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 32, Number 9—September 2026
Research Letter
Southern Tick–Associated Rash Illness in Pediatric Patient, New York, USA, 2025
Suggested citation for this article
Abstract
Southern tick–associated rash illness (STARI) is a tickborne disease of unknown etiology characterized by an erythema migrans–like skin lesion. We report a STARI case in New York in a child after an Amblyomma americanum tick bite; we detected Borrelia lonestari, a disputed cause of STARI, in the tick.
Southern tick–associated rash illness (STARI) is a tickborne disease of unknown etiology. Its hallmark finding is an erythema migrans (EM)–like skin lesion after a lone star tick (Amblyomma americanum) bite. Although it is considered self-limited, STARI is difficult to diagnose and manage because of characteristics similar to Lyme disease. STARI is not known to cause any sequelae after rash resolution; the role of antimicrobial drugs in proven cases is therefore undetermined (1).
Previous descriptions of STARI focused on the southern United States. Because lone star tick populations have increased in the mid-Atlantic and northeastern United States, regions highly endemic to Lyme disease, differentiating STARI from Lyme disease has become a challenge (2). We describe the case of a child evaluated in Long Island, New York, USA for an EM-like skin lesion.
An 8-year-old girl with a history of asthma and allergic rhinitis living in eastern Long Island was brought in June 2025 for evaluation of a recent EM-like lesion. Approximately 2 weeks before her visit, she had a 5-cm annular lesion with peripheral erythema and a central nodule on the upper back (Figure 1). She also experienced low-grade fever, posterior cervical lymphadenopathy, and myalgia. A tick had been removed from the lesion site and stored in a sealed bag 12 days before the rash began. The patient did not receive doxycycline postexposure prophylaxis. Because early localized Lyme disease was suspected, her pediatrician prescribed a 2-week course of amoxicillin. The rash and associated symptoms resolved within 1 week. She was asymptomatic at the time of the follow-up consultation.
Although care providers initially suspected Lyme disease, the biting tick was identified as an adult male lone star tick (Figure 2), which does not transmit Borrelia burgdorferi, which mean the patient’s signs and symptoms were consistent with a diagnosis of STARI. We extracted DNA from the tick, performed nested PCR targeting the Borrelia flagellin gene (3), and confirmed the presence of a B. lonestari–specific sequence (GenBank accession no. PZ457021).
A. americanum, an aggressive tick species, has expanded across the United States (2,3). In the US Northeast, diagnosing STARI is challenging because of a high rate of B. burgdorferi–infected Ixodes scapularis ticks (2). As A. americanum tick populations have increased across Long Island, the proportion of EM lesions caused by Lyme disease has decreased, likely because of higher STARI incidence (2). National STARI incidence remains unknown because the condition is not reportable and is often presumed to be the result of B. burgdorferi infection.
STARI was described in 1995 in 45 patients with EM-like lesions in Missouri, USA, in a region without Lyme disease (4). Study participants had negative serology results for Lyme disease and negative B. burgdorferi culture results from skin lesion biopsies, which raised suspicion of an alternative diagnosis (4). B. lonestari was identified as a potential cause of STARI after it was identified in both skin biopsy and the associated tick in a patient bitten by a female A. americanum tick in North Carolina (5). A subsequent Missouri study assessed B. burgdorferi and B. lonestari in skin biopsies from patients with EM-like lesions (6); results from 16S eubacterial rDNA PCR, glpQ PCR for B. lonestari DNA detection, and B. burgdorferi culture were negative (6). In a later study, 16s rRNA metagenomic sequencing of blood samples collected during 2018–2019 from STARI patients did not identify any tickborne bacteria (7). Consequently, it has been suggested that STARI is caused not by an infection but rather a hypersensitivity reaction (8), possibly related to alpha-gal syndrome, which is also caused by the bite of a lone star tick (8). B. lonestari prevalence on Long Island is uncommon (detected in 1% of A. americanum ticks) (9), which made identification in our case particularly interesting. Because our patient did not undergo testing for B. lonestari infection, we cannot determine if that bacterium caused her symptoms.
STARI diagnosis is difficult because it shares features with Lyme disease; however, subtle clinical differences exist. Compared with EM patients from New York, a highly Lyme disease–endemic state, patients from Missouri, who presumably had STARI, experienced a shorter duration from tick bite to skin lesion onset; had fewer associated symptoms; were less likely to experience multiple lesions; had lesions that were smaller, more circular, and had more central clearing; and recovered more quickly (10). Although withholding antimicrobial treatment might be reasonable in confirmed cases of STARI, doing so in B. burgdorferi–endemic regions poses the risk of undertreating Lyme disease. As our case demonstrated, STARI can be diagnosed only if a lone star tick is identified, underscoring the importance of preserving the biting tick.
The etiology of STARI remains unknown; whether B. lonestari is the causative agent is not clear (5,6). Although detection of B. lonestari does not establish it as the cause, our findings raise questions about B. lonestari pathogenicity and underscore the need for improved diagnostics for patients with EM-like lesions.
Dr. Handel is a clinical associate professor of pediatrics in the Division of Infectious Diseases at the Renaissance School of Medicine at Stony Brook University in New York, USA. His research focuses on recognized and emerging tickborne infections and congenital cytomegalovirus.
Acknowledgments
We thank Jorge Benach for his critical review of this manuscript.
The patient’s parent or guardian provided written permission to publish this case report.
We are grateful for ongoing research support from the Long Island Network for Clinical and Translational Science fellowship (A.S.H.), National Institute of Allergy and Infectious Diseases of the National Institutes of Health (grant nos. AI152208 and AI179732 to H.K.K.), and Stony Brook University (A.S.H., H.K.K.). The funders had no role in study design, data collection, interpretation, or the decision to submit the work for publication. The authors declare no competing interests.
A.S.H. has received honoraria from GSK for serving in an expert panel on invasive meningococcal disease.
References
- Lantos PM, Rumbaugh J, Bockenstedt LK, Falck-Ytter YT, Aguero-Rosenfeld ME, Auwaerter PG, et al. Clinical practice guidelines by the Infectious Diseases Society of America (IDSA), American Academy of Neurology (AAN), and American College of Rheumatology (ACR): 2020 guidelines for the prevention, diagnosis and treatment of Lyme disease. Clin Infect Dis. 2021;72:e1–8. DOIPubMedGoogle Scholar
- Schutzer SE, Wellins A-M, Dattwyler RJ. Borrelia burgdorferi infection and erythema migrans. N Engl J Med. 2026;394:302–3. DOIPubMedGoogle Scholar
- Stromdahl EY, Williamson PC, Kollars TM Jr, Evans SR, Barry RK, Vince MA, et al. Evidence of Borrelia lonestari DNA in Amblyomma americanum (Acari: Ixodidae) removed from humans. J Clin Microbiol. 2003;41:5557–62. DOIPubMedGoogle Scholar
- Campbell GL, Paul WS, Schriefer ME, Craven RB, Robbins KE, Dennis DT. Epidemiologic and diagnostic studies of patients with suspected early Lyme disease, Missouri, 1990–1993. J Infect Dis. 1995;172:470–80. DOIPubMedGoogle Scholar
- James AM, Liveris D, Wormser GP, Schwartz I, Montecalvo MA, Johnson BJB. Borrelia lonestari infection after a bite by an Amblyomma americanum tick. J Infect Dis. 2001;183:1810–4. DOIPubMedGoogle Scholar
- Wormser GP, Masters E, Liveris D, Nowakowski J, Nadelman RB, Holmgren D, et al. Microbiologic evaluation of patients from Missouri with erythema migrans. Clin Infect Dis. 2005;40:423–8. DOIPubMedGoogle Scholar
- Lindell K, Sheldon S, Kingry L, Mead PS, Molins C, Hinckley AF. Epidemiologic and clinical characteristics and outcomes of patients diagnosed with southern tick–associated rash illness (STARI), 2018–2019. Diagn Microbiol Infect Dis. 2025;113:
116928 . DOIPubMedGoogle Scholar - Wormser GP, Shishido A. Could alpha-gal syndrome be the cause of southern tick-associated rash illness (STARI)? Wien Klin Wochenschr. 2025;137:800–1. DOIPubMedGoogle Scholar
- Sanchez-Vicente S, Tagliafierro T, Coleman JL, Benach JL, Tokarz R. Polymicrobial nature of tick-borne diseases. MBio. 2019;10:e02055-19. DOIPubMedGoogle Scholar
- Wormser GP, Masters E, Nowakowski J, McKenna D, Holmgren D, Ma K, et al. Prospective clinical evaluation of patients from Missouri and New York with erythema migrans-like skin lesions. Clin Infect Dis. 2005;41:958–65. DOIPubMedGoogle Scholar
Figures
Suggested citation for this article: Handel AS, Ahmed S, Rochlin I, Kim HK. Southern tick–associated rash illness in pediatric patient, New York, USA, 2025. Emerg Infect Dis. 2026 Sep [date cited]. https://doi.org/10.3201/eid3209.260871
Original Publication Date: July 24, 2026
Table of Contents – Volume 32, Number 9—September 2026
| EID Search Options |
|---|
|
|
|
|
|
|


Please use the form below to submit correspondence to the authors or contact them at the following address:
Andrew S. Handel, Stony Brook University Renaissance School of Medicine, 101 Nicolls Rd, HSC-T11, Stony Brook, NY 11794, USA
Top