scholarly journals Detection of Toxoplasma gondii-specific immunoglobulin (IgG) antibodies in meat juice of beef

2021 ◽  
Vol 35 (2) ◽  
pp. 319-324
Author(s):  
Raafat Shaapan ◽  
Nagwa Toaleb ◽  
Eman Abdel-Rahman
Author(s):  
Jasem Saki ◽  
Karim Mowla ◽  
Reza Arjmand ◽  
Forough Kazemi ◽  
Somayeh Fallahizadeh

Introduction: Parasitic myositis is caused by some parasites such as T. gondii and T. canis. So, the aim of the study was to evaluate the prevalence T. gondii and T. canis in patients with myositis and healthy individuals. Methods: A total of 108 samples were randomly selected as the control (54 healthy individuals) and test (54 myositis patients) groups. IgG and IgM antibodies against T. gondii and IgG antibodies against T. canis were measured by the ELISA. The detection of chronic and acute toxoplasmosis was performed by the ELISA IgG avidity. The presence of T. gondii in blood was evaluated by the nested-PCR. Results: Of 108, 33 (30.6%) cases were detected positive for IgG against T. gondii that 19 (35.2%) and 14 (25.9%) were observed in myositis patients and healthy individuals, respectively (P=0.296). Of 19 positive cases, 12 (63.2%) and 7 (36.8%) cases were detected as chronic and acute toxoplasmosis, respectively, while, all positive cases in the control group had chronic toxoplasmosis (P=0.013). One (1.9%) sample was detected positive for anti- Toxoplasma gondii IgM and two (3.7%) samples were found positive for IgG against T. canis by the ELISA that these positive cases were observed only in myositis patients (P=1.000 P=0.495, respectively). B1 T. gondii gene was amplified in 12 (63.2%) and 1 (7.1%) in myositis patients and healthy subjects (P=0.001). Conclusions: Our findings showed that there was a relatively high prevalence of acute toxoplasmosis in myositis patients in comparison with the control subjects in southwest of Iran.


2002 ◽  
Vol 9 (2) ◽  
pp. 496-498
Author(s):  
Mardjan Arvand ◽  
Ilkay Kazak ◽  
Sergije Jovanovic ◽  
Hans-Dieter Foss ◽  
Oliver Liesenfeld

ABSTRACT We report on a young patient with chronic cervical lymphadenopathy and serological and histological evidence for infection with Bartonella henselae and Toxoplasma gondii. Serological follow-up studies, including testing for avidity of Toxoplasma-specific immunoglobulin G antibodies, assisted in the determination of the cause of the acute lymphadenitis. Our results suggest that the clinical symptoms were most likely due to cat scratch disease rather than to acute toxoplasmosis.


2015 ◽  
Vol 64 (1) ◽  
pp. 55-59 ◽  
Author(s):  
JUSTYNA M. GATKOWSKA ◽  
BOŻENA DZIADEK ◽  
JAROSŁAW DZIADEK ◽  
KATARZYNA DZITKO ◽  
HENRYKA DŁUGOŃSKA

The aim of this study was to evaluate the potential diagnostic usefulness of the full-length recombinant Toxoplasma gondii MAG1 protein by determining the levels of specific IgM and IgG antibodies in mouse and human sera obtained from individuals with acute and chronic toxoplasmosis. The obtained results revealed that IgG antibodies against MAG1 are a sensitive and specific marker of T. gondii infection since the protein was recognized by both mouse and human sera, 100% and 94.3%, respectively, rendering the full-length rMAG1 a prospective alternative for the polyvalent native antigen (TLA).


Author(s):  
Margarita VILLAVEDRA ◽  
Hernán CAROL ◽  
Alberto NIETO

The recognition profile of the tissue cysts antigens by IgG antibodies was studied during acute and chronic human toxoplasmic infection. Thus the IgG response against Toxoplasma gondii was investigated by immunoblotting in two patients accidentally infected with the RH strain as well as in group of naturally infected patients at acute and chronic phase. There was an overall coincidence of molecular mass among antigens of tachyzoites and tissue cysts recognized by these sera, however, they appear not to be the same molecules. The response against tissue cysts starts early during acute infection, and the reactivity of antibodies is strong against a wide range of antigens. Six bands (between 82 and 151 kDa) were exclusively recognized by chronic phase sera but only the 132 kDa band was positive in more than 50% of the sera analysed. A mixture of these antigens could be used to discriminate between the two infection phases. The most important antigens recognized by the acute and the chronic phase sera were 4 clusters in the ranges 20-24 kDa, 34-39 kDa, 58-80 kDa and 105-130 kDa as well as two additional antigens of 18 and 29 kDa. Both accidentally infected patients and some of the naturally infected patients showed a weak specific response against tissue cyst antigens.


2020 ◽  
Vol 7 (2) ◽  
pp. e676 ◽  
Author(s):  
Kayluz F. Boligan ◽  
Johanna Oechtering ◽  
Christian W. Keller ◽  
Benjamin Peschke ◽  
Robert Rieben ◽  
...  

ObjectiveTo explore the repertoire of glycan-specific immunoglobulin G (IgG) antibodies in treatment-naive patients with relapsing-remitting multiple sclerosis (RRMS).MethodsA systems-level approach combined with glycan array technologies was used to determine specificities and binding reactivities of glycan-specific IgGs in treatment-naive patients with RRMS compared with patients with noninflammatory and other inflammatory neurologic diseases.ResultsWe identified a unique signature of glycan-binding IgG in MS with high reactivities to the dietary xenoglycan N-glycolylneuraminic acid (Neu5Gc) and the self-glycan N-acetylneuraminic acid (Neu5Ac). Increased reactivities of serum IgG toward Neu5Gc and Neu5Ac were additionally observed in an independent, treatment-naive cohort of patients with RRMS.ConclusionPatients with MS show increased IgG reactivities to structurally related xenogeneic and human neuraminic acids. The discovery of these glycan-specific epitopes as immune targets and potential biomarkers in MS merits further investigation.


2004 ◽  
Vol 53 (12) ◽  
pp. 1183-1186 ◽  
Author(s):  
Süleyman Yazar ◽  
Ozan Yaman ◽  
Bülent Eser ◽  
Fevzi Altuntaş ◽  
Fatih Kurnaz ◽  
...  

This study aimed to determine the prevalence of anti-Toxoplasma gondii antibodies in patients with neoplasia. One hundred and eight patients with neoplasia and 108 healthy controls were studied for the presence of anti-T. gondii antibodies using a micro ELISA and peroxidase-labelled anti-human IgG (rabbit) and IgM (goat). Anti-T. gondii IgG antibodies were detected in 68 (63.0 %) patients and in 21 (19.4 %) of the controls, which was a statistically significant difference. In addition, anti- T. gondii IgM antibodies were detected in seven (6.5 %) patients and in one (0.9 %) control. A high percentage of positivity for Toxoplasma antibodies in patients with neoplasia was detected. Therefore, parasitological surveys of this patient group should be periodically performed.


2014 ◽  
Vol 62 (4) ◽  
pp. 272 ◽  
Author(s):  
Bronwyn A. Fancourt ◽  
Robert B. Jackson

Toxoplasma gondii is a cosmopolitan protozoan parasite of felids that also has significant implications for the health of wildlife, livestock and humans worldwide. In Australia, feral, stray and domestic cats (Felis catus) are the most important definitive host of T. gondii as they are the only species that can excrete the environmentally resistant oocysts that provide a major source of infection for mammals and birds. In Tasmania, the rapid decline of the Tasmanian devil (Sarcophilus harrisii) may allow an increase in feral cat abundance, thereby increasing the risk of T. gondii infection to a range of susceptible wildlife species. At present, there is scant information on the prevalence of T. gondii infection in feral cat populations across Tasmania. We tested feral cats from 13 regions across Tasmania for the presence of T. gondii–specific IgG antibodies using a modified agglutination test. Results were combined with serosurveys from three previous studies to enable a comparison of seroprevalence among 14 regions across Tasmania. We found that 84.2% (224 of 266) of cats tested positive for T. gondii IgG antibodies. This is among the highest rates of prevalence recorded from Australia, and significantly higher than for most other countries. Adult cats had higher seroprevalence than kittens but there was no difference between sexes. In Tasmania, seroprevalence was high in 12 of 14 regions (range: 79.3–100.0%), with only two regions (Tasman Island and Southern Tasmania) recording significantly lower seroprevalence (≤50%). This suggests a high risk of infection across Tasmania, and has significant implications for wildlife conservation should feral cat abundance increase with the ongoing declines in Tasmanian devils.


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