Open Access Brief Communication

Use of a doxycycline-enrofloxacin-metronidazole combination with/without diminazene diaceturate to treat naturally occurring canine babesiosis caused by Babesia gibsoni Abstract Canine babesiosis is an important worldwide, tick-borne disease caused by hemoprotozoan parasites of the genus Babesia. Babesia gibsoni is the predominant species that causes canine babesiosis in Taipei, Taiwan. It is a small pleomorphic intraerythrocytic parasite that can cause erythrocyte destruction and hemolytic anemia. Efficacy of oral administration of a doxycycline-enrofloxacin-metronidazole combination with and without injections of diminazene diaceturate in the management of naturally occurring canine babesiosis caused by B. gibsoni was evaluated retrospectively. The overall efficacy of this combination of doxycycline-enrofloxacin-metronidazole in conjunction with and without administration of diminazene diaceturate was 85.7% and 83.3%, respectively; with a mean recovery time of 24.2 and 23.5 days, respectively. Concomitant use of intramuscular diminazene diaceturate may not improve the efficacy of a doxycycline-enrofloxacin-metronidazole combination in management of canine babesiosis caused by B. gibsoni. Findings Canine babesiosis is an important worldwide, tick-borne disease caused by hemoprotozoan parasites of the genus Babesia, and the predominant species infecting dogs is B. vogeli [1]. In a previous study, B. gibsoni was found to be the major causative agent of canine babesiosis in Taipei, Taiwan [2]. Babesia gibsoni is a small pleomorphic, intra-erythrocytic parasite that can cause erythrocyte destruction and hemolytic anemia [1]. This parasite is suspected to be transmitted through the bite of ixodid ticks, such as Rhipicephalus sanguineus [1,3-8]. Clinical signs of canine babesiosis are characterized by lethargy, anorexia, fever, hemolytic anemia, thrombocy-topenia, splenomegaly and even septic shock [2,9-14]. Chronic infection is common. Definitive diagnosis of canine babesiosis is based on medical history and clinical signs together with the identification of Babesia spp. within infected erythrocytes, positive serologic results, and detection of amplification of nucleic acid extracted from blood or tissues [4,5,15]. Many drugs have been applied in management of canine babesiosis, including babesiacidal agents (dimina-zene aceturate, imidocarb diproprionate), antibiotics (azithromycin, clindamycin, doxycycline, metronidazole), and an antiprotozoal agent (Atovaquone). However, no single drug has successfully eliminated B. gibsoni from infected dogs [9,10,12,13,15-18]. Addictive or synergistic effects of these drugs in combination have not been fully evaluated. The babesiacide diminazene diaceturate is mainly used in horses, donkeys and cows [19-21]. Efficacy of diminazene diaceturate in management of canine babesiosis is limited, but this is the only diminazene available for veterinary use in Taiwan, whereas atovaquone is not yet available. The aim of this study was to evaluate …


Findings
Canine babesiosis is an important worldwide, tick-borne disease caused by hemoprotozoan parasites of the genus Babesia, and the predominant species infecting dogs is B. vogeli [1]. In a previous study, B. gibsoni was found to be the major causative agent of canine babesiosis in Taipei, Taiwan [2]. Babesia gibsoni is a small pleomorphic, intraerythrocytic parasite that can cause erythrocyte destruction and hemolytic anemia [1]. This parasite is suspected to be transmitted through the bite of ixodid ticks, such as Rhipicephalus sanguineus [1,[3][4][5][6][7][8].
Many drugs have been applied in management of canine babesiosis, including babesiacidal agents (diminazene aceturate, imidocarb diproprionate), antibiotics (azithromycin, clindamycin, doxycycline, metronidazole), and an antiprotozoal agent (Atovaquone). However, no single drug has successfully eliminated B. gibsoni from infected dogs [9,10,12,13,[15][16][17][18]. Addictive or synergistic effects of these drugs in combination have not been fully evaluated. The babesiacide diminazene diaceturate is mainly used in horses, donkeys and cows [19][20][21]. Efficacy of diminazene diaceturate in management of canine babesiosis is limited, but this is the only diminazene available for veterinary use in Taiwan, whereas atovaquone is not yet available. The aim of this study was to evaluate the efficacy of a doxycycline-enrofloxacin-metronidazole (D-E-M) combination with and without administration of diminazene diaceturate to manage naturally occurring canine babesiosis caused by B. gibsoni.
Medical records of dogs in which babesiosis was diagnosed at the National Taiwan University Veterinary Hos-pital from January 2005 to December 2006 were reviewed. Inclusion criteria were history of tick infestation, presence of anemia, and identification of B. gibsoni in the stained blood films, and treatment with an oral doxycycline (7-10 mg/Kg, q 12 hours; China Chemical & Pharmaceutical Co. Ltd., Taipei, Taiwan)-enrofloxacin (2-2.5 mg/Kg, q 12 hours; Baytril ® , Bayer HealthCare AG, Leverkusen, Germany)-metronidazole (5-15 mg/Kg, q 12 hours; Sinphar Pharmaceutical Co. Ltd. Taipei, Taiwan; D-E-M) combination of six weeks with and without two intramuscular injections of diminazene diaceturate (3 mg/Kg, q 7 days; Tricip Plus ® , Cipla Ltd., Mumbai, India). Informed consent of using diminazene diaceturate had been obtained from the owners of dogs. Breed, sex, age, pre-treatment complete cell counts, bi-weekly follow-up complete cell counts, and the outcome for each case were recorded. Co-infection with other tick-borne diseases, such as Anaplasma phagocytophilum and Ehrlichia canis were excluded using a commercially available immunoenzymatic dot-ELISA assays (Snap 4Dx, Idexx Laboratories Inc., Maine, U.S.A.).
In this study, identification of B. gibsoni was based on morphological characteristics of intraerythrocytic parasites found in the stained blood films. Dogs affected with other babesia species, such as B. canis and B. vogeli were excluded from this study. Efficacy of treatment was defined as elimination of B. gibsoni in blood films, and clinical remission for seven weeks after the treatment was discontinued.
Comparison of the time to reach clinical remission between two treatment protocols was performed by means of repeated-measures ANOVAs. Associations between sex, age, treatment protocols, and time to reach clinical remission were evaluated by means of ANOVA. Variables that might have influenced relapse of anemia and persistent parasitemia were analyzed by use of a Cox proportional hazard model. Such variables included sex, age and severity of anemia at diagnosis, and treatment protocol. Data for dogs that failed to response (relapse of anemia and persistent parasitemia) were censored. All statistical analyses were performed using SPSS software (Statistical Package for the Social Sciences, version 13.0; SSPS Inc, Illinois, USA). Continuous data are presented as mean ± SD. Statistical significance was set at P ≤ 0.05.
Medical records of 6789 dogs from January 2005 to December 2006 were screened. Of these, 118 cases was diagnosed as babesiosis and caused by B. gibsoni. Breeds of the 40 dogs included in this study were: 10 Maltese terriers; four each of Beagles, mixed breeds and miniature Schnauzers; three of Labrador retrievers and Yorkshire terriers; two each of Pit bull terriers, Golden retrievers, and Pomeranians; one each of Chihuahua, Siberian Husky, Old English sheepdog, miniature Poodle, Pug and Shih Tzu. The mean age of the dogs included in the study was 5.3 ± 3.9 years, and ranged from 9 months to 14 years old. The ratio of male to female was 3 to 1.
Twenty-eight dogs were treated with an oral combination of D-E-M for six weeks plus two intramuscular injections of diminazene diaceturate, whereas 12 dogs received only the oral combination of D-E-M for six weeks.
Of 28 dogs (mean age: 6.0 ± 3.8 years) treated with oral D-E-M combination and two intramuscular injections of diminazene diaceturate, 4 dogs showed relapse of anemia and parasitemia after 14, 28, 35 and 42 days, respectively, and 24 dogs had clinical remission. The overall efficacy of multiple antibiotics combined with diminazene diaceturate was 85.7%, with a mean recovery time of 24.2 days (n = 24, Table 1).
Of 12 dogs (mean age: 3.6 ± 3.8 years) treated with D-E-M, but were not given injections of diminazene diaceturate relapsed anemia was identified in 2 dogs after 45 and 73 days, while another 10 dogs reached clinical remission. The overall efficacy of management of canine babesiosis using only multiple antibiotics was 83.3%, with a mean recovery time of 23.5 days (n = 10, Table 2).
No significant difference was seen in management efficacy between the two protocols (P = 0.36). The time to reach clinical remission was not affected by sex, age or treatment protocols (P = 0.88, P = 0.36, P = 0.38, respectively).
Results of the Cox proportional hazard model indicated that relapse of anemia and persistent parasitemia was not associated with sex, age or severity of anemia at diagno- sis, or treatment protocol (P = 0.72, P = 0.72, P = 0.65, P = 0.52, respectively) In this study, the overall prevalence of canine babesiosis caused by B. gibsoni was 1.7%, which was only slightly higher than the prevalence established in a similar study conducted 10 years earlier (1.6%) [2].
In our previous study, Maltese terriers seemed to be predisposed to babesiosis [2]. In the present study, the Maltese terrier was accounting for 25% of the cases of babesiosis, but no further statistical analyses were carried out to assert that Maltese terrier was predisposing to canine babesiosis. Maltese terrier is, however, much less popular compared to 10 years ago. A large scale study of breed predisposition to this disease is warranted. Certain breeds, such as American Pit Bull terriers and Tosa dogs [5,22], have also been found to having higher rates of subclinical infection with B. gibsoni. Particularly dogs that have been bitten were found to have a higher subclinical infection with B. gibsoni [5,22,23].
The efficacy of treatment of babesiosis caused by B. gibsoni with either doxycycline or metronidazole has been evaluated, but the ability of each drug alone to successfully treat B. gibsoni is still controversial [18]. In the present study, synergistic efficacy of the D-E-M combination was 83.3%. Relapse of anemia and persistent parasitemia was not associated with sex, age or severity of anemia at diagnosis, or D-E-M combination with or without diminazene diaceturate.
Diminazene aceturate, an aromatic diamidine compound, can interfere with the synthesis of DNA and aerobic glycolysis and has been commonly used against infection of canine babesiosis caused by B. gibsoni [18]. Diminazene diaceturate has also been widely used against infection of babesiosis in horses, donkeys and cows [13,20,21]. In a comparative study, diminazene aceturate exhibited a higher efficacy than diminazene diaceturate in the treatment of babesiosis in horses [21]. In the present study, efficacy and the time to achieve clinical remission did not differ between the two treatment protocols. Although the efficacy of the administration of diminazene diaceturate alone against B. gibsoni was not evaluated in our study, it suggested that concomitant use of diminazene diaceturate may not improve the efficacy of a D-E-M combination treatment of canine babesiosis caused by B. gibsoni.
All cases of subclinical infection of B. gibsoni may not be detected solely by, morphological identification in blood smears, and polymerase chain reaction assay should therefore be included in further studies in order to identify subclinical carriers after treatment.
Concomitant use of intramuscular diminazene diaceturate may not improve the efficacy of a doxycycline-enrofloxacin-metronidazole combination in management of canine babesiosis caused by B. gibsoni.