scholarly journals Pregnancy Diagnosis with Progesterone ELISA Kit in Farm Animals, Its Accuracy and Application

2019 ◽  
Vol 36 ◽  
pp. 111-117
Author(s):  
Sambriddhi Nepal ◽  
Deepak Subedi ◽  
Krishna Kaphle

 Pregnancy is a special condition where a female lodges one or more young ones within her uterus. It is maintained by various endocrine physiology and metabolic changes between maternal and fetal circumstances. Space dine secreted by corpus luteum increases extraordinarily throughout the pregnancy, estrogen increases rapidly during first trimester and prolonged lifespan of corpus luteum and small quantity of estrogen prevents prostaglandins pulsatic secretion. We reviewed available literature to evaluate the accuracy of progesterone ELISA test kit in pregnancy diagnosis in farm animals. We found varying accuracy in global and Nepalese context but found that this is an important tool for early pregnancy diagnosis and infertility monitoringwith high accuracy which contributes to increase economic efficiency of a farm. This kit has been used for qualitative and quantitative study of progesterone to understand the reproductive status of animals. Therefore, its use is increasing in globally and in Nepal. This kit has been used at various breeding centers, and livestock service centers of Nepal. However, wider level use is still difficult due to lack of infrastructuresand subsistence farming.

1996 ◽  
Vol 32 (5) ◽  
pp. 397-400
Author(s):  
SD Babyak ◽  
MG Groves ◽  
DS Dimski ◽  
J Taboada

An enzyme-linked immunosorbent assay (ELISA) test kit for the detection of feline leukemia virus (FeLV) antigen in saliva was evaluated in 150 cats. Saliva and blood samples from all cats were tested for FeLV using the saliva ELISA kit and a plasma ELISA kit, respectively. These results were compared with indirect immunofluorescent antibody (IFA) testing of blood smears also obtained from each cat. The proportion of cats that tested positive were 10%, 7%, and 8% for each test, respectively. Using the IFA test as the gold standard, the saliva FeLV test had a sensitivity of 91.7% and specificity of 97.1%, while the plasma ELISA test had a sensitivity of 91.7% and specificity of 100%.


2011 ◽  
Vol 35 (2) ◽  
pp. 61-65
Author(s):  
Maithem Ihsan Abdulrasool

This study was conducted for rapid detection of contamination of meat products with E. coli 0157 by usage of ELISA test kit as one of the most rapid and newest test. The study showed the efficiency of ELISA test kit used in this study in detection of bacteria antigen in meat products samples of raw beef meat , kabab and beef burger which subjected to improper storage conditions or undercooked and hence when some peoples uptake some of these products they suffered from clinical intoxication signs like diarrhea ,vomiting and hyperthermia. The kit showed the presence of (9) samples positive among (90) samples ; (2) positive out of (30) kabab samples,(3) positive out of (30) beef burger and (4) positive out of (30) raw beef meat after 16 hrs of enrichment of all samples in EC Modified broth including Novobiocin supplement as inhibitor of other bacteria and then the liquid supernatants from all prepared samples got tested by ELISA kit used in this study and the data recovered in less than 1 hr.The study indicated the ability of using ELISA kit for detection of E. coli 0157 antigens in food stuffs and reduce the time for releasing the results in less than 24 hrs when compared with conventional culturing procedure which reuiqred more than 3 days and launch the food products for consumption with focusing on the main point here which is the protection of our consumer safety.


Author(s):  
Rongqing Zhao ◽  
Maohua Li ◽  
Hao Song ◽  
Jianxin Chen ◽  
Wenlin Ren ◽  
...  

WHO has declared COVID-19 a pandemic with more than 300,000 confirmed cases and more than 14,000 deaths. There is urgent need for accurate and rapid diagnostic kits. Here we report the development and validation of a COVID-19/SARS-CoV-2 S1 serology ELISA kit for the detection of total anti-virus antibody (IgG+IgM) titers in sera from either the general population or patients suspected to be infected. For indirect ELISA, CHO-expressed recombinant full length SARS-CoV-2-S1 protein with 6* His tag was used as the coating antigen to capture the SARS-CoV-2-S1 antibodies specifically. The specificity of the ELISA kit was determined to be 97.5%, as examined against total 412 normal human sera including 257 samples collected prior to the outbreak and 155 collected during the outbreak. The sensitivity of the ELISA kit was determined to be 97.5% by testing against 69 samples from hospitalized and/or recovered COVID-19 patients. The overall accuracy rate reached 97.3%. Most importantly, in one case study, the ELISA test kit was able to identify an infected person who had previously been quarantined for 14 days after coming into contact with a confirmed COVID-19 patient, and discharged after testing negative twice by nucleic acid test. With the assays developed here, we can screen millions of medical staffs in the hospitals and people in residential complex, schools, public transportations, and business parks in the epidemic centers of the outbreaks to fish out the “innocent viral spreaders”, and help to stop the further spreading of the virus.


Author(s):  
B. T. Stegniy ◽  
S. S. Drahut ◽  
V. A. Kutsenko ◽  
T. P. Ramazanova ◽  
N. V. Marchenko ◽  
...  

The purpose of the work. Comparison the diagnostic ability of the ELISA test kits «DIA®-Brucella ab. combi-V» and «ID Screen® Brucellosis Serum Indirect Multi-species» for the detection of antibodies to brucellosis pathogens in various farm animals. Materials and methods. For the analysis there were used 29 positive samples to brucellosis with specific antibodies in different concentrations, 26 of which are serums (22 — from cattle, 2 — from pigs, 1 — from goat, 1 — from camel) and 3 — milk samples from cows. There were used 32 serums (23 — from cattle, 6 — from sheep, 2 — from pigs, 1 — from goat), and 2 milk samples from cows that don’t contain antibodies to brucellosis pathogens for determining the ability of test kits to detect correctly negative samples. There were also used serums from cattle containing antibodies that can lead to false positive results, 1 sample with antibodies to Francisella tularensis, 1 — to Yersinia 03 and 1 — to Yersinia 09. To compare the results in the two test kits, comparative ratios were used that allowed to determine how many times the result obtained in both test kits was higher or less than cut off, that differentiated positive samples from negative. Results of the work. When analyzing 22 cattle serums containing antibodies to B. abortus, the “DIA®-Brucella ab. combi-V” kit determined all samples positive with a results 5.3–10.6 times higher than cut off. The “ID Screen® Brucellosis Serum Indirect Multi-species” test kit identified only 18 positive serums with a maximum value of 1.3 above the cut off. The result of the analysis of 3 samples was doubtful and 1 serum was negative. When analyzing 4 sera from different animals containing antibodies to brucellosis pathogens, the “DIA®-Brucella ab. combi-V” test kit identified all positive samples with the results 8.1–9.4 times higher than cut off. The “ID Screen® Brucellosis Serum Indirect Multi-species” test kit detected specific antibodies in only 3 serums — from pigs and camel. When the goat serum was tested, a doubtful (uncertain) result of the analysis was obtained. When analyzing 3 milk samples from cows containing antibodies to B. abortus in different concentrations there was received a positive result to brucellosis in both test kits. However, ability of the “DIA®-Brucella ab. combi-V” test kit to detect specific antibodies was significantly higher than in comparison test kit. When investigating 32 serums from different animals and 2 milk samples that didn’t contain antibodies to the brucellosis pathogens, a negative result of the analysis was obtained in both test kits. When analyzing cattle serums containing antibodies that can lead to false positive results, both test kits identified 1 sample with antibodies to Francisella tularensis and 1 serum with antibodies to Yersinia 03 with negative result. When analyzing 1 serum with antibodies to Yersinia 09 the result of the analysis was false positive. Conclusions. Studies have shown that the “DIA®-Brucella ab. combi-V” test kit has a high diagnostic capacity. When analyzing 29 blood serums, including samples from different animals, and milk samples from cows containing antibodies to brucellosis pathogens, the test kit identified all samples as positive with results 5.3–10.8 times above the cut off. The “ID Screen® Brucellosis Serum Indirect Multi-species” test kit detected antibodies to brucellosis pathogens only in 24 samples with a maximum value 1.3 times higher than cut off. When investigating 4 serums, 3 samples of which are from cattle and 1 — from goat, the result of the analysis was doubtful (uncertain), 1 cattle serum was identified as negative. The ability of test kits to detect correctly negative samples was comparable. When analyzing 32 serums from different animals and 2 milk samples from cows that do not contain antibodies to brucellosis pathogens, in both test kits, a negative result of the analysis was obtained. For the 3 negative cattle serums, the analysis of which on brucellosis may be incorrect (the presence of antibodies to Yersinia О3, Yersinia О9, Francisella tularensis), in both test kits, for 1 sample with antibodies to Yersinia О9 a false positive result was obtained


2015 ◽  
Vol 46 (2) ◽  
pp. 362-367 ◽  
Author(s):  
Monique Tomazele Rovani ◽  
Alfredo Skrebsky Cezar ◽  
Melânia Lazzari Rigo ◽  
Bernardo Garziera Gasperin ◽  
Janduí Escarião da Nóbrega Júnior ◽  
...  

ABSTRACT: Pregnancy diagnosis is an important tool for farm management. Ultrasonography is the main technique used for pregnancy diagnosis in ewes. As an alternative, radioimmunoassay (RIA) allows accurate and early detection of pregnancy-associated glycoproteins (PAGs) in sheep blood. However, radioactive-based techniques, as RIA, have been increasingly inadvisable due to environmental risk. Homology between ovine and bovine PAGs is high, and ELISA kits used for PAGs detection in cattle are safer than RIA. Thus, this study aimed to evaluate the feasibility of PAGs detection for pregnancy diagnosis in sheep serum samples using an ELISA kit produced for cattle. The sensitivity and specificity of the ELISA kit were 93.5% and 98.9%, respectively, whereas positive and negative predictive values were 99.0% and 93.1%, respectively, in comparison to ultrasonography diagnostic (control). PAGs reached consistently detectable concentrations in ovine serum around 33 days after mating. Accuracy of the ELISA test was 96.1% from 33 days of pregnancy until lambing. After parturition, PAGs were still detectable seven days post-lambing. However, from 21 days post-parturition, PAGs from the previous pregnancy were no longer detected in serum samples. In conclusion, the bovine ELISA kit can accurately detect pregnancy in sheep 33 days following mating, while PAGs levels from the previous gestation are no longer detected from 21 days post-partum. The evaluated ELISA test is a reliable tool for pregnancy diagnosis in sheep at random stages and as a complementary exam at early gestation.


2017 ◽  
Vol 1 (1) ◽  
Author(s):  
Turabian Jose Luis ◽  
Minier-Rodriguez Luis Enoc ◽  
Moreno-Ruiz Sandra ◽  
Rodriguez-Almonte Francis Eliant ◽  
Cucho-Jove Raul ◽  
...  

2016 ◽  
Vol 18 (2) ◽  
pp. 140-148 ◽  
Author(s):  
Silvia Tommaso ◽  
Carlo Cavallotti ◽  
Antonio Malvasi ◽  
Daniele Vergara ◽  
Antonio Rizzello ◽  
...  

Behaviour ◽  
2014 ◽  
Vol 151 (12-13) ◽  
pp. 1663-1686 ◽  
Author(s):  
Kasey D. Fowler-Finn ◽  
Emilia Triana ◽  
Owen G. Miller

When mating interactions are influenced by multiple sources of selection, they may involve multiple stages of mate assessment. At each stage, a different set of morphological and behavioural traits may be important in determining the outcome of the interaction. Here, we test the potential for multiple sources of selection to shape mating interactions in Leiobunum vittatum harvestmen, commonly known as ‘daddy longlegs’. We provide a qualitative and quantitative study of mating interactions, and investigate the influence of multiple morphological traits on each of several distinct stages of their mating interactions. Mating interactions start with a struggle between males and females during which the male attempts to secure the females in a mating embrace. Success at this stage depends on the length of the male’s clasping pedipalps: those with shorter pedipalps (and thus greater mechanical advantage) were more successful. Male size relative to the female determines how quickly males achieve this embrace. Mating interactions then proceed to tactile exchanges between males and females, indicating the potential for mutual mate choice and/or peri- and post-copulatory selection. We found no morphological predictors of the timing of these later stages of the mating interactions, and suggest that the exchange of a nuptial gift is important for the dynamics of these stages. Overall, our results highlight L. vittatum as a potentially highly informative group for studying how traits involved in mating are shaped by the interaction of selection across multiple stages in mating interactions.


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