• Parasites, Hosts and Diseases
• /
• 제31권1호
• /
• pp.49-56
• /
• 1993

현재 유구낭미충증을 혈청학적으로 진단하는 데에는 낭액항원을 이용한 특이항체검사법으로 micro-ELISA를 널리 이용하고 있다. 이 실험은 효소부착 이차항체를 사용하는 micro-ELISA방법 대신 민감도가 뛰어난 것으로 알려진 ABC-ELISA나 Protein-ELISA로 바꾸어 사용하면 검사의 민감도를 보다 개선할 수 있는지를 알기 위하여 실시하였다. ABC-ELISA에 의한 항체검사는 낭액항원 단백질 $2.5{\;}\mu\textrm{g}/ml$, 혈청 희석 1:10,000, biotinylated no-hmn IgG 1:100,000 회석, peroxidase conjugated streptavidin 1:40,000 희석 및 2,2-azino-di(3-ethylbenztlllazoline) sulfnnlc acid발색제를 사용하는 조건으로 실시하였고 415 nm에서 흡광도를 측정하였다. Protein A-ELISA는 항원단백질 $2.5{\;}\mu\textrm{g}/ml$, 혈청은 1:200 회석, HRP-Protein A 1:20,000 희석 및 ABTS 발색제를 사용하는 조건으로 실시하고 415 nm에서 흡광도를 측정하였다. 유구낭미충증 환자 115 명의 혈청을 검사한 바 민감도는 micro-ELISA 81.7%, Protein A-ELISA 82.6%, ABC-ELISA 86. 1%이었다. 다른 기생충성 질환자, 비기생충성 질환자 및 대조군 등 165명 혈청에서 특이도는 각각 88.5%, 93.3%, 93.8%이었다 세 가지 ELISA방법에 의한 항체가 사이에는 상관계수 0.84~0.86의 높은 상관관계가 성립하였다. 이상의 결과 ABC-ELISA는 micro-ELISA에 비하여 민감한 혈청학적 방법이고 실제 유구낭미충 특이항체 검사상의 특이도에서도 차이가 있다는 것을 알 수 있었다. 따라서 ABC-ELISA는 유구낭미충증의 혈청학적 진단에서 혈청 및 뇌척수액 등 검체를 적게 사용할 수 있다는 장점이 있다는 것을 알 수 있었다.

• 한국응용곤충학회지
• /
• 제14권4호
• /
• pp.193-198
• /
• 1975

벼줄무늬잎마름병 바이러스에 대한 혈청학적인 검토결과를 다음과 같이 적요한다. 1. 벼줄무늬잎마름병 바이러스는 항원성을 갖고 있으며 항체와 특이적인 혈청반응을 타나냈다. 2. 가토 정맥주사에 의한 항혈청의 항체가는 아주 낮아 16배에 불과하였다. 3. 벼 품종 $\ulcorner$사도미노리$\lrcorner$에 있어서 침강반응혼합법으로 측정한 결과 이병엽의 병징정도에 따라 바이러스 농도에 차이가 인정되는데 병징정도가 심할수록 바이러스농도가 높았다. 4. 동정도의 병징이라도 벼품종에 따라 바이러스농도가 달랐는데 저항성품종인 $\ulcorner$통일$\lrcorner$에서는 높았고 이병성인 $\ulcorner$사도미노리$\lrcorner$, $\ulcorner$팔굉$\lrcorner$, $\ulcorner$만경$\lrcorner$, $\ulcorner$니혼바레$\lrcorner$에서는 낮았다. 그러나 저항성 품종인 $\ulcorner$유신$\lrcorner$에서는 낮았다. 5. 항체감작적혈구 응집반응에 의한 항체가는 아주 높아 512배였으며 보독충의 검정시험에서도 반응이 잘 나타나 $38\%$라는 보독충율을 나타냈다.

• 식물병연구
• /
• 제12권2호
• /
• pp.144-147
• /
• 2006

닭을 이용한 egg yolk immunoglobulin (IgY)의 생산과 이용 가능성을 조사하기 위하여 pepper mild mottle virus (PMMoV)로 닭을 면역하였다. Ring-test로 달걀의 난황에서 분리 정제한 IgY의 역가를 조사한 결과 IgY의 최고 역가는 1:2,560이었고 달걀 l 개에서 대략 $60{\sim}80 mg$의 IgY를 얻을 수 있었다. 최고역가를 갖는 IgY를 이용하여 Gelrite gel 이중확산법, 효소면역항체법 (ELISA), 조직자국면역반응법을 실시한 결과 간접면역효소항체법의 PMMoV 검출 감도는 1 ng/ml 이었고, 검정법의 바이러스 검출감도와 특이도는 IgG와 비슷한 경향을 보였다. 그러므로 한 마리의 닭으로부터 대량으로 생산 가능한 IgY는 식물바이러스에 대한 항체생산과 혈청학적 검정에 유용할 것으로 생각한다.

• Parasites, Hosts and Diseases
• /
• 제47권4호
• /
• pp.427-429
• /
• 2009

To establish a definite diagnosis for pulmonary hydatid disease, combination of radiology and serology is useful. In this study, 19 preoperative sera from patients with surgically confirmed pulmonary hydatidosis, 40 sera from patients with other parasitosis and pulmonary diseases, and 20 sera from healthy donors were evaluated using 4 different serological tests, i.e., the commercial ELISA (ELISA-kit) test, the ELISA (ELISA-lab) test prepared in our laboratory, the commercial indirect hemagglutination assay kit (IHA-kit) test, and the IHA test using sensitized sheep red blood cells with tannic acid (IHA-TA). The ELISA-kit was the most sensitive (84.2%) and the most specific test (100.0%). The ELISA-kit also demonstrated the highest positive (100.0%) and negative (95.2%) predictive values. The sensitivity of the ELISA-lab test, that we prepared, was found to be 73.6%, whereas the IHA-kit test and the IHA-TA test were found to be 73.6% and 68.4%, respectively. The specificity of these tests was 96.6%, 98.3%, and 83.3%, respectively. When all 4 tests were assessed together, it was found that the sensitivity had risen to 94.7%. When the ELISA-kit was assessed with the IHA-kit and IHA-TA together, it was found that the sensitivity was 89.5% and 84.2%, respectively. Likewise, the combination of the ELISA-lab and IHA-kit or IHA-TA allowed us to achieve a sensitivity of 84.2% in cases of pulmonary echinococcosis. In conclusion, the diagnosis would be imminent if least 2 tests were applied together.

• 대한수의학회지
• /
• 제61권2호
• /
• pp.19.1-19.7
• /
• 2021

Feline panleukopenia virus (FPV) causes leukopenia and severe hemorrhagic diarrhea, killing 50% of naturally infected cats. Although intact FPV can serve as an antigen in the hemagglutination inhibition (HI) test, an accidental laboratory-mediated infection is concern. A non-infectious diagnostic reagent is required for the HI test. Here, we expressed the viral protein 2 (VP2) gene of the FPV strain currently prevalent in South Korea in a baculovirus expression system; VP2 protein was identified by an indirect immunofluorescence assay, electron microscopy (EM), Western blotting (WB), and a hemagglutination assay (HA). EM showed that the recombinant VP2 protein self-assembled to form virus-like particles. WB revealed that the recombinant VP2 was 65 kDa in size. The HA activity of the recombinant VP2 protein was very high at 1:2¹⁵. A total of 143 cat serum samples were tested using FPV (HI-FPV test) and the recombinant VP2 protein (HI-VP2 test) as HI antigens. The sensitivity, specificity, and accuracy of the HI-VP2 test were 99.3%, 88.9%, and 99.3%, respectively, compared to the HI-FPV test. The HI-VP2 and HI-FPV results correlated significantly (r = 0.978). Thus, recombinant VP2 can substitute for intact FPV as the serological diagnostic reagent of the HI test for FPV.

• 대한수의학회지
• /
• 제10권1호
• /
• pp.11-23
• /
• 1970

Recently Carter(1952) reported the capsule antigens of Pasteurella multocida could be divided into four serological types A,B,C and D by means of precipitation tests. Subsequently he showed that the most sensitive for identification of these types involved the use of capsule substance adsorbed by erythrocytes in hemagglutination test. It may be somewhat difficult to conduct the hemagglutination test in small laboratory, because relatively large amounts of antisera and erythrocytes of the human O type are required for the test. A simple method for serological typing of P. multocida was the slide agglutination test employed by Little et al. (1943) and Namioka et al. (1962), but this method is still in controversy. The author tried adapting Carter's hemagglutination method to the slide method so called "micromethod technique", and studied on the stabilization of erythrocytes for use of slide hemagglutination to P. multocida although many invesigators reported the stabilization of erythrocytes. The results obtained are summarized as follows: 1. A simplified method (slide method) for capsule typing of the organism was developed by adapting Carter's hemagglutination reaction(tube method). Antibody-containing serum can be diluted serially on Boerner's microtest slide with capillary or serological pipetts with a considerable accuracy. The slide reaction can be carried out with case on the slide by adding $0.05m{\ell}$ of antigen-sensitized erythrocytes suspension diluted to one percent on $0.05m{\ell}$ of serially diluted antibody-containing sera, and the final result can be read after 60 minutes at the room temperature ($15^{\circ}C$). 2. It is difficult to determine superiority of inferiority between the slide method and the tube method on the pattern of the reaction of hemagglutination. 3. The pH range of 6.6 to 8.3 is optimal for the slide hemagglutination reaction. 4. The antigen-sensitization against erythrocytes at $37^{\circ}C$ is optimal for the slide hemagglutination. 5. Both the doses and concentration of antigen do not influence the antigen-adsorbing capacity of erythrocytes. 6. The reduction of antigen-sensitizing hours does not influence the antigen-adsorbing capacity of erythrocytes even 30 minutes. 7. The tannic acid treatment against formalinized and non-formalinized erythrocytes showed no effect on the reaction of hemagglutination. 8. The erythrocytes preserved at $4^{\circ}C$ in the ACD solution do not decrease the reactivity on the reaction of hemagglutination for 60 days, while they begin slight hemolysis 30 days after preserving. 9. The stable preparation of erythrocytes can be obtained by treating the cells at $37^{\circ}C$ for 20 hours with from 4 to 8 percent of formalin in saline or buffer. These cells can be preserved at $4^{\circ}C$ for more than 8 months experimented without hemolysis. With low concentration of formalin, the cells were not sufficiently stabilized resulting in the hemolysis after short period of preservation at $4^{\circ}C$. 10. The erythrocytes treated with 16 percent of formalin remain constantly or increase the reactivity for the reaction of hemagglutination. On the contrary, the cells treated with I to 8 percent of formalin decrease the reactivity. 11. There is no difference between nontreated fresh erythrocytes and the erythrocytes preserved in the ACD solution on the reactivity against the hemagglutination, and the erythrocytes treated with 16 percent of formalin showed the reactivity of higher level than that of the above two kinds of erythrocytes. 12. There is no difference between the saline and the isotonic buffer solution on the reaction of hemagglutination.

• 한국동물위생학회지
• /
• 제26권1호
• /
• pp.11-18
• /
• 2003

A total of 1,024 sera were collected from cattle(227), pigs(465), chickens(257) and dogs(75) raised or slaughtered in Daejeon metropolitan city from April to September 2002. Japanses encephalitis virus(JEV) antibodies in sera were detected by the haemagglutination inhibition test. The prevalence rates of JEV antibodies were 99.1 %, 54.0 %, 63.0 % and 98.7 % in cattle, pigs, chickens and dogs, respectively. In case of cattle and dogs, the monthly antibody-positive rates were as high as 85.7∼100.0 % and there were no differences among six months. In case of pigs, the monthly antibody-positive rate showed the lowest in April(6.4 %) and the highest in July(100.0 %) and it remained above 50 % during the summer-time. In case of chickens, the monthly antibody-positive rate was 100.0 % in July & August, 80.5 % in June, 40.0 % in May, 7.5 % in September and 5.0 % in April in order and there were distinct differences in seasons.

• 대한수의학회지
• /
• 제38권4호
• /
• pp.818-822
• /
• 1998

The persistence of porcine epidemic diarrhea virus(PEDV) infection was demonstrated in 7 swine farms employing continuous pig flow management even after seasonal outbreaks. Clinically, sporadic postweaning diarrhea was a major concern in those farms. Subsequently circulatory antibody detection using serum neutralizing test made useful for confirmation of PEDV persistent infections. The persistence of PEDV in the premise might have induced recurrence over the period of time.

• 한국동물위생학회지
• /
• 제14권2호
• /
• pp.154-158
• /
• 1991

To investigate the Akabane antibody in the cattle with the serological test in Chung Chung Buk Do from May to Nov 1191. The result are summarized as follows. 1. Breed in cattle reacted as positive condition in Akabane antibody 76 heads(42%) in 180 cattles reacted as positive condition in Akabane antibody, 23 heads(51%) in 45 Korea native cattle reacted as positive condition in Akabane antibody. 2. During 5, 9, 10, 11 month, Akabane antibody in cattle is over 45%. 3. Less of 2 years old and over 4 years old cattle are Akabane antibody in cattle is over 40%. 4. The relation of titer of 2 folds of dilution HA and 10 folds of dilution TCID$_{50}$ was same relation.n.

• Environmental Analysis Health and Toxicology
• /
• 제7권3_4호
• /
• pp.37-55
• /
• 1992

Effect of Synethrin on the Toxicity of Dichlorvos in Rats. Hematological, biological and enzymatic effects were investigated in rats treated with DDVP and synethrin. Mutagenicity was also examined. In serological analysis, LDH and ALP were more significantly increased in rats treated with the mixture of DDVP (10mg/kg) and synethrin (250mg/kg) than with either DDVP or synethrin. DDVP alone slightly increased cytochrome P-450 in the liver while synethrin or the mixture decreased it. Lipid peroxidation was significantly increased in the liver when rats were treated with both DDVP and the mixture. Cholinesterase activity was significantly decreased in the liver and serum when treated with DDVP as well as with the mixture. In mutagenicity test, DDVP was shown to be weakly positive to TA 97a, TA 100 and TA 102, but negative to TA 1537. Synethrin showed negative in all strains tested. These results suggest that the mixture of DDVP and synethrin increased the toxicities but not the mutagenicity.