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পাতার বিষয়বস্তু আরও ভালো করতে চান? একটি পরিবর্তনের প্রস্তাব দিন।

Kimberly E. Mace, PhD1; Daniel Jacobs, MS2; Carolyn V. Gould, MD1; J. Erin Staples, MD, PhD1; Shelby L. Lyons, MPH1 (

Summary

What is already known about this topic?

West Nile virus (WNV) is the leading cause of arthropodborne viral (arboviral) disease, manifesting as acute febrile or neurologic illness in the United States. Several other arboviruses transmitted through bites of infected mosquitoes or ticks also occur in the United States and cause similar illnesses. Transmission through blood transfusion or organ transplantation has been reported.

What is added by this report?

In 2024, arboviral disease cases were reported from 48 states and the District of Columbia. WNV was most common, followed by Powassan virus disease, which increased to a new record high. La Crosse virus disease was the most common arboviral disease among children; the case-fatality rate was highest for eastern equine encephalitis.

What are the implications for public health practice?

Clinicians should consider arboviral testing for patients with fever or neurologic illness, particularly when mosquitoes and ticks are active. Timely surveillance can be used to identify geographic areas at risk for arboviral infection. Reducing arboviral diseases depends on personal protective measures, vector control, and screening blood and organ donors for WNV.

Tables

Related Materials

Abstract

In the United States, arthropodborne viruses (arboviruses) are primarily transmitted by infected mosquitoes or ticks; rarely, they can be transmitted through blood transfusion or organ transplantation. Whereas a majority of arboviral infections are asymptomatic, symptomatic infections range from mild febrile illness to severe neuroinvasive disease. This report summarizes data for nationally notifiable domestic arboviral diseases with illness onset in 2024. Forty-eight states and the District of Columbia reported 1,955 arboviral disease cases, including 189 (10%) deaths. Although the number of West Nile virus (WNV) disease cases in 2024 was below the 10-year median (2,162), WNV caused most reported arboviral disease cases (1,808; 92%). Powassan virus disease was the second most commonly reported arboviral disease (60; 3%), increasing from a previous high of 49 cases in 2023. A majority of patients with arboviral disease were aged ≥60 years (1,133; 58%), were male (1,223; 63%), and had illness onset during July–September (1,603; 82%). However, La Crosse virus disease occurred almost exclusively among children aged

Introduction

Arboviruses are maintained in transmission cycles among arthropods and vertebrate hosts, including humans and other animals (1). In the United States, humans typically acquire arboviral infections when they are bitten by an infected mosquito or tick and, although rare, through other routes such as blood transfusion and organ transplantation (2). Of the most common nationally notifiable domestic arboviral diseases in the continental United States, five are mosquitoborne (West Nile, La Crosse, Jamestown Canyon, eastern equine encephalitis, and St. Louis encephalitis virus diseases) and one (Powassan virus disease) is tickborne. The majority of arboviral infections are asymptomatic, but disease can range from mild febrile illness to severe, potentially fatal, neuroinvasive disease. Older age, certain chronic medical conditions (e.g., cancer, diabetes, high blood pressure, or kidney disease), and immunosuppression are risk factors for neuroinvasive disease. No prophylactic agents or treatments are available for arboviral diseases; therefore, timely and accurate surveillance is critical to help focus prevention measures (e.g., personal protection against mosquito bites and vector control) to reduce disease morbidity and mortality. This report provides an annual update on domestic arboviral disease case numbers and incidence to increase awareness of the occurrence and characteristics of arboviral diseases in the United States (3,4).

Data Source

State health departments voluntarily report cases of nationally notifiable domestic arboviral diseases to CDC by location of patient residence through ArboNET, the national arbovirus surveillance system, using standard surveillance case definitions that include clinical and laboratory criteria. Confirmed and probable cases are included in this report; ­cases are further characterized as neuroinvasive (i.e., those with meningitis, encephalitis, acute flac­cid paralysis, or other unspecified neurologic manifestation) or nonneuroinvasive (all other cases).

Analysis

Confirmed and probable cases with clinically compatible disease and supporting laboratory results were combined in the analysis. The case features of six domestic arboviral diseases (West Nile, Powassan, La Crosse, Jamestown Canyon, eastern equine encephalitis, and St. Louis encephalitis virus diseases) are described and compared with previous years’ data reported to ArboNET to identify trends. Incidence was calculated using U.S. Census Bureau 2024 midyear population estimates as denominators and limited to neuroinvasive disease cases because these cases are more severe and therefore more consistently diagnosed and reported (1). A negative binomial regression was chosen for the Powassan case trend analysis to account for overdispersion of the annual count data, with the year variable centered to limit multicollinearity; this analysis was conducted using the SAS proc genmod procedure; all analyses were conducted using SAS (version 9.4; SAS Institute). This activity was reviewed by CDC, deemed not research, and conducted consistent with applicable federal law and CDC policy.*

Reported Arboviral Disease Cases

CDC received 1,955 reports of confirmed (594; 30%) and probable (1,361; 70%) arboviral disease cases with illness onset in 2024; 1,485 cases (76%) were neuroinvasive (

WNV disease cases were reported from 591 (19%) of 3,143 counties in 48 states and DC. Texas (363 cases), California (103), and New York (69) accounted for 40% of all U.S. WNV neuroinvasive disease cases. The national incidence of WNV neuroinvasive disease was 0.40 per 100,000 population (

Powassan Virus Disease

In 2024, a total of 60 Powassan virus disease cases were reported. The median patient age was 69 years (IQI = 60–75 years), with four patients (7%) aged Powassan virus disease cases were reported from 45 counties across 10 states. Nationally, the incidence of neuroinvasive Powassan virus disease was 0.02 per 100,000 population, with the highest incidence in Maine (0.43), Minnesota (0.24), New Hampshire (0.21), and Wisconsin (0.20) (Table 2). From 2023 to 2024, Minnesota and Wisconsin experienced a combined 160% relative increase in cases, from 10 to 26. Nationally, the number of cases reported in 2024 was above the 10-year median of 23 cases (IQI = 21–43), and during the previous 21 years, cases increased with an annual growth rate of 17.5% (95% CI = 13.6–21.6; negative binomial regression; pIn 2024, a total of 37 La Crosse virus disease cases were reported; 35 (95%) occurred among children aged In 2024, a total of 27 cases of Jamestown Canyon virus disease was reported; the median patient age was 66 years (IQI = 53–76 years), and 19 (70%) patients were male. Twenty-one (78%) patients were hospitalized, 20 (74%) had neuroinvasive disease, and two (7%) died (CFR = 10% among patients with neuroinvasive disease) (Table 1). Illness onset occurred during July–September for 13 (48%) patients and April–June for 10 (37%). Cases were reported from 23 counties in six states. The highest numbers of cases were reported from Wisconsin (10), Michigan (eight), and Minnesota (four). The national incidence of neuroinvasive Jamestown Canyon virus disease was 0.01 per 100,000 population, with the highest incidences in New Hampshire (0.14), Wisconsin (0.10), Rhode Island (0.09), and Michigan (0.08) (Table 2). The number of Jamestown Canyon virus disease cases in 2024 was similar to the 10-year median (21 cases; IQI = 12–41).

Eastern Equine Encephalitis Virus Disease

In 2024, a total of 19 cases of eastern equine encephalitis virus disease were reported; the median patient age was 68 years (IQI = 53–78 years), and 15 (79%) patients were male. All patients were hospitalized with neuroinvasive disease, and five died (CFR = 26%) (Table 1). Eighteen (95%) patients had illness onset during July–September. Cases were reported from 12 counties in nine states. The highest numbers of cases were reported by New Hampshire (five) and Massachusetts (four). The national incidence of neuroinvasive eastern equine encephalitis virus disease was 0.01 per 100,000, and rates were highest in New Hampshire (0.35) and Vermont (0.31) (Table 2). The number of reported eastern equine encephalitis disease cases in 2024 was the highest since 2019 and higher than the 10-year median of 6.5 (IQI = 5–8).

St. Louis Encephalitis Virus Disease

Two cases of St. Louis encephalitis virus disease were reported in 2024, both in men aged

Discussion

Domestic arboviruses occur in arthropod and animal hosts throughout the continental United States. Local ecology and climate, especially temperature and moisture, host immunity, and human activities all influence disease occurrence. In 2024, WNV was the most common domestic arbovirus, but the number of reported cases was below the 10-year median. High case counts are often driven by regional outbreaks, as in 2024 when 456 WNV disease cases reported from Texas accounted for 25% of all WNV cases, highlighting geographic heterogeneity in transmission. The numbers of eastern equine encephalitis and Powassan virus disease cases in 2024 were higher than the previous 10-year medians, which is especially concerning because these two arboviral diseases are associated with the highest CFRs among domestic arboviral diseases (26% and 15%, respectively). Eastern equine encephalitis is characterized by periodic surges over time and in certain geographic areas; the number of cases reported in 2024 (19) was the third highest reported since 2003, following 2019 (38) and 2005 (21) (5–7). In contrast, the number of Powassan virus disease cases has been increasing by an average of 17.5% annually during the past 21 years. The reasons for this might be related to an actual increase in incidence, improved health care provider awareness, expanded availability of diagnostic testing at commercial and state public health laboratories, or potential expansion of the vector range (8).

In the United States, although adults aged ≥60 years are at higher risk for most neuroinvasive arboviral disease and poor outcomes compared with younger persons, who are more likely to have an asymptomatic or mild, febrile illness (1,9), La Crosse virus disease occurs more commonly among children. In 2024, La Crosse virus disease accounted for 54% of the 63 neuroinvasive arboviral disease cases reported among children aged 10).

One WNV transplant cluster associated with two neuroinvasive disease deaths was identified in 2024. Although rare, arboviral transmission through solid organ transplantation is often associated with high morbidity and mortality among organ recipients, likely related to their immunosuppression (2). Organ donors in the United States, unlike blood donors, were not universally screened for WNV. However, a policy that requires seasonal WNV screening (July 1–October 31) for all potential living and deceased solid organ donors was implemented in June 2026.

Limitations

The findings in this report are subject to at least three limitations. First, cases can be misclassified because inclusion in ArboNET does not require clinical signs and symptoms or diagnostic laboratory test results. Second, ArboNET is a passive surveillance system that relies on patients seeking health care, appropriate testing by clinicians, and reporting of arboviral disease cases; thus, prevalence is likely underestimated. Conservative estimates based on historical ratios and assuming comparable national reporting patterns, population characteristics, and environmental conditions demonstrated that 30–70 nonneuroinvasive disease cases occur for every reported case of WNV neuroinvasive disease (9); accordingly, 40,410–94,290 nonneuroinvasive WNV disease cases likely occurred nationally in 2024, although only 461 (0.5%–1% of the estimated total) were reported. Finally, the average annual growth rate estimated for the Powassan virus disease trend is limited to the 21-year historical period and is not necessarily a predictor of future trends.

Implications for Public Health Practice

High-quality and timely surveillance is critical to understanding the epidemiology, seasonality, and geographic distribution of domestic arboviruses, which can facilitate clinical recognition, identification of outbreaks, messaging activities to the public and health care providers, and vector-control activities. WNV and other arboviral disease testing should be considered by clinicians for patients with acute febrile or neurologic illness, including recipients of organ transplants or blood transfusions, particularly during times when mosquitoes and ticks are active. Health care providers who order testing for a specific causative agent should take into consideration the timing of illness onset, type and location of exposures, patient age, and underlying health status.

The seasonality of arboviral diseases varies according to the vectors responsible for transmitting them; ticks, which transmit Powassan virus, are active earlier and later during the season compared with mosquitoes that typically have peak activity during July–September. Therefore messaging (e.g., media, newsletters, and education at trailheads or parks) to increase public and health care provider awareness can be tailored based on locally circulating arboviruses and the activity of their vectors.

Approximately 25 years after the detection of WNV in the United States, effective tools for diagnosis, prevention, and treatment are lacking. Consistently high WNV disease incidence each year indicates that further research and development of additional strategies, such as human vaccines and prophylactic or therapeutic monoclonal antibodies for persons at high risk for severe illness, are needed. Development of rapid diagnostic tests can facilitate earlier and more reliable diagnosis, which would also improve patient care, disease surveillance, timely public health messaging, and the ability to conduct clinical trials.

Because no specific treatments (e.g., antiviral medications) are available for domestic arboviral diseases, clinical management is supportive. Likewise, no prophylactic agents (e.g., human vaccines) are available to prevent domestic arboviral diseases; therefore, prevention and control rely on use of personal protective measures (e.g., using insect repellent registered by the Environmental Protection Agency and wearing protective clothing), vector-control activities both at household and community levels (CDC | Ticks | Preventing Tick Bites and CDC | Mosquitoes | Mosquito Control), and WNV blood and organ donor screening to minimize transfusion- and transplant-associated transmission.

Acknowledgments

National Arboviral Surveillance System surveillance coordinators in state and local health departments; Surveillance and Epidemiology Team, Arboviral Diseases Branch, CDC.

Corresponding author: Kimberly E. Mace, kmace@cdc.gov.

1Division of Vector-Borne Diseases, National Center for Emerging and Zoonotic Infectious Diseases, CDC; 2Alaka`ina Foundation, Orlando, Florida.

All authors have completed and submitted the International Committee of Medical Journal Editors form for disclosure of potential conflicts of interest. No potential conflicts of interest were disclosed.

  • 45 C.F.R. part 46, 21 C.F.R. part 56; 42 U.S.C. Sect. 241(d); 5 U.S.C. Sect. 552a; 44 U.S.C. Sect. 3501 et seq.

† Unspecified California serogroup virus reports belong to the California serogroup (e.g., La Crosse, Jamestown Canyon, snowshoe hare, and California encephalitis viruses), but the specific virus is unknown or not identified.

References

  • Committee on Infectious Diseases, American Academy of Pediatrics. Arboviruses [Chapter 7]. In: Red book: 2024–2027 report of the Committee on Infectious Diseases. Itasca, IL: American Academy of Pediatrics; 2024:237–44.
  • Soto RA, McDonald E, Annambhotla P, et al. West Nile virus transmission by solid organ transplantation and considerations for organ donor screening practices, United States. Emerg Infect Dis 2022;28:403–6. https://doi.org/10.3201/eid2802.211697 PMID:34843660
  • Padda H, Jacobs D, Gould CV, et al. West Nile Virus and other nationally notifiable arboviral diseases—United States, 2023. MMWR Morb Mortal Wkly Rep 2025;74:358–64. https://doi.org/10.15585/mmwr.mm7421a1 PMID:40504766
  • Sutter RA, Lyons S, Gould CV, Staples JE, Lindsey NP. West Nile virus and other nationally notifiable arboviral diseases—United States, 2022. MMWR Morb Mortal Wkly Rep 2024;73:484–8. https://doi.org/10.15585/mmwr.mm7321a2 PMID:38814815
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  • Lindsey NP, Martin SW, Staples JE, Fischer M. Notes from the field: multistate outbreak of eastern equine encephalitis virus—United States, 2019. MMWR Morb Mortal Wkly Rep 2020;69:50–1. https://doi.org/10.15585/mmwr.mm6902a4 PMID:31945032
  • CDC. Eastern equine encephalitis—New Hampshire and Massachusetts, August–September 2005. MMWR Morb Mortal Wkly Rep 2006;55:697–700. PMID:16810146
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CharacteristicVirus type, no. (%)** of cases
West NilePowassanLa CrosseJamestown CanyonEastern equine encephalitisSt. Louis encephalitis
Total, no. (N = 1,953)1,808603727192
Age group, yrs
  • A confirmed case meets clinical criteria for arboviral disease and at least one of the following laboratory criteria: 1) isolation of virus from, or demonstration of specific viral antigen or nucleic acid in tissue, blood, CSF, or other body fluid; 2) fourfold or higher change in virus-specific quantitative antibody titers in paired sera; 3) virus-specific IgM antibodies in serum with confirmatory virus-specific neutralizing antibodies in the same or a later specimen; or 4) virus-specific IgM antibodies in CSF and a negative test result for other IgM antibodies in CSF for arboviruses endemic in the region where exposure occurred.
    † A probable case meets clinical criteria for arboviral infection and virus-specific IgM antibodies in CSF or serum but without other testing.
    § Two unspecified California serogroup virus cases were reported but are not included in the table.
    ¶ United States refers to all U.S. states, territories, and the District of Columbia.
    ** Percentages might not sum to 100 because of rounding.
    †† Percentages of cases of encephalitis, meningitis, AFP, and unspecified neurologic signs or symptoms are percentages of neuroinvasive cases.
    §§ Among the 55 West Nile virus disease cases with AFP, 15 (27%) also had encephalitis or meningitis. Among the four Powassan virus disease cases with AFP, all four (100%) also had encephalitis or meningitis.
U.S. Census Bureau division/JurisdictionVirus type, no. (incidence) of cases
West NilePowassanLa CrosseJamestown CanyonEastern equine encephalitisSt. Louis encephalitis
United States1,347 (0.40)60 (0.02)36 (0.01)20 (0.01)19 (0.01)1 (0)
New England32 (0.21)28 (0.18)—**3 (0.02)13 (0.08)
Connecticut10 (0.27)6 (0.16)
Maine1 (0.07)6 (0.43)1 (0.07)
Massachusetts16 (0.22)11 (0.15)4 (0.06)
New Hampshire1 (0.07)3 (0.21)2 (0.14)5 (0.35)
Rhode Island3 (0.27)2 (0.18)1 (0.09)1 (0.09)
Vermont1 (0.15)2 (0.31)
Middle Atlantic149 (0.35)6 (0.01)1 (0)4 (0.01)
New Jersey33 (0.35)2 (0.02)1 (0.01)2 (0.02)
New York69 (0.35)3 (0.02)2 (0.01)
Pennsylvania47 (0.36)1 (0.01)
East North Central128 (0.27)12 (0.03)4 (0.01)14 (0.03)1 (0)
Illinois56 (0.44)
Indiana10 (0.14)
Michigan24 (0.24)8 (0.08)
Ohio12 (0.10)4 (0.03)
Wisconsin26 (0.44)12 (0.20)6 (0.10)1 (0.02)
West North Central142 (0.65)14 (0.06)2 (0.01)2 (0.01)
Iowa16 (0.49)
Kansas11 (0.37)
Minnesota26 (0.45)14 (0.24)1 (0.02)2 (0.03)
Missouri12 (0.19)1 (0.02)
Nebraska50 (2.49)
North Dakota22 (2.76)
South Dakota5 (0.54)
South Atlantic130 (0.19)17 (0.02)1 (0)
Delaware1 (0.10)
District of Columbia2 (0.28)
Florida15 (0.06)
Georgia39 (0.35)
Maryland24 (0.38)
North Carolina27 (0.24)15 (0.14)1 (0.01)
South Carolina15 (0.27)1 (0.02)
Virginia5 (0.06)
West Virginia2 (0.11)1 (0.06)
East South Central87 (0.44)12 (0.06)
Alabama27 (0.52)
Kentucky8 (0.17)
Mississippi42 (1.43)
Tennessee10 (0.14)12 (0.17)
West South Central450 (1.04)1 (0)1 (0)
Arkansas12 (0.39)
Louisiana38 (0.83)
Oklahoma37 (0.90)
Texas363 (1.16)1 (0)1 (0)
Mountain124 (0.47)
Arizona23 (0.30)
Colorado40 (0.67)
Idaho4 (0.20)
Montana3 (0.26)
Nevada15 (0.46)
New Mexico24 (1.13)
Utah14 (0.40)
Wyoming1 (0.17)
Pacific105 (0.19)
Alaska
California103 (0.26)
Hawaii1 (0.07)
Oregon
Washington1 (0.01)
  • Cases per 100,000 population, based on July 1, 2024, U.S. Census Bureau population estimates.
    † A confirmed case meets clinical criteria for arboviral disease and at least one of the following laboratory criteria: 1) isolation of virus from, or demonstration of specific viral antigen or nucleic acid in tissue, blood, CSF, or other body fluid; 2) fourfold or higher change in virus-specific quantitative antibody titers in paired sera; 3) virus-specific IgM antibodies in serum with confirmatory virus-specific neutralizing antibodies in the same or a later specimen; or 4) virus-specific IgM antibodies in CSF and a negative test result for other IgM antibodies in CSF for arboviruses endemic in the region where exposure occurred.
    § A probable case meets clinical criteria for arboviral infection and virus-specific IgM antibodies in CSF or serum but without other testing.
    ¶ United States refers to all U.S. states, territories, and the District of Columbia.
    ** Dashes indicate no reported cases.

###

Abbreviations: CSF = cerebrospinal fluid; DC = District of Columbia; IgM = immunoglobulin M.

  • Cases per 100,000 population, based on July 1, 2024, U.S. Census Bureau population estimates.

† A confirmed case meets clinical criteria for arboviral disease and at least one of the following laboratory criteria: 1) isolation of virus from, or demonstration of, specific viral antigen or nucleic acid in tissue, blood, CSF, or other body fluid; 2) fourfold or higher change in virus-specific quantitative antibody titers in paired sera; 3) virus-specific IgM antibodies in serum with confirmatory virus-specific neutralizing antibodies in the same or a later specimen; or 4) virus-specific IgM antibodies in CSF and a negative test result for other IgM antibodies in CSF for arboviruses endemic in the region where exposure occurred.

§ A probable case meets clinical criteria for arboviral infection and virus-specific IgM antibodies in CSF or serum but without other testing.

¶ United States refers to all U.S. states, territories, and DC.

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