• 제목/요약/키워드: drug-resistant mutants

검색결과 21건 처리시간 0.023초

Understanding Rifampicin Resistance in Tuberculosis through a Computational Approach

  • Kumar, Satish;Jena, Lingaraja
    • Genomics & Informatics
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    • 제12권4호
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    • pp.276-282
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    • 2014
  • The disease tuberculosis, caused by Mycobacterium tuberculosis (MTB), remains a major cause of morbidity and mortality in developing countries. The evolution of drug-resistant tuberculosis causes a foremost threat to global health. Most drug-resistant MTB clinical strains are showing resistance to isoniazid and rifampicin (RIF), the frontline anti-tuberculosis drugs. Mutation in rpoB, the beta subunit of DNA-directed RNA polymerase of MTB, is reported to be a major cause of RIF resistance. Amongst mutations in the well-defined 81-base-pair central region of the rpoB gene, mutation at codon 450 (S450L) and 445 (H445Y) is mainly associated with RIF resistance. In this study, we modeled two resistant mutants of rpoB (S450L and H445Y) using Modeller9v10 and performed a docking analysis with RIF using AutoDock4.2 and compared the docking results of these mutants with the wild-type rpoB. The docking results revealed that RIF more effectively inhibited the wild-type rpoB with low binding energy than rpoB mutants. The rpoB mutants interacted with RIF with positive binding energy, revealing the incapableness of RIF inhibition and thus showing resistance. Subsequently, this was verified by molecular dynamics simulations. This in silico evidence may help us understand RIF resistance in rpoB mutant strains.

CTL과 바이러스 변이를 고려한 HIV 모형과 최적 제어를 이용한 약물 투여 전략 (An HIV model with CTL and drug-resistant mutants, and optimal drug scheduling)

  • 이지형;윤태웅
    • 대한전자공학회:학술대회논문집
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    • 대한전자공학회 2009년도 정보 및 제어 심포지움 논문집
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    • pp.135-137
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    • 2009
  • Mathematical models for describing the Human Immunodeficiency Virus(HIV) infection can be devised to better understand how the HIV causes Acquired Immune Deficiency Syndrome(AIDS). The HIV models can then be used to find clues to curing AIDS from a control theoretical point of view. Some models take Cytotoxic T Lymphocytes(CTL) response to HIV infection into account, and others consider mutants against the drugs. However, to the best of our knowledge, there has been no model developed, which describes CTL response and mutant HIV together. Hence we propose a unified model to consider both of these. On the basis of the resulting model, we also present a Model Predictive Control(MPC) scheme to find an optimal treatment strategy. The optimization is performed under the assumption that the Structured Treatment Interruption(STI) policy is employed.

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표고버섯의 영양요구성 및 약물내성주의 분리 (Isolation of auxotrophs and drug resistant mutants of Lentinus edodes)

  • 김채균;심미자;최응칠;김병각
    • 한국균학회지
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    • 제24권2호통권77호
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    • pp.135-141
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    • 1996
  • 맛과 향이 탁월하며 항암작용을 지닌 표고버섯 Lentinus edodes의 균사체 균질액에 자외선을 조사하여 돌연변이주를 유도, 선발하였다. 자외선 조사시 생존율은 3분 조사시 2.45%, 10분 조사시 0.024%이었다. 자외선 조사에 의한 돌연변이주 선발율은 0.40%이며, ethidium bromide (EtBr) 농화 법에 의해 glycerol 함유 배지에서 자라지 못하는 균주 34종을 선발하였다. 독립영양형으로 되돌아가는 비율은 $4.81{\times}10^{-4}{\sim}8.46{\times}10^{-4}$이었다. 돌연변이 주의 영양요구성을 검정하여 다양한 amino acid, nucleic acid, vitamin 요구성 균주를 선발하였다. 항진균성 약물의 MIC는 cycloheximide 2.0 ug/ml, p-fluorophenylalanine 1000 ug/ml, benomyl 2000 ug/ml이었다. p-fluorophenylalanine 1000 ug/ml에 내성 균주 5종과 benomyl 1000 ug/ml에 내성인 균주 8종을 선발하였다.

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A Forward Genetic Approach for Analyzing the Mechanism of Resistance to the Anti-Cancer Drug, 5-Fluorouracil, Using Caenorhabditis elegans

  • Kim, Seongseop;Shim, Jaegal
    • Molecules and Cells
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    • 제25권1호
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    • pp.119-123
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    • 2008
  • Pyrimidine antagonists including 5-Fluorouracil (5-FU) have been used in chemotherapy for cancer patients for over 40 years. 5-FU, especially, is a mainstay treatment for colorectal cancer. It is a pro-drug that is converted to the active drug via the nucleic acid biosynthetic pathway. The metabolites of 5-FU inhibit normal RNA and DNA function, and induce apoptosis of cancer cells. One of the major obstacles to successful chemotherapy is the resistance of cancer cells to anti-cancer drugs. Therefore, it is important to elucidate resistance mechanisms to improve the efficacy of chemotherapy. We have used C. elegans as a model system to investigate the mechanism of resistance to 5-FU, which induces germ cell death and inhibits larval development in C. elegans. We screened 5-FU resistant mutants no longer arrested as larvae by 5-FU. We obtained 18 mutants out of 72,000 F1 individuals screened, and mapped them into three complementation groups. We propose that C. elegans could be a useful model system for studying mechanisms of resistance to anti-cancer drugs.

Characterization of Muations in DNA Gyrase and Topoisomerase IV Involved in Resistant Mutants to DW-286a, a Novel Quinolone Antibiotic, in Streptococcus pneumoniae

  • Seol, Min-Jeong;Kim, Hyun-Joo;Park, Hee-Soo;Kwak, Jin-Hwan
    • 대한약학회:학술대회논문집
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    • 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2-2
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    • pp.70.2-71
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    • 2003
  • Quinolone resistance in Streptococcus pneumoniae is related to mutations in the DNA gyrase and topoisomerase IV genes. DW-286a displayed potent activity against S. pneumoniae C9211 (MIC, 0.015 ${\mu}$g/ml) compared with gemifloxacin (MIC, 0.06 ${\mu}$g/ml). This study was performed to analyze the ability of DW-286a to cause resistance development in S. pneumoniae and to establish whether DNA gyrase or topoisomerase IV is primary target. DW-286a resistant mutants of S. pneumoniae C9211 were generated by stepwise selection at increasing drug concentration. (omitted)

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Comparative Phenotypic Analysis of Anabaena sp. PCC 7120 Mutants of Porin-like Genes

  • Schatzle, Hannah;Brouwer, Eva-Maria;Liebhart, Elisa;Stevanovic, Mara;Schleiff, Enrico
    • Journal of Microbiology and Biotechnology
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    • 제31권5호
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    • pp.645-658
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    • 2021
  • Porins are essential for the viability of Gram-negative bacteria. They ensure the uptake of nutrients, can be involved in the maintenance of outer membrane integrity and define the antibiotic or drug resistance of organisms. The function and structure of porins in proteobacteria is well described, while their function in photoautotrophic cyanobacteria has not been systematically explored. We compared the domain architecture of nine putative porins in the filamentous cyanobacterium Anabaena sp. PCC 7120 and analyzed the seven candidates with predicted OprB-domain. Single recombinant mutants of the seven genes were created and their growth capacity under different conditions was analyzed. Most of the putative porins seem to be involved in the transport of salt and copper, as respective mutants were resistant to elevated concentrations of these substances. In turn, only the mutant of alr2231 was less sensitive to elevated zinc concentrations, while mutants of alr0834, alr4741 and all4499 were resistant to high manganese concentrations. Notably the mutant of alr4550 shows a high sensitivity against harmful compounds, which is indicative for a function related to the maintenance of outer membrane integrity. Moreover, the mutant of all5191 exhibited a phenotype which suggests either a higher nitrate demand or an inefficient nitrogen fixation. The dependency of porin membrane insertion on Omp85 proteins was tested exemplarily for Alr4550, and an enhanced aggregation of Alr4550 was observed in two omp85 mutants. The comparative analysis of porin mutants suggests that the proteins in parts perform distinct functions related to envelope integrity and solute uptake.

Mycobacterium smegmatis를 이용한 Viomycin의 내성 및 작용 기전에 관한 연구 (Studies on the Mechanism of Resistance to and Mode of Action of Viomycin in Mycobacterium smegmatis)

  • 최응칠
    • 약학회지
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    • 제24권1호
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    • pp.1-10
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    • 1980
  • Viomycin inhibited polypeptide biosynthesis, initiation complex formation and translocation of peptidyl-tRNA on ribosomes derived from a sensitive strain of Mycobacterium smegmatis (R-15), but not significantly on ribosomes from viomycin-resistant mutants(R-31 and R-43). The inhibition of translocation was stronger than that of initiation complex formation in the sensitive strain. The binding of [$^{14}C$] tuberactinomycin O, a viomycin analog, to ribosomal particles was studied by Millipore filter method. The sensitive ribosome exhibited higher affinity for the antibiotic than the resistant ribosomes. The resistance was localized on the large ribosomal subunit in a mutant(R-31), and on the small subunit in another mutant(R-43). The binding of the drug to the sensitive ribosomal subunit was markedly reduced by combination with the resistant pair subunit, and the entire ribosome became resistant to the antibiotic.

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Mycobacterium bovis 균주들이 nitroimidazopyran 항생제에 내성을 갖게 해주는 PPE 유전자들의 돌연변이들 (Mutations in the PPE Genes that Confer Resistance to a Nitroimidazopyran Drug on Mycobacterium bovis Strains)

  • 배영민
    • 생명과학회지
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    • 제15권2호
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    • pp.182-185
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    • 2005
  • IS1096 transposon을 사용하여 결핵균군에 작용하는 항생제인 PA-824에 내성을 나타내는 Mycobacterium bovis BCG의 돌연변이 균주를 얻고자 하였고, 그 결과 24종류의 서로 다른 돌연변이 균주를 얻을 수 있었다. Transposon이 insertion된 부위를 알아내기 위해서 각각의 돌연변이 균주로 inverse PCR을 수행하였고, PPE 유전자를 포함한 여러 가지 부위에 insertion된 transposon의 위치를 확인할 수 있었다. PPE 유전자에 insertion돌연변이가 발생한 5개 균주의 세포 추출물을 HPLC로 분석한 결과, 3개에서는 야생균주에서 관찰되는 coenzyme $F^{420}$이 존재하지 않았고, 그 생합성 경로의 중간산물인 F0만 존재하였다. 또한 나머지 2개에서는 F0 또는 $F^{420}$어느 것도 존재하지 않았다. 이 결과는 PPE 유전자들의 산물들이 coenzyme $F^{420}$에 어떤 식으로든 관여하고 있음을 나타낸다고 할 수 있다.

Genetic characteristics of Phytophthora capsici mutants induced by dimethomorph

  • Nam Moon;Lee, Kyoung-Mi;Jang, Kuang-Il;Jeong young Song;Kim, Hong-Gi
    • 한국식물병리학회:학술대회논문집
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    • 한국식물병리학회 2003년도 정기총회 및 추계학술발표회
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    • pp.117.1-117
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    • 2003
  • Phytophthora blight, caused by P. capsici, is very important disease of pepper. Many fungicides to control of Phytophthora blight have been developed, but most of fungicides disappeared in short periods. Nowadays dimethomorph was known as one of the most effective to control of this disease. P. capsici isolates from pepper fields were collected and surveyed their growth in dimethomorph amended V8 medium in order to evaluate their fungicides resistance. The fungicide resistant isolates were not founded among them. Most of the sensitive isolates were inhibited perfectly in V8 medium amended with 10ppm dimethomorph. Mutants of P. capsici by dimethomorph, was grown very well in 250ppm. The difference of pathogenicity, colony morphology, drug response, RT-PCR results was identified between sensitive and resistance isolates. This study should be provided a basic information about the occurrence of dimethomorph resistant isolates and genetic changes in P. capsici population.

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AIDS환자 치료를 위한 NvBAT 치료기법: RTI에 대한 PI의 우수성 (NvBAT Treatment for AIDS Patients: The Superiority of PI Over RTI)

  • 조남훈
    • 전기학회논문지
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    • 제56권10호
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    • pp.1836-1843
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    • 2007
  • In this paper, we study the NvBAT treatment for AIDS patients that is combined with PI rather than RTI, while the Previous results have been focused on the NvBAT in conjuction with RTI. To this end, we obtain a bifurcation diagram which shows a change in the equilibrium points, and in their stability properties as the PI drug effect is varied. Based on the bifurcation diagram, we show that the NvBAT can be combined with drug PI for the treatment of AIDS patients. Various computer simulation results are included, which show the superiority of the NvBAT with PI over that with RTI. Accordition to simulation result, the NvBAT combined with PI is able to keep virus load level lower than that combined with RTI, which is crucial to avoid the emergence of drug-resistant mutants. Moreover, it is shown that, for some AIDS patients, NvBAT with RTI cannot make patients into long term non-progressor, while NvBAT with PI can.