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Volume 31, Number 4—April 2025
Research Letter

Increased Recognition of Human Anaplasmosis, Ontario, Canada, 2021

Author affiliation: Queen’s University, Kingston, Ontario, Canada (C. Dai, D. Good, E. Wilson, S. Srivastava); Kingston Health Sciences Center, Kingston (C. Dai, D. Good, E. Wilson, S. Srivastava); University of Ottawa School of Epidemiology and Public Health, Ottawa, Ontario (A. Slatculescu, M.A. Kulkarni); Kingston, Frontenac, and Lennox & Addington Public Health, Kingston, Ontario (T.H. Guan)

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Abstract

Human granulocytic anaplasmosis is a tickborne infection characterized by fever, thrombocytopenia, leukopenia, transaminitis, or a combination of those. Treatment must be prompt and appropriately targeted to prevent clinical decompensation. We discuss an unusual cluster of 16 probable cases in Ontario, Canada, during June–August 2021.

Human granulocytic anaplasmosis (HGA) is a tickborne infection caused by the intracellular, gram-negative bacteria Anaplasma phagocytophilium (1). The infection is transmitted to people via bites from infected blacklegged ticks (Ixodes scapularis) (1). HGA has been historically limited to the northeastern and upper midwestern portions of the United States (2). However, factors such as climate change (3,4) and the spread of ticks via migratory birds from the United States to Canada (5) have contributed to the northward spread of the range of blacklegged tick populations at an estimated rate of 33–55 km/year (4). Reports of anaplasmosis in Canada emerged in 2009 (6), and the first locally acquired case was reported in eastern Ontario in 2018 (7). We describe a cluster of 16 probable anaplasmosis cases requiring admission to an academic hospital in eastern Ontario, Canada, during June–August 2021.

At the time of our study, anaplasmosis was not a reportable disease of public health concern in Ontario. It became reportable in 2023. We identified cases using data abstraction from electronic health records. We flagged adults >18 years of age who visited a tertiary care hospital in eastern Ontario and whose records showed hematopathologist-reported inclusions on peripheral blood smears. We performed manual abstraction and verification and collected demographic data, clinical notes, and diagnosis and treatment data for descriptive analysis. We performed geographic spatial visualization using the forward sortation area, and we overlaid those data with tick-dragging data from public health units (Appendix). We obtained ethics approval through the Queen’s University Research Ethics board.

Figure

Peripheral blood smear from a sample studied as part of an investigation into increased recognition of human anaplasmosis, Ontario, Canada, 2021. Morulae (deep purple inclusions) can be visualized within the neutrophil. Wright’s stain, original magnification ×100.

Figure. Peripheral blood smear from a sample studied as part of an investigation into increased recognition of human anaplasmosis, Ontario, Canada, 2021. Morulae (deep purple inclusions) can be visualized within the...

We identified 16 probable cases of HGA infection as defined by US Centers for Disease Control and Prevention criteria (8). Of note, none met the Centers’ case definition for confirmed HGA infection because of a lack of follow-up serology or PCR testing. Fourteen (87.5%) cases met supportive laboratory criteria, with morulae seen in neutrophils on peripheral blood smear (Figure). Two (12.5%) cases had a single indirect fluorescent antibody IgG titer of >1:64. None of the cases involved PCR testing. The mean age of case-patients was 69 (range 32–91; median 70) years, and the mean Charlson Comorbidity Index was 3.3. Seven case-patients were female, and 9 were male.

All case-patients were febrile and had laboratory abnormalities, most commonly transaminitis (85%) or thrombocytopenia (76%). Ten (62.5%) case-patients required hospital admission, and median length-of-stay was 5 (range 3–13) days. Clinical deterioration in patients corresponded with delays in appropriate treatment.

Two (12.5%) case-patients required intensive care unit (ICU) admission. Both were elderly (73 and 70 years of age), and both had a Charlson Comorbidity Index of 4, slightly above the 3.3 mean. Both patients entered the hospital with initially stable, undifferentiated febrile illness. They decompensated over 3–4 days, requiring transfer to the ICU without a clear diagnosis of HGA infection. One patient developed severe hypoxic respiratory failure and the other progressed to septic shock, requiring vasopressor support. Both patients encountered associated complications, including new atrial fibrillation, acute renal injury, and hyponatremia. Administration of doxycycline resulted in clinical improvement within 48 hours, and both patients were able to transfer out of the ICU. We observed similar prompt improvement across all cases in which patients received appropriate treatment.

HGA is typically mild and self-limiting, but patients can develop life-threatening complications, particularly if they are elderly, have comorbidities, or if they experience delays in diagnosis and treatment (2). The number of patients with serious complications requiring hospitalization and ICU admission seen here likely reflects delayed clinician recognition of HGA. This series of 16 probable HGA cases identified in 1 hospital over 3 months raises concern that infection rates are increasing locally. Because of a lack of PCR confirmation or follow-up serology in the cases we reviewed, a limitation of this study was that none of the probable cases could be considered epidemiologically confirmed. Research suggests, however, that tickborne infections like HGA will continue to become more prevalent throughout Canada (3,4,6). High incidences of blacklegged ticks and Lyme disease are known in southeastern Ontario (9).

In 2023, the first year that HGA was reportable in Ontario, researchers identified 40 cases of anaplasmosis, with 17 cases confirmed (10). Those data likely emerged consequentially with increased rates of PCR and serology testing and increasing local HCP awareness of HGA resulting from public health involvement. Our study demonstrates the potential severity of HGA infections in cases where diagnosis and appropriate treatment is delayed and illustrates how continuing advancements in education of HCPs could help in increasing recognition of this emerging infectious disease in Canada.

In conclusion, healthcare providers (HCPs) should consider HGA when treating patients with fever, thrombocytopenia, transaminitis, or leukopenia during spring, summer, and fall. When encountering potential cases, HCPs should treat promptly with doxycycline rather than await confirmatory testing results. Improved awareness regarding the most appropriate confirmatory testing for HGA would help HCPs in establishing a diagnosis. In treating patients in the acute phase of illness, HCPs should request PCR testing, rather than serology.

Dr. Dai was a fellow in the general internal medicine subspecialty training program at Queen’s University, Kingston, Ontario at the time of data collection and analysis. She is now a practicing general internist at Markham Stouffville Hospital in Markham, Ontario. Dr Dai’s areas of clinical interest include care of acutely ill hospitalized patients, perioperative evaluation and risk assessment, and quality improvement.

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Acknowledgment

We acknowledge and thank Public Health Ontario, the Canadian Lyme Disease Research Network, and the Public Health Agency of Canada’s National Microbiology Laboratory for their contributions to the tick data.

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References

  1. Ismail  N, McBride  JW. Tick-borne emerging infections: ehrlichiosis and anaplasmosis. Clin Lab Med. 2017;37:31740. DOIPubMedGoogle Scholar
  2. Biggs  HM, Behravesh  CB, Bradley  KK, Dahlgren  FS, Drexler  NA, Dumler  JS, et al. Diagnosis and management of tickborne rickettsial diseases: Rocky Mountain spotted fever and other spotted fever group rickettsioses, ehrlichioses, and anaplasmosis—United States. MMWR Recomm Rep. 2016;65:144. DOIPubMedGoogle Scholar
  3. Ogden  NH, Maarouf  A, Barker  IK, Bigras-Poulin  M, Lindsay  LR, Morshed  MG, et al. Climate change and the potential for range expansion of the Lyme disease vector Ixodes scapularis in Canada. Int J Parasitol. 2006;36:6370. DOIPubMedGoogle Scholar
  4. Leighton  PA, Koffi  JK, Pelcat  Y, Lindsay  LR, Ogden  NH. Predicting the speed of tick invasion: an empirical model of range expansion for the Lyme disease vector Ixodes scapularis in Canada. J Appl Ecol. 2012;49:45764. DOIGoogle Scholar
  5. Ogden  NH, Lindsay  LR, Hanincová  K, Barker  IK, Bigras-Poulin  M, Charron  DF, et al. Role of migratory birds in introduction and range expansion of Ixodes scapularis ticks and of Borrelia burgdorferi and Anaplasma phagocytophilum in Canada. Appl Environ Microbiol. 2008;74:178090. DOIPubMedGoogle Scholar
  6. Parkins  MD, Church  DL, Jiang  XY, Gregson  DB. Human granulocytic anaplasmosis: First reported case in Canada. Can J Infect Dis Med Microbiol. 2009;20:e1002. DOIPubMedGoogle Scholar
  7. Edginton  S, Guan  TH, Evans  G, Srivastava  S. Human granulocytic anaplasmosis acquired from a blacklegged tick in Ontario. CMAJ. 2018;190:E3636. DOIPubMedGoogle Scholar
  8. Centers for Disease Control and Prevention. National Notifiable Diseases Surveillance System–2008. Ehrlichiosis and anaplasmosis case definition [cited 2023 August 20]. https://ndc.services.cdc.gov/case-definitions/ehrlichiosis-and-anaplasmosis-2008/
  9. Werden  L, Lindsay  LR, Barker  IK, Bowman  J, Gonzales  EK, Jardine  CM. Prevalence of Anaplasma phagocytophilum and Babesia microti in Ixodes scapularis from a newly established Lyme disease endemic area, the Thousand Islands Region of Ontario, Canada. Vector Borne Zoonotic Dis. 2015;15:6279. DOIPubMedGoogle Scholar
  10. Ontario Agency for Health Protection and Promotion/Public Health Ontario. Summary report: anaplasmosis and babesiosis in Ontario: 2023. Toronto (ON): King’s Printer for Ontario; 2024.

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Figures

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Suggested citation for this article: Dai C, Good D, Slatculescu A, Kulkarni MA, Guan TH, Wilson E, et al. Increased recognition of human anaplasmosis, Ontario, Canada, 2021. Emerg Infect Dis. 2025 Apr [date cited]. https://doi.org/10.3201/eid3104.231435

DOI: 10.3201/eid3104.231435

Original Publication Date: March 17, 2025

Table of Contents – Volume 31, Number 4—April 2025

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Corresponding author: Dr. Cathy Dai, Division of Internal Medicine, Markham Stouffville Hospital, 381 Church Street, Markham, Ontario, Canada L3P 7P3

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Page created: March 17, 2025
Page updated: March 17, 2025
Page reviewed: March 17, 2025
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.
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