Ixodes scapularis Tick Parasitizing Dog in Dawson County, Montana, USA, 2023
Philip E. Stewart, Justin B. Lack, Marni Rolston, Kimmo Virtaneva, Paul A. Beare, Craig M. Martens, Marshall E. Bloom, Tom G. Schwan

TL;DR
A tick species known as Ixodes scapularis was found on a dog in Montana, indicating a possible expansion of its geographic range.
Contribution
The discovery of I. scapularis in Montana suggests a geographic range expansion and highlights the need for public health monitoring.
Findings
A partially engorged Ixodes scapularis tick was identified from a dog in Bozeman, Montana.
The tick was confirmed as I. scapularis using morphologic and genomic methods.
The finding suggests a potential expansion of the tick's geographic distribution.
Abstract
In October 2023, a partially engorged female Ixodes tick was removed from a dog in Bozeman, Montana, USA, that had recently spent time in eastern Montana. The tick was identified as I. scapularis according to morphologic characteristics and genomic sequencing, suggesting an expanded geographic distribution requiring continued public health surveillance.
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Figure 1
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Taxonomy
TopicsViral Infections and Vectors · Vector-borne infectious diseases · Vector-Borne Animal Diseases
The blacklegged tick, Ixodes scapularis, is the vector of several human pathogens and the primary vector of the Lyme disease spirochete Borrelia burgdorferi in the eastern half of the continental United States (1). During the past 40 years, intensive investigations of this tick’s geographic distribution have documented its spread north and west, with new populations established in eastern North and South Dakota (2,3). Montana has remained free of I. scapularis ticks and their western counterparts, I. pacificus ticks (2). As part of a citizen science investigation during 2016–2017, a specimen of I. scapularis tick was submitted from Liberty County, Montana; however, the tick stage and host were not given, and the authors concluded that either the tick had been recently imported to the area or had been misidentified (4).
On October 12, 2023, a partially engorged female Ixodes tick was removed from the lower neck of a 7.5-year-old female French Brittany hunting dog in Bozeman, Montana, USA; the dog had recently returned with its owners from a pheasant hunting trip north of Ritchey, Dawson County, in eastern Montana. The specimen was submitted to the Schutter Diagnostic Laboratory at Montana State University in Bozeman for identification, and subsequently stored in alcohol and forwarded to the Rocky Mountain Laboratories, National Institutes of Health (Hamilton, MT, USA) for further examination. The specimen lacked the hypostome and 1 palp but, when examined microscopically, the characteristics were consistent with an I. scapularis tick (Figure 1, panels A–D). The specimen and 3 other museum specimens of unengorged female I. scapularis ticks matched I. scapularis (5,6) but not any of the 9 Ixodes spp. previously recorded in Montana (Appendix Table). The dog had not traveled outside the state before acquiring the tick, and the presumed time of attachment correlated with the trip to Dawson County (Appendix Figure 1).
Because of the condition of the specimen and potential significance of its identity, we processed the tick for genomic sequencing. We removed the tick from alcohol, froze it in liquid nitrogen, then pulverized it and extracted genomic DNA by using the MagAttract HMW DNA Kit (QIAGEN, https://www.qiagen.com) according to the manufacturer’s protocol. DNA isolated from this tick was partially degraded and produced a low yield, likely because of the long-term storage in alcohol; however, we performed whole-genome sequencing.
Sequencing coverage was ≈1× for the nuclear genome; the median mitochondrial genome coverage mapped to the published I. scapularis mitochondrial DNA sequence (GenBank accession no. MZ645749.1) (7). We extracted the cox1 gene consensus sequence from the data and generated a maximum-likelihood phylogeny that had 100% bootstrap support for identity between I. scapularis and this specimen. The uncorrected pairwise identity between I. scapularis and this specimen was 99.49%, whereas pairwise identity with several other Ixodes spp. established in Montana was <89% (Figure 2). We deposited the cox1 sequence into GenBank (accession no. PQ284574).
As an independent approach separate from mapping to the I. scapularis reference genome, we mapped the Illumina sequencing reads from this specimen to a database of >5 million cox1 sequences (8). The highest count (6,174,692 reads) mapped to I. scapularis, far more than the next highest count, which was I. ricinus (718,590 reads). In addition, we analyzed the microbial sequences from this tick specimen and identified 340,000 reads mapping to the I. scapularis–specific endosymbiont bacterium Rickettsia buchneri (Appendix Figure 2) (9), further supporting the identification of this tick. A relatively low number (1,509) of reads mapped to the family Borreliaceae, which includes the causative agents of Lyme disease and relapsing fever. Although this low number of reads requires independent verification, it suggests the tick specimen might have been infected with a member of the genus Borrelia.
In conclusion, the continued range expansion of I. scapularis ticks is thought to be complex and multifactorial (10). Here, we confirmed that a tick acquired in eastern Montana was I. scapularis by using 2 independent methods: morphologic characterization and genomic DNA sequence alignments. Identification is further supported by the presence of R. buchneri in the tick’s microbiome. In 2023, the Centers for Disease Control and Prevention predicted the western boundary of the I. scapularis tick range terminated in the middle of North Dakota (Appendix Figure 1). The collection of a single specimen does not signify an established population in Montana, but the public health concern regarding this tick species warrants further investigation into the potential range expansion of the I. scapularis tick. If an established I. scapularis tick population is confirmed, continued surveillance and characterization of any corresponding human pathogens will be required.
The reference list from the paper itself. Each links out to its DOI / PubMed record.
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