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Articles from Emerging Infectious Diseases

Perspective

Medscape CME Activity
Archaea in the Human Microbiome and Potential Effects on Human Infectious Disease [PDF - 991 KB - 9 pages]
S. Duller and C. Moissl-Eichinger

Archaea represent a separate domain of life, next to bacteria and eukarya. As components of the human microbiome, archaea have been associated with various diseases, including periodontitis, endodontic infections, small intestinal bacterial overgrowth, and urogenital tract infections. Archaea are generally considered nonpathogenic; the reasons are speculative because of limited knowledge and gene annotation challenges. Nevertheless, archaeal syntrophic principles that shape global microbial networks aid both archaea and potentially pathogenic bacteria. Evaluating archaea interactions remains challenging, requiring clinical studies on inflammatory potential and the effects of archaeal metabolism. Establishing a culture collection is crucial for investigating archaea functions within the human microbiome, which could improve health outcomes in infectious diseases. We summarize potential reasons for archaeal nonpathogenicity, assess the association with infectious diseases in humans, and discuss the necessary experimental steps to enable mechanistic studies involving archaea.

EID Duller S, Moissl-Eichinger C. Archaea in the Human Microbiome and Potential Effects on Human Infectious Disease. Emerg Infect Dis. 2024;30(8):1505-1513. https://doi.org/10.3201/eid3008.240181
AMA Duller S, Moissl-Eichinger C. Archaea in the Human Microbiome and Potential Effects on Human Infectious Disease. Emerging Infectious Diseases. 2024;30(8):1505-1513. doi:10.3201/eid3008.240181.
APA Duller, S., & Moissl-Eichinger, C. (2024). Archaea in the Human Microbiome and Potential Effects on Human Infectious Disease. Emerging Infectious Diseases, 30(8), 1505-1513. https://doi.org/10.3201/eid3008.240181.
Synopses

Outbreak of Intermediate Species Leptospira venezuelensis Spread by Rodents to Cows and Humans in L. interrogans–Endemic Region, Venezuela [PDF - 762 KB - 9 pages]
L. Caraballo et al.

Leptospirosis is a common but underdiagnosed zoonosis. We conducted a 1-year prospective study in La Guaira State, Venezuela, analyzing 71 hospitalized patients who had possible leptospirosis and sampling local rodents and dairy cows. Leptospira rrs gene PCR test results were positive in blood or urine samples from 37/71 patients. Leptospira spp. were isolated from cultured blood or urine samples of 36/71 patients; 29 had L. interrogans, 3 L. noguchii, and 4 L. venezuelensis. Conjunctival suffusion was the most distinguishing clinical sign, many patients had liver involvement, and 8/30 patients with L. interrogans infections died. The Leptospira spp. found in humans were also isolated from local rodents; L. interrogans and L. venezuelensis were isolated from cows on a nearby, rodent-infested farm. Phylogenetic clustering of L. venezuelensis isolates suggested a recently expanded outbreak strain spread by rodents. Increased awareness of leptospirosis prevalence and rapid diagnostic tests are needed to improve patient outcomes.

EID Caraballo L, Rangel Y, Reyna-Bello A, Muñoz M, Figueroa-Espinosa R, Sanz-Rodriquez CE, et al. Outbreak of Intermediate Species Leptospira venezuelensis Spread by Rodents to Cows and Humans in L. interrogans–Endemic Region, Venezuela. Emerg Infect Dis. 2024;30(8):1514-1522. https://doi.org/10.3201/eid3008.231562
AMA Caraballo L, Rangel Y, Reyna-Bello A, et al. Outbreak of Intermediate Species Leptospira venezuelensis Spread by Rodents to Cows and Humans in L. interrogans–Endemic Region, Venezuela. Emerging Infectious Diseases. 2024;30(8):1514-1522. doi:10.3201/eid3008.231562.
APA Caraballo, L., Rangel, Y., Reyna-Bello, A., Muñoz, M., Figueroa-Espinosa, R., Sanz-Rodriquez, C. E....Takiff, H. E. (2024). Outbreak of Intermediate Species Leptospira venezuelensis Spread by Rodents to Cows and Humans in L. interrogans–Endemic Region, Venezuela. Emerging Infectious Diseases, 30(8), 1514-1522. https://doi.org/10.3201/eid3008.231562.

Systematic Review of Prevalence of Histoplasma Antigenuria in Persons with HIV in Latin America and Africa [PDF - 911 KB - 8 pages]
P. Sekar et al.

Histoplasmosis is a fungal disease associated with substantial mortality rates among persons with advanced HIV disease. Our systematic review synthesized data on the global prevalence of Histoplasma­-caused antigenuria in persons with HIV. We searched PubMed/Medline, Embase, and Scopus databases on January 3, 2023, to identify cross-sectional and cohort studies evaluating Histoplasma antigenuria prevalence among adults with HIV infection. We calculated point estimates and 95% CIs to summarize prevalence. Of 1,294 studies screened, we included 15. We found Histoplasma antigenuria among 581/5,096 (11%; 95% CI 11%–12%) persons with HIV and 483/3,789 persons with advanced HIV disease (13%; 95% CI 12%–14%). Among persons with HIV and symptoms consistent with histoplasmosis, Histoplasma antigenuria prevalence was 14% (95% CI 13%–15%; 502/3,631 participants). We determined that persons with advanced HIV disease, inpatients, and symptomatic persons might benefit from a systematic approach to early detection of histoplasmosis using urine antigen testing.

EID Sekar P, Hale G, Gakuru J, Meya DB, Boulware DR, Ellis J, et al. Systematic Review of Prevalence of Histoplasma Antigenuria in Persons with HIV in Latin America and Africa. Emerg Infect Dis. 2024;30(8):1523-1530. https://doi.org/10.3201/eid3008.231710
AMA Sekar P, Hale G, Gakuru J, et al. Systematic Review of Prevalence of Histoplasma Antigenuria in Persons with HIV in Latin America and Africa. Emerging Infectious Diseases. 2024;30(8):1523-1530. doi:10.3201/eid3008.231710.
APA Sekar, P., Hale, G., Gakuru, J., Meya, D. B., Boulware, D. R., Ellis, J....Rajasingham, R. (2024). Systematic Review of Prevalence of Histoplasma Antigenuria in Persons with HIV in Latin America and Africa. Emerging Infectious Diseases, 30(8), 1523-1530. https://doi.org/10.3201/eid3008.231710.
Research

Environmental Hot Spots and Resistance-Associated Application Practices for Azole-Resistant Aspergillus fumigatus, Denmark, 2020–2023 [PDF - 1.74 MB - 11 pages]
M. Arendrup et al.

Azole-resistant Aspergillus fumigatus (ARAf) fungi have been found inconsistently in the environment in Denmark since 2010. During 2018–2020, nationwide surveillance of clinical A. fumigatus fungi reported environmental TR34/L98H or TR46/Y121F/T289A resistance mutations in 3.6% of isolates, prompting environmental sampling for ARAf and azole fungicides and investigation for selection of ARAf in field and microcosmos experiments. ARAf was ubiquitous (20% of 366 samples; 16% TR34/L98H- and 4% TR46/Y121F/T289A-related mechanisms), constituting 4.2% of 4,538 A. fumigatus isolates. The highest proportions were in flower- and compost-related samples but were not correlated with azole-fungicide application concentrations. Genotyping showed clustering of tandem repeat–related ARAf and overlaps with clinical isolates in Denmark. A. fumigatus fungi grew poorly in the field experiment with no postapplication change in ARAf proportions. However, in microcosmos experiments, a sustained complete (tebuconazole) or partial (prothioconazole) inhibition against wild-type A. fumigatus but not ARAf indicated that, under some conditions, azole fungicides may favor growth of ARAf in soil.

EID Arendrup M, Hare R, Jørgensen K, Bollmann UE, Bech TB, Hansen C, et al. Environmental Hot Spots and Resistance-Associated Application Practices for Azole-Resistant Aspergillus fumigatus, Denmark, 2020–2023. Emerg Infect Dis. 2024;30(8):1531-1541. https://doi.org/10.3201/eid3008.240096
AMA Arendrup M, Hare R, Jørgensen K, et al. Environmental Hot Spots and Resistance-Associated Application Practices for Azole-Resistant Aspergillus fumigatus, Denmark, 2020–2023. Emerging Infectious Diseases. 2024;30(8):1531-1541. doi:10.3201/eid3008.240096.
APA Arendrup, M., Hare, R., Jørgensen, K., Bollmann, U. E., Bech, T. B., Hansen, C....Jørgensen, L. (2024). Environmental Hot Spots and Resistance-Associated Application Practices for Azole-Resistant Aspergillus fumigatus, Denmark, 2020–2023. Emerging Infectious Diseases, 30(8), 1531-1541. https://doi.org/10.3201/eid3008.240096.

Medscape CME Activity
Retrospective Study of Infections with Corynebacterium diphtheriae Species Complex, French Guiana, 2016–2021 [PDF - 1.81 MB - 10 pages]
M. Gaillet et al.

Human infections with Corynebacterium diphtheriae species complex (CdSC) bacteria were rare in French Guiana until 2016, when the number of cases diagnosed increased. We conducted an epidemiologic, multicenter, retrospective study of all human CdSC infections diagnosed in French Guiana during January 1, 2016–December 31, 2021. A total of 64 infectious episodes were observed in 60 patients; 61 infections were caused by C. diphtheriae and 3 by C. ulcerans. Estimated incidence increased from 0.7 cases/100,000 population in 2016 to 7.7 cases/100,000 population in 2021. The mean patient age was 30.4 (+23.7) years, and male-to-female ratio was 1.7:1 (38/22). Of the 61 C. diphtheriae isolates, 5 tested positive for the diphtheria toxin gene, and all results were negative by Elek test; 95% (61/64) of cases were cutaneous, including the C. ulcerans cases. The increase in reported human infections underscores the need to raise awareness among frontline healthcare practitioners to improve prevention.

EID Gaillet M, Hennart M, Rose V, Badell E, Michaud C, Blaizot R, et al. Retrospective Study of Infections with Corynebacterium diphtheriae Species Complex, French Guiana, 2016–2021. Emerg Infect Dis. 2024;30(8):1545-1554. https://doi.org/10.3201/eid3008.231671
AMA Gaillet M, Hennart M, Rose V, et al. Retrospective Study of Infections with Corynebacterium diphtheriae Species Complex, French Guiana, 2016–2021. Emerging Infectious Diseases. 2024;30(8):1545-1554. doi:10.3201/eid3008.231671.
APA Gaillet, M., Hennart, M., Rose, V., Badell, E., Michaud, C., Blaizot, R....Brisse, S. (2024). Retrospective Study of Infections with Corynebacterium diphtheriae Species Complex, French Guiana, 2016–2021. Emerging Infectious Diseases, 30(8), 1545-1554. https://doi.org/10.3201/eid3008.231671.

Emergence of Bluetongue Virus Serotype 3, the Netherlands, September 2023 [PDF - 2.35 MB - 10 pages]
M. Holwerda et al.

Since 1998, notifiable bluetongue virus (BTV) serotypes 1–4, 6, 8, 9, 11, and 16 have been reported in Europe. In August 2006, a bluetongue (BT) outbreak caused by BTV serotype 8 began in northwestern Europe. The Netherlands was declared BT-free in February 2012, and annual monitoring continued. On September 3, 2023, typical BT clinical manifestations in sheep were notified to the Netherlands Food and Product Safety Consumer Authority. On September 6, we confirmed BTV infection through laboratory diagnosis; notifications of clinical signs in cattle were also reported. We determined the virus was serotype 3 by whole-genome sequencing. Retrospective analysis did not reveal BTV circulation earlier than September. The virus source and introduction route into the Netherlands remains unknown. Continuous monitoring and molecular diagnostic testing of livestock will be needed to determine virus spread, and new prevention strategies will be required to prevent BTV circulation within the Netherlands and Europe.

EID Holwerda M, Santman-Berends I, Harders F, Engelsma M, Vloet R, Dijkstra E, et al. Emergence of Bluetongue Virus Serotype 3, the Netherlands, September 2023. Emerg Infect Dis. 2024;30(8):1552-1561. https://doi.org/10.3201/eid3008.231331
AMA Holwerda M, Santman-Berends I, Harders F, et al. Emergence of Bluetongue Virus Serotype 3, the Netherlands, September 2023. Emerging Infectious Diseases. 2024;30(8):1552-1561. doi:10.3201/eid3008.231331.
APA Holwerda, M., Santman-Berends, I., Harders, F., Engelsma, M., Vloet, R., Dijkstra, E....van Rijn, P. A. (2024). Emergence of Bluetongue Virus Serotype 3, the Netherlands, September 2023. Emerging Infectious Diseases, 30(8), 1552-1561. https://doi.org/10.3201/eid3008.231331.

Phylogeographic Analysis of Mycobacterium kansasii Isolates from Patients with M. kansasii Lung Disease in Industrialized City, Taiwan [PDF - 2.08 MB - 9 pages]
P. Tobias Cudahy et al.

Little is known about environmental transmission of Mycobacterium kansasii. We retrospectively investigated potential environmental acquisition, primarily water sources, of M. kansasii among 216 patients with pulmonary disease from an industrial city in Taiwan during 2015–2017. We analyzed sputum mycobacterial cultures using whole-genome sequencing and used hierarchical Bayesian spatial network methods to evaluate risk factors for genetic relatedness of M. kansasii strains. The mean age of participants was 67 years; 24.1% had previously had tuberculosis. We found that persons from districts served by 2 water purification plants were at higher risk of being infected with genetically related M. kansasii isolates. The adjusted odds ratios were 1.81 (1.25–2.60) for the Weng Park plant and 1.39 (1.12–1.71) for the Fongshan plant. Those findings unveiled the association between water purification plants and M. kansasii pulmonary disease, highlighting the need for further environmental investigations to evaluate the risk for M. kansasii transmission.

EID Tobias Cudahy P, Liu P, Warren JL, Sobkowiak B, Yang C, Ioerger TR, et al. Phylogeographic Analysis of Mycobacterium kansasii Isolates from Patients with M. kansasii Lung Disease in Industrialized City, Taiwan. Emerg Infect Dis. 2024;30(8):1562-1570. https://doi.org/10.3201/eid3008.240021
AMA Tobias Cudahy P, Liu P, Warren JL, et al. Phylogeographic Analysis of Mycobacterium kansasii Isolates from Patients with M. kansasii Lung Disease in Industrialized City, Taiwan. Emerging Infectious Diseases. 2024;30(8):1562-1570. doi:10.3201/eid3008.240021.
APA Tobias Cudahy, P., Liu, P., Warren, J. L., Sobkowiak, B., Yang, C., Ioerger, T. R....Lin, H. (2024). Phylogeographic Analysis of Mycobacterium kansasii Isolates from Patients with M. kansasii Lung Disease in Industrialized City, Taiwan. Emerging Infectious Diseases, 30(8), 1562-1570. https://doi.org/10.3201/eid3008.240021.

Potential of Pan-Tuberculosis Treatment to Drive Emergence of Novel Resistance [PDF - 1.16 MB - 9 pages]
C. McQuaid et al.

New tuberculosis (TB) drugs with little existing antimicrobial resistance enable a pan-TB treatment regimen, intended for universal use without prior drug-susceptibility testing. However, widespread use of such a regimen could contribute to an increasing prevalence of antimicrobial resistance, potentially rendering the pan-TB regimen ineffective or driving clinically problematic patterns of resistance. We developed a model of multiple sequential TB patient cohorts to compare treatment outcomes between continued use of current standards of care (guided by rifampin-susceptibility testing) and a hypothetical pan-TB approach. A pan-TB regimen that met current target profiles was likely to initially outperform the standard of care; however, a rising prevalence of transmitted resistance to component drugs could make underperformance likely among subsequent cohorts. Although the pan-TB approach led to an increased prevalence of resistance to novel drugs, it was unlikely to cause accumulation of concurrent resistance to novel drugs and current first-line drugs.

EID McQuaid C, Ryckman TS, Menzies NA, White RG, Cohen T, Kendall EA. Potential of Pan-Tuberculosis Treatment to Drive Emergence of Novel Resistance. Emerg Infect Dis. 2024;30(8):1571-1579. https://doi.org/10.3201/eid3008.240541
AMA McQuaid C, Ryckman TS, Menzies NA, et al. Potential of Pan-Tuberculosis Treatment to Drive Emergence of Novel Resistance. Emerging Infectious Diseases. 2024;30(8):1571-1579. doi:10.3201/eid3008.240541.
APA McQuaid, C., Ryckman, T. S., Menzies, N. A., White, R. G., Cohen, T., & Kendall, E. A. (2024). Potential of Pan-Tuberculosis Treatment to Drive Emergence of Novel Resistance. Emerging Infectious Diseases, 30(8), 1571-1579. https://doi.org/10.3201/eid3008.240541.

Wastewater Surveillance to Confirm Differences in Influenza A Infection between Michigan, USA, and Ontario, Canada, September 2022–March 2023 [PDF - 906 KB - 9 pages]
R. Corchis-Scott et al.

Wastewater surveillance is an effective way to track the prevalence of infectious agents within a community and, potentially, the spread of pathogens between jurisdictions. We conducted a retrospective wastewater surveillance study of the 2022–23 influenza season in 2 communities, Detroit, Michigan, USA, and Windsor-Essex, Ontario, Canada, that form North America’s largest cross-border conurbation. We observed a positive relationship between influenza-related hospitalizations and the influenza A virus (IAV) wastewater signal in Windsor-Essex (ρ = 0.785; p<0.001) and an association between influenza-related hospitalizations in Michigan and the IAV wastewater signal for Detroit (ρ = 0.769; p<0.001). Time-lagged cross correlation and qualitative examination of wastewater signal in the monitored sewersheds showed the peak of the IAV season in Detroit was delayed behind Windsor-Essex by 3 weeks. Wastewater surveillance for IAV reflects regional differences in infection dynamics which may be influenced by many factors, including the timing of vaccine administration between jurisdictions.

EID Corchis-Scott R, Beach M, Geng Q, Podadera A, Corchis-Scott O, Norton J, et al. Wastewater Surveillance to Confirm Differences in Influenza A Infection between Michigan, USA, and Ontario, Canada, September 2022–March 2023. Emerg Infect Dis. 2024;30(8):1580-1588. https://doi.org/10.3201/eid3008.240225
AMA Corchis-Scott R, Beach M, Geng Q, et al. Wastewater Surveillance to Confirm Differences in Influenza A Infection between Michigan, USA, and Ontario, Canada, September 2022–March 2023. Emerging Infectious Diseases. 2024;30(8):1580-1588. doi:10.3201/eid3008.240225.
APA Corchis-Scott, R., Beach, M., Geng, Q., Podadera, A., Corchis-Scott, O., Norton, J....McKay, R. (2024). Wastewater Surveillance to Confirm Differences in Influenza A Infection between Michigan, USA, and Ontario, Canada, September 2022–March 2023. Emerging Infectious Diseases, 30(8), 1580-1588. https://doi.org/10.3201/eid3008.240225.

Fatal SARS-CoV-2 Infection among Children, Japan, January–September 2022 [PDF - 852 KB - 10 pages]
S. Mitsushima et al.

To determine the characteristics of pediatric patients 0–19 years of age who died after onset of SARS-CoV-2 infection in Japan during January 1–September 30, 2022, we reviewed multiple sources. We identified 62 cases, collected detailed information from medical records and death certificates, and conducted interviews, resulting in 53 patients with detailed information for our study. Among 46 patients with internal causes of death (i.e., not external causes such as trauma), 15% were <1 year of age, 59% had no underlying disease, and 88% eligible for vaccination were unvaccinated. Nonrespiratory symptoms were more common than respiratory symptoms. Out-of-hospital cardiac arrest affected 46% of patients, and time from symptom onset to death was <7 days for 77%. Main suspected causes of death were central nervous system abnormalities (35%) and cardiac abnormalities (20%). We recommend careful follow-up of pediatric patients after SARS-CoV-2 infection during the first week after symptom onset, regardless of underlying diseases.

EID Mitsushima S, Yahata Y, Tsuchihashi Y, Ikenoue C, Fukusumi M, Otake S, et al. Fatal SARS-CoV-2 Infection among Children, Japan, January–September 2022. Emerg Infect Dis. 2024;30(8):1589-1598. https://doi.org/10.3201/eid3008.240031
AMA Mitsushima S, Yahata Y, Tsuchihashi Y, et al. Fatal SARS-CoV-2 Infection among Children, Japan, January–September 2022. Emerging Infectious Diseases. 2024;30(8):1589-1598. doi:10.3201/eid3008.240031.
APA Mitsushima, S., Yahata, Y., Tsuchihashi, Y., Ikenoue, C., Fukusumi, M., Otake, S....Sunagawa, T. (2024). Fatal SARS-CoV-2 Infection among Children, Japan, January–September 2022. Emerging Infectious Diseases, 30(8), 1589-1598. https://doi.org/10.3201/eid3008.240031.

Metagenomic Detection of Bacterial Zoonotic Pathogens among Febrile Patients, Tanzania, 2007–2009 [PDF - 1.13 MB - 10 pages]
R. J. Rolfe et al.

Bacterial zoonoses are established causes of severe febrile illness in East Africa. Within a fever etiology study, we applied a high-throughput 16S rRNA metagenomic assay validated for detecting bacterial zoonotic pathogens. We enrolled febrile patients admitted to 2 referral hospitals in Moshi, Tanzania, during September 2007–April 2009. Among 788 participants, median age was 20 (interquartile range 2–38) years. We performed PCR amplification of V1–V2 variable region 16S rRNA on cell pellet DNA, then metagenomic deep-sequencing and pathogenic taxonomic identification. We detected bacterial zoonotic pathogens in 10 (1.3%) samples: 3 with Rickettsia typhi, 1 R. conorii, 2 Bartonella quintana, 2 pathogenic Leptospira spp., and 1 Coxiella burnetii. One other sample had reads matching a Neoerhlichia spp. previously identified in a patient from South Africa. Our findings indicate that targeted 16S metagenomics can identify bacterial zoonotic pathogens causing severe febrile illness in humans, including potential novel agents.

EID Rolfe RJ, Sheldon SW, Kingry LC, Petersen JM, Maro VP, Kinabo GD, et al. Metagenomic Detection of Bacterial Zoonotic Pathogens among Febrile Patients, Tanzania, 2007–2009. Emerg Infect Dis. 2024;30(8):1599-1608. https://doi.org/10.3201/eid3008.240529
AMA Rolfe RJ, Sheldon SW, Kingry LC, et al. Metagenomic Detection of Bacterial Zoonotic Pathogens among Febrile Patients, Tanzania, 2007–2009. Emerging Infectious Diseases. 2024;30(8):1599-1608. doi:10.3201/eid3008.240529.
APA Rolfe, R. J., Sheldon, S. W., Kingry, L. C., Petersen, J. M., Maro, V. P., Kinabo, G. D....Crump, J. A. (2024). Metagenomic Detection of Bacterial Zoonotic Pathogens among Febrile Patients, Tanzania, 2007–2009. Emerging Infectious Diseases, 30(8), 1599-1608. https://doi.org/10.3201/eid3008.240529.

SARS-CoV-2 Seropositivity in Urban Population of Wild Fallow Deer, Dublin, Ireland, 2020–2022 [PDF - 2.56 MB - 12 pages]
K. Purves et al.

SARS-CoV-2 can infect wildlife, and SARS-CoV-2 variants of concern might expand into novel animal reservoirs, potentially by reverse zoonosis. White-tailed deer and mule deer of North America are the only deer species in which SARS-CoV-2 has been documented, raising the question of whether other reservoir species exist. We report cases of SARS-CoV-2 seropositivity in a fallow deer population located in Dublin, Ireland. Sampled deer were seronegative in 2020 when the Alpha variant was circulating in humans, 1 deer was seropositive for the Delta variant in 2021, and 12/21 (57%) sampled deer were seropositive for the Omicron variant in 2022, suggesting host tropism expansion as new variants emerged in humans. Omicron BA.1 was capable of infecting fallow deer lung type-2 pneumocytes and type-1–like pneumocytes or endothelial cells ex vivo. Ongoing surveillance to identify novel SARS-CoV-2 reservoirs is needed to prevent public health risks during human–animal interactions in periurban settings.

EID Purves K, Brown H, Haverty R, Ryan A, Griffin LL, McCormack J, et al. SARS-CoV-2 Seropositivity in Urban Population of Wild Fallow Deer, Dublin, Ireland, 2020–2022. Emerg Infect Dis. 2024;30(8):1609-1620. https://doi.org/10.3201/eid3008.231056
AMA Purves K, Brown H, Haverty R, et al. SARS-CoV-2 Seropositivity in Urban Population of Wild Fallow Deer, Dublin, Ireland, 2020–2022. Emerging Infectious Diseases. 2024;30(8):1609-1620. doi:10.3201/eid3008.231056.
APA Purves, K., Brown, H., Haverty, R., Ryan, A., Griffin, L. L., McCormack, J....Fletcher, N. F. (2024). SARS-CoV-2 Seropositivity in Urban Population of Wild Fallow Deer, Dublin, Ireland, 2020–2022. Emerging Infectious Diseases, 30(8), 1609-1620. https://doi.org/10.3201/eid3008.231056.

Detection of Nucleocapsid Antibodies Associated with Primary SARS-CoV-2 Infection in Unvaccinated and Vaccinated Blood Donors [PDF - 1.11 MB - 10 pages]
E. Grebe et al.

Nucleocapsid antibody assays can be used to estimate SARS-CoV-2 infection prevalence in regions implementing spike-based COVID-19 vaccines. However, poor sensitivity of nucleocapsid antibody assays in detecting infection after vaccination has been reported. We derived a lower cutoff for identifying previous infections in a large blood donor cohort (N = 142,599) by using the Ortho VITROS Anti-SARS-CoV-2 Total-N Antibody assay, improving sensitivity while maintaining specificity >98%. We validated sensitivity in samples donated after self-reported swab-confirmed infection diagnoses. Sensitivity for first infections in unvaccinated donors was 98.1% (95% CI 98.0–98.2) and for infection after vaccination was 95.6% (95% CI 95.6–95.7) based on the standard cutoff. Regression analysis showed sensitivity was reduced in the Delta compared with Omicron period, in older donors, in asymptomatic infections, <30 days after infection, and for infection after vaccination. The standard Ortho N antibody threshold demonstrated good sensitivity, which was modestly improved with the revised cutoff.

EID Grebe E, Stone M, Spencer BR, Akinseye A, Wright DJ, Di Germanio C, et al. Detection of Nucleocapsid Antibodies Associated with Primary SARS-CoV-2 Infection in Unvaccinated and Vaccinated Blood Donors. Emerg Infect Dis. 2024;30(8):1621-1630. https://doi.org/10.3201/eid3008.240659
AMA Grebe E, Stone M, Spencer BR, et al. Detection of Nucleocapsid Antibodies Associated with Primary SARS-CoV-2 Infection in Unvaccinated and Vaccinated Blood Donors. Emerging Infectious Diseases. 2024;30(8):1621-1630. doi:10.3201/eid3008.240659.
APA Grebe, E., Stone, M., Spencer, B. R., Akinseye, A., Wright, D. J., Di Germanio, C....Busch, M. P. (2024). Detection of Nucleocapsid Antibodies Associated with Primary SARS-CoV-2 Infection in Unvaccinated and Vaccinated Blood Donors. Emerging Infectious Diseases, 30(8), 1621-1630. https://doi.org/10.3201/eid3008.240659.

Standardized Phylogenetic Classification of Human Respiratory Syncytial Virus below the Subgroup Level [PDF - 1.88 MB - 11 pages]
S. Goya et al.

A globally implemented unified phylogenetic classification for human respiratory syncytial virus (HRSV) below the subgroup level remains elusive. We formulated global consensus of HRSV classification on the basis of the challenges and limitations of our previous proposals and the future of genomic surveillance. From a high-quality curated dataset of 1,480 HRSV-A and 1,385 HRSV-B genomes submitted to GenBank and GISAID (https://www.gisaid.org) public sequence databases through March 2023, we categorized HRSV-A/B sequences into lineages based on phylogenetic clades and amino acid markers. We defined 24 lineages within HRSV-A and 16 within HRSV-B and provided guidelines for defining prospective lineages. Our classification demonstrated robustness in its applicability to both complete and partial genomes. We envision that this unified HRSV classification proposal will strengthen HRSV molecular epidemiology on a global scale.

EID Goya S, Ruis C, Neher RA, Meijer A, Aziz A, Hinrichs AS, et al. Standardized Phylogenetic Classification of Human Respiratory Syncytial Virus below the Subgroup Level. Emerg Infect Dis. 2024;30(8):1631-1641. https://doi.org/10.3201/eid3008.240209
AMA Goya S, Ruis C, Neher RA, et al. Standardized Phylogenetic Classification of Human Respiratory Syncytial Virus below the Subgroup Level. Emerging Infectious Diseases. 2024;30(8):1631-1641. doi:10.3201/eid3008.240209.
APA Goya, S., Ruis, C., Neher, R. A., Meijer, A., Aziz, A., Hinrichs, A. S....Viegas, M. (2024). Standardized Phylogenetic Classification of Human Respiratory Syncytial Virus below the Subgroup Level. Emerging Infectious Diseases, 30(8), 1631-1641. https://doi.org/10.3201/eid3008.240209.

Geographic Distribution of Rabies Virus and Genomic Sequence Alignment of Wild and Vaccine Strains, Kenya [PDF - 1.61 MB - 9 pages]
E. N. Wambugu et al.

Rabies, a viral disease that causes lethal encephalitis, kills ≈59,000 persons worldwide annually, despite availability of effective countermeasures. Rabies is endemic in Kenya and is mainly transmitted to humans through bites from rabid domestic dogs. We analyzed 164 brain stems collected from rabid animals in western and eastern Kenya and evaluated the phylogenetic relationships of rabies virus (RABV) from the 2 regions. We also analyzed RABV genomes for potential amino acid changes in the vaccine antigenic sites of nucleoprotein and glycoprotein compared with RABV vaccine strains commonly used in Kenya. We found that RABV genomes from eastern Kenya overwhelmingly clustered with the Africa-1b subclade and RABV from western Kenya clustered with Africa-1a. We noted minimal amino acid variances between the wild and vaccine virus strains. These data confirm minimal viral migration between the 2 regions and that rabies endemicity is the result of limited vaccine coverage rather than limited efficacy.

EID Wambugu EN, Kimita G, Kituyi SN, Washington MA, Masakhwe C, Mutunga LM, et al. Geographic Distribution of Rabies Virus and Genomic Sequence Alignment of Wild and Vaccine Strains, Kenya. Emerg Infect Dis. 2024;30(8):1642-1650. https://doi.org/10.3201/eid3008.230876
AMA Wambugu EN, Kimita G, Kituyi SN, et al. Geographic Distribution of Rabies Virus and Genomic Sequence Alignment of Wild and Vaccine Strains, Kenya. Emerging Infectious Diseases. 2024;30(8):1642-1650. doi:10.3201/eid3008.230876.
APA Wambugu, E. N., Kimita, G., Kituyi, S. N., Washington, M. A., Masakhwe, C., Mutunga, L. M....Waitumbi, J. N. (2024). Geographic Distribution of Rabies Virus and Genomic Sequence Alignment of Wild and Vaccine Strains, Kenya. Emerging Infectious Diseases, 30(8), 1642-1650. https://doi.org/10.3201/eid3008.230876.

Scrapie versus Chronic Wasting Disease in White-Tailed Deer [PDF - 1.89 MB - 9 pages]
Z. J. Lambert et al.

White-tailed deer are susceptible to scrapie (WTD scrapie) after oronasal inoculation with the classical scrapie agent from sheep. Deer affected by WTD scrapie are difficult to differentiate from deer infected with chronic wasting disease (CWD). To assess the transmissibility of the WTD scrapie agent and tissue phenotypes when further passaged in white-tailed deer, we oronasally inoculated wild-type white-tailed deer with WTD scrapie agent. We found that WTD scrapie and CWD agents were generally similar, although some differences were noted. The greatest differences were seen in bioassays of cervidized mice that exhibited significantly longer survival periods when inoculated with WTD scrapie agent than those inoculated with CWD agent. Our findings establish that white-tailed deer are susceptible to WTD scrapie and that the presence of WTD scrapie agent in the lymphoreticular system suggests the handling of suspected cases should be consistent with current CWD guidelines because environmental shedding may occur.

EID Lambert ZJ, Bian J, Cassmann ED, Greenlee M, Greenlee JJ. Scrapie versus Chronic Wasting Disease in White-Tailed Deer. Emerg Infect Dis. 2024;30(8):1651-1659. https://doi.org/10.3201/eid3008.240007
AMA Lambert ZJ, Bian J, Cassmann ED, et al. Scrapie versus Chronic Wasting Disease in White-Tailed Deer. Emerging Infectious Diseases. 2024;30(8):1651-1659. doi:10.3201/eid3008.240007.
APA Lambert, Z. J., Bian, J., Cassmann, E. D., Greenlee, M., & Greenlee, J. J. (2024). Scrapie versus Chronic Wasting Disease in White-Tailed Deer. Emerging Infectious Diseases, 30(8), 1651-1659. https://doi.org/10.3201/eid3008.240007.
Dispatches

Highly Pathogenic Avian Influenza Virus A(H5N1) Clade 2.3.4.4b Infection in Free-Ranging Polar Bear, Alaska, USA [PDF - 876 KB - 4 pages]
R. Stimmelmayr et al.

We report a natural infection with a Eurasian highly pathogenic avian influenza A(H5N1) clade 2.3.4.4b virus in a free-ranging juvenile polar bear (Ursus maritimus) found dead in North Slope Borough, Alaska, USA. Continued community and hunter-based participation in wildlife health surveillance is key to detecting emerging pathogens in the Arctic.

EID Stimmelmayr R, Rotstein D, Torchetti M, Gerlach R. Highly Pathogenic Avian Influenza Virus A(H5N1) Clade 2.3.4.4b Infection in Free-Ranging Polar Bear, Alaska, USA. Emerg Infect Dis. 2024;30(8):1660-1663. https://doi.org/10.3201/eid3008.240481
AMA Stimmelmayr R, Rotstein D, Torchetti M, et al. Highly Pathogenic Avian Influenza Virus A(H5N1) Clade 2.3.4.4b Infection in Free-Ranging Polar Bear, Alaska, USA. Emerging Infectious Diseases. 2024;30(8):1660-1663. doi:10.3201/eid3008.240481.
APA Stimmelmayr, R., Rotstein, D., Torchetti, M., & Gerlach, R. (2024). Highly Pathogenic Avian Influenza Virus A(H5N1) Clade 2.3.4.4b Infection in Free-Ranging Polar Bear, Alaska, USA. Emerging Infectious Diseases, 30(8), 1660-1663. https://doi.org/10.3201/eid3008.240481.

Rustrela Virus in Wild Mountain Lion (Puma concolor) with Staggering Disease, Colorado, USA [PDF - 1.93 MB - 4 pages]
K. A. Fox et al.

We identified a rustrela virus variant in a wild mountain lion (Puma concolor) in Colorado, USA. The animal had clinical signs and histologic lesions compatible with staggering disease. Considering its wide host range in Europe, rustrela virus should be considered as a cause for neurologic diseases among mammal species in North America.

EID Fox KA, Breithaupt A, Beer M, Rubbenstroth D, Pfaff F. Rustrela Virus in Wild Mountain Lion (Puma concolor) with Staggering Disease, Colorado, USA. Emerg Infect Dis. 2024;30(8):1664-1667. https://doi.org/10.3201/eid3008.240411
AMA Fox KA, Breithaupt A, Beer M, et al. Rustrela Virus in Wild Mountain Lion (Puma concolor) with Staggering Disease, Colorado, USA. Emerging Infectious Diseases. 2024;30(8):1664-1667. doi:10.3201/eid3008.240411.
APA Fox, K. A., Breithaupt, A., Beer, M., Rubbenstroth, D., & Pfaff, F. (2024). Rustrela Virus in Wild Mountain Lion (Puma concolor) with Staggering Disease, Colorado, USA. Emerging Infectious Diseases, 30(8), 1664-1667. https://doi.org/10.3201/eid3008.240411.

Hepatitis B Virus Reactivation after Switch to Cabotegravir/Rilpivirine in Patient with Low Hepatitis B Surface Antibody [PDF - 340 KB - 4 pages]
E. Adachi et al.

A patient in Japan with HIV began antiretroviral therapy because of acute hepatitis B virus (HBV) 15 years ago, with low hepatitis B surface antibody, and experienced breakthrough HBV reactivation 4 months after switching from bictegravir/emtricitabine/tenofovir alafenamide to cabotegravir/rilpivirine. An immune escape mutation, E164V, was identified in the isolated HBV DNA.

EID Adachi E, Sedohara A, Arizono K, Takahashi K, Otani A, Kanno Y, et al. Hepatitis B Virus Reactivation after Switch to Cabotegravir/Rilpivirine in Patient with Low Hepatitis B Surface Antibody. Emerg Infect Dis. 2024;30(8):1668-1671. https://doi.org/10.3201/eid3008.240019
AMA Adachi E, Sedohara A, Arizono K, et al. Hepatitis B Virus Reactivation after Switch to Cabotegravir/Rilpivirine in Patient with Low Hepatitis B Surface Antibody. Emerging Infectious Diseases. 2024;30(8):1668-1671. doi:10.3201/eid3008.240019.
APA Adachi, E., Sedohara, A., Arizono, K., Takahashi, K., Otani, A., Kanno, Y....Yotsuyanagi, H. (2024). Hepatitis B Virus Reactivation after Switch to Cabotegravir/Rilpivirine in Patient with Low Hepatitis B Surface Antibody. Emerging Infectious Diseases, 30(8), 1668-1671. https://doi.org/10.3201/eid3008.240019.

Characterization of Influenza D Virus Reassortant Strain in Swine from Mixed Pig and Beef Farm, France [PDF - 833 KB - 4 pages]
S. Gorin et al.

Influenza D virus was isolated from pigs on a mixed pig and beef farm in France. Investigation suggested bull-to-pig transmission and spread among pigs. The swine influenza D virus recovered was a reassortant of D/660 and D/OK lineages. Reported mutations in the receptor binding site might be related to swine host adaptation.

EID Gorin S, Richard G, Hervé S, Eveno E, Blanchard Y, Jardin A, et al. Characterization of Influenza D Virus Reassortant Strain in Swine from Mixed Pig and Beef Farm, France. Emerg Infect Dis. 2024;30(8):1672-1676. https://doi.org/10.3201/eid3008.240089
AMA Gorin S, Richard G, Hervé S, et al. Characterization of Influenza D Virus Reassortant Strain in Swine from Mixed Pig and Beef Farm, France. Emerging Infectious Diseases. 2024;30(8):1672-1676. doi:10.3201/eid3008.240089.
APA Gorin, S., Richard, G., Hervé, S., Eveno, E., Blanchard, Y., Jardin, A....Simon, G. (2024). Characterization of Influenza D Virus Reassortant Strain in Swine from Mixed Pig and Beef Farm, France. Emerging Infectious Diseases, 30(8), 1672-1676. https://doi.org/10.3201/eid3008.240089.

Spatiotemporal Modeling of Cholera, Uvira, Democratic Republic of the Congo, 2016−2020 [PDF - 1.25 MB - 6 pages]
R. Ratnayake et al.

We evaluated the spatiotemporal clustering of rapid diagnostic test−positive cholera cases in Uvira, eastern Democratic Republic of the Congo. We detected spatiotemporal clusters that consistently overlapped with major rivers, and we outlined the extent of zones of increased risk that are compatible with the radii currently used for targeted interventions.

EID Ratnayake R, Knee J, Cumming O, Saidi J, Rumedeka B, Finger F, et al. Spatiotemporal Modeling of Cholera, Uvira, Democratic Republic of the Congo, 2016−2020. Emerg Infect Dis. 2024;30(8):1677-1682. https://doi.org/10.3201/eid3008.231137
AMA Ratnayake R, Knee J, Cumming O, et al. Spatiotemporal Modeling of Cholera, Uvira, Democratic Republic of the Congo, 2016−2020. Emerging Infectious Diseases. 2024;30(8):1677-1682. doi:10.3201/eid3008.231137.
APA Ratnayake, R., Knee, J., Cumming, O., Saidi, J., Rumedeka, B., Finger, F....Gallandat, K. (2024). Spatiotemporal Modeling of Cholera, Uvira, Democratic Republic of the Congo, 2016−2020. Emerging Infectious Diseases, 30(8), 1677-1682. https://doi.org/10.3201/eid3008.231137.

Surge in Ceftriaxone-Resistant Neisseria gonorrhoeae FC428-Like Strains, Asia-Pacific Region, 2015−2022 [PDF - 956 KB - 4 pages]
L. Xiu et al.

Ceftriaxone-resistant Neisseria gonorrhoeae FC428-like strains have disseminated across the Asia-Pacific region, with a continuous rise in prevalence during 2015–2022. To mitigate the effect of these strains, we advocate for enhanced molecular diagnostics, expanded surveillance networks, and a regionally coordinated effort to combat the global spread of FC428-like strains.

EID Xiu L, Zhang L, Peng J. Surge in Ceftriaxone-Resistant Neisseria gonorrhoeae FC428-Like Strains, Asia-Pacific Region, 2015−2022. Emerg Infect Dis. 2024;30(8):1683-1686. https://doi.org/10.3201/eid3008.240139
AMA Xiu L, Zhang L, Peng J. Surge in Ceftriaxone-Resistant Neisseria gonorrhoeae FC428-Like Strains, Asia-Pacific Region, 2015−2022. Emerging Infectious Diseases. 2024;30(8):1683-1686. doi:10.3201/eid3008.240139.
APA Xiu, L., Zhang, L., & Peng, J. (2024). Surge in Ceftriaxone-Resistant Neisseria gonorrhoeae FC428-Like Strains, Asia-Pacific Region, 2015−2022. Emerging Infectious Diseases, 30(8), 1683-1686. https://doi.org/10.3201/eid3008.240139.

Real-Time Enterovirus D68 Outbreak Detection through Hospital Surveillance of Severe Acute Respiratory Infection, Senegal, 2023 [PDF - 1.24 MB - 5 pages]
M. Jallow et al.

In December 2023, we observed through hospital-based surveillance a severe outbreak of enterovirus D68 infection in pediatric inpatients in Dakar, Senegal. Molecular characterization revealed that subclade B3, the dominant lineage in outbreaks worldwide, was responsible for the outbreak. Enhanced surveillance in inpatient settings, including among patients with neurologic illnesses, is needed.

EID Jallow M, Mendy M, Barry M, Diagne M, Sagne S, Tall F, et al. Real-Time Enterovirus D68 Outbreak Detection through Hospital Surveillance of Severe Acute Respiratory Infection, Senegal, 2023. Emerg Infect Dis. 2024;30(8):1687-1691. https://doi.org/10.3201/eid3008.240410
AMA Jallow M, Mendy M, Barry M, et al. Real-Time Enterovirus D68 Outbreak Detection through Hospital Surveillance of Severe Acute Respiratory Infection, Senegal, 2023. Emerging Infectious Diseases. 2024;30(8):1687-1691. doi:10.3201/eid3008.240410.
APA Jallow, M., Mendy, M., Barry, M., Diagne, M., Sagne, S., Tall, F....Dia, N. (2024). Real-Time Enterovirus D68 Outbreak Detection through Hospital Surveillance of Severe Acute Respiratory Infection, Senegal, 2023. Emerging Infectious Diseases, 30(8), 1687-1691. https://doi.org/10.3201/eid3008.240410.

Macrolide-Resistant Mycoplasma pneumoniae Infections among Children before and during COVID-19 Pandemic, Taiwan, 2017–2023 [PDF - 926 KB - 5 pages]
T. Wu et al.

Before the COVID-19 pandemic, Mycoplasma pneumoniae infections emerged during spring to summer yearly in Taiwan, but infections were few during the pandemic. M. pneumoniae macrolide resistance soared to 85.7% in 2020 but declined to 0% during 2022–2023. Continued molecular surveillance is necessary to monitor trends in macrolide-resistant M. pneumoniae.

EID Wu T, Fang Y, Liu F, Pan H, Yang Y, Song C, et al. Macrolide-Resistant Mycoplasma pneumoniae Infections among Children before and during COVID-19 Pandemic, Taiwan, 2017–2023. Emerg Infect Dis. 2024;30(8):1692-1696. https://doi.org/10.3201/eid3008.231596
AMA Wu T, Fang Y, Liu F, et al. Macrolide-Resistant Mycoplasma pneumoniae Infections among Children before and during COVID-19 Pandemic, Taiwan, 2017–2023. Emerging Infectious Diseases. 2024;30(8):1692-1696. doi:10.3201/eid3008.231596.
APA Wu, T., Fang, Y., Liu, F., Pan, H., Yang, Y., Song, C....Lee, C. (2024). Macrolide-Resistant Mycoplasma pneumoniae Infections among Children before and during COVID-19 Pandemic, Taiwan, 2017–2023. Emerging Infectious Diseases, 30(8), 1692-1696. https://doi.org/10.3201/eid3008.231596.

Group B Streptococcus Sequence Type 103 as Human and Bovine Pathogen, Brazil [PDF - 842 KB - 5 pages]
L. Oliveira et al.

Group B Streptococcus sequence type 103 is known primarily as a bovine mastitis pathogen. In Brazil, it has circulated in cattle and humans since the 1990s. It lacks scpB and, in humans, was found only among carriage isolates. Bovine–human interspecies transmission may have contributed to its evolution and spread.

EID Oliveira L, Simões LC, Crestani C, Costa NS, Pantoja JF, Rabello RF, et al. Group B Streptococcus Sequence Type 103 as Human and Bovine Pathogen, Brazil. Emerg Infect Dis. 2024;30(8):1697-1701. https://doi.org/10.3201/eid3008.231575
AMA Oliveira L, Simões LC, Crestani C, et al. Group B Streptococcus Sequence Type 103 as Human and Bovine Pathogen, Brazil. Emerging Infectious Diseases. 2024;30(8):1697-1701. doi:10.3201/eid3008.231575.
APA Oliveira, L., Simões, L. C., Crestani, C., Costa, N. S., Pantoja, J. F., Rabello, R. F....Zadoks, R. N. (2024). Group B Streptococcus Sequence Type 103 as Human and Bovine Pathogen, Brazil. Emerging Infectious Diseases, 30(8), 1697-1701. https://doi.org/10.3201/eid3008.231575.

Recurrent Occupational Hantavirus Infections Linked to Feeder Rodent Breeding Farm, Taiwan, 2022 [PDF - 1.44 MB - 4 pages]
K. Wang et al.

We investigated 2 acute cases and 1 previous case of Seoul hantavirus infection in workers in a feeder rodent breeding farm in Taiwan. Prevalence of hantavirus IgG among the tested feeder rats was 37.5%. Appropriate prevention measures, including using disinfection protocols and personal protective equipment, are crucial to lowering risk.

EID Wang K, Chang C, Chang S, Shu P, Wang H, Su S, et al. Recurrent Occupational Hantavirus Infections Linked to Feeder Rodent Breeding Farm, Taiwan, 2022. Emerg Infect Dis. 2024;30(8):1702-1705. https://doi.org/10.3201/eid3008.230875
AMA Wang K, Chang C, Chang S, et al. Recurrent Occupational Hantavirus Infections Linked to Feeder Rodent Breeding Farm, Taiwan, 2022. Emerging Infectious Diseases. 2024;30(8):1702-1705. doi:10.3201/eid3008.230875.
APA Wang, K., Chang, C., Chang, S., Shu, P., Wang, H., Su, S....Su, C. (2024). Recurrent Occupational Hantavirus Infections Linked to Feeder Rodent Breeding Farm, Taiwan, 2022. Emerging Infectious Diseases, 30(8), 1702-1705. https://doi.org/10.3201/eid3008.230875.

Crimean-Congo Hemorrhagic Fever Virus Kinetics in Serum, Saliva, and Urine, Iran, 2018 [PDF - 1.12 MB - 4 pages]
M. Metanat et al.

Little is known about using noninvasive samples for diagnosing Crimean-Congo hemorrhagic fever (CCHF). We investigated detection of CCHF virus in serum, saliva, and urine samples. Our results indicate that serum is the best sample type for CCHF diagnosis; saliva can be used for noninvasive sampling.

EID Metanat M, Nasab S, Jalali T, Amiri F, Jahromi N, Tavakoli M, et al. Crimean-Congo Hemorrhagic Fever Virus Kinetics in Serum, Saliva, and Urine, Iran, 2018. Emerg Infect Dis. 2024;30(8):1706-1709. https://doi.org/10.3201/eid3008.240036
AMA Metanat M, Nasab S, Jalali T, et al. Crimean-Congo Hemorrhagic Fever Virus Kinetics in Serum, Saliva, and Urine, Iran, 2018. Emerging Infectious Diseases. 2024;30(8):1706-1709. doi:10.3201/eid3008.240036.
APA Metanat, M., Nasab, S., Jalali, T., Amiri, F., Jahromi, N., Tavakoli, M....Salehi-Vaziri, M. (2024). Crimean-Congo Hemorrhagic Fever Virus Kinetics in Serum, Saliva, and Urine, Iran, 2018. Emerging Infectious Diseases, 30(8), 1706-1709. https://doi.org/10.3201/eid3008.240036.

Multiplex Dual-Target Reverse Transcription PCR for Subtyping Avian Influenza A(H5) Virus [PDF - 578 KB - 4 pages]
M. K. Sahoo et al.

An increased risk for human infection with avian influenza A(H5N1) viruses is of concern. We developed an internally controlled, dual-target reverse transcription PCR for influenza A(H5) subtyping. This test could be used to detect influenza A(H5) in clinical samples.

EID Sahoo MK, Morante I, Huang C, Solis D, Yamamoto F, Ohiri UC, et al. Multiplex Dual-Target Reverse Transcription PCR for Subtyping Avian Influenza A(H5) Virus. Emerg Infect Dis. 2024;30(8):1710-1713. https://doi.org/10.3201/eid3008.240785
AMA Sahoo MK, Morante I, Huang C, et al. Multiplex Dual-Target Reverse Transcription PCR for Subtyping Avian Influenza A(H5) Virus. Emerging Infectious Diseases. 2024;30(8):1710-1713. doi:10.3201/eid3008.240785.
APA Sahoo, M. K., Morante, I., Huang, C., Solis, D., Yamamoto, F., Ohiri, U. C....Pinsky, B. A. (2024). Multiplex Dual-Target Reverse Transcription PCR for Subtyping Avian Influenza A(H5) Virus. Emerging Infectious Diseases, 30(8), 1710-1713. https://doi.org/10.3201/eid3008.240785.

ST913-IVa-t991 Methicillin-Resistant Staphylococcus aureus among Pediatric Patients, Israel [PDF - 1.51 MB - 5 pages]
M. Baum et al.

In Israel, prevalence of sequence type 913, staphylococcal cassette chromosome mecIVa, spa type t991 methicillin-resistant Staphylococcus aureus lineage has surged among pediatric populations, predominantly in Arab and Orthodox Jewish communities. Antimicrobial resistance patterns vary by demographics. This lineage's spread and microevolution in the Middle East underscore the need for ongoing surveillance.

EID Baum M, Anuka E, Davidovich-Cohen M, Rokney A. ST913-IVa-t991 Methicillin-Resistant Staphylococcus aureus among Pediatric Patients, Israel. Emerg Infect Dis. 2024;30(8):1714-1718. https://doi.org/10.3201/eid3008.230981
AMA Baum M, Anuka E, Davidovich-Cohen M, et al. ST913-IVa-t991 Methicillin-Resistant Staphylococcus aureus among Pediatric Patients, Israel. Emerging Infectious Diseases. 2024;30(8):1714-1718. doi:10.3201/eid3008.230981.
APA Baum, M., Anuka, E., Davidovich-Cohen, M., & Rokney, A. (2024). ST913-IVa-t991 Methicillin-Resistant Staphylococcus aureus among Pediatric Patients, Israel. Emerging Infectious Diseases, 30(8), 1714-1718. https://doi.org/10.3201/eid3008.230981.
Research Letters

Emayella augustorita, New Member of Pasteurellaceae, Isolated from Blood Cultures of Septic Patient [PDF - 544 KB - 3 pages]
S. Meyer et al.

We report discovery of a new bacterial genus and species of the family Pasteurellaceae by using phylogenetic and metabolic analysis. The bacterium, Emayella augustorita, was isolated from blood cultures of a patient in France diagnosed with an adenocarcinoma of the intestines and who was treated with a biliary prosthesis placement.

EID Meyer S, Tilloy V, Durand-Fontanier S, Lafon T, Garnier F, Martin C, et al. Emayella augustorita, New Member of Pasteurellaceae, Isolated from Blood Cultures of Septic Patient. Emerg Infect Dis. 2024;30(8):1719-1721. https://doi.org/10.3201/eid3008.231651
AMA Meyer S, Tilloy V, Durand-Fontanier S, et al. Emayella augustorita, New Member of Pasteurellaceae, Isolated from Blood Cultures of Septic Patient. Emerging Infectious Diseases. 2024;30(8):1719-1721. doi:10.3201/eid3008.231651.
APA Meyer, S., Tilloy, V., Durand-Fontanier, S., Lafon, T., Garnier, F., Martin, C....Barraud, O. (2024). Emayella augustorita, New Member of Pasteurellaceae, Isolated from Blood Cultures of Septic Patient. Emerging Infectious Diseases, 30(8), 1719-1721. https://doi.org/10.3201/eid3008.231651.

Persistence of Influenza H5N1 and H1N1 Viruses in Unpasteurized Milk on Milking Unit Surfaces [PDF - 493 KB - 3 pages]
V. Le Sage et al.

Examining the persistence of highly pathogenic avian influenza A(H5N1) from cattle and human influenza A(H1N1)pdm09 pandemic viruses in unpasteurized milk revealed that both remain infectious on milking equipment materials for several hours. Those findings highlight the risk for H5N1 virus transmission to humans from contaminated surfaces during the milking process.

EID Le Sage V, Campbell A, Reed DS, Duprex W, Lakdawala SS. Persistence of Influenza H5N1 and H1N1 Viruses in Unpasteurized Milk on Milking Unit Surfaces. Emerg Infect Dis. 2024;30(8):1721-1723. https://doi.org/10.3201/eid3008.240775
AMA Le Sage V, Campbell A, Reed DS, et al. Persistence of Influenza H5N1 and H1N1 Viruses in Unpasteurized Milk on Milking Unit Surfaces. Emerging Infectious Diseases. 2024;30(8):1721-1723. doi:10.3201/eid3008.240775.
APA Le Sage, V., Campbell, A., Reed, D. S., Duprex, W., & Lakdawala, S. S. (2024). Persistence of Influenza H5N1 and H1N1 Viruses in Unpasteurized Milk on Milking Unit Surfaces. Emerging Infectious Diseases, 30(8), 1721-1723. https://doi.org/10.3201/eid3008.240775.

Panton-Valentine Leukocidin–Positive Staphylococcus aureus in Family and Pet Cat [PDF - 426 KB - 3 pages]
A. Bethe et al.

Continued detection of Panton-Valentine leukocidin–positive Staphylococcus aureus in samples from a family with severe repeated skin infections and their pet cat suggests transmission between the family and the cat. Decolonizing the pet led to successful elimination of the bacteria from the household. Clinicians should consider pet cats as possible reinfection sources.

EID Bethe A, Schink A, Brombach J, Epping L, Semmler T, Reinhardt S, et al. Panton-Valentine Leukocidin–Positive Staphylococcus aureus in Family and Pet Cat. Emerg Infect Dis. 2024;30(8):1724-1726. https://doi.org/10.3201/eid3008.231255
AMA Bethe A, Schink A, Brombach J, et al. Panton-Valentine Leukocidin–Positive Staphylococcus aureus in Family and Pet Cat. Emerging Infectious Diseases. 2024;30(8):1724-1726. doi:10.3201/eid3008.231255.
APA Bethe, A., Schink, A., Brombach, J., Epping, L., Semmler, T., Reinhardt, S....Lübke-Becker, A. (2024). Panton-Valentine Leukocidin–Positive Staphylococcus aureus in Family and Pet Cat. Emerging Infectious Diseases, 30(8), 1724-1726. https://doi.org/10.3201/eid3008.231255.

Rare Case of Echinostoma cinetorchis Infection, South Korea [PDF - 1011 KB - 4 pages]
S. Hong et al.

A woman in South Korea who underwent a colonoscopy for occasional gastrointestinal discomfort had 4 adult flukes of Echinostoma cinetorchis showing 37 collar spines around the oral sucker recovered from the terminal ileum through the ascending colon. Partial gene sequencing showed high identity with E. cinetorchis.

EID Hong S, Shin H, Lee Y, Hong S, Kim S, Kim Y, et al. Rare Case of Echinostoma cinetorchis Infection, South Korea. Emerg Infect Dis. 2024;30(8):1726-1729. https://doi.org/10.3201/eid3008.240289
AMA Hong S, Shin H, Lee Y, et al. Rare Case of Echinostoma cinetorchis Infection, South Korea. Emerging Infectious Diseases. 2024;30(8):1726-1729. doi:10.3201/eid3008.240289.
APA Hong, S., Shin, H., Lee, Y., Hong, S., Kim, S., Kim, Y....Jung, B. (2024). Rare Case of Echinostoma cinetorchis Infection, South Korea. Emerging Infectious Diseases, 30(8), 1726-1729. https://doi.org/10.3201/eid3008.240289.

Vibrio mimicus Lineage Carrying Cholera Toxin and Vibrio Pathogenicity Island, United States and China [PDF - 583 KB - 4 pages]
S. Morgado et al.

Vibrio mimicus bacteria have caused sporadic cases and outbreaks of cholera-like diarrhea throughout the world, but the association of lineages with such events is unexplored. Genomic analyses revealed V. mimicus lineages carrying the virulence factors cholera toxin and toxin coregulated pilus, one of which has persisted for decades in China and the United States.

EID Morgado S, dos Santos Freitas F, Lourenço da Fonseca E, Vicente A. Vibrio mimicus Lineage Carrying Cholera Toxin and Vibrio Pathogenicity Island, United States and China. Emerg Infect Dis. 2024;30(8):1729-1732. https://doi.org/10.3201/eid3008.240252
AMA Morgado S, dos Santos Freitas F, Lourenço da Fonseca E, et al. Vibrio mimicus Lineage Carrying Cholera Toxin and Vibrio Pathogenicity Island, United States and China. Emerging Infectious Diseases. 2024;30(8):1729-1732. doi:10.3201/eid3008.240252.
APA Morgado, S., dos Santos Freitas, F., Lourenço da Fonseca, E., & Vicente, A. (2024). Vibrio mimicus Lineage Carrying Cholera Toxin and Vibrio Pathogenicity Island, United States and China. Emerging Infectious Diseases, 30(8), 1729-1732. https://doi.org/10.3201/eid3008.240252.

Fecal Microbiota Transplantation for Severe Infant Botulism, China [PDF - 485 KB - 3 pages]
C. Fan et al.

Infant botulism in a 4-month-old boy in China who continued to excrete toxins for over a month despite antitoxin therapy was further treated with fecal microbiota transplantation. After treatment, we noted increased gut microbial diversity and altered fecal metabolites, which may help reduce intestinal pH and enhance anti-inflammatory capabilities.

EID Fan C, Li R, Wang L, Li K, Jia X, Gao H, et al. Fecal Microbiota Transplantation for Severe Infant Botulism, China. Emerg Infect Dis. 2024;30(8):1732-1734. https://doi.org/10.3201/eid3008.231702
AMA Fan C, Li R, Wang L, et al. Fecal Microbiota Transplantation for Severe Infant Botulism, China. Emerging Infectious Diseases. 2024;30(8):1732-1734. doi:10.3201/eid3008.231702.
APA Fan, C., Li, R., Wang, L., Li, K., Jia, X., Gao, H....Qian, S. (2024). Fecal Microbiota Transplantation for Severe Infant Botulism, China. Emerging Infectious Diseases, 30(8), 1732-1734. https://doi.org/10.3201/eid3008.231702.

Infective SARS-CoV-2 in Skull Sawdust at Autopsy, Finland [PDF - 276 KB - 3 pages]
J. N. Kantonen et al.

We assessed the distribution of SARS-CoV-2 at autopsy in 22 deceased persons with confirmed COVID-19. SARS-CoV-2 was found by PCR (2/22, 9.1%) and by culture (1/22, 4.5%) in skull sawdust, suggesting that live virus is present in tissues postmortem, including bone. Occupational exposure risk is low with appropriate personal protective equipment.

EID Kantonen JN, Kuivanen S, Smura T, Puttonen H, Kekäläinen E, Sajantila A, et al. Infective SARS-CoV-2 in Skull Sawdust at Autopsy, Finland. Emerg Infect Dis. 2024;30(8):1735-1737. https://doi.org/10.3201/eid3008.240145
AMA Kantonen JN, Kuivanen S, Smura T, et al. Infective SARS-CoV-2 in Skull Sawdust at Autopsy, Finland. Emerging Infectious Diseases. 2024;30(8):1735-1737. doi:10.3201/eid3008.240145.
APA Kantonen, J. N., Kuivanen, S., Smura, T., Puttonen, H., Kekäläinen, E., Sajantila, A....Carpén, O. (2024). Infective SARS-CoV-2 in Skull Sawdust at Autopsy, Finland. Emerging Infectious Diseases, 30(8), 1735-1737. https://doi.org/10.3201/eid3008.240145.

Novel Genotypes of Highly Pathogenic Avian Influenza H5N1 Clade 2.3.4.4b Viruses, Germany, November 2023 [PDF - 282 KB - 3 pages]
A. Ahrens et al.

Several subtypes and many different genotypes of highly pathogenic avian influenza viruses of subtype H5 clade 2.3.4.4b have repeatedly caused outbreaks in Germany. Four new highly pathogenic avian influenza genotypes emerged in November 2023 after reassortment with low pathogenicity precursors, replacing genotype BB, which had dominated in Europe since 2022.

EID Ahrens A, Pohlmann A, Grund C, Harder T, Beer M. Novel Genotypes of Highly Pathogenic Avian Influenza H5N1 Clade 2.3.4.4b Viruses, Germany, November 2023. Emerg Infect Dis. 2024;30(8):1737-1739. https://doi.org/10.3201/eid3008.240103
AMA Ahrens A, Pohlmann A, Grund C, et al. Novel Genotypes of Highly Pathogenic Avian Influenza H5N1 Clade 2.3.4.4b Viruses, Germany, November 2023. Emerging Infectious Diseases. 2024;30(8):1737-1739. doi:10.3201/eid3008.240103.
APA Ahrens, A., Pohlmann, A., Grund, C., Harder, T., & Beer, M. (2024). Novel Genotypes of Highly Pathogenic Avian Influenza H5N1 Clade 2.3.4.4b Viruses, Germany, November 2023. Emerging Infectious Diseases, 30(8), 1737-1739. https://doi.org/10.3201/eid3008.240103.
Letters

Transmission and Surveillance of Rat Hepatitis E Virus in Swine [PDF - 236 KB - 1 page]
M. Bezerra et al.
EID Bezerra M, Oliveira da Paz M, de Oliveira-Filho E, de Souza Reis C. Transmission and Surveillance of Rat Hepatitis E Virus in Swine. Emerg Infect Dis. 2024;30(8):1739. https://doi.org/10.3201/eid3008.240484
AMA Bezerra M, Oliveira da Paz M, de Oliveira-Filho E, et al. Transmission and Surveillance of Rat Hepatitis E Virus in Swine. Emerging Infectious Diseases. 2024;30(8):1739. doi:10.3201/eid3008.240484.
APA Bezerra, M., Oliveira da Paz, M., de Oliveira-Filho, E., & de Souza Reis, C. (2024). Transmission and Surveillance of Rat Hepatitis E Virus in Swine. Emerging Infectious Diseases, 30(8), 1739. https://doi.org/10.3201/eid3008.240484.
Etymologia

Microbiota [mī′′-krō-bī′-ō-′tә], microbiome [mī′′-krō-bī′-ōm] [PDF - 480 KB - 1 page]
J. Cabrera and D. Monte
EID Cabrera J, Monte D. Microbiota [mī′′-krō-bī′-ō-′tә], microbiome [mī′′-krō-bī′-ōm]. Emerg Infect Dis. 2024;30(8):1663. https://doi.org/10.3201/eid3008.230677
AMA Cabrera J, Monte D. Microbiota [mī′′-krō-bī′-ō-′tә], microbiome [mī′′-krō-bī′-ōm]. Emerging Infectious Diseases. 2024;30(8):1663. doi:10.3201/eid3008.230677.
APA Cabrera, J., & Monte, D. (2024). Microbiota [mī′′-krō-bī′-ō-′tә], microbiome [mī′′-krō-bī′-ōm]. Emerging Infectious Diseases, 30(8), 1663. https://doi.org/10.3201/eid3008.230677.
Online Reports

Proposal for a Global Classification and Nomenclature System for A/H9 Influenza Viruses [PDF - 3.71 MB - 13 pages]
A. Fusaro et al.

Influenza A/H9 viruses circulate worldwide in wild and domestic avian species, continuing to evolve and posing a zoonotic risk. A substantial increase in human infections with A/H9N2 subtype avian influenza viruses (AIVs) and the emergence of novel reassortants carrying A/H9N2-origin internal genes has occurred in recent years. Different names have been used to describe the circulating and emerging A/H9 lineages. To address this issue, an international group of experts from animal and public health laboratories, endorsed by the WOAH/FAO Network of Expertise on Animal Influenza, has created a practical lineage classification and nomenclature system based on the analysis of 10,638 hemagglutinin sequences from A/H9 AIVs sampled worldwide. This system incorporates phylogenetic relationships and epidemiologic characteristics designed to trace emerging and circulating lineages and clades. To aid in lineage and clade assignment, an online tool has been created. This proposed classification enables rapid comprehension of the global spread and evolution of A/H9 AIVs.

EID Fusaro A, Pu J, Zhou Y, Lu L, Tassoni L, Lan Y, et al. Proposal for a Global Classification and Nomenclature System for A/H9 Influenza Viruses. Emerg Infect Dis. 2024;30(8):1-13. https://doi.org/10.3201/eid3008.231176
AMA Fusaro A, Pu J, Zhou Y, et al. Proposal for a Global Classification and Nomenclature System for A/H9 Influenza Viruses. Emerging Infectious Diseases. 2024;30(8):1-13. doi:10.3201/eid3008.231176.
APA Fusaro, A., Pu, J., Zhou, Y., Lu, L., Tassoni, L., Lan, Y....Liu, J. (2024). Proposal for a Global Classification and Nomenclature System for A/H9 Influenza Viruses. Emerging Infectious Diseases, 30(8), 1-13. https://doi.org/10.3201/eid3008.231176.

Wastewater Target Pathogens of Public Health Importance for Expanded Sampling, Houston, Texas, USA [PDF - 685 KB - 4 pages]
K. Sheth et al.

Building on the success of initiatives put forth during the COVID-19 pandemic response, US health officials are expanding wastewater surveillance programs to track other target pathogens and diseases of public health interest. The Houston Health Department in Houston, Texas, USA, conducted a hypothesis-generating study whereby infectious disease subject matter experts suggested potential targets. This study addressed 2 criteria recommended by the National Academies of Sciences, Engineering, and Medicine for selecting wastewater targets. Results can be used as a basis of a questionnaire for a future population-based study to recommend targets of highest priority to include for expanded wastewater sampling.

EID Sheth K, Hopkins L, Domakonda K, Stadler L, Ensor KB, Johnson CD, et al. Wastewater Target Pathogens of Public Health Importance for Expanded Sampling, Houston, Texas, USA. Emerg Infect Dis. 2024;30(8):14-17. https://doi.org/10.3201/eid3008.231564
AMA Sheth K, Hopkins L, Domakonda K, et al. Wastewater Target Pathogens of Public Health Importance for Expanded Sampling, Houston, Texas, USA. Emerging Infectious Diseases. 2024;30(8):14-17. doi:10.3201/eid3008.231564.
APA Sheth, K., Hopkins, L., Domakonda, K., Stadler, L., Ensor, K. B., Johnson, C. D....Septimus, E. (2024). Wastewater Target Pathogens of Public Health Importance for Expanded Sampling, Houston, Texas, USA. Emerging Infectious Diseases, 30(8), 14-17. https://doi.org/10.3201/eid3008.231564.
About the Cover

The Tree of Life, Archetype and Artifice [PDF - 2.24 MB - 3 pages]
B. Breedlove
EID Breedlove B. The Tree of Life, Archetype and Artifice. Emerg Infect Dis. 2024;30(8):1740-1742. https://doi.org/10.3201/eid3008.ac3008
AMA Breedlove B. The Tree of Life, Archetype and Artifice. Emerging Infectious Diseases. 2024;30(8):1740-1742. doi:10.3201/eid3008.ac3008.
APA Breedlove, B. (2024). The Tree of Life, Archetype and Artifice. Emerging Infectious Diseases, 30(8), 1740-1742. https://doi.org/10.3201/eid3008.ac3008.
Page created: July 19, 2024
Page updated: July 23, 2024
Page reviewed: July 23, 2024
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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