중합효소연쇄반응을 이용한 자돈 혈청형에 따른 Salmonellosis의 신속한 검출

최경성,박진호,권오덕,이주묵,Choi, Kyoung-seong,Park, Jin-ho,Kwon, Oh-deog,Lee, Joo-mook 대한수의학회 1998 大韓獸醫學會誌 Vol.38 No.4

Salmonella typhimurium is a causitive agent of diarrhea, fever, gastroenteritis, septicemia and sudden death in piglet. The currently used methods such as IFA, ELISA, DNA hybridization assay is needed a long-time and difficult to detect the organism in carrier animal or contaminated sample with other agents. However, it is important to detect rapidly and sensitively S typhimurium in piglet with other infectious pathogens to minimize an economic loss. Two sets of PCR primer, rfbJ forward primer(5'-AGAATATGTAATTGTCAG-3') and reverse primer(5'-TAACCGTTTCAGTAGTTC-3') were designed to amplify a 882 by fragment of Salmonella serovar type B gene. The target genomic DNA for PCR was extracted from the cultivated materials with various enrichment periods in a nonselective enrichment agar and broth with clinical specimens. The PCR is carried out here made it possible to detect the gene from two hours. Also, the amplified fragment with PCR was cloned into pGEM-T vector and digested with restrict enzyme, and sequenced for the identification of Salmonella serotype B rfbJ gene. Duplicated cultivation agar-broth followed by PCR were performed to develop a rapid and sensitive detection of S typhlmurium based on serovar type. This duplicated cultivation-PCR method provides a sensitive and rapid diagnostic tool to detect Salmonella from infected piglet with improved sensitivity.

Epidemiological Investigation of Diseases in Korean Native Suckling Calves

권오덕,최경성,이승옥,정환,이주묵,Kwon, Oh-Deog,Choi, Kyoung-Seong,Lee, Seung-Ok,Jang, Hwan,Lee, Joo-Mook The Korean Society of Veterinary Clinics 2000 한국임상수의학회지 Vol.17 No.1

This study was carried out to investigate the epidemiological prevalence of diseases from birth to weaning in 268 Koeran native calves which was delivered from three stock farm in Chonbuk area. We examined body weight gain, incidence rate of diseases and mortality rate in relation to age, season, environmental temperature and rearing management conditions for one year. The results of this experiment were as follows: Birth weight and body weight gain of Korean native calves born of primiparae were lower than those of multiparae. Body weight gain of diseased calves was lower than normal calves. Of 268 delivered calves, 242 calves(90.3%) were affected with gastronistestinal and/or respiratory diseases. The prevalence of the diseases were gastronitestinal disease(54.1%), gastronitestinal and respiratory disease(21.6%), and respiratory disease(14.5%). Of 242 diseased calves, 33 calves(13.6%) were occurred gastronitestinal disease and respiratory disease at different time respectively. Of 268 delivered calves, 126 calves were died(47%). The prevalence of the death were gastronitestinal disease(31.4%), gastronitestinal and respiratory disease(14.5%), and respiratory disease(1.1%). 81% of the diseases and 76.2% of the death were occurred in winter and a change of season(December to May). 59.1% of the diseases and 52.4% of the death were occurred at atmospheric temperatures below 1$0^{\circ}C$. 91.7% of the diseased calves and 96.8% of the dead calves were born of primiparae. 77.2% of the gastronitestinal disease were occurred within 2 weeks old, and the incidence was decreased with increasing age. Whereas the incidence of respiratory disease was incidence with ageing, and 69.2% of the respiratory disease were occurred between 2 weeks and 5 weeks old. And 62% of the gastronitestinal and respiratory disease wre occurred between 1 week and 3 weeks old. 65.1% of the dead calves were died within 2 weeks old. The morbidity and population mortality rate in each farm stock were 56.5%-104.9%, and 14.5%-64.2%, respectively.

TaqMan 실시간 중합 효소 연쇄반응에 의한 살모넬라속의 검출 및 ompC 항원단백 유전자의 비교

이영성,최경성,김명철,한재철,채준석,Lee, Young-Sung,Choi, Kyoung-Seong,Kim, Myeong-Chul,Han, Jae-Cheol,Chae, Joon-Seok 대한수의학회 2002 大韓獸醫學會誌 Vol.42 No.4

Antigenic ompC genes of S. gallinarum, S. pullorum and S. dublin were characterized among Salmonella spp. isolated from chickens and other animals to identify genetic variation. Salmonella ompC gene fragment (1,027 bp) was amplified by PCR and the amplicons were cloned for comparison of nucleotide sequences. The identity of the sequences between S. gallinarum and S. pullorum, S. gallinarum and S. dublin, S. pullorum and S. dublin was 99.8%, 97.6% and 97.8%, respectively. Also, we found that ompC has some diversity between S. gallinarum and S. pullorum, and other Salmonella spp. which may be useful to type the organisms. Similar to diagnosis in other organisms, the TaqMan PCR method can be applied to rapid and accurate diagnosis of salmonellosis in chickens and other animals. We designed PCR primers and TaqMan probe for flagellin gene (fliC) for detection of Salmonella spp. by TaqMan PCR. The TaqMan PCR method was 10,000 times more sensitive than conventional PCR.

겨울철에 발생한 Holstein 송아지의 Anaplasma marginale 감염

이주묵,권오덕,송희종,박진호,최경성,Lee, Joo-mook,Kwon, Oh-deog,Song, Hee-jong,Park, Jin-ho,Choi, Kyoung-seong 대한수의학회 1997 大韓獸醫學會誌 Vol.37 No.4

We observed an outbreak of calf anaplasmosis at a farm in Chonbuk area during winter season, which was diagnosed by the hematological and serological tests. The results are as follow. On hematological observation for infected thirteen calves (ages 1 to 25 days) showed anemia with hematocrit $27.7{\pm}7.7%$, erythrocyte $6.9{\pm}1.9{\times}10^6/{\mu}l$, hemoglobin $11.3{\pm}3.2g/dl$, MCV $40.6{\pm}1.5fl$, MCH $16.3{\pm}1.6pg$ and MCHC $40.5{\pm}3.6g/dl$. Anaplasma marginale was observed in all of the calves's erythrocytes by Diff-Quick and acridine orange staining, and were reacted by ELISA.

TaqMan 실시간 PCR법에 의한 개 전염성 간염 바이러스의 검출

왕혜영,최재용,이미진,박진호,조매림,한재철,최경성,채준석,Wang, Hye-young,Choi, Jae-yong,Lee, Mi-jin,Park, Jin-ho,Cho, Mae-Rim,Han, Jae-cheol,Choi, Kyoung-seong,Chae, Joon-seok 대한수의학회 2004 大韓獸醫學會誌 Vol.44 No.4

The aim of this work was the validation of a rapid real-time PCR assay based on TaqMan technology for the unequivocal identification of infectious canine hepatitis (ICH) virus, to be used directly on DNA purified from blood specimens. A real-time PCR system targeting at the E3 ORFA gene sequence of canine adenovirus type 1 was optimized and validated through comparative analysis of samples using conventional PCR system. The real-time PCR assay based on TaqMan technology could disclose 23 (37.7%) out of 61 samples as PCR positive. In contrast, 18 (29.5%) samples were found PCR positive when conventional PCR was applied on these samples. The use of the ABI Prism 7700 sequence detection system allowed the efficient determination of the amplified product accumulation through a fluorogenic probe. The entire real-time TaqMan PCR assay, including DNA extraction, amplification, and detection could be completed within 3 hours. The detection method of real-time TaqMan PCR assay was 1,000 times more sensitive than conventional PCR. Real-time TaqMan probe and primer set developed and optimized in this study is a sensitive, rapid and accurate method for detection of ICH virus and can be effective screening tool for the detection of ICH in a diagnostic laboratory routines.

관악산에서 참진드기 조사 및 중증열성혈소판감소증후군 바이러스 검출

채정병,김태희,정지호,박윤지,박진호,최경성,유도현,박배근,채준석,Chae, Jeong-Byoung,Kim, Tae-Hee,Jung, Jee-Ho,Park, Yoon-Ji,Park, Jin-Ho,Choi, Kyoung-Seong,Yu, Do-Hyeon,Park, Bae-Keun,Chae, Joon-Seok 대한수의학회 2017 大韓獸醫學會誌 Vol.57 No.3

This study was performed to investigate the distribution of ticks and the rate of infection with severe fever with thrombocytopenia syndrome (SFTS) virus in ticks collected at Mt. Gwanak and the Seoul National University campus, Korea. Ticks (n = 273) were collected from May to October and included 76 Haemaphysalis longicornis (4 adult females, 72 nymphs), 49 Haemaphysalis flava (9 adult females, 3 adult males, 37 nymphs), and 148 Haemaphysalis spp. larvae. SFTS virus detection was performed by using one-step RT PCR and nested PCR. The SFTS virus was detected in 7 samples (1 Haemaphysalis longicornis nymph, 3 Haemaphysalis flava nymphs, and 3 Haemaphysalis spp. larva). The overall minimum field infection rate was 2.6%, whereas the minimum field infection rates of adult, nymphal, and larval ticks were 0%, 3.2%, and 2.0%, respectively. For a more accurate indication of the prevalence of SFTS virus in Korea, further in-depth investigations of tick species and SFTS virus occurrence over a larger area and longer period are needed.