SYSTEMATIC REVIEW article

Front. Vet. Sci., 18 January 2023

Sec. Comparative and Clinical Medicine

Volume 9 - 2022 | https://doi.org/10.3389/fvets.2022.1080139

A review of foodborne Toxoplasma gondii with a special focus on its prevalence in Pakistan from 2000 to 2022

  • 1. Department of Parasitology, University of Agriculture, Faisalabad, Pakistan

  • 2. Department of Veterinary Medicine, College of Agriculture and Veterinary Medicine, Qassim University, Buraidah, Saudi Arabia

Abstract

Third-world countries have a higher prevalence of food-related disorders than developed nations. Millions of people in underdeveloped countries are seriously at risk from the potential water supply contamination with protozoan diseases. Toxoplasma gondii is one of the important protozoans causing diseases in livestock and humans. Despite the standard tests for diagnosing this parasite and different treatment methods, the spread of these parasites is uncontrollable and rising every year due to other management disorders. In this review, we summarize etiopathogenesis and prevalence in Pakistan. We looked for papers reporting the seroprevalence of T. gondii in people and animals between 2000 and 2022 in different databases: PubMed, Google Scholar, ScienceDirect, Scopus, and Web of Science. Data on the seroprevalence of T. gondii in Pakistan's domestic animals (sheep and goats, horses, donkeys, mules, cattle, and buffaloes), domestic pets (cats and dogs), poultry and rodents, and humans were gathered. According to the findings, sheep had an estimated pooled seroprevalence of T. gondii that varied from 11.20 to 26.50 %, and goats from 24.50 to 38.40%. Whereas in buffalo the opposite trend was followed, and the prevalence was observed is 0% in 2022, in horses, donkeys, and mules, only one study was reported according to which a high prevalence was observed in mules (28.60%) followed by donkeys (23.50%) and horses (23.50%), in cats 38.5% prevalence was observed in a recent study and in dogs 28.43% observed, and in humans from 22 to 60%. Human beings are found to be the most affected species showing high prevalence among all. According to our findings, animals and pets not only serve as a reservoir for the parasite but also serve as a direct route for human infection with T. gondii. The diagnostic techniques used in the observed studies were mostly serological testing whereas only a few studies have only been observed with molecular testing. To know the exact pattern of the disease for its control, the trend of molecular and advanced testing should be adopted as it is more reliable. Moreover, to decrease the transmission chances of T. gondii to humans, it is crucial to manage T. gondii infections in non-human species.

1. Introduction

Infections caused by food and water have attracted a lot of attention recently. The term “foodborne sickness” refers to a set of diseases that develop after consuming microbially or chemically contaminated food. Even contaminated water, utensils, as well as the hands of the diner can spread the disease. Third-world countries have a higher prevalence of food-related disorders than developed nations. Most people in the world still lack access to clean water and sanitary facilities, and households in rural areas where untreated water used for drinking, cooking, washing fruits, bathing, and swimming expose them to various pathogens including protozoan parasites (, ). Millions of people in underdeveloped countries are seriously at risk from the potential water supply contamination with protozoan diseases. There are many basic signs of food-related diseases, and gastrointestinal dysfunction is commonly used to diagnose them.

Parasites are capable of causing an acute, chronic, and debilitating type of diseases (). In nature, parasitic protozoa may be found almost everywhere. In both developed and developing nations, they are accountable for epidemics and chronic poverty (). Since certain parasites are zoonotic in nature and consequently exist in animals, their food and water prevalence should be considered a public health problem (). The prevalence of food- and waterborne parasites has increased throughout time due to several past disease outbreaks linked to parasites. The World Health Organization (WHO) and the Food and Agriculture Organization of the United Nations (FAO) published their worldwide risk rating of foodborne parasites (FBPs) in 2014 (). It was followed in 2015 as a global burden related to foodborne pathogens (). Despite being acknowledged as significant foodborne pathogens, parasites are still underappreciated when compared to bacterial and viral foodborne pathogens ().

Toxoplasma spp is one of the important protozoans causing disease in livestock and humans (). Across the world, this parasite has posed a serious threat. Despite the standard test for diagnosing this parasite and different treatment methods, the spread of these parasites is uncontrollable due to the other management disorders (). This review summarizes etiopathogenesis, epidemiology in Pakistan from 2000 to 2022, and preventive measures for zoonotic toxoplasmosis.

2. Material and methods

2.1. Search technique

We searched databases (PubMed, Embase, Google Scholar, ScienceDirect, Scopus, ProQuest, and Web of Science) for articles reporting the seroprevalence of T. gondii in Pakistan from 2000 to 2022 to conduct this systematic review. The searches were limited to English-language articles. Electronic searches mostly employed the MeSH keywords (Human, Animal) AND (Toxoplasma gondii OR toxoplasmosis; Prevalence and seroprevalence OR serology).

For management, the citations were observed keenly. The final article choice was made after screening each article's title and abstract by eliminating duplicate records.

2.2. Criteria for inclusion and exclusion

Using the titles as a guide, references were screened, and unnecessary and duplicate references were removed. A flow chart of the article identification, screening, eligibility, and inclusion criteria is shown in Figure 1. The last search was conducted on October 6th, 2022.

Figure 1

3. Toxoplasmosis

Toxoplasma gondii is a member of the phylum Apicomplexa, which is made up of a variety of protists, most of which are intracellular parasites capable of inflicting potentially life-threatening diseases in both humans and animals. Given its ability to infect virtually all warm-blooded vertebrates, T. gondii is the most prevalent. It is also thought to infect about one-third of the world's population of humans (). According to the nation or region under consideration, seropositivity rates in the human population vary from < 10 to over 90%, partly due to local socio-economic conditions and population patterns (). For instance, there is a more significant incidence in continental Europe, South America, and the United Kingdom than in the United States or the United Kingdom. Both wild and domestic animals have high seroprevalence, making them essential T. gondii reservoirs and sources for human contamination through meat intake (). In addition to being an issue for human contamination, toxoplasmosis in farm animals has a significant negative impact on the livestock (on milk production and reproductive performance), which results in a high cost for the industry ().

Only one species has been identified for the genus Toxoplasma, yet many clonal lineages have varying degrees of pathogenicity. Four primary clonal types I, II, III, and XII dominate the population pattern of T. gondii in Europe and North America (). The most common strains in a wild and domestic context in Europe are type II (and type III, though to a lesser extent) (, ). Domestic isolates from North America are comparable to those from Europe (types II and III), while in the wild, strains from type XII prevail (, ). More contrast exists in other regions of the world. For instance, South America has a lot more genetic variety (, ), which suggests that recombination occurs more frequently there. Following T. gondii infection, the host's type, genetic makeup, and of course, the host's immune status all play a role in the development of the disease. Some species appear to be innately resistant to T. gondii infection. In contrast, others are highly susceptible, partly due to variables like their habitat's closeness to the parasite's definitive hosts (). However, the host immune system and how parasite factors affect it continue to be one of the most critical factors affecting susceptibility to T. gondii ().

4. Life cycle and routes of transmission of Toxoplasma

The life cycle of T. gondii includes both, asexual replication in a range of vertebrate hosts (intermediate hosts) and sexual replication in felids (definitive hosts). Felids consume the T. gondii by consuming encysted bradyzoites on infected intermediate hosts. Under the influence of digestive enzymes and acid, bradyzoites are liberated from cysts and enter the small intestine's epithelial cells. Although the parasite may spread throughout the body of the final host and cause clinical symptoms, this is uncommon (). More typically, bradyzoites transform into schizonts in the intestine before reaching the merozoite stage (). Merozoites differentiate into male and female gametes after a few cycles of asexual division. After that, male and female gametes combine to form diploid oocysts, which are enclosed in a solid, impenetrable wall. The millions of them contaminate the ecosystem that the felids excrete. The oocysts are resilient and survive in the environment, allowing them to spread (, ). Intermediate hosts consume sporulated oocysts by drinking or eating contaminated water and foods. Invading sporozoites quickly transform into the tachyzoite form inside a transitory parasitophorous vacuole (PV) that stays in the host cells (). Tachyzoites are proliferative forms of toxoplasmosis that spread throughout the body and cause acute symptoms. They can move between tissues via blood vessels or the lymphatic system. At least when felids can prey on the intermediate host, this ensures parasite transmission to the final host to finish the cycle. Even when intermediate hosts aren't the felids who are often their prey, the parasites can still spread to new intermediate hosts through carnivory, keeping the parasite transmission cycle going without the necessity for sexual reproduction. The life cycle of T. gondii is shown in Figure 2.

Figure 2

Human infection can occur through food consumption, such as raw or undercooked meat containing cysts or vegetables, fruits, or water that has sporulated oocysts (). To prevent foodborne toxoplasmosis, it is crucial to wash produce, cook meat properly, and adequately treat sewage or water (). Congenital transfer of tachyzoites from a woman who is mainly infected to the growing fetus through the placenta is one of the alternative ways of transmission ().

Congenital toxoplasmosis must be managed with precautions that restrict the mother's exposure to established transmission channels while pregnant and with quick identification and treatment beginning following infection. Although uncommon, blood transfusion (41) or organ transplantation (42) from sick donors are potential sources of contamination in people.

5. Clinical manifestations of toxoplasmosis

In immunocompetent people, toxoplasmosis can cause a minor, self-limiting disease or remain unnoticed in most cases (43). In pregnant women, congenital toxoplasmosis may develop because, during the parasite's dissemination phase, the parasite passes through the placenta and infect the growing fetus. Depending on the gestational stage at the time of maternal infection, it might result in varying degrees of neurological, ophthalmic, or systemic damage. For instance, a maternal illness in the first trimester may result in more severe symptoms (44). Although some of them can also happen later in life, hydrocephalus, mental retardation, epilepsy, and blindness are the most significant sequelae for newborns (45).

Even though acute acquired infection can occur, immunodeficiency in adults can also result in severe toxoplasmosis.

People who have impaired immune systems or immunosuppression [such as those with HIV (46), cancer patients (47), or transplant recipients] are particularly vulnerable. Toxoplasmic encephalitis may be the most severe outcome because it causes significant tissue damage and inflammation when toxoplasmosis from parasites ensconced in the central nervous system returns (48). Left untreated, this cerebral toxoplasmosis can be potentially fatal and frequently manifest as headache, fever, ataxia, or seizures. Acute toxoplasmosis has harmful effects, but chronic toxoplasmosis—the parasite's long-term persistence in the body as tissue cysts—may also have significant effects on behavioral changes and psychiatric problems, especially because it affects the central nervous system (49).

6. Prevalence of toxoplasmosis in humans and animals of Pakistan

Human studies that assessed the seroprevalence of T. gondii among the various individual groups listed in Table 1 have been published in Pakistan. Seroprevalence of T. gondii in dogs and cats, small ruminants, large ruminants, equines and camels, and poultry are mentioned in Tables 26, respectively. Pregnant women's seroprevalence has received the majority of attention in research (5052), followed by patients with illnesses (53), The sociodemographic information, epidemiological profile, potential risk factors for transmitting the T. gondii infection, and the source of detection and diagnostic approach is also the focus of these investigations. Variable seroprevalence levels have been observed with a rise in percentage between 2001 and 2022.

Table 1

SpeciesArea of studyPrevalence rate (%)Source of detectionNo. of samples testedDiagnostic approachAge of animalYear of studyReferences
HumanLahore22%Serum150LAT< 15 years to >40 yearsN/A(59)
Kohat, Khyber-Pakhtunkhwa14.4%Serum180 pregnantELISAN/AJune–September 2007(60)
Lahore11.33%Serum300LATNot mentioned for rats ≥45 years in humans2012(61)
Rajanpur, Bahawalnagar, and Multan29.45%Serum550LAT1–70 years2010(62)
Khyber-Pakhtunkhwa65.71%Serum420ELISA10 to >51 yearsN/A(63)
Multan19.4% pregnant women
15.2% non-pregnant women
Serum232 pregnant women
171 non-pregnant women
ELISA20–40 years2017(64)
Khyber-Pakhtunkhwa1.32%Serum150 pregnant womenELISA20–40 yearsFebruary–November 2015(65)
Charsadda21%Serum300LAT15–75 yearsMay–July 2017(66)
Sub-Tropical Areas20.37%Serum1,659ELISA< 10 to >40 monthsN/A(67)
Punjab7.42%Serum593ELISA< 20 to >40 yearsJanuary 1–December 31, 2017(68)
Bahawalpur21.2% farmer
6.8% non-farmer
Serum160 farmer
160 non-farmer
LATN/AMay 2016–April 2017(69)
Swat25.92%Serum216Lateral flow chromatographic immune-assay31–40 yearsJune–September 2016(70)
Khyber-Pakhtunkhwa40.6%Serum360ELISA16–40 yearsN/A(53)
Peshawar21.3%Serum94 Pregnant womenICT21–53 yearsSeptember–December 2017(52)
Sahiwal24.5%Serum200ELISAN/AMay–November 2020(71)
KPK39.94%Serum425ELISA15–50 yearsN/A(72)
Khanewal52%Serum200ELISAN/AMay–November 2020(71)

Reported prevalence of Toxoplasma gondii in human population of Pakistan.

Table 2

SpeciesArea of studyPrevalence rate (%)Source of detectionNo. of samples testedDiagnostic approachAge of animalYear of studyReferences
CatsFaisalabad60%Serum10LAT6 months to >4 yearsN/A(73)
Lahore56% catsSerum50LAT6 monthsN/A(59)
Sub-tropical Arid parts26.43% catsSerum420ELISA1–2 yearsJanuary–December 2012(74)
Lahore2.3%Feces470PCRN/AJune 2013–May 2014(75)
KPK25.4% catsSerum and blood50PCR2–4 yearsN/A(76)
KPK74.6%Serum and blood147ELISA2–4 yearsN/A(76)
KPK2.50%Feces40Centrifugal sedimentation leading to PCRN/AJanuary–December 2019(77)
Sahiwal and Khanewal6.5%Feces200Floatation/sedimentationN/AMay–November 2020(71)
KPK12.22%Serum40LATN/AJanuary–December 2019(77)
Sahiwal and Khanewal38.46%Feces13PCRN/AMay–November 2020(71)
DogsFaisalabad50% dogsSerum40LAT6 months to >4 yearsN/A(73)
Lahore39% dogsSerum100LAT6 months to >7 yearsN/A(59)
Lahore46.88%Serum305LAT6 months to >4 yearsN/A(78)
Sub-tropical Arid parts28.43% DogsSerum408ELISA1–2 yearsJanuary–December 2012(74)

Reported prevalence of Toxoplasma gondii in cats and dogs in Pakistan.

Table 3

SpeciesArea of studyPrevalence rate (%)Source of detectionNo. of samples testedDiagnostic approachAge of animalYear of studyReferences
SheepRahim Yar Khan11.2%Serum90LATN/A2006–2007(79)
Mardan44.13% sheepSerum290IHA1–2 yearsN/A(80)
Pothwar Region18.16% sheepSerum413ELISA1–3 yearsSeptember 2011–December 2012(81)
Southern Punjab37.31%Serum335LATN/AMay 2012–April 2013(82)
Northeast Punjab26.2% sheepSerum470ELISA1–3 yearsJanuary–December 2013(83)
Multan34.02%Serum288LAT4–73 monthsApril 2012–June 2013(84)
Khanewal33.01%Serum212LAT4–73 monthsApril 2012–June 2013(84)
Cholistan desert (Punjab)37.31%Serum335LAT1 to >25 monthsN/A(84)
Cholistan desert (Punjab)29.13%Serum865LAT1 to >25 monthsN/A(74)
Multan44.80%Serum125LAT< 1 to > 2 yearsN/A(85)
Charsadda40.55% sheepSerum143LAT1–4 yearsN/A(86)
Dera Gazi Khan23% ELISA
25% LAT
Serum103ELISA and LAT8–42 monthsN/A(87)
Bahawalpur36.25% sheepSerum160LATN/AMay 2016–April 2017(69)
Peshawar49% sheepSerum360IHT< 1 to < 2 yearsN/A(88)
Khyber-Pakhtunkhwa52.69%Serum167ELISA1 to > 3 years2018–2020(54)
Jhang31.49% sheepSerum181LAT< 12 to >24 monthsN/A(90)
Sahiwal23.5%Serum1,000ELISAN/AMay–November 2020(71)
Khanewal26.5%Serum1,000ELISAN/AMay–November 2020(71)
GoatsRahim Yar Khan24.5%Serum110LATN/A2006–2007(79)
Mardan42.28% goatsSerum350IHA1–2 yearsN/A(80)
Pothwar Region14.32% goatsSerum419ELISA1–3 yearsSeptember 2011–December 2012(81)
Northeast Punjab42.8% goatSerum530ELISA1–3 yearsJanuary–December 2013(83)
Multan40.80Serum125LAT< 1 to >2 yearsN/A(85)
Charsadda41.61%Serum149LAT1 to >3 yearsN/A(65)
Bahawalpur28.1% goatSerum160LATN/AMay 2016–April 2017(69)
Dera Gazi Khan32.67% ELISA
35.64% LAT goat
Serum101ELISA and LAT8–42 monthsN/A(87)
Khyber Pakhtunkhwa7.9%Serum70ELISA1 month to < 2 years2018–2020(54)
Dera Ghazi Khan10%Serum410LAT1–3 years6 months(77)
Khyber-Pakhtunkhwa18.25 %Serum126ELISA1 to >3 years2018–2020(54)
Faisalabad33.59%Serum384LAT< 2 to >5 yearsOctober 2016–March 2017(91)
Peshawar45.7% goatsSerum420IHA< 1 to < 2 yearsN/A(88)
Faisalabad53.15%Serum380LAT1–6 yearsN/A(89)
Khanewal5.3%Blood898PCR1–3 yearsMarch 2019–February 2020(92)
Faisalabad17.9%Serum240LAT< 1 to >3 yearsSeptember 2016, February 2017(93)
Khanewal29.2%Serum1,000ELISAN/AMay–November 2020(71)
Jhang36.52% goatSerum219LAT< 12 months to >24 monthsN/A(90)
Sahiwal38.4%Serum1,000ELISAN/AMay–November 2020(71)

Reported prevalence of Toxoplasma gondii in small ruminants (sheep and goats) in Pakistan.

Table 4

SpeciesArea of studyPrevalence rate (%)Source of detectionNo. of samples testedDiagnostic approachAge of animalYear of studyReferences
CattleNorthern Punjab19.75% cattleSerum400ELISA>24 to >48 monthsJanuary–December 2012(94)
Charsadda55.39%Serum139LAT1 to >5 yearsN/A(65)
Khyber Pakhtunkhwa13%Serum100ELISA1 month to < 2 years2018–2020(54)
Khyber-Pakhtunkhwa18 %Serum100ELISA1 to >3 years2018–2020(54)
Rajanpur12.2% cattleBlood190PCR≥5 years to < 5 yearsJuly–October 2019(95)
Pakistan29.75%Serum90ELISAN/AN/A(96)
Pakistan35.75%Serum400LAT>5 yearsN/A(96)
BuffaloNorthern Punjab15.16% buffaloSerum422ELISA>24 to >48 monthsJanuary–December 2012(94)
Charsadda17.32% BuffaloSerum127LAT1–4 yearsN/A(86)
KPK15.51 %Serum58ELISA1 to >3 years2018–2020(54)
Rajanpur0% BuffaloBlood120PCR≥5 to < 5 yearsJuly–October, 2019(95)

Reported prevalence of Toxoplasma gondii in large ruminants (cattle and buffalo) in Pakistan.

Table 5

SpeciesArea of studyPrevalence rate (%)Source of detectionNo. of samples testedDiagnostic approachAge of animalYear of studyReferences
EquinesFaisalabad, Lahore, and GujranwalaHorses 23.5%Serum183 horsesLAT≥5 years to < 10 yearsN/A(101)
Faisalabad, Lahore, and GujranwalaMule 28.6%Serum14 mulesLAT≥5 years to < 10 yearsN/A(101)
Faisalabad, Lahore, and GujranwalaDonkey 58.7%Serum75 donkeyLAT≥5 years to < 10 yearsN/A(101)
CamelsBahawalpur Region10%Serum100 camelsLAT1–15 yearsN/A(102)
Bhawalpur, Punjab17.9%Serum201 camelLAT1–>13 yearsFebruary–December, 2015(103)
Punjab40.1%Serum897 one-humped camelIndirect ELISA3–7 yearsJuly–August, 2016(104)
Mianwali district38%Serum350 camelsIndirect ELISA3–7 yearsN/A(105)

Reported prevalence of Toxoplasma gondii in equines and camels of Pakistan.

Table 6

SpeciesArea of studyPrevalence rate (%)Source of detectionNo. of samples testedDiagnostic approachAge of animalYear of studyReferences
PoultryMardan18.85%Serum536IHAN/AN/A(96)
Faisalabad36.33%Serum300LAT< 1 to >2 yearsJuly 2011–June 2012(97)
Kasur12.5 %Serum200 wild birdsLATN/AN/A(98)
Upper dir and Peshawar10.84295 tissue samples295PCR30 days to 2 yearsN/A(99)
Upper Dir and Peshawar26.6%398 serum398ELISA30 days to 2 yearsN/A(99)
Punjab38.3%Brain sample120 rock birdsPCRN/AJuly 2018–October 2018(100)
RatsLahore58.57% of ratsSerumRat 210LATN/A2012(61)

Reported prevalence of Toxoplasma gondii in poultry and rats in Pakistan.

IFA, indirect fluorescent assay; IHA, indirect hemagglutination test; ELISA, enzyme-linked immunosorbent assay; LAT, latex agglutination test; PCR, polymerase chain reaction.

The procedure used in the publications is often the collection of a blood sample from the population and testing it for anti-toxoplasma antibodies in the sera. The ELISA, latex agglutination (LA) test, and other serological assays were often employed (54, 55). Although their sensitivity and specificity varied, commercial test kits were employed, and the results were occasionally inconclusive.

In the food chain, which serves as a source of nutrition for humans and other animals, animals play a crucial role. The bradyzoite cyst is present in the body tissues of animals, and the parasite then transmits to new hosts by eating a raw or undercooked piece of the infected tissues (56). This situation raises the risk of zoonotic infection by foodborne pathogens since a particular group of humans, such as hunters, butchers, and consumers may get infected by ingesting domestic or wild meat (57). Only wild and domestic cats excrete the oocyst infective stage, which may infect humans when eaten in tainted food, water, or vegetables, which is especially noteworthy (58).

According to an analysis of the records currently available over the previous 20 years (2001–2022), domestic animals in Pakistan have a relatively high and rising seroprevalence rate of T. gondii as a zoonotic infection, except for buffalo, cats, and dogs. The comparison is shown in Figure 3. Although the prevalence level may have decreased and increased in different species, caution is advised.

Figure 3

All the data mentioned in the previous study of Figure 1 is collected from the year 2022 except for equines, dogs, and rats because the previous study performed in equine was in the year 2015, and for rat, it was in 2012. Whereas in dogs, the last study was performed in 2014 in Pakistan.

7. Methods used for the detection of T. gondii

Examining the levels of immunoglobulin G (IgG), immunoglobulin M (IgM), and IgG avidity in a sample—typically serum from the blood of a particular host population—the serological test assesses the antibodies and calculates the seroprevalence of infection. Although it is the simplest and most straightforward test, it frequently yields false-positive or false-negative findings (106). Most of the studies in Pakistan have been diagnosed through Latex Agglutination Test (LAT). Cd4 mentioned in Table 1. The tests using molecular methods are reliable, perceptive, and accurate (107). Few studies have been reported and mentioned in Table 1, which have been diagnosed with Molecular methods. They use a variety of samples to find a specific gene of interest that is unique to this particular organism. Numerous techniques are routinely used, including loop-mediated amplification (LAMP), quantitative PCR, and traditional polymerase chain reaction (PCR) (108). This technique is seldom employed in histological procedures. It is primarily concerned with identifying the bradyzoite stage in. tissues such as the heart, liver, and brain. The bradyzoite stage is primarily detected in tissues, including the heart, liver, and brain (109). Before being examined under a microscope, such tissues are mounted on a glass slide and stained with hematoxylin and eosin (H&E). Another method of evaluating suspected samples, such as cat feces, liver, lung, and brain homogenates of intermediate hosts by inoculation and then testing the animal for the presence of an infection, is bioassay/in vivo using an animal model (mice/rat) (110). The test is costly and time-consuming, but it is an accurate approach to assessing the sustainability and pathogenicity of the various strains. Through the establishment of an enclosed environment where suspected specimens, such as blood, are cultured in a medium, the in vitro/tissue culture technique removes the usage of animals (111). Microscopy is used to assess the sample's motility or viability for the tissue culture endpoint. Most intuitive findings that can identify the parasite's morphology nevertheless rely heavily on microscopy as their foundation. Other tests like tissue culture and histology consistently rely on it because of its adaptability (112).

8. Comparison of serological techniques for T. gondii antibody detection in Pakistan

All studies employed convenient sampling to gather data, and two serological tests—the Latex Agglutination Test (LAT) and Enzyme-Linked Immunosorbent Assay (ELISA)—are mostly used to assess the outcomes based on the detection of IgG, IgM, and avidity test of T. gondii antibodies (Table 1) (96, 99). Most studies did not follow established procedures for collecting and processing specimens, and most did not have information on the control group. However, since a different company produced each ELISA and LAT test, it was challenging to evaluate and confirm each assay's specificities and sensitivities. Except for a few recent studies, further PCR validation of the data was not done (75, 77, 95, 100). Because of differences in the experimental design and the commercial kits utilized, some of the results are thus disputed.

9. Prevention of toxoplasmosis

The foundation for the current strategies employed to control T. gondii infection has been supplied by the exponential growth in our understanding of T. gondii biology, epidemiology, and ecology during the past few decades. Limiting contact with available transmission channels and minimizing exposure to the parasite's infectious phases are the main goals of preventative interventions.

As previously indicated, people contract T. gondii either by eating or drinking raw or undercooked meat with parasite cysts on it or by drinking water contaminated with oocysts deposited in cat feces. Additionally, eating raw shellfish can result in illness (106).

Therefore, seronegative should only consume fully cooked meat, refrain from consuming raw shellfish, carefully wash their hands after coming into contact with raw meat, avoid gardening and soil handling without gloves, and thoroughly clean fruits and vegetables.

People who take care of the litter box should make it a habit to wear disposable gloves and wash their hands thoroughly with antiseptic. Seronegative should refrain from adopting or handling stray cats, and cats should stay indoors whenever feasible. They should also not be fed raw or undercooked meat. The suggestions mentioned above for preventing T. gondii infection also apply to people in other particular at-risk groups. Soon after HIV diagnosis, standardized guidelines advise testing all for serological signs of prior T. gondii infection (107).

Primary prophylaxis should be given to those who are also seropositive for T. gondii and have peripheral blood CD4 T cell levels of 100/L (107). People receiving cART who have had more than 200 CD4 T cells/L for 3 months can stop using primary prophylaxis without risk. When they reach more than 200 CD4 T cells/L for 6 months, PLWH who have undergone effective therapy for TE and are getting cART can stop receiving maintenance treatment (107). It is important to remember that despite these precautions, T. gondii infection cannot be entirely avoided.

10. Conclusion

Infectious diseases of animals including parasitic infestations pose significant threats to health and productivity potential of animals (113116) which leads to heavy economic losses (117122). Parasitic infections lead to chronic and debilitating types of diseases and have zoonotic implications as well (, 123126). Results of the current evaluation on toxoplasmosis research in Pakistan from 2001 to 2022 revealed little information on animal seroprevalence in cases of humans, cattle, buffaloes, sheep, goats, cats, dogs, camels, and horses. In Pakistan, the seroprevalence among human females is rising. The frequency of toxoplasmosis in cattle, mainly chicken intended for human consumption, is also little understood. The T. gondii strain prevalent in Pakistan from HIV patients, pregnant women, livestock, and domestic cats has not yet been genetically characterized. Alarming reports of toxoplasmosis in the KPK population have been observed in humans. Despite the widespread occurrence and severe effects of toxoplasmosis, which are mostly seen in immunocompromised patients, there are significant flaws in the present control programs, particularly in the diagnostic resources available. The prevalence throughout the country is increasing every year. The majority of diagnostic procedures also frequently misdiagnose the illness in endemic regions. It is necessary to create molecular approaches that are sensitive, specific, straightforward to use, affordable, and high throughput because early detection is the most effective way to combat the illness. Researchers, healthcare professionals, veterinary professionals, and politicians can benefit from the current review on toxoplasmosis. Therefore, there is an urgent need to inform and educate the public about the risk factors for toxoplasmosis infection in humans and animals. That may be accomplished by running health-related advertisements and educational campaigns in regional newspapers, television, radio, and, more recently, social media platforms.

Statements

Data availability statement

All data supporting the conclusions of this article are included within the article.

Author contributions

WQ and AA worked on the development of this unique title of review, planned, designed, and structured the layout of the article. WQ wrote the article. AA reviewed the article. All authors finally approved this review article.

Acknowledgments

The researcher would like to thank the Deanship of Scientific Research, Qassim University, Saudi Arabia, for funding the publication of this review.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

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Summary

Keywords

Toxoplasma, life cycle, transmission, symptoms, prevalence, diagnostic methods/prevention

Citation

Qamar W and Alsayeqh AF (2023) A review of foodborne Toxoplasma gondii with a special focus on its prevalence in Pakistan from 2000 to 2022. Front. Vet. Sci. 9:1080139. doi: 10.3389/fvets.2022.1080139

Received

25 October 2022

Accepted

07 December 2022

Published

18 January 2023

Volume

9 - 2022

Edited by

Kun Li, Nanjing Agricultural University, China

Reviewed by

Shahbaz Ul Haq, Lanzhou Institute of Husbandry and Pharmaceutical Sciences (CAAS), China; Muhammad Ehsan, Islamia University of Bahawalpur, Pakistan; Qaisar Tanveer, University of Edinburgh, United Kingdom

Updates

Copyright

*Correspondence: Abdullah F. Alsayeqh ✉

This article was submitted to Comparative and Clinical Medicine, a section of the journal Frontiers in Veterinary Science

Disclaimer

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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