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Article

Seroprevalence and Risk Factors for Toxoplasma gondii Infection in Horses

by
Mohamed Marzok
1,2,3,*,
Omar A. AL-Jabr
4,
Mohamed Salem
1,3,5,
Khalid Alkashif
6,
Mohamed Sayed-Ahmed
7,8,
Majed H. Wakid
9,10,
Mahmoud Kandeel
11,12 and
Abdelfattah Selim
13,*
1
Department of Clinical Sciences, College of Veterinary Medicine, King Faisal University, Al-Hofuf 31982, Saudi Arabia
2
Department of Surgery, Faculty of Veterinary Medicine, Kafr El Sheikh University, Kafr El Sheikh 33511, Egypt
3
King Faisal University Veterinary Hospital, Al-Asha 31982, Saudi Arabia
4
Department of Microbiology, College of Veterinary Medicine, King Faisal University, Al-Asha 31982, Saudi Arabia
5
Department of Medicine and Infectious Diseases, Faculty of Veterinary Medicine, Cairo University, Cairo 12613, Egypt
6
Department of Pharmacology and Toxicology, College of Pharmacy, Jazan University, Jazan 82722, Saudi Arabia
7
Department of Clinical Pharmacy, College of Pharmacy, Jazan University, Jazan 82722, Saudi Arabia
8
Department of Internal Medicine and Infectious Diseases, Faculty of Veterinary Medicine, Mansoura University, Mansoura 35516, Egypt
9
Department of Medical Laboratory Technology, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah 21589, Saudi Arabia
10
Special Infectious Agents Unit, King Fahd Medical Research Center, King Abdulaziz University, Jeddah 21589, Saudi Arabia
11
Department of Pharmacology, Faculty of Veterinary Medicine, Kafr El Sheikh University, Kafr El Sheikh 33511, Egypt
12
Department of Biomedical Sciences, College of Veterinary Medicine, King Faisal University, Al-Ahsa 31982, Saudi Arabia
13
Department of Animal Medicine (Infectious Diseases), Faculty of Veterinary Medicine, Benha University, Toukh 13736, Egypt
 
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*
Authors to whom correspondence should be addressed.
Vet. Sci. 2023, 10(3), 237; https://doi.org/10.3390/vetsci10030237
Submission received: 21 February 2023 / Revised: 14 March 2023 / Accepted: 16 March 2023 / Published: 22 March 2023
(This article belongs to the Special Issue Immunological Study of Toxoplasma gondii Infection in Animals)
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Abstract

:

Simple Summary

Toxoplasma gondii is classified as intracellular protozoa and is one of the major zoonotic parasites. Mares, horses of mixed breeds, and older than five years are substantially more likely to contract T. gondii infection. In addition, horses raised in contact with cats or domestic ruminants are more likely to test positive for T. gondii infection. This study confirms that horses in Northern Egypt are exposed to T. gondii and raises the possibility that people and other animals could contract the disease.

Abstract

Background: Toxoplasma gondii is classified as intracellular protozoa and is one of the major zoonotic parasites. Most warm-blooded intermediate hosts, including humans, are commonly infected by this parasite. The epidemiology of T. gondii infection in Egyptian horses is currently poorly understood. Methods: 420 blood samples were randomly collected from horses raised in four governorates in Northern Egypt (110 each from Giza and Kafr El Sheikh, and 100 each from Qalyubia and Gharbia) to investigate the existence of antibodies against T. gondii using a commercial ELISA kit, and to ascertain the risk factors for the infection. Results: the antibodies for T. gondii were found in 16.2% (68/420) of the examined horses, with no significant differences among the four studied governorates. The highest prevalence rate was observed in Giza. The results revealed that sex, breed, age, and contact with domestic ruminants or cats were recognized as potential risk factors. The high prevalence rate was found in mixed breed horses (OR = 2.63, 95% CI: 0.95–7.26), mares (OR = 2.35, 95% CI: 1.31–4.19), and horses aged over 10 years (OR = 2.78, 95% CI: 1.30–3.44). Moreover, the likelihood of seropositivity for T. gondii infection was higher in horses raised in environments with cats (OR = 1.97, 95% CI: 1.13–3.44, p = 0.017) or domestic ruminants (OR = 2.16, 1.21–3.86, p = 0.010). This report confirms that horses in Northern Egypt are exposed to T. gondii and thus raises the possibility that people and other animals could contract the disease. Conclusions: routine examination and management of T. gondii infection in horses in these governorates is advised.

1. Introduction

Toxoplasma gondii is classified as a globally prevalent intracellular protozoan, which causes toxoplasmosis [1,2,3]. Domestic cats and other felids are the definitive hosts for T. gondii [4]. Only these hosts can release oocysts into the environment, which can contaminate pastures, food, and water. Around 100 million non-sporulated oocysts can be passed by a single cat, and these oocysts become infective between one and five days later [5]. Nevertheless, the parasite has a variety of intermediate hosts, including mammals, such as humans, and birds that harbour the cyst stage in their tissues [6,7].
T. gondii infection in herbivores and equines mostly happens through water or food contaminated with sporulated oocysts, however, transplacental transmission of tachyzoites from mother to foetus is also possible [8,9].
Toxoplasmosis is a chronic disease causing cystic formation in the tissues of the hosts [10], however, the life cycle of T. gondii depends on oocysts, which become infectious to a wide range of warm-blooded intermediate hosts if consumed after one to a few days of maturation (sporulation) in the environment. Oocysts are not the only infective stages of T. gondii; there are also tachyzoites and bradyzoites, the latter of which is seen in tissue cysts. Tachyzoites infiltrate host cells after infection and grow there. When the parasite forms parasitophorous vacuoles, this replication is strictly intracytoplasmic. Parallel to this, the parasite creates internal tissue cysts that contain bradyzoites that are no longer multiplying or are only replicating slowly after multiple rounds of multiplication [11]. The infected intermediate hosts’ brain tissue, skeletal and cardiac muscles, and even their retinas, are the preferred locations for tissue cyst formation. The parasite has a complicated life cycle, and there are numerous ways for infection [12].
The majority of infections in people are asymptomatic, but congenital Toxoplasma infections can have serious side effects, including stillbirth, abortion, mortality, and hydrocephalus in newborns, as well as retinochoroidal lesions that cause retinitis, chronic ocular disease, lymphadenopathy, and encephalitis in people with compromised immune systems [8].
Since it was originally isolated in 1908, T. gondii has spread globally. In northern Iraq, a serosurvey of sheep and goats revealed seroprevalences of Toxoplasma infection of 42.1% and 36.1%, respectively [13]. In addition, T. gondii infection in canine was detected in Brazil and revealed a seropositivity of 9.54% [14]. The seroprevalence of T. gondii in animals ranged from 6% to 33%, according to statistical analysis of the positive rates of T. gondii infection in five different animal species in the Nordic-Baltic region [15]. T. gondii infection may affect one-third of the global population according to the Centers for Disease Control and Prevention (CDC), T. gondii infects approximately 22.5% of Americans over 12 years old in the United States, although recent years have seen a slight reduction in prevalence [16].
In Egypt, anti-T. gondii antibodies were found in 10.8% of cattle based on ELISA test results [17] and in 43.7% or 41.7% of sheep examined by a modified agglutination test or ELISA [18], respectively. Furthermore, donkeys and horses have high corresponding seroprevalences of 65.6% and 48.1%, respectively [19,20].
T. gondii is a significant contributor to small ruminant reproductive problems, resulting in abortion, stillbirth, mummification, infertility, and the delivery of poor lambs [21,22]. Although T. gondii infection in horses is typically asymptomatic [23], fever, abortion, degeneration in retina, and stillbirth were recorded in infected pregnant mares [24,25].
Moreover, one of the main ways that humans become infected is through the ingestion of undercooked, contaminated meat, although eating horse meat is not common for people in Egypt [1], and eating horse meat from the Americas has been epidemiologically associated to serious sickness in Europeans [26,27]. Toxoplasma infection can also develop through other means, such as eating undercooked, contaminated meat (particularly lamb, pork, and venison) or shellfish (such as clams or mussels) [28]. Because humans can become infected by consuming contaminated meat, T. gondii infection not only results in financial and reproductive losses but also has an impact on public health [12,29].
The incidence of T. gondii in human across Egypt is not well-documented. The majority of serological reports are founded on convenience samples, including those taken from pregnant women and patients with illnesses. Moreover, T. gondii DNA was discovered in 10% (15/150) of Alexandria blood donors [30] and in 6% of the blood donors from the Qalubiya governorate [31].
A common reference test for the serosurvey of toxoplasmosis in various animal species is the latex agglutination test (LAT) [32]. However, the ELISA test displays greater potency, sensitivity, and specificity when compared to other reference serodiagnostic tests, such as the LAT, the modified agglutination test, the direct agglutination test, and the indirect fluorescent antibody test, which are used to identify anti-T. gondii antibodies in serum samples from various animals [33,34,35].
Although monitoring of T. gondii infection is crucial to prevent its proliferation, Egypt has limited information on its prevalence in horses [19,36]. Understanding the frequency of T. gondii in horses is vital to prevent infection through consumption of contaminated meat, as Egypt’s carnivorous zoo animals are routinely given raw horse meat [36].
Consequently, the purpose of this study was to evaluate the risk factors for T. gondii infection in horses in four governorates of northern Egypt and to ascertain the seroprevalence of T. gondii therein.

2. Material and Methods

2.1. Ethical Statement

Benha University’s Animal Ethics Committee approved this work (Approval no. BUFVTM02-10-22, Benha). Serum samples were obtained and handled in conformity with the Animal Ethics Procedures and Guidelines of the Committee. This study was conducted according to ARRIVE guidelines. In this study, we worked on live horses and we did not anesthetize and/or sacrifice those animals.

2.2. Study Area

The study was conducted in northern Egypt, specifically in the governorates of Giza, Kafr El Sheikh, Qalyubia, and Gharbia, which are geographically situated at 29°59′13.2″ N 31°12′42.48″ E, 31°06′42″ N 30°56′45″ E, 30°24′36″ N 31°12′36″ E, 30°52′1.2″ N 31°1′40.8″ E, respectively (Figure 1). The large equine population in these regions led to their selection for this research.
Egypt has a predominantly hot, arid environment (Köppen climatic classification BWh). The country’s climate is often rather dry, except the northern Mediterranean coast. The climate in Giza is arid. Summers are quite warm and winters are mild in this type of environment. Here, rain rarely falls.
The other governorates are situated in the Nile Delta of Egypt. The climate of these areas, much like the rest of Egypt, is a hot desert climate (Köppen: BWh), but its northernmost area, like the rest of Egypt’s northern coast, which is the country’s wettest region, has more moderate temperatures, with summer highs typically not exceeding 31 °C. On average, the delta region receives only 100–200 mm (4–8 in) of rain each year, with the majority of this precipitation occurring in the winter.

2.3. Sample Collection and Preparation

A cross-sectional study was conducted between January and December of 2020. By using simple random sampling, blood samples from horses were obtained.
On the basis of the 48.1% prevalence rate of T. gondii in horses in Egypt as reported by Ghazy, et al. [20], the predicted prevalence was set as 48.1% (P), with a 5% (d) absolute precision and a 95% confidence level (z = 1.96). The sample size of 420 exceeds the minimum sample size (383) according to the following formula: N = P (1 − P)z2/d2 [37].
Blood samples were taken from horses raised in the four selected areas. Each animal had a jugular vein venipuncture, and sterile 10-mL tubes free of anticoagulant were used to collect 5 mL of blood from each horse. The blood samples were labelled, preserved in an icebox, and then transported to the Veterinary Diagnostic Laboratory at the Faculty of Veterinary Medicine at Benha University. Prior to further serological investigation, the sera were separated by centrifugation for 10 min at 3000 xg, and then stored in 1.5 mL tubes at −20 °C.
At the time of sample collection, the data of each animal was collected through a questionnaire filled in by the owner or veterinarian. According to collected data, animals were categorised according to region (Giza, Kafr El Sheikh, Qalyubia, or Gharbia), breed (Arabian, thoroughbred, or mixed), sex (male or female), and age groups (<5, 5–10, or >10 years old). The questionnaire also included questions about farm biosecurity, such as if cats or other domestic ruminants were present. The details of examined horses are presented in Table 1. All of the horses under investigation were fed wheat bran, some green grass, and agricultural waste items, such as barley and maize. In addition, water was provided three times per day.

2.4. Serological Examination

Horse serum samples were examined using the commercial kit ID Screen® Toxoplasmosis Indirect Multi-species Indirect ELISA (ID Vet, Montpellier, France) for T. gondii immunoglobulin G (IgG) antibodies. The kit uses a multi-species peroxidase as a conjugate and the P30 T. gondii protein as a substrate to detect specific IgG antibodies following T. gondii infection.
The testing was performed in accordance with the manufacturer’s recommendations, and the optical densities (ODs) of the ELISA findings were read at 450 nm. Each test serum’s sample (S) to positive (P) ratio (S/P%) was determined using the following formula:
S P % = O D s a m p l e − O D n e g a t i v e   c o n t r o l O D p o s i t i v e   c o n t r o l − O D n e g a t i v e   c o n t r o l × 100
According to the manufacturer guidelines, samples with S/P% readings above 50% were regarded as positive, below 40% were considered negative and those between 40 to 50% considered doubtful.

2.5. Statistical Analysis

The SPSS software version24.0 (IBM, New York, NY, USA) was used for data analysis. The differences in the seroprevalences of variable categories were determined by Chi-square test, with p-values of <0.05 considered as significant. The relationship between T. gondii infection and the relevant risk variables was examined using univariate analysis. Multivariate logistic regression models were then fitted for all variables in the univariate analysis with a p-value less than 0.25. To determine the degree of relation between the presence of T. gondii and variables, the odds ratios (ORs) and 95% confidence intervals (95% CIs) were calculated. The model fit was assessed using the Hosmer and Lemeshow goodness-of-fit test.

3. Results

T. gondii had a 16.2% seroprevalence in the examined horses, with 68 samples from 420 horses testing positive for T. gondii via an ELISA test. T. gondii antibodies were detected in samples from all four governorates, with 20.9% in Giza, 17.3% in Kafr El Sheikh, 12% in Qalyubia and 14% in Gharbia. The difference was statistically non-significant (p = 0.31), Table 2.
Interestingly, statistically significant differences (p < 0.05) occurred in the seroprevalence of T. gondii between horse breeds and sexes. T. gondii seroprevalence was higher in females (20.9%) than in males (10.5%), and higher in mixed breed (21.3%) than in Arabian (8.3%) and thoroughbred horses (14.5%), as shown in Table 3.
Furthermore, T. gondii seroprevalence was 22.7% in horses older than 10 years, a value which was significantly higher than the rates of other age groups (16.7% for horses aged 5 to 10 years and 10% for those under 5 years; p = 0.02). The results highlight the fact that higher T. gondii seroprevalence (p < 0.05) was found in horses raised in contact with cats (21.1%) or domestic ruminants (23.3%) (Table 3).
Multivariate analysis results in Table 4 established that the variables of breed, sex, age, presence of cats, and presence of domestic ruminants, were all independently associated with T. gondii infection in horses in Egypt. The risk for mares was 2.35 times (95% CI: 1.31–4.19) greater than for male horses. Mixed breed horses were had 2.63 times (95% CI: 0.95–7.26) greater risk than their Arabian counterparts. Further, horses aged 5–10 years have a 2.23 times (95% CI: 1.06–4.70) greater risk, and those >10 years have a 2.78 times (95% CI: 1.30–5.95) greater risk, than those younger than 5 years old. Both the presence of domestic ruminants (OR = 2.16, 95% CI: 1.21–3.86, p = 0.010) and cats (OR = 1.97, 95% CI: 1.13–3.44, p = 0.017) in close proximity to horses increased the risk of T. gondii seroprevalence in horses, Table 4.

4. Discussion

T. gondii is one of the most significant zoonotic pathogens, as T. gondii infection in horses has become one of the most significant possible causes of human toxoplasmosis [1]. Unfortunately, little information is available about the epidemiology of T. gondii infection in horses in Egypt, and the majority of existing research is outdated [19,20]. The present study aimed to determine the seroprevalence of T. gondii in horses in northern Egypt using the ELISA technique, as well as to ascertain the risk factors for T. gondii infection.
In this work, T. gondii seroprevalence was 16.2% in horses, a value which is lower than previous reported rate (25%) in Egypt by Haridy, et al. [38], but is close to value of (17.92%) observed in northern Chinese horses [39]. However, the seroprevalence rates in the present study were lower than those reported by Almeida et al. [40] (23.64% in Brazil); Saqib et al. [41] (23.50% in Pakistan); Bártová et al. [42] (24.17% in Nigeria); Razmi et al. [43] (20.30% in Iran); and Alanazi and Alyousif [44] (31.58% in Saudi Arabia). By contrast, the seroprevalence rates of this work were higher than those reported by Aharonson-Raz et al. [45] (3.25% in Israel); García-Bocanegra et al. [23] (10.79% in Spain); Lopes et al. [46] (13.29% in Portugal); Boughattas et al. [47] (17.72% in Tunisia); and Karatepe et al. [48] (7.20% in Turkey). Moreover, relatively lower seroprevalence levels were found in Sweden (0.5–1%) [49] and Greece (1.8%) [50] and relatively higher values were found in Italy (30.7%) [51], in numerous studies in Turkey (20.6–28%) [52,53] and in recently conducted studies in the Czech Republic (23%) [54].
The following factors may be responsible for the variations in seroprevalence: time of sampling, sample size, differences in the sensitivity of the detection methods, the cut off titer utilised in the interpretation of findings, animal susceptibility, the number and age of examined horses, location, feeding practices, sanitation, and farming management [23,39,40,55,56,57,58,59]. Additionally, climate-linked influences that include regional distribution, density of population, and the presence or absence of cats or of animals that serve as reservoir hosts or transport hosts, are crucial to the emergence, survival, dispersion, and transmission of T. gondii [3,60,61,62,63,64,65].
This work did not detect significant differences in T. gondii seroprevalence according to sampling location, an outcome similar to that of a study from Japan [10]. Nevertheless, T. gondii seroprevalence varied in the examined areas, being notably higher in the Giza governorate in comparison to other locations. This may be due to the Giza governorate’s very hospitable climate for the growth of oocysts, especially its humidity and temperature, as well as the governorate’s substantial animal populations that are bred in big groups.
There is currently no proof that T. gondii infects horses spontaneously or through experimental exposure to induce clinical illness [66]. Nonetheless, live T. gondii has been identified from naturally exposed horses [36], and people in France who ate raw imported horse meat had severe clinical toxoplasmosis. According to findings obtained by Shaapan and Ghazy [36], the prevalence of T. gondii in Egypt is very high. Moreover, they isolated viable T. gondii by mouse bioassay in 79 of 150 pools of tissue samples from 150 horses slaughtered in the Giza Zoo abattoir. As a result, eating horseflesh could potentially infect humans as well as captive felines in zoos. T. gondii-infected horsemeat should not be offered to cats or consumed by humans, as a study shown that it may survive in edible tissues of living horses for up to 476 days [66]. Hence, equids might be involved in the spread of T. gondii to humans and cats in Egypt.
Furthermore, T. gondii seroprevalence varied significantly amongst equine breeds. El-Ghaysh [19] suggested that being kept as free-ranging animals explained the higher seroprevalence of T. gondii among mixed breeds and thoroughbreds relative to the Arabian counterpart. That is, the non-Arabian breeds may come into contact with oocysts in the contaminated environment more frequently. These findings were consistent with those of García-Bocanegra, et al. [23] who found that seroprevalence was higher in crossbred horses than in stabled thoroughbreds because the former frequently roam more freely and have greater access to parasites. Finally, the type of activity and location have been proven to exert a substantial impact on the presence of T. gondii infection in horses in Egypt [36,67,68,69,70,71].
The available data about the seroprevalences of T. gondii in other equids than horses are very little. The few published studies on donkeys establish the high seroprevalence of T. gondii in Egypt, at a range between 45% and 66% [19,72]. Mules, which are more closely related to donkeys than horses, demonstrated intermediate T. gondii levels between that of horses and donkeys, an outcome which is consistent with findings from China (8.6% seroprevalence in mules against 4.5% in horses) [72].
The present findings support the previous observation of Haridy, et al. [38] which indicates that females have more contact with contaminated environments than males, but contradict the outcomes from previous studies in Tunisia and Turkey [47,48]. Also, it implies that female horses are more susceptible to parasite infection than male and gelding horses, which is consistent with the findings of an earlier study conducted in Egypt [38]. Similar findings were also found in Spain [23], northwest Algeria [73], and Xinjiang, northwestern China [74], however unlike our study, their difference was not demonstrated to be statistically significant.
In line with earlier findings, younger horses have a lower seroprevalence, and statistically significant differences occur between age groups [50]. This result implies that equids contract an infection during their first few years of life and that the exposure remains continuous as they age, thereby explaining the higher prevalence of T. gondii infection in older horses [47,74,75,76]. By contrast, other research revealed a negative relationship between age and T. gondii infection in horses as well as a high prevalence rate in younger horses, the latter of which may be mostly due to underdeveloped immune systems [39] or as a result of trans-placental transmission and horizontal infection of T. gondii resulting from the consumption of oocyst-contaminated food or water. In addition, recent research from other nations, in contrast to our findings, revealed no appreciable variation in the seroprevalence of T. gondii in horses from Mexico, southern Spain, Korea, and southern Italy within age classes [23,77,78,79,80].
Equines and other intermediate hosts for T. gondii, such as ruminants, can only get infected after eating or drinking products contaminated with sporulated T. gondii oocysts from cats, or through congenital transmission [1,2]. High seroprevalence has been seen in felid species in the past, including domestic cats (50%) and Iberian lynx (Lynx pardinus) (62.8%) in Andalusia [81,82]. T. gondii oocysts are believed to have been released into the environment by seropositive felids.
In addition, it has been noted that the presence of cats is one of the major contributors to T. gondii seroprevalence in other domestic animals, including pigs [82] and small ruminants [83]. It should be highlighted that the present findings may have been impacted by the challenge of accurately estimating the amount of cats in shelters or even pastures where horses are housed.
The present work confirmed that raising horses in contact with cats was a risk factor for T. gondii infection, which is consistent with findings of previous studies [4,13,47]. The variations in the environment’s level of contamination by cats, which are the definitive hosts of T. gondii, and other mechanical carriers of oocysts, such as rodents, may be the cause of the disparities in seroprevalence.
The presence of domestic ruminants was associated with the seroprevalence of T. gondii in equids as determined in a study in Spain [23]. In Egypt, T. gondii is regarded as one of the major causes of small ruminant abortion and neonatal death. In Egypt, research on T. gondii seroprevalence in domestic ruminants revealed significant antibody prevalence levels in cattle (10.8%), sheep (98.4%), goats (41.7%), and camels (46.9%) [3,35].

5. Conclusions

This study confirmed that T. gondii circulates in the horse populations in four governorates in Egypt, thereby posing a concern to the health of both animals and people. In addition, breed, sex, age, the presence of cats, and the presence of domestic ruminants, are identified as risk factors for the infection. These results are intended to provide Egyptian authorities with helpful information for managing and preventing toxoplasmosis in horses and/or other hosts. Finally, further seroepidemiological studies are necessary to investigate the prevalence of T. gondii in wider areas in Egypt, and to identify the epidemiological situation of the parasite across the country.

Author Contributions

Conceptualization, methodology, formal analysis, investigation, resources, data curation, writing—original draft preparation, A.S., M.M., M.S.-A., O.A.A.-J., K.A. and M.S.-A.; writing—review and editing, A.S., M.M., M.S., O.A.A.-J., K.A., M.H.W., M.K. and M.S.-A.; project administration, A.S., M.M., M.S., M.H.W., M.K. and O.A.A.-J.; funding acquisition, A.S., M.M., M.S., M.H.W., M.K., M.S.-A. and O.A.A.-J. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported through the Annual Funding track by the Deanship of Scientific Research, Vice Presidency for Graduate Studies and Scientific Research, King Faisal University, Saudi Arabia (Grant Number 2950).

Institutional Review Board Statement

Consent was obtained from Benha University’s Animal Ethics Committee BUFVTM02-10-22.

Informed Consent Statement

The owners were informed and permission was taken before sampling.

Data Availability Statement

This article contains all of the data that was created or analyzed throughout the investigation.

Acknowledgments

The authors would like to acknowledge the Deanship of Scientific Research, Vice Presidency for Graduate Studies and Scientific Research, King Faisal University, Saudi Arabia for the financial support of this research through the Grant Number 2950.

Conflicts of Interest

The authors declare no conflict of interest.

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Vetsci 10 00237 g001 550
Figure 1. Map showing four the Egyptian governorates where horses were sampled (map generated by QGIS software 3.18.3).
Figure 1. Map showing four the Egyptian governorates where horses were sampled (map generated by QGIS software 3.18.3).
Vetsci 10 00237 g001
Table
Table 1. Descriptive analysis of the factors used to determine the seroprevalence of T. gondii infection in Egyptian horses.
Table 1. Descriptive analysis of the factors used to determine the seroprevalence of T. gondii infection in Egyptian horses.
VariableCategoryNo. of HorsesDistribution
LocalityGiza11026.2%
Kafr El Sheikh11026.2%
Qalyubia10023.8%
Gharbia10023.8%
BreedArabian6014.3%
Thoroughbred20047.6%
Mixed16038.1%
SexMale19045.2%
Female23054.7%
Age<5 year13031%
5–1018042.8%
>1011026.2%
Presence of catsYes18042.9%
No24057.1%
Presence of domestic ruminantsYes12028.6%
No30071.4%
Table
Table 2. Seroprevalence of T. gondii in horses from different governorates under the study.
Table 2. Seroprevalence of T. gondii in horses from different governorates under the study.
FactorNo. of Examined HorsesNo. of Positive% of Positive95% CIp-Value
Locality
Giza1102320.914.36–29.43
Kafr El Sheikh1101917.311.34–25.41
Qalyubia1001212.07–19.810.31
Gharbia1001414.08.53–22.14
Table
Table 3. Univariate analysis of the association of focal variables with seropositivity to T. gondii in horses (N = 420) in Egypt.
Table 3. Univariate analysis of the association of focal variables with seropositivity to T. gondii in horses (N = 420) in Egypt.
FactorNo. of Examined HorsesNo. of Positive% of Positive95% CIStatistics
Breed
Arabian6058.33.61–18.06χ2 = 6.167 df = 2
p = 0.04 *
Thoroughbred2002914.510.29–20.05
Mixed1603421.315.62–28.22
Sex
Male1902010.56.92–15.7χ2 = 8.203 df = 1
p = 0.004 *
Female2304820.916.12–26.58
Age
<5 years1301310.05.94–16.36χ2 = 7.165 df = 2
p = 0.02 *
5–10 years1803016.711.93–22.8
>10 years1102522.715.9–31.4
Presence of cats
Yes1803821.115.78–27.64χ2 = 5.621 df = 1
p = 0.02 *
No2403012.58.9–17.28
Presence of domestic ruminants
Yes1202823.316.66–31.65χ2 = 6.317 df = 1
p = 0.01 *
No3004013.39.94–17.64
Total4206816.212.98–20.02
* The result considered significant at p < 0.05.
Table
Table 4. Final multivariate mode of the risk factors for Toxoplasma gondii infection in horses in Egypt.
Table 4. Final multivariate mode of the risk factors for Toxoplasma gondii infection in horses in Egypt.
VariableBS.E.OR95% CI for ORp-Value
LowerUpper
Breed
Thoroughbred0.5740.5191.780.644.900.268
Mixed0.9650.5192.630.957.260.063
Sex
Female0.8520.2962.351.314.190.004
Age
5–10 years0.8030.3802.231.064.700.034
>10 years1.0230.3882.781.305.950.008
Presence of cats
Yes0.6790.2831.971.133.440.017
Presence of domestic ruminants
Yes0.7690.2972.161.213.860.010
B—logistic regression coefficient; SE—standard error; OR—odds ratio; CI—confidence interval.
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Marzok, M.; AL-Jabr, O.A.; Salem, M.; Alkashif, K.; Sayed-Ahmed, M.; Wakid, M.H.; Kandeel, M.; Selim, A. Seroprevalence and Risk Factors for Toxoplasma gondii Infection in Horses. Vet. Sci. 2023, 10, 237. https://doi.org/10.3390/vetsci10030237

AMA Style

Marzok M, AL-Jabr OA, Salem M, Alkashif K, Sayed-Ahmed M, Wakid MH, Kandeel M, Selim A. Seroprevalence and Risk Factors for Toxoplasma gondii Infection in Horses. Veterinary Sciences. 2023; 10(3):237. https://doi.org/10.3390/vetsci10030237

Chicago/Turabian Style

Marzok, Mohamed, Omar A. AL-Jabr, Mohamed Salem, Khalid Alkashif, Mohamed Sayed-Ahmed, Majed H. Wakid, Mahmoud Kandeel, and Abdelfattah Selim. 2023. "Seroprevalence and Risk Factors for Toxoplasma gondii Infection in Horses" Veterinary Sciences 10, no. 3: 237. https://doi.org/10.3390/vetsci10030237

APA Style

Marzok, M., AL-Jabr, O. A., Salem, M., Alkashif, K., Sayed-Ahmed, M., Wakid, M. H., Kandeel, M., & Selim, A. (2023). Seroprevalence and Risk Factors for Toxoplasma gondii Infection in Horses. Veterinary Sciences, 10(3), 237. https://doi.org/10.3390/vetsci10030237

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