First description of Bartonella koehlerae infection in a Spanish dog with infective endocarditis
© The Author(s). 2017
Received: 13 January 2017
Accepted: 11 May 2017
Published: 19 May 2017
Bartonella koehlerae has been recently described as a new cat- and cat fleas-associated agent of culture-negative human endocarditis. It has been also encountered in one dog from Israel and six dogs from the USA, but other clinically relevant reports involving this bacterium are lacking.
A 7-year-old intact male mixed dog presented with clinico-pathological signs consistent with mitral endocarditis and cutaneous hemangiosarcoma. Molecular studies revealed the presence of Bartonella koehlerae DNA in samples from blood and mitral valve tissue.
This is the first description of B. koehlerae in Spain, corroborating that it can also be detected in dogs. Bartonella koehlerae infection should also be considered in Spain in humans and dogs presenting with clinical disease suggestive of it, such as culture-negative endocarditis.
Bartonella spp. are the etiological agents in humans and animals of several emergent and re-emergent vector-borne diseases that have a broad spectrum of clinical presentations including endocarditis, granulomatous diseases, meningoencephalitis, polyarthritis, uveitis or hemolytic anemia .
Bartonella koehlerae has been documented as a human pathogen and it has been increasingly detected in the last years [2, 3]. There are sporadic isolated descriptions of this bacterium in dogs. Bartonella koehlerae has been described in seven dogs from Israel and the USA with endocarditis, splenic disease, with suspicion of having a vector-transmitted infection or with hyperinsulinemic hypoglycemia syndrome [4–7].
A case report of a dog with endocarditis is herein presented. Clinical investigation was performed and complemented with postmortem evaluation at Hospital Veterinario San Vicente (San Vicente del Raspeig, Alicante, Spain). Techniques employed for laboratory workup were Procyte Dx Hematology Analyzer-Idexx, Catalyst Dx Chemistry Analyzer and IDEXX VetLab® UA™. Serologies were performed with rapid tests (Test SNAP® Leishmania and test SNAP 4Dx, IDEXX). Histopathology was performed at Histovet (Servicio de Diagnóstico Histopatológico Veterinario, Sant Quirze del Vallés, Barcelona, Spain).
Molecular investigation was initially performed at the SVGM (Servei Veterinari de Genètica Molecular, Facultat de Veterinaria, Universitat Autònoma de Barcelona, Spain) with EDTA-blood samples and freshly frozen tissue samples and further investigation was completed at the Intracellular Pathogens Research Laboratory (Center for Comparative Medicine and Translational Research, College of Veterinary Medicine, North Carolina State University, Raleigh, NC, USA). Samples shipped to the Intracellular Pathogens Research Laboratory consisted on DNA previously extracted at SVGM, EDTA-blood sample and paraffin-embedded tissue.
PCR screening of Bartonella ITS region was performed by real-time PCR using oligonucleotides BsppITS325s: 5'-CTT CAG ATG ATG ATC CCA AGC CTT YTG GCG-3' and BsppITS543as: 5'-TAA AYT GGT GGG CCT GGG AGG ACT TG-3' as forward and reverse primers, respectively, to increase the sensitivity of the detection of a broader range of Bartonella species . Amplification was performed in a 25-μl final volume reaction containing 12.5 μl of 2× Sso Advanced Universal Sybr Green Supermix (BioRad), 0.2 μl of 100 μM of each forward and reverse primer (IDT® DNA Technology) and 5 μl of DNA from each sample tested. PCR negative controls were prepared using 5 μl of DNA from blood of a healthy dog. Positive controls for PCR were prepared by serial dilution (using dog blood DNA) of genomic DNA from B. henselae down to 0.001 pg/μl (equivalent to 0.5 bacteria per μl). qPCR was performed in an BioRad CFX96 Real-Time System, under the following conditions: a single hot-start cycle at 95 °C for 2 min followed by 55 cycles of denaturing at 94 °C for 10 s, annealing at 66 °C for 10 s, and extension at 72 °C for 15 s. Amplicons products were sequenced to establish species strain identification. The sensitivity of the qPCR assay is 98% at 0.001 pg/μl (0.5 bacteria genomes per μl).
A 7-year-old intact male mixed dog was presented for a three-week history of anorexia, weight loss, polyuria and polydipsia that had worsened to severe generalized weakness at presentation time. There was also a cutaneous mass located in the right flank that had ruptured some days before resulting in serosanguinolent discharge. The dog lived outdoors, was regularly vaccinated and dewormed. Physical examination abnormalities included poor body condition (BCS, 2/9), fever (40 °C), tachycardia, grade 3-heart apex systolic murmur, pain in several joints, abdominal discomfort and an ulcerated cutaneous mass in the abdomen.
Laboratory workup revealed left shift leukocytosis (45.53 M/μl; reference range, 5.5–16.9 M/μl), neutrophilia (37.01 K/μl; reference range, 2–12 K/μl), thrombocytopenia (114 K/μl; reference range, 175–500 K/μl), azotemia (creatinine 2.1 mg/dl; reference range, 0.5–1.8 mg/dl, blood urea nitrogen, BUN 60 mg/dl; reference range, 7–27 mg/dl), increased ALP (388 U/l; reference range, 23–212 U/l), hypoalbuminemia (1.6 g/dl; reference range, 2.3–4.0 g/dl), low USG (1.020) and proteinuria (dipstick analyses ≥ 500 mg/dl). Microbiologic urine and blood cultures, and Leishmania and SNAP 4Dx (Ehrlichia canis, Dirofilaria immitis, Anaplasma platys, Anaplasma phagocythophilum and Borrelia burgdorferi) serologies were negative.
Abdominal ultrasound evidenced generalized splenomegaly and diffuse nodular hypoechoic peripheral lesions in both kidneys. Thorax radiographs showed an alveolar pattern on right lung lobes and left cranial lung lobes. Thickened mitral valve with regurgitation was detected on echocardiography. Fine needle aspiration of the cutaneous mass and spleen were consistent with a mesenchymal neoplasm and reactive splenomegaly, respectively.
Here, we report the first description of Bartonella koehlerae in Spain, as the causative agent of Bartonella endocarditis involving the mitral valve in a dog.
Infective endocarditis is an uncommon and often deadly disease in dogs that represents a diagnostic challenge in most of the cases because echocardiogram can be normal, and blood cultures can yield false-negative results due to the low-grade and intermittent bacteremia associated to Bartonella infection at the time of blood collection. Previous research has emphasized that negative blood cultures are especially frequent in Bartonella-induced endocarditis and other techniques are needed for diagnosis . The combination of a pre-enrichment liquid culture with PCR amplification enhances the detection of Bartonella species . Previous studies have shown that B. vinsonii berkhoffii is one of the most common agents found in canine Bartonella endocarditis, where infection often involves the aortic valve . However other species, such as B. koehlerae and B. henselae, have been recently implicated in canine endocarditis in the USA and Israel [4, 11]. In Spain, several cases of endocarditis due to Bartonella spp. has been reported in people in the past ten years and the number of cases is likely to be underestimated .
Interestingly, recent reports suggest that Bartonella spp. should be investigated as a cause of vasoproliferative tumors in both humans and dogs, due to their ability of enhancing endothelial cell proliferation in conjunction with inhibition of apoptosis [13, 14]. Species of Bartonella involved are B. bacilliformis, B. quintana, B. henselae, B. vinsonii berkhoffi and B. koehlerae. Unfortunately, definitive association of Bartonella and the skin hemangiosarcoma could not be established in this study since Bartonella DNA could not be amplified from the skin tumor. False-negative PCR results could be caused by prolonged period of formalin fixation [15, 16]. Further research is needed to test the potential role of the genus Bartonella as cofactor in the development of cancer [13, 14].
In Spanish dogs, presence of canine bartonellosis has been demonstrated with serological studies . Moreover, there is molecular evidence of this infection in a recently described dog with generalised pyogranulomatous disease and hyperviscosity syndrome . Several reports have confirmed that Bartonella infection is present in people in the Valencian Community and Catalonia (Spain) [19, 20].
Definitive documentation of the causative Bartonella spp. in dogs may prove to be a legitimate medical concern, as dogs have been also implicated in the transmission of bartonellosis following a bite or a scratch [21, 22]. Bartonella koehlerae has been described as a cat-associated agent of culture-negative human endocarditis , and this case report corroborates that it can also be detected in dogs.
The findings presented in this manuscript reinforce the concept of “One Health” approach, which requires close communication in all aspects of health care for humans and animals, with the aim of supporting public health in general. It is worth highlighting that there are many vectors that could harbor Bartonella organisms as sand flies, human body lice, cat fleas, ear mites, and ticks have been described as potential vectors . Therefore the risk of both animal and human exposure to Bartonella spp. may be more substantial than is currently believed and, until an effective vaccine in the protection against Bartonella spp. could be available, ectoparasites control measures should be implemented in both dogs and cats to avoid the potential of zoonotic transmission of this severe infection to humans.
To our knowledge, this is the first description of Bartonella koehlerae in Spain, corroborating that the parasite can also be detected in dogs. Bartonella spp. infection should also be considered in Spain in humans and dogs presenting with features suggestive of it, such as blood culture-negative endocarditis.
The paper has been sponsored by Bayer Animal Health in the framework of the 12th CVBD World Forum Symposium.
Availability of data and materials
Alignment of the ITS region sequences comparing the dog sequences with Bartonella henselae and B. koehlerae is provided in Additional file 1: Figure S1.
MDT wrote the manuscript and was the clinician who made the diagnostic work up and treatment of the dog. LA and RGM performed the genetics tests and identify the final pathogen involved in the case report. JA performed the histological examination. XR was involved in drafting the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
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