• 한국동물위생학회지
• /
• 제30권3호
• /
• pp.385-391
• /
• 2007

A novel enzyme linked immunosorbent assay (ELISA) is described and compared with other established serologic tests for bovine brucellosis, namely the rose bengal test (RBT), the complement fixation test (CFT), and the tube agglutination test (TAT) approved and used in Korea. A total of 109 bovine serum samples were tested using all the 4 assays and analyzed as to specificity, sensitivity, reproducibility and predictive value. The ELISA showed 100% agreement with the CFT. The least agreement between ELISA was observed with the TAT. The agreement between the ELISA and RBT was not significantly different from that observed between the CFT and the ELISA. It is concluded that the new assay would be a good candidate for routine serologic survey for brucellosis in Korea. A protocol combining the ELISA and the CFT would increase the power for detection of serologically positive individuals and herds.

• 대한미생물학회지
• /
• 제34권6호
• /
• pp.555-559
• /
• 1999

The 38 kDa protein of Mycobacterium tuberculosis, which was known previously as antigen 5, has been extensively used in the serodiagnosis of tuberculosis. In an attempt to develop and evaluate a serodiagnostic test using the antigen, we expressed the 38 kDa protein in BCG and its seroreactivity was compared to that expressed in Escherichia coli. The coding region of the 38 kDa protein was amplified by PCR, and the gene was cloned into a Mycobacterium-E. coli shuttle expression vector pYMC-his and pQE30 expression vector and expressed in BCG and E. coli, respectively. Both recombinant 38 kDa proteins showed strong seroreactivity against pooled serum from tuberculosis patients. There was no significant difference in seroreactivity between the two recombinant antigens in sera from the far advanced tuberculosis patients. However, of 25 tuberculosis patients graded as "minimal" by chest X-ray, 5 (20.0%) were seropositive by r38 kDa expressed in E. coli, while 8 (32.0%) by that expressed in BCG. Likewise, higher seroreactivity by r38 kDa expressed in BCG was found in sera from the moderately advanced tuberculosis. This study thus indicates that the recombinant 38 kDa expressed in BCG is more effective than that expressed in E. coli in detecting antibodies to the native 38 kDa protein of M. tuberculosis in sera from minimally affected tuberculosis patients.

• Parasites, Hosts and Diseases
• /
• 제51권4호
• /
• pp.433-440
• /
• 2013

Toxocariasis is a worldwide zoonosis caused by larvae of ascarid nematodes of dogs or cats, Toxocara canis or T. cati. Diagnosis of human toxocariasis currently relies on serology that uses T. canis excretory-secretory antigen to detect specific IgG antibodies by ELISA. We investigated the serodiagnostic efficacy of ELISA using crude antigen of T. canis larvae (TCLA). Serum specimens of 64 clinically confirmed toxocariasis, 115 healthy controls, and 119 other tissue-invading helminthiases were screened by ELISA using TCLA. The ELISA using TCLA showed 92.2% (59/64 patient samples) sensitivity and 86.6% (103/119) specificity. Its positive diagnostic predictivity was 78.7% and negative predictivity was 97.8%. No serum of healthy controls reacted but that of anisakiasis (45.5%), gnathostomiasis (19.2%), clonorchiasis (15.8%), sparganosis (11.1%), and cysticercosis (6.3%) cross-reacted. Immunoblot analysis on TCLA recognized antigenic proteins of 28- and 30-kDa bands in their dominant protein quantity and strong blotting reactivity. The present results indicate that the ELISA using our TCLA antigen is acceptable by the sensitivity and specificity for serodiagnosis of human toxocariasis. ELISA with TCLA is recommended to make differential diagnosis for patients with any sign of organ infiltration and eosinophilia.

• Parasites, Hosts and Diseases
• /
• 제51권5호
• /
• pp.503-510
• /
• 2013

Toxoplasma gondii is an apicomplexan parasite with a broad host range of most warm-blooded mammals including humans, of which one-thirds of the human population has been infected worldwide which can cause congenital defects, abortion, and neonatal complications. Here, we developed a rapid diagnostic test (RDT) for T. gondii infection. Antigenic N-terminal half of the major surface antigen (SAG1) was linked with intrinsically unstructured domain (IUD) of dense granule protein 2 (GRA2). The recombinant GST-GRA2-SAG1A protein was successfully expressed and purified as 51 kDa of molecular weight. Furthermore, antigenicity and solubility of the rGST-GRA2-SAG1A protein were significantly increased. The overall specificity and sensitivity of GST-GRA2-SAG1A loaded RDT (TgRDT) were estimated as 100% and 97.1% by comparing with ELISA result which uses T. gondii whole cell lysates as the antigen. The TgRDT tested with Uganda people sera for field trial and showed 31.9% of seroprevalence against T. gondii antibody. The TgRDT is proved to be a kit for rapid and easy to use with high accuracy, which would be a suitable serodiagnostic tool for toxoplasmosis.

• 대한수의학회지
• /
• 제31권4호
• /
• pp.501-507
• /
• 1991

Diagnosis of cryptosporidiosis is currently confirmed by the detection of the oocysts or endogenous stages in fecal or tissue samples. Various conventional staining methods and serodiagnostic techniques have been reported, but the latter has far been limited to a few laboratories. Cryptosporidium has recently been reported in mice and chiekens in Korea, but there has been no report on staining methods to the oocysts. The present study was performed by light and scanning electron microscopic observations, and discussed with staining properties of four conventional methods such as dichromate solution floatation method, Carbol fuchsin stain, Auramine-O stain and Giemsa stain method. Cryptosporidial oocysts were isolated from the laboratory mouse. In tissue sections of duodenum, jejunum, ileum, cecum and upper colon, numerous very small, basophilic bodies were observed on the border of mucosal epithelial cells. In scanning electron microscopic observations, a few of developmental stages of Cryptosporidium were seen. Two types of thick and thin-walled oocysts were recognized in the intestinal contents. Mean size of its were $5.19{\pm}0.23{\times}4.31{\pm}0.32{\mu}m$ and $5.14{\pm}0.25{\times}4.27{\pm}0.4{\mu}m$, respectively. Carbol fuchsin and Auramine-O stain methods are recommended as the satisfactory ones for the identification of Cryptosporidium oocysts. Giemsa stain was also recommended as available in the laboratory, because a few of developmental stage fo Cryptosporidium could be seen by it.

• 농촌의학ㆍ지역보건
• /
• 제12권1호
• /
• pp.117-123
• /
• 1987

Detection of IgG antibody in clonorchiasis has been accomplished through various serodiagnostic procedure including complement fixation test, gel diffusion test, indirect fluorescent antibody test, indirect hemagglutination test etc. In this report enzyme immunoassay (ELISA) and indirect hemagglutination test (IHA) were used to determine IgG serum antibody levels before and after therapy with praziquantel. Briefly, sera from 62 cases of confirmed human clonorchiasis were examined before and after treatment with praziquantel. Among 62 cases treated 25 cases were categorized as completely cured groups by formalin-ether and careful examination of 4 cellophane thick smered slides at 18 months after treatment. The sera of 25 cases of cured groups were examined again by ELISA and IHA, and com-pared to the previous data. The results obtained were as follows; 1) Sensitivity of IHA test was 83.6% when cut-off titer of 1:8 was applied. No sera obtained from 10 normal healthy control showed positive reaction. 2) Twenty cases (80.0%) out of 25 cured one showed negative results by IHA at 18 months after treatment. 3) Although 5 cases showed positive titer even 18 months after treatment 3 cases of them showed decreased antibody titer. However 2 cases did not show any response. 4) Even though almost all cases showed de- creased ELISA value, only 11 cases (44.0%) out of 25 patients showed negative results by ELISA at 18 months after treatment. In conclusion, it is suggested that, while IgG ELISA for detecting long persisting antibody was more sensitive than IHA, IHA results more conclusively indicated effective treatment in clonorchiasis by negative conversion than did the results of ELISA.

• Parasites, Hosts and Diseases
• /
• 제44권1호
• /
• pp.49-54
• /
• 2006

In order to develop tools for an early serodiagnosis of Plasmodium falciparum infection, we evaluated the usefulness of P. falciparum liver stage antigen-3 (LSA-3) as a serodiagnostic antigen. A portion of LSA-3 gene was cloned, and its recombinant protein (rLSA-3) was expressed in Escherichia coli and purified by column chromatography. The purified rLSA-3 and 120 test blood/serum samples collected from inhabitants in malaria-endemic areas of Mandalay, Myanmar were used for this study. In microscopic examinations of blood samples, P. falciparum positive rate was $39.1\%$ (47/120) in thin smear trials, and $33.3\%$ (40/120) in thick smear trials. Although the positive rate associated with the rLSA-3 $(30.8\%)$ was lower than that of the blood stage antigens $(70.8\%)$, rLSA-3 based enzyme-linked immunosorbent assay could detect 12 seropositive cases $(10.0\%),$ in which blood stage antigens were not detected. These results indicate that the LSA-3 is a useful antigen for an early serodiagnosis of P. falciparum infection.

• 대한수의학회지
• /
• 제36권4호
• /
• pp.845-858
• /
• 1996

The purpose of this study was to establish early diagnostic methods for the detection of Aujeszky's disease viral antigens and nucleic acid in nasal cells, and buffy coats from experimentally infected living pigs by a combination of immunocytochemistry, in situ hybridization with digoxigenin(DIG)-labled probe and electron microscopy. Forty days old piglets were inoculated intranasally with $10^{7.0}TCID_{50}$ of Aujeszky's disease virus (ADV, NYJ-1-87 strain). The viral antigens and nucleic acid of ADV were detected in nasal cells, and buffy coat for 20 days after inoculation by immunocytochemistry, in situ hybridization with DIG-labeled probe and electron microscopical method. The results were compared with conventional methods such as a porcine Aujeszky's disease serodiagnostic(PAD) kit, neutralization test(NT) and virus isolation. 1. The viral antigens, nucleic acids and capsids of ADV were detected in nasal cells, buffy coats from 3 days to 20 days after inoculation by immunocytochemistry, in situ hybridization with DIG-labeled probe and electron microscopy, respectively. 2. When viral antigens were detected by the immunocytochemical technique, a diffuse brown deposit was observed in the nucleus and cytoplasm of nasal cells, buffy coats and PK-15 cells under a microscope. 3. DIG-labeled DNA probe was prepared by amplification of conserved sequence of recombinant ADV-gp50 clone with polymerase chain reacction. When ADV-DNA was detected by ISH with DIG-labeled probe, purplish blue pigmentation were observed in the nuclei and cytoplasms of ADV-infected cells under a microscope. Positive signals were observed in nasal cells and in the buffy coat and PK-15 cells at the first day after inoculation. 4. Where ADV-capsids were detected by transmission electron microscopical method, aggregation of capsids was observed in the nuclei and cytoplasms of nasal cells, buffy coats and PK-15 cells. The results suggested that these methods were considered as the highly sensitive and reliable tools for rapid and confirmative diagnosis of Aujeszky's disease in living pigs.

• Journal of Yeungnam Medical Science
• /
• 제12권1호
• /
• pp.48-55
• /
• 1995

1995년 1월에서 1995년 3월까지 심근 손상이 의심되는 환자 및 정상대조군에 대한 TnT, 총 LD, 총 CK 및 각 동위효소에 대한 고찰에서 다음과 같은 결과를 얻었다. Tropohin T는 정상인에서 $0.01{\pm}0.02{\mu}g/L$, 급성심근경색환자에서 최고치는 4.7-24.2 ${\mu}g/L$로 나타났으며, 초기검사에서 정상범위에 속한 환자에서 6시간 후 추적조사에서는 모든 증례에서 1.0 ${\mu}g/L$이상으로 나타났다. 총 LD는 1-3일경에 최고치를 보인 후 점차적으로 감소되었으나, LD1/LD2 비율은 대부분의 환자에서 10일 이상 1.0이상으로 유지되므로, 상대적으로 늦은 시간에 내원한 경우 총 LD와 LD1/LD2 비율이 진단에 유용할 것으로 사료되었다. 총 CK 및 CK-MB인 경우 대부분의 환자에서 3-4일 후 정상 범위로 떨어지므로, 조기진단에는 도움이 되나, 장기간의 추적조사에는 유용성이 없는 것으로 사료되었다. 총 Lactate Dehydrogenase, LD1/LD2 비율, 총 Creatine Kinase, CK-MB와 Troponin T의 상호비교에서 Troponin T가 상대적으로 초기 혹은 장기간 경과된 경우에도 유용한 지표로 사료되었다.

• Tuberculosis and Respiratory Diseases
• /
• 제48권3호
• /
• pp.315-323
• /
• 2000

연구배경 : 현행 도말 및 배양등의 미생물학적 검사법의 제한점을 보완 또는 보조할 수 있는 신속한 결핵진단 방법의 하나로서 가장 많이 연구 되어온 분야가 혈청학적인 방법이다. 이 중 현재까지 결핵의 혈청학적 진단에 유용성이 높은 것으로 평가되는 항원의 하나가 38KDa으로 대표되는 결핵균 분비항원이다. 마침, 이 38KDa 항원을 주항원 성분으로 하여, 간편하게 실험할 수 있도록 kit화된 제품이 국내외에서 널리 시판되고 있기에(ICT-TB, 호주 ICT Diagnostics사) 이를 이용, 결핵의 혈청학적 진단이 얼마나 유용할 것인지를 평가하고자 하였다. 방 법 : 결핵이 없는 7세 이하 아동 21명과 건강 성인 47명 등 총 68명의 대조군과, 치료 개시 전에는 균양성이었으나 ICT 검사 당시는 균이 나오지는 않았던 치료 중인 폐결핵환자 82명 (결핵성 흉막염 환자 3명 포함) 및 균양성으로 당시 치료 중이던 폐결핵환자 40명 등, 총 122명의 결핵환자를 대상으로 하여 결핵의 혈청학적 진단용 kit인 ICT를 이용하여 시험하였다. 결 과 : 1. 결핵환자가 아닌 대조용 대상자 68명(7세 이하 아동 21명 포함)에 대한 ICT의 양성반응률 (위양성률)은 13.2%였고, 음성반응률 (결핵환자가 아닌 것으로 판정되는 율, true negative)은 86.8%였다. 2. 시험된 대상 결핵환자 122명에 대한 ICT에 의한 양성반응률은 86.9%, 음성반응률은 13.1%였다. 3. 균양성 폐결핵 환자 40명에 대한 ICT 양성률은 95.0% (38명), 음성률은 5.0% (2명)였다. 4. 폐외결핵환자 3명을 포함한, 현재 치료 중에 있는 균음성 결핵환자에 82명에 대한 ICT의 양성반응률은 82.9%(68 명), 음성반응률은 17.1%(14명)였다. 그러나, 균양성 결핵환자와 균음성인 결핵환자간 ICT 양성률에는 통계적으로 유의한 차이가 없었다(P>0.05). 5.ICT의 민강도와 특이도는 모두 87%였으며, 위양성률과 위음성률도 같은 13%였다. 또 유병율이 64% 수준일 때의 양성예측률은 92.2%, 음성예측률은 78.7%였다. 결 론 : ICT의 높은 위양성률과 진단능률(diagnosability) 등을 고려할 때, 결핵이 의심되지만 기존의 도말 및 배양검사 결과를 얻기 어려운 대상자에게만 필요에 따라 제한적으로 활용해볼 수 있는 검사인 것으로 판단되었다.