Access Restriction

Author Burk, Steffanie V. ♦ Dangoudoubiyam, Sriveny ♦ Brewster Barnes, Tammy ♦ Bryant, Uneeda K. ♦ Howe, Daniel K. ♦ Carter, Craig N. ♦ Vanzant, Eric S. ♦ Harmon, Robert J. ♦ Kazacos, Kevin R. ♦ Rossa, Mary G.
Source SpringerLink
Content type Text
Publisher Springer Berlin Heidelberg
File Format PDF
Copyright Year ©2014
Language English
Subject Domain (in DDC) Technology ♦ Medicine & health
Subject Keyword Parascaris equorum ♦ Western blot ♦ Baylisascaris procyonis ♦ Equine ♦ Toxocara canis ♦ Antibody ♦ Medical Microbiology ♦ Microbiology ♦ Immunology
Abstract Currently, diagnosis of Parascaris equorum infection in equids is limited to patent infections. The goals of this study were to culture P. equorum larvae in vitro and identify excretory-secretory (ES) products for prepatent diagnostic testing. Parascaris equorum L2/L3 larvae were hatched and cultured for up to 3 weeks for ES product collection. Fifth stage (L5) P. equorum were also cultured for ES product collection. Examination of ES fractions by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) and silver stain revealed L2/L3 products ranging from 12–94 kDa and L5 products ranging from 12–189 kDa. Western blot analyses were conducted using polyclonal antibodies produced against P. equorum or Baylisascaris procyonis L2/L3 ES products, sera from rabbits inoculated with B. procyonis or Toxocara canis eggs, and sera from animals naturally infected with P. equorum or T. canis. Western blot results indicated parasite antigens migrating at 19 and 34 kDa may be useful for specifically detecting P. equorum infections.
ISSN 09320113
Age Range 18 to 22 years ♦ above 22 year
Educational Use Research
Education Level UG and PG
Learning Resource Type Article
Publisher Date 2014-09-11
Publisher Place Berlin/Heidelberg
e-ISSN 14321955
Journal Parasitology Research
Volume Number 113
Issue Number 11
Page Count 8
Starting Page 4217
Ending Page 4224

Open content in new tab

   Open content in new tab
Source: SpringerLink