Toxoplasmosis in Cats and Public Health: Risks During Pregnancy and Prevention

Etiology and Life Cycle of Toxoplasma gondii

Toxoplasmosis is caused by the obligate intracellular apicomplexan parasite Toxoplasma gondii. The definitive host is the domestic cat and other felids, in which the parasite completes its sexual cycle and produces oocysts [1]. The life cycle involves both sexual reproduction in the feline intestinal epithelium and asexual replication in a wide range of intermediate hosts, including mammals and birds [2]. Cats become infected by ingesting tissue cysts from intermediate hosts or by ingesting sporulated oocysts from the environment [3]. After ingestion, the parasite invades the intestinal epithelium and undergoes a series of developmental stages culminating in the production of unsporulated oocysts that are shed in feces [1]. Shedding typically begins 3 to 10 days after primary infection and can last for 1 to 3 weeks, during which millions of oocysts may be released [4]. Once shed, oocysts sporulate in the environment and become infectious to intermediate hosts, including humans [5].

The pre-sexual stages of T. gondii within the feline gut have been characterized at the cellular level, revealing a proliferative phase that precedes gametogenesis [2]. A single-cell atlas of sexual development in the feline intestinal tract has further elucidated the transcriptional programs governing this process [1]. The parasite also induces dynamic changes in the microRNA expression profile of the feline small intestine during infection, which may modulate host immune responses [6].

Epidemiology and Seroprevalence in Cats

Seroprevalence of T. gondii in domestic cat populations varies widely by geographic region, management practices, and lifestyle. In a study from Hong Kong, seroprevalence in privately owned cats and community cats was associated with demographic factors such as age, outdoor access, and diet [7]. In Jordan, seroprevalence and molecular detection of T. gondii in cats revealed significant associations with risk factors including stray status and raw meat consumption [3]. In Bangkok, Thailand, PCR detection of T. gondii DNA in fecal samples from stray cats demonstrated a notable prevalence of oocyst shedding, highlighting the potential for environmental contamination [4].

Seroprevalence studies in other animal species provide indirect evidence of environmental contamination. High seroprevalence rates have been reported in dogs in Brazil [8], dairy cattle in Turkey [9], goats in Nigeria [10], and deer in Iraq [11]. These findings underscore the widespread distribution of T. gondii and the role of cats as the primary source of environmental oocysts [5, 12]. In Bangladesh, genotype distribution and risk factor analysis in animals further confirmed the presence of T. gondii in domestic and peridomestic settings [12].

Clinical Signs and Pathology in Cats

Most immunocompetent cats infected with T. gondii remain asymptomatic [13]. Clinical disease is more common in kittens, immunocompromised cats, or those co-infected with other pathogens. When clinical signs occur, they may include fever, lethargy, anorexia, dyspnea, and ocular or neurological signs [14]. Pyogranulomatous and neutrophilic lymphadenitis has been described in cats with toxoplasmosis, and a subset of cases may present with steroid-responsive lymphadenitis [14]. Neurological manifestations can result from cerebral involvement, and ocular toxoplasmosis may present as uveitis or retinochoroiditis [15].

The AB blood group system phenotype does not appear to play a role in T. gondii infection in cats, suggesting that genetic susceptibility is not linked to this particular blood group [13]. Reproductive tissues of cats from a municipal neutering program have been found to harbor T. gondii, indicating potential vertical transmission or tissue tropism [16].

Pathogenesis and Host Cell Interactions

After ingestion, T. gondii tachyzoites invade host cells through an active process involving the formation of a parasitophorous vacuole. The parasite evades host immune responses by modulating signaling pathways and inhibiting apoptosis. In the feline gut, sexual development is restricted to the intestinal epithelium, where the parasite undergoes gametogenesis and oocyst formation [1]. The molecular mechanisms governing this stage conversion are under active investigation, with recent advances in gene-edited live-attenuated vaccines targeting these processes [17].

The parasite can alter host behavior in intermediate hosts, a phenomenon that has been documented in rodents and may have implications for transmission to felids [18]. The mechanisms underlying these behavioral changes involve neurotropic effects and modulation of neurotransmitter pathways [19].

Diagnosis of Feline Toxoplasmosis

Diagnosis of toxoplasmosis in cats relies on a combination of serological, molecular, and histopathological methods. Serological detection of anti-T. gondii antibodies is commonly performed using commercial ELISA kits or immunofluorescence assays [20]. A double-antigen sandwich colloidal gold immunochromatographic strip has been developed and field-validated for detection of T. gondii antibodies in multiple host species, including cats [20]. Similarly, a SAG1-based colloidal gold immunochromatographic strip has been developed for serological detection in swine, with potential cross-species applicability [21].

Molecular detection of T. gondii DNA in feline feces, blood, or tissues is achieved through PCR-based assays. An antisense PCR assay has been developed and evaluated for detection of T. gondii in domestic cats, offering improved sensitivity for low-parasite-burden samples [22]. PCR detection in fecal samples from stray cats has been used to estimate environmental contamination risk [4]. The MIC17A antigen has been identified as a potential marker for both entero-epithelial and chronic stage infection, which may improve diagnostic accuracy for feline toxoplasmosis [23].

Histopathological examination of tissues, particularly lymph nodes, can reveal pyogranulomatous inflammation and the presence of tachyzoites or tissue cysts [14]. Immunohistochemistry and in situ hybridization provide additional specificity for confirming T. gondii infection in tissue sections.

Treatment and Management

Treatment of clinical toxoplasmosis in cats typically involves administration of antiprotozoal agents such as clindamycin, which is the drug of choice for feline toxoplasmosis. Supportive care, including fluid therapy and nutritional support, is indicated for severely affected animals. In cases of ocular toxoplasmosis, topical corticosteroids may be used in conjunction with systemic antiprotozoal therapy to control inflammation [15]. Treatment should be guided by clinical signs and confirmed diagnosis, as asymptomatic cats generally do not require therapy.

Zoonotic Risk and Public Health Significance

T. gondii is a zoonotic parasite of major public health importance. Humans can become infected through ingestion of sporulated oocysts from contaminated soil, water, or food, or through consumption of undercooked meat containing tissue cysts [5, 10]. Direct contact with cats is not considered a primary route of transmission, as oocysts require 1 to 5 days to sporulate after shedding [24]. However, handling of cat litter boxes or contaminated soil poses a risk, particularly for pregnant women and immunocompromised individuals [24].

The risk of congenital toxoplasmosis is a primary public health concern. Primary infection acquired during pregnancy can lead to transplacental transmission and fetal infection, resulting in miscarriage, stillbirth, or congenital abnormalities including hydrocephalus, intracranial calcifications, and chorioretinitis [25, 26]. Seroprevalence studies in women with a history of abortion or stillbirth have identified T. gondii seropositivity as a potential contributing factor [25]. In Algeria, molecular and histopathological detection of T. gondii in aborted fetal goat myocardium has been reported, with associated risk factors including contact with cats [26]. Similarly, T. gondii has been detected in an aborted equine fetus in Brazil, with serological evidence of infection in mares [27].

The term "cat toxoplasmosis baby" is often used in public discourse to describe the risk of congenital infection from maternal exposure to feline-derived oocysts. While the risk is real, it is important to contextualize it within the broader epidemiology of T. gondii infection. Many pregnant women acquire infection from undercooked meat or contaminated produce rather than from direct contact with cats [24]. Nevertheless, seronegative pregnant women who own cats should receive specific advice on preventive measures [24].

Seroprevalence of T. gondii in veterinary medicine professionals and students has been documented, indicating occupational exposure risk [28]. Knowledge and practices regarding toxoplasmosis among pregnant women in some regions remain suboptimal, highlighting the need for targeted health education [29, 30]. In Côte d'Ivoire, a first report of knowledge and practices among pregnant women in primary care revealed gaps in awareness of transmission routes and prevention [29]. In Iraq, university students demonstrated variable knowledge of toxoplasmosis, suggesting that educational interventions are warranted [30].

Prevention Strategies for Pregnant Women

Prevention of toxoplasmosis in pregnant women centers on avoiding ingestion of oocysts and tissue cysts. Specific recommendations for cat owners include the following:

• Daily cleaning of litter boxes, preferably by a non-pregnant individual, to remove oocysts before they sporulate [24].
• Use of gloves and hand washing after handling cat litter or gardening.
• Keeping cats indoors to prevent hunting and ingestion of intermediate hosts.
• Feeding cats commercial cooked or canned food rather than raw meat.
• Avoiding stray cats and kittens during pregnancy.

Environmental contamination with oocysts is a significant risk factor, particularly in areas with large populations of free-roaming cats [5, 4]. Social marginalisation and environmental degradation have been associated with increased T. gondii exposure in urban informal settlements, underscoring the role of socioeconomic factors in transmission risk [5]. In Quilombola communities, risk factors and ocular health associated with toxoplasmosis have been identified, further emphasizing the need for community-level interventions [31].

Vaccine Development and One Health Approaches

Significant research efforts are directed toward developing vaccines against T. gondii for both cats and intermediate hosts. Gene-edited live-attenuated vaccines have shown promise in preclinical studies, with recent advances focusing on deletion of genes essential for virulence or persistence [17]. A comprehensive review of vaccine development from antigen discovery to mRNA platforms has highlighted the potential for One Health strategies that target both animal and human populations [32]. Vaccination of cats could reduce oocyst shedding and environmental contamination, thereby decreasing zoonotic risk.

Diagnostic Advances and Surveillance

Recent diagnostic innovations include the development of antisense PCR assays for improved sensitivity in feline samples [22] and colloidal gold immunochromatographic strips for rapid serological screening in multiple species [20, 21]. These tools facilitate large-scale surveillance and point-of-care testing in veterinary practice. Molecular detection of T. gondii in fecal samples from stray cats provides a means of monitoring environmental contamination and assessing public health risk [4].

The following table summarizes key diagnostic methods for feline toxoplasmosis:

Decision Tree for Management of Toxoplasmosis Risk in Pregnant Cat Owners

The following Mermaid diagram outlines a clinical decision tree for veterinary professionals advising pregnant women who own cats.

flowchart TD
    A[Pregnant woman owns cat], > B{Is woman seronegative for Toxoplasma?}
    B, >|Yes| C[Provide preventive counseling]
    B, >|No / Unknown| D[Refer for human serological testing]
    C, > E[Advise daily litter box cleaning by non-pregnant person]
    C, > F[Advise keeping cat indoors]
    C, > G[Advise feeding only cooked/commercial food]
    C, > H[Advise hand hygiene after gardening or soil contact]
    E, > I[Monitor cat for clinical signs of toxoplasmosis]
    I, > J{Does cat have clinical signs?}
    J, >|Yes| K[Perform feline serology and PCR]
    J, >|No| L[No further action needed]
    K, > M{Is cat actively shedding oocysts?}
    M, >|Yes| N[Isolate cat from pregnant woman; treat if indicated]
    M, >|No| O[Reassure; continue preventive measures]
    N, > P[Re-test after treatment to confirm cessation of shedding]

Conclusion

Toxoplasmosis in cats represents a significant zoonotic concern, particularly for pregnant women and immunocompromised individuals. The feline definitive host is central to the environmental dissemination of T. gondii oocysts, which are the primary source of infection for humans and other animals [1, 24]. Advances in molecular diagnostics, including antisense PCR and immunochromatographic assays, have improved the detection of infection in cats and facilitated surveillance of environmental contamination [20, 21, 22]. Vaccine development using gene-edited live-attenuated strains holds promise for reducing oocyst shedding and breaking the transmission cycle [17, 32]. Preventive measures, including proper litter box management, indoor confinement, and dietary precautions, remain the cornerstone of risk reduction for pregnant women [24]. Public health education targeting both veterinary professionals and the general public is essential to mitigate the risks associated with this widespread parasite [29, 30].

References

[1] Alrubaye HS, Reilly SM, da Silva R, et al. A single-cell atlas of Toxoplasma sexual development in the feline intestinal tract. Nat Microbiol. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/42020723/

[2] Sena F, Hakimi M-A, Francia ME. Proliferating toward sex: characterization of cell division of Toxoplasma gondii's pre-sexual stages. mBio. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/42153709/

[3] Alkhatatbeh SK, Lafi SQ, Hammad HB, et al. The first seroprevalence and molecular detection of toxoplasmosis infecting cats in Jordan with associated risk factors. Vet Parasitol Reg Stud Reports. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/41741047/

[4] Kengradomkij C, Chimnoi W, Kamyingkird K, et al. PCR detection of Toxoplasma gondii DNA in fecal samples from stray cats in Bangkok Metropolitan, Thailand. Food Waterborne Parasitol. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/42094705/

[5] Eyre MT, Wang JY, Carneiro IO, et al. Social marginalisation, environmental degradation and Toxoplasma gondii exposure in urban informal settlements in Brazil. PLoS Negl Trop Dis. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/42330015/

[6] Zhai B, Bao B, Xie SC, et al. Dynamic landscape of microRNA expression in the feline small intestine during Toxoplasma gondii infection. Parasit Vectors. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/41965856/

[7] Elsohaby I, Zubair M, Baqar Z, et al. Seroprevalence of Toxoplasma gondii and associated demographic factors in privately-owned dogs, cats, and community cats in Hong Kong. BMC Vet Res. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/42135800/

[8] Artiaga-Silva GL, de Lima Ruy Dias ÁF, Carvalho MR, et al. High Seroprevalence Rates of Toxoplasma gondii and Neospora caninum in Dogs in the Pantanal Region of Mato Grosso, Brazil. Acta Parasitol. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/41843222/

[9] Hanedan B, Taş BZ, Yıldırım E, et al. Investigation of Toxoplasma gondii seroprevalence and associated risk factors in dairy cattle in the Eastern Anatolia region of Türkiye. Vet Parasitol Reg Stud Reports. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/41819961/

[10] Muhammad AS, Kudi AC, Mohammed A, et al. Public health significance of prevalence and risk factors associated with Toxoplasma gondii infection in goats sampled from two quarantine facilities and an institutional farm in Maiduguri metropolis, Borno state, Nigeria. Sci Rep. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/42020619/

[11] Aziz KJ, Mikaeelb FB, Nasrullah OJ, et al. Seroepidemiological investigation of Toxoplasma gondi and Neospora caninum in local Deers in Erbil, Iraq. Vet Parasitol Reg Stud Reports. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/42034957/

[12] Biswas PK, Aryal D, Tarak AN, et al. Genotype distribution and risk factors of Toxoplasma gondii infection in animals of Trishal, Bangladesh. PLoS One. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/41528989/

[13] Spada E, Tattarletti G, Proverbio D, et al. The AB Blood Group System Phenotype Does Not Play a Role in Toxoplasma gondii Infection in Cats. Pathogens. 2025. URL: https://pubmed.ncbi.nlm.nih.gov/41471183/ *** Disclaimer: This article is for educational and informational purposes only. It is not intended to substitute for professional veterinary advice, diagnosis, treatment, or regulatory guidance. Always consult a licensed veterinarian or qualified specialist regarding animal health, disease diagnosis, and therapeutic decisions.

[14] Doyle E, Walker J. Diagnosis of pyogranulomatous and neutrophilic lymphadenitis in 72 cats presenting to a referral hospital: with a focus on nine cats with steroid-responsive lymphadenitis. J Feline Med Surg. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/41527158/

[15] Askaryanzardak A, Kakkassery V, Tartaglione Gracia GP, et al. [Ocular toxoplasmosis in adults : Refresher course]. Ophthalmologie. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/41603939/

[16] Murata FHA, Barboza JP, de Souza CAG, et al. Investigation of Toxoplasma gondii in reproductive tissues of companion animals from a municipal neutering program. Vet Parasitol Reg Stud Reports. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/41651631/

[17] Sang X, Zhang H, Zhang Y, et al. Gene-edited live-attenuated vaccines against Toxoplasma gondii: recent advances and future frontiers. Parasit Vectors. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/42252477/

[18] Loeb J. Thrill seekers: how parasites change host behaviour. Vet Rec. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/41481034/

[19] Jesuthasan J, Merritt K, Solmi F, et al. The association between childhood Toxoplasma gondii, psychotic experiences and grey matter volume: A population-based cohort study. Schizophr Res. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/41643571/

[20] Mu X, Chen C, Pu X, et al. Development and Field Validation of a Double-Antigen Sandwich Colloidal Gold Immunochromatographic Strip for Detection of Toxoplasma gondii Antibodies in Multiple Host Species. Transbound Emerg Dis. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/42253330/

[21] Chen XX, Sun H, Liang Y, et al. Development of a SAG1-based colloidal gold immunochromatographic strip for rapid serological detection of swine Toxoplasma gondii. Parasit Vectors. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/42169035/

[22] Li YY, Bai SY, Yu HQ, et al. Development and evaluation of an antisense PCR assay for Toxoplasma gondii detection in domestic cats. Vet Parasitol. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/41724116/

[23] Günay-Esiyok Ö, Koçkaya ES, Yılmaz R, et al. The Potential of MIC17A both as an Entero-epithelial and Chronic Stage Marker for Detection of Feline Toxoplasmosis. Curr Microbiol. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/41874672/

[24] Gharbi M, Yera H, Dupouy-Camet J. [The cat, the women and the toxoplasma: What advice should be given to a pregnant woman who is seronegative for toxoplasmosis and owns a cat?]. Gynecol Obstet Fertil Senol. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/41628830/

[25] Karacali B, Mor N. Investigation of anti-Toxoplasma gondii antibody seropositivity and possible risk factors in women with abortion or stillbirth history in Kars, Turkey. Afr J Reprod Health. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/42202767/

[26] Ait Issad N, Mohamed Cherif A, Mebkhout F, et al. First report of molecular and histopathological detection of Toxoplasma gondii in aborted fetal goat myocardium in Algeria with associated risk factors. Parasitol Int. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/41864556/

[27] Pinto GOA, Silva RAD, Oliveira PRF, et al. Molecular detection of Toxoplasma gondii in an aborted equine fetus and serological evidence of infection in mares enrolled in embryo transfer programs in Brazil. J Equine Vet Sci. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/42252005/

[28] de Velasco-Reyes I, Torres-García SE, Hernández-Rangel JJ, et al. Seroprevalence of Toxoplasma gondii Infection in Veterinary Medicine Professionals and Students in Aguascalientes, Mexico. Epidemiologia (Basel). 2026. URL: https://pubmed.ncbi.nlm.nih.gov/42201205/

[29] Henriette BA, Jémima EK, Jean-Sébastien MA, et al. First report of knowledge and practices towards toxoplasmosis among pregnant women in primary care in Abidjan, Côte d'Ivoire. Trop Parasitol. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/42199683/

[30] Chalabi KN, Jabar Bakr E. Toxoplasmosis - knowledge among university students in Erbil, Iraq: a cross-sectional study. Int J Environ Health Res. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/41873025/

[31] Filho SCC, Moron SE, Ferreira RG, et al. Risk Factors and Ocular Health Associated with Toxoplasmosis in Quilombola Communities. Microorganisms. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/41597614/

[32] Qadeer A, Tharwat M, Khan MZ, et al. Advances and Translational Challenges in Toxoplasma gondii Vaccine Development: From Antigen Discovery to mRNA and One Health Strategies. Vet Sci. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/42188907/

[33] Orish VN, Tetteh RE, Adzah D, et al. Toxoplasma gondii seropositivity among patients with sickle cell disease: Prevalence and association with blood transfusion history. PLoS One. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/41931585/

[34] Mihaljević D, Sitaš Z, Hanulak J, et al. Cerebral Toxoplasmosis in a Renal Transplant Recipient-A Rare Complication. Life (Basel). 2026. URL: https://pubmed.ncbi.nlm.nih.gov/41900989/

[35] Marín-García PJ, Ballesteros-García O, Martínez-Sáez L, et al. Low seroprevalence of Toxoplasma gondii in pig farms (Sus scrofa domesticus) of eastern Spain in intensive farms with control of animal entry. Vet Parasitol Reg Stud Reports. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/41741032/