Anti-Trichinella antibodies detected in chronically infected horses by IFA and Western blot, but not by ELISA.
Abstract: In the Balkan countries, where trichinellosis is a re-emerging zoonosis, it is of great importance to determine Trichinella infection prevalence among the major hosts, including horses. One method for monitoring prevalence is serological surveillance; however, the validity of serological methods in horses is not well understood. The dynamics of anti-Trichinella IgG production and circulating excretory/secretory (ES) antigens were investigated in three horses experimentally-infected with Trichinella spiralis. Horses were slaughtered at 32 week post infection (p.i.). Low worm burdens were found in all three animals. Anti-Trichinella IgG was detected up to 32 weeks p.i. by an indirect immunofluorescence assay (IFA) and by Western blot (Wb), but not by ELISA. The ELISA test detected antibodies for only a short period of time (up to 18 weeks p.i. using ES antigen or up to 20 weeks p.i. using tyvelose-BSA antigen). The presence of circulating muscle larvae ES antigen in sera of infected horses was observed by dot blot from the 4th week p.i. up to the 32nd week p.i.
Publication Date: 2005-07-05 PubMed ID: 15992997DOI: 10.1016/j.vetpar.2005.05.037Google Scholar: Lookup
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- Journal Article
- Research Support
- Non-U.S. Gov't
- Antibodies
- Diagnostic Technique
- Disease Prevalence
- Disease Surveillance
- Enzyme-Linked Immunosorbent Assay (ELISA)
- Epidemiology
- Equine Health
- Horses
- Immunofluorescence Assay
- Immunoglobulin G
- Infection
- Infectious Disease
- Parasites
- Public Health
- Serological Surveys
- Seroprevalence
- Veterinary Medicine
- Western Blot
- Zoonotic Diseases
Summary
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The article is centered on the prevalence and detection of Trichinella infection in horses in Balkan countries where trichinellosis is re-emerging. The study indicates that the indirect immunofluorescence assay (IFA) and Western blot techniques were effective in detecting anti-Trichinella IgG in horses up to 32 weeks post infection (p.i.), while the ELISA method was only effective in a short period of time.
Objective and Methodology
- The main objective of the research was to investigate and understand the prevalence of Trichinella infection among horses in the Balkan regions, and to validate the effectiveness of different serological methods in detecting this infection.
- Three horses were chosen as the experimental subjects and each of them was intentionally infected with a specific species of parasite, Trichinella spiralis.
- The study monitored the production of anti-Trichinella IgG and the circulation of Excretory/Secretory (ES) antigens in the horses, which were slaughtered 32 weeks after the infection.
Results
- At the point of termination, all three horses were found to have low worm burdens, indicating minimal infections.
- Two serological methods – Indirect Immunofluorescence Assay (IFA) and Western blot could detect the presence of the anti-Trichinella IgG up to 32 weeks p.i, indicating that these methods may indeed be effective in long-term monitoring of the infection in horses.
- On the other hand, ELISA could only detect the presence of the anti-Trichinella antibodies for a short duration (up to 18 weeks using ES antigen and 20 weeks using Tyvelose-BSA antigen), indicating that ELISA might not be as accurate for long-term monitoring.
Significance
- These findings are very important for disease control and prevention in regions where trichinellosis is a re-emerging problem. It proves the need for effective surveillance methods for monitoring the infection in major hosts like horses.
- Our results give valuable insights into the patterns of immune response against Trichinella infection in horses – a low burden of worms can elicit a lasting immune response, which can be effectively detected by certain lab techniques bu not by others.
- This highlights the importance of selecting the right techniques for disease surveillance, prevention and control.
Cite This Article
APA
Sofronic-Milosavljevic Lj, Ilic N, Djordjevic M, Savic M, Gruden-Movsesijan A, Cuperlovic K, Murrell KD.
(2005).
Anti-Trichinella antibodies detected in chronically infected horses by IFA and Western blot, but not by ELISA.
Vet Parasitol, 132(1-2), 107-111.
https://doi.org/10.1016/j.vetpar.2005.05.037 Publication
Researcher Affiliations
- Institute for the Application of Nuclear Energy (INEP), Banatska 31b, 11080 Belgrade, Serbia and Montenegro. sofronic@inep.cp.yu
MeSH Terms
- Animals
- Antibodies, Helminth / blood
- Antigens, Helminth / chemistry
- Blotting, Western / veterinary
- Enzyme-Linked Immunosorbent Assay / veterinary
- Fluorescent Antibody Technique, Indirect / veterinary
- Helminth Proteins / chemistry
- Hexoses / chemistry
- Horse Diseases / blood
- Horse Diseases / immunology
- Horse Diseases / parasitology
- Horses
- Tongue / parasitology
- Trichinella / growth & development
- Trichinella / immunology
- Trichinellosis / blood
- Trichinellosis / immunology
- Trichinellosis / parasitology
- Trichinellosis / veterinary
- Yugoslavia
Citations
This article has been cited 5 times.- Ilic N, Bojic-Trbojevic Z, Lundström-Stadelmann B, Cujic D, Mitic I, Gruden-Movsesijan A. Immunomodulatory components of Trichinella spiralis excretory-secretory products with lactose-binding specificity. EXCLI J 2022;21:793-813.
- Bruschi F, Gómez-Morales MA, Hill DE. International Commission on Trichinellosis: Recommendations on the use of serological tests for the detection of Trichinella infection in animals and humans. Food Waterborne Parasitol 2019 Mar;14:e00032.
- Frey CF, Schuppers ME, Nöckler K, Marinculić A, Pozio E, Kihm U, Gottstein B. Validation of a Western Blot for the detection of anti-Trichinella spp. antibodies in domestic pigs. Parasitol Res 2009 Jun;104(6):1269-77.
- Nagano I, Wu Z, Takahashi Y. Species-specific antibody responses to the recombinant 53-kilodalton excretory and secretory proteins in mice infected with Trichinella spp. Clin Vaccine Immunol 2008 Mar;15(3):468-73.
- Pietkiewicz H, Hiszczyńska-Sawicka E, Kur J, Petersen E, Nielsen HV, Paul M, Stankiewicz M, Myjak P. Usefulness of Toxoplasma gondii recombinant antigens (GRA1, GRA7 and SAG1) in an immunoglobulin G avidity test for the serodiagnosis of toxoplasmosis. Parasitol Res 2007 Jan;100(2):333-7.
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