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Abstract

In July 2019, Bourbon virus RNA was detected in anAmblyomma americanum tick removed from a resident of Long Island, New York, USA. Tick infection and white-tailed deer (Odocoileus virginianus) serosurvey results demonstrate active transmission in New York, especially Suffolk County, emphasizing a need for surveillance anywhereA. americanum ticks are reported.

In July 2019, New York State Department of Health (NYSDOH) epidemiologists were notified that BRBV RNA was detected in an individual, partially engorged femaleA. americanum tick removed from a Long Island, New York, resident. Comprehensive testing performed through the University of Massachusetts TickReport service (https://www.tickreport.com) revealed the tick was also positive forEhrlichia ewingiibacteria. Notes on the tick submission form indicated the person was experiencing fever, chills, and fatigue; officials with NYSDOH and Suffolk County Department of Health Services (SCDHS) attempted to contact the resident for a follow-up investigation. No additional information was provided, and no blood samples were available to assess potential infection with BRBV.

In 2016, NYSDOH and SCDHS initiated active tick surveillance targetingA. americanum ticks for BRBV and Heartland virus (HRTV). HRTV-infected ticks and seropositive deer were detected on Long Island in 2018 and reported in 2021 (11). We used standardized flag sampling for the collection of host-seekingA. americanum ticks on public lands in Suffolk County. During 2016–2020, a total of 1,265 pools, representing 4,189 adults, 7,227 nymphs, and 97 larvae, tested negative for BRBV RNA by real-time reverse transcription PCR using an in-house multiplex assay to detect HRTV and BRBV (11). The BRBV primers for this assay were designed based on the St. Louis strain (GenBank accession no. MK453528) (12). During 2021, we expanded sampling forA. americanum ticks on Long Island to collect a greater number of ticks from more locations, and we modified molecular detection protocols to use BRBV-specific primers developed at TickReport (Table 1). We designed BRBV-specific primers based on the original virus strain deposited in GenBank (accession no. KU708254) (13). We collected a total of 1,058 pools, consisting of 4,406 adults (460 pools) and 9,972 nymphs (598 pools) from 12 sites in Suffolk County, New York. Pool sizes ranged from 1–10 adults and 5–20 nymphs. We detected BRBV RNA in 5 pools of unengorged nymphs. We collected positive pools at 1 site in Smithtown, New York (n = 3), on May 3, 2021, and 2 sites, 1 positive pool each, in Brookhaven, New York, on June 9 and July 8, 2021. We isolated infectious virus from all BRBV RNA-positive tick pools after incubation on Vero cells (ATCC, Manassas, VA, USA). We confirmed that the isolates were BRBV by real-time reverse transcription PCR.

Figure 1

Figure 1. Sampling of hunter-harvested white-tailed deer blood and Bourbon virus seropositivity by county, New York, NY, USA. Locations (open circles) of harvested deer are randomly jittered within townships to avoid overplotting.

Figure 2

Figure 2. Suffolk County tick collection sites for study of Bourbon virus seropositivity, New York, NY, USA. Circles within townships indicate tick collection sites. Open circles are sites with no evidence of...

Serologic testing of hunter-harvested white-tailed deer blood submitted for arbovirus serosurveys has been conducted in New York since 2007 using plaque reduction neutralization tests, as described (14). BRBV was included in these assays starting in 2019 for deer harvested in Suffolk County and the Hudson Valley Region and 2020 for deer harvested in central and western New York. We screened a total of 881 serum samples at 1:20 for the presence of neutralizing antibodies to BRBV (Table 2;Figure 1). We serially diluted samples testing positive for endpoint titers. Statewide, 37.7% of the deer were seropositive; 89.2% of the seropositive deer had titers >20. The seropositivity was 66.5% for deer harvested in Suffolk County (Table 2;Figures 1,2). Seroprevalence was lower in western New York (3.8%), the Hudson Valley (1.7%), and central New York (1.2%). We did not detect BRBV neutralizing antibodies in 7 deer harvested in the northern New York region (Table 2;Figure 1). We testedA. americanum ticks (n = 1,641) collected from 145 deer harvested from Suffolk County for BRBV RNA; the virus was not detected.

Isolation of BRBV from the local tick population and high seropositivity in hunter-harvested white-tailed deer demonstrated active transmission throughout Suffolk County, New York, since 2019. In addition, serologic evidence suggests the virus is present in other regions of New York. Consistent with previous BRBV field studies and the recent discovery of a closely related virus transmitted byAmblyomma species ticks in Japan,A. americanum ticks were implicated in local transmission of BRBV (2,6). Tick minimal infection rates were 0%–0.77%. It is unclear whether the unengorged nymphs had acquired the virus as larvae feeding on viremic hosts, through co-feeding transmission, or transovarially. These routes of transmission have been demonstrated in laboratory studies (5). BRBV was not detected in adult ticks tested during surveillance despite high numbers collected. Considering the overlap of adult and nymphal tick activity on Long Island, future surveillance campaigns should study the effect of phenology on BRBV transmission.

Of interest, of the 5 BRBV positive pools detected by the TickReport primer set, 1 pool was positive with the primer set used during previous surveillance seasons despite similar assay limits of detection; this result suggested genetic differences in the primer target regions. We plan to conduct phylogenetic analyses and in-vitro growth characteristic studies.

White-tailed deer are a sensitive sentinel model for many arboviruses because of their overall abundance and distribution, small home ranges, and the frequency on which they are fed upon by ticks and other hematophagous arthropods (14,15). Seroprevalence in Suffolk County deer (66.5%) was higher than that reported in North Carolina deer (56%), but lower than deer harvested in Missouri (86%) (8,9). BRBV seroprevalence rates of white-tailed deer harvested from various areas in Suffolk County (Table 2) were similar to Oz virus seroprevalence rates (30.0%–73.7%) in wild sika deer (Cervus nippon) in Japan sampled from prefectures located near the initial detection of the virus (3). The lower seroprevalence in regions of New York outside of Long Island can be attributed to fewer established populations ofA. americanum ticks or incidental transmission by bird-dispersed immatures originating from established regions. To date, no competent vertebrate host, including deer, has been implicated in BRBV amplification.

Our findings emphasize the need to include emerging pathogens such as BRBV and HRTV in surveillance programs wherever lone star ticks are distributed. Clinicians outside of the midwestern United States should be aware of the potential for human disease. It is unclear if the symptoms of the person who removed the BRBV-positive tick were the result of potential infection with BRBV,Ehrlichia ewingii, or an unrelated etiology, because patient blood samples were not available. Considering the overlapping symptomologies of BRBV (fever, fatigue, loss of appetite, thrombocytopenia, and leukopenia) with other tickborne infections, including ehrlichiosis and Heartland virus disease, diagnosis is difficult without specific testing. Currently, testing is only available at the Centers for Disease Control and Prevention and a few state health laboratories. Providers should request BRBV and HRTV testing for patients with history of tick exposure or travel to regions whereA. americanum ticks are reported and who are displaying clinical symptoms, including leukopenia and thrombocytopenia, that do not respond with antimicrobial treatment.

Mr. Dupuis is a research scientist at the Wadsworth Center, New York State Department of Health. His research interests include the role of the vertebrate host in the ecology of mosquitoborne and tickborne viruses.

Please use the form below to submit correspondence to the authors or contact them at the following address:

Alan P. Dupuis II, The Arbovirus Laboratory, New York State Department of Health, 5668 State Farm Rd, Slingerlands, NY 12159, USA

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