Articles from Emerging Infectious Diseases
Volume 30, Number 11—November 2024
Perspective
Flexible Development Programs for Antibacterial Drugs to Address Unmet Medical Needs
The US Food and Drug Administration recognizes the unmet medical need for antibacterial drugs to treat serious bacterial diseases caused by resistant pathogens for which effective therapies are limited or lacking. The agency also recognizes that designing and conducting clinical trials to assess the safety and efficacy of drugs to treat resistant infections is challenging, especially for drugs only active against a single or a few bacterial species, and that a more flexible development program might be appropriate. In this article, we discuss several regulatory considerations for flexible development programs for antibacterial drugs intended to meet an unmet medical need. As an example, we use the recent approval of sulbactam for injection and durlobactam for injection (XACDURO) for the treatment of hospital-acquired bacterial pneumonia and ventilator-associated bacterial pneumonia caused by susceptible isolates of Acinetobacter baumannii-calcoaceticus complex.
EID | Ghosh M, Iarikov D, Qi X, Rubin D, Shurland S, Goodwin A, et al. Flexible Development Programs for Antibacterial Drugs to Address Unmet Medical Needs. Emerg Infect Dis. 2024;30(11):2227-2230. https://doi.org/10.3201/eid3011.231416 |
---|---|
AMA | Ghosh M, Iarikov D, Qi X, et al. Flexible Development Programs for Antibacterial Drugs to Address Unmet Medical Needs. Emerging Infectious Diseases. 2024;30(11):2227-2230. doi:10.3201/eid3011.231416. |
APA | Ghosh, M., Iarikov, D., Qi, X., Rubin, D., Shurland, S., Goodwin, A....Sherwat, A. (2024). Flexible Development Programs for Antibacterial Drugs to Address Unmet Medical Needs. Emerging Infectious Diseases, 30(11), 2227-2230. https://doi.org/10.3201/eid3011.231416. |
Conceptual Framework for Community-Based Prevention of Brown Dog Tick–Associated Rocky Mountain Spotted Fever
Rocky Mountain spotted fever (RMSF) is a severe tickborne disease that can reach epidemic proportions in communities with certain social and ecologic risk factors. In some areas, the case-fatality rate of brown dog tick-associated RMSF is up to 50%. Because of the spread of brown dog tick–associated RMSF in the southwestern United States and northern Mexico, the disease has the potential to emerge and become endemic in other communities that have large populations of free-roaming dogs, brown dog ticks, limited resources, and low provider awareness of the disease. By using a One Health approach, interdisciplinary teams can identify communities at risk and prevent severe or fatal RMSF in humans before cases occur. We have developed a conceptual framework for RMSF prevention to enable communities to identify their RMSF risk level and implement prevention and control strategies.
EID | Brophy MK, Weis E, Drexler NA, Paddock CD, Nicholson WL, Kersh GJ, et al. Conceptual Framework for Community-Based Prevention of Brown Dog Tick–Associated Rocky Mountain Spotted Fever. Emerg Infect Dis. 2024;30(11):2231-2240. https://doi.org/10.3201/eid3011.240293 |
---|---|
AMA | Brophy MK, Weis E, Drexler NA, et al. Conceptual Framework for Community-Based Prevention of Brown Dog Tick–Associated Rocky Mountain Spotted Fever. Emerging Infectious Diseases. 2024;30(11):2231-2240. doi:10.3201/eid3011.240293. |
APA | Brophy, M. K., Weis, E., Drexler, N. A., Paddock, C. D., Nicholson, W. L., Kersh, G. J....Salzer, J. S. (2024). Conceptual Framework for Community-Based Prevention of Brown Dog Tick–Associated Rocky Mountain Spotted Fever. Emerging Infectious Diseases, 30(11), 2231-2240. https://doi.org/10.3201/eid3011.240293. |
Synopses
Reemergence of Oropouche Virus in the Americas and Risk for Spread in the United States and Its Territories, 2024
Oropouche virus has recently caused outbreaks in South America and the Caribbean, expanding into areas to which the virus was previously not endemic. This geographic range expansion, in conjunction with the identification of vertical transmission and reports of deaths, has raised concerns about the broader threat this virus represents to the Americas. We review information on Oropouche virus, factors influencing its spread, transmission risk in the United States, and current status of public health response tools. On the basis of available data, the risk for sustained local transmission in the continental United States is considered low because of differences in vector ecology and in human–vector interactions when compared with Oropouche virus–endemic areas. However, more information is needed about the drivers for the current outbreak to clarify the risk for further expansion of this virus. Timely detection and control of this emerging pathogen should be prioritized to mitigate disease burden and stop its spread.
EID | Guagliardo SJ, Connelly C, Lyons S, Martin SW, Sutter R, Hughes HR, et al. Reemergence of Oropouche Virus in the Americas and Risk for Spread in the United States and Its Territories, 2024. Emerg Infect Dis. 2024;30(11):2241-2249. https://doi.org/10.3201/eid3011.241220 |
---|---|
AMA | Guagliardo SJ, Connelly C, Lyons S, et al. Reemergence of Oropouche Virus in the Americas and Risk for Spread in the United States and Its Territories, 2024. Emerging Infectious Diseases. 2024;30(11):2241-2249. doi:10.3201/eid3011.241220. |
APA | Guagliardo, S. J., Connelly, C., Lyons, S., Martin, S. W., Sutter, R., Hughes, H. R....Staples, J. (2024). Reemergence of Oropouche Virus in the Americas and Risk for Spread in the United States and Its Territories, 2024. Emerging Infectious Diseases, 30(11), 2241-2249. https://doi.org/10.3201/eid3011.241220. |
Congregate homeless shelters are disproportionately affected by infectious disease outbreaks. We describe enterovirus epidemiology across 23 adult and family shelters in King County, Washington, USA, during October 2019–May 2021, by using repeated cross-sectional respiratory illness and environmental surveillance and viral genome sequencing. Among 3,281 participants >3 months of age, we identified coxsackievirus A21 (CVA21) in 39 adult residents (3.0% [95% CI 1.9%–4.8%] detection) across 7 shelters during October 2019–February 2020. We identified enterovirus D68 (EV-D68) in 5 adult residents in 2 shelters during October–November 2019. Of 812 environmental samples, 1 was EV-D68–positive and 5 were CVA21–positive. Other enteroviruses detected among residents, but not in environmental samples, included coxsackievirus A6/A4 in 3 children. No enteroviruses were detected during April 2020–May 2021. Phylogenetically clustered CVA21 and EV-D68 cases occurred in some shelters. Some shelters also hosted multiple CVA21 lineages.
EID | Cox SN, Casto AM, Franko NM, Chow EJ, Han PD, Gamboa L, et al. Clinical and Genomic Epidemiology of Coxsackievirus A21 and Enterovirus D68 in Homeless Shelters, King County, Washington, USA, 2019–2021. Emerg Infect Dis. 2024;30(11):2250-2260. https://doi.org/10.3201/eid3011.240687 |
---|---|
AMA | Cox SN, Casto AM, Franko NM, et al. Clinical and Genomic Epidemiology of Coxsackievirus A21 and Enterovirus D68 in Homeless Shelters, King County, Washington, USA, 2019–2021. Emerging Infectious Diseases. 2024;30(11):2250-2260. doi:10.3201/eid3011.240687. |
APA | Cox, S. N., Casto, A. M., Franko, N. M., Chow, E. J., Han, P. D., Gamboa, L....Chu, H. Y. (2024). Clinical and Genomic Epidemiology of Coxsackievirus A21 and Enterovirus D68 in Homeless Shelters, King County, Washington, USA, 2019–2021. Emerging Infectious Diseases, 30(11), 2250-2260. https://doi.org/10.3201/eid3011.240687. |
Mortality Rates after Tuberculosis Treatment, Georgia, USA, 2008–2019
Limited data exist on mortality rates after tuberculosis (TB) treatment in the United States. We analyzed mortality rates for all adults in Georgia, USA, who had a TB diagnosis and finished treatment during January 1, 2008–December 31, 2019. We obtained posttreatment mortality rate data from the National Death Index and calculated standardized mortality ratios (SMRs) for TB treatment survivors and the general Georgia population. Among 3,182 TB treatment survivors, 233 (7.3%) had died as of December 31, 2019. The overall TB cohort age- and sex-adjusted SMR was 0.89 (95% CI 0.73–1.05). The SMR among US-born TB treatment survivors was 1.56 (95% CI 1.36–1.77). In the TB cohort, US-born status, HIV co-infection, excess alcohol use, diabetes mellitus, and end-stage renal disease were associated with increased risk for death after TB treatment. TB treatment survivors could benefit from improved linkage to primary and HIV comprehensive care to prevent posttreatment death.
EID | Gorvetzian S, Pacheco AG, Anderson E, Ray SM, Schechter MC. Mortality Rates after Tuberculosis Treatment, Georgia, USA, 2008–2019. Emerg Infect Dis. 2024;30(11):2261-2270. https://doi.org/10.3201/eid3011.240329 |
---|---|
AMA | Gorvetzian S, Pacheco AG, Anderson E, et al. Mortality Rates after Tuberculosis Treatment, Georgia, USA, 2008–2019. Emerging Infectious Diseases. 2024;30(11):2261-2270. doi:10.3201/eid3011.240329. |
APA | Gorvetzian, S., Pacheco, A. G., Anderson, E., Ray, S. M., & Schechter, M. C. (2024). Mortality Rates after Tuberculosis Treatment, Georgia, USA, 2008–2019. Emerging Infectious Diseases, 30(11), 2261-2270. https://doi.org/10.3201/eid3011.240329. |
Vibrio parahaemolyticus Foodborne Illness Associated with Oysters, Australia, 2021–2022
The bacterium Vibrio parahaemolyticus is ubiquitous in tropical and temperate waters throughout the world and causes infections in humans resulting from water exposure and from ingestion of contaminated raw or undercooked seafood, such as oysters. We describe a nationwide outbreak of enteric infections caused by Vibrio parahaemolyticus in Australia during September 2021–January 2022. A total of 268 persons were linked with the outbreak, 97% of whom reported consuming Australia-grown oysters. Cases were reported from all states and territories of Australia. The outbreak comprised 2 distinct strains of V. parahaemolyticus, sequence types 417 and 50. We traced oysters with V. parahaemolyticus proliferation back to a common growing region within the state of South Australia. The outbreak prompted a national recall of oysters and subsequent improvements in postharvest processing of the shellfish.
EID | Fearnley E, Leong L, Centofanti A, Dowsett P, Combs BG, Draper A, et al. Vibrio parahaemolyticus Foodborne Illness Associated with Oysters, Australia, 2021–2022. Emerg Infect Dis. 2024;30(11):2271-2278. https://doi.org/10.3201/eid3011.240172 |
---|---|
AMA | Fearnley E, Leong L, Centofanti A, et al. Vibrio parahaemolyticus Foodborne Illness Associated with Oysters, Australia, 2021–2022. Emerging Infectious Diseases. 2024;30(11):2271-2278. doi:10.3201/eid3011.240172. |
APA | Fearnley, E., Leong, L., Centofanti, A., Dowsett, P., Combs, B. G., Draper, A....Wright, R. (2024). Vibrio parahaemolyticus Foodborne Illness Associated with Oysters, Australia, 2021–2022. Emerging Infectious Diseases, 30(11), 2271-2278. https://doi.org/10.3201/eid3011.240172. |
Wastewater Surveillance for Poliovirus in Selected Jurisdictions, United States, 2022–2023
Wastewater testing can inform public health action as a component of polio outbreak response. During 2022–2023, a total of 7 US jurisdictions (5 states and 2 cities) participated in prospective or retrospective testing of wastewater for poliovirus after a paralytic polio case was identified in New York state. Two distinct vaccine-derived poliovirus type 2 viruses were detected in wastewater from New York state and New York City during 2022, representing 2 separate importation events. Of those viruses, 1 resulted in persistent community transmission in multiple New York counties and 1 paralytic case. No poliovirus was detected in the other participating jurisdictions (Connecticut, New Jersey, Michigan, and Illinois and Chicago, IL). The value of routine wastewater surveillance for poliovirus apart from an outbreak is unclear. However, these results highlight the ongoing risk for poliovirus importations into the United States and the need to identify undervaccinated communities and increase vaccination coverage to prevent paralytic polio.
EID | Whitehouse ER, Gerloff N, English R, Reckling SK, Alazawi MA, Fuschino M, et al. Wastewater Surveillance for Poliovirus in Selected Jurisdictions, United States, 2022–2023. Emerg Infect Dis. 2024;30(11):2279-2287. https://doi.org/10.3201/eid3011.240771 |
---|---|
AMA | Whitehouse ER, Gerloff N, English R, et al. Wastewater Surveillance for Poliovirus in Selected Jurisdictions, United States, 2022–2023. Emerging Infectious Diseases. 2024;30(11):2279-2287. doi:10.3201/eid3011.240771. |
APA | Whitehouse, E. R., Gerloff, N., English, R., Reckling, S. K., Alazawi, M. A., Fuschino, M....Kidd, S. (2024). Wastewater Surveillance for Poliovirus in Selected Jurisdictions, United States, 2022–2023. Emerging Infectious Diseases, 30(11), 2279-2287. https://doi.org/10.3201/eid3011.240771. |
Rocky Mountain Spotted Fever in Children along the US‒Mexico Border, 2017–2023
Rocky mountain spotted fever (RMSF) causes significant illness and death in children. Although historically rare in California, USA, RMSF is endemic in areas of northern Mexico that border California. We describe 7 children with RMSF who were hospitalized at a tertiary pediatric referral center in California during 2017–2023. Five children had recent travel to Mexico with presumptive exposure, but 2 children did not report any travel outside of California. In all 7 patients, Rickettsia rickettsii DNA was detected by plasma microbial cell-free next-generation sequencing, which may be a useful diagnostic modality for RMSF, especially early in the course of illness, when standard diagnostic tests for RMSF are of limited sensitivity. A high index of suspicion and awareness of local epidemiologic trends remain most critical to recognizing the clinical syndrome of RMSF and initiating appropriate antimicrobial therapy in a timely fashion.
EID | Chiang L, Ramchandar N, Aramkul J, Fireizen Y, Beatty ME, Monroe M, et al. Rocky Mountain Spotted Fever in Children along the US‒Mexico Border, 2017–2023. Emerg Infect Dis. 2024;30(11):2288-2293. https://doi.org/10.3201/eid3011.231760 |
---|---|
AMA | Chiang L, Ramchandar N, Aramkul J, et al. Rocky Mountain Spotted Fever in Children along the US‒Mexico Border, 2017–2023. Emerging Infectious Diseases. 2024;30(11):2288-2293. doi:10.3201/eid3011.231760. |
APA | Chiang, L., Ramchandar, N., Aramkul, J., Fireizen, Y., Beatty, M. E., Monroe, M....Coufal, N. G. (2024). Rocky Mountain Spotted Fever in Children along the US‒Mexico Border, 2017–2023. Emerging Infectious Diseases, 30(11), 2288-2293. https://doi.org/10.3201/eid3011.231760. |
Research
Mycobacterium abscessus infection is challenging to treat. Extrapulmonary M. abscessus infections (EP-MAB) are less common than pulmonary M. abscessus infections. To evaluate treatment regimens, we retrospectively analyzed consecutive microbiologically confirmed EP-MAB cases diagnosed in France during 2012–2020. We studied 45 patients with EP-MAB, including 14 bone and joint infections, 10 skin and soft tissue infections, and 8 lymph node infections. Most (62%) patients had no reported immunodeficiency. In 27 patients, EP-MAB followed healthcare-associated (44%) or environmental (16%) injuries. Of the 45 isolates, 25 were subspecies abscessus, 10 bolletii, and 9 massiliense; 1 was unidentified. Cure was achieved for 36 (80%) patients who received a median antimicrobial regimen of 6 months; 22 (55%) also underwent surgery. Four patients died, and 5 were unavailable for follow-up. EP-MAB predominantly affects immunocompetent patients after an injury; outcomes are favorable. We propose a >6-month regimen of antimicrobial therapy with consideration for surgery and regular patient reassessment.
EID | Heid-Picard B, Mougari F, Pouvaret A, Lanternier F, Awad Z, Bille E, et al. Extrapulmonary Mycobacterium abscessus Infections, France, 2012–2020. Emerg Infect Dis. 2024;30(11):2294-2302. https://doi.org/10.3201/eid3011.240459 |
---|---|
AMA | Heid-Picard B, Mougari F, Pouvaret A, et al. Extrapulmonary Mycobacterium abscessus Infections, France, 2012–2020. Emerging Infectious Diseases. 2024;30(11):2294-2302. doi:10.3201/eid3011.240459. |
APA | Heid-Picard, B., Mougari, F., Pouvaret, A., Lanternier, F., Awad, Z., Bille, E....Cambau, E. (2024). Extrapulmonary Mycobacterium abscessus Infections, France, 2012–2020. Emerging Infectious Diseases, 30(11), 2294-2302. https://doi.org/10.3201/eid3011.240459. |
Antiviral Susceptibility of Swine-Origin Influenza A Viruses Isolated from Humans, United States
Since 2013, a total of 167 human infections with swine-origin (variant) influenza A viruses of A(H1N1)v, A(H1N2)v, and A(H3N2)v subtypes have been reported in the United States. Analysis of 147 genome sequences revealed that nearly all had S31N substitution, an M2 channel blocker-resistance marker, whereas neuraminidase inhibitor–resistance markers were not found. Two viruses had a polymerase acidic substitution (I38M or E199G) associated with decreased susceptibility to baloxavir, an inhibitor of viral cap-dependent endonuclease (CEN). Using phenotypic assays, we established subtype-specific susceptibility baselines for neuraminidase and CEN inhibitors. When compared with either baseline or CEN-sequence–matched controls, only the I38M substitution decreased baloxavir susceptibility, by 27-fold. Human monoclonal antibodies FI6v3 and CR9114 targeting the hemagglutinin’s stem showed variable (0.03 to >10 µg/mL) neutralizing activity toward variant viruses, even within the same clade. Methodology and interpretation of laboratory data described in this study provide information for risk assessment and decision-making on therapeutic control measures.
EID | Gao R, Pascua PQ, Chesnokov A, Nguyen HT, Uyeki TM, Mishin VP, et al. Antiviral Susceptibility of Swine-Origin Influenza A Viruses Isolated from Humans, United States. Emerg Infect Dis. 2024;30(11):2303-2312. https://doi.org/10.3201/eid3011.240892 |
---|---|
AMA | Gao R, Pascua PQ, Chesnokov A, et al. Antiviral Susceptibility of Swine-Origin Influenza A Viruses Isolated from Humans, United States. Emerging Infectious Diseases. 2024;30(11):2303-2312. doi:10.3201/eid3011.240892. |
APA | Gao, R., Pascua, P. Q., Chesnokov, A., Nguyen, H. T., Uyeki, T. M., Mishin, V. P....Gubareva, L. V. (2024). Antiviral Susceptibility of Swine-Origin Influenza A Viruses Isolated from Humans, United States. Emerging Infectious Diseases, 30(11), 2303-2312. https://doi.org/10.3201/eid3011.240892. |
Risk for Facial Palsy after COVID-19 Vaccination, South Korea, 2021–2022
We conducted a self-controlled case series study to investigate the association between COVID-19 vaccination and facial palsy (FP) in South Korea. We used a large immunization registry linked with the national health information database. We included 44,564,345 patients >18 years of age who received >1 dose of COVID-19 vaccine (BNT162b2, mRNA-1273, ChAdOx1 nCoV-19, or Ad.26.COV2.S) and had an FP diagnosis and corticosteroid prescription within 240 days postvaccination. We compared FP incidence in a risk window (days 1–28) with a control window (the remainder of the 240-day observation period, excluding any risk windows). We found 5,211 patients experienced FP within the risk window and 10,531 experienced FP within the control window. FP risk increased within 28 days postvaccination, primarily after first and second doses and was observed for both mRNA and viral vaccines. Clinicians should carefully assess the FP risk-benefit profile associated with the COVID-19 vaccines and monitor neurologic signs after vaccination.
EID | Yoon D, Jung K, Kim J, Ko H, Yoon B, Shin J. Risk for Facial Palsy after COVID-19 Vaccination, South Korea, 2021–2022. Emerg Infect Dis. 2024;30(11):2313-2322. https://doi.org/10.3201/eid3011.240610 |
---|---|
AMA | Yoon D, Jung K, Kim J, et al. Risk for Facial Palsy after COVID-19 Vaccination, South Korea, 2021–2022. Emerging Infectious Diseases. 2024;30(11):2313-2322. doi:10.3201/eid3011.240610. |
APA | Yoon, D., Jung, K., Kim, J., Ko, H., Yoon, B., & Shin, J. (2024). Risk for Facial Palsy after COVID-19 Vaccination, South Korea, 2021–2022. Emerging Infectious Diseases, 30(11), 2313-2322. https://doi.org/10.3201/eid3011.240610. |
Detection in Orchards of Predominant Azole-Resistant Candida tropicalis Genotype Causing Human Candidemia, Taiwan
Fluconazole-resistant clade 4 Candida tropicalis causing candidemia in humans has been detected in tropical/subtropical areas, including those in China, Singapore, and Australia. We analyzed 704 individual yeasts isolated from fruits, soil, water, and farmers at 80 orchards in Taiwan. The most common pathogenic yeast species among 251 isolates recovered from farmers were Candida albicans (14.7%) and C. parapsilosis (11.6%). In contrast, C. tropicalis (13.0%), C. palmioleophila (6.6%), and Pichia kudriavzevii (6.0%) were prevalent among 453 environmental isolates. Approximately 18.6% (11/59) of C. tropicalis from the environment were resistant to fluconazole, and 81.8% (9/11) of those belonged to the clade 4 genotype. C. tropicalis susceptibility to fluconazole correlated with susceptibilities to the agricultural azole fungicides, difenoconazole, tebuconazole, and triadimenol. Tandem gene duplications of mutated ERG11 contributed to azole resistance. Agriculture environments are a reservoir for azole-resistant C. tropicalis; discontinuing agricultural use of azoles might reduce emergence of azole-resistant Candida spp. strains in humans.
EID | Tseng K, Chen Y, Zhou Z, Tsai J, Tseng M, Liu H, et al. Detection in Orchards of Predominant Azole-Resistant Candida tropicalis Genotype Causing Human Candidemia, Taiwan. Emerg Infect Dis. 2024;30(11):2323-2332. https://doi.org/10.3201/eid3011.240545 |
---|---|
AMA | Tseng K, Chen Y, Zhou Z, et al. Detection in Orchards of Predominant Azole-Resistant Candida tropicalis Genotype Causing Human Candidemia, Taiwan. Emerging Infectious Diseases. 2024;30(11):2323-2332. doi:10.3201/eid3011.240545. |
APA | Tseng, K., Chen, Y., Zhou, Z., Tsai, J., Tseng, M., Liu, H....Lo, H. (2024). Detection in Orchards of Predominant Azole-Resistant Candida tropicalis Genotype Causing Human Candidemia, Taiwan. Emerging Infectious Diseases, 30(11), 2323-2332. https://doi.org/10.3201/eid3011.240545. |
Spatiotemporal Ecologic Analysis of COVID-19 Vaccination Coverage and Outcomes, Oklahoma, USA, February 2020–December 2021
Data on COVID-19 cases, deaths, hospitalizations, and vaccinations in Oklahoma, USA, have not been systematically described. The relationship between vaccination and COVID-19–related outcomes over time has not been investigated. We graphically described data collected during February 2020–December 2021 and conducted spatiotemporal modeling of monthly increases in COVID-19 cumulative death and hospitalization rates, adjusting for cumulative case rate, to explore the relationship. A 1 percentage point increase (absolute change) in the cumulative vaccination rate was associated with a 6.3% (95% CI 1.4%–10.9%) relative decrease in death outcome during April–June 2021, and a 1.9% (95% CI 1.1%–2.6%) relative decrease in death outcome and 1.1% (95% CI 0.5%–1.7%) relative decrease in hospitalization outcome during July–December 2021; the effect on hospitalizations was driven largely by data from urban counties. Our findings from Oklahoma suggest that increasing cumulative vaccination rates might reduce the increase in cumulative death and hospitalization rates from COVID-19.
EID | Ding K, Naqvi OH, Seeberger R, Bratzler DW, Wendelboe AM. Spatiotemporal Ecologic Analysis of COVID-19 Vaccination Coverage and Outcomes, Oklahoma, USA, February 2020–December 2021. Emerg Infect Dis. 2024;30(11):2333-2342. https://doi.org/10.3201/eid3011.231582 |
---|---|
AMA | Ding K, Naqvi OH, Seeberger R, et al. Spatiotemporal Ecologic Analysis of COVID-19 Vaccination Coverage and Outcomes, Oklahoma, USA, February 2020–December 2021. Emerging Infectious Diseases. 2024;30(11):2333-2342. doi:10.3201/eid3011.231582. |
APA | Ding, K., Naqvi, O. H., Seeberger, R., Bratzler, D. W., & Wendelboe, A. M. (2024). Spatiotemporal Ecologic Analysis of COVID-19 Vaccination Coverage and Outcomes, Oklahoma, USA, February 2020–December 2021. Emerging Infectious Diseases, 30(11), 2333-2342. https://doi.org/10.3201/eid3011.231582. |
SARS-CoV-2 Infection in School Settings, Okinawa Prefecture, Japan, 2021–2022
During the COVID-19 pandemic, widespread school closures were implemented globally based on the assumption that transmission among children in the school environment is common. However, evidence regarding secondary infection rates by school type and level of contact is lacking. Our study estimated the frequency of SARS-CoV-2 infection in school settings by examining the positivity rate according to school type and level of contact by using data from a large-scale school-based PCR project conducted in Okinawa, Japan, during 2021–2022. Our results indicate that, despite detection of numerous positive cases, the average number of secondary infections remained relatively low at ≈0.5 cases across all types of schools. Considering the profound effects of prolonged closures on educational access, balancing public health benefits against potential long-term effects on children is crucial.
EID | Takayama Y, Shimakawa Y, Matsuyama R, Chowell G, Omori R, Nagamoto T, et al. SARS-CoV-2 Infection in School Settings, Okinawa Prefecture, Japan, 2021–2022. Emerg Infect Dis. 2024;30(11):2343-2351. https://doi.org/10.3201/eid3011.240638 |
---|---|
AMA | Takayama Y, Shimakawa Y, Matsuyama R, et al. SARS-CoV-2 Infection in School Settings, Okinawa Prefecture, Japan, 2021–2022. Emerging Infectious Diseases. 2024;30(11):2343-2351. doi:10.3201/eid3011.240638. |
APA | Takayama, Y., Shimakawa, Y., Matsuyama, R., Chowell, G., Omori, R., Nagamoto, T....Mizumoto, K. (2024). SARS-CoV-2 Infection in School Settings, Okinawa Prefecture, Japan, 2021–2022. Emerging Infectious Diseases, 30(11), 2343-2351. https://doi.org/10.3201/eid3011.240638. |
Quantitative SARS-CoV-2 Spike Receptor-Binding Domain and Neutralizing Antibody Titers in Previously Infected Persons, United States, January 2021–February 2022
We studied SARS-CoV-2 binding and neutralizing antibody titers among previously infected persons in the United States over time. We assayed SARS-CoV-2 spike protein receptor-binding domain and neutralizing antibody titers for a convenience sample of residual clinical serum specimens that had evidence of prior SARS-CoV-2 infection gathered during January 2021–February 2022. We correlated titers and examined them by age group (<18, 18–49, 50–64, and >65 years) across 4 different SARS-CoV-2 variant epochs. Among selected specimens, 30,967 had binding antibody titers and 744 had neutralizing titers available. Titers in specimens from children and adults correlated. In addition, mean binding antibody titers increased over time for all age groups, and mean neutralization titers increased over time for persons 16–49 and >65 years of age. Incorporating binding and neutralization antibody titers into infectious disease surveillance could provide a clearer picture of overall immunity and help target vaccination campaigns.
EID | Bratcher A, Kao S, Chun K, Petropoulos CJ, Gundlapalli AV, Jones J, et al. Quantitative SARS-CoV-2 Spike Receptor-Binding Domain and Neutralizing Antibody Titers in Previously Infected Persons, United States, January 2021–February 2022. Emerg Infect Dis. 2024;30(11):2352-2361. https://doi.org/10.3201/eid3011.240043 |
---|---|
AMA | Bratcher A, Kao S, Chun K, et al. Quantitative SARS-CoV-2 Spike Receptor-Binding Domain and Neutralizing Antibody Titers in Previously Infected Persons, United States, January 2021–February 2022. Emerging Infectious Diseases. 2024;30(11):2352-2361. doi:10.3201/eid3011.240043. |
APA | Bratcher, A., Kao, S., Chun, K., Petropoulos, C. J., Gundlapalli, A. V., Jones, J....Clarke, K. (2024). Quantitative SARS-CoV-2 Spike Receptor-Binding Domain and Neutralizing Antibody Titers in Previously Infected Persons, United States, January 2021–February 2022. Emerging Infectious Diseases, 30(11), 2352-2361. https://doi.org/10.3201/eid3011.240043. |
Estimating Influenza Illnesses Averted by Year-Round and Seasonal Campaign Vaccination for Young Children, Kenya
In Kenya, influenza virus circulates year-round, raising questions about optimum strategies for vaccination. Given national interest in introducing influenza vaccination for young children 6–23 months of age, we modeled total influenza-associated illnesses (inclusive of hospitalizations, outpatient illnesses, and non‒medically attended illnesses) averted by multiple potential vaccination strategies: year-round versus seasonal-campaign vaccination, and vaccination starting in April (Southern Hemisphere influenza vaccine availability) versus October (Northern Hemisphere availability). We modeled average vaccine effectiveness of 50% and annual vaccination coverage of 60%. In the introduction year, year-round vaccination averted 6,410 total illnesses when introduced in October and 7,202 illnesses when introduced in April, whereas seasonal-campaign vaccination averted 10,236 (October) to 11,612 (April) illnesses. In the year after introduction, both strategies averted comparable numbers of illnesses (10,831–10,868 for year-round, 10,175–11,282 for campaign). Campaign-style vaccination would likely have a greater effect during initial pediatric influenza vaccine introduction in Kenya; however, either strategy could achieve similar longer-term effects.
EID | Gharpure R, Yoo YM, Andagalu B, Tempia S, Loayza S, Machingaidze C, et al. Estimating Influenza Illnesses Averted by Year-Round and Seasonal Campaign Vaccination for Young Children, Kenya. Emerg Infect Dis. 2024;30(11):2362-2369. https://doi.org/10.3201/eid3011.240375 |
---|---|
AMA | Gharpure R, Yoo YM, Andagalu B, et al. Estimating Influenza Illnesses Averted by Year-Round and Seasonal Campaign Vaccination for Young Children, Kenya. Emerging Infectious Diseases. 2024;30(11):2362-2369. doi:10.3201/eid3011.240375. |
APA | Gharpure, R., Yoo, Y. M., Andagalu, B., Tempia, S., Loayza, S., Machingaidze, C....Emukule, G. O. (2024). Estimating Influenza Illnesses Averted by Year-Round and Seasonal Campaign Vaccination for Young Children, Kenya. Emerging Infectious Diseases, 30(11), 2362-2369. https://doi.org/10.3201/eid3011.240375. |
Dispatches
Fatal Oropouche Virus Infections in Nonendemic Region, Brazil, 2024
We report acute Oropouche virus infections in 2 previously healthy women from a nonendemic region of Brazil outside the Amazon Basin. Infections rapidly progressed to hemorrhagic manifestations and fatal outcomes in 4–5 days. These cases highlight the critical need for enhanced surveillance to clarify epidemiology of this neglected disease.
EID | Bandeira A, Pereira F, Leal A, Santos S, Barbosa A, Souza M, et al. Fatal Oropouche Virus Infections in Nonendemic Region, Brazil, 2024. Emerg Infect Dis. 2024;30(11):2370-2374. https://doi.org/10.3201/eid3011.241132 |
---|---|
AMA | Bandeira A, Pereira F, Leal A, et al. Fatal Oropouche Virus Infections in Nonendemic Region, Brazil, 2024. Emerging Infectious Diseases. 2024;30(11):2370-2374. doi:10.3201/eid3011.241132. |
APA | Bandeira, A., Pereira, F., Leal, A., Santos, S., Barbosa, A., Souza, M....Araújo, M. (2024). Fatal Oropouche Virus Infections in Nonendemic Region, Brazil, 2024. Emerging Infectious Diseases, 30(11), 2370-2374. https://doi.org/10.3201/eid3011.241132. |
Co-Circulation of 2 Oropouche Virus Lineages, Amazon Basin, Colombia, 2024
In early 2024, explosive outbreaks of Oropouche virus (OROV) linked to a novel lineage were documented in the Amazon Region of Brazil. We report the introduction of this lineage into Colombia and its co-circulation with another OROV lineage. Continued surveillance is needed to prevent further spread of OROV in the Americas.
EID | Usuga J, Limonta D, Perez-Restrepo LS, Ciuoderis KA, Moreno I, Arevalo A, et al. Co-Circulation of 2 Oropouche Virus Lineages, Amazon Basin, Colombia, 2024. Emerg Infect Dis. 2024;30(11):2375-2380. https://doi.org/10.3201/eid3011.240405 |
---|---|
AMA | Usuga J, Limonta D, Perez-Restrepo LS, et al. Co-Circulation of 2 Oropouche Virus Lineages, Amazon Basin, Colombia, 2024. Emerging Infectious Diseases. 2024;30(11):2375-2380. doi:10.3201/eid3011.240405. |
APA | Usuga, J., Limonta, D., Perez-Restrepo, L. S., Ciuoderis, K. A., Moreno, I., Arevalo, A....Osorio, J. E. (2024). Co-Circulation of 2 Oropouche Virus Lineages, Amazon Basin, Colombia, 2024. Emerging Infectious Diseases, 30(11), 2375-2380. https://doi.org/10.3201/eid3011.240405. |
Analysis of Monkeypox Virus Exposures and Lesions by Anatomic Site
We used cross-sectional data from 226 patients with monkeypox virus to investigate the association between anatomic exposure site and lesion development. Penile, anorectal, and oral exposures predicted lesion presence at correlating anatomic sites. Exposure site also predicted the first lesion site of the penis and anus.
EID | Guagliardo SJ, Smith T, Hamer DH, Huits R, Kozarsky P, Libman M, et al. Analysis of Monkeypox Virus Exposures and Lesions by Anatomic Site. Emerg Infect Dis. 2024;30(11):2381-2384. https://doi.org/10.3201/eid3011.241120 |
---|---|
AMA | Guagliardo SJ, Smith T, Hamer DH, et al. Analysis of Monkeypox Virus Exposures and Lesions by Anatomic Site. Emerging Infectious Diseases. 2024;30(11):2381-2384. doi:10.3201/eid3011.241120. |
APA | Guagliardo, S. J., Smith, T., Hamer, D. H., Huits, R., Kozarsky, P., Libman, M....Angelo, K. M. (2024). Analysis of Monkeypox Virus Exposures and Lesions by Anatomic Site. Emerging Infectious Diseases, 30(11), 2381-2384. https://doi.org/10.3201/eid3011.241120. |
Emerging Monkeypox Virus Sublineage C.1 Causing Community Transmission, Vietnam, 2023
We studied a community cluster of 25 mpox cases in Vietnam caused by emerging monkeypox virus sublineage C.1 and imported into Vietnam through 2 independent events; 1 major cluster carried a novel APOBEC3-like mutation. Three patients died; all had advanced HIV co-infection. Viral evolution and its potential consequences should be closely monitored.
EID | Hoa H, Dung N, Hung L, Hong N, Quy V, Thao N, et al. Emerging Monkeypox Virus Sublineage C.1 Causing Community Transmission, Vietnam, 2023. Emerg Infect Dis. 2024;30(11):2385-2390. https://doi.org/10.3201/eid3011.240729 |
---|---|
AMA | Hoa H, Dung N, Hung L, et al. Emerging Monkeypox Virus Sublineage C.1 Causing Community Transmission, Vietnam, 2023. Emerging Infectious Diseases. 2024;30(11):2385-2390. doi:10.3201/eid3011.240729. |
APA | Hoa, H., Dung, N., Hung, L., Hong, N., Quy, V., Thao, N....Van Tan, L. (2024). Emerging Monkeypox Virus Sublineage C.1 Causing Community Transmission, Vietnam, 2023. Emerging Infectious Diseases, 30(11), 2385-2390. https://doi.org/10.3201/eid3011.240729. |
Dengue Outbreak Caused by Multiple Virus Serotypes and Lineages, Colombia, 2023–2024
Dengue cases rose to record levels during 2023–2024. We investigated dengue in Valle del Cauca, Colombia, to determine if specific virus serotypes or lineages caused its large outbreak. We detected all 4 serotypes and multiple lineages, suggesting that factors such as climatic conditions were likely responsible for increased dengue in Colombia.
EID | Grubaugh ND, Torres-Hernández D, Murillo-Ortiz MA, Dávalos DM, Lopez P, Hurtado IC, et al. Dengue Outbreak Caused by Multiple Virus Serotypes and Lineages, Colombia, 2023–2024. Emerg Infect Dis. 2024;30(11):2391-2395. https://doi.org/10.3201/eid3011.241031 |
---|---|
AMA | Grubaugh ND, Torres-Hernández D, Murillo-Ortiz MA, et al. Dengue Outbreak Caused by Multiple Virus Serotypes and Lineages, Colombia, 2023–2024. Emerging Infectious Diseases. 2024;30(11):2391-2395. doi:10.3201/eid3011.241031. |
APA | Grubaugh, N. D., Torres-Hernández, D., Murillo-Ortiz, M. A., Dávalos, D. M., Lopez, P., Hurtado, I. C....López-Medina, E. (2024). Dengue Outbreak Caused by Multiple Virus Serotypes and Lineages, Colombia, 2023–2024. Emerging Infectious Diseases, 30(11), 2391-2395. https://doi.org/10.3201/eid3011.241031. |
Evidence of Human Bourbon Virus Infections, North Carolina, USA
Bourbon virus is a tickborne virus that can cause human disease. Cases have been reported in Kansas, Oklahoma, and Missouri, USA. We identified Bourbon virus–specific neutralizing antibodies in patients from North Carolina. Bourbon virus infections are likely more common than previously thought, highlighting the need for improved diagnostics and surveillance.
EID | Zychowski DL, Bamunuarachchi G, Commins SP, Boyce RM, Boon A. Evidence of Human Bourbon Virus Infections, North Carolina, USA. Emerg Infect Dis. 2024;30(11):2396-2399. https://doi.org/10.3201/eid3011.240499 |
---|---|
AMA | Zychowski DL, Bamunuarachchi G, Commins SP, et al. Evidence of Human Bourbon Virus Infections, North Carolina, USA. Emerging Infectious Diseases. 2024;30(11):2396-2399. doi:10.3201/eid3011.240499. |
APA | Zychowski, D. L., Bamunuarachchi, G., Commins, S. P., Boyce, R. M., & Boon, A. (2024). Evidence of Human Bourbon Virus Infections, North Carolina, USA. Emerging Infectious Diseases, 30(11), 2396-2399. https://doi.org/10.3201/eid3011.240499. |
Clinical and Molecular Characterization of Human Burkholderia mallei Infection, Brazil
We report a case of Burkholderia mallei causing glanders in a 73-year-old patient from the Northeast Region of Brazil. The patient was hospitalized with severe pneumonia. PCR and genomic sequencing confirmed B. mallei in pleural drainage. Genotyping revealed a novel genotype, emphasizing the need for genetic surveillance in zoonotic infections.
EID | Luz KG, Bezerra F, Sicolo MA, Silva A, Egito AA, Suniga P, et al. Clinical and Molecular Characterization of Human Burkholderia mallei Infection, Brazil. Emerg Infect Dis. 2024;30(11):2400-2403. https://doi.org/10.3201/eid3011.240549 |
---|---|
AMA | Luz KG, Bezerra F, Sicolo MA, et al. Clinical and Molecular Characterization of Human Burkholderia mallei Infection, Brazil. Emerging Infectious Diseases. 2024;30(11):2400-2403. doi:10.3201/eid3011.240549. |
APA | Luz, K. G., Bezerra, F., Sicolo, M. A., Silva, A., Egito, A. A., Suniga, P....Araújo, F. R. (2024). Clinical and Molecular Characterization of Human Burkholderia mallei Infection, Brazil. Emerging Infectious Diseases, 30(11), 2400-2403. https://doi.org/10.3201/eid3011.240549. |
Computerized Decision Support Systems Informing Community-Acquired Pneumonia Surveillance, France, 2017–2023
We show the value of real-time data generated by a computerized decision support system in primary care in strengthening pneumonia surveillance. The system showed a 66% (95% CI 64%–67%) increase in community-acquired pneumonia from 2018 to 2023 for the population of France, 1 month before a national alert was issued.
EID | Delory T, Le Bel J, Métras R, Guerrisi C, Suhanda IE, Bouvet E, et al. Computerized Decision Support Systems Informing Community-Acquired Pneumonia Surveillance, France, 2017–2023. Emerg Infect Dis. 2024;30(11):2404-2408. https://doi.org/10.3201/eid3011.240072 |
---|---|
AMA | Delory T, Le Bel J, Métras R, et al. Computerized Decision Support Systems Informing Community-Acquired Pneumonia Surveillance, France, 2017–2023. Emerging Infectious Diseases. 2024;30(11):2404-2408. doi:10.3201/eid3011.240072. |
APA | Delory, T., Le Bel, J., Métras, R., Guerrisi, C., Suhanda, I. E., Bouvet, E....Jeanmougin, P. (2024). Computerized Decision Support Systems Informing Community-Acquired Pneumonia Surveillance, France, 2017–2023. Emerging Infectious Diseases, 30(11), 2404-2408. https://doi.org/10.3201/eid3011.240072. |
Invasive Group A Streptococcus Hypervirulent M1UK Clone, Canada, 2018–2023
To determine invasive group A Streptococcus trends in Canada, we characterized emm1 isolates collected during 2018–2023. The percentage of hypervirulent M1UK lineage isolates increased significantly, from 22.1% in 2018 to 60.2% in 2023. Genomic analysis identified geographically and temporally associated clusters and genes associated with virulent bacteriophage acquisition.
EID | Golden AR, Griffith A, Tyrrell GJ, Kus JV, McGeer A, Domingo M, et al. Invasive Group A Streptococcus Hypervirulent M1UK Clone, Canada, 2018–2023. Emerg Infect Dis. 2024;30(11):2409-2413. https://doi.org/10.3201/eid3011.241068 |
---|---|
AMA | Golden AR, Griffith A, Tyrrell GJ, et al. Invasive Group A Streptococcus Hypervirulent M1UK Clone, Canada, 2018–2023. Emerging Infectious Diseases. 2024;30(11):2409-2413. doi:10.3201/eid3011.241068. |
APA | Golden, A. R., Griffith, A., Tyrrell, G. J., Kus, J. V., McGeer, A., Domingo, M....Martin, I. (2024). Invasive Group A Streptococcus Hypervirulent M1UK Clone, Canada, 2018–2023. Emerging Infectious Diseases, 30(11), 2409-2413. https://doi.org/10.3201/eid3011.241068. |
Genomic Epidemiology of Human Respiratory Syncytial Virus, Minnesota, USA, July 2023–February 2024
We recently expanded the viral genomic surveillance program in Minnesota, USA, to include human respiratory syncytial virus. We performed whole-genome sequencing of 575 specimens collected at Minnesota healthcare facilities during July 2023–February 2024. Subgroups A and B differed in their genomic landscapes, and we identified 23 clusters of genetically identical genomes.
EID | Evans D, Kunerth H, Mumm E, Namugenyi S, Plumb M, Bistodeau S, et al. Genomic Epidemiology of Human Respiratory Syncytial Virus, Minnesota, USA, July 2023–February 2024. Emerg Infect Dis. 2024;30(11):2414-2418. https://doi.org/10.3201/eid3011.241000 |
---|---|
AMA | Evans D, Kunerth H, Mumm E, et al. Genomic Epidemiology of Human Respiratory Syncytial Virus, Minnesota, USA, July 2023–February 2024. Emerging Infectious Diseases. 2024;30(11):2414-2418. doi:10.3201/eid3011.241000. |
APA | Evans, D., Kunerth, H., Mumm, E., Namugenyi, S., Plumb, M., Bistodeau, S....Wang, X. (2024). Genomic Epidemiology of Human Respiratory Syncytial Virus, Minnesota, USA, July 2023–February 2024. Emerging Infectious Diseases, 30(11), 2414-2418. https://doi.org/10.3201/eid3011.241000. |
Transmission of Severe Fever with Thrombocytopenia Syndrome Virus to Human from Nonindigenous Tick Host, Japan
We report a human case of severe fever with thrombocytopenia syndrome virus infection transmitted by a tick, confirmed by viral identification. Haemaphysalis aborensis, a tick species not native to Japan that has been observed to transmit the virus to humans, is now recognized as a potential vector of this virus in Japan.
EID | Xu Q, Nabeshima T, Hamada K, Sugimoto T, Tun M, Morita K, et al. Transmission of Severe Fever with Thrombocytopenia Syndrome Virus to Human from Nonindigenous Tick Host, Japan. Emerg Infect Dis. 2024;30(11):2419-2423. https://doi.org/10.3201/eid3011.240912 |
---|---|
AMA | Xu Q, Nabeshima T, Hamada K, et al. Transmission of Severe Fever with Thrombocytopenia Syndrome Virus to Human from Nonindigenous Tick Host, Japan. Emerging Infectious Diseases. 2024;30(11):2419-2423. doi:10.3201/eid3011.240912. |
APA | Xu, Q., Nabeshima, T., Hamada, K., Sugimoto, T., Tun, M., Morita, K....Takamatsu, Y. (2024). Transmission of Severe Fever with Thrombocytopenia Syndrome Virus to Human from Nonindigenous Tick Host, Japan. Emerging Infectious Diseases, 30(11), 2419-2423. https://doi.org/10.3201/eid3011.240912. |
Research Letters
Outbreak of Listeriosis Likely Associated with Baker’s Yeast Products, Switzerland, 2022–2024
We traced back a nationwide outbreak of human listeriosis in Switzerland to a persisting production line contamination of a factory producing baker’s yeast with Listeria monocytogenes serotype 1/2a sequence type 3141. We used whole-genome sequencing to match clinical isolates to isolates from product samples.
EID | Stephan R, Horlbog J, Nüesch-Inderbinen M, Dhima N. Outbreak of Listeriosis Likely Associated with Baker’s Yeast Products, Switzerland, 2022–2024. Emerg Infect Dis. 2024;30(11):2424-2426. https://doi.org/10.3201/eid3011.240764 |
---|---|
AMA | Stephan R, Horlbog J, Nüesch-Inderbinen M, et al. Outbreak of Listeriosis Likely Associated with Baker’s Yeast Products, Switzerland, 2022–2024. Emerging Infectious Diseases. 2024;30(11):2424-2426. doi:10.3201/eid3011.240764. |
APA | Stephan, R., Horlbog, J., Nüesch-Inderbinen, M., & Dhima, N. (2024). Outbreak of Listeriosis Likely Associated with Baker’s Yeast Products, Switzerland, 2022–2024. Emerging Infectious Diseases, 30(11), 2424-2426. https://doi.org/10.3201/eid3011.240764. |
Influenza A(H5N1) Virus Resilience in Milk after Thermal Inactivation
Highly pathogenic avian influenza A(H5N1) detected in dairy cows raises concerns about milk safety. The effects of pasteurization-like temperatures on influenza viruses in retail and unpasteurized milk revealed virus resilience under certain conditions. Although pasteurization contributes to viral inactivation, influenza A virus, regardless of strain, displayed remarkable stability in pasteurized milk.
EID | Caceres C, Gay L, Faccin F, Regmi D, Palomares R, Perez DR. Influenza A(H5N1) Virus Resilience in Milk after Thermal Inactivation. Emerg Infect Dis. 2024;30(11):2426-2429. https://doi.org/10.3201/eid3011.240772 |
---|---|
AMA | Caceres C, Gay L, Faccin F, et al. Influenza A(H5N1) Virus Resilience in Milk after Thermal Inactivation. Emerging Infectious Diseases. 2024;30(11):2426-2429. doi:10.3201/eid3011.240772. |
APA | Caceres, C., Gay, L., Faccin, F., Regmi, D., Palomares, R., & Perez, D. R. (2024). Influenza A(H5N1) Virus Resilience in Milk after Thermal Inactivation. Emerging Infectious Diseases, 30(11), 2426-2429. https://doi.org/10.3201/eid3011.240772. |
Prevalence of Pertactin-Deficient Bordetella pertussis Isolates, Slovenia
In Slovenia, primary acellular pertussis vaccines (ACVs) containing pertactin (PRN) were mostly used during 1999–2016; ACVs without PRN were introduced in 2017. Among 123 Bordetella pertussis strains collected during 2002–2020, a total of 48 were PRN-deficient; 44 were collected after 2017. Changes to ACVs could increase PRN-deficient B. pertussis and infections.
EID | Barkoff A, Kastrin T, Seme K, Vitek M, Mertsola J, He Q. Prevalence of Pertactin-Deficient Bordetella pertussis Isolates, Slovenia. Emerg Infect Dis. 2024;30(11):2429-2432. https://doi.org/10.3201/eid3011.231393 |
---|---|
AMA | Barkoff A, Kastrin T, Seme K, et al. Prevalence of Pertactin-Deficient Bordetella pertussis Isolates, Slovenia. Emerging Infectious Diseases. 2024;30(11):2429-2432. doi:10.3201/eid3011.231393. |
APA | Barkoff, A., Kastrin, T., Seme, K., Vitek, M., Mertsola, J., & He, Q. (2024). Prevalence of Pertactin-Deficient Bordetella pertussis Isolates, Slovenia. Emerging Infectious Diseases, 30(11), 2429-2432. https://doi.org/10.3201/eid3011.231393. |
Suspected Acute Pulmonary Coccidioidomycosis in Traveler Returning to Switzerland from Peru
We report a suspected case of acute pulmonary coccidioidomycosis contracted in Peru, where the disease is not known to occur, in a patient from Switzerland. Although not confirmed by direct diagnostic testing, the clinical manifestations and serologic testing results of this case are highly suggestive of coccidioidomycosis.
EID | Neumayr A, Rickerts V, Ackermann S, Castelblanco F, Kuenzli E, Durovic A, et al. Suspected Acute Pulmonary Coccidioidomycosis in Traveler Returning to Switzerland from Peru. Emerg Infect Dis. 2024;30(11):2432-2435. https://doi.org/10.3201/eid3011.241034 |
---|---|
AMA | Neumayr A, Rickerts V, Ackermann S, et al. Suspected Acute Pulmonary Coccidioidomycosis in Traveler Returning to Switzerland from Peru. Emerging Infectious Diseases. 2024;30(11):2432-2435. doi:10.3201/eid3011.241034. |
APA | Neumayr, A., Rickerts, V., Ackermann, S., Castelblanco, F., Kuenzli, E., Durovic, A....Seas, C. (2024). Suspected Acute Pulmonary Coccidioidomycosis in Traveler Returning to Switzerland from Peru. Emerging Infectious Diseases, 30(11), 2432-2435. https://doi.org/10.3201/eid3011.241034. |
Epidemiology of Streptococcus pyogenes Disease before, during, and after COVID-19 Pandemic, Germany, 2005–2023
We analyzed 3,081 invasive and noninvasive Streptococcus pyogenes cases (January 2005–December 2023) at a tertiary care hospital in southwest Germany. Absolute numbers of case-patients increased each year from 2005 until the COVID-19 pandemic. Odds ratios for invasive streptococcal disease were significantly influenced by year, male sex, and older age.
EID | Burckhardt I, Burckhardt F. Epidemiology of Streptococcus pyogenes Disease before, during, and after COVID-19 Pandemic, Germany, 2005–2023. Emerg Infect Dis. 2024;30(11):2435-2438. https://doi.org/10.3201/eid3011.231667 |
---|---|
AMA | Burckhardt I, Burckhardt F. Epidemiology of Streptococcus pyogenes Disease before, during, and after COVID-19 Pandemic, Germany, 2005–2023. Emerging Infectious Diseases. 2024;30(11):2435-2438. doi:10.3201/eid3011.231667. |
APA | Burckhardt, I., & Burckhardt, F. (2024). Epidemiology of Streptococcus pyogenes Disease before, during, and after COVID-19 Pandemic, Germany, 2005–2023. Emerging Infectious Diseases, 30(11), 2435-2438. https://doi.org/10.3201/eid3011.231667. |
Wastewater Surveillance for Norovirus, California, USA
Norovirus is a leading cause of acute gastroenteritis and imposes a substantial disease burden. In California, USA, norovirus surveillance is limited. We evaluated correlations between wastewater norovirus concentrations and available public health surveillance data. Wastewater surveillance for norovirus genotype GII in California provided timely, localized, and actionable data for public health authorities.
EID | Yu AT, Burnor E, Rabe A, Rutschmann S, Wolfe MK, Burmester J, et al. Wastewater Surveillance for Norovirus, California, USA. Emerg Infect Dis. 2024;30(11):2438-2441. https://doi.org/10.3201/eid3011.241001 |
---|---|
AMA | Yu AT, Burnor E, Rabe A, et al. Wastewater Surveillance for Norovirus, California, USA. Emerging Infectious Diseases. 2024;30(11):2438-2441. doi:10.3201/eid3011.241001. |
APA | Yu, A. T., Burnor, E., Rabe, A., Rutschmann, S., Wolfe, M. K., Burmester, J....Vugia, D. J. (2024). Wastewater Surveillance for Norovirus, California, USA. Emerging Infectious Diseases, 30(11), 2438-2441. https://doi.org/10.3201/eid3011.241001. |
Environmental Vibrio cholerae Strains Harboring Cholera Toxin and Vibrio Pathogenicity Island 1, Nigeria, 2008–2015
Analysis of clinical and environmental Vibrio cholerae O1 strains obtained during 2008–2015 in Nigeria showed that lineages Afr9 and Afr12 carrying cholera toxin and Vibrio pathogenicity island 1 can be isolated from water. Our findings raise concerns about the role of the environment in maintenance and emergence of cholera outbreaks in Nigeria.
EID | Morgado S, Adewale A, Abiodun I, Lawal S, Freitas F, Fonseca É, et al. Environmental Vibrio cholerae Strains Harboring Cholera Toxin and Vibrio Pathogenicity Island 1, Nigeria, 2008–2015. Emerg Infect Dis. 2024;30(11):2441-2444. https://doi.org/10.3201/eid3011.240495 |
---|---|
AMA | Morgado S, Adewale A, Abiodun I, et al. Environmental Vibrio cholerae Strains Harboring Cholera Toxin and Vibrio Pathogenicity Island 1, Nigeria, 2008–2015. Emerging Infectious Diseases. 2024;30(11):2441-2444. doi:10.3201/eid3011.240495. |
APA | Morgado, S., Adewale, A., Abiodun, I., Lawal, S., Freitas, F., Fonseca, É....Vicente, A. (2024). Environmental Vibrio cholerae Strains Harboring Cholera Toxin and Vibrio Pathogenicity Island 1, Nigeria, 2008–2015. Emerging Infectious Diseases, 30(11), 2441-2444. https://doi.org/10.3201/eid3011.240495. |
Mpox Hepatic and Pulmonary Lesions in HIV/Hepatitis B Virus Co-Infected Patient, France
We report a case of persistent disseminated mpox evolving over >6 months in an HIV/hepatitis B virus co-infected patient in France who had <200 CD4+ cells/mm3, pulmonary and hepatic necrotic lesions, persistent viremia, and nasopharyngeal excretion. Clinical outcome was favorable after 90 days of tecovirimat treatment and administration of human vaccinia immunoglobulins.
EID | Calin R, Périllaud-Dubois C, Marot S, Kerrou K, Peytavin G, Bachir M, et al. Mpox Hepatic and Pulmonary Lesions in HIV/Hepatitis B Virus Co-Infected Patient, France. Emerg Infect Dis. 2024;30(11):2445-2447. https://doi.org/10.3201/eid3011.241331 |
---|---|
AMA | Calin R, Périllaud-Dubois C, Marot S, et al. Mpox Hepatic and Pulmonary Lesions in HIV/Hepatitis B Virus Co-Infected Patient, France. Emerging Infectious Diseases. 2024;30(11):2445-2447. doi:10.3201/eid3011.241331. |
APA | Calin, R., Périllaud-Dubois, C., Marot, S., Kerrou, K., Peytavin, G., Bachir, M....Pialoux, G. (2024). Mpox Hepatic and Pulmonary Lesions in HIV/Hepatitis B Virus Co-Infected Patient, France. Emerging Infectious Diseases, 30(11), 2445-2447. https://doi.org/10.3201/eid3011.241331. |
Iquitos Virus in Traveler Returning to the United States from Ecuador
We describe the case of a returned traveler to the United States from Ecuador who had an acute febrile illness, initially diagnosed as Oropouche fever. This illness was later confirmed to be a rare infection with Iquitos virus, a related bunyavirus that shares 2 of 3 genome segments with Oropouche virus.
EID | Baer K, Arora I, Kimbro J, Haider A, Mott M, Marshall K, et al. Iquitos Virus in Traveler Returning to the United States from Ecuador. Emerg Infect Dis. 2024;30(11):2447-2451. https://doi.org/10.3201/eid3011.240708 |
---|---|
AMA | Baer K, Arora I, Kimbro J, et al. Iquitos Virus in Traveler Returning to the United States from Ecuador. Emerging Infectious Diseases. 2024;30(11):2447-2451. doi:10.3201/eid3011.240708. |
APA | Baer, K., Arora, I., Kimbro, J., Haider, A., Mott, M., Marshall, K....Waggoner, J. J. (2024). Iquitos Virus in Traveler Returning to the United States from Ecuador. Emerging Infectious Diseases, 30(11), 2447-2451. https://doi.org/10.3201/eid3011.240708. |
Letters
Estimating Underdetection of Foodborne Disease Outbreaks
EID | Hedberg CW, Firestone MJ, Kim TN, Edmundson AR, Bender JB. Estimating Underdetection of Foodborne Disease Outbreaks. Emerg Infect Dis. 2024;30(11):2451. https://doi.org/10.3201/eid3011.240198 |
---|---|
AMA | Hedberg CW, Firestone MJ, Kim TN, et al. Estimating Underdetection of Foodborne Disease Outbreaks. Emerging Infectious Diseases. 2024;30(11):2451. doi:10.3201/eid3011.240198. |
APA | Hedberg, C. W., Firestone, M. J., Kim, T. N., Edmundson, A. R., & Bender, J. B. (2024). Estimating Underdetection of Foodborne Disease Outbreaks. Emerging Infectious Diseases, 30(11), 2451. https://doi.org/10.3201/eid3011.240198. |
Estimating Underdetection of Foodborne Disease Outbreaks (Response)
EID | Ford L, Self JL, Wong KK, Hoekstra RM, Tauxe RV, Rose E, et al. Estimating Underdetection of Foodborne Disease Outbreaks (Response). Emerg Infect Dis. 2024;30(11):2452. https://doi.org/10.3201/eid3011.241351 |
---|---|
AMA | Ford L, Self JL, Wong KK, et al. Estimating Underdetection of Foodborne Disease Outbreaks (Response). Emerging Infectious Diseases. 2024;30(11):2452. doi:10.3201/eid3011.241351. |
APA | Ford, L., Self, J. L., Wong, K. K., Hoekstra, R. M., Tauxe, R. V., Rose, E....Bruce, B. B. (2024). Estimating Underdetection of Foodborne Disease Outbreaks (Response). Emerging Infectious Diseases, 30(11), 2452. https://doi.org/10.3201/eid3011.241351. |
Books and Media
Revenge of the Microbes: How Bacterial Resistance Is Undermining the Antibiotic Miracle, 2nd Edition
EID | Caruso I. Revenge of the Microbes: How Bacterial Resistance Is Undermining the Antibiotic Miracle, 2nd Edition. Emerg Infect Dis. 2024;30(11):2453. https://doi.org/10.3201/eid3011.240228 |
---|---|
AMA | Caruso I. Revenge of the Microbes: How Bacterial Resistance Is Undermining the Antibiotic Miracle, 2nd Edition. Emerging Infectious Diseases. 2024;30(11):2453. doi:10.3201/eid3011.240228. |
APA | Caruso, I. (2024). Revenge of the Microbes: How Bacterial Resistance Is Undermining the Antibiotic Miracle, 2nd Edition. Emerging Infectious Diseases, 30(11), 2453. https://doi.org/10.3201/eid3011.240228. |
Online Reports
Rapid Decision Algorithm for Patient Triage during Ebola Outbreaks
The low specificity of Ebola virus disease clinical signs increases the risk for nosocomial transmission to patients and healthcare workers during outbreaks. Reducing this risk requires identifying patients with a high likelihood of Ebola virus infection. Analyses of retrospective data from patients suspected of having Ebola virus infection identified 13 strong predictors and time from disease onset as constituents of a prediction score for Ebola virus disease. We also noted 4 highly predictive variables that could distinguish patients at high risk for infection, independent of their scores. External validation of this algorithm on retrospective data revealed the probability of infection continuously increased with the score.
EID | Ardiet D, Nsio J, Komanda G, Coulborn RM, Grellety E, Grandesso F, et al. Rapid Decision Algorithm for Patient Triage during Ebola Outbreaks. Emerg Infect Dis. 2024;30(11):1-11. https://doi.org/10.3201/eid3011.231650 |
---|---|
AMA | Ardiet D, Nsio J, Komanda G, et al. Rapid Decision Algorithm for Patient Triage during Ebola Outbreaks. Emerging Infectious Diseases. 2024;30(11):1-11. doi:10.3201/eid3011.231650. |
APA | Ardiet, D., Nsio, J., Komanda, G., Coulborn, R. M., Grellety, E., Grandesso, F....Ahuka-Mundeke, S. (2024). Rapid Decision Algorithm for Patient Triage during Ebola Outbreaks. Emerging Infectious Diseases, 30(11), 1-11. https://doi.org/10.3201/eid3011.231650. |
About the Cover
Not Everything Is as It First Appears
EID | Breedlove B. Not Everything Is as It First Appears. Emerg Infect Dis. 2024;30(11):2454-2455. https://doi.org/10.3201/eid3011.ac3011 |
---|---|
AMA | Breedlove B. Not Everything Is as It First Appears. Emerging Infectious Diseases. 2024;30(11):2454-2455. doi:10.3201/eid3011.ac3011. |
APA | Breedlove, B. (2024). Not Everything Is as It First Appears. Emerging Infectious Diseases, 30(11), 2454-2455. https://doi.org/10.3201/eid3011.ac3011. |