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Emerg Infect Dis. Dec 2004; 10(12): 2261–2262.
PMCID: PMC3323364
Bartonella clarridgeiae and B. henselae in Dogs, Gabon
Vijay A.K.B. Gundi,* Olivier Bourry, Bernard Davoust, Didier Raoult,* and Bernard La Scolacorresponding author*
*Faculté de Médecine, Marseille, France;
Centre International de Recherches Médicales, Franceville, Gabon;
Direction Régionale du Service de Santé des Armées, Lyon, France
corresponding authorCorresponding author.
Address for correspondence: Bernard La Scola, Unité des Rickettsies, CNRS UMR 6020, IFR 48, Faculté de Médecine, 27 Boulevard Jean Moulin, 13385 Marseille Cedex 05, France; fax: 33-91-83-03-90; email: bernard.lascola/at/medecine.univ-mrs.fr
Keywords: letter, Bartonella, cat scratch disease, bartonellosis, dog, Gabon
To the Editor: The genus Bartonella contains several recently described species, many of which are emerging human pathogens. Human infections are mostly due to Bartonella henselae and B. quintana. Like many vectorborne disease agents, Bartonella species have a natural cycle. This cycle contains a reservoir host, in which Bartonella species cause an intraerythrocytic bacteremia, and a vector, which transmits the bacteria from the reservoir host to a new susceptible host (usually the uninfected reservoir host) (1). In the case of B. quintana and B. bacilliformis, the natural host is human. In Bartonella diseases, humans act as accidental hosts. Among the nonhuman Bartonella species that infect humans, B. henselae is most commonly encountered and usually causes cat-scratch disease. However, several cases of infections in humans attributable to other Bartonella species, including B. elizabethae, B. grahamii, B. vinsonii arupensis, B. vinsonii berkhoffii, and possibly B. clarridgeiae, have been reported (1). Isolation of Bartonella species in animals that have contact with humans can help identify new human pathogens or new diseases. We report results of isolation of Bartonella spp. from the blood of 258 dogs in Gabon.
The study was performed in the Ogooué-Ivindo province of Gabon, a country of Central Africa with an equatorial climate. Blood samples were taken from dogs in the town of Mékambo and in all villages connecting Mékambo and Mazingo (nine villages) and Mékambo and Ekata (seven villages) during July and August 2003. Each dog brought by its owner for the study was weighed and sedated by injection with 50 μg/kg of medetomidine (Pfizer Santé Animal, Orsay, France). After the dog was examined, a blood sample was drawn from the jugular vein by Vacutainer (Becton Dickinson, Meylan, France). Each dog was tattooed with an identification number and given both antihelminthic and external antiparasitic treatments. During the examination, the dogs were treated with care; upon completion of the examination, the dogs were given 250 μg/kg of the reversal agent atipamezola (Pfizer Santé Animal) intramuscularly. A physical examination form and a questionnaire were completed for each test participant by its owner. A total of 258 dogs (155 males and 103 females) were examined and had blood samples drawn during the study. All animals were of mixed breeds and were 6 months to 14 years old (average 3 years 1 month). The Vacutainer tubes were kept on ice until blood samples were dispensed into cryotubes and frozen in liquid nitrogen. Samples were stored at –80°C until isolation attempts were made on Columbia agar (Biomérieux, Marcy l'étoile, France) as described previously (2). In this study, six Bartonella isolates were obtained and identified as B. clarridgeiae (five isolates) and B. henselae (one isolate), by internal transcribed spacer amplification and sequencing (3).
B. vinsonii subsp. berkhoffii was the first Bartonella species found in dogs (1). Isolation of B. clarridgeiae (4,5) and B. washoensis (6) in dogs was recently reported. Infection of dogs by other Bartonella species was also detected in the DNA of B. henselae (7,8), B. clarridgeiae (7), and B. elizabethae (8). The presence of these Bartonella species is not surprising, since Ctenocephalides felis, the vector of B. henselae in cats, has a wide range of hosts, including the domestic dog. However, attempts to isolate this species in samples collected from 211 dogs in the United Kingdom failed (9). Bartonella species are supposedly difficult to isolate in dogs because of a low concentration of bacteria in the blood (1). This supposition was apparent in our study; we identified approximately 100 bacterial colonies per milliliter of blood from three of the six dogs in our study. From the other three dogs in our study, including the dog infected with B. henselae, we identified two to four bacterial colonies per milliliter of blood.
Most of the data pertaining to Bartonella have been obtained in the United States and Europe. Increasingly, Bartonella infections are being reported in Africa, especially in southern Africa (10). We report here the first isolation of B. henselae from a dog and the first isolation of B. clarridgeiae in Central Africa. That dogs also act as reservoirs of B. henselae likely has implications in Africa where HIV infections are prevalent.
Footnotes
Suggested citation for this article: Gundi VAKB, Bourry O, Davoust B, Raoult D, La Scola B. Bartonella clarridgeiae and B. henselae in dogs, Gabon [letter]. Emerg Infect Dis [serial on the Internet] 2004 Dec [date cited]. http://dx.doi.org/10.3201/eid1012.040359
1. 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. doi: 10.1128/CMR.13.3.428-438.2000. [PMC free article] [PubMed] [Cross Ref]
2. La Scola B, Davoust B, Boni M, Raoult D Lack of correlation between Bartonella DNA detection within fleas, serological results, and results of blood culture in a Bartonella-infected stray cat population. Clin Microbiol Infect. 2002;8:345–51. doi: 10.1046/j.1469-0691.2002.00434.x. [PubMed] [Cross Ref]
3. Houpikian P, Raoult D 16S/23S rRNA intergenic spacer regions for phylogenetic analysis identification and subtyping of Bartonella species. J Clin Microbiol. 2001;39:2768–78. doi: 10.1128/JCM.39.8.2768-2778.2001. [PMC free article] [PubMed] [Cross Ref]
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6. Chomel BB, Wey AC, Kasten RW Isolation of Bartonella washoensis from a dog with mitral valve endocarditis. J Clin Microbiol. 2003;41:5327–32. doi: 10.1128/JCM.41.11.5327-5332.2003. [PMC free article] [PubMed] [Cross Ref]
7. Gillespie TN, Washabau RJ, Goldschmidt MH, Cullen JM, Rogala AR, Breitschwerdt EB Detection of Bartonella henselae and Bartonella clarridgeiae DNA in specimens from two dogs with hepatic disease. J Am Vet Med Assoc. 2003;222:47–51. doi: 10.2460/javma.2003.222.47. [PubMed] [Cross Ref]
8. Mexas AM, Hancock SI, Breitschwerdt EB Bartonella henselae and Bartonella elizabethae as potential canine pathogens. J Clin Microbiol. 2002;40:4670–4. doi: 10.1128/JCM.40.12.4670-4674.2002. [PMC free article] [PubMed] [Cross Ref]
9. Birtles RJ, Laycock G, Kenny MJ, Shaw SE, Day MJ Prevalence of Bartonella species causing bacteremia in domesticated companion animals in the United Kingdom. Vet Rec. 2002;151:225–9. doi: 10.1136/vr.151.8.225. [PubMed] [Cross Ref]
10. Pretorius AM, Kelly PJ An update on human bartonelloses. Cent Afr J Med. 2000;46:194–200. [PubMed]
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