• Journal of Animal Science and Technology
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• 제46권5호
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• pp.729-734
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• 2004

본 연구는 한우의 mtDNA D-loop 영역 염기 변이가 산유량에 미치는 효과를 검증하기 위하여 수행하였다. 젖소의 mtDNA D-loop 영역에서 단일염기의 치환이 20 개의 지역에서 확인되었다. 그중 8, 169, 16042, 16051, 16057, 16093, 16119, 16122, 16209, 16255, 16302 bp 지역에서 높은 빈도의 염기치환이 검출되었다. 16119bp 지역에서는 T가 C로 치환된 빈도가 0 .138로 검출되었으며, 이 위치에서의 염기치환에 의한 산유량 효과는 -1.61 (p<0.1)로 나타났다. 16185bp 지역에서의 염기치환에 의한 산유량 효과는 3.557(p<0.05)로 나타났으며 G가 A로 치환된 빈도는 0.063로 나타났다. 본 연구에서 검출한 한우 다유계통 집단의 mtDNA내 D- loop 영역의 염기서열 변이 빈도와 유량과의 연관성분석 결과 등은 한우 집단의 유전적 변이성 추정과 좀 더 다양한 경제형질과의 관련성 분석으로 다양한 유전적 지표인자 발굴에 도움 될 것이며 이를 통해 분자유전학적 기법을 이용한 한우의 육종 전략을 확립하논데 기초 자료가 되는 것은 물론 우려나라 고유 품종인 한우의 유전자원 보존과 분자육종학적인 연구에 기초 자료로서 유용하게 활용 할 수 있을 것으로 기대된다.

• The Plant Pathology Journal
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• 제35권6호
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• pp.635-643
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• 2019

To detect Xanthomonas arboricola pv. pruni, a loopmediated isothermal amplification (LAMP) detection method were developed. The LAMP assay was designed to test crude plant tissue without pre-extraction, or heating incubation, and without advanced analysis equipment. The LAMP primers were designed by targeting an ABC transporter ATP-binding protein, this primer set was tested using the genomic DNA of Xanthomonas and non-Xanthomonas strains, and a ladder product was generated from the genomic DNA of X. arboricola pv. pruni strain but not from 12 other Xanthomonas species strains and 6 strains of other genera. The LAMP conditions were checked with the healthy leaves of 31 peach varieties, and no reaction was detected using either the peach leaves or the peach DNA as a template. Furthermore, the high diagnostic accuracy of the LAMP method was confirmed with 13 X. arboricola pv. pruni strains isolated from various regions in Korea, with all samples exhibiting a positive reaction in LAMP assays. In particular, the LAMP method successfully detected the pathogen in diseased peach leaves and fruit in the field, and the LAMP conditions were proven to be a reliable diagnostic method for the specific detection and identification of X. arboricola pv. pruni in peach orchards.

• Journal of Animal Science and Technology
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• 제45권6호
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• pp.911-916
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• 2003

돼지 Duroc 품종의 mitochondria DNA D-loop전체 유전자를 증폭하기 위하여 많은 동물에서 고도로 상동성이 높은 tRNA-Pro와 tRNA-Phe 염기서열 일부를 이용하여 oligonucleotide primer를 제작하였다. 그 결과 Duroc 품종의 D-loop 전체 유전자는 1,145 base pairs 였으며, 그 중간위치에 10bp의 Sus Scrofa-specific sequence (TACACGTGCG)가 10개 존재하고 있었다. 돌연변이 검출을 위하여 가장 변이가 심한 지역을 primer 제작하여 345 bp의 DNA 단편을 증폭하였으며, Single Stranded Conformation Polymorphism(SSCP) 분석은 8% polyacrylamide gel에서 200 V, 16시간 전기영동하여 ethidium bromide (EtBr)로 10분간 염색하여 UV image analyzer로 관찰하였다. 그 결과 두 개의 서로 다른 밴드유형을 관찰하였으며, 21개 부위에서 염기서열 변이가 관찰되었다. 이러한 결과는 유전적 다양성 변이를 검출하는데 SSCP 분석이 유용한 도구라고 사료된다.

• The Plant Pathology Journal
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• 제33권2호
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• pp.184-192
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• 2017

Tylenchulus semipenetrans is an important and widespread plant-parasitic nematode of citrus worldwide and can cause citrus slow decline disease leading to significant reduction in tree growth and yield. Rapid and accurate detection of T. semipenetrans in soil is important for the disease forecasting and management. In this study, a loop-mediated isothermal amplification (LAMP) assay was developed to detect T. semipenetrans using DNA extracted from soil. A set of five primers was designed from the internal transcribed spacer region (ITS1) of rDNA, and was highly specific to T. semipenetrans. The LAMP reaction was performed at $63^{\circ}C$ for 60 min. The LAMP product was visualized directly in one reaction tube by adding SYBR Green I. The detection limit of the LAMP assay was $10^{-2}J2/0.5g$ of soil, which was 10 times more sensitive than conventional PCR ($10^{-1}J2/0.5g$ of soil). Examination of 24 field soil samples revealed that the LAMP assay was applicable to a range of soils infested naturally with T. semipenetrans, and the total assay time was less than 2.5 h. These results indicated that the developed LAMP assay is a simple, rapid, sensitive, specific and accurate technique for detection of T. semipenetrans in field soil, and contributes to the effective management of citrus slow decline disease.

• 한국동물위생학회지
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• 제40권1호
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• pp.15-20
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• 2017

A two-tube reverse transcription loop-mediated isothermal amplification (RT-LAMP) assay was designed for the rapid visual detection of the M gene of all subtypes of avian influenza virus (AIV) and the H5 gene of the H5 subtype of highly pathogenic AIV (HPAIV). The reaction carried out in two tubes in a single step at $58^{\circ}C$ for 40 min, and the assay results could be visually detected by using hydroxynaphthol blue dye. Using M or H5 gene-specific primers, the assay successfully detected all subtypes or H5 subtypes of AIVs, including the Korean representative H5N1 and H5N8 HPAIVs. The detection limit of the assay was approximately $10^{2.0}$ $EID_{50}/reaction$ for the M and H5 genes of H5N1 HPAIV, respectively, and was more sensitive than that of previously reported RT-LAMP and comparable to that of real-time RT-PCR. These results suggest that the present RT-LAMP assay, with its high specificity, sensitivity, and simplicity, will be a useful diagnostic tool for surveillance of currently circulating H5 HPAIVs and other subtypes of AIV in bird population, even in under-equipped laboratories.

• Parasites, Hosts and Diseases
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• 제51권2호
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• pp.237-241
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• 2013

Giardia lamblia is recognized as one of the most prevalent parasites in dogs. The present study aimed to establish a loop-mediated isothermal amplification (LAMP) assay for rapid and specific detection of G. lamblia from dogs. The fecal samples were collected and prepared for microscopic analysis, and then the genomic DNA was extracted directly from purified cysts. The concentration of DNA samples of G. lamblia were diluted by 10-fold serially ranging from $10^{-1}$ to $10^{-5}ng/{\mu}l$ for LAMP and PCR assays. The LAMP assay allows the amplification to be finished within 60 min under isothermal conditions of $63^{\circ}C$ by employing 6 oligonucleotide primers designed based on G. lamblia elongation factor 1 alpha ($EF1{\alpha}$) gene sequence. Our tests showed that the specific amplification products were obtained only with G. lamblia, while no amplification products were detected with DNA of other related protozoans. Sensitivity evaluation indicated that the LAMP assay was sensitive 10 times more than PCR. It is concluded that LAMP is a rapid, highly sensitive and specific DNA amplification technique for detection of G. lamblia, which has implications for effective control and prevention of giardiasis.

• Journal of Microbiology and Biotechnology
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• 제23권2호
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• pp.246-250
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• 2013

In this study, a loop-mediated isothermal amplification (LAMP) method to rapidly detect Staphylococcus aureus strains was developed and evaluated by extensively applying a large number of S. aureus isolates from clinical and food samples. Six primers were specially designed for recognizing eight distinct sequences on the species-specific femA gene of S. aureus. The detection limits were 100 fg DNA/tube and $10^4$ CFU/ml. The LAMP assay was applied to 432 S. aureus strains isolated from 118 clinical and 314 food samples. Total detection rates for the LAMP and polymerase chain reaction assays were 98.4% (306/311) and 89.4% (278/311), respectively.

• Journal of Microbiology and Biotechnology
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• 제31권4호
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• pp.501-509
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• 2021

More than half the world's population is thought to be infected with Helicobacter pylori. Although the majority of infected people are asymptomatic, H. pylori infection may cause gastric ulcers and deadly gastric cancer. Owing to the difficulty and invasiveness of current routine culture and diagnostic methods, a highly sensitive and specific noninvasive assay for H. pylori is of interest. This study highlighted the design and performance of a colorimetric magneto loop-mediated isothermal amplification (CM-LAMP) assay to detect H. pylori in spiked saliva samples. LF primers were coated on magnetic nanoparticles by carbodiimide-induced immobilization and functionally used for solid-phase amplification. During the LAMP reaction at 66℃, biotin-tagged FIPs were incorporated into LAMP amplicons. The colorimetric signal developed after the addition of NeutrAvidin horseradish peroxidase conjugate (NA-HRP) and ABTS. None of the tested microorganisms, including closely related bacteria, was shown positive by the CM-LAMP assay except H. pylori isolates. This novel platform was highly specific and 100-fold more sensitive (40 CFU/ml or 0.2 CFU per reaction) than the PCR and conventional LAMP assays for the detection of H. pylori in spiked saliva. Our results demonstrated the feasibility of using this noninvasive molecular diagnostic test to detect H. pylori in saliva samples.

• Journal of Forest and Environmental Science
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• 제28권4호
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• pp.278-281
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• 2012

Comparative sequence analyses were conducted on complete mtDNA sequences from four small mammal species in Korea and revealed the presence of 30 well conserved sequences in various regions of the complete mtDNA sequences. The conserved sequences were found in 9 regions in protein coding genes, 10 regions in tRNA genes, 10 in rRNA genes, one region in replication origin and 2 regions in D loop. They could be used to design primers for amplifying complete mtDNA sequences of small mammals.

• Journal of Animal Science and Technology
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• 제44권2호
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• pp.181-190
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• 2002

본 연구는 한우 mt DNA 염기서열 가운데 $tRNA^{Pro}$와 $tRNA^{Pre}$ 유전자 사이에 위치하고 있는 D-loop 영역의 염기서열을 결정하고 한우의 염기변이 다형성을 분석하기 위하여 mt DNA의 D-loop 영역내 404번부터 15061까지 1142bp 크기의 염기서열 부위를 특이적인 primer를 이용하여 PCR로 증폭하였다. 한우의 mt DNA내 D-loop 영역에서 단일염기의 치환 및 삽입에 의해 총 24개의 polymorphic site가 확인되었다. 한우 mt DNA D-loop 영역 가운데 16042～16122번째에 위치하고 있는 영역의 염기치환율이 다른 염기서열 영역에 비하여 약 50%를 점유하고 있었으며 이들 polymorphic site에서 16055, 16230 및 16260 번의 염기치환은 한우에서만 검출된 새로운 염기변이로 확인되었다. 따라서, 한우 D-loop 영역내 특이적인 염기변이는 모계 및 세포질 DNA marker로서 한우품종을 특정하는데 활용할 수 있는 가능성을 시사하였다. Polymorphic site의 출현빈도는 169번째 염기가 81.3%로 가장 출현율이 높았고 다음으로 16302번과 16093번째는 56.3% 그리고 16042번와 16119번째 염기가 각각 50.0%와 43.8%의 치환율을 보였으며 나머지 14개 염기는 6.3%에서 25.0% 수준의 출현율을 나타냈다. 한우와 타 품종간의 유전적 근연관계를 추정한 결과 Bos taurus 계통의 유럽종과 유전적 유사도가 높은 것으로 추정되었고, Africa와 India의 Bos indicus 계통의 품종과는 상대적으로 근연관계가 먼 것으로 나타났다. 본 연구에서 검출한 mt DNA내 D-loop 영역의 염기서열 다형성은 한우집단의 유전적 변이성 추정과 모계유전 분석 및 나아가 경제적으로 중요한 형질들과의 연관성 분석에 유용하게 활용할 수 있을 것으로 기대된다.