scholarly journals NextGen sequencing reveals short double crossovers contribute disproportionately to genetic diversity in Toxoplasma gondii

BMC Genomics ◽  
2014 ◽  
Vol 15 (1) ◽  
pp. 1168 ◽  
Author(s):  
Asis Khan ◽  
Jahangheer S Shaik ◽  
Michael Behnke ◽  
Qiuling Wang ◽  
Jitender P Dubey ◽  
...  
Author(s):  
Jitender P. Dubey ◽  
Fernando H.A. Murata ◽  
Camila K. Cerqueira-Cézar ◽  
Oliver C.H. Kwok ◽  
Yurong Yang ◽  
...  

2008 ◽  
Vol 157 (3-4) ◽  
pp. 299-305 ◽  
Author(s):  
J.P. Dubey ◽  
G.V. Velmurugan ◽  
A. Chockalingam ◽  
H.F.J. Pena ◽  
L. Nunes de Oliveira ◽  
...  

2014 ◽  
Vol 37 (3) ◽  
pp. 173-179 ◽  
Author(s):  
Marija Marković ◽  
Vladimir Ivović ◽  
Tijana Štajner ◽  
Vitomir Djokić ◽  
Ivana Klun ◽  
...  

2017 ◽  
Vol 258 ◽  
pp. 38-49 ◽  
Author(s):  
Mehdi Sharif ◽  
Afsaneh Amouei ◽  
Shahabeddin Sarvi ◽  
Azadeh Mizani ◽  
Mohsen Aarabi ◽  
...  

2011 ◽  
Vol 11 (6) ◽  
pp. 1378-1387 ◽  
Author(s):  
A. Mercier ◽  
D. Ajzenberg ◽  
S. Devillard ◽  
M.P. Demar ◽  
B. de Thoisy ◽  
...  

2022 ◽  
Vol 18 (1) ◽  
Author(s):  
Luis Fernando Valenzuela-Moreno ◽  
Sara Teresa Méndez-Cruz ◽  
Claudia Patricia Rico-Torres ◽  
Carlos Cedillo-Peláez ◽  
Dolores Correa ◽  
...  

Abstract Background Currently, more than 300 genotypes of Toxoplasma gondii (T. gondii) have been described throughout the world, demonstrating its wide genetic diversity. The SAG3 locus is one of the genes included in the genotyping panel of this parasite. It is associated with its virulence since it participates during the invasion process of the host cells. Therefore, cloning, sequencing, and bioinformatic analysis were used to deepen the understanding of the SAG3 locus genetic diversity of T. gondii in blood samples from feral cats. Results Six different SAG3 sequences were detected, five of which were detected in one feline. Three sequences were first reported here; one of them was an intragenic recombinant. In the cladogram, four out of ten SAG3 sequences did not share nodes with others reported worldwide. Conclusions Cloning and sequencing of samples with more than one restriction pattern by PCR-RFLP were very helpful tools to demonstrate the presence of more than three genotypes of T. gondii in the blood of feral cats from southeastern Mexico. This suggests a potential mixed infection of multiple T. gondii strains and high genetic diversity of the parasites in felines in this tropical region of Mexico.


2017 ◽  
Vol 22 (4) ◽  
pp. 203-209 ◽  
Author(s):  
Mehdi Tavalla ◽  
Fatemeh Asgarian ◽  
Forough Kazemi

Parasitology ◽  
2019 ◽  
Vol 147 (3) ◽  
pp. 295-302 ◽  
Author(s):  
J. P. Dubey ◽  
C. K. Cerqueira-Cézar ◽  
F. H. A. Murata ◽  
S. K. Verma ◽  
O. C. H. Kwok ◽  
...  

AbstractFeral swine are known reservoirs of various pathogens, including Toxoplasma gondii. Here, we report the first national survey of viable T. gondii in feral swine in the USA. We paired serological surveys with parasite isolation and bioassay to evaluate the prevalence and genetic diversity of these parasites. From 2012–2017, sera and tissues from 1517 feral swine across the USA were collected for the isolation of viable T. gondii. Serum samples were initially screened for antibodies to T. gondii, and then the tissues of seropositive feral swine were bioassayed in mice. Antibodies were detected in 27.7% of feral swine tested by the modified agglutination test (1:25 or higher). Antibody positive rates increased significantly with age, with 10.1% of juveniles, 16.0% of sub-adults and 38.4% of adults testing seropositive. Myocardium (50 g) from 232 seropositive feral swine was digested in pepsin and bioassayed in mice. Viable T. gondii was isolated from 78 feral swine from 21 states. Twelve of the 78 isolates were pathogenic to outbred Swiss Webster mice and 76 of the 78 isolates could be propagated further in cell culture and were genotyped. For genotyping, deoxyribonucleic acid extracted from cell culture-derived tachyzoites was characterized by polymerase chain reaction restriction fragment length polymorphism using the genetic markers SAG1, SAG2, SAG3, BTUB, GRA6, c22-8, c29-2, L358, PK1 and Apico. Genotyping revealed 15 ToxoDB genotypes, including 43 isolates for genotype #5 (haplogroup 12), 11 isolates for #24, four isolates for #2 (haplogroup 3), two isolates for each of genotypes #3 (haplogroup 2), #4 (haplogroup 12), #216, #221, #289 and #297 and one isolate for each of genotypes #1 (haplogroup 2), #39, #66, #260, #261 and #299. Genotype #5 was the most frequently isolated, accounted for 57% (43/76) of the isolates, followed by #24, accounted for 14% (11/76). Genotypes #260, #289, #297 and #299 are new types. Genotype #289 was highly virulent to mice and originated from feral swine collected in Louisiana on the same day at the same location. Genotype #216 was previously demonstrated to be highly virulent to mice. Our results indicate moderate genetic diversity of T. gondii in feral swine in the USA, with the genotype #5 (haplogroup 12) dominant in the continental USA, whereas genotype #24 (10/14) was dominant in Hawaii, suggesting different population structures of the parasites among the two distinct geographical locations.


Parasitology ◽  
2020 ◽  
Vol 147 (7) ◽  
pp. 775-781 ◽  
Author(s):  
J. P. Dubey ◽  
C. K. Cerqueira-Cézar ◽  
F. H. A. Murata ◽  
S. K. Verma ◽  
O. C. H. Kwok ◽  
...  

AbstractTo assess the role of white-tailed deer (Odocoileus virginianus, WTD) in the epidemiology of toxoplasmosis, we conducted a national survey of WTD across the USA for Toxoplasma gondii infection. To do this, we combined serology with parasite isolation to evaluate the prevalence and genetic diversity of T. gondii in this game species. From October 2012 to March 2019, serum and tissues were collected from 914 WTD across the USA. Serum samples were screened for antibodies to T. gondii, and then the tissues of seropositive WTD were bioassayed in mice. Antibodies were detected in 329 (36%) of 914 WTD tested by the modified agglutination test (positive reaction at 1:25 or higher). Viable T. gondii was isolated from the heart of 36 WTD from 11 states. Three of the 36 isolates were pathogenic but not highly virulent to outbred Swiss Webster mice and all 36 isolates could be propagated further in cell culture and were genotyped. For genotyping, DNA extracted from cell culture-derived tachyzoites was characterized by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) using the genetic markers SAG1, SAG2, SAG3, BTUB, GRA6, c22-8, c29-2, L358, PK1 and Apico. Genotyping revealed seven ToxoDB PCR-RFLP genotypes, including 24 isolates for genotype #5 (haplogroup 12), four isolates for #2 (type III, haplogroup 3), three isolates for genotypes #1 (type II, haplogroup 2), two isolates for genotypes #3 (type II, haplogroup 2) and one isolate each for #39, #221 and #224. Genotype #5 was the most frequently isolated, accounting for 66.6% (24 of 36) of the isolates. Combining the 36 isolates from this study with previously reported 69 isolates from WTD, 15 genotypes have been identified. Among these, 50.4% (53/105) isolates belong to genotype #5. Our results indicate moderate genetic diversity of T. gondii in WTD. The results also indicate that undercooked venison should not be consumed by humans or fed to cats.


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