• 제목/요약/키워드: Mycoplasma spp.

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경기지역 도축우 및 도축돈의 폐렴병변에서 Mycoplasma spp. 원인체에 관한 연 (Prevalence of Mycoplasma spp. in Slaughtered Cows and Pigs with Pneumonic Lung Lesion in Gyeonggi Province)

  • 제미성;이찬희;김용백;박건택;정우경;박용호
    • 한국식품위생안전성학회지
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    • 제33권4호
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    • pp.306-309
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    • 2018
  • 본 연구는 경기지역 도축돈 및 도축우의 폐렴병변에서 Mycoplasma spp.의 발생 분포를 조사하고자 수행하였다. 부천 소재 도축장에 출하된 소와 돼지의 폐에 대하여 육안적 검사를 하고, 이 중 병변을 보인 소 192두와 돼지 257두의 폐에 대한 PCR 검사 결과, Mycoplasma spp.는 소에서 147두(76.5%), 돼지에서는 203두(80.9%) 에서 각각 검출되었다. 소, 돼지 각각의 Mycoplasma spp.에 대한 세부 primer를 이용한 검사 결과에서는 소에서 M. agalactiae가 16두(8.3%)에서 검출되었으나, M. dispar, M. bovis 및 M. bovirhinis는 검출되지 않았다. 돼지에서는 M. hyopneumoniae가 74두(28.8%), M. hyorhinis가 13두(5.1%) 검출되었다. M. hyosynoviae는 검출되지 않았다. 본 연구를 통해 경기지역 도축우 및 도축돈에서 Mycoplasma성 폐렴이 상재하고 있음을 확인하였다.

국내 사육 유우군의 마이코플라스마균 유방감염에 관한 연구 (Epidemiological studies on Mycoplasma mastitis of dairy cows in South Korea)

  • 한홍율;황철용;손대호;김미경;유종현;박선일;오태호
    • 대한수의학회지
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    • 제40권3호
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    • pp.645-652
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    • 2000
  • This study was performed to investigate Mycoplasma (M) spp. infection status of dairy cow in South Korea. Among 8,485 bulk tank milk collected from dairy farms of the 5 areas, 26 samples (0.30%) were positive for Mycoplasma by direct culture method. The isolation rates of Mycoplasma spp. according to the areas were 0.51% in Kyonggi, 0.16% in Cholla, 0.23% in Gyoungsang, 0.12% in Chungchong, and 0.08% in Kangwon. In the species identification test by indirect immunoperoxidase test, 16 out of 26 isolates were identified as M bovis (61.53%), M bovigenitalium (23.07%), M californicum (7.69%), M alkalescens and Acholeplasma laidlawii (3.84%), respectively. The isolation rate of Mycoplasma spp. from 208 quarter milk samples in culling cows due to severe clinical mastitis was 3.0%. These Mycoplasma spp. were identified as M bovis (62.0%), M bovigenitalium (12.0%), M californicaum (12.0%), and M alkalescens (12.0%). This study shows that the bovine mammary gland infected by Mycoplasma spp. is present in some dairy farms and the routine culture test of bulk tank milk samples for Mycoplasma is needed for a high quality milk promotion services.

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영남지방 도축돈에 대한 폐렴발생 조사 (Survey on Pneumonia of Slaughter Pigs in Youngnam)

  • 조광현;박인화;도재철;장성준;박노찬;권헌일;박덕상
    • 한국동물위생학회지
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    • 제19권2호
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    • pp.126-138
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    • 1996
  • Lungs from 109 slaughter pigs with gross lesions indicating enzootic Pneumonia of pigs(EPP) and 16 grossly normal lungs, all originating from seven different herds, were subjected to microbiological examinations. The microbiological studies were included both bacterial and mycoplasmal culture. From lungs of 125 slaughter pigs, 87.2% pigs were pneumonia lesions alone or complexly Mycoplasma spp., pasteurella multocidu(p. multocida), Streptococcus spp., and Actinobacillus pleuropneumoniue(A. pleuropneumoniae) were detected in 39.4%, 42.2%, 13.8%, and 3.7% of the pneumonic lungs, respectively. P. multocida was the most frequently isolated organism in pneumonic lungs. Mycoplasmas not isolated organism in 33.9% the pneumonic lungs even If [here are gross lessions mycoplasmas. The amounts of pneumonia in lungs with Mycoplasma spp. alone, a concurrence of Mycoplasma spp. and P. multocida, p. multocida alone, a concurrence of P. multocida and A. pleuropneumoniae, and a concurrence of Mycoplasma spp. and A pleurdpneumoniae were 10.1%, 22.7%, 18.7%, 25%, and 30%, respectively These findings indicated that p. multocida might be involved in the pathogenesis of pneumonia in slaughter pigs. Mycoplasma spp. was also, in this study, associated with higher frequency of pneumonia. The frequency of pigs snout lesion grade 0∼5 inclusive were 27.2%, 28%, 19.2%, 16%, 6.4%, and 3.2% from 125 slaughter pigs. 32(25.6%) pigs were positive and 13~30% in the pigs from seven herds were found to be infected with atrophic rhintis (AR). A total of 46 P. multocida strains In pneumonic lungs were further characterized by capsular serotyping and testing for production of dermonecrotic toxin. 42(91.3%) of strains were capsular A and 4(8.7%) were type D. Out of the type A and type D strains, 86% and 75% were toxigenic, respectively.

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동물용 생 바이러스 백신에서 Mycoplasma 검출을 위한 PCR 기법 적용 (Application of a PCR Method for the Detection of Mycoplasma in Veterinary Live Viral Vaccines)

  • 전우진;김병한;정병열;안동준;이철현;장환;정갑수
    • 미생물학회지
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    • 제41권4호
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    • pp.269-274
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    • 2005
  • 동물용 생 바이러스 백신 내에 mycoplasma를 검출하기 위해 polymerase chain reaction (PCR)기법과 2가지의 상품화된 PCR 검출킷트를 평가하였다. PCR기법은 시험에 사용된 모든 mycoplasma를 특이적으로 검출할 수 있었으나, 2가지의 상품화된 PCR 검출킷트는 일부의 mycoplasma를 검출하지 못하였다. 또한, PCR기법의 검출 특이도는 조류 유래 mycoplasma에 속한 4주의 표준주 및 7주의 야외분리주를 모두 검출할 수 있었다. PCR기법의 민감도는 9 CFR Mycoplasma액체배지에서 배양한 Mycoplasma 속균 및 Acholeplasma속균에 대해 $1\~100$ colony forming units/ml까지 검출할 수 있었다. 동물용생 바이러스 백신에 대해 PCR기법의 적용가능성을 평가하기 위해, 돼지 전염성위장염 및 로타바이러스 흔합백신과 개 파보바이러스 백신내에 A. laidlawii를 인공적으로 접종한 후, PCR기법의 민감도를 조사하였을 때 배양액을 이용한 검출한계와 유사하였다. 본 연구에서 사용된 PCR 기법은 동물용 생 바이러스 백신내의 mycoplasma를 신속하고 민감하게 검출할 수 있을 것으로 판단되었다.

Detection of Respiratory Viral Pathogens and Mycoplasma spp from Calves with Summer Pneumonia in Korea

  • Park, Jung-hoon;Kim, Doo
    • 한국임상수의학회지
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    • 제36권4호
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    • pp.185-189
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    • 2019
  • Respiratory pathogens of calves including bovine parainfluenza type 3 virus (BPI3V), bovine respiratory syncytial virus (BRSV), infectious bovine rhinotracheitis virus (IBRV) and Mycoplasma spp is well-known for winter pathogens. However, there are no studies about summer pneumonia pathogens of calves in Korea. The aim of this study was to detect respiratory pathogens from calves with summer pneumonia. Eighty calves from 5 regions were chosen and their nasal swabs were used to detect respiratory pathogens with real-time PCR. Mycoplasma spp was major primary respiratory pathogens in calves with summer pneumonia. Although, the detection rates of respiratory viruses were very low, serological assays showed that respiratory viruses exist widely in farms.

Detection of Mycoplasma felis from the kenneled cats with pneumonia

  • Hong, Sunhwa;Lee, Hak-Yong;Kim, Tae-Wan;Kim, Okjin
    • 한국동물위생학회지
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    • 제38권1호
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    • pp.31-36
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    • 2015
  • Two cats were obtained from a cat kennel. Over the previous 7 days, the cats had shown cough, anorexia, depression and nasal discharge. In this study, the consensus PCR was able to detect successfully Mycoplasma species in nasal swab samples of the cats. To identify feline mycoplasma species from the lung tissue of the cats with pneumonia, Mycoplasma species-specific PCR reactions were conducted. As the results, we could identify M. felis by the positive amplified DNAs. On the other hand, we could not detect any positive reactions with the PCR reaction for M. arginini, M. canis, M. edwardii, M. cynos, M. gateae, M. maculosum, M. molared, M. opalescens, M. spumans and Mycoplasma HRC-689. In conclusion, we detected M. felis from the kenneled cats with pneumonia. We suggested that this consensus PCR would be useful and effective for monitoring Mycoplasma species in various kinds of animals including cats. The application of preceding consensus PCR before the species-specific PCRs may be the most recommended strategy for the identification of Mycoplasma spp.

Molecular Detection of Mycoplasma felis Infection in a Cat with Respiratory Symptoms

  • Lee, Hyun-A;Hong, Sunhwa;Chung, Yungho;Kim, Okjin
    • 한국임상수의학회지
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    • 제35권6호
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    • pp.273-275
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    • 2018
  • A 6-month-old male cat was presented for investigation of depression, loss of appetite, dehydration, pale conjunctival mucous membrane, weight loss, fast heart and respiratory rates, nasal discharge and cough. Nasal swabs collected from the studied cat. As the results of bacterial culture with nasal swabs, it was suspected with Mycoplasma spp. Also, Mycoplasma species was detected by the PCR reaction with Mycoplasma genus primers. At species PCR assay, the specimens evaluated for the presence of M. felis, M. arginini, M. gateae, and Acholeplasma laidlawii and the result was visualization of bands from 238 bp in agarose gel 1.5% showing M. felis amplicons in samples. In conclusion, we detected M. felis in a cat with respiratory disease. PCR was able to detect successfully M. felis infection in cats.

도축돈의 폐렴병소에서 분리한 세균의 항생제 감수성 (Antibiotic susceptibility of microorganisms isolated from Pneumonic lungs of slaughtered pig in northern Chungnam area)

  • 이종훈;김성민;배영재;나기복;박일규;정영재
    • 한국동물위생학회지
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    • 제19권2호
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    • pp.115-125
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    • 1996
  • A total of 315 microorgainisms were isolated from 256 pneumonic lung samples of pig in abattoirs of northern Chungnam area during February to November 1994, and Identified 97 strains as Pusteurella multocida, 89 strains as Staphylococcus spp, 54 strains as Streptococcus spp, 22 strains as Mycoplasma spp, 21 strains as Escherichia coli, 18 strains as Haemophilus parsuis, 11 strains as Corymebacteroi, pyogenes, and 3 strains as Acrinobacillus spp by Gram's and Dienes stain, and biological properties test Involved API system. After that, they were examined anti biotic susceptibility for ampicillin(AM), cephalothin(CF), chloramphenicol(CP), erythromycin(EM), kanamycin(KM), gentamicin(GM), neomycin(NM), penicillin(PC), streptomycin(SM), tetracycline(TE), tiamulin(TIA), tylosin(TYL), methicillin(DP), colistin(CL) and trimet hoprim(SXT). In antibiotics susceptibility test, 293 isolates except Mycoplasma spp 22 strain were highly susceptible to DF(79.2%) and AM(76.2%), but resistant to PC(14.0%), NM(19.5%) and KM (23.2%) The multiple drug resistant patterns were noted in most isolates, whereas only 7 isolates resistant to single drugs.

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영남지방 도축돈의 Mycoplasma 폐렴조사 및 분리균에 대한 약제 감수성 (Survey on mycoplasmal pneumonia of swine in Youngnam area and antimicrobial susceptibility of Mycoplasma hyopneumoniae isolated from Slaughter pigs)

  • 조광현;최정수;김봉환
    • 대한수의학회지
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    • 제39권1호
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    • pp.96-103
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    • 1999
  • The present study was carried out to investigate the prevalence of mycoplasmal pneumonia of slaugter pigs in Youngnam area during the period from 1995 to 1997. The prevalence and pathomorphology of gross lung lesions were studied from 682 slaughter pigs in 8 swine herds. Gross lesions of pneumonia were recorded in the lungs of 442(64.8%), from 367 out of them(83.0%) were diagnosed as mycoplasmal pneumonia. Microbiological examination was performed with 197 lungs with gross lesions of mycoplasmal pneumonia of slaughter pigs from 8 different swine herds. M hyopneumoniae, P multocida, A pleuropneumoniae, Streptococcus spp, Corynebacterium spp, and H parasuis were detected in 24. 4%, 48.2%, 2.5%, 11.2%, 3.6%, and 1.0% of the pneumonic lungs, respectively. A total of 48 strains of M hyopneumoniae was investigated for their in vitro susceptibility to 8 antibiotics. Among the drugs tested, lincomycin, oxytetracycline, tiamulin and tylosin showed the high activity in minimal inhibitory concentration(MIC) of $0.04{\sim}5{\mu}g/ml$ while erythromycin showed low activity in MIC values($1.25{\sim}{\geq}40{\mu}g/ml$).

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돼지 희석정액의 세균오염도 및 유효 항생제 선발 (Bacterial contaminants in extended boar semen and selection of effective antimicrobials)

  • 김하영;변재원;신동호;김형순;윤하정;박최규;이오수;정병열
    • 대한수의학회지
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    • 제50권2호
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    • pp.125-131
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    • 2010
  • Bacterial contamination is an unavoidable finding of the semen collection process in boar and can lead in deleterious effects on semen quality and longevity if left uncontrolled. The purpose of this study is to identify the bacteria in extended boar semen and to select the effective antimicrobials to control of the contaminants. Of 116 extended boar semen samples submitted from eight AI centers in Korea, 39 (33.6%) samples were positive for bacterial contamination. Among 39 contaminated semen, most of them (84.6%) were contaminated with one or two bacterial species and there was no significant difference between two age groups $(\leq\;24\;and\;>\;24\;month\;old).$ Stenotrophomonas maltophilia (n = 18) was the most predominant bacterium followed by Elizabethkingia meningoseptica (n = 12), Sphingomonas paucimobilis (n = 12), Myroides spp. (n = 5), Ochrobactrum anthropi (n = 3), and so on. Enrofloxacin (72.9%), florfenicol (72.9%), bacitracin (49.2%) and tylosin (49.2%) showed higher sensitivity compared with penicillin (13.6%) or aminoglycosides (6.8%-18.6%). Brucella spp., Leptospira spp., Mycoplasma hyopneumoniae, Mycoplasma hyorhinis, Mycobacterium tuberculosis complex were not detected in semen by PCR.