emerging Infectious Diseases. 2026;32(4):619-622. doi:10.3201/eid3204.251135.
APA León, T. M., McCready, J., Chutaro, E., McAllister, J., Solomon, B., & Hapairai, L. K. (2026). Outbreak of Dengue Virus Serotype 3, Republic of the Marshall Islands, 2019–2021. Emerging Infectious Diseases, 32(4), 619-622. https://doi.org/10.3201/eid3204.251135.

Treatment of Severe Ocular Mpox with Cidofovir and Tecovirimat [PDF - 1.74 MB - 4 pages]
X. Brousse et al.

Mpox, a reemerging zoonotic disease since 2022, primarily affects the skin; ocular involvement is rarely reported. We present a case of mpox-caused disciform keratitis treated with a combination of cidofovir and tecovirimat. The patient recovered without residual ocular sequelae, suggesting these drugs are an option to treat ocular mpox manifestations.

EID Brousse X, Kreidie R, Mourgues E, Fraysse L, Lahouati M, Servant V, et al. Treatment of Severe Ocular Mpox with Cidofovir and Tecovirimat. Emerg Infect Dis. 2026;32(4):623-626. https://doi.org/10.3201/eid3204.250882
AMA Brousse X, Kreidie R, Mourgues E, et al. Treatment of Severe Ocular Mpox with Cidofovir and Tecovirimat. Emerging Infectious Diseases. 2026;32(4):623-626. doi:10.3201/eid3204.250882.
APA Brousse, X., Kreidie, R., Mourgues, E., Fraysse, L., Lahouati, M., Servant, V....Cazanave, C. (2026). Treatment of Severe Ocular Mpox with Cidofovir and Tecovirimat. Emerging Infectious Diseases, 32(4), 623-626. https://doi.org/10.3201/eid3204.250882.

Disseminated Acanthamoeba Infection with Necrotic Skin Lesions and Granulomatous Vasculitis, United States [PDF - 1.34 MB - 4 pages]
M. Koshy et al.

An elderly man, on dupilumab therapy for asthma and sinus polyposis, sought care for necrotic skin lesions. Biopsy revealed granulomatous vasculitis and he received immunosuppressive therapy but worsened. We diagnosed an Acanthamoeba infection that was treated with multidrug therapy including nitroxoline. Clinicians should be aware of this rare etiology for infectious vasculitis.

EID Koshy M, Flynn C, Kribis M, McNiff J, Grant M, Gleeson S. Disseminated Acanthamoeba Infection with Necrotic Skin Lesions and Granulomatous Vasculitis, United States. Emerg Infect Dis. 2026;32(4):627-630. https://doi.org/10.3201/eid3204.251201
AMA Koshy M, Flynn C, Kribis M, et al. Disseminated Acanthamoeba Infection with Necrotic Skin Lesions and Granulomatous Vasculitis, United States. Emerging Infectious Diseases. 2026;32(4):627-630. doi:10.3201/eid3204.251201.
APA Koshy, M., Flynn, C., Kribis, M., McNiff, J., Grant, M., & Gleeson, S. (2026). Disseminated Acanthamoeba Infection with Necrotic Skin Lesions and Granulomatous Vasculitis, United States. Emerging Infectious Diseases, 32(4), 627-630. https://doi.org/10.3201/eid3204.251201.

Cardiomyopathy Caused by Coxsackievirus Strain A9 in Previously Healthy Child, Northeastern France, 2024 [PDF - 2.14 MB - 5 pages]
A. Lebreil et al.

We characterized a recombinant mosaic coxsackievirus A9 strain responsible for severe inflammatory cardiomyopathy in a previously healthy child in northeastern France in 2024 by using whole-genome sequencing. This case highlights that enterovirus species other than coxsackievirus strain B3 can cause cardiomyopathy in otherwise healthy pediatric patients.

EID Lebreil A, Bisseux M, Mirand A, Glenet M, N’Guyen Y, Taha N, et al. Cardiomyopathy Caused by Coxsackievirus Strain A9 in Previously Healthy Child, Northeastern France, 2024. Emerg Infect Dis. 2026;32(4):631-635. https://doi.org/10.3201/eid3204.251574
AMA Lebreil A, Bisseux M, Mirand A, et al. Cardiomyopathy Caused by Coxsackievirus Strain A9 in Previously Healthy Child, Northeastern France, 2024. Emerging Infectious Diseases. 2026;32(4):631-635. doi:10.3201/eid3204.251574.
APA Lebreil, A., Bisseux, M., Mirand, A., Glenet, M., N’Guyen, Y., Taha, N....Andreoletti, L. (2026). Cardiomyopathy Caused by Coxsackievirus Strain A9 in Previously Healthy Child, Northeastern France, 2024. Emerging Infectious Diseases, 32(4), 631-635. https://doi.org/10.3201/eid3204.251574.

Whole-Genome Analysis of Treponema pallidum Subspecies endemicum among Men Who Have Sex with Men, Japan, 2020–2023 [PDF - 547 KB - 4 pages]
Y. Ohama et al.

Whole-genome sequencing of Treponema pallidum subsp. endemicum strains from men who have sex with men in Japan revealed a genetically distinct lineage from other geographic regions circulating via sexual transmission. Strengthening global molecular epidemiologic surveillance is essential for clarifying epidemiologic trends, clinical characteristics, and transmission pathways of this subspecies.

EID Ohama Y, Imai K, Kotaka Y, Lee K, Itoda I, Nakayama S, et al. Whole-Genome Analysis of Treponema pallidum Subspecies endemicum among Men Who Have Sex with Men, Japan, 2020–2023. Emerg Infect Dis. 2026;32(4):636-639. https://doi.org/10.3201/eid3204.251045
AMA Ohama Y, Imai K, Kotaka Y, et al. Whole-Genome Analysis of Treponema pallidum Subspecies endemicum among Men Who Have Sex with Men, Japan, 2020–2023. Emerging Infectious Diseases. 2026;32(4):636-639. doi:10.3201/eid3204.251045.
APA Ohama, Y., Imai, K., Kotaka, Y., Lee, K., Itoda, I., Nakayama, S....Akeda, Y. (2026). Whole-Genome Analysis of Treponema pallidum Subspecies endemicum among Men Who Have Sex with Men, Japan, 2020–2023. Emerging Infectious Diseases, 32(4), 636-639. https://doi.org/10.3201/eid3204.251045.

Panton-Valentine Leukocidin–Encoding Methicillin-Resistant Staphylococcus aureus, the Netherlands, 2023–2024 [PDF - 874 KB - 4 pages]
P. van Schelven et al.

We describe a community outbreak of Panton-Valentine leukocidin–positive methicillin-resistant Staphylococcus aureus (MRSA) during November 2023–June 2024 in the Netherlands. We identified a massage center as the source. Case-patients experienced skin infections and abscesses. This study highlights the importance of genomic surveillance of MRSA in distinguishing Panton-Valentine leukocidin–positive MRSA.

EID van Schelven P, Nijhuis R, Jamin C, Goemans S, Hintaran P, van der Jagt-Zwetsloot M, et al. Panton-Valentine Leukocidin–Encoding Methicillin-Resistant Staphylococcus aureus, the Netherlands, 2023–2024. Emerg Infect Dis. 2026;32(4):640-643. https://doi.org/10.3201/eid3204.251646
AMA van Schelven P, Nijhuis R, Jamin C, et al. Panton-Valentine Leukocidin–Encoding Methicillin-Resistant Staphylococcus aureus, the Netherlands, 2023–2024. Emerging Infectious Diseases. 2026;32(4):640-643. doi:10.3201/eid3204.251646.
APA van Schelven, P., Nijhuis, R., Jamin, C., Goemans, S., Hintaran, P., van der Jagt-Zwetsloot, M....Raven, S. (2026). Panton-Valentine Leukocidin–Encoding Methicillin-Resistant Staphylococcus aureus, the Netherlands, 2023–2024. Emerging Infectious Diseases, 32(4), 640-643. https://doi.org/10.3201/eid3204.251646.

Guillain-Barré Syndrome and Visual Impairment Associated with Emerging Oropouche Virus Lineage, Brazil, 2024 [PDF - 844 KB - 5 pages]
C. Filho et al.

We report a case of Guillain-Barré syndrome with visual impairment after confirmed Oropouche virus infection during the 2024 outbreak in Ceará, Brazil. Whole-genome sequencing revealed infection by a novel reassortant viral lineage (OROVBR_2025_2024), raising concern about the neurovirulence of this emerging orthobunyavirus strain.

EID Filho C, Carvalho F, Neto A, Maia A, Rossi M, Pitombeira M, et al. Guillain-Barré Syndrome and Visual Impairment Associated with Emerging Oropouche Virus Lineage, Brazil, 2024. Emerg Infect Dis. 2026;32(4):644-648. https://doi.org/10.3201/eid3204.250617
AMA Filho C, Carvalho F, Neto A, et al. Guillain-Barré Syndrome and Visual Impairment Associated with Emerging Oropouche Virus Lineage, Brazil, 2024. Emerging Infectious Diseases. 2026;32(4):644-648. doi:10.3201/eid3204.250617.
APA Filho, C., Carvalho, F., Neto, A., Maia, A., Rossi, M., Pitombeira, M....de Góes Cavalcanti, L. (2026). Guillain-Barré Syndrome and Visual Impairment Associated with Emerging Oropouche Virus Lineage, Brazil, 2024. Emerging Infectious Diseases, 32(4), 644-648. https://doi.org/10.3201/eid3204.250617.

Rapid Spread of Recombinant African Swine Fever Virus Genotypes I and II, Vietnam, 2023–2024 [PDF - 1.09 MB - 4 pages]
T. Nguyen et al.

Molecular analyses of African swine fever (ASF) outbreaks in northern and central Vietnam during 2023–2024 revealed a rapid expansion (14.1%–42.2%) of recombinant ASF virus genotypes I and II. Increased prevalence and resistance to commercial ASF vaccines underscore the urgent need for better ASF control and an updated vaccine in Vietnam.

EID Nguyen T, Kim Y, Nguyen V, Tran T, Vu N, Vu T, et al. Rapid Spread of Recombinant African Swine Fever Virus Genotypes I and II, Vietnam, 2023–2024. Emerg Infect Dis. 2026;32(4):649-652. https://doi.org/10.3201/eid3204.251688
AMA Nguyen T, Kim Y, Nguyen V, et al. Rapid Spread of Recombinant African Swine Fever Virus Genotypes I and II, Vietnam, 2023–2024. Emerging Infectious Diseases. 2026;32(4):649-652. doi:10.3201/eid3204.251688.
APA Nguyen, T., Kim, Y., Nguyen, V., Tran, T., Vu, N., Vu, T....Hong, S. (2026). Rapid Spread of Recombinant African Swine Fever Virus Genotypes I and II, Vietnam, 2023–2024. Emerging Infectious Diseases, 32(4), 649-652. https://doi.org/10.3201/eid3204.251688.
Photo Quizzes

Photo Quiz [PDF - 1.23 MB - 4 pages]
N. Hoffmann
EID Hoffmann N. Photo Quiz. Emerg Infect Dis. 2026;32(4):653-656. https://doi.org/10.3201/eid3204.251083
AMA Hoffmann N. Photo Quiz. Emerging Infectious Diseases. 2026;32(4):653-656. doi:10.3201/eid3204.251083.
APA Hoffmann, N. (2026). Photo Quiz. Emerging Infectious Diseases, 32(4), 653-656. https://doi.org/10.3201/eid3204.251083.
Research Letters

Acute Febrile Illness Surveillance for Estimating Population Immunity, Dominican Republic, 2021 [PDF - 655 KB - 4 pages]
E. J. Nilles et al.

We assessed whether acute febrile illness surveillance could provide timely estimates of population immunity. In the Dominican Republic, antibody levels and inferred protection were similar between surveillance data and household survey serum samples, suggesting that surveillance platforms may offer a scalable approach to track population-level protection.

EID Nilles EJ, Paulino C, Vasquez M, Duke W, Jarolim P, Ramm R, et al. Acute Febrile Illness Surveillance for Estimating Population Immunity, Dominican Republic, 2021. Emerg Infect Dis. 2026;32(4):660-663. https://doi.org/10.3201/eid3204.251205
AMA Nilles EJ, Paulino C, Vasquez M, et al. Acute Febrile Illness Surveillance for Estimating Population Immunity, Dominican Republic, 2021. Emerging Infectious Diseases. 2026;32(4):660-663. doi:10.3201/eid3204.251205.
APA Nilles, E. J., Paulino, C., Vasquez, M., Duke, W., Jarolim, P., Ramm, R....Lau, C. L. (2026). Acute Febrile Illness Surveillance for Estimating Population Immunity, Dominican Republic, 2021. Emerging Infectious Diseases, 32(4), 660-663. https://doi.org/10.3201/eid3204.251205.

Seroepidemiologic Study of Oropouche Virus, Amazonas State, Brazil, 2015–2016 [PDF - 1.21 MB - 3 pages]
J. Forato et al.

We conducted a cross-sectional serosurvey for Oropouche virus (OROV) among residents of Amazonas State, Brazil, during 2015–2016. We detected OROV neutralizing antibodies in 85/814 (10.4%) participants; seroprevalence was higher in Manaus (49/440 [11.1%]) than in Coari (36/374 [9.6%]). Those findings suggest OROV circulation in Amazonas State before 2015.

EID Forato J, Scachetti GC, Salgado BB, Singh C, Pereira NC, dos Santos Reis R, et al. Seroepidemiologic Study of Oropouche Virus, Amazonas State, Brazil, 2015–2016. Emerg Infect Dis. 2026;32(4):663-665. https://doi.org/10.3201/eid3204.250917
AMA Forato J, Scachetti GC, Salgado BB, et al. Seroepidemiologic Study of Oropouche Virus, Amazonas State, Brazil, 2015–2016. Emerging Infectious Diseases. 2026;32(4):663-665. doi:10.3201/eid3204.250917.
APA Forato, J., Scachetti, G. C., Salgado, B. B., Singh, C., Pereira, N. C., dos Santos Reis, R....Lalwani, P. (2026). Seroepidemiologic Study of Oropouche Virus, Amazonas State, Brazil, 2015–2016. Emerging Infectious Diseases, 32(4), 663-665. https://doi.org/10.3201/eid3204.250917.

Rickettsia lanei Rickettsiosis, Oregon, USA, 2025 [PDF - 637 KB - 3 pages]
S. G. Ladd-Wilson et al.

Using metagenomic sequencing, we identified a patient infected with Rickettsia lanei who was initially diagnosed with Rocky Mountain spotted fever (RMSF), a clinically similar disease caused by infection with R. rickettsii. Our investigation highlights the importance of clinical, epidemiologic, and laboratory partnerships to leverage the discovery of novel pathogens.

EID Ladd-Wilson SG, Fawcett RW, Park SY, Venkatasubrahmanyam S, Lindner MS, Davis S, et al. Rickettsia lanei Rickettsiosis, Oregon, USA, 2025. Emerg Infect Dis. 2026;32(4):666-668. https://doi.org/10.3201/eid3204.251962
AMA Ladd-Wilson SG, Fawcett RW, Park SY, et al. Rickettsia lanei Rickettsiosis, Oregon, USA, 2025. Emerging Infectious Diseases. 2026;32(4):666-668. doi:10.3201/eid3204.251962.
APA Ladd-Wilson, S. G., Fawcett, R. W., Park, S. Y., Venkatasubrahmanyam, S., Lindner, M. S., Davis, S....Paddock, C. D. (2026). Rickettsia lanei Rickettsiosis, Oregon, USA, 2025. Emerging Infectious Diseases, 32(4), 666-668. https://doi.org/10.3201/eid3204.251962.
Another Dimension

The Weight of Waiting [PDF - 549 KB - 3 pages]
M. Diagne

In Ebola outbreaks, families wait to bury their dead until a PCR whispers yes or no. Amid outbreaks of hemorrhagic fever in Senegal, laboratories raced clocks they could not command as loved ones stood by. This essay explores the ethics and emotion of that fragile interval between sample and answer.

EID Diagne M. The Weight of Waiting. Emerg Infect Dis. 2026;32(4):657-659. https://doi.org/10.3201/eid3204.251540
AMA Diagne M. The Weight of Waiting. Emerging Infectious Diseases. 2026;32(4):657-659. doi:10.3201/eid3204.251540.
APA Diagne, M. (2026). The Weight of Waiting. Emerging Infectious Diseases, 32(4), 657-659. https://doi.org/10.3201/eid3204.251540.
Etymologia

Anopheles stephensi [ә-nah′-fuhl-ēz ste′-fen-zī] [PDF - 340 KB - 1 page]
G. Kumar and J. Kaur
EID Kumar G, Kaur J. Anopheles stephensi [ә-nah′-fuhl-ēz ste′-fen-zī]. Emerg Infect Dis. 2026;32(4):562. https://doi.org/10.3201/eid3204.241933
AMA Kumar G, Kaur J. Anopheles stephensi [ә-nah′-fuhl-ēz ste′-fen-zī]. Emerging Infectious Diseases. 2026;32(4):562. doi:10.3201/eid3204.241933.
APA Kumar, G., & Kaur, J. (2026). Anopheles stephensi [ә-nah′-fuhl-ēz ste′-fen-zī]. Emerging Infectious Diseases, 32(4), 562. https://doi.org/10.3201/eid3204.241933.
Corrections

Correction: Vol. 31, No. 4 [PDF - 207 KB - 1 page]
EID Correction: Vol. 31, No. 4. Emerg Infect Dis. 2026;32(4):668. https://doi.org/10.3201/eid3204.c13204
AMA Correction: Vol. 31, No. 4. Emerging Infectious Diseases. 2026;32(4):668. doi:10.3201/eid3204.c13204.
APA (2026). Correction: Vol. 31, No. 4. Emerging Infectious Diseases, 32(4), 668. https://doi.org/10.3201/eid3204.c13204.
About the Cover

Giovanni Battista Grassi and Malaria [PDF - 1.33 MB - 3 pages]
S. Pozzi and M. A. Riva
EID Pozzi S, Riva MA. Giovanni Battista Grassi and Malaria. Emerg Infect Dis. 2026;32(4):669-671. https://doi.org/10.3201/eid3204.ac3204
AMA Pozzi S, Riva MA. Giovanni Battista Grassi and Malaria. Emerging Infectious Diseases. 2026;32(4):669-671. doi:10.3201/eid3204.ac3204.
APA Pozzi, S., & Riva, M. A. (2026). Giovanni Battista Grassi and Malaria. Emerging Infectious Diseases, 32(4), 669-671. https://doi.org/10.3201/eid3204.ac3204.
Page created: April 10, 2026
Page updated: April 16, 2026
Page reviewed: April 16, 2026
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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