scholarly journals Prevalence and genotyping of Toxoplasma gondii in stray cats in Mashhad area, Iran.

2019 ◽  
Author(s):  
Majid Khodaverdi ◽  
Gholamreza Razmi

Abstract Background: Cats as a definitive host have an important role in the epidemiology of toxoplasmosis in humans and animals. The aim of the study was to determine the frequency of Toxoplasma gondii infection and isolate and identify the genotypes of T. gondii in stray cats in the Mashhad suburb. Methods: From April 2016 to August 2017, 175 fecal samples from stray cats and 31 brain samples from cats killed in driving accidents were collected. The fecal samples were examined by fecal flotation technique and T. gondii-specific PCR. The brain samples were investigated by T. gondii-specific PCR and consequently examined by mice bioassay. The DNA of T. gondii isolated was genotyped using SAG1, SAG2, SAG3, BTUB and GRA6 as PCR-restriction fragment length polymorphism (PCR-RFLP) markers. Results: In the present study, Toxoplasma-like oocysts were microscopically observed in 2.2% (4/175) fecal samples. The presence of Toxoplasma oocysts was confirmed in one microscopy-positive sample by PCR. In addition, T. gondii DNA was detected in 4% (7/175) microscopy-negative samples using PCR. T. gondii was isolated from one brain PCR-positive sample by mice bioassay. The isolate was avirulent and many T. gondii cysts were observed in mice brain. The isolate was successfully genotyped by PCR-RLFP analysis .The isolated genotyped was type II. Besides, eight Toxoplasma-positive fecal samples contained insufficient DNA and only amplified at SAG-3 locus in PCR. These samples were also showed type II pattern at this locus. Conclusions: Parasitological and molecular results showed low frequency of Toxoplasma infection in the stray cats, and identified the genotype of T. gondii isolate as type II, for the first time in Mashhad area, Khorasan Razavi Province.

2019 ◽  
Author(s):  
Majid Khodaverdi ◽  
Gholamreza Razmi

Abstract Background: Cats as a definitive host have an important role in the epidemiology of toxoplasmosis in humans and animals. The aim of the study was to determine the frequency of Toxoplasma gondii infection and isolate and identify the genotypes of T. gondii in stray cats in Mashhad suburb. Methods: From April 2016 to August 2017, 175 fecal samples from stray cats and 31 brain samples from cats killed in driving accidents were collected. The fecal samples were examined by fecal flotation technique and T. gondii -specific PCR. The brain samples were investigated by T. gondii -specific PCR and consequently examined by mice bioassay. The DNA of T. gondii isolated was genotyped using SAG1, SAG2, SAG3, BTUB and GRA6 as PCR-restriction fragment length polymorphism (PCR-RFLP) markers. Results: In the present study, Toxoplasma -like oocysts were microscopically observed in 2.2% (4/175) fecal samples. The presence of Toxoplasma oocysts was confirmed in one microscopy-positive sample by PCR. In addition, T . gondii DNA was detected in 4% (7/175) microscopy-negative samples using PCR. T. gondii was isolated from one brain PCR-positive sample by mice bioassay. The isolate was avirulent and many T. gondii cysts were observed in mice brain. The isolate was successfully genotyped by PCR-RLFP analysis .The isolated genotyped was type II. Beside, eight Toxoplasma- positive fecal samples contained insufficient DNA and only amplified at SAG-3 locus in PCR. These samples were also showed type II pattern at this locus. Conclusions: Parasitological and molecular results showed low frequency of Toxoplasma infection in the stray cats, and identified the genotype of T. gondii isolate as type II, for the first time in Mashhad area, Khorasan Razavi Province.


2019 ◽  
Author(s):  
Majid Khodaverdi ◽  
Gholamreza Razmi

Abstract Background: Cats as a definitive host have an important role in the epidemiology of toxoplasmosis in humans and animals. The aim of the study was to determine the frequency of Toxoplasma gondii infection and isolate and identify the genotypes of T. gondii in stray cats in Mashhad suburb. Methods: From April 2016 to August 2017, 175 fecal samples from stray cats and 31 brain samples from cats killed in driving accidents were collected. The fecal samples were examined by fecal flotation technique and T. gondii-specific PCR. The brain samples were investigated by T. gondii-specific PCR and consequently examined by mice bioassay. The DNA of T. gondii isolated was genotyped using SAG1, SAG2, SAG3, BTUB and GRA6 as PCR-restriction fragment length polymorphism (PCR-RFLP) markers. Results: In the present study, Toxoplasma-like oocysts were microscopically observed in 2.2% (4/175) fecal samples. The presence of Toxoplasma oocysts was confirmed in one microscopy-positive sample by PCR. In addition, T. gondii DNA was detected in 4% (7/175) microscopy-negative samples using PCR. T. gondii was isolated from one brain PCR-positive sample by mice bioassay. The isolate was avirulent and many T. gondii cysts were observed in mice brain. The isolate was successfully genotyped by PCR-RLFP analysis .The isolated genotyped was type II. Beside, eight Toxoplasma-positive fecal samples contained insufficient DNA and only amplified at SAG-3 locus in PCR. These samples were also showed type II pattern at this locus. Conclusions: Parasitological and molecular results showed low frequency of Toxoplasma infection in the stray cats, and identified the genotype of T. gondii isolate as type II, for the first time in Mashhad area, Khorasan Razavi Province.


2019 ◽  
Author(s):  
Majid Khodaverdi ◽  
Gholamreza Razmi

Abstract Background: Cats as a definitive host have an important role in the epidemiology of toxoplasmosis in humans and animals. The aim of the study was to determine the frequency of Toxoplasma gondii infection and isolate and identify the genotypes of T. gondii in stray cats in Mashhad suburb . Methods: From April 2016 to August 2017, in this study, 175 fecal samples from stray cats and 31 brain samples from cats killed in driving accidents were collected. The fecal samples were examined by fecal flotation technique and T. gondii -specific PCR. The brain samples were investigated by T. gondii -specific PCR and consequently examined by mice bioassay. The DNA of T. gondii isolated were genotyped using SAG1, SAG2, SAG3, BTUB and GRA6 as PCR-restriction fragment length polymorphism (PCR-RFLP) markers . Results: In the present study, oocysts-like Toxoplasma were microscopically observed in 2.2% (4/175) fecal samples. The presence of Toxoplasma oocysts was confirmed in one microscopy-positive sample by PCR. In addition, T. gondii DNA was detected in 4% (7/175) microscopy-negative samples using PCR. T. gondii was isolated from one brain PCR-positive sample by mice bioassay. The isolate was avirulent and many T. gondii cysts were observed in mice brain. The isolate was successfully genotyped by PCR-RLFP analysis .The isolated genotyped was type II. Beside, eight Toxoplasma- positive fecal samples contained insufficient DNA and only amplified at SAG-3 locus in PCR. These samples were also showed type II pattern at this locus. Conclusions: Parasitological and molecular results showed low frequency of Toxoplasma infection in the stray cats, and identified the genotype of T. gondii isolate as type II, for the first time in Mashhad area, Khorasan Razavi Province.


2019 ◽  
Vol 15 (1) ◽  
Author(s):  
Majid Khodaverdi ◽  
Gholamreza Razmi

Abstract Background Cats as a definitive host have an important role in the epidemiology of toxoplasmosis in humans and animals. The aim of the study was to determine the frequency of Toxoplasma gondii infection and isolate and identify the genotypes of T. gondii in stray cats in the Mashhad suburb. Methods From April 2016 to August 2017, 175 fecal samples from stray cats and 31 brain samples from cats killed in driving accidents were collected. The fecal samples were examined by fecal flotation technique and T. gondii-specific PCR. The brain samples were investigated by T. gondii-specific PCR and consequently examined by mice bioassay. The DNA of T. gondii isolated was genotyped using SAG1, SAG2, SAG3, BTUB and GRA6 as PCR-restriction fragment length polymorphism (PCR-RFLP) markers. Results In the present study, Toxoplasma-like oocysts were microscopically observed in 2.2% (4/175) fecal samples. The presence of Toxoplasma oocysts was confirmed in one microscopy-positive sample by PCR. In addition, T. gondii DNA was detected in 4% (7/175) microscopy-negative samples using PCR. T. gondii was isolated from one brain PCR-positive sample by mice bioassay. The isolate was avirulent and many T. gondii cysts were observed in mice brain. The isolate was successfully genotyped by PCR-RLFP analysis. The isolated genotyped was type II. Besides, eight Toxoplasma-positive fecal samples contained insufficient DNA and only amplified at SAG-3 locus in PCR. These samples were also showed type II pattern at this locus. Conclusions Parasitological and molecular results showed low frequency of Toxoplasma infection in the stray cats, and identified the genotype of T. gondii isolate as type II, for the first time in Mashhad area, Khorasan Razavi Province.


2020 ◽  
Vol 41 (1) ◽  
pp. 213
Author(s):  
Keila Jimenez Torrico ◽  
Nelson Jessé Rodrigues dos Santos ◽  
Hugo Luca Abate ◽  
Felippe Danyel Cardoso Martins ◽  
Luiz Daniel de Barros ◽  
...  

Protozoans are widely distributed, and several species may parasitize the digestive tracts of cats (Felis catus), and can be transmitted to humans. The present study aimed to evaluate the species and occurrence of gastrointestinal protozoans in cats in the city of Londrina, Paraná, Brazil. A total of 206 cat fecal samples were tested, of which 141 were from shelter animals, and 65 were from pets owned by local people. Samples were processed by parasitological techniques. Coproparasitological techniques (Willis, Faust and Ziehl-Neelsen) were performed for detection of protozoan parasites. Subsequently, all samples were processed by PCR protocols specific to Toxoplasma gondii, Giardia spp., and Cryptosporidium spp. PCR products from positive samples were selected for sequencing. No samples were found to be positive for Cryptosporidium spp. using the Ziehl-Neelsen technique. Using specific PCR protocols, 1/206 (0.48%) samples tested positive for Cryptosporidium spp. After purification, this one positive sample was sequenced, and it demonstrated a 100% identity match to Cryptosporidium muris. Using specific PCR protocols, 13/206 (9.22%) cat fecal samples tested, including 2/65 (3.08%) pet cat fecal samples, were positive for T. gondii. PCR analysis revealed that 37/206 (17.96%) of cat fecal samples were positive for Giardia spp., including 27/141 (19.15%) of shelter cat fecal samples, and 10/65 (15.38%) pet cat fecal samples (p = 0.5124). When sequenced, these positive samples showed a 100% identity match with Giardia duodenalis. This study demonstrated that infections with Cryptosporidium spp., Toxoplasma gondii, and Giardia duodenalis are present in the population of both pet cats and shelter cats in the city of Londrina. This poses a risk to public health, because these parasites have a high zoonotic potential.


2010 ◽  
Vol 19 (3) ◽  
pp. 152-156 ◽  
Author(s):  
Piassa Franciele Rossandra ◽  
Jacqueline Baptista de Araújo ◽  
Ronaldo César da Rosa ◽  
Rodrigo José Mattei ◽  
Rodrigo Costa da Silva ◽  
...  

Toxoplasma gondii infection has been diagnosed in pigs all over the world. Economical losses are generally related to reproductive disorders. Toxoplasma infection is also a matter of public health because tissue cysts of the parasite may remain in pork and pork products, and become sources of human infection. The objective of this study was to evaluate the frequency and risk factors associated with Toxoplasma infection in certified and non-certified pig breeding farms in the Toledo microregion, in the State of Paraná, Brazil which includes the cities of Toledo, Nova Santa Rosa, Sao José das Palmeiras and Sao Pedro do Iguaçu. Relative frequency of infection was 13.4%, independently of the type of farm. Logistic regression analysis showed that the following factors were associated with infection: absence of workers exclusive for each area of the farm, access of other animals to feeders and drinkers, lack of lids in drinkers, lack of rodent control measures, mean piglet number and weight at weaning per female.


Parasitology ◽  
2013 ◽  
Vol 140 (14) ◽  
pp. 1768-1776 ◽  
Author(s):  
A. BURRELLS ◽  
P. M. BARTLEY ◽  
I. A. ZIMMER ◽  
S. ROY ◽  
A. C. KITCHENER ◽  
...  

SUMMARYToxoplasma gondiiis a zoonotic pathogen defined by three main clonal lineages (types I, II, III), of which type II is most common in Europe. Very few data exist on the prevalence and genotypes ofT. gondiiin the UK. Wildlife can act as sentinel species forT. gondiigenotypes present in the environment, which may subsequently be transmitted to livestock and humans. DNA was extracted from tissue samples of wild British carnivores, including 99 ferrets, 83 red foxes, 70 polecats, 65 mink, 64 badgers and 9 stoats. Parasite DNA was detected using a nested ITS1 PCR specific forT. gondii, PCR positive samples were subsequently genotyped using five PCR–RFLP markers.Toxoplasma gondiiDNA was detected within all these mammal species and prevalence varied from 6·0 to 44·4% depending on the host. PCR–RFLP genotyping identified type II as the predominant lineage, but type III and type I alleles were also identified. No atypical or mixed genotypes were identified within these animals. This study demonstrates the presence of alleles for all three clonal lineages with potential for transmission to cats and livestock. This is the first DNA-based study ofT. gondiiprevalence and genotypes across a broad range of wild British carnivores.


2019 ◽  
Vol 113 (8) ◽  
pp. 453-462 ◽  
Author(s):  
Maryam Sadeghi ◽  
Seyed Mohammad Riahi ◽  
Mona Mohammadi ◽  
Vafa Saber ◽  
Somayeh Aghamolaie ◽  
...  

Abstract Toxoplasma gondii is a neurotropic pathogen with worldwide distribution. To evaluate the association between Toxoplasma infection and the risk of epilepsy by meta-analysis, observational peer-reviewed studies were retrieved from PubMed, Embase, Web of Science, Scopus and Google Scholar (up to 10 October 2018) and by reference review. Pooled risk estimates were calculated using a random effects model. Heterogeneity was assessed using Cochrane’s Q-test and I2. In total, 16 eligible studies involving 19 data sets were included for the final analysis. A total 7897 participants (3771 epileptic patients, 4026 healthy controls) were included. The pooled odds ratio (OR) for Toxoplasma infection was increased to 1.72 (95% confidence interval [CI] 1.37 to 2.16) among patients with epilepsy. There was moderate heterogeneity among the studies (χ2=39.8, I2=62.3%, p=0.001). The ORs from subgroup analyses showed that both cryptogenic epilepsy (OR 2.65 [95% CI 1.91 to 3.68]) and active convulsive epilepsy (OR 1.37 [95% CI 1.09 to 1.72]) were significantly associated with Toxoplasma infection. Another subgroup analyses according to age showed a significant positive association in children (OR 1.33), adults (OR 1.57) and in all ages (OR 1.89). Our findings support the association between Toxoplasma infection and epilepsy. More prospective studies with larger sample sizes and more experimental studies are recommended to elucidate a causative relationship.


2021 ◽  
Author(s):  
Joshua Mayoral ◽  
Rebekah B. Guevara ◽  
Yolanda Rivera-Cuevas ◽  
Vincent Tu ◽  
Tadakimi Tomita ◽  
...  

The intracellular parasite Toxoplasma gondii adapts to diverse host cell environments within a replicative compartment that is heavily decorated by secreted proteins. In attempts to identify novel parasite secreted proteins that influence host cell activity, we identified and characterized a trans-membrane dense granule protein dubbed GRA64 (TGME49_202620). We found that GRA64 is on the parasitophorous vacuolar membrane (PVM) and is partially exposed to the host cell cytoplasm in both tachyzoite and bradyzoite parasitophorous vacuoles. Using co-immunoprecipitation and proximity-based biotinylation approaches, we demonstrate that GRA64 appears to interact with certain components of the host Endosomal Sorting Complexes Required for Transport (ESCRT). Genetic disruption of GRA64 does not affect acute Toxoplasma virulence in mice nor encystation as observed via tissue cyst burdens in mice during chronic infection. However, ultrastructural analysis of Dgra64 tissue cysts using electron tomography revealed enlarged vesicular structures underneath the cyst membrane, suggesting a role for GRA64 in organizing the recruitment of ESCRT proteins and subsequent intracystic vesicle formation. This study uncovers a novel host-parasite interaction that contributes to an emerging paradigm in which specific host ESCRT proteins are recruited to the limiting membranes (PVMs) of tachyzoite and bradyzoite vacuoles formed during acute and chronic Toxoplasma infection.


Blood ◽  
2014 ◽  
Vol 124 (21) ◽  
pp. 1187-1187
Author(s):  
Sairah Ahmed ◽  
Elizabeth J Shpall ◽  
Alison Gulbis ◽  
Roy Jones ◽  
Charles S. Martinez ◽  
...  

Abstract Background Toxoplasma gondii infection is a catastrophic infectious complication with a high rate of mortality in immune compromised patients and particularly stem cell transplant (SCT) recipients. Incidence of infection is variable from 0.1 % to 6% and higher in Europe and Latin America compared to US. Mortality rate is 60-90% in SCT patients compared to 30% in AIDS patients (Clin Infect Dis 2005;40:67–68). Most cases of toxoplasmosis among SCT recipients are due to disease reactivation from previously acquired infection. Per ASBMT guidelines of 2009, incidence of clinical reactivation is 2-6% of seropositive recipients, and cord blood recipients are at highest risk. Allogeneic SCT candidates should be tested for toxoplasma IgG antibody and patients who are seropositive should be treated empirically if develop CNS or pulmonary lesions. The introduction of trimethoprim/sulfamethoxazole (TMP/SMX) prophylaxis (Br J Haematol 2002;117:370–386) has led to a decrease of toxoplasmosis, however patients can still develop infection while on TMP/SMX. This is a rare infectious complication in recipients of allogeneic SCT, and can be difficult to diagnose. Methods We retrospectively reviewed patients who received an allogeneic (allo) SCT at MD Anderson from 1994 to 2013. In period from 1994-2009 routine serologic testing for toxoplasma was not done and from 2010 – 2013 SCT patients were routinely tested for toxoplasma IgG antibody. Diagnosis made in first cohort by: autopsy (3), brain biopsy (4), PCR CSF and cytopathology (1), PCR blood (1). Diagnosis in second cohort was made by PCR blood (5), PCR CSF (5), autopsy (1), characteristic findings on imaging + improvement on therapy (1). Results From 1994-2009 nine of 3623 allo SCT patients had a clinical toxoplasma infection, of which 4 were international patients and 5 were from the US; total incidence of 0.25%; 4/246 international patients: 1.6% and 5/3380 US patients 0.15% (p=0.002). In time period from 2010-2013 of 1047 transplanted patients, 9 cases of toxoplasma diagnosed of which 3 patients from high incidence countries. Time to presentation is bimodal; early (1 month) and late (3-6 months) post transplant. From 1994-2009, 9 patients presented with toxoplasma infection of which 8 died - 3 presented with disseminated infection/pulmonary symptoms while 6 had neurologic symptoms. Type of donor: matched related donor (MRD) (6), matched unrelated donor (MUD) (1), haploidentical donor (2). In the 2nd cohort 2 cases didn't have serology done but serology in entire patient population revealed toxoplasma IgG (+) equaled 97/1047 (9.2%), clinical cases of all tested patients, 7/1047 (0.7%) and all clinical cases with positive toxoplasma IgG pretransplant 7/97 for an incidence of 7.2%. From 2010-2013, 9 patients presented with toxoplasma infection, 4 died of toxoplasmosis while 5 survived of which 1 died of relapse. Five patients presented with sepsis, 2 with pneumonia and 1 with myocarditis, while 8 patients had CNS symptoms including meningoencephalitis and classic presentation of brain lesions. Six patients had concomitant CMV reactivation and 3 were on corticosteroids. Remaining patients had no other predisposing conditions. Type of donor: MRD (1), MUD (5), haploidentical (2), cord blood (1). Three cases were second transplants and all those patients died. The 5 patients who survived all received treatment within 6 days of presentation. (Table 1) Conclusions The most common presentations of toxoplasma infection in SCT patients are meningoencephalitis and sepsis. Only 2 patients in our most recent patient population had classic brain disease. Five of nine survived in our more recent cohort compared to 1/9 in previous time period. It appears that delayed treatment (³6 days) may be related to increased mortality. Although toxoplasma infection in SCT patients carries a high mortality, identifying patients at higher risk and early treatment may improve outcomes. TABLE 1 Type of transplant SCT to illness Site of infection Days to Treatment Primary Cause of Death MUDSCT 33 Sepsis/Pneumonia 6 Protozoal infection MUDSCT (2nd) 94 Brain 4 MUDSCT 100 Meningoencephalitis 2 MUDSCT 166 Brain UNK HAPLO 34 Sepsis/CNS 4 HAPLO (2nd) 165 Sepsis/CNS NO TX Autopsy: Cardiac/Lung/CNS Toxo MUDSCT 13 Sepsis/ meningoencephalitis 6 Autopsy: Recurrence/persistence of disease Cord 30 Sepsis/Meningitis 7 Protozoal infection AlloMRD (2nd) 10 Meningoencephalitis 8 Protozoal infection Disclosures No relevant conflicts of interest to declare.


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