Next Article in Journal
Green Veterinary Pharmacology Applied to Parasite Control: Evaluation of Punica granatum, Artemisia campestris, Salix caprea Aqueous Macerates against Gastrointestinal Nematodes of Sheep
Previous Article in Journal
In Situ Hybridization of PRRSV-1 Combined with Digital Image Analysis in Lung Tissues of Pigs Challenged with PRRSV-1
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Seroprevalence and Risk Factors Associated with Canine Leishmaniasis in Egypt

by
Abdelfattah Selim
1,*,
Salma Shoulah
1,
Abdelhamed Abdelhady
2,
Abdulaziz Alouffi
3,4,
Yasser Alraey
5 and
Waleed S. Al-Salem
6,7
1
Department of Animal Medicine (Infectious Diseases), College of Veterinary Medicine, Benha University, Toukh 13736, Egypt
2
Department of Parasitology and Animal Diseases, National Research Center, Giza 8655, Egypt
3
King Abdulaziz City for Science and Technology, Riyadh 12354, Saudi Arabia
4
Chair Vaccines Research of Infectious Diseases, King Saud University, Riyadh 11495, Saudi Arabia
5
Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Khalid University, Abha 62529, Saudi Arabia
6
Department of Parasitology, Liverpool School of Tropical Medicine, Liverpool L3 5QA, UK
7
Minister of Environment, Water and Agriculture, Riyadh 11195, Saudi Arabia
*
Author to whom correspondence should be addressed.
Submission received: 21 September 2021 / Revised: 9 October 2021 / Accepted: 13 October 2021 / Published: 15 October 2021

Abstract

:
Background: Canine leishmaniasis (CanL) is caused by Leishmania infantum (L. infantum) that is transmitted by sand fly vectors with dogs acting as the main reservoir. Methods: The present study aimed to determine the seroprevalence of CanL in dogs from Egypt and assessed the associated risk factors. The study was conducted from 2019 to 2020 in five governorates situated in Northern Egypt. Serum samples from 450 asymptomatic dogs were serologically examined by use of enzyme-linked immunosorbent assay (ELISA). Results: Overall, the seroprevalence rate of CanL was 21.3% and the highest rates were observed in Cairo and Giza governorates. The univariable analysis revealed that the seropositivity of CanL was strongly related to the dogs’ ages, length of hair, absence of veterinary care or application of insecticides, and the type of floor of their shelters. The risk factors that were found to be associated with CanL in exposed dogs were: age group 2–4 years old (OR = 12, 95% CI: 1.6–92.3); short hair (OR = 2.07, 95% CI: 1.2–3.6); absence of veterinary care (OR = 2.7, 95% CI: 1.3–5.8); no application of insecticides (OR = 3.09, 95% CI: 1.5–6.5) and their residence in a shelter with an earthen floor (OR = 1.42, 95% CI: 0.7–2.9). Conclusions: Based on the present results, CanL is present in Egyptian dogs and this increases the possibility of transmission by sand fly to humans with whom they have contact. Consequently, an efficient monitoring programme and effective control measures are important to reduce the risk of infection.

1. Introduction

Canine leishmaniasis (CanL) is a neglected zoonotic disease that is caused by Leishmania spp. [1]. Leishmaniasis is a vector-borne disease that is caused by protozoan flagellates. It affects several animal species including humans and is transmitted via bites of the infected female Phlebotomus sand fly [2,3].
The disease is endemic in tropical and temperate regions in 98 countries, and visceral leishmaniasis (VL) is the most fatal and common form in the Mediterranean region [4,5]. Zoonotic leishmaniasis caused by Leishmania infantum (L. infantum) is endemic in most of the Middle East, North Africa and the Mediterranean, including Egypt [6].
Domestic dogs are the main reservoir for leishmaniasis and can become infected at any age [7]. The clinical features of CanL vary from asymptomatic through self-limiting to severe viscero-cutaneous infection [8,9]. However, asymptomatic dogs can develop clinical signs during their lives, while L. infantum can spread unnoticed within the dog population and remain as a source of infection for sand flies, which transmit the parasite to other hosts [10]. Hence, early diagnosis of these asymptomatic carriers is critical for disease control in both endemic and non-endemic countries [11].
Leishmaniasis was reported in Egypt over 4000 years ago, in ancient Egyptian mummies. In past decades, L. major has been detected in dogs from Egypt [12] and antibodies against Leishmania spp. were detected in dogs from Egypt by Morsy, et al. [13]. In addition, there have been several reports from the mid to late 20th century of sporadic cases of cutaneous leishmaniasis (CL) and VL among Egyptian people, particularly those in the Suez Canal, Sinai and Agamy regions in Alexandria [4,14,15,16,17,18]. Recently, the presence of L. tropica in humans and L. infantum in dogs has been proven [1].
Serological examination is a useful tool to detect specific antibodies and to determine the spread of the disease, because a large proportion of dogs are asymptomatic [19]. Enzyme-linked immunosorbent assay (ELISA) and indirect fluorescent antibody tests (IFAT) are the most widely used serological methods [20]. ELISA shows potential as a sensitive tool for mass screening in epidemiological studies and is suited to field conditions [21,22].
In Egypt, the prevalence of L. infantum in dogs is uncertain, especially with changes of climatic conditions, dog populations and distributions of sand flies, all of which affect the epidemiology of the disease.
To fill this knowledge gap, the present study aimed to determine the seroprevalence of CanL and the risk factors that were associated with infection among dogs in some governorates in Northern Egypt.

2. Materials and Methods

2.1. Ethics Statement

All procedures involving the handling and collection of samples from dogs used in this study were approved by the ethical committee for Animal Experiment of Benha University and informed consent was obtained from owners. All methods regarding animals and human participant in the study were performed in accordance with the relevant guidelines and regulations and were approved by ethical committee of faculty of veterinary medicine, Benha University.

2.2. Study Area

The study was conducted during the period from June 2019 to May 2020 in five governorates located in Northern Egypt. These governorates were Cairo (30.0444° N, 31.2357° E), Giza (30.0131° N, 31.2089° E), Qalyubia (30.3292° N, 31.2168° E), Kafr ElSheikh (31.1107° N, 30.9388° E) and Gharbia (30.8754° N, 31.0335° E), Figure 1. The climate of the selected areas is Mediterranean with dry, hot summers and wet winters.

2.3. Sampling and Data Collection

The required samples size was determined using Danial′s formula as follows:
n = z 2 p ( 1 P ) d 2
where n is number of appropriate sample, z is level of confidence (z value is 1.96 if 95% confidence level is conventional), P is prevalence level which was 10% based on previously study of [12] and e is precision whereas this study’s precision (e) was 5% based on [23]. According to dog population in each examined area and based on Danial’s formula, the estimated sample size from each area was 95, 115, 75, 80 and 85 from Cairo, Giza, Qalyubia, Kafr ElSheikh and Gharbia governorates.
During June 2019 to May 2020, a total of 450 blood samples (2 mL) were collected from the saphenous or cephalic veins of dogs that had been admitted to veterinary clinics distributed across the five governorates. Serum samples were separated by centrifugation at 3500× g for 10 min and preserved at −20 ℃ for serological examination. In addition, the data for each dog were gathered when the samples were collected. These data included location of the dog, its age, sex and hair length. Additionally, owners were questioned regarding the veterinary care they supplied to the dog, whether any insecticides had been applied to the animals against sand flies and the type of floor on which they slept.

2.4. Statistical Analysis

The study data were analysed through use of the statistical package for the social sciences (SPSS) software (ver. 24.0, IBM, Endicott, NY, USA). A chi-square test was applied to compare seropositivity to each variable for L. infantum and the results were considered significant if p was ≤0.05. Univariate logistic regression was performed to determine any association between the seropositivity of exposed dogs for L. infantum and variables of location (five governorates), age (6–12 months, 1–2 years, 2–4 years, 4–6 years or >6 years old), sex (male or female), hair length (short or long), floor of shelter (paved or soil), level of veterinary care and whether or not insecticide had been applied. The variables with p ≤ 0.2 were included in a multivariable logistic model to determine risk factors, odds ratios (ORs) and confidence intervals (CIs) for each significant variable. The Hosmer–Lemeshow goodness-of-fit test was used to determine the fit of the multivariable logistic regression model.

3. Results

A total of 450 blood samples were collected from asymptomatic dogs that were distributed across five governorates of Northern Egypt. In this study, antibodies against L. infantum were detected in 96 (21.3%) of 450 examined dogs. In general, there were significant differences (p ≤ 0.05) between the different localities that were visited in the study. The seroprevalence rate ranged between 17.6% and 28.4%. The governorates of Cairo (28.4%) and Giza (21.7%) showed the highest rates of infection, Table 1.
According to univariate analysis, the seroprevalence rate increased significantly with exposed dogs in the >2–4-year age group that were most likely to be infected. However, no association (p > 0.05) was found between sex and CanL infection.
A further analysis revealed that the seropositive rate was higher among German Shepherd (18.2%, 95% CI: 13.2–24.7) and rottweiler (27%, 95% CI: 19.3–36.4) vs another breed and in short-haired dogs (25%, 95% CI: 20.3–30.4) was higher than that in long-haired dogs, particularly among those raised in earthen-floor shelters (36.4%, 95% CI: 28.5–45). Likewise, the seroprevalence of L. infantum was strongly associated with lack of veterinary care (33.7%, 95% CI: 27–40.9) and with no insecticide having been applied (35.6%, 95% CI: 28.7–43.1), Table 1.
Application of a multivariate logistical regression model identified age, hair length, veterinary care, application of insecticides and life in a shelter with earthen floor as definitive predictors of L. infantum infection in exposed dogs. According to the multivariate model, the risk of infection increased in middle age, peaking in dogs aged 2–4 years old (OR = 12, 95% CI: 1.6–92.3), male dogs (OR = 1.93, 95% CI: 1.1–3.3) German Shepherd breed (OR = 1.59, 95% CI: 0.9–2.9) and in short-haired dogs (OR = 2.07, 95% CI: 1.2–3.6). Moreover, an absence of veterinary care (OR = 2.7, 95% CI: 1.3–5.8) or no application of insecticides (OR = 3.09, 95% CI: 1.5–6.5) were associated with higher risk of seropositivity. Regarding the floor of the shelter, dogs that lived in earthen-floored shelters seemed to be at higher risk of infection (OR = 1.42, 95% CI: 0.7–2.9), Table 2.

4. Discussion

CanL caused by L. infantum is an emerging parasitic disease in the Mediterranean region, including Egypt. Dogs form the main reservoir and remain asymptomatic for long periods of their lives, so are considered to be a source of infection for other hosts. Until now, data on CanL in Egypt are fragmented and scarce. This first survey presents a picture of the current epidemiology of CanL in Egypt, including the associated risk factors.
In order to facilitate and improve disease control, sensitive diagnostic tests that may be used in the field are becoming increasingly important. IFATs, ELISAs and direct agglutination tests (DATs) are the most widely used serological tests in CanL screening [14,20]. ELISA is a highly applicable technique that is characterised by high sensitivity, but its specificity depends on the antigen. The specificity and sensitivity of the ELISA test that was employed to detect CanL in this investigation were 99.1% and 98.5%, respectively [21].
Overall, the seroprevalence rate of CanL in exposed dogs was 21.3%, which was in accordance with a previous rate (19.5%) that was reported in the North-Eastern and Pyrenean areas of Spain [19]. In the present study, the seroprevalence rate showed non-significant disparity (p = 0.382) between governorates that were visited for the study. The highest prevalence rates among the governorates were observed in Cairo and Giza. In previous studies performed in Egypt, the prevalence rate of CanL was estimated to be 66.6% by polymerase chain reaction [1] and 10% according to immunochromatography [12].
In other studies, the seroprevalence rate of CanL in exposed dogs as measured by ELISA was estimated to be 15.4% in Iran [21], 10.5% in the west of Iran [24], 5.5% in Palestine [25] and 26.6% in Pakistan [26]. Through use of IFAT, the seroprevalence rate was estimated to be 15.4% in Sardinia, Italy [5] and ranged between 42.9% and 74.3% in Sudan [27].
These disparities could be explained by differences in sampling techniques, serological tests, ecological factors and encroachment on urban areas [2,6,12,28,29,30].
In the present study, dogs older than two years were more likely to become infected. This finding was in accordance with those of previous studies, which confirmed that the risk of infection increased with the age of the dogs [20,31,32]. A popular explanation is that adult dogs remain outside for long periods and that increases their chance of contact with vectors [33,34,35,36], and that the immune response against latent infection in resistant dogs may develop in older dogs [37].
Concerning the sex of the dogs, the males showed higher prevalence rates but without significant differences. This finding is consistent with those of [5,37]. This result may be attributable to the roaming behaviour of males [20] or a host immune response that results from the properties of the testosterone hormone in males [38,39,40,41].
CanL susceptibility is known to vary depending on a variety of host-related factors, such as dog breed. German Shephered was more likely to get an infection than other examined breeds. This result ties well with previous studies [42] wherein certain breeds such as German Shephered and Rottweiler are more susceptible to being infected. It has been suggested that the breed’s relative immunocompetence derived from a cellular, parasite-specific immune response, which is linked to clinical wellness [43].
Interestingly, the risk of being seropositive to L. infantum increased significantly among short-haired dogs, which was also in agreement with other previous studies [44,45]. Indeed, phlebotomine sand flies are known to feed on hairless areas such as the border of the canine muzzle, which is always exposed [44]. Moreover, long hair decreases emissions of CO2 and heat radiation from the host’s body, making it less appealing to vectors [46].
Furthermore, the strong association that was found between the seropositivity of the exposed dogs and the absence of veterinary care or application of insecticides was also as previously reported [5]. This result could be due to the ineffectiveness of control measures such as use of repellent collars or insecticides and the absence of a vaccination protocol against CanL, which is related to a high risk of infection [47].
Another important risk factor that was identified in this study was the material used for the floor of the shelter. The risk of infection with L. infantum increased significantly among dogs that were raised in shelters made of earthen floors in comparison with those that were kept in shelters with paved floors. Since paved floors are easy to clean and covered with less organic matter than soil floors, they offer unfavourable conditions for the spreading of the vector larvae [48,49].

5. Conclusions

The results that were obtained in this study confirm the presence of antibodies against CanL in exposed dogs in some governorates of Northern Egypt and identify the risk factors that are associated with the infection. A high L. infantum seroprevalence rate was observed in older, male, short-haired dogs that were kept in earthen-floor shelters, particularly in the absence of veterinary care or any application of insecticides. Thus, the results show an increased number of asymptomatic dogs that acted as reservoirs for the disease and should be considered a great risk to public health. Consequently, additional information about risk factors and application of efficient control measures is a potential tool to reduce the zoonotic hazard.

Author Contributions

Conceptualization, A.S., A.A. (Abdulaziz Alouffi), Y.A., S.S. and A.A. (Abdelhamed Abdelhady); methodology, A.S.; formal analysis, A.S.; investigation, A.S.; resources, A.A. (Abdelhamed Abdelhady) and Y.A.; data curation, A.A. (Abdelhamed Abdelhady); writing—original draft preparation, A.S.; writing—review and editing, A.S., A.A. (Abdelhamed Abdelhady), Y.A., S.S. and W.S.A.-S.; project administration, A.A. (Abdulaziz Allouffi); funding acquisition, A.A. (Abdelhamed Abdelhady). All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Benha University, and approved by Ethics Committee of Faculty of Veterinary Medicine, Benha Univeristy (BUFVTM).

Informed Consent Statement

Informed consent was obtained from all owner involved in the study.

Data Availability Statement

All data analyzed during this study are included in this published article.

Acknowledgments

The authors also thank the veterinarians for their support and help in providing data and samples collection throughout the study.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Abuowarda, M.; AbuBakr, H.O.; Ismael, E.; Shaalan, M.; Mohamed, M.A.; Aljuaydi, S.H. Epidemiological and genetic characteristics of asymptomatic canine leishmaniasis and implications for human Leishmania infections in Egypt. Zoonoses Public Health 2021, 68, 413–430. [Google Scholar] [CrossRef]
  2. Malmasi, A.; Janitabar, S.; Mohebali, M.; Akhoundi, B.; Maazi, N.; Aramoon, M.; Khorrami, N.; Seifi, H.A. Seroepidemiologic survey of canine visceral leishmaniasis in Tehran and Alborz Provinces of Iran. J. Arthropod Borne Dis. 2014, 8, 132. [Google Scholar] [PubMed]
  3. Cardoso, L.; Rodrigues, M.; Santos, H.; Schoone, G.J.; Carreta, P.; Varejão, E.; van Benthem, B.; Afonso, M.O.; Alves-Pires, C.; Semião-Santos, S.J. Sero-epidemiological study of canine Leishmania spp. infection in the municipality of Alijó (Alto Douro, Portugal). Vet. Parasitol. 2004, 121, 21–32. [Google Scholar] [CrossRef] [PubMed]
  4. Alvar, J.; Vélez, I.D.; Bern, C.; Herrero, M.; Desjeux, P.; Cano, J.; Jannin, J.; Boer, M.D.; Team, W.L.C. Leishmaniasis worldwide and global estimates of its incidence. PLoS ONE 2012, 7, e35671. [Google Scholar] [CrossRef] [PubMed]
  5. Tamponi, C.; Scarpa, F.; Carta, S.; Knoll, S.; Sanna, D.; Gai, C.; Pipia, A.P.; Dessì, G.; Casu, M.; Varcasia, A. Seroprevalence and risk factors associated with Leishmania infantum in dogs in Sardinia (Italy), an endemic island for leishmaniasis. Parasitol. Res. 2020, 120, 289–300. [Google Scholar] [CrossRef]
  6. Tabbabi, A. Review of leishmaniasis in the Middle East and North Africa. Afr. Health Sci. 2019, 19, 1329–1337. [Google Scholar] [CrossRef] [Green Version]
  7. Medkour, H.; Davoust, B.; Dulieu, F.; Maurizi, L.; Lamour, T.; Marié, J.-L.; Mediannikov, O. Potential animal reservoirs (dogs and bats) of human visceral leishmaniasis due to Leishmania infantum in French Guiana. PLoS Negl. Trop. Dis. 2019, 13, e0007456. [Google Scholar] [CrossRef]
  8. Dantas-Torres, F.; de Brito, M.E.F.; Brandão-Filho, S.P. Seroepidemiological survey on canine leishmaniasis among dogs from an urban area of Brazil. Vet. Parasitol. 2006, 140, 54–60. [Google Scholar] [CrossRef]
  9. Najafi, L.; Omidian, M.; Rezaei, Z.; Shahabi, S.; Ghorbani, F.; Arefkhah, N.; Mohebali, M.; Zaraei, Z.; Sarkari, B. Molecular and serological evaluation of zoonotic visceral leishmaniasis in dogs in a rural area of Fars province, southern Iran, as a source of Leishmania infantum infection. Vet. Med. Sci. 2021, 7, 1082–1089. [Google Scholar] [CrossRef]
  10. Solano-Gallego, L.; Miró, G.; Koutinas, A.; Cardoso, L.; Pennisi, M.G.; Ferrer, L.; Bourdeau, P.; Oliva, G.; Baneth, G. LeishVet guidelines for the practical management of canine leishmaniosis. Parasites Vectors 2011, 4, 1–16. [Google Scholar] [CrossRef] [Green Version]
  11. Esteva, L.; Vargas, C.; de León, C.V. The role of asymptomatics and dogs on leishmaniasis propagation. Math. Biosci. 2017, 293, 46–55. [Google Scholar] [CrossRef]
  12. Rosypal, A.C.; Bowman, S.S.; Epps, S.A.; El Behairy, A.; Hilali, M.; Dubey, J. Serological survey of dogs from Egypt for antibodies to Leishmania species. J. Parasitol. 2013, 99, 170–171. [Google Scholar] [CrossRef]
  13. Morsy, T.A.; Schnur, L.F.; Feinsod, F.M.; Salem, A.M.; Wahba, M.M.; El Said, S.M. Natural infections of Leishmania major in domestic dogs from Alexandria, Egypt. Am. J. Trop. Med. Hyg. 1987, 37, 49–52. [Google Scholar] [CrossRef]
  14. Bessat, M.; Okpanma, A.; Shanat, E. Leishmaniasis: Epidemiology, control and future perspectives with special emphasis on Egypt. J. Trop. Dis. 2015, 2, 1–10. [Google Scholar]
  15. Awadalla, H.; Mansour, N.; Mohareb, E. Further characterization of Leishmania isolates from children with visceral infection in Alexandria area, Egypt. Trans. R. Soc. Trop. Med. Hyg. 1987, 81, 915–917. [Google Scholar] [CrossRef]
  16. Faris, R.; Massoud, A.; El Said, S.; Gadallah, M.; Feinsod, F.; Saar, A.; Londner, M.; Rosen, G. The epidemiology of human visceral leishmaniasis in El Agamy (Alexandria Governorate), Egypt: Serosurvey and case/control study. Ann. Trop. Med. Parasitol. 1988, 82, 445–452. [Google Scholar] [CrossRef] [PubMed]
  17. Fryauff, D.J.; Modi, G.B.; Mansour, N.S.; Kreutzer, R.D.; Soliman, S. Epidemiology of Cutaneous Leishmaniasis at a Focus Monitored by the Multinational Force and Observers in the Northeastern Sinai Desert of Egypt. Am. J. Trop. Med. Hyg. 1993, 49, 598–607. [Google Scholar] [CrossRef] [PubMed]
  18. Hamadto, H.A.; El Fkahany, A.F.; Morsy, T.A.; Farrag, A.; MK, A.M. Re-evaluation of zoonotic cutaneous leishmaniasis status in North Sinai Governorate, Egypt. J. Egypt. Soc. Parasitol. 2003, 33, 687–694. [Google Scholar]
  19. Vélez, R.; Ballart, C.; Domenech, E.; Abras, A.; Fernández-Arévalo, A.; Gómez, S.A.; Tebar, S.; Muñoz, C.; Cairó, J.; Gállego, M. Seroprevalence of canine Leishmania infantum infection in the Mediterranean region and identification of risk factors: The example of North-Eastern and Pyrenean areas of Spain. Prev. Vet. Med. 2019, 162, 67–75. [Google Scholar] [CrossRef]
  20. Rombolà, P.; Barlozzari, G.; Carvelli, A.; Scarpulla, M.; Iacoponi, F.; Macrì, G. Seroprevalence and risk factors associated with exposure to Leishmania infantum in dogs, in an endemic Mediterranean region. PLoS ONE 2021, 16, e0244923. [Google Scholar] [CrossRef]
  21. Mahshid, M.; Baharak, A.; Iraj, S.; Sina, K.; Javad, K.; Mehdi, B. Seroprevalence of canine visceral leishmaniasis in southeast of Iran. J. Parasit. Dis. 2014, 38, 218–222. [Google Scholar] [CrossRef] [Green Version]
  22. Costa, M.M.; Penido, M.; Dos Santos, M.S.; Doro, D.; de Freitas, E.; Michalick, M.S.M.; Grimaldi, G.; Gazzinelli, R.T.; Fernandes, A.P. Improved canine and human visceral leishmaniasis immunodiagnosis using combinations of synthetic peptides in enzyme-linked immunosorbent assay. PLoS Negl. Trop. Dis. 2012, 6, e1622. [Google Scholar] [CrossRef] [PubMed]
  23. Pourhoseingholi, M.A.; Vahedi, M.; Rahimzadeh, M. Sample size calculation in medical studies. Gastroenterol. Hepatol. Bed Bench 2013, 6, 14. [Google Scholar] [PubMed]
  24. Gharekhani, J.; Pourmahdi Borujeni, M.; Sazmand, A. Seroprevalence of Visceral Leishmaniosis in Stray Dogs of Hamedan, West of Iran in 2018. J. Med Microbiol. Infect. Dis. 2020, 8, 71–75. [Google Scholar] [CrossRef]
  25. Abdeen, Z.A.; Sawalha, S.S.; Eisenberger, C.L.; Khanfar, H.M.; Greenblatt, C.L.; Yousef, O.; Schnur, L.F.; Azmi, K.; Warburg, A.; Bader, K.A. Epidemiology of visceral leishmaniasis in the Jenin District, West Bank: 1989–1998. Am. J. Trop. Med. Hyg. 2002, 66, 329–333. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  26. Rab, M.; Frame, I.; Evans, D. The role of dogs in the epidemiology of human visceral leishmaniasis in northern Pakistan. Trans. R. Soc. Trop. Med. Hyg. 1995, 89, 612–615. [Google Scholar] [CrossRef]
  27. Dereure, J.; El-Safi, S.H.; Bucheton, B.; Boni, M.; Kheir, M.M.; Davoust, B.; Pratlong, F.; Feugier, E.; Lambert, M.; Dessein, A. Visceral leishmaniasis in eastern Sudan: Parasite identification in humans and dogs; host-parasite relationships. Microbes Infect. 2003, 5, 1103–1108. [Google Scholar] [CrossRef]
  28. Selim, A.; Almohammed, H.; Abdelhady, A.; Alouffi, A.; Alshammari, F.A. Molecular detection and risk factors for Anaplasma platys infection in dogs from Egypt. Parasites Vectors 2021, 14, 1–6. [Google Scholar] [CrossRef]
  29. Selim, A.; Manaa, E.; Khater, H. Seroprevalence and risk factors for lumpy skin disease in cattle in Northern Egypt. Trop. Anim. Health Prod. 2021, 53, 1–8. [Google Scholar] [CrossRef]
  30. Selim, A.; Manaa, E.A.; Waheed, R.M.; Alanazi, A.D. Seroprevalence, associated risk factors analysis and first molecular characterization of chlamydia abortus among Egyptian sheep. Comp. Immunol. Microbiol. Infect. Dis. 2021, 74, 101600. [Google Scholar] [CrossRef]
  31. Martín-Sánchez, J.; Morales-Yuste, M.; Acedo-Sánchez, C.; Barón, S.; Díaz, V.; Morillas-Márquez, F. Canine leishmaniasis in southeastern Spain. Emerg. Infect. Dis. 2009, 15, 795. [Google Scholar] [CrossRef]
  32. Sauda, F.; Malandrucco, L.; Macrì, G.; Scarpulla, M.; De Liberato, C.; Terracciano, G.; Fichi, G.; Berrilli, F.; Perrucci, S. Leishmania infantum, Dirofilaria spp. and other endoparasite infections in kennel dogs in central Italy. Parasite 2018, 25, 2–10. [Google Scholar] [CrossRef] [Green Version]
  33. Matos, M.M.; Filgueira, K.D.; Amora, S.; Suassuna, A.; Ahid, S.M.M.; Alves, N. Ocorrência da leishmaniose visceral em cães em Mossoró, Rio Grande do Norte. Ciênc. Anim. 2006, 16, 51–54. [Google Scholar]
  34. Selim, A.; Megahed, A.A.; Kandeel, S.; Abdelhady, A. Risk factor analysis of bovine leukemia virus infection in dairy cattle in Egypt. Comp. Immunol. Microbiol. Infect. Dis. 2020, 72, 101517. [Google Scholar] [CrossRef]
  35. Selim, A.; Radwan, A. Seroprevalence and molecular characterization of West Nile Virus in Egypt. Comp. Immunol. Microbiol. Infect. Dis. 2020, 71, 101473. [Google Scholar] [CrossRef] [PubMed]
  36. Selim, A.; Radwan, A.; Arnaout, F.; Khater, H. The Recent Update of the Situation of West Nile Fever among Equids in Egypt after Three Decades of Missing Information. Pak. Vet. J. 2020, 40, 390–393. [Google Scholar]
  37. Gálvez, R.; Miró, G.; Descalzo, M.; Nieto, J.; Dado, D.; Martín, O.; Cubero, E.; Molina, R. Emerging trends in the seroprevalence of canine leishmaniosis in the Madrid region (central Spain). Vet. Parasitol. 2010, 169, 327–334. [Google Scholar] [CrossRef] [PubMed]
  38. Živičnjak, T.; Martinković, F.; Marinculić, A.; Mrljak, V.; Kučer, N.; Matijatko, V.; Mihaljević, Ž.; Barić-Rafaj, R. A seroepidemiologic survey of canine visceral leishmaniosis among apparently healthy dogs in Croatia. Vet. Parasitol. 2005, 131, 35–43. [Google Scholar] [CrossRef]
  39. Selim, A.; Abdelhady, A. The first detection of anti-West Nile virus antibody in domestic ruminants in Egypt. Trop. Anim. Health Prod. 2020, 52, 3147–3151. [Google Scholar] [CrossRef]
  40. Selim, A.; Ali, A.-F. Seroprevalence and risk factors for C. burentii infection in camels in Egypt. Comp. Immunol. Microbiol. Infect. Dis. 2020, 68, 101402. [Google Scholar] [CrossRef]
  41. Selim, A.; Marawan, M.A.; Ali, A.-F.; Manaa, E.; AbouelGhaut, H.A. Seroprevalence of bovine leukemia virus in cattle, buffalo, and camel in Egypt. Trop. Anim. Health Prod. 2020, 52, 1207–1210. [Google Scholar] [CrossRef]
  42. Burnham, A.C.; Ordeix, L.; Alcover, M.M.; Martínez-Orellana, P.; Montserrat-Sangrà, S.; Willen, L.; Spitzova, T.; Volf, P.; Solano-Gallego, L. Exploring the relationship between susceptibility to canine leishmaniosis and anti-Phlebotomus perniciosus saliva antibodies in Ibizan hounds and dogs of other breeds in Mallorca, Spain. Parasites Vectors 2020, 13, 1–15. [Google Scholar] [CrossRef] [PubMed]
  43. Solano-Gallego, L.; Llull, J.; Ramis, A.; Fernández-Bellon, H.; Rodriguez, A.; Ferrer, L.; Alberola, J. Longitudinal study of dogs living in an area of Spain highly endemic for leishmaniasis by serologic analysis and the leishmanin skin test. Am. J. Trop. Med. Hyg. 2005, 72, 815–818. [Google Scholar] [CrossRef] [PubMed]
  44. Cortes, S.; Vaz, Y.; Neves, R.; Maia, C.; Cardoso, L.; Campino, L. Risk factors for canine leishmaniasis in an endemic Mediterranean region. Vet. Parasitol. 2012, 189, 189–196. [Google Scholar] [CrossRef] [PubMed]
  45. Silva, J.C.F.D.; Costa, R.T.D.; Siqueira, A.M.; Coelho, G.L.L.M.; Costa, C.A.D.; Mayrink, W.; Vieira, E.P.; Silva, J.C.D. Epidemiology of canine visceral leishmaniasis in the endemic area of Montes Claros Municipality, Minas Gerais State, Brazil. Vet. Parasitol. 2003, 111, 161–173. [Google Scholar] [CrossRef]
  46. Belo, V.S.; Struchiner, C.J.; Werneck, G.L.; Barbosa, D.S.; de Oliveira, R.B.; Neto, R.G.T.; da Silva, E.S. A systematic review and meta-analysis of the factors associated with Leishmania infantum infection in dogs in Brazil. Vet. Parasitol. 2013, 195, 1–13. [Google Scholar] [CrossRef] [PubMed]
  47. Lopes, P.M.; Sorte, E.D.C.B.; Gasparetto, N.D.; Oliveira, C.M.; Almeida, A.D.B.P.F.D.; Sousa, V.R.F. Seroprevalence and risk factors associated with visceral leishmaniasis in dogs in Jaciara, State of Mato Grosso. Rev. Soc. Bras. Med. Trop. 2014, 47, 791–795. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  48. Coura-Vital, W.; Marques, M.J.; Veloso, V.M.; Roatt, B.M.; Aguiar-Soares, R.D.D.O.; Reis, L.E.S.; Braga, S.L.; Morais, M.H.F.; Reis, A.B.; Carneiro, M. Prevalence and factors associated with Leishmania infantum infection of dogs from an urban area of Brazil as identified by molecular methods. PLoS Negl. Trop. Dis. 2011, 5, e1291. [Google Scholar] [CrossRef] [Green Version]
  49. De Almeida Leal, G.G.; Carneiro, M.; da Costa Pinheiro, A.; Marques, L.A.; Ker, H.G.; Reis, A.B.; Coura-Vital, W. Risk profile for Leishmania infection in dogs coming from an area of visceral leishmaniasis reemergence. Prev. Vet. Med. 2018, 150, 1–7. [Google Scholar] [CrossRef]
Figure 1. Map of Egypt showing governorates that were considered in the study.
Figure 1. Map of Egypt showing governorates that were considered in the study.
Vetsci 08 00236 g001
Table 1. Seroprevalence of canine leishmaniasis in relation to different variables.
Table 1. Seroprevalence of canine leishmaniasis in relation to different variables.
FactorNo of Examined DogsNo of PositiveNo of Negative%95% CIStatistics
Location
Cairo 95276828.420.33–38.19
Giza115338221.715.2–30.1χ2 = 4.179
df = 4
p = 0.382
Qalyubia7596618.711.5–28.9
Kafr ElSheikh80126818.811.7–28.7
Gharbia85157017.611–27.1
Age
6–12 months301293.30.2–19.1χ2 = 11.483
df = 4
p = 0.02 *
1–2 years6595613.86.0–25.2
2–4 years2306017026.120.6–32.3
4–6 years95217422.114.5–32.0
>6 years3052516.76.3–35.4
Sex
Male2806721323.919.1–29.5χ2 = 2.975
df = 1
p = 0.08
Female1702914117.111.9–23.7
Breed
German Shepherd1703113918.213.2–24.7χ2 = 2.891
df = 2
p = 0.236
Rott Weiler10027732719.3–36.4
Mongrel1803814221.115.7–27.6
Hair length
Long15021129149.1–20.8χ2 = 7.210 df = 1
p = 0.007 *
Short300752252520.3–30.4
Veterinary care
Yes2603222812.38.7–17.1χ2 = 29.891
df = 1
p = 0.0001 *
No1906412633.727.0–40.9
Application of insecticides
Yes2703223811.98.4–16.5χ2 = 36.158
df = 1
p = 0.0001 *
No1806411635.628.7–43.1
Floor of shelter
Paved3104526514.510.8–19.1χ2 = 27.594
df = 1
p = 0.0001 *
Soil140518936.428.5–45.0
* The result is significant at p < 0.05.
Table 2. Multivariable logistic analysis for risk factors of Leishmania infantum infection in dogs.
Table 2. Multivariable logistic analysis for risk factors of Leishmania infantum infection in dogs.
VariableB aSE bOR c95% CI dp Value
Age
1–2 years1.6021.0944.960.6–42.30.143
2–4 years2.4851.04112.001.6–92.30.017 *
4–6 years2.2491.0609.481.2–75.80.034 *
>6 years1.6781.1465.350.6–50.60.143
Sex
Male0.6550.2691.931.1–3.30.015 *
Breed
German Shepherd0.4620.3201.590.9–2.90.15
Hair length
Short0.7290.2852.071.2–3.60.011 *
Veterinary Care
No0.9940.3872.71.3–5.80.010 *
Application of Insecticides
No1.1270.3783.091.5–6.50.003 *
Floor of shelter
Soil0.3530.3731.420.7–2.90.343
a Logistic regression coefficient; b Standard error; c Odds ratio; d Confidence interval; * The result is significant at p < 0.05.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Selim, A.; Shoulah, S.; Abdelhady, A.; Alouffi, A.; Alraey, Y.; Al-Salem, W.S. Seroprevalence and Risk Factors Associated with Canine Leishmaniasis in Egypt. Vet. Sci. 2021, 8, 236. https://0-doi-org.brum.beds.ac.uk/10.3390/vetsci8100236

AMA Style

Selim A, Shoulah S, Abdelhady A, Alouffi A, Alraey Y, Al-Salem WS. Seroprevalence and Risk Factors Associated with Canine Leishmaniasis in Egypt. Veterinary Sciences. 2021; 8(10):236. https://0-doi-org.brum.beds.ac.uk/10.3390/vetsci8100236

Chicago/Turabian Style

Selim, Abdelfattah, Salma Shoulah, Abdelhamed Abdelhady, Abdulaziz Alouffi, Yasser Alraey, and Waleed S. Al-Salem. 2021. "Seroprevalence and Risk Factors Associated with Canine Leishmaniasis in Egypt" Veterinary Sciences 8, no. 10: 236. https://0-doi-org.brum.beds.ac.uk/10.3390/vetsci8100236

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop