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A study on canine dirofilariasis in selected areas of Sri Lanka

BMC Research Notes volume 15, Article number: 137 (2022) Cite this article

Abstract

Objectives

Canine dirofilariasis is a mosquito borne zoonotic filarial parasitic disease caused by Dirofilaria species. In Sri Lanka, human dirofilariasis is endemic and well documented. Even though canine dirofilariasis is an established infection among dog populations in Sri Lanka, the prevalence and risk factors were not documented in Kanthale divisional secretariat, Eastern Province of Sri Lanka. Therefore, the main objective of this study is to determine the prevalence of dirofilariasis and to identify the exposure-related risk factors in dogs using an interviewer administered questionnaire in Kanthale divisional secretariat.

Results

Out of 162 blood samples collected from dogs, 47.5% (n = 77/162) were positive for the presence of microfilariae by direct smear. Of 162 samples 58.6% (n = 95/162) were molecularly identified as D. repens. Species-specific primer pair DIR3/DIR4 that amplified 5S rRNA was used. The current study observed a significant association between mongrels and canine dirofilariasis (p = 0.049), where 61.3% (n = 95) out of 155 mongrels showed PCR positivity. This study showed no significant association between the occurrence of dirofilariasis and the age, sex, rearing method, presence or absence of skin rash, and stray or domestic dogs. Dirofilaria immitis was not identified in direct smear test and PCR.

Introduction

Canine dirofilariasis is a mosquito borne zoonotic filarial parasitic disease caused by Dirofilaria species. Dirofilaria immiitis and autochtonous Dirofilaria repens are the etiological agents responsible for pulmonary dirofilariasis and subcutaneous dirofilarisis, respectively, in dogs [1]. Dirofilaria repens infection in dogs is limited to Asia, Africa and Europe [2]. Higher prevalence of D. repens is reported in Spain (84.6%) [3], France (35.2%) [4], and Greece (30%) [3]. Prevalence of D. repens reported in Sri Lanka ranged between 30% and 60% [5,6,7]. Dirofilaria immitis was not reported in Sri Lanka yet.

Age, sex, breed, climate, size, provenance, management system, and pollution source, can be potential risk factors for canine dirofilariasis [1, 8]. The common clinical presentation of D. repens infection includes subcutaneous nodules, subconjuctival lesions and meningo encephalitis in dogs [9]. Progression of D. repens in dogs is mainly asymptomatic causing silent spread of infection among dogs [8]. Thus, eventually increases human infection [10]. Human acts as an accidental host for this infection [11]. In humans, it presents as localized nodules in skin, sub conjunctival, or peri-orbital tissues [6, 12].

Even though this infection is known for a period of 80 years, only few studies have been carried out on canine dirofilariasis [6]. A study carried out in Sri Lanka has shown an increased dog population (ratio of 1:4.6 dog to human population) [13]. Therefore, this study was designed to detect the prevalence of canine dirofilariasis and to identify the risk factors of Dirofilaria infection in dogs in Kanthale divisional secretariat in Trincomalee district in Sri Lanka.

Main text

Method

Study area

The study was conducted in Kanthale divisional secretariat, Trincomalee district, located in the Eastern Province of Sri Lanka. Blood samples were collected from the dogs attending Anti-rabies vaccination program from four village officers (VO) divisions. The VO divisions were randomly selected. Dog population was determined according to the Department of Animal Production and Health calculation with a dog to human population ratio of 1:6 and calculated dog population in the study area was 11,000 and confidence interval (CI) was 95%.

Sample collection

A total of 162 samples were collected from stray and domestic dogs, which were brought to the anti-rabies vaccination programs in the study area. All dogs aged above 6 months were included in this study. Blood samples were collected by the veterinary surgeon from the cephalic vein using sterile disposable syringe into EDTA tubes under strict aseptic conditions. The samples were stored at 4 ºC until dispatched to the Department of Parasitology, Faculty of Medicine, and University of Peradeniya. Demographical data and noduleswere recorded using an interviewer administered questionnaire. The questionnaires were filled by the author.

Detection of microfilariae (mf)

Thick blood smear

Thick blood smear was carried out according to the method described by Phuakrod et al. [14]. The smears were incubated at 37 °C overnight. The samples were hemolyzed with clean water and fixed with methanol for 30 s and fixed samples were covered with 5–10 drops of Giemsa stain (1:10 dilution) for 10–15 min and excess stain was washed with running tap water and air dried. The stained smears were observed under light microscope in higher magnification (× 100 objective lens). Microfilariae were identified based on the morphological key published by Mallawarachchi et al. [15] and Liotta et al. [16].

DNA extraction

Genomic DNA was extracted from all blood samples using commercially available DNA extraction kit (Gene JET Genomic DNA Purification Kit) according to the manufacturer’s guidelines.

Amplification of Dirofilaria species

PCR was done for all 162 samples using D. immitis and D. repens specific primers separately (Table 1). Tenfold dilution of extracted DNA was used to carry out PCR to identify 13 mf positive but PCR negative samples.

Table 1 Primers used for Dirofilaria species identification
Full size table

Amplification for D. immitis was carried out in 25 μl reaction mixture composed of 2.5 μl of PCR buffer, 2 μl of 2.5 mM dNTP, 1.5 μl of forward and reverse primer (10 pmol), 0.25 μl of Taq DNA polymerase, 4 μl of 25 mM MgCl2, 5 μl of template DNA and 8.25 μl of nuclease free water. The temperature profile was initial denaturation at 94 ºC for 2 min followed by 32 cycles each at 94 ºC for 30 s, the annealing 60 ºC for 30 s, 72 ºC for 1 min with final extension at 72 ºC for 5 min [19]. The temperature profile for D. repens amplification was initial denaturation at 94 ºC for 3 min followed by 40 cycles each at 94 ºC for 30 s, the annealing at 55 ºC for 30 s, 72 ºC for 1 min and the final extension was at 72 ºC for 5 min [20]. Amplified products were analyzed by agarose gel electrophoresis. All raw gel images are given in Additional file 1.

Statistical analysis

Descriptive statistical analysis was used to identify the relationship between the occurrence of canine dirofilariasis and breed, rearing method, stray vs. domestic, skin rash, age and gender. The statistical significance of relationships among selected variables and mf positivity was determined using Chi square test and the Fishers exact test. Statistical analysis was carried out by GraphPad Prism 9.1.0 (221) [21]. p < 0.05 was considered statistically significant.

Results

Demography of study population

A total of 162 blood samples were collected from four VO division; Sooriyapura (22, 14%), Wanela (28, 17%), Agbopura (62, 38%), and Thalgaswewa (50, 31%). Of the total of 162 samples the majority (n = 103, 64.6%) were males. Large proportion (n = 140, 86.4%) of the study group were aged above one year. Of the study population 17 (10.5%) were stray dogs and 145 (89.5%) were domestic dogs. Majority were reared outdoor (n = 127, 78.4%). Large number of dogs in the study population were mongrel (n = 155, 95.7%) (Table 2).

Table 2 PCR positivity by demographic and other factors of the study population
Full size table

Microfilariae (mf) positivity

Examination of direct smear revealed 77 (47.5%) unsheathed mf out of 162 samples. Sixty-four mf samples had the morphological features of D. repens with cephalic end obtuse, two of cephalic nuclei, sharp tail, and a filiform with an umbrella handing, with a width ranging from 6 to 8 μm and length ranging from 310 to 355 μm. Rest of the mf (n = 13/77) were slightly different, where they had a blunt anterior end and unsheathed posteriror ending with button hook.

Molecular identification

Sixty-four microfilariae samples with morphological features of D. repens and 31 samples out of 85 smear negative samples were positive for D. repens species-specific primers, where the rest of the 13 mf samples were PCR negative for both onefold and tenfold dilution (Fig. 1). None were positive for D. immitis species-specific primers.

Fig. 1
figure 1

Amplification of D. repens 5s rRNA gene using species-specific primers DIR 3 and DIR 4. M molecular marker with 100 bp DNA ladder, PC positive control, NC negative control. Samples 1–18, 21–33, 35–36, 38–44, 48, 50–55, 57–63, 66–72, 74–76, 80, 82–84, 86, 89–90, 96–98, 105, 107–114, 115, 117–119, 122–127, 139–140 were PCR positive

Full size image

Factors associated with dirofilaria infection

All PCR positives were considered D. repens infected dogs (n = 95, 58.6%). Compared to female dogs (30, 50.8%), males (65, 63.1%) showed higher D. repens infection. Higher percentage of stray (n = 17/17, 100.0%) were infected with Dirofilaria infection. Dogs aged more than 1 years showed high rate of infection (n = 85/140, 55.7%) in comparison to dogs aged above 6 months to less than 1 year (n = 10/22, 45.4%). With regard to type of rearing, outdoor reared dogs were highly infected (Table 2). Out of 95 Dirofilaria positive 40 (48.6%) were presented with skin rashes. There was a statistically significant difference (p = 0.049) of PCR positivity and the breed of the dog, showing high percentage (61.3%) of PCR positivity in mongrels (Table 2).

Discussion

Dirofilariasis is an established infection among dogs in Sri Lanka and the main causative parasite is known to be D. repens [6]. Microfilaremic dogs present in an area can increase the risk of transmitting the infection to humans through competent mosquito vectors [11]. Studies conducted several decades ago revealed 30–60% prevalence of infection in dogs in some areas of Sri Lanka [6]. In the present study, the overall prevalence of 58.6% of canine dirofilariasis by D. repens was recorded in Kanthale divisional secretariat which includes 4 VO divisions.

Similarly, previous Sri Lankan studies reported prevalence between 44% and 54.4% in Western and North Western Provinces [6]. In contrast to present study low prevalence has been reported in India (26.5%), USA and Canada (12%) [1, 22]. Current study did not identify D. immitis. The only case of D. immitis that was reported in the country was in a dog imported from China [23].

In this study, majority of the infected dogs were males (63.1%) though it is not statistically significant (p > 0.05). Several studies have documented the similar findings [24, 25]. The current study identified a significant association of mongrels with canine dirofilariasis (p = 0.049), similar to the previous studies; that of mongrels being more prone to D. repens infection [15, 25].

The present study failed to identify statistically significant difference between age groups and the infection. But, the accumulation of infection transmission increases with age [26]. However, the majority of infected dogs (n = 85/95, 89.5%) were older than one year. Similar results were documented in several other studies [24,25,26,27,28,29]. Even though the mode of rearing and dirofilarial infection did not show a significant association, the current study observed high rate of infection in the outdoor reared dogs. A previous study has showed a significantly high infection in outdoor reared dogs [29]. In contrast to a previous study [30], the presence of skin rash with dirofilariasis infection did not show any significant association.

The results did not show any significant association with dogs being stray or domestic. The majority of the dogs having the infection were stray dogs (100.0%). Almost all the stray dogs had not been treated with anti-parasitic drugs before and this may have been the reason for the high occurrence of dirofilariasis among stray dogs. Further, studies are required to identify the factors affecting canine dirofilariasis among domestic dogs in Sri Lanka.

Out of the 77 (47.5%) microfilariae positive samples, 64 (83.1%) and 31 out of 85 smear negative samples were identified as D. repens by PCR. Thirteen microfilariae positive samples did not belong either to D. repens or D. immitis. There are several other Dirofilaria species causing canine dirofilariasis [30, 31]. Therefore, further studies are needed to identify these 13 mf positive samples. In Sri Lanka, the dirofilariasis infection in humans is on the rise [32, 33] and the local studies have identified lack of public awareness on this illness [34, 35].

In conclusion this study showed high prevalence of canine dirofilariasis due D. repens among dogs and mf of D. immitis were not detected in Kanthale division in consistent with previous reports. Further, this study identified the breed of the dog as a significant risk factor for dirofilarial infection. The current study recommends to enhance prophylaxis to prevent Dirofilaria species infection, treatment of infective dogs, increased public awareness, responsible dog ownership, and vector control programs in Sri Lanka in order to reduce the human and canine exposure to this zoonotic infection in Sri Lanka. Further studies are needed to further characterize dirofilarial species.

Limitations

The sample size was limited and could not use the universal primers for Cox 1 or 12S. Sequencing was not able to carryout to identify 13 unknown microfilariae.

Availability of data and materials

The datasets used and/or analyzed during the current study are available within the manuscript and Additional file.

Abbreviations

PCR:

Polymerase chain reaction

5S rRNA:

Ribosomal 5S ribonucleic acid

VO:

Village officers

CI:

Confidence interval

DNA:

Deoxyribonucleic acid

ITS:

Internal transcribed spacer

DNTP::

Deoxyribonucleotide triphosphate

Bp:

Base pair

MF:

Microfilariae

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Acknowledgements

RD is thankful to Dr. M.KU.T. Amarasiri, veterinary surgeon, Kanthale. The authors would like to thank Mr. M. Sanger, Mrs. D.R.L.N. Bandara, Mr. W.M.H.G. Wickramanayaka, S.G. Wathsala, and Mrs. H.M.L.M.K Herath for their generous support and assistant during the sample processing and laboratory analysis.

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  1. Animal Quarantine Office, Bandaranayake International Airport, Katunayake, Sri Lanka

    Randima Dasanayake

  2. Department of Parasitology, Faculty of Medicine, University of Peradeniya, Peradeniya, Sri Lanka

    Thivya Balendran, Dhilma Atapattu & Devika Iddawela

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  1. Randima Dasanayake
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Contributions

RD participated in data collection, methodology, formal analysis, investigation and writing original draft. DI and DA participated in conceptualization, project administration, supervision and writing, review and editing the manuscript. TB participated in writing, review and editing the manuscript. All the authors read and approved the final manuscript.

Corresponding author

Correspondence to Devika Iddawela.

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Ethical approval and consent to participate

All the procedures and the protocols related to the study were approved by the institutional animal ethics committee of Postgraduate Institute of Science (PGIS), University of Peradeniya, Sri Lanka. Informed written consent was obtained from each dog owner before collecting blood samples.

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Not applicable.

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The author declare that they have no competing interests.

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Supplementary Information

Additional file 1.

Original unprocessed gel images.

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Dasanayake, R., Balendran, T., Atapattu, D. et al. A study on canine dirofilariasis in selected areas of Sri Lanka. BMC Res Notes 15, 137 (2022). https://doi.org/10.1186/s13104-022-06024-0

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Keywords

  • Canine dirofilariasis
  • Dirofilaria repens
  • Dirofilaria immitis
  • Mongrels
  • Sri Lanka

BMC Research Notes

ISSN: 1756-0500

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