Molecular detection of Bartonella clarridgeiae in domestic cats from Midwest Brazil

Dear Editor,

Cat scratch disease (CSD) is caused by Bartonella henselae a hemotropic bacterium that infects human, domestic and wild mammals. Closely related to B. henselae, the B. clarridgeiae comprises approximately 10-30% of Bartonella isolates from clinically healthy cats and was found in cardiac and hepatic lesions in dogs.¹ Moreover, B. clarridgeiae has been serologically associated with CSD-like illness in humans.²

Cats are considered the major reservoir and carriers of B. henselae, B. clarridgeiae and B. koehlerae. Bartonella spp. can be a vector transmitted by flea to susceptible cats. Few cats naturally infected have clinical signs. Medical problems of cats associated with Bartonella infections are variable, ranging from transient fever and lymphadenopathy to abscesses or microabscesses in different organs, endocarditis, and central nervous signs.¹ Transmission from cats to humans and dogs mainly occurs through cat scratches or bites. In humans, this infection may be asymptomatic and can disappear spontaneously without any treatment; however, in some cases the disease may be fatal if left untreated.³

In order to identify arthropod-borne pathogens in domestic feline, 182 cats from different places of Cuiabá and Varzea Grande cities, both located in Mato Grosso State, Midwest Brazil, have been analyzed. Cats were seen at the Veterinary Hospital of the Federal University of Mato Grosso (HOVET-UFMT), Veterinary Hospital of the University of Cuiabá (UNIC-HV), and animal shelters and Zoonosis Control Centers (ZCC) of Cuiabá and Várzea Grande cities. Sample collection was conducted in agreement with the Ethical Principles for Animal Research under the institutional watch of the UFMT Committee for Ethics in Animal Research.

Collected blood samples were subjected to a DNA extraction using the Axyprep Blood Genomic DNA Miniprep Kit (Axygen Biosciences, Hangzhou, China). Extracted DNA was then used as a template for Bartonella spp. PCR assay usingvthe primer BARTON-1 (5t -TAACCGATATTGGTTGTGTTGAAG-3t) and BARTON-2 (5t -TAAAGCTAGAAAGTCTGGCAACATAACG-3t ), which amplifies a segment of 585-588 bp of Riboflavin synthase C (ribC) gene of Bartonella genus.⁴

Three (1.6%) cats were positive to the presence of Bartonella DNA according to PCR targeting portions of the ribC gene. Partial DNA sequences of all PCR-positive samples were generated yielding a sequence (GenBank accession: KR092386) that was identical to KC331014 and HM588660 and 99% similarity to HQ012585, KC331017, KC331014, which corresponds to B. clarridgeiae sequences available in GenBank.

The positive cats were found in the ZCC of Várzea Grande city. Usually, these animals are taken off the streets and kept until adoption. Boulouis et al. observed that stray cats present higher prevalence of Bartonella spp. infection than pet cats, mainly due to close contact between infected animals in large groups of cats, demonstrating that differences in the occurrence of the infection are associated with the type of feline population studied.⁵ Due to vigorous flea control among cat populations, the prevalence of Bartonella infection in cats have reduced and the risk of Bartonella-associated disease in pet owners decreased. However, cat owners and animal health professionals should be cautioned to avoid behaviors that increase the risk of animal bites or scratches, since the feline population acts as a source of zoonotic agents and represents a potential risk of infection.¹

In Brazil, the occurrence of Bartonella infection in human was previously described. In the State of Rio de Janeiro, 41.6% of clinically asymptomatic HIV-positive patients were found seropositive for Bartonella species.³ In fact, veterinarians and medical doctors should consider the presence of these zoonotic pathogens in their diagnostic routine.

Acknowledgements

The authors gratefully acknowledge the scholarships granted by FAPEMAT (Research Support Foundation of the State of Mato Grosso) to IAB and CNPq (National Council for Scientific and Technological Development) to ISOD and DMA. We also thank for the support offered by Valeria Dutra and Luciano Nakazato for laboratory resources.

REFERENCES

• ¹
  Kordick DL, Hilyard EJ, HadfieldTL, et al. Bartonella clarridgeiae, a newly recognized zoonoticpathogen causing inoculation papules, fever, and lymphadenopathy (cat scratch disease). J Clin Microbiol. 1997;35:1813-8.
• ²
  Breitschwerdt EB, Kordick DL. Bartonella infection in animals: carriership, reservoir potential, pathogenicity and zoonotic potential for human infection. Clin Microbiol Rev. 2000;13:428-38.
• ³
  Lamas C, Rozental T, Favacho A, et al. Bartonella sp. infections in HIV positive individuals in Rio de Janeiro, Brazil. Int J Infect Dis. 2006;10:S176.
• ⁴
  Bereswill S, Hinkelmann S, Kist M, Sander A. Molecular analysis of rib of lavinsyn the sisgenes in Bartonella henselae and use of the rib C gene for differentiation of Bartonella speciesby PCR. J Clin Microbiol.1999;37:3159-66.
• ⁵
  Boulouis HJ, Chang CC, Henn JB, Kasten RW, Chomel BB. Factors associated with the rapid emergence of zoonotic Bartonella infections. Vet Res. 2005;36:383-410.

Publication Dates

• Publication in this collection
  Jul-Aug 2015

History

• Received
  15 Apr 2015
• Accepted
  12 May 2015