scholarly journals Trichinelloscopy of domestic and wild animal carcasses

2021 ◽  
Vol 15 (3) ◽  
pp. 71-75
Author(s):  
A. V. Uspensky ◽  
O. B. Zhdanova ◽  
O. N. Andreyanov ◽  
L. A. Napisanova ◽  
N. S. Malysheva

The purpose of the research is analyze the localization of Trichinella sp. in animals muscle and to evaluate the methods of intravital and post-mortem diagnosis of trichinellosis in domestic, wild and game animals.Materials and methods. In order to prevent trichinellosis in human population and animals, life-time and post-mortem diagnosis methods for trichinellosis are widely used. Life-time diagnosis of trichinellosis is based on detection of specific antibodies in blood serum of sick animals. Modern immunological assays allow detecting specific antibodies (immunoglobulins J and M) at 10–12 days after infection. Enzyme-linked immunosorbent assay (ELISA) with fractionated antigen has the greatest real possibility of application for individual and mass seroepizootic studies of pigs and horses; ELISA is a highly sensitive and specific test. Veterinary and sanitary examination is conducted by methods of compressor trichinelloscopy and peptolysis (muscle tissue digested in artificial gastric juice). For the compression research method, in particular for pig carcasses, 2 samples of the diaphragmatic peduncles of 60 g each are taken. It is also possible to study samples from masticatory muscles, tongue, intercostal space or esophagus. Twelve sections are made from each sample (24 in total). A more sensitive and productive method is the digestion of muscle tissue using a set of diagnostic devices and instruments such as AVT. The method is based on peptolysis of crushed muscle tissue in technological reactors. Diagnosis of trichinellosis using such devices makes it possible to automate and mechanize all processes associated with the isolation of Trichinella larvae. The main application areas of the devices are meat processing factories, fur farms or veterinary and sanitary examination laboratories in the markets.Results and discussion. We presented data on the role of veterinary and sanitary examination for trichinellosis in susceptible animals as the core measure in the system of measures to prevent this infection. We analyzed indicators of diagnostic efficiency, performance and usability of methods of compressor trichinelloscopy and digestion of muscle tissue in artificial gastric juice. Factors of diagnostic efficiency, performance and usability of methods of compressor trichinelloscopy and digestion of muscle tissue in artificial gastric juice were analyzed. Information was given on localization of Trichinella larvae in various species of domestic and wild animals, optimal sampling sites and volumes of muscle tissue samples with the existing methods of examination for trichinellosis. To study fresh carcasses for trichinellosis at meat processing factories, the peptolysis method is recommended.

Viruses ◽  
2021 ◽  
Vol 13 (2) ◽  
pp. 303
Author(s):  
Wei-Ting Hsu ◽  
Chia-Yu Chang ◽  
Chih-Hsuan Tsai ◽  
Sung-Chan Wei ◽  
Huei-Ru Lo ◽  
...  

Porcine epidemic diarrhea virus (PEDV) is a coronavirus that causes serious and highly contagious enteric disease in swine worldwide. In this study, we constructed a recombinant baculovirus (S-Bac) expressing full-length spike protein of the virulent epidemic genotype 2b (G2b) PEDV strain for serological studies of infected pigs. We found that most spike-specific antibodies produced upon PEDV infection in pigs are conformation-specific and they could be detected on S-Bac-infected insect cells by immunofluorescent assay, but they were insensitive to Western blot analysis, the typical method for antiserum analysis. These results indicated that spike conformation is crucial for serum recognition. Since it is difficult to purify trimeric spike membrane protein for conventional enzyme-linked immunosorbent assay (ELISA), we used S-Bac to generate a novel cell-based ELISA for convenient PEDV detection. We analyzed 100 pig serum samples, and our cell-based ELISA exhibited a sensitivity of 100%, a specificity of 97%, and almost perfect agreement [Cohen’s kappa coefficient value (κ) = 0.98] with immunocytochemical staining results. Our cell-based ELISA rapidly presented antigen for proper detection of conformation-specific antibodies, making PEDV detection more convenient, and it will be useful for detecting many viral diseases in the future.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Markus H. Kainulainen ◽  
Eric Bergeron ◽  
Payel Chatterjee ◽  
Asheley P. Chapman ◽  
Joo Lee ◽  
...  

AbstractSARS-CoV-2 emerged in late 2019 and has since spread around the world, causing a pandemic of the respiratory disease COVID-19. Detecting antibodies against the virus is an essential tool for tracking infections and developing vaccines. Such tests, primarily utilizing the enzyme-linked immunosorbent assay (ELISA) principle, can be either qualitative (reporting positive/negative results) or quantitative (reporting a value representing the quantity of specific antibodies). Quantitation is vital for determining stability or decline of antibody titers in convalescence, efficacy of different vaccination regimens, and detection of asymptomatic infections. Quantitation typically requires two-step ELISA testing, in which samples are first screened in a qualitative assay and positive samples are subsequently analyzed as a dilution series. To overcome the throughput limitations of this approach, we developed a simpler and faster system that is highly automatable and achieves quantitation in a single-dilution screening format with sensitivity and specificity comparable to those of ELISA.


Author(s):  
Eide Dias Camargo ◽  
Paulo Mutuko Nakamura ◽  
Adelaide José Vaz ◽  
Marcos Vinícius da Silva ◽  
Pedro Paulo Chieffi ◽  
...  

The dot-enzyme-linked immunosorbent assay (dot-ELISA) was standardized using somatic (S) and excretory-secretory (ES) antigens of Toxocara-canis for the detection of specific antibodies in 22 serum samples from children aged 1 to 15 years, with clinical signs of toxocariasis. Fourteen serum samples from apparently normal individuals and 28 sera from patients with other pathologies were used as controls. All samples were used before and after absorption with Ascaris suum extract. When the results were evaluated in comparison with ELISA, the two tests were found to have similar sensitivity, but dot-ELISA was found to be more specific in the presence of the two antigens studied. Dot-ELISA proved to be effective for the diagnosis of human toxocariasis, presenting advantages in terms of yield, stability, time and ease of execution and low cost.


1998 ◽  
Vol 5 (5) ◽  
pp. 613-616 ◽  
Author(s):  
Felix Grimm ◽  
Friedrich E. Maly ◽  
Jian Lü ◽  
Roberto Llano

ABSTRACT The potential roles of specific antibodies of the different immunoglobulin G (IgG) subclasses in the serological diagnosis of cystic echinococcosis (CE) and alveolar echinococcosis (AE) were investigated by an enzyme-linked immunosorbent assay based on hydatid fluid as antigen. Specific antibodies of subclass 1 were found to be of major importance. In sera collected at the time of diagnosis (i.e., before any therapeutic intervention was initiated) they could be demonstrated in 14 of 15 sera from patients with CE and in all 12 sera from patients with AE. The most discriminatory and the most specific antibodies found in this study belonged to IgG subclass 4. Only one false-positive reaction was observed with 253 sera from healthy volunteers, and no cross-reactions occurred in 80 sera from patients with different parasitic infections. Specific IgG4 antibodies could be demonstrated in 61.0 to 66.7% (CE) or 47.6 to 66.7% (AE) of the cases. Antibody levels of IgG subclass 2 were elevated only moderately, and subclass 3 antibodies were detected in a few cases only. In addition, nonspecific reactions in sera of healthy volunteers or patients with other parasitic infections could partially be attributed to antibodies of subclasses 2 and 3.


2007 ◽  
Vol 5 (5) ◽  
pp. 637-644 ◽  
Author(s):  
An Rykx ◽  
Sadia Vancauwenbergh ◽  
Line De Kimpe ◽  
Katrien Janssens ◽  
Sandy Vandoninck ◽  
...  

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