Interpretation of Coagulation Tendency Contributing to Thrombosis in Vector-Borne Diseases (Ehrlichiosis, Anaplasmosis, Leishmaniosis, and Dirofilariasis) among Dogs
DOI:
https://doi.org/10.22456/1679-9216.80033Keywords:
vector-borne, disease, dog, D-dimer, coagulation, thrombocytopeniaAbstract
Background: Vector-borne infectious and zoonotic diseases are an important health problem that directly affects human and animal health negatively. Results through evaluation of coagulation disorders among vector-borne diseases should be of beneficial for both human and dogs studies. According to the present author’s knowledge reports regarding changes in platelet (PLT) count, prothrombin time (PT), activated partial thromboplastin time (APTT), fibrinogen (FIB) and D-dimer levels in dogs naturally infected with one or more vector-borne pathogens are lacking. Therefore, the present study was aimed to detecting those parameters for relation between diagnosis and prognosis of vector-borne diseases among dogs.
Materials, Methods & Results: The material of this study was 46 dogs (36 were naturally infected with vector-borne diseases and 10 were healthy) from different breed, age and of both sexes. Venous blood samples were obtained to detect PLT counts, antibodies of ehrlichiosis, anaplasmosis, borreliosis, leishmaniosis and antigens of Dirofilaria immitis. The diagnosis of vector-borne diseases was performed by using a commercial ELISA assay kits. PLT count was performed with an automated blood cell counter analyser. In addition, PT, APTT and FIB concentrations were measured using a microcoagulometer. D-dimer concentrations were determined using fluorescence immunoassay rapid quantitave test analyser. Subgroups were formed according to the number of cases and the distribution of vector-borne agent. Statistically significant decreased PLT count was found in dogs mono infected with ehrlichiosis compared to healthy dogs (P < 0.001). Changes in mean PT value in the studied animals did not show statistically significant differences among the groups
(P > 0.05). APTT values in the ehrlichiosis mono infection group were significantly higher than that of the healthy control
(P < 0.01). A significant increase in FIB levels were detected for ehrlichiosis mono infection and ehrlichiosis - leishmaniosis co infection versus healthy control (P < 0.001). Plasma D-dimer concentrations were found to be higher in all groups infected with vector borne diseases compared to healthy group (P < 0.001) and the differences between infected groups were not statistically significant.
Discussion: Bleeding disorders such as epistaxis, haematuria and haemorrhagic diarrhoea has been reported in dogs with vector-borne diseases. These disorders represent the main cause of death in dogs. In the present study, thrombocytopenia was observed in dogs mono infected with ehrlichiosis compared to healthy. This finding is in agreement with those reported in dogs with ehrlichiosis. Plasma FIB is one of the most important factors in the coagulation cascade. In the present study, a significant difference between dogs with ehrlichiosis mono infection and ehrlichiosis - leishmaniosis co infection versus healthy controls group was observed. PT and APTT are commonly used in evaluating dogs with bleeding tendencies. In the present study, a significant difference between dogs with ehrlichiosis and with healthy control was observed in APTT values, however, differences in PT values compared to healthy dogs were insignificant. No statistical difference in PT values might be related to the lower sensitivity of the commercial PT assays. In dogs, D-dimer concentrations can be elevated due to disseminated intravascular coagulopathy, infections, metabolic disorders, neoplasia and post-surgically. In the present study, a significant increase in D-dimer concentration was observed in all dogs with vector-borne diseases. This finding points to the activation of the fibrinolysis system in consequence of thrombophilia. In conclusion, elevations presented in coagulation biomarkers such as APTT, FIB and D-dimer in the present study were interpreted as with the effects of vector-borne diseases. It may be briefly suggested that D-dimer levels as a marker of pro-coagulatory activity, as well as fibrinolysis, indicates the highly active and excessive coagulation, and all through are risk factors for thromboembolic disorders. Therefore, these findings should be considered in the diagnosis, treatment and prognosis of the vector-borne diseases in dogs.
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References
Baneth G., Harrus S., Ohnona F.S. & Schlesinger Y. 2009. Longitudinal quantification of Ehrlichia canis in experimental infection with comparison to natural infection. Veterinary Microbiology. 136: 321-325.
Bhadesiya C.M. & Raval S.K. 2015. Hematobiochemical changes in ehrlichiosis in dogs of Anand region, Gujarat. Veterinary World. 8(6): 713-717.
Blomback B. 1996. Fibrinogen and fibrin-proteins withcomplex roles in hemostasis and thrombosis. Thrombosis Research. 83: 1-75.
Bulla C., Kiomi Takahira R., Pessoa Araújo J., Aparecida Trinca L., Souza Lopes R. & Wiedmeyer C.E. 2004. The relationship between the degree of thrombocytopenia and infection with Ehrlichia canis in an endemic area. Veterinary Research. 35(1): 141-146.
Carretón E., Corbera J.A., Juste M.C., Morchón R., Simón F. & Montoya-Alonso J.A. 2011. Dirofilaria immitis infection in dogs: cardiopulmonary biomarker levels. Veterinary Parasitology. 176: 313-316.
Ciaramella P., Pelagalli A., Cortese L., Pero M.E., Corona M., Lombardi P., Avallone L. & Persechino A. 2005. Altered platelet aggregation and coagulation disorders related to clinical findings in 30 dogs naturally infected by Leishmania infantum. Veterinary Journal. 169: 465-467.
Cortese L., Pelagalli A., Piantedosi D., Mastellone V., Manco A., Lombardi P., Ciaramella P. & Avallone L. 2006. Platelet aggregation and haemostatic response in dogs naturally co-infected by Leishmania infantum and Ehrlichia canis. Journal of Veterinary Medicine. 53: 546-548.
Caprariis D., Dantas-Torres F., Capelli G., Mencke N., Stanneck D., Breitschwerdt E.B. & Otranto D. 2011. Evolution of clinical, haematological and biochemical findings in young dogs naturally infected by vector-borne pathogens. Veterinary Microbiology. 149(1-2): 206-212.
Edirimanne E.R.K.V., Ariyarathna H.S., Beijerink N.J. & de Silva D.D.N. 2014. Latest clinical manifestations of canine ehrlichiosis: “The Pup Killer” - A Preliminary Communication. Wayamba Journal of Animal Science. 1397905837: 880-892.
Elhamiani Khatat S., Defauw P., Marynissen S., Van de Maele I., van Dongen A. & Daminet S. 2015. Exposure to Anaplasma phagocytophilum in two dogs in Belgium. Vlaams Diergeneeskundig Tijdschrift. 84(1): 39-46.
Epstein S.E., Hopper K., Mellema M.S. & Johnson L.R. 2013. Diagnostic utility of D-dimer concentrations in dogs with pulmonary embolism. Journal of Veterinary Internal Medicine. 27: 1646-1649.
Everse S.J., Spraggon G., Veerapandian L., Riley M. & Doolittle R.F. 1998. Crystal structure of fragment double-D from human fibrin with two different bound ligands. Biochemistry. 37(24): 8637-8642.
Gaunt S.D., Baker D.C. & Babin S.S. 1990. Platelet aggregation studies in dogs with acute Ehrlichia platys infection. American Journal of Veterinary Research. 51(2): 290-293.
Grisi L., Leite R.C., Martins J.R., Barros A.T., Andreotti R. & Cançado P.H. 2014. Reassessment of the potential economic impact of cattle parasites in Brazil. Revista Brasileira de Parasitologia Veterinária. 23: 150-156.
Hajsadeghi S., Kerman S.R., Khojandi M., Vaferi H., Ramezani R., Jourshari N.M., Mousavi S.A. & Pouraliakbar H. 2012. Accuracy of D-dimer:fibrinogen ratio to diagnose pulmonary thromboembolism in patients admitted to intensive care units. Cardiovascular Journal of Africa. 23(8): 446-456.
Harrus S., Waner T., Eldor A., Zwang E. & Bark H. 1996. Platelet dysfunction associated with experimental acute canine ehrlichiosis. Veterinary Record. 139(12): 290-293.
Herring J. & Mc Michael M. 2012. Diagnostic approach to small animal bleeding disorders. Topics in Companion Animal Medicine. 27: 73-80.
Irwin PJ. 2014. It shouldn’t happen to a dog … or a veterinarian: clinical paradigms for canine vector-borne diseases. Trends in Parasitology. 30: 104-112.
Jimenez C. & Fernandez F. 2000. Inflammation, kinins, and complement. System interaction with haemostasis. In: B.F. Feldman, J.G. Zinkl & N.C. Jain (Eds). Schalm’s Veterinary Hematology. 5th edn. Philadelphia: Lippincott Williams and Wilkins, pp.549-551.
Kang M.H., Heo R.Y. & Park H.M. 2016. Evaluation of D-dimer concentrations in clinically ill dogs with high risk of thromboembolic disease. Pakistan Veterinary Journal. 36(2): 219-223.
Kebapcilar A.G., Kulaksizoglu M., Ipekci S.H., Korkmaz H., Kebapcilar L., Akyurek F., Taner C.E. & Gonen M.S. 2013. Relationship between mean platelet volume and low-grade systemic coagulation with vitamin D deficiency in primary ovarian insufficiency. Archives of gynecology and obstetrics. 288(1): 207-212.
Koenig W. 1998. Haemostatic risk factors for cardiovascular diseases. European Heart Journal. 19: 39-43.
Kubo S., Tateno M., Ichikawa Y. & Endo Y. 2015. A molecular epidemiological survey of Babesia, Hepatozoon, Ehrlichia and Anaplasma infections of dogs in Japan. Journal of Veterinary Medicine and Science. 77: 1275-1279.
Lakkawar W.A., Nair G.M., Varshney C.K., Sreekrishnan R. & Rao V.N. 2003. Pathology of canıne monocytic ehrlichiosis in a German shepherd dog. Slovenian Veterinary Research. 40 (2): 119-128.
Otranto D. & Dantas-Torres F. 2010. Canine and feline vector-borne diseases in Italy: current situation and perspectives. Parasite & Vectors. 3: 2.
Otranto D., Dantas-Torres F. & Breitschwerdt E.B. 2009. Managing canine vector-borne diseases of zoonotic concern: part one. Trends in Parasitology. 25: 157-163.
Ruiz de Gopegui R., Peñalba B., Goicoa A., Espada Y., Fidalgo L.E. & Espino L. 2007. Clinico-pathological findings and coagulation disorders in 45 cases of canine babesiosis in Spain. Veterinary Journal. 174(1): 129-132.
Santamaria A., Calzada J.E., Saldaña A., Yabsley M.J. & Gottdenker N.L. 2014. Molecular diagnosis and species identification of Ehrlichia and Anaplasma infections in dogs from Panama, Central America. Vector Borne Zoonotic Diseases. 14: 368-370.
Schetters T.P., Kleuskens J.A., Van De Crommert J., De Leeuw P.W., Finizio A.L. & Gorenflot. A. 2009. Systemic inflammatory responses in dogs experimentally infected with Babesia canis; a haematological study. Veterinary Parasitology. 162: 7-15.
Scott-Moncrieff J.C., Treadwell N.G., McCullough S.M. & Brooks M.B. 2001. Hemostatic abnormalities in dogs with primary immune-mediated hemolytic anemia. Journal of American Animal Hospital Association. 37: 220-227.
Shipov A., Klement E., Reuveni-Tager L., Waner T. & Harrus S. 2008. Prognostic indicators for canine monocytic ehrlichiosis. Veterinary Parasitology. 153(1-2): 131-138.
Stokol T., Brooks M.B., Erb H.N. & Mauldin G.E. 2000. D-dimer concentrations in healthy dogs and dogs with disseminated intravascular coagulation. American Journal of Veterinary Research. 61: 393-398.
Sumathi D., Selvaraj P., Nambi A.P., Prathaban S. & Enbavelan P.A. 2012. Assessment of prothrombin and activated partial thromboplastin time in dogs. Tamilnadu Journal of Veterinary & Animal Sciences. 8(4): 238-240.
Torres Mde M., Almeida Ado B., Paula D.A., Mendonça A.J., Nakazato L., Pescador C.A. & Sousa V.R. 2016. Hemostatic assessment of dogs associated with hepatic parasite load of Leishmania infantum chagasi. Revista Brasileira de Parasitologia Veterinária. 25(2): 244-247.
Tripodi A., Branchi A. & Chantarangkul V. 2011. Hypercoagulability in patients with type 2 diabetes mellitus detected by a thrombin generation assay. Journal of Thrombosis and Thrombolysis. 31: 165-172.
Ural K., Gultekin M., Atasoy A. & Ulutas B. 2014. Spatial distribution of vector borne disease agents in dogs in Aegean region, Turkey. Revista MVZ Córdoba. 19(2): 4086-4098.
Zoia A., Augusto M., Drigo M. & Caldin M. 2012. Evaluation of hemostatic and fibrinolytic markers in dogs with ascites attributable to right-sided congestive heart failure. Journal of American Veterinary Medical Association. 241: 1336-1343.
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