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Revista Brasileira de Parasitologia Veterinária

On-line version ISSN 1984-2961

Rev. Bras. Parasitol. Vet. (Online) vol.19 no.4 Jaboticabal Oct./Dec. 2010

https://doi.org/10.1590/S1984-29612010000400003 

FULL ARTICLE

 

Serological survey of Rickettsia sp. in horses and dogs in an non-endemic area in Brazil

 

Identificação sorológica de Rickettsia sp. em equinos e cães de área não endêmica no Brasil

 

 

Fernanda Gonçalves BatistaI; Daniella Matos da SilvaI; Kerriel Thandile GreenI; Louise Boulsfield de Lorenzi TezzaI; Sâmara Pereira de VasconcelosI; Suelen Graziele Soares de CarvalhoI; Iara SilveiraII; Jonas Moraes-FilhoII; Marcelo Bahia LabrunaII; Fernanda Silva FortesI; Marcelo Beltrão MolentoI

ILaboratory of Parasitic Diseases, Federal University of Paraná – UFPR
IIDepartment of Preventative Veterinary Medicine, University of São Paulo – USP

Corresponding author

 

 


ABSTRACT

Brazilian Spotted Fever (BSF) is a lethal rickettsiosis in humans caused by the bacteria Rickettsia rickettsii, and is endemic in some areas of Brazil. Horses and dogs are part of the disease's life cycle and they may also serve as sentinel animals in epidemiological studies. The first human BSF case in the State of Paraná was reported in 2005. The present study was conducted in the municipality of Almirante Tamandaré, where no previous case of BSF was reported. Serum samples were collected from 71 horses and 20 dogs from nine properties in the area. Ticks were also collected from these animals. All farmers completed a questionnaire about their knowledge of BSF and animal health management. Serum samples were analyzed by indirect immunofluorescent-antibody assay (IFA) using R. rickettsii and R. parkeri as antigens. Ticks were analyzed by PCR for Rickettsia sp., and all of them were PCR-negative. Six horses (8.45%) and 4 dogs (20%) were identified as seropositive. Farmers were not aware of the correlation between the presence of ticks and risk of BSF. Although a non-endemic area, Almirante Tamandaré is a vulnerable environment for BSF and effective tick control measures are required.

Keywords: Ticks, brazilian spotted fever, emerging zoonosis.


RESUMO

A Febre Maculosa Brasileira (FMB) é uma riquetsiose letal para humanos, causada pela bactéria Rickettsia rickettsii, e é endêmica em algumas regiões brasileiras. Equinos e cães podem participar do ciclo da doença e podem também servir como sentinelas em estudos epidemiológicos. O primeiro caso humano relatado no Estado do Paraná ocorreu em 2005. O presente estudo foi realizado no município de Almirante Tamandaré, região onde não há relatos de casos de FMB. Foram coletadas amostras de sangue de 71 cavalos e 20 cães em nove propriedades rurais na região. Carrapatos também foram colhidos dos animais. Todos os proprietários responderam a um questionário sobre o manejo sanitário dos animais e o conhecimento a respeito da FMB. As amostras de soro foram processadas pela técnica de Reação de Imunofluorescência Indireta (RIFI), utilizando-se os antígenos de R. rickettsii e R. parkeri. Os carrapatos foram analisados por PCR para Rickettsia sp. e todos foram negativos. Seis cavalos (8,45%) e 4 cães (20%) foram identificados como soropositivos. Todos os proprietários desconheciam a relação de carrapatos com a FMB. Embora considerada uma área não endêmica, Almirante Tamandaré é um ambiente vulnerável à FMB e um controle eficiente de carrapatos deve ser implementado.

Palavras-chave: Carrapatos, febre maculosa brasileira, zoonose emergente.


 

 

Introduction

Rickettsiae are gram-negative, obligate intracellular bacteria that inhabit salivary glands and ovaries of their arthropod hosts (BILLINGS et al., 1998). Rickettsia rickettsii is the primary etiological agent of Brazilian spotted fever (BSF) but Rickettsia parkeri and Rickettsia felis have also been described as causative agents. However, lethal human cases have been confirmed as caused only by R. rickettsii (SILVA, 2007). BSF is acquired through the bite of an infected tick that remains attached to the host for at least four to six hours (RICKETTS, 1906).

In humans these bacteria replicate in the vascular endothelium, causing vasculitis and leading to the activation of platelets and coagulation system, thrombosis and increased vascular permeability. Hemostatic disorders, including thrombocytopenia and prolonged clotting time, are attributed to cytopathic effects and cellular activity of R. rickettsii endotoxins (DAVIDSON et al., 1990). BSF is characterized by sudden onset of high fever, headache, myalgia, and prostration, followed by a maculopapular rash predominantly on palms and sole. Patients who do not receive early treatment can develop serious complications, and approximately 50% of these patients may die (WALKER, 2002).

Clinical cases have been described in dogs in the United States (McDADE; NEWHOUSE, 1986), but there have been no reported cases in Brazil (SANGIONI et al., 2005). In horses, there are no descriptions of clinical signs or symptoms, even when these animals have high titers (>1:1024) against R. rickettsii (LEMOS et al., 1996).

The tick Amblyomma cajennense is the main vector of BSF. However, disease transmission is not exclusively associated to this tick species, as verified in a study by Pinter and Labruna (2006) in São Paulo that reported A. aureolatum as a vector; and Rozental et al. (2002) reported the tick Rhipicephalus sanguineus as a potential vector. Cunha et al. (2009) reported the first molecular detection by PCR of R. rickettsii on R. sanguineus naturally infected in Rio de Janeiro. These tick species are also responsible for maintenance of R. rickettsii in the environment through transovarial and transtadial transmission, and a single female can transmit the agent to all its progenies. Besides the tick, other amplified hosts of the disease include wild animals such as capybaras (SOUZA et al., 2008). Dogs and horses may help to maintain the cycle of disease as they are potential hosts for R. sanguineus (FREITAS, 2007) and Amblyomma cajennense ticks (TIRIBA, 1972; LABRUNA et al., 2002).

Cardoso et al. (2006) among others described that seropositive horses and dogs are often reported in endemic areas, serving as sentinel animals in epidemiological studies. Labruna (2009) remarked that horses and capybaras are also sentinel animals and that few populations of ticks are infected by pathogenic Rickettsia. Pinter et al. (2008) reported that dogs are important sentinels for the presence of the bacterium R. rickettsii in areas where the tick A. aureolatum is the main vector of BSF.

BSF can be considered a reemerging zoonosis in Brazil, and information about disease transmission is still incipient (SANGIONI et al., 2005). Cases have been underdiagnosed because of the lack of awareness of health providers about this disease and difficult clinical and laboratorial diagnosis in humans and animals (PADDOCK et al., 1999). According to the Brazilian Ministry of Health (2005) BSF was first reported in Brazil in 1929. Between 1995 and 2005, 386 cases were reported in Southeastern States of São Paulo and Minas Gerais and in the Southern State of Santa Catarina. The first human case in the State of Paraná was reported in April, 2005, in a 45-year-old male owner of a rural property in the municipality of São José dos Pinhais (FREITAS, 2007). Freitas (2007) reported for the first time anti-Rickettsia antibodies of the spotted fever group in horses and dogs from that area.

The objective of the present study was to provide epidemiological input on BSF in the State of Paraná, Brazil, by determining the presence of anti-R. rickettsii and R. parkeri antibodies by IFA in sera of horses and dogs from the municipality of Almirante Tamandaré.

 

Material and Methods

1. Study area

The study was conducted in the municipality of Almirante Tamandaré, which is part of the metropolitan area of Curitiba, State of Paraná, Southern Brazil. The city has a population of 93,055 inhabitants and is located at latitude of 25º 19' 29" S and longitude 49º 18' 36" W. It has an altitude of 945 m above sea level. The climate is subtropical with temperatures varying from 18 to 22 ºC.

2. Local knowledge of BSF

During field work, a questionnaire was applied to 17 residents including questions about their knowledge on the importance of ticks, the presence of ticks on animals and whether ticks could pose any risk to animals or transmit any disease.

3. Animals and techniques

A total of 71 horses and 20 dogs living in nine rural properties were sampled from August and September, 2008. A record was kept for each animal including information such as age and name. In addition, a questionnaire about husbandry practices was filled out for each property. Blood samples were collected from jugular vein using vacutainer needles and adapters (BD Vacutainer, England), centrifuged to separate the serum and frozen before analysis.

Each serum was tested by indirect immunofluorescent-antibody assay (IFA) using crude R. rickettsii and R. parkeri antigens as previously described (LABRUNA et al., 2007). Individual sera were initially screened at a dilution 1:64 against each of the rickettsial antigens. In case of a positive reaction, serum serial dilutions at two-fold increments were tested up to the endpoint titer.

Ticks found attached to horses and dogs were collected and preserved in isopropyl alcohol. They were individually identified to species and submitted to DNA extraction by guanidine thiocyanate as previously described by Sangioni et al. (2005). Ticks were processed in pools of up to three specimens, and tested by PCR with primers CS-78 and CS-323, which target a 401-bp fragment of the gltA gene of Rickettsia spp. These procedures were performed as previously described by Labruna et al. (2004).

 

Results

Overall, 8.5% (6/71) of horses and 20% (4/20) of dogs showed positive anti-Rickettsia reactions (Table 1), with titers ranging from 1:64 to 1:1024 for both R. rickettsii or R. parkeri (Table 2). All sera reactive to R. rickettsii were also reactive to R. parkeri, usually with similar endpoint titers with at most 2-fold difference between them. One serum (horse 30) showed a 4-fold difference between anti-R. rickettsii and anti-R. parkeri endpoint titers.

Eleven horses (15.5%) were infested with Dermacentor nitens. Seven dogs (35%) were found infested, six with Amblyomma aureolatum and one with Rhipicephalus microplus. No rickettsial DNA was amplified by PCR from these ticks.

The questionnaire showed that 42.9% (6/14) farmers had no knowledge on BSF, 71.4% (10/14) did not know how the pathogen is transmitted, and none of them knew any clinical signs of BSF. Fifteen farmers (80%) reported having seen wild animals in the area in the following order of frequency: hares (100%), capybaras (16.7%), and deers (8.3%).

Acaricide treatment was provided for 60 (7.1%), 90 (25%) or 180 days (21.4%) based on the presence of ticks reported by the owners (7.8%) and during summer months (3.6%). Only 21.5% of the owners did not use acaricides.

Regarding the origin of the horses studied, 60.7% (17/28) were from Almirante Tamandaré, and were used for different purposes (horseback riding, rodeos, and work). The average age of these animals was 9.5 years (range: 1 to 20 years). The dogs had an average age of 2.5 years (range: 0.3 to 9 years). All dogs were mostly reared unrestrained with free outdoor access.

 

Discussion

Almirante Tamandaré is in an area where rural tourism is of significant economic importance, with several horse stables and training centers. This is an area of rivers, abundant vegetation and reported wild animals such as capybaras, which can all favor the maintenance of many tick species and consequently of Rickettsia. The fact that antibodies against Rickettsia from the spotted fever group have been found in animals in Almirante Tamandaré, a non-endemic area, reinforces the notion that BSF is an important reemerging zoonosis in Brazil.

Negative PCR tests for ticks could be explained by the small sample of ticks examined and also the varying refractory effect to the pathogen (LABRUNA et al., 2008), with lethal effect from R. rickettsii (NIEBYLSKI et al., 1999) that may alter the host-pathogen relationship.

In the present study, the seroprevalence of rickettsial antibodies in horses was 8.45% which is low compared to that reported (25 and 27.3%) in other studies in non-endemic areas of Brazil (LEMOS, 1996; HORTA et al., 2004; GALVÃO et al., 2005; CARDOSO et al., 2006; FREITAS, 2007; FREITAS et al., 2010). However Freitas (2007) investigated an area where there was an outbreak of BSF and a human case reported. Also, Vianna et al. (2008) reported that 100% of the sampled horses where positive to R. rickettsii in Minas Gerais. The prevalence of rickettsial antibodies in dogs in this study (20%) was higher than that found by Lemos et al. (1996) and Freitas (2007) of 12.9 and 12.5%, respectively.

In the present study all five properties that were crossed or delimited by rivers were considered BSF niches by IFA (Figure 1). Therefore, the city is within an area of biotic potential for the development of free-living ticks and hosts and the occurrence of BSF. The study showed positive animals living under environment conditions favorable to ticks where rivers and wild animals such as capybaras (MOLENTO, personal communication) may serve as reservoirs of Rickettsia sp. (LEMOS et al., 1996, 2001; MILAGRES, 2004; HORTA et al., 2004; SOUZA et al., 2009; FORTES et al., 2010).

 

 

Conclusion

There is serological evidence showing the presence of rickettsiae from the spotted fever group in the area of Almirante Tamandaré. Further studies are needed and although this is a non-endemic area, humans are vulnerable to BSF due to their close proximity to positive animals.

 

References

BILLINGS, A. N. et al. Detection of a spotted fever group Rickettsia in Amblyomma cajennense (Acari: Ixodidae) in South Texas. Journal of Medical Entomology, v. 35, n. 4, p. 474-478, 1998.         [ Links ]

BRAZILIAN MINISTRY OF HEALTH (MINISTÉRIO DA SÁUDE). Guia de vigilância epidemiológica. 6ª. ed. Brasília: Ministry of Health, 2005, 816 p.         [ Links ]

CARDOSO, L. D. et al. Caracterização de Rickettsia spp. Circulante em Foco Silencioso de Febre Maculosa Brasileira no município de Caratinga, Minas Gerais, Brasil. Caderno de Saúde Pública, v. 22, n. 3, p. 495-501, 2006.         [ Links ]

CUNHA, N. C. et al. First identification of natural infection of Rickettsia rickettsii in the Rhipicephalus sanguineus tick, in the State of Rio de Janeiro. Pesquisa Veterinária Brasileira, v. 29, n. 2, p. 105-108, 2009.         [ Links ]

DAVIDSON, M. G. et al. Vascular permeability and coagulation during Rickettsia rickettsii infection in dogs. American Journal of Veterinary Research, v. 51, n. 1, p. 165-170, 1990.         [ Links ]

FORTES, F. S. et al. Frequency of antibodies against Rickettsia spp. in free-ranging and captive capybaras (Hydrochaeris hydrochaeris) from Southern Brazil. Pesquisa Veterinária Brasileira, 2010. in press.         [ Links ]

FREITAS, M. C. D. Detecção de Rickettsias do grupo febre maculosa em cães e eqüinos em São José dos Pinhais, PR. 2007. 79 f. Dissertação (Mestrado)-Universidade Federal do Paraná, Curitiba, 2007.         [ Links ]

FREITAS, M. C. D. O. et al. Brazilian spotted fever in cart horses in a non-endemic area in Southern Brazil. Revista Brasileira de Parasitologia Veterinária, v. 19, n. 2, p. 130-131, 2010.         [ Links ]

GALVÃO, M. A. M. et al. Riquetsioses no Brasil e Portugal: ocorrência, distribuição e diagnóstico. Revista de Saúde Pública de São Paulo, v. 39, n. 5, p. 850-856, 2005.         [ Links ]

HORTA, M. C. et al. Prevalence of antibodies to spotted fever group rickettsiae in humans and domestic animals in a Brazilian spotted fever-endemic area in the state of São Paulo, Brazil: serologic evidence for infection by Rickettsia rickettsii and another spotted fever group rickettsia. American Journal of Tropical Medicine and Hygiene, v. 71, n. 1, p. 93-97, 2004.         [ Links ]

LABRUNA, M. B. Ecology of Rickettsia in South America. Annals of the New York Academy of Science, v. 1166, p. 156-166, 2009.         [ Links ]

LABRUNA, M. B. et al. Comparative susceptibility of larval stages of Amblyomma aureolatum, Amblyomma cajennense, and Rhipicephalus sanguineus to infection by Rickettsia rickettsii. Journal of Medical Entomology, v. 45, n. 6, p. 1156-1159, 2008.         [ Links ]

LABRUNA, M. B. et al. Prevalence of Rickettsia infection in dogs from the urban and rural areas of Monte Negro municipality, Western Amazon, Brazil. Vector Borne Zoonotic Disease. v. 7, n. 2, p. 249-256, 2007.         [ Links ]

LABRUNA, M. B. et al. Rickettsia species infecting Amblyomma cooperi ticks from an area in the State of São Paulo, Brazil, where Brazilian spotted fever is endemic. Journal of Clinical Microbiology, v. 42, n. 1, p. 90-98, 2004.         [ Links ]

LABRUNA, M. B. et al. Ticks (Acari: Ixodidae) on Wild Animals from the Porto-Primavera Hydroeletric Power Station Area, Brazil. Memórias do Instituto Oswaldo Cruz, v. 97, n. 8, p. 1133-1136, 2002.         [ Links ]

LEMOS, E. R. et al. Spotted fever in Brazil: a seroepidemiological study and description of clinical cases in an endemic area in the state of São Paulo. American Journal of Tropical Medicine and Hygiene, v. 65, n. 4, p. 329-334, 2001.         [ Links ]

LEMOS, E. R. S. et al. Epidemiological aspects of the Brazilian spotted fever: serological survey of dogs and horses in a endemic area in the state of São Paulo, Brazil. Revista do Instituto de Medicina Tropical de São Paulo, v. 38, n. 6, p. 427-430, 1996.         [ Links ]

McDADE, J. E.; NEWHOUSE, V. F. Natural history of Rickettsia rickettsii. Annual Review of Microbiology, v. 40, p. 287-309, 1986.         [ Links ]

MILAGRES, B. S. Perfil sorológico de algumas infecções em capivaras (Hydrochaeris hydrochaeris) capturadas nos estados de São Paulo e Minas Gerais, Brasil. 2004. 77 f. Dissertação (Mestrado)-Universidade Federal de Viçosa, Minas Gerais, 2004.         [ Links ]

NIEBYLSKI, M. L.; PEACOCK, M. G.; SCHWAN, T. G. Lethal effect of Rickettsia rickettsii on its tick vector (Dermacentor andersoni). Applied and Environmental Microbiology, v. 65, n. 2, p. 773-778, 1999.         [ Links ]

PADDOCK, C. D. et al. Hidden mortality attributable to Rocky Mountain spotted fever: immunohistochemical detection of fatal, serologically unconfirmed disease. Journal of Infection Diseases, v. 179, n. 6, p. 1469-1476, 1999.         [ Links ]

PINTER, A. et al. Serosurvey of Rickettsia spp in dogs and humans from an endemic area for Brazilian spotted Fever in the state of São Paulo, Brazil. Cadernos de Saúde Pública, v. 24, n. 2, p. 247-252, 2008.         [ Links ]

PINTER, A.; LABRUNA, M. B. Isolation of Rickettsia rickettsii and Rickettsia bellii in cell culture from the tick Amblyomma aureolatum in Brazil. Annals of the New York Academy of Sciences, v. 1078, n. 1, p. 523-529, 2006.         [ Links ]

RICKETTS, H. T. The transmission of Rocky Mountain spotted fever by the bite of the wood tick (Dermacentor occidentalis). Journal of the American Medical Association, v. 47, n. 5, p. 358, 1906.         [ Links ]

ROZENTAL, T. et al. Evidence of spotted fever group rickettsiae in state of Rio de Janeiro, Brazil. Revista do Instituto de Medicina Tropical de São Paulo, v. 44, n. 3, p. 155-158, 2002.         [ Links ]

SANGIONI, L. A. et al. Rickettsial infection in animals and Brazilian spotted fever endemicity. Emerging Infectious Diseases, v. 11, n. 2, p. 265-270, 2005.         [ Links ]

SILVA, M. E. Freqüência de anticorpos anti-Rickettsia spp. em cães da cidade de Belo Horizonte, Minas Gerais, Brasil, 2005. 2007. 35 f. Dissertação (Mestrado)-Universidade Federal de Minas Gerais, Belo Horizonte, 2007.         [ Links ]

SOUZA, C. E. et al. Experimental infection of capybaras Hydrochoerus hydrochaeris by Rickettsia rickettsii and evaluation of the transmission of the infection to ticks Amblyomma cajennense. Veterinary Parasitology, v. 161, n. 1-2, p. 116-121, 2009.         [ Links ]

SOUZA, C. E. et al. Serological identification of Rickettsia spp from the Spotted Fever group in capybaras in the region of Campinas - SP - Brazil. Ciência Rural, v. 38, n. 6, p. 1694-1699, 2008.         [ Links ]

TIRIBA, A. C. Geografia médica das riquetsioses. In: LACAZ, C. S.; BURUZZI, R. G.; SIQUEIRA, J. R. Introdução a geografia médica do Brasil. São Paulo: Edgard Blucher, 1972. p. 388-397.         [ Links ]

VIANNA, M. C. B. et al. Rickettsial Spotted Fever in Capoeirão Village, Itabira, Minas Gerais, Brazil. Revista do Instituto de Medicina Tropical de São Paulo, v. 50, n. 5, p. 297-301, 2008.         [ Links ]

WALKER, D. H. Rickettsia rickettsii: as virulent as ever. American Journal of Tropical Medicine and Hygiene, Northbroock, v. 66, n. 5, p. 448-449, 2002.         [ Links ]

 

 

Corresponding author:
Marcelo Beltrão Molento
Laboratory of Parasitic Diseases
Federal University of Paraná – UFPR
Rua dos Funcionários, 1540
CEP 80035-080, Curitiba - PR, Brazil
e-mail: molento@ufpr.br

Received April 20, 2010
Accepted September 23, 2010

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