Canine Visceral Leishmaniasis in Kerman, Southeast of Iran: A Seroepidemiological, Histopathological and Molecular Study

Abstract

Canine visceral leishmaniasis (CVL) is a systemic disease with a high mortality rate, caused by a diphasic protozoan parasite, Leishmania infantum/chagasi in the world. The objective of the present study was to determine the presence of CVL in the city and suburbs of Kerman, using a range of serological, histopathological and molecular methods. Blood samples were taken from 80 clinically symptomatic stray dogs All the collected blood samples were tested by direct agglutination test (DAT) to detect the anti-Leishmania antibodies in dogs, using a cut-off value of ≥1:320. Pathological specimens including spleen, liver and lymph nodes were prepared for paraffin blocks, sectioning, staining and final microscopic examination in the pathology laboratory. PCR amplification of kDNA from 9 samples of DAT positive stray dogs was studied. The anti-Leishmania antibody was detected in 9 dogs (11.25 %) of the total 80 studied dogs. No significant difference was found between VL infection and gender. In contrast, there was a significant difference between seropositivity and age (P<0.05). Pathological samples showed changes including hyperplasia of infected macrophages and inflammatory cells that occupied sinusoids and splenic cords. Among the samples which was characterized by PCR, only one specimen revealed to be mixed infection between L. infantum and L. tropica. The results revealed a high prevalence of L. infantum infection in stray dogs in Kerman. This kind of information is needed for implementation of future control programs.

Headnote

Received 11 Feb 2014

Accepted 18 Jun 2014

Keywords:

Seroepidemiology,

Histopathology,

Canine visceral leishmaniasis,

Molecular identification,

Iran

Abstract

Background: Canine visceral leishmaniasis (CVL) is a systemic disease with a high mortality rate, caused by a diphasic protozoan parasite, Leishmania infantum/chagasi in the world. The objective of the present study was to determine the presence of CVL in the city and suburbs of Kerman, using a range of serological, histopathological and molecular methods.

Methods: Blood samples were taken from 80 clinically symptomatic stray dogs All the collected blood samples were tested by direct agglutination test (DAT) to detect the anti-Leishmania antibodies in dogs, using a cut-off value of ≥1:320. Pathological specimens including spleen, liver and lymph nodes were prepared for paraffin blocks, sectioning, staining and final microscopic examination in the pathology laboratory. PCR amplification of kDNA from 9 samples of DAT positive stray dogs was studied.

Results: The anti-Leishmania antibody was detected in 9 dogs (11.25 %) of the total 80 studied dogs. No significant difference was found between VL infection and gender. In contrast, there was a significant difference between seropositivity and age (P<0.05). Pathological samples showed changes including hyperplasia of infected macrophages and inflammatory cells that occupied sinusoids and splenic cords. Among the samples which was characterized by PCR, only one specimen revealed to be mixed infection between L. infantum and L. tropica.

Conclusion: The results revealed a high prevalence of L. infantum infection in stray dogs in Kerman. This kind of information is needed for implementation of future control programs.

Introduction

Leishmania infantum is the main etio- logical agent of canine visceral leishmaniasis (CVL) around the Mediterranean Basin including Iran (1). CVL due to L. infantum, is transmitted by different species of Phlebotomus sand flies which is con- sidered one of the most important canine pro- tozoal diseases of zoonotic concern (2). Dog has also been shown to carry L. infantum, main causative agent of human visceral leish- maniasis (HVL) in Iran (3). Eventually, VL results in death if left untreated. The majority of leishmaniasis deaths go unrecognized, and even with treatment access, VL may result in case-fatality rates of 10-20% (4-7).

National experts provided leishmaniasis case data for the last 5 years and information regarding treatment and control in their re- spective countries and a comprehensive litera- ture review was conducted covering publi- cations on leishmaniasis in 98 countries and territories (8). The prevalence and incidence of canine infection are important parameters and the estimation of which depend on the reliable identification of infected dogs (9). In humans, symptoms of the disease include fever, spleen and liver enlargement, immunosuppression, anemia and weight loss (10). VL is the most severe form of leishmaniasis in the world, which is responsible for approximately 500,000 cases each year, worldwide (11). The parasite migrates to the reticuloendothelial system (RES) including liver, spleen and bone marrow (12).

VL is endemic in various parts of Iran in- cluding Ardabil, East Azerbaijan, Fars and to some extent sporadic in Boushehr, Kerman and recently in Qom and northern Khorasan province. Sporadic cases of VL are also re- ported from other parts of the country (7). CVL is not only a veterinary problem but is also a serious public health concern. Serologic testing can identify exposure to the parasite. Rapid detection of CVL is highly important for controlling HVL. Serological methods are highly sensitive and fairly non-invasive and they are appropriate to be used in field condi- tions (13). In this study, direct agglutination test (DAT) was used as a sero-diagnostic tool because it is a simple and valid test and does not require sophisticated equipments (3, 14,15). In the last decade, the use of polymer- ase chain reaction (PCR) for detection of Leishmania DNA was shown to be highly sen- sitive and specific. A variety of canine tissues, including bone marrow, spleen, lymph nodes, skin, and conjunctival biopsy specimens, have been used for identification (16).

The objective of this study was to determine the seroepidemiological, histopathological and molecular identity of CVL in the city and sub- urbs of Kerman in southeastern Iran. The rea- son for selection of this place was due to the previous reported cases of VL from this area (17). This kind of information is essential for planning an effective future control strategy and to identify the animal reservoir hosts of the disease for implementation of control pro- grams.

Material and Methods

Study area

This study was carried out in the city and suburbs of Kerman. This province is located in southeastern Iran with arid and semiarid climate which is the largest province of Iran and constitutes 11% of the total area of the country. The province has a population of about 2.5 million.

Sampling

The survey was carried out from January 2012 to April 2013. Blood samples were taken from 80 clinically symptomatic stray dogs in the city and suburbs of Kerman. The authori- zation for shooting dogs and necropsy was obtained from the Kerman municipality office. In fact, the phenomenon of stray dogs and its related public health concern are respon- sibilities of the local municipalities in the country. A considerable number of dogs more frequently in the winter will be sacrificed each year by shooting and their corpse will be bur- ied in a defined area.

A questionnaire was completed for each dog, recording sex, age and any clinical manifesta- tions of VL including skin lesions, alopecia, nose hyperkeratosis and cachexia. Five ml pe- ripheral blood samples were taken from the cephalic vein of each dog and transported to the Leishmaniasis Research Center at School of Medicine in Kerman University of Medical Sci- ences. Blood samples were centrifuged at 3000 rpm for 3-5 min and the separated sera were stored at -20°C for serological examination.

Serological test

The sera were tested by DAT. An initial screening DAT was performed at dilutions of 1:80 and 1:320. Samples with titers of 1:320 in dogs were further diluted to endpoint titer of 1:20480 in dog's samples. Control wells (anti- gen only on each plate) with confirmed nega- tive and positive control sera were tested in each plate daily. The cut- off value was de- fined as the highest dilution at which aggluti- nation was visible, as a blue mat, compared with negative control wells, which had clear blue dots. The positive standard control serum was prepared from dogs with L. infantum in- fection in an endemic area and confirmed by parasitological methods. Quantitative results obtained with DAT are expressed as an anti- body titer, the reciprocal of the highest dilu- tion at which agglutination (large diffuse blue mats) was visible after 12-18 h incubation at room temperature (18, 19). The cut-off was based on previous studies (3, 20-22). The anti- Leishmania antibody titers at ≥1:320 were con- sidered positive for L. infantum infection in dogs.

Histopathological study

At necropsy, suspected dogs were inspected and evaluated for enlargement of reticuloen- dotelial system (RES) organs such as spleen, liver and lymph nodes. The RES organs were transported to the pathology laboratory at School of Medicine in Kerman University of Medical Sciences. Tissue slices of 1cm3 were preserved in 10% formalin and embedded in paraffin. Four μm thick tissue sections were stained with routine Haematoxylin and Eosin (H&E) for histopathological study.

Molecular identification

DNA extraction

DNA from tissues of samples which were positive for DAT test extracted by using DNA extraction kit for cells and tissues (Roche, Germany, Product No. 11814770001) and quantified with a spectrophotometer (Nano Drop-2000c; Thermo Scientific).

Amplification

Kinetoplastic minicircle DNA was amplified with specific primers, upstream 5'-TCG- CAGAACGCCCCTACC-3' and downstream 5'-AGGGGTTGGTGTAAAATAGGC-3' according to the method described by Mahboudi et al. (23). The 25 µl amplification reaction was carried out with 12.5 µl master mix (Ampliqon, Product Number, 160301) and 50 ng/reaction of DNA extract and 1 µl of 10 picoM of each primers. The mixture was incubated in a thermo cycler (Felx Cycler, An- alyticgena) for 5 min at 94°C followed by 16 cycles, each was consisting of 30s at 94°C, 30s at 72°C, and 30 s at 72°C. Annealing temper- ature was decreased to 0.5 degree in each cycle. Then, new 15 cycles were consisted of 30s at 94°C, 30s at 72°C, and 30s at 72°C. Extension was continued for a further 10 min and 6 µl of the amplification reaction product was visual- ized in 2% agarose gel and stained with ethidi- um bromide.

Data analysis

Analyses were performed using SPSS soft- ware ver. 15 and positive DAT test was set as an outcome variable. Sex and age were used as independent variables. A primary screening was performed using two K contingency table (cross-tab) of exposure variables by chi-square and fisher exact tests and P<0.05 was defined significant.

Results

Serological examination

In this study, anti-Leishmania antibodies at the titers of ≥1:320 were detected in 9 (11.25 %) out of 80 studied dogs (Table 1). No significant difference was found between VL infection and gender. In contrast, there was a significant difference between seroposi- tivity and age (P<0.05).

Histopathological finding

Samples prepared from spleen, liver, lymph nodes and skin of 9 sero-positive dogs showed the following pathological changes: prolifera- tion of amastigote laden macrophages (leish- man bodies) (Fig.1). Focal periadnexal and perivascular lymphocytic infiltration of the skin (dermatitis) (Fig. 2), relative lymphoid hyperplasia of the spleen and lymph nodes, inflammatory cell infiltration and vasculitis in various organs.

Molecular study

PCR amplification of kDNA from samples of DAT positive stray dogs was studied. Among the samples only one dog was identi- fied as positive for L. infantum, alt- hough molecular study revealed mixed infec- tion between L. infantum and L. tropica with corresponding electrophoretic bands. (Fig.3). Based on expectation pattern on bands of Leishmania species, L. infantum with a band at 650 bp and L. tropica with a band at 830 bp could be differentiated at species level (23). In this study, the ampliqon reaction from positive sample shows both bands (Fig. 3).

Discussion

Visceral leishmaniasis remains a significant disease with high mortality rate (11). This dis- ease is endemic in some parts of Iran includ- ing Ardabil, Fars, East Azerbaijan and to some extent sporadic in Bushehr, North Khorasan, Kerman and Qum provinces (13, 24), and sporadic foci of the disease are also reported from other parts of the country (7). Based on these results, seroprevalence of CVL in Ker- man was determined to be 11.25% using the cut-off value of ≥1:320. The seropositivity rate was lower than those found by Gavgani et al (25), and Mohebali et al (3), who reported 21.6% and 18.2%, respectively, seroprevalence in dogs from northwest of Iran.

Dogs and wild canines are the animal reser- voir hosts for L. infantum in both Old and New Worlds (26). Determination of the prevalence of canine Leishmania infection is necessary to define and plan control measures for zoonotic visceral leishmaniasis (27). Ac- cording to the previous studies (20, 28, 29) the performance of DAT for detection of L. infan- tum infection in humans and dogs was desira- ble. Therefore, we used DAT to determine seroprevalence of canine Leishmania infection. In our study, no statistical difference was found between gender and seropositivity. This finding is consistent with those reported in Portugal (30), Greece (31) and Iran (32, 33).

In our study 5% of the sero-positive cases (≥1:320) were male and 6.25% female dogs. No significant difference was observed among male and female animals. In the current study, we found canine Leishmania infection mostly in older dogs (≥3 years of age). In contrast, there was a significant difference regarding the age and seropositivity. Statistical analysis re- vealed a greater seroprevalence rate in the groups of older dogs, suggesting that the probability of exposure to the bite of sand flies infected with L. infantum enhanced with increasing age of dogs (30, 34).

The pathology of CVL shows that resistant animals exhibit low parasite burden and re- duced inflammatory responses, making it diffi- cult to find parasites in the mononuclear phagocytic cells of RES organs (35, 36). Ac- cording to the study of Sanchez et al. (37), or- ganic response in CVL varies from individual to individual and within the same individual, with a strong evidence of being organ-specific. The pathological finding of the present study showed hyperplasia of macrophages, inflam- mations, vasculitis in various organs and der- matitis by focal lesions.

Molecular study revealed mixed infection of L. infantum and L. tropica in one dog with their relative specific electrophoresis bands. Ma- deira et al (38) reported the first case of co- infection with Leishmania (Viannia) braziliensis and Leishmania (Leishmania) chagasi in a natu- rally infected dog from Rio de Janeiro, Bra- zil. Bakhshi et al. (39) reported that in their molecular detection on sand fly specimens against Leishmania parasites, two of their posi- tive samples revealed mixed infection of both L. turanica and L. gerbilli. Although some stud- ies report mixed infection with other species, there is no report on mixed infection between L. tropica and L. infantum in literature. To our knowledge this is the first documentation re- port indicating the concurrent infection be- tween L.tropica and L. infantum in dog. The re- sults of the present study indicated a high prevalence of L. infantum infection in stray dogs in Kerman, especially in dogs older than 3 years of age, indicating a high public health concern due to their contribution to the trans- mission of infection to humans by sand fly vectors. Therefore, it is necessary to prevent CVL by controlling animal reservoirs and sand fly vectors and taking steps to avoid exposure to sandflies bites.

Conclusion

This finding revealed a high prevalence of L. infantum infection in stray dogs in the city and suburbs of Kerman. Mixed infection with L. infantum and L. tropica could be occurred. This kind of information is required for implemen- tation of future control programs.

Acknowledgements

This study was supported by the Vice-Chan- cellor for Research, Kerman University of Medical Sciences (project no. 91.56), Kerman, Iran. We thank Prof. Dabiri for his help in performance of pathological examinations at Dept. of Pathology, Kerman University of Medical Sciences as well as Dr. Behnaz Ak- houndi for preparation of DAT antigen in leishmaniasis Lab. in the School of Public Health, Tehran University of Medical Sciences. The authors declare that there is no conflict of interests.

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