Skip directly to site content Skip directly to page options Skip directly to A-Z link Skip directly to A-Z link Skip directly to A-Z link

Disclaimer: Early release articles are not considered as final versions. Any changes will be reflected in the online version in the month the article is officially released.

Volume 30, Number 9—September 2024
Research Letter

Powassan Virus Encephalitis After Tick Bite, Manitoba, Canada

Author affiliation: University of Manitoba, Winnipeg, Manitoba, Canada

Suggested citation for this article

Abstract

A case of Powassan encephalitis occurred in Manitoba, Canada, after the bite of a black-legged tick. Awareness of this emerging tickborne illness is needed because the number of vector tick species is growing. No specific treatment options exist, and cases with illness and death are high. Prevention is crucial.

Figure

Black-legged tick (Ixodes scapularis) after removal with tweezers from a patient in Manitoba, Canada, who was later diagnosed with Powassan virus.

Figure. Black-legged tick (Ixodes scapularis) after removal with tweezers from a patient in Manitoba, Canada, who was later diagnosed with Powassan virus.

On October 2, 2022, a 60-year-old male hobbyist outdoor photographer in southern Manitoba, Canada, noticed a black-legged tick (Ixodes scapularis) attached to his neck (Figure). The patient sought treatment for possible Lyme disease and was prescribed doxycycline.

On October 16, 2 weeks after the tick bite, the patient had complaints of diarrhea, nausea, and malaise. He also had a fever that reached 40°C (104°F), a 10–15-pound weight loss, difficulty concentrating, and a bilateral headache, and he became bedbound from weakness and ataxia. He was admitted to a hospital in Winnipeg, Manitoba on November 1. He had a history of hypertension for which he was taking ramipril and right arm thrombosis for which he was taking apixaban.

The patient complained of radicular pain in his arms and legs requiring opioids. He recalled no recent travel, immunizations, or mosquito bites. Physical examination revealed tachycardia, confusion, dysarthria, and difficulty following commands. He did not have fever, rash, or nuchal rigidity. A neurologic examination demonstrated a bilateral intention tremor, twitching, dysmetria, and ataxia.

Laboratory testing of the patient’s blood samples showed mild hypokalemia and leukopenia (4.1 cells/μL). Magnetic resonance imaging of the patient’s brain revealed a punctate T2 hyperintensity in the right frontal lobe white matter. Electroencephalography revealed mild bilateral fronto-temporal cerebral dysfunction. Cerebrospinal fluid (CSF) examination showed 41 nucleated cells/mm3 (89% lymphocytes) and a protein level of 1.41 g/L (reference range 0.2–0.4 g/L); glucose level was within reference range. Results of laboratory testing of the CSF was negative for West Nile virus IgM, Epstein-Barr virus, cytomegalovirus, herpes simplex virus 1 and 2, and varicella zoster virus; bacterial and viral cultures yielded negative results. PCR testing of the CSF was negative for human herpesvirus 6. Additional serum testing was negative for HIV, syphilis, hepatitis B and C, and Lyme disease. PCR testing on a stool sample was negative for enteroviruses.

We ordered Powassan virus (POWV) testing of convalescent serum, and results were positive for IgM. A 90% plaque reduction neutralization test (PRNT90) resulted in antibody neutralization at a dilution of 1:80 on November 3 and then 1:160 on November 6. On the basis of clinical symptoms, timeline from tick attachment to symptom onset, and confirmatory PRNT90, we made a diagnosis of Powassan encephalitis. After 1 week, the patient improved and was discharged. Repeat serologic testing on July 14, 2023, showed that PRNT90 had decreased to 1:20.

POWV is a flavivirus transmitted by tick species that also act as reservoirs (1). The most consequential vectors are black-legged ticks, which are known to bite humans and can spread other tickborne pathogens such as Borrelia burgdorferi (Lyme disease), Anaplasma phagocytophilum (anaplasmosis), and Babesia microti (babesiosis) (2). Those pathogens require tick attachment periods >24 hours (2), but according to animal studies, the transmission time of POWV from vector to host can occur in 15 minutes (2), although transmission typically occurs after 3 hours in humans (3). No human-to-human transmission has been reported.

POWV is found in Canada, the United States, and Russia (1). In the northeastern United States, >200 cases have been reported. The highest incidence is in Wisconsin and Minnesota, both bordering Manitoba (1,4). Cases occur predominantly in May–November, when ticks are active (4). Only 21 cases have been reported in Ontario, New Brunswick, and Quebec (1), Canada. The true prevalence in Canada is unknown because POWV is not a reportable disease. Serologic surveys from 1968–1969 in British Columbia found antibodies in 0.129% of those tested and higher rates of 12.4% in outdoor workers (5). Studies in Ontario from the 1970s found antibodies in 0.70% of persons tested (1). The range of black-legged ticks is expanding up to 46 km annually, so exposure is likely increasing (6). No data on the prevalence of POWV in black-legged ticks in Manitoba have been published.

The incubation period of POWV is 7–34 days, after which 1–3 days of influenza-like prodrome occurs (7). Central nervous system infection with encephalitis is common (7). During 2011–2020, the United States reported 194 cases; 91.75% were neuroinvasive, and 10%–15% resulted in death (4,7). Fevers, weakness, headaches, and altered sensorium are the most common patient complaints reported (7,8). Other complaints include gastrointestinal involvement, focal neurologic signs, seizures, ataxia, twitching, tremors, and radiculitis (7). Magnetic resonance imaging findings commonly include T2/flair hyperintensities in the brainstem, cortex, and deep gray structures (9). Electroencephalography slowing has been described (8). Those findings are corroborated by autopsy results showing high POWV RNA levels in brain tissue (10). Neurologic sequelae occur in >50% of survivors. In the case we report, the patient reported persistent ataxia for months. Because no specific antiviral drug is available, disease management consists of supportive measures for airway protection and cerebral edema and analgesia for radiculitis.

A lack of reporting, limited awareness of POWV as a causative agent of encephalitis, expanding tick range, and incomplete knowledge of prevalence has led to a lack of action against this emerging virus. Prevention strategies include avoiding ticks, using insect repellant, treating clothing with 0.5% permethrin in endemic areas, and frequent tick checks.

Dr. Smith is a second-year core internal medicine resident with the Max Rady College of Medicine at the University of Manitoba. Research interests include infectious disease and general internal medicine.

Top

References

  1. Corrin  T, Greig  J, Harding  S, Young  I, Mascarenhas  M, Waddell  LA. Powassan virus, a scoping review of the global evidence. Zoonoses Public Health. 2018;65:595624. DOIPubMedGoogle Scholar
  2. Eisen  L. Pathogen transmission in relation to duration of attachment by Ixodes scapularis ticks. Ticks Tick Borne Dis. 2018;9:53542. DOIPubMedGoogle Scholar
  3. Feder  HM Jr, Telford  S III, Goethert  HK, Wormser  GP. Powassan virus encephalitis following brief attachment of Connecticut deer ticks. Clin Infect Dis. 2021;73:e23504. DOIPubMedGoogle Scholar
  4. Centers for Disease Control and Prevention. Powassan virus [cited 2022 Dec 1]. https://www.cdc.gov/powassan/statistics.html.
  5. Kettyls  GD, Verrall  VM, Wilton  LD, Clapp  JB, Clarke  DA, Rublee  JD. Arbovirus infections in man in British Columbia. Can Med Assoc J. 1972;106:11759.PubMedGoogle Scholar
  6. Clow  KM, Leighton  PA, Ogden  NH, Lindsay  LR, Michel  P, Pearl  DL, et al. Northward range expansion of Ixodes scapularis evident over a short timescale in Ontario, Canada. PLoS One. 2017;12:e0189393. DOIPubMedGoogle Scholar
  7. Kemenesi  G, Bányai  K. Tickborne flaviviruses, with a focus on Powassan virus. Clin Microbiol Rev. 2018;32:e0010617. DOIPubMedGoogle Scholar
  8. El Khoury  MY, Camargo  JF, White  JL, Backenson  BP, Dupuis  AP II, Escuyer  KL, et al. Potential role of deer tick virus in Powassan encephalitis cases in Lyme disease-endemic areas of New York, U.S.A. Emerg Infect Dis. 2013;19:192633. DOIPubMedGoogle Scholar
  9. Piantadosi  A, Rubin  DB, McQuillen  DP, Hsu  L, Lederer  PA, Ashbaugh  CD, et al. Emerging cases of Powassan virus encephalitis in New England: clinical presentation, imaging, and review of the literature. Clin Infect Dis. 2016;62:70713. DOIPubMedGoogle Scholar
  10. Normandin  E, Solomon  IH, Zamirpour  S, Lemieux  J, Freije  CA, Mukerji  SS, et al. Powassan virus neuropathology and genomic diversity in patients with fatal encephalitis. Open Forum Infect Dis. 2020;7:ofaa392. DOIPubMedGoogle Scholar

Top

Figure

Top

Suggested citation for this article: Smith N, Keynan Y, Wuerz T, Sharma A. Powassan virus encephalitis after tick bite, Manitoba, Canada. Emerg Infect Dis. 2024 September [date cited]. https://doi.org/10.3201/eid3009.231344

DOI: 10.3201/eid3009.231344

Original Publication Date: August 09, 2024

1These senior authors contributed equally to this article.

Table of Contents – Volume 30, Number 9—September 2024

EID Search Options
presentation_01 Advanced Article Search – Search articles by author and/or keyword.
presentation_01 Articles by Country Search – Search articles by the topic country.
presentation_01 Article Type Search – Search articles by article type and issue.

Top

Comments

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

Nathan Smith, University of Manitoba, 561 Trent Ave, Winnipeg, MB R2K1G2, Canada

Send To

10000 character(s) remaining.

Top

Page created: July 30, 2024
Page updated: August 09, 2024
Page reviewed: August 09, 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.
file_external