The aim of the present study was to determine the prevalence of Dirofilaria immitis in stray, pet, and working dogs (n = 413, 266, and 103, resp.) from Guwahati (Assam) and Aizawl (Mizoram), areas located in two Northeastern States of India. Diagnostic methods applied were microscopy (wet film and Knott's concentration technique), immunological test (Ag ELISA by SNAP 4Dx ELISA kit), and molecular tools (polymerase chain reaction and sequencing), which evidenced 11.38, 18.03, and 13.93% of positive animals, respectively. No significant differences were observed by area (18.23% versus 17.68%) nor by sex (18.1% versus 17.9%), whereas stray dogs proved more infected than other groups (P < 0.05). ELISA test evidenced an overall 22.69% of occult infections, mainly in working dogs (60%), and molecular techniques detected Dirofilaria (Nochtiella) repens in 4 stray dogs from Guwahati. Characterization of D. immitis isolates for ITS-2 region showed close identity with South Asian isolates.

The objective of the study was to detect Babesia infections in pet dogs of a north-eastern state of India. The diagnostic efficacy of Babesia infection by polymerase chain reaction (PCR) technique has been compared with microscopy examination. For this, a total of 111 blood samples of pet dogs presented at clinical complex of the College of Veterinary Science, Guwahati, Assam with clinical signs suspected for Babesia infection subjected to the study. A total of 44 (39.63 %) dogs were diagnosed as positive for Babesia infections after microscopic examination. Among these, Babesia canis infection was diagnosed in 5 dogs (4.50 %) and B. gibsoni infection in 39 (35.13 %) dogs microscopically in Giemsa stained blood smears. Molecular diagnosis using PCR detected 63 (56.75 %) dogs positive for Babesia infection. Single infection with B. canis was found in 9 (8.10 %) dogs while B. gibsoni alone was detected in 3 (2.70 %) dogs. Mixed infections by both these species were detected in 51 (45.94 %) dogs. Overall, PCR detected 54 (48.64 %) dogs as B. gibsoni and 60 (54.05 %) dogs as B. canis positive.

Background: Trichomonas gallinae is a flagellated protozoa, infects the upper digestive system of pigeon and causing a condition called canker, characterized by development of granulomatous lesions in the buccal cavity, crop, proventriculus, gizzard and liver of affected birds causing mortality upto 90% in squabs. Systemic research on prevalence and pathology of T. gallinae in pigeons are scant in India. The present work was carried out to document the prevalence and pathology of T. gallinae in pigeons of Assam.Methods: During the one- year study period, throat swab samples were collected from households, market places and temple premises in 4 districts of Assam. A total of 324 birds were examined by wet mount and Giemsa staining methods for detection of T. gallinae. Naturally died carcasses were studied for gross and histopathological alteration in different organs.Result: In the present study prevalence of T. gallinae was found 26.85% and squabs were highly susceptible with 56.25 percent. Sex wise, comparatively higher prevalence was observed in females (33.54%) than in the males (20.48%). Seasonality study revealed highest prevalence during winter. Gross pathological alteration characterized by yellowish white caseo-necrotic haemorrhagic lesion in the upper digestive tract beginning with the oral cavity and lesions also found in liver and lungs. Histopathological alteration also recorded in different organs. In the liver sinusoidal congestion and kupffer cell hyperplasia were observed. Infiltration of polymorphonuclear cells in the thickened inter alveolar space of lungs also recorded. Further study is required to identify the prevalent strains of T. gallinae on the basis of pathogenicity in this geographic region and immunology of T. gallinae in pigeons and other hosts remain to be explored.

Aim:The aim of the present study was to investigate the presence of Theileria in blood samples of crossbred and indigenous adult cows raised under unorganized small scale farming system in a Babesia and Anaplasma endemic geographical area from Assam, India and to see its transmission through Rhipicephalus (Boophilus) microplus ticks.Materials and Methods:For the present study, 57 clinical cases of cattle suspected to be of hemoparasitic infections were taken into consideration. The parasites were identified based on morphology in giemsa stained blood smear followed by polymerase chain reaction (PCR). Sera samples were tested for T. annulata antibodies in plate and Dot-ELISA. PCR was also conducted in eggs of Rhipicephalus (Boophilus) microplus tick collected from a Theileria orientalis positive animal.Results:PCR amplified 1124, 776, and 160 bp DNA fragments of B. bigemina (64.91%), T. orientalis (21.05%) and A. marginale (14.03%), respectively. This assay further conducted in 12 T. orientalis positive blood samples with primers of Buffeli, Chitose, and Ikeda variants of T. orientalis showed 3 samples positive to Ikeda type and none for Buffeli and Chitose. Babesia bovis and Theileria annulata specific primers also did not amplify any fragment during the PCR assay of the blood samples. Further, all sera samples tested negative to T. annulata antibodies in Plate and Dot-ELISA. PCR conducted in eggs of R (B).microplus tick collected from a T. orientalis positive animal revealed presence of the parasite DNA. Gradual improvement in physical condition leading to complete recovery in 10 out of 12 T. orientalis infected clinical cases treated with buparvaquone(at 2.5mg/kg.b.wt I/M) was the feedback obtained from field veterinarians and the cattle owners.Conclusion:The present investigation represents the first report of occurrence of T. orientalis in cattle of Assam with involvement of pathogenic Ikeda strain in clinical outbreaks and its possible natural transmission by R (B). microplus through the transovarian mode.

Aim: This research work is aimed to find out the prevalence of haemoparasitic infections in different categories of dogs.Materials and Methods: Out of 2104 dogs registered in the Teaching Veterinary Clinical Complex of the College of Veterinary Science, Khanapara, Guwahati during January 2009 to December 2010, blood of 424 cases suspected for haemoparasites on the basis of clinical history were microscopically examined in wet blood film and giemsa stained blood smears. Results:The prevalence was 57.31% in the hospital population comprising pet (58.03%) and working (54.54%) dogs and 63.64% in stray dog population. A total of 7 species viz. Babesia gibsoni (47.16%), Ehrlichia (Anaplasma) platys (8.49%), Dirofilaria immitis (2.83%), Ehrlichia canis (2.12%), Babesia canis (1.41%), Hepatozoon canis (1.41%) and Ehrlichia ewingii (0.47%) in single or mixed infections were recorded. B. gibsoni was found to be most predominant haemoprotozoan species. However, B. canis, the large form of Babesia was detected in very few dogs. Similarly, inclusion of E. platys inside blood platelets, although rare in occurrence, was more easily detectable than that of E. canis inside the monocytes and lymphocytes. Infection with D. immitis in pet dogs (2.38%) was comparatively lower than in working dogs (4.54%) and found in single and mixed infections with B. gibsoni, B. canis and E. platys. Hepatozoon canis was recorded in 6 hospital dogs either in single or mixed infection with B. gibsoni and E. platys. Six species of haemoparasites namely B. gibsoni (47.72%), D. immitis (27.27%), E. platys (4.54%), E. canis (2.27%), E. ewingii (2.27%) and H. canis (2.27%) were detected in blood of stray dogs. Trypanosoma evansi as recorded in dogs from other parts of the country was not detected in this study. Conclusion:Present findings led to a significant conclusion that Assam and adjoining states of North East region of India are highly enzootic for the vector borne haemoparasites of dog.