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Volume 25, Number 12—December 2019
Research Letter

Fatal Brazilian Spotted Fever Associated with Dogs and Amblyomma aureolatum Ticks, Brazil, 2013

Elisa S.M.M. Savani, Francisco B. Costa, Elisabete A. Silva, Ana C.F. Couto, Melanie Gutjahr, Juliana N.M.O. Alves, Fabiana C.P. Santos, and Marcelo B. LabrunaComments to Author 
Author affiliations: Prefeitura de São Paulo, São Paulo, Brazil (E.S.M.M. Savani, E.A. Silva, A.C.F. Couto, M. Gutjahr, J.N.M.O. Alves); Universidade de São Paulo, São Paulo (F.B. Costa, M.B. Labruna); Instituto Adolfo Lutz, São Paulo (F.C.P. Santos)

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Abstract

In São Paulo metropolitan area, Brazil, Amblyomma aureolatum ticks are the main vector of Rickettsia rickettsii, which causes Brazilian spotted fever. In 2013, a boy in São Paulo died of Brazilian spotted fever associated with household dogs and A. aureolatum ticks. Prompt recognition and treatment of this illness might prevent deaths.

The bacterium Rickettsia rickettsii is the etiologic agent of Rocky Mountain spotted fever; in Brazil, this illness is called Brazilian spotted fever and is a national notifiable tickborne disease with fatality rates ≈50% (1,2). Since the 1920s, the vector of R. rickettsii in the southern São Paulo metropolitan area has been the Amblyomma aureolatum tick (3,4). In this area, free-roaming domestic dogs (major hosts of A. aureolatum ticks) are presumed to play a role in carrying R. rickettsii–infected ticks from forest fragments (A. aureolatum tick habitat) to household interiors (4,5). Dogs could thus be associated with the higher incidence of Brazilian spotted fever in women and children, who usually spend more time indoors, in close contact with dogs (5).

In November 2013, a 12-year-old boy died after 8 days of an acute febrile illness. He lived in the neighborhood of Sete Praias, near Atlantic forest remnants in the southern São Paulo metropolitan area. On day 3 of illness, he was admitted to the Nasf-Unifesp Hospital in the city of São Paulo with fever (temperature 39.5°C), headache, nausea, asthenia, and abdominal rash. The patient’s mother informed the physician that her son had been bitten by a tick on his nape ≈1 week before disease onset; the tick was removed and discarded. The boy was medicated with dipyrone and sent home. On day 6, the patient was returned to the hospital, unconscious, with jaundice and seizures. He was transferred to the intensive care unit; meningitis was suspected. The next day, his condition worsened, and when hematologic and biochemical examinations indicated thrombocytopenia and hepatic alterations, meningitis was ruled out. A blood serum sample was submitted for leptospirosis and spotted fever testing by serologic and molecular analysis, respectively. Results for leptospirosis were negative. The patient died on day 8 of illness. While the body was being prepared for the funeral, a tick was found attached behind the ear and was sent to the laboratory of the Prefeitura de São Paulo, where it was identified as an A. aureolatum unengorged female.

DNA extracted from the serum sample by use of PureLink Viral RNA/DNA Mini Kit (Invitrogen, https://www.thermofisher.com) was positive by Taqman real-time PCR for the genus Rickettsia (6). We therefore next performed 2 conventional PCRs, 1 targeting a 401-bp fragment of the rickettsial gltA gene (7) and the other targeting a 631-bp fragment of the rickettsial ompA gene (8). Both yielded amplicons that, after DNA sequencing, had sequences 100% identical to R. rickettsii (GenBank accession no. CP003305) by BLAST analyses (http://blast.ncbi.nlm.nih.gov/Blast.cgi).

Immediately after the patient’s death, the hospital notified the São Paulo Board of Health of this case, and we performed an epidemiologic investigation. In the patient’s household, we collected blood samples from 3 dogs and 11 cats, all adults, born and raised in the area, with free access to surrounding forests and the dwelling interior. Direct contact between the patient and his pets was reportedly common. Serum from the dogs and cats was tested for R. rickettsii IgG by immunofluorescence assay, as described (3). Seroreactivity was detected in the 3 dogs (endpoint titers 512, 2,048, and 4,096) and 3 of the cats (titers 64, 64, and 512).

During animal sampling, we collected 13 ticks from 1 dog and 1 tick from 1 cat; all ticks were A. aureolatum adults. These 14 ticks, plus the 1 from the patient’s body, were submitted for DNA extraction (5) and tested by the same 2 conventional PCRs. Two ticks (1 from the dog and the 1 from the patient) yielded gltA and ompA amplicons, which generated DNA sequences 100% identical to R. rickettsii (CP003305).

This fatal case of Brazilian spotted fever was epidemiologically associated with A. aureolatum ticks and domestic dogs. Because the patient had no recent history of traveling outside his neighborhood, we infer that he acquired the infection in his neighborhood, where R. rickettsii was circulating between ticks and his dogs. Although the A. aureolatum tick collected postmortem from the patient harbored R. rickettsii, we cannot be sure that this particular tick was the primary vector of the bacterium to the patient because the tick would certainly have been exposed to an infected blood meal during the last days of the patient’s life. We can, however, confirm that the patient was exposed in his neighborhood to A. aureolatum ticks, competent vectors of R. rickettsii (5). Because fed adult A. aureolatum ticks need only 10 minutes of attachment to transmit R. rickettsii to hosts (5), the likelihood of such transmission for this patient was high, considering his close contact with his pets. Had the physicians suspected Brazilian spotted fever when the boy was first admitted to the hospital on day 3 of febrile illness, treatment with appropriate antimicrobial drugs might have prevented his death (9).

Dr. Savani is an epidemiologist at the São Paulo City Board of Health. Her research interests are epidemiology and control of urban zoonoses.

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Acknowledgment

This work was performed at the University of São Paulo, Prefeitura de São Paulo, and Adolfo Lutz Institute, São Paulo, SP, Brazil.

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References

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Cite This Article

DOI: 10.3201/eid2512.191146

Original Publication Date: 11/12/2019

Table of Contents – Volume 25, Number 12—December 2019

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Marcelo B. Labruna, Universidade de São Paulo, Departamento de Medicina Veterinária Preventiva e Saúde Animal, Faculdade de Medicina Veterinária e Zootecnia, Av. Prof. Orlando Marques de Paiva, 87 Cidade Universitaria, São Paulo, SP 05508-270, Brazil

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Page created: November 18, 2019
Page updated: November 18, 2019
Page reviewed: November 18, 2019
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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