돼지 정액 채취과정은 무균적으로 진행되기가 어려우므로 채취된 정액의 세균오염 (bacteriospermia)은 일반적인 것으로 알려져 있다. 돼지 정액에서 주로 분리되는 오염 세 균은 그람음성균이고, 장내세균과(Enterobacteriaceae)에 속하는 것으로 조사되고 있다. 정액 내 세균오염은 오염 정도에 따라 정액의 품질과 수명에 부정적인 영향을 미치는 것 으로 보고되고 있다. 본 실험에서는 돼지 정액에서 순수분리한 대장균을 실험적으로 농 도별로 오염시켜 돼지 정액의 활력, 생존율 및 pH에 대한 대장균 오염의 영향을 확인코 자 하였다. 정자 농도와 세균오염 정도를 조절하기 위하여 항생제가 첨가되지 않은 시판 돼지 정 액 희석제(Seminark Pro)를 이용하였고 돼지 정자수 대비 대장균수가 4,000 : 1(T1), 400 : 1(T2), 40 : 1(T3), 4 : 1(T4)이 되도록 액상정액 시료를 제조하였다. 모든 시료는 17℃ 저온배양기에 보존하면서 유세포분석기(flow cytometer)를 이용하여 0일차, 1일차, 3일차 및 5일차에 각 시료별 정자 활력(미토콘드리아 함량 측정)과 생존율(Live/DeadⓇ 염색)을 측정하였고, 산도측정기(pH meter)로 정액 pH를 측정하였다. 정자의 활력은 T3, T4에서 0일차(17℃, 4시간 배양)부터 대조군(C)에 비하여 유의성 있 게 감소하였고, 모든 시료에서 3일차 이후부터 활력이 감소(p<0.05)하였다. 정자 생존율 의 경우에도 T3, T4에서 0일차부터 C에 비하여 유의성 있게 감소하였고, 모든 시료에서 3일차부터 생존율이 감소(p<0.05)하였다. 보존일 경과에 따른 정액의 pH 변화의 경우, C, T1 및 T2에서는 0일차에 pH 7.00 정도에서 5일차(p<0.05)에 pH 7.10 이상으로 높아진 반면, T3에서는 3일차(p<0.05)부터 pH 6.90 이하로 낮아져 5일차에는 pH 6.86이었고, T4 에서는 1일차(p<0.05)부터 pH 6.86 이하로 낮아져 3일차(p<0.05)와 5일차(p<0.05)에는 pH 6.65 이하로 낮아졌다. 본 결과로부터 돼지 정자수 대비 대장균수가 40 : 1(20×106 sperm cells/ml : 5×105 cfu/ ml) 이상으로 오염되었을 경우 오염 당일부터 5일차까지 대조군에 비하여 정자의 활력과 생존율이 유의성 있게 감소되었으며 40 : 1의 경우는 3일차부터, 4 : 1의 경우는 1일차부 터 정자의 사멸 혹은 세균오염에 의한 산패로 정액의 pH가 낮아지는 경향을 확인할 수 있었다. 이는 정액 내 세균오염이 정액의 품질과 수명에 부정적인 영향을 미친다는 보고 와 일치하며 위생적인 정액 채취를 위한 노력과 고품질 정액 공급을 위한 정기적인 모니 터링 검사 및 보존액 내 유효한 항생제 첨가가 중요할 것으로 사료된다.

Erysipelothrix rhusiopathiae is a causative agent of erysipelas in avian and mammalian species globally. Eight dead 5-week-old Ross broiler chickens were submitted for diagnostic tests in September 2005. Typical signs including white necrotic foci on the liver, focal congestion of the pancreas, severe atrophy and hardening of the bursa of Fabricius were detected. E. rhusiopathiae was isolated from haemorrhagic lung samples. However, no specific PCR product for the viral diseases tested was detected in these chicken samples. To our best knowledge, this is the first report of the isolation of E. rhusiopathiae in broiler chickens in Korea.

There are many researches about the contribution of virginiamycin use in animals to quinupristin/dalfopristin (Q/D) resistance in humans. In this study, the prevalence and mechanisms of streptogramin resistance in Enterococcus faecium from chickens were investigated. A total of 170 E. faecium isolates from 38 chicken farms was tested for antimicrobial susceptibility. Eleven (6.5%) E. faecium isolates were found to be resistant to Q/D. The vatE and ermB genes were detected in 2 (18%) and 6 (55%) of Q/D-resistant E. faecium respectively. By using pulsed-field gel electrophoresis (PFGE), 6 distinct PFGE patterns were identified. These data indicate that Q/D resistance among E. faecium from chickens remains low despite the long history of virginiamycin use. However, we have to concern over antimicrobial resistance in bacteria originated from animals, including the possibility of transfer of resistance genes from animal to human.

The present study was conducted to investigate serotype distribution and biofilm formation of Actinobacillus (A.) pleuropneumoniae isolated from pneumonic lungs of pigs. A total of 37 A. pleuropneumoniae were isolated between January 2009 and June 2010. Serotypes of A. pleuropneumoniae isolates were determined using two different PCRs. The majority of isolates belonged to serotype 5 (n=31, 83.8%), and the others belonged to serotype 1 (n=4, 10.8%), and 2 (n=2, 5.4%), respectively. The ability of biofilm formation of the isolates was also determined by quantitative microtiter plate assay. Biofilm formation was observed in both 23 (62.2%) of the 37 field isolates and seven (43.8%) of the 16 reference strains. On the other hand, biofilm formation was various according to the serotypes: 20 (64.5%) of serotype 5, and three (75.0%) of serotype 1. However, two isolates of serotype 2 did not produce the biofilm in this study. Consequently, A. pleuropneumoniae serotype 5 was the most frequently detected (83.8% of the isolates), and 23 (62.2%) of 37 isolates exhibited biofilm positive phenotype in this study.

Aflatoxins produced by Aspergillus spp. are recognized as a major concern in animal and human health. In pigs, ingestion of aflatoxin-contaminated feeds causes immunosuppression, hepatotoxicosis and poor feed efficiency. In this study, we screened the contaminated level of aflatoxins in 449 pig feeds from 12 swine farms in Korea. For rapid and efficient screening of aflatoxins in pig feeds we evaluated the feasibility of three commercial ELISA kits for the screening of aflatoxins in pig feeds. Twenty-nine pig feed samples were examined for total aflatoxins using three ELISA kits, simultaneously. From three repetitions of each assay, the average intra-assay precisions and the average inter-assay precisions expressed as coefficient of variation (CV, %) for VeratoxⓇ Quantitative Aflatoxin test were 6.90 and 12.29, respectively. A statistical comparison of the results between HPLC and ELISAs showed that the correlation coefficient values for VeratoxⓇ was 0.96. The results demonstrated that we can apply the VeratoxⓇ Quantitative Aflatoxin test for the detection of aflatoxins in pig feed from the field. The screening of field samples with this ELISA kit showed that 11 out of 265 pig feeds for growers and weaners were contaminated with total aflatoxin levels exceeding 10 ppb, maximum tolerable limits for their compound feeds and the aflatoxins levels of remaining 184 pig feeds for other age groups of pigs were confirmed as below 20 ppb. The results from the screening indicated overall low levels of aflatoxins contamination in pig feeds.