Detailed Information on Publication Record
2016
Toxoplasma gondii and Neospora caninum in wild small mammals: seroprevalence, DNA detection and genotyping
MACHAČOVÁ, Tereza, Daniel AJZENBERG, Alena ŽÁKOVSKÁ, Kamil SEDLÁK, Eva BÁRTOVÁ et. al.Basic information
Original name
Toxoplasma gondii and Neospora caninum in wild small mammals: seroprevalence, DNA detection and genotyping
Authors
MACHAČOVÁ, Tereza (203 Czech Republic, guarantor), Daniel AJZENBERG (250 France), Alena ŽÁKOVSKÁ (203 Czech Republic, belonging to the institution), Kamil SEDLÁK (203 Czech Republic) and Eva BÁRTOVÁ (203 Czech Republic)
Edition
Veterinary Parasitology, Elsevier Science, 2016, 0304-4017
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30102 Immunology
Country of publisher
Netherlands
Confidentiality degree
není předmětem státního či obchodního tajemství
Impact factor
Impact factor: 2.356
RIV identification code
RIV/00216224:14310/16:00089871
Organization unit
Faculty of Science
UT WoS
000377317200015
Keywords (in Czech)
Toxoplasmosis neosporosis hlodavci genotyp
Keywords in English
Toxoplasmosis neosporosis rodents genotype Czech Republic
Tags
International impact, Reviewed
Změněno: 14/4/2017 20:58, Ing. Andrea Mikešková
Abstract
V originále
Generally, rodents and other small mammals are considered as one of the sources of Toxoplasma gondii or Neospora caninum infection for cats and dogs as the definitive hosts of these two parasites, respectively. The aim of the study was to find out the prevalence of these two parasites in wild small mammals from the Czech Republic and to characterize T. gondii isolates by methods of molecular biology. A total of 621 wild small mammals were caught in the Czech Republic during years 2002 – 2014. Antibodies to T. gondii were detected by latex agglutination test in six (2.5 percent) of 240 small mammals (in two A. agrarius and four A. flavicollis). Antibodies to N. caninum were detected by commercially available competitive-inhibition enzyme-linked immunosorbent assay (percent inhibition value is more than 30 percent) in one A. flavicolis (0.4 percent). Three of 427 (0.7 percent) liver samples were positive for T. gondii by PCR while negative for N. caninum. All embryo samples (n = 102) were negative for both T. gondii and N. caninum. Three T. gondii isolates (two A. flavicollis and one A. sylvaticus) were genotyped by microsatellite markers and characterized as type II. To our knowledge, this is the first information about genetic characterization of T. gondii isolates in small mammals from Europe and the first detection of N. caninum antibodies in wild rodents from the Czech Republic.