• 제목/요약/키워드: Rapid detection kit

검색결과 95건 처리시간 0.036초

Rapid Detection of Infectious Bursal Disease Virus (IBDV) in Chickens by an Immunochromatographic Assay Kit

  • Choi, Kang-Seuk;Oh, Jin-Sik;Jeon, Woo-Jin;Na, Keon-Sok;Lee, Eun-Kyoung;Lee, Youn-Jeong;Sung, Hwan-Woo;Ha, Gun-Woo;Kwon, Jun-Hun
    • 한국가금학회지
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    • 제37권2호
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    • pp.167-172
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    • 2010
  • 닭 전염성 F낭병 (IBD)은 닭에서 전염성이 강하고 발병으로 인하여 양계 산업에 막대한 경제적 피해를 입히는 닭의 바이러스성 전염병이다. 이 연구에서는 수 분 이내에 검사 시료로부터 닭 전염성 F낭병 바이러스를 검출할 수 있는 시판용 면역크로마토그래피법 검사 킷트를 이용하여 IBD 진단에 있어서의 유용성을 조사하였다. 사용한 면역크로마토그래피법 검사 킷트는 닭 전염성 F낭병 바이러스 VP2에 특이적인 단클론 항체를 이용하여 닭 전염성 F낭병 바이러스를 검출하도록 고안되었다. 바이러스 감염 역가를 알고 있는 IBDV를 사용하여 조사한 결과, IC 검사 킷트의 검출 한계는 $10^{3.1}$ 내지 $10^{3.9}$ $EID_{50}$/mL이었다. 이 검사 킷트는 닭의 다른 전염성 바이러스인 뉴캣슬병 바이러스, 닭 전염성 기관지염 바이러스, 조류인플루엔자 바이러스 및 전염성 후두기관염 바이러스에 대하여 비특이 반응을 나타내지 않았다. 고병원성의 IBDV를 실험적으로 감염시킨 후 3일 내지 4일에 폐사한 닭의 장기별로 조사한 결과, 모든 폐사 닭의 F낭, 장편도, 비장, 신장 시료들은 면역크로마토그래피법 검사 킷트에서 강한 양성반응을 나타내었다. 검사 시료 중 F낭 시료가 IC 검사 킷트에서 가장 강한 양성반응을 나타내었다. 폐사 닭의 간, 흉선, 선위의 경우, 각각 검사시료의 87.5%, 37.5% and 0%가 양성 반응을 나타내었다. 면역크로마토그래피법 검사 킷트에서 음성이었던 시료 중 흉선 시료 한 점을 제외한 모든 시료는 DAS-ELISA와 동일한 검사 결과를 나타내었으나, 검사 시료 중 흉선과 선위 일부에서 RT-PCR 검사에서 양성 반응을 나타내었다. 야외 IBD 발생 농장과 비발생 농장에서 수거한 폐사닭 231수의 조직을 면봉으로 도말하여 채취한 시료를 조사하여 RT-PCR법과 비교한 결과, 상대적 민감도와 특이도는 각각 100% (109/109) 및 97.5% (119/122)를 나타났으며, 두 검사 방법간 kappa value는 0.97이었다. 우리의 연구 결과는 IC 검사 킷트는 야외 양계 농장에서 폐사 닭을 대상으로 IBD를 진단하는 데 적용하기에 매우 유용하다는 것을 말해준다.

마비성패류독소 검출을 위한 분석법 비교 (Comparison of Analytical Methods for the Detection of Paralytic Shellfish Toxins (PSTs))

  • 이가정;권순재;정연중;손광태;하광수;목종수;김지회
    • 한국수산과학회지
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    • 제50권6호
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    • pp.669-674
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    • 2017
  • Paralytic shellfish toxins (PSTs) are produced by marine dinoflagellate phytoplankton Alexandrium spp. and Gymnodinium spp. These toxins accumulate in filter feeding organisms such as bivalves and the ingestion of contaminated shellfish can cause illness in humans. The mouse bioassay (MBA) has been the preferred PST testing method worldwide for more than 50 years. However, this assay has several disadvantages, such as detection limits, non-toxic-profiles, and the ethical issues of using animals. The aim of this study was to establish an alternative to the MBA method for testing for PSTs. We optimized the analysis conditions of a post-column oxidation-high performance liquid chromatography (PCOX-HPLC) method and the Scotia Rapid Test Kit, and then compared the accuracy of these methods to the MBA method. The results demonstrated a strong correlation between the PCOX-HPLC method and the MBA, although the PCOX-HPLC method required expensive equipment and standard material, and was time consuming. The Scotia Rapid Test Kit promises to be a useful tool, as it provided rapid and qualitative results, although the method sometimes gave a false positive result that could not be explained by toxin profiles.

결핵진단에서 Xeniss Rapid TB kit의 임상적 유용성 (Evaluation of the Clinical Usefulness of the Xeniss Rapid TB kit for the Diagnosis of Tuberculosis)

  • 박승규;이우철;황수희;권은시;이흥순;이덕형
    • Tuberculosis and Respiratory Diseases
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    • 제53권4호
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    • pp.389-400
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    • 2002
  • 배 경 :결핵의 조기치료와 전염방지를 위해서 신속하고 간편한 결핵진단법의 개발이 요구되고 있는 실정에서 결핵균에 특이한 38-kDa단백을 포함하여 금 콘쥬게이트에 결합된 유전자재조합 항원을 혈청과 반응시켜 항결핵 항체를 발견하도록 고안된 카드형태의 혈청학적 진단기법인 Xeniss Rapid TB kit가 결핵의 진단에 유용하게 이용될 수 있는 지를 알아보고자 하였다.방 법 :188명의 결핵환자(폐결핵 177명, 폐외결핵 11명)와 82명의 접촉자, 그리고 57명의 건강한 성인을 대상으로 하였으며, 연구대상자의 혈청을 이용하여 Xeniss Rapid TB kit의 민감도, 특이도, 양성예측율, 그리고 음성예측율을 조사하였다. 결 과 : 전체적인 민감도는 73.9%, 특이도 81.3%, 양상예측율 84.2%, 그리고 음성예측율은 85.8%였다. 진단시점부터 검사시점간의 시간간격에 따라서는 1개월 이내에서 61.5%로 가장 낮고 점차 증가하여 4-6개월 시점에 94.4%로 가장 높았으며 이후 점차 감소하여 12개월 이상 경과한 시점에서는 67.4%의 양성반응율을 보였다. 페외결핵 환자(90.9%)에서는 폐결핵 환자(72.8%)보다 양성반응율이 높았다. 객담도말양성 (76.2 대 68.4%), 방사선 사진상 중증 (79.3 대 63.3%), 공동성 병소(75.7 대 70.0%), 과거 치료력 (76.3 대 73.3%)이 있는 환자군에서 상대적으로 높은 양성반응율을 보였으며, 당뇨병을 동반한 환자군(69.0 대 74.8%)과 노인환자군(68.l 대 100%)에서는 상대적으로 낮은 양성반응율을 보였다. 건강성인군 7.0%, 환자가족군 17.5%에 비해 병원직원군에서 57.9%의 양성반응율을 보여 활동성 결핵환자와 장기간 지속적으로 접촉한 군에서 높은 양성반응율을 보였다. 결 론 : Xeniss Rapid TB kit는 신속하고 간편하며, 민감도와 특이도가 비교적 높고 특히, 폐외결핵에서는 높은 양성반응율을 보여 폐결핵, 폐외결핵, 그리고 감염자의 진단에 보조적 검사법으로 유용하게 이용될 수 있을 것으로 생각된다.

Development of a Disperse Dye Immunoassay Technique for Detection of Antibodies against Neospora caninum in Cattle

  • Selahi, Fatemeh;Namavari, Mehdi;Hosseini, Mohammad Hossein;Mansourian, Maryam;Tahamtan, Yahya
    • Parasites, Hosts and Diseases
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    • 제51권1호
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    • pp.129-132
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    • 2013
  • In this study a disperse dye immunoassay method was standardized and evaluated for detection of antibodies against Neospora caninum in cattle. Sera from 150 cattle with a recent history of abortion were collected and tested by commercial ELISA kit and a standardized in-house dye immunoassay system. The positivity rate for the sera used in this study was 34.6% for the disperse dye immunoassay (DDIA) compared to 32% obtained by ELISA kit. This study showed no significant difference between DDIA and ELISA. The results indicated that the DDIA provide an economic, simple, rapid and robust test for detection of N. caninum infection in cattle.

Development and Clinical Evaluation of a Rapid Serodiagnostic Test for Toxoplasmosis of Cats Using Recombinant SAG1 Antigen

  • Chong, Chom-Kyu;Jeong, Woo-Seog;Kim, Hak-Yong;An, Dong-Jun;Jeoung, Hye-Young;Ryu, Jeong-Eun;Ko, A-Ra;Kim, Yong-Joo;Hong, Sung-Jong;Yang, Zhaoshou;Nam, Ho-Woo
    • Parasites, Hosts and Diseases
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    • 제49권3호
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    • pp.207-212
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    • 2011
  • Rapid serodiagnostic methods for Toxoplasma gondii infection in cats are urgently needed for effective control of transmission routes toward human infections. In this work, 4 recombinant T. gondii antigens (SAG1, SAG2, GRA3, and GRA6) were produced and tested for the development of rapid diagnostic test (RDT). The proteins were expressed in Escherichia coli, affinity-purified, and applied onto the nitrocellulose membrane of the test strip. The recombinant SAG1 (rSAG1) showed the strongest antigenic activity and highest specificity among them. We also performed clinical evaluation of the rSAG1-loaded RDT in 182 cat sera (55 household and 127 stray cats). The kit showed 0.88 of kappa value comparing with a commercialized ELISA kit, which indicated a significant correlation between rSAG1-loaded RDT and the ELISA kit. The overall sensitivity and specificity of the RDT were 100% (23/23) and 99.4% (158/159), respectively. The rSAG1-loaded RDT is rapid, easy to use, and highly accurate. Thus, it would be a suitable diagnostic tool for rapid detection of antibodies in T. gondii-infected cats under field conditions.

맥주오염미생물의 동정과 specific PCR primer의한 신속한 검출 방법 (Characterization of beer-spoilage microorganism and its rapid detection by specific PCR primer)

  • 이택인;최신건
    • 산업기술연구
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    • 제28권A호
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    • pp.141-147
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    • 2008
  • Several contaminated bacteria such as Lactobacillus brevis and Pediococcus damnosus in beer production cause beer spoilage by producing off flavours and turbidity. Detection of these organisms is complicated by the strict anaerobic conditions and lengthy incubation times required for their cultivation, consequently there is a need for more rapid detection methods. Recently, two contaminated strains were isolated from vessel of beer production and identified as Lactobacillus species by API kit identificaton as well as 16S-23S ITS sequencing analyses. Two isolated strains were named as Lactobacillus sp. HLA1 and Lactobacillus HLB2, respectively. A polymerase chain reaction (PCR) method was developed for the rapid and specific detection of Lactobacillus sp.. Two sets of primer pairs (HLA1-F/HLA1-R and HLB2-F/HLB2-R) were designed for the amplification of a 1576 base pair (bp) fragment of the HLA1 16S-23S rRNA gene and 1888 bp fragement of the HLB2 16S-23S rRNA. Amplified PCR products were highly specific to detect corresponding bacteria when other contaminated strains were used as PCR templates. However, detection of both strains were limited when $100{\mu}{\ell}$ of cultured samples were mixed with $100m{\ell}$ of beer sample in arbitrary manner. The sensitivity of the assay still needs to be improved for direct detection of the small amounts of bacteria present in beer.

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Comparative Analysis of the Multiple Test Methods for the Detection of Pandemic Influenza A/H1N1 2009 Virus

  • Choi, Young-Jin;Nam, Hae-Seon;Park, Joon-Soo;Kim, Hwi-Jun;Park, Kyung-Bae;Jeon, Min-Hyok;Kim, Chang-Jin;HwangBo, Young;Park, Kwi-Sung;Baek, Kyoung-Ah
    • Journal of Microbiology and Biotechnology
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    • 제20권10호
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    • pp.1450-1456
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    • 2010
  • Accurate and rapid diagnosis of Pandemic Influenza A/H1N1 2009 virus (H1N1 2009) infection is important for the prevention and control of influenza epidemics and the timely initiation of antiviral treatment. This study was conducted to evaluate the performance of several diagnostic tools for the detection of H1N1 2009. Flocked nasopharyngeal swabs were collected from 254 outpatients of suspected H1N1 2009 during October 2009. This study analyzed the performances of the RealTime Ready Inf A/H1N1 Detection Set (Roche), Influenza A (H1N1) Real-Time Detection Kit (Bionote), Seeplex Influenza A/B OneStep Typing Set [Seeplex Reverse Transcriptase PCR (RT-PCR)], BinaxNow Influenza A & B Test Kit [Binax Rapid Antigen Test (RAT)], and SD BIOLINE Influenza Ag kit (SD RAT). Roche and Bionote real-time RT-PCR showed identical results for the H1N1 2009 hemagglutinin gene. Compared with real-time RT-PCR, the sensitivities and specificities were 83.7% and 100% for Seeplex RT-PCR, 64.5% and 94.7% for Binax RAT, and 69.5% and 100% for SD RAT. The sensitivities of Seeplex RT-PCR, Binax RAT, and SD RAT in patients aged over 21 years were 73.7%, 47.4%, and 57.9%, respectively. The sensitivities of Seeplex RT-PCR, Binax RAT, and SD RAT on the day of initial symptoms were mostly lower (68.8%, 56.3%, and 31.3%, respectively). In conclusion, multiplex RT-PCR and RAT for the detection of H1N1 2009 were significantly less sensitive than real-time RT-PCR. Moreover, a negative RAT may require more sensitive confirmatory assays, because it cannot be ruled out from influenza infection.

면역크로마토그라피 기법을 이용한 Salmonella 속균 신속 검출킷트 개발 (Development of the rapid detection kit for Salmonella spp. using immunochromatographic assay)

  • 정병열;정석찬
    • 대한수의학회지
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    • 제45권2호
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    • pp.191-197
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    • 2005
  • An immunochromatographic (IC) strip for the rapid detection of Salmonella spp. in the enriched sample was developed. Affinity purified Salmonella polyclonal antibody was conjugated with 40 nm colloidal gold particles which were prepared by citrate method in our laboratory. The antigen-antibody-gold complex was captured by Salmonella antibody attached to test line of nitrocellulose membrane during the capillary migration of sample. Specificity of the IC strip was calculated to be 100% (12/12) and sensitivity was 97.6% (41/42) in the test with pure cultured bacteria. Salmonella was artificially inoculated into raw pork macerated with enrichment broth. And then it was 10-fold diluted from $5.2{\times}10^{8}CFU/ml$ to 5.2 CFU/ml. The IC strip could detect $5.2{\times}10^{6}CFU/ml$ before enrichment. However, the lowest limit of detection was 5.2 CFU/ml after overnight incubation. The results indicated that the IC assay was a rapid, economical and simple method with high specificity and sensitivity for the detection of Salmonella spp. without using any equipment.

신속 진단 킷트를 활용한 한우 송아지의 설사증 원인체 검사 (Use of rapid diagnostic kit for the diagnosis of Korean native calf diarrhea)

  • 최창용;정영훈;도윤정;조아라;김성범;강희성;류재규;박진호
    • 한국동물위생학회지
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    • 제40권1호
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    • pp.61-66
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    • 2017
  • Calf diarrhea is a disease experienced by almost all of calves after birth and is one of the representative causes of damage to farmers due to mass mortality and of economic losses to them by inhibiting normal growth. In this study, we conducted quick detection of etiologic agents of diarrhea by using a rapid diagnostic kit to multiply diagnose antigens of five etiologic agents of calf diarrhea (rotavirus, coronavirus, Escherichia coli, Cryptosporidium, Giardia) in Hanwoo (Korean native cattle) calves. When the positive antigen proportion of the calf diarrheal feces for each farm was analyzed, rotavirus, coronavirus, Escherichia coli, Cryptosporidium, and Giardia showed antigen positive rates of 0~67%, 0~20%, 0~60%, 0~20%, and 0~67%, respectively. With regard to the antigen positive rate by age in days after birth, 1-week-old calves showed the antigen positive rate of 20% in rotavirus and 20% in Giardia, and 2-week-old calves showed that of 50% in rotavirus. In addition, 4-week-old calves showed the antigen positive rate of 10% in rotavirus, 10% in coronavirus, 10% in Escherichia coli, and 30% in Giardia, and 8-week-old calves showed the antigen positive rate of 17% in coronavirus, 50% in Escherichia coli, 17% in Cryptosporidium, and 33% in Giardia. Based on the results of this study, the etiologic agents of diarrhea in Hanwoo calves for each farm are widely distributed. Although younger than 2-week-old calves were strongly positive for rotavirus, older than 4-week-old calves were highly positive for Giardia and Escherichia coli. In conclusion, we considered that a rapid diagnostic kit is an effective method for quick detection of etiologic agents and would be helpful for cattle farmers and veterinarians to select appropriate therapeutic method.

PCR Kit와 선택배지를 이용한 계란의 병원성세균 검출 비교 평가 (Comparison of a PCR Kit and a Selective Medium to Detect Pathogenic Bacteria in Eggs)

  • 김동호;윤혜정;송현파;임상용;조민호;조철훈
    • 한국식품저장유통학회지
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    • 제16권6호
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    • pp.965-970
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    • 2009
  • 유통중인 계란의병원성균 오염상태를 시판되는 multiplex polymerase chain reaction (mPCR) kit로 검사한 결과, 총 90개의 검사시료 가운데 한 가지 이상의 미생물이 검출된 계란시료는 30개로, 검사시료의 미생물 오염도는 약 33.3% 수준이었다. 미생물별 검출 빈도는 B. cereus가 17개 시료(18.9%)에서 검출되어 가장 높은 빈도를 보였으며 Y. enterocolitica는 16개(17.8%), L. monocytogenes 15개(16.7%), St. aureus 12개(13.3%), E. coli O157:H7 4개(4.4%)의 검출빈도를 보였다. 한편, 선택배지를 이용한 viable cell count 방법에서는 27개의 시료에서 미생물이 검출되어 검사시료의 미생물 오염도는 약 30.0% 수준이였으며, 미생물별 검출 빈도는 B. cereus가 17개 시료(18.9%)에서 14개(15.6%) 시료로, Y. enterocolitica는 16개(17.8%)에서 12개(13.3%)로, L. monocytogenes는 15개(16.7%)에서 13개(14.4%)로, St. aureus는 12개(13.3%)에서 10개(11.1%)로 감소하였으며, E. coli O157:H7은 두 가지 검출방법간의 차이가 나타나지 않았다. 검출 대상 미생물 9종 가운데 Campylobacter jejuni, Vibrio parahaemolyticus, Salmonella spp., 및 Shigella spp.는 두 방법 모두에서 검출되지 않았다. 이상의 결과에서 살펴본 바와 같이 PCR을 이용한 병원성 미생물의 검출 방법은 viable cell count 방법보다 감도가 높음을 알 수 있었다.