• 제목/요약/키워드: serology

검색결과 132건 처리시간 0.03초

Malignant Catarrhal Fever의 병리조직학적 진단과 혈청학적 진단 및 PCR 진단법의 비교 (Comparison of Histopathology, Serology and PCR for the Diagnosis of Malignant Catarrhal Fever)

  • 김옥진
    • 대한수의학회지
    • /
    • 제43권3호
    • /
    • pp.471-476
    • /
    • 2003
  • Malignant catarrhal fever (MCF) is a systemic disease of ruminants caused by ovine herpesvirus 2 (OvHV-2). OvHV-2 is a gamma herpesvirus, which induces frequent latent infection and often difficult to detect its antigens and even specific nucleic acids because of its low viral copies in the infected tissues. Histopathology, serology and polymerase chain reaction (PCR) were compared for the diagnosis of MCF using 10 bison infected with OvHV-2. Histopathological diagnosis was performed using the criteria which was based upon the pathognomic lesions. Serological diagnosis was conducted using its serum with competitive ELISA for the detection of antibodies of OvHV-2. Also, the nest PCR was performed with peripheral blood leukocytes for the detection of OvHV-2-specific DNAs. Primers 556 and 775 were used for the primary amplification, and primers 556 and 555 were used for the secondary amplification. As the results, positive cases were 6 by histopahology, 9 by serology and 10 by PCR. As comparing with other diagnostic methods, PCR was found to be more sensitive than histopathology and serology. The recent development of molecular diagnostic assays has provided powerful tools for investigating how viruses survive in nature. Development of PCR specific for viruses has dramatically improved the accuracy of diagnosis of viruses in clinically infected animals. Furthermore, amplification of viral genomic material by nest PCR represents the most sensitive method for the detection of viruses and might be detected successfully even though very low viral DNA copies. So, it could be used as the first choice for the detection of viral DNAs with low copies such as the status of latent infection. However, it has also some limitation of application like as false negative results by PCR inhibitors and false positive results by contamination. The results of this study suggest that the use of molecular biological methods like PCR may increase the accuracy for the diagnosis of infectious diseases. However, in diagnostic laboratory, it is recommended that PCR assay must be conducted with other diagnostic methods for more reliable diagnosis.

녹(鹿)의 혈청단백(血淸蛋白)에 관한 연구(硏究) (Studies on the Blood Protein Polymorphisms of Deer: Cervus nippon, Cervus unicolor)

  • 임영재;송영의;스즈키 쇼조;타나카 카즈;아마노 타카시;쿠로사와 야츠;카츠마타 마코토
    • 대한수의학회지
    • /
    • 제25권1호
    • /
    • pp.19-25
    • /
    • 1985
  • 한국(韓國), 대만(臺灣), 일본(日本)에서 사육(飼育)하고 있는 꽃사슴(Cervus nippon) 129두(頭)와 물사슴(Cervus unicolor) 7두(頭)에서 hemoglobin, transferrin, albumin carbonic anhydrase, slow-${\alpha}_2$ 및 amylase형(型)을 전기영동(電氣泳動)에 의(依)하여 분석(分析)한 결과(結果) 다음과 같은 결론(結論)을 얻었다. 1. cellulose acetate에 의(依)한 전기영동(電氣泳動)이 starch gel에 의(依)한 전기영동(電氣泳動)보다 hemoglobin형(型) 분리(分離)에 있어서 더 간편하며 시간이 적게 걸리고, 선명(鮮明)할 뿐만 아니라 영구보존(永久保存)이 가능(可能)하다. 2. 꽃사슴의 hemoglobin형(型)은 $Hb^F$, $Hb^{FS}$, $Hb^S$형(型)으로 분리(分離)되었으나 물사슴에 있어서는 전부(全部) $Hb^F$형(型)으로 나타났다. 3. hemoglobin ${\beta}$ chain은 4가지형(型) 즉 ${\beta}$-1, ${\beta}$-2, ${\beta}$-3 및 ${\beta}$-4로 분리(分離)되었다. 4. hemoglobin ${\alpha}$ chain은 ${\alpha}_1$${\alpha}_1{\alpha}_2$형(型)으로 분리(分離)되었다. 5. slow-${\alpha}_2$형(型)은 A형(型)과 AB형(型)으로 분리(分離)되었으며, 꽃사슴에 있어서는 AB형(型)이 12% 출현(出現)하였으나 물사슴에서는 전부(全部) A형(型)으로 AB형(型)은 없었다. 6. albumin형(型)에서는 F형(型)과 S형(型)으로 분리(分離)되었으며 꽃사슴은 전부(全部) F형(型)이였고, 물사슴은 전부(全部) S형(型)이였다. 7. transferrin형(型), carbonic anhydrase형(型) 및 amylase형(型)은 전부(全部) 각각(各各) 1종류(種類)의 형(型)이였다.

  • PDF

SEROLOGY

  • 이승우
    • 대한치과의사협회지
    • /
    • 제9권9호
    • /
    • pp.527-529
    • /
    • 1971
  • PDF

Molecular Analysis of HLA-C Using Polymerase Chain Reaction-Sequence Specific Primers

  • Lee, Kyung-Ok;Hong, Sung-Hoi;Kim, Min-Jung;Park, Taek-Kyu;Kim, Yoon-Jung;Lee, Kyu-Pum
    • BMB Reports
    • /
    • 제30권1호
    • /
    • pp.26-32
    • /
    • 1997
  • Of all HLA class I molecules, HLA-C gene products are most poorly understood because they express at a low level on the cell surface compared to HLA-A and -B. In order to identify serologically detectable and undetectable HLA-C antigens, we have established a DNA-based tissue typing method for the HLA-C locus by PCR-SSP (polymerase chain reaction-sequence specific primers). Genomic DNA prepared from Iymphoblastoid 21 B-cell lines and 120 Korean individuals by proteinase K digestion and pheno/chloroform extractions have been typed by PCR-SSP (23 primer mixes were used). The PCR-SSP results of control cell lines were discrepant from serology in 1 case among 21 cases: Cw6 which was negative by serology but positive by PCR-SSP (cell line: MANIKA). Twenty four HLA-Cw "blank" antigens among fifty Korean individuals were completely determined by PCR-SSP DNA typing. HLA-Cw*0101 (15.3%), Cw*1401 (12.3%) and Cw*0701 (11.7%) alleles were frequently found in 120 Korean individual samples. In conclusion. the high level of discrimination for HLA-C alleles may prove useful and informative in the study of transplant survival, and identify the importance of allelic differences, not readily detectable by serology, on host and donor compatibility.

  • PDF

Antiserum Preparation of Recombinant Sweet Potato Latent Virus-Lotus (SPLV-Lotus) Coat Protein and Application for Virus-Infected Lotus Plant Detection

  • He, Zhen;Dong, Tingting;Chen, Wen;Wang, Tielin;Gan, Haifeng;Li, LiangJun
    • The Plant Pathology Journal
    • /
    • 제36권6호
    • /
    • pp.651-657
    • /
    • 2020
  • Lotus is one of the most important aquatic vegetables in China. Previously, we detected sweet potato latent virus from lotus (SPLV-lotus) and found that it has highly significant sequence diversity with SPLV-sweet potato isolates (SPLV-sp). Here, we developed serological methods for the detection of SPLV-lotus in Chinese lotus cultivation areas. Based on the high sensitivity of SPLV-lotus coat protein antiserum, rapid, sensitive and large-scale diagnosis methods of enzyme-linked immunosorbent assay (ELISA) and dot blot in lotus planting area were developed. The established ELISA and dot blot diagnostic methods can be used to detect SPLV-lotus from samples successfully. And our results also showed that the SPLV-lotus and sweet potato isolates appeared clearly distinction in serology. Our study provides a high-throughput, sensitive, and rapid diagnostic method based on serology that can detect SPLV on lotus, which is suggested to be included in viral disease management approach due to its good detection level.

Incidence of Infection among Subjects with Helicobacter pylori Seroconversion

  • Young Jung Kim;Sun-Young Lee;Jeong Hwan Kim;In-Kyung Sung;Hyung Seok Park
    • Clinical Endoscopy
    • /
    • 제55권1호
    • /
    • pp.67-76
    • /
    • 2022
  • Background/Aims: Helicobacter pylori (H. pylori) seroconversion may occur during screening for gastric cancer. Our study aimed to assess the number of seroconverted subjects with H. pylori and their results in follow-up tests. Methods: Data were consecutively collected on subjects who were H. pylori-seronegative and presented for gastric cancer screening. Subjects who were followed up using the same serology test and pepsinogen (PG) assays on the day of endoscopy were included in the study. Results: During the follow-up of 57.7±21.4 months, 61 (15.0%) of 407 seronegative subjects showed seroconversion. H. pylori infection was detected in six (9.8%) of 61 seroconverted subjects. A diffuse red fundal appearance, with a significant increase in the Kyoto classification scores for gastritis, was observed in the infected subjects (p<0.001). Compared to the false-seropositive subjects, infected subjects showed higher serology titers (p<0.001) and PG II levels (p<0.001) and lower PG I/II ratios (p=0.002), in the follow-up tests. Conclusions: Seroconversion occurred in 3.3% of seronegative subjects per year; however, only 9.8% had H. pylori infection. The majority (90.2%) of the seroconverted subjects showed false seropositivity without significant changes in the follow-up test results. The diffuse red fundal appearance could be an indicator of H. pylori infection.

위암 환자의 헬리코박터 파이로리 감염 진단에 있어서 위절제술 직후 생검된 위점막 조직을 이용한 신속 요소 분해 효소 검사법 도입의 의의 (An Alternative Method for a Rapid Urease Test Using Back-table Gastric Mucosal Biopsies from Gastrectomy Specimen for Making the Diagnosis of Helicobacter pylori Infection in Patients with Gastric Cancer)

  • 김신일;진성호;이재환;민재석;방호윤;이종인
    • Journal of Gastric Cancer
    • /
    • 제9권4호
    • /
    • pp.172-176
    • /
    • 2009
  • 목적: 신속 요소 분해 효소 검사법은 헬리코박터 파이로리 감염의 진단에 있어서 빠르고 신뢰성 높은 검사이다. 그러나 내시경을 통한 위점막의 생검이 필요할 뿐 아니라 국내의 의료보험에서는 위암 환자에 대해 급여 인정이 되지 않는 제한점이 있다. 따라서 저자들은 대체 방법으로 위절제술 직후 생검된 위점막 검체를 이용하여 신속 요소 분해 효소 검사를 시행하였고 이를 소개하고자 한다. 대상 및 방법: 위절제술을 시행 받은 위선암 환자들 중 90명을 대상으로 헬리코박터 파이로리에 대한 IgG 항체 검사를 시행하였으며, 위절제술 직후 위전정부와 위체부 각각에서 점막 생검을 하여 신속 요소 분해 효소 검사 키트에 고정한 후 24시간 이내에 색깔변화를 통해 양성 여부를 판독하였다. 본 연구에서는 면역 혈청학적 검사에서 양성이거나 신속 요소 분해 효소 검사에서 양성인 경우 헬리코박터 파이로리 감염이 있다고 정의하였다. 결과: 신속 요소 분해 효소 검사와 면역 혈청학적 검사에서 양성인 경우가 각각 91.1%와 77.8%였다. 신속 요소 분해 효소 검사의 민감도, 특이도, 양성 예측률, 음성 예측률은 94.3%, 100%, 100%, 37.5%였으며, 면역 혈청학적 검사는 80.5%, 100%, 100%, 15%로 나타났다. 신속 요소 분해 효소검사의 정확도는 94.4%로 면역 혈청학적 검사의 81.1%보다 높았다. 신속 요소 분해 효소 검사의 헬리코박터 파이로리 감염 진단률이 면역 혈청학적 검사보다 더 높았다. 결론: 본 연구에서 위선암 환자에서 위절제술 후 생검된 위점막 검체를 이용한 신속 요소 분해 효소 검사법은 문헌상에 보고된 통상적인 신속 요소 분해 효소 검사법의 진단률과 대등하였다. 따라서 위절제술을 시행 받는 환자에서 헬리코박터 파이로리 감염의 대체 검사법으로 유용할 것으로 기대된다.

  • PDF