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Rapid Increase in Seroprevalence of <em>Borrelia burgdorferi</em> Antibodies among Dogs, Northwestern North Carolina, USA, 2017-2021


Rapid Increase in Seroprevalence of <em>Borrelia burgdorferi</em> Antibodies among Dogs, Northwestern North Carolina, USA, 2017-2021

Exploratory geographic analysis included 2,739 client households within Watauga County. Canine B. burgdorferi seroprevalence in 2017 appeared higher in more population-dense areas, such as Boone and the primarily residential areas south of Boone (Figure; Appendix Figure 2). In contrast, in 2021, when canine B. burgdorferi seroprevalence was significantly higher, we did not observe an apparent geographic correlation. The Moran's I values for canine B. burgdorferi seroprevalence were positive and significant for 2017 (p = 0.002), 2018 (p<0.001), and 2019 (p<0.001), indicating geographic clustering (Table 3). In the 2017 bivariate regression analysis (Table 4), elevation was positively associated with canine B. burgdorferi seroprevalence, and slope was negatively associated with seroprevalence in the 0.5-mile, 1-mile, and 3-mile buffer regions surrounding households. Aspect was positively associated with canine B. burgdorferi seroprevalence, and density of forest land cover was negatively associated with seroprevalence at the 3-mile level. In the 2021 bivariate regression analysis, only the slope was positively associated with canine B. burgdorferi seroprevalence at the household level.

Seroprevalence and incident seropositivity of B. burgdorferi antibodies among domestic dogs in Watauga County, North Carolina, increased substantially from 2017 to 2021; the largest relative difference in proportions of newly positive test results occurred in 2020. Although less frequent, Anaplasma spp. seroprevalence and incident seropositivity also increased during 2017-2021, possibly indicating emergence of Anaplasma spp. in southern states. However, that result might indicate exposure to A. platys, which is not spread by Ixodes sp. ticks, unlike A. phagocytophilum.

Doxycycline was prescribed for ≈50% of dogs that had a positive test result. We used concurrent doxycycline prescriptions to measure symptomatic illness; however, this might have led to an overestimate because doxycycline could have also been prescribed for asymptomatic cases. Over the study period, canine B. burgdorferi seroprevalence shifted from clustering in distinct geographic areas to having no distinct clusters within the county. Moreover, the observed B. burgdorferi seroprevalence in 2021 (11.2%) falls within the sensitivity indicator (>5%) for human infection risk (20) and is comparable to rates found in traditionally high-incidence states. For example, the Companion Animal Parasite Council reported an annual canine B. burgdorferi seroprevalence of 8.8% in Rhode Island, 11.9% in Connecticut, and 12.4% in Maine in 2021 (40). Therefore, our overall findings provide compelling evidence of change in canine B. burgdorferi seropositivity, supporting the conclusion that Lyme disease is rapidly emerging and is likely established in northwestern North Carolina (14).

Geographic analysis results were generally consistent with trends observed in the epidemiologic analysis. For example, in 2017, specific environmental factors were associated with canine B. burgdorferi seroprevalence, including elevation, slope, aspect, and density of forest land cover. This finding is consistent with previous research in southwestern Virginia that found associations between Lyme disease incidence and higher geographic elevation (41). In addition, others have found slope to be negatively associated with tick densities, and higher tick densities were associated with northerly aspects (42), consistent with our findings. Forest land cover density was negatively associated with B. burgdorferi seroprevalence in our study, consistent with a report that found Lyme disease risk was inversely related to forest patch area; small patches had higher risk because of a higher density of infected vectors (e.g., white-footed mouse) that thrive in fragmented forest areas (43). The absence of clustering or geographic associations seen in 2021 data suggests that Lyme disease risk is becoming widespread within the county without regard to specific environmental or ecologic factors.

Surveillance reports using human data have shown a similar Lyme disease trend in Watauga County; the number of reported human cases increased from 7 in 2017 to 31 in 2021 (44). However, well-documented limitations of traditional surveillance systems, such as underreporting, often underestimate the true risk for human infection and can, therefore, limit public health responses (10-12). Evidence of underreporting can clearly be seen during the COVID-19 pandemic, when surveillance reports from 2020 identified no human Lyme disease cases in Watauga County, despite being listed as a high-incidence North Carolina county several consecutive years before that time (15). This distinction is further exemplified in our findings for the year 2021, which identified 231 newly positive tests among dogs at 1 veterinary clinic in Watauga County alone compared with 31 human cases reported through traditional surveillance systems (44). Although data for both humans and dogs showed similar Lyme disease trends in Watauga County, monitoring changes in canine B. burgdorferi seroprevalence might help to overcome limitations of traditional surveillance systems by providing a more consistent, robust, and accessible data source. Furthermore, sentinel-based surveillance at veterinary clinics could be used to monitor Lyme disease risk in emergent areas at the leading edge of Ixodes sp. tick and B. burgdorferi endemicity through regular reporting of canine B. burgdorferi seroprevalence to local or state health departments. Observed changes in seroprevalence estimates could subsequently trigger public health interventions, such as targeted entomologic surveillance, educational efforts for clinical providers, and public awareness campaigns. Surveillance is likely to be most effective in areas where the ecology is suitable for vectors and where variations in land cover and ecologic features occur (45).

Most research evaluating trends in canine B. burgdorferi seroprevalence have used cross-sectional analysis and ecologic data (19,20). A previous observational study using data from the IDEXX Reference Laboratories network and from veterinarians who used the IDEXX VetLab Stations and software found that canine B. burgdorferi seroprevalence increased in North Carolina from 1.9% in 2010 to 2.3% in 2017; Watauga County was listed as 1 of the 12 counties contributing to the observed increase (19). Our results support and build upon those findings. However, our analysis differs because we evaluated our data on an individual level, further demonstrating the ability of canine seroprevalence to identify Lyme disease emergence into nonendemic areas, where populations might be at increased risk (18-20). By working directly with a local veterinary clinic, we obtained client addresses to further evaluate geographic risk factors associated with canine B. burgdorferi seroprevalence. Individual-level canine B. burgdorferi seroprevalence data has additional applications for human health that should be evaluated in future research. For example, knowledge of the dog's serostatus could be used to target educational and behavioral interventions for owners of B. burgdorferi-positive dogs, prioritizing prevention, control, and even vaccine efforts for high-risk persons. If a human Lyme disease vaccine becomes available, veterinary clinic visits could be used as an opportunity to inform the owner about the human vaccine and discuss their risk according to their dog's B. burgdorferi serostatus. This type of intervention might improve acceptance of human Lyme disease vaccines and could help counter vaccine hesitancy with nontraditional sources, such as veterinarians, providing education and individualized risk assessments to human clients (46,47).

Our study has notable strengths, including the use of a large individual-level dataset. However, the first limitation of our study is that we only collected data from 1 veterinary clinic within the county, which might limit the generalizability of our overall findings and interpretations. In addition, our results might also be less generalizable than previous studies that used publicly available data, which enabled larger scale analysis. However, we believe that the study population was representative of domestic dogs in Watauga County because our partner clinic is a large and established veterinary hospital in the community, completing >2,000 SNAP 4DX Plus tests annually. Second, the definition used to measure incident seropositivity might have included some dogs that were not tested before receiving their first positive result and, therefore, might not represent a true incident infection. However, we believe this number is low because of the relatively small proportion of dogs that tested positive during the first year of the study. Third, associated behavioral data was absent. Understanding the extent to which certain confounders influence B. burgdorferi seropositivity among dogs is crucial, especially among previously unexposed populations, where less is known about behavioral risk factors (14). For example, we did not collect information regarding the use of tick prevention or control products among dogs, which might influence a dog's susceptibility for infection and eventually human risk for tick exposure (48), although we have no reason to believe that marketing or use of those products during the study period would have changed. Future research should evaluate the extent to which covariates influence exposure and outcome relationships between humans and their pet dogs to help develop and implement community awareness and prevention campaigns in areas where Lyme disease is emerging. Furthermore, some tested dogs might have had antibodies against B. burgdorferi that reflect exposure from other higher transmission areas for various reasons, such as relocation of owners, recreational activities outside northwestern North Carolina (e.g., hiking, hunting), and movement of animals from breeders or shelters before residing with their current owner. Not adjusting for travel history might overestimate the human Lyme disease risk in Watauga County, especially in study years before 2020, because we believe travel might have been limited because of the COVID-19 pandemic. Future research should control for this potential bias by documenting residence and travel histories of both owners and animals.

In conclusion, our findings provide support for leveraging canine B. burgdorferi seroprevalence in sentinel surveillance to monitor human Lyme disease risk in Lyme disease-emergent areas. Sentinel veterinary clinics might also serve as critical partners, providing opportunities for education and individualized risk assessment delivered by trusted veterinarians. Our findings in Watauga County indicate the use of canine B. burgdorferi seroprevalence might help overcome limitations of traditional human surveillance systems by providing more accessible and cost-effective estimates of human Lyme disease risk.

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