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Image Search Results
Journal: Journal of Clinical Microbiology
Article Title: MGIT Enriched Shotgun Metagenomics for Routine Identification of Nontuberculous Mycobacteria: a Route to Personalized Health Care
doi: 10.1128/jcm.01318-22
Figure Lengend Snippet: M. avium complex phylogeny and M. avium in more detail. The phylogeny illustrates that the NGS-WG typing is perfectly able to identify the species of MAC. However, it has some trouble in determining the M. avium subspecies. This is mainly because the phylogeny shows multiple small subclusters of M. avium . fastBAPS cluster 3 (on level 2) shows distinct Mycobacterium avium subsp. paratuberculosis cluster. fastBAPS cluster 4 (on level 2) shows a distinct M. avium 104-like cluster. CF, cystic fibrosis; TB, tuberculosis; QC, quality control; nod/bronch, nodule/bronchiole; HIV, human immunodeficiency viruses.
Article Snippet: Stored
Techniques: Control
Journal: Journal of Clinical Microbiology
Article Title: MGIT Enriched Shotgun Metagenomics for Routine Identification of Nontuberculous Mycobacteria: a Route to Personalized Health Care
doi: 10.1128/jcm.01318-22
Figure Lengend Snippet: Flowchart of routine use of MGIT enriched shotgun metagenomics for identification of nontuberculous mycobacteria. All the steps are shown in the flowchart and projected onto our weekly planning. As this workflow is repeated weekly. the maximum time from positive MGIT to DNA isolation is 7 days, meaning the TAT is 4 to 11 days. Icons are obtained from flaticon and are free to use.
Article Snippet: Stored
Techniques: DNA Extraction
Journal: Current HIV/AIDS reports
Article Title: The Impact of Treatment as Prevention on the HIV Epidemic in British Columbia, Canada
doi: 10.1007/s11904-020-00482-6
Figure Lengend Snippet: List of AIDS-defining illnesses used in this study
Article Snippet:
Techniques: Infection
Journal: BMC Microbiology
Article Title: Detection of clinically important non tuberculous mycobacteria (NTM) from pulmonary samples through one-step multiplex PCR assay
doi: 10.1186/s12866-020-01952-y
Figure Lengend Snippet: Amplified PCR product. Image showing genus specific ( 16S rRNA) bands M: Marker 100 bp; Lane1; Mycobacterium tuberculosis (H37Rv), Lane 2; Mycobacterium fortuitum ; Lane 3, 4, 5 & 6: clinically confirmed MTBC; NC: negative control
Article Snippet: Hu C, et al. , [ ] observed five different species of NTM causing pulmonary disease with the help of
Techniques: Amplification, Marker, Negative Control
Journal: BMC Microbiology
Article Title: Detection of clinically important non tuberculous mycobacteria (NTM) from pulmonary samples through one-step multiplex PCR assay
doi: 10.1186/s12866-020-01952-y
Figure Lengend Snippet: Oligonucleotide used as primer for amplification
Article Snippet: Hu C, et al. , [ ] observed five different species of NTM causing pulmonary disease with the help of
Techniques:
Journal: Heliyon
Article Title: Facile green synthesis of silver nanoparticles derived from the medicinal plant Clerodendrum serratum and its biological activity against Mycobacterium species
doi: 10.1016/j.heliyon.2024.e31116
Figure Lengend Snippet: (a) The figure shows the zone of inhibition of PEG-AgNPs, AgNPs, PLE, and AgNO 3 with Linezolid taken as a standard drug against the three Mycobacterium species i.e., (1) M. smegmatis (2) M. fortuitum, and (3) M. marinum. (b) Hemolytic activity of PEG-AgNPs (100 μg/mL), AgNPs (100 μg/mL), PLE (500 mg/mL), Linezolid (100 μg/mL), AgNO 3 (1 mM), and Triton X-100 (0.5 % v/v) on human blood agar. Triton X-100 and Linezolid were taken as positive control. (c) Flow cytometric analysis to determine the membrane damage of (1) M. smegmatis (2) M. fortuitum, and (3) M. marinum . (i–x) PI staining of all three Mycobacterium species (i) control without PI treatment, (ii) control with PI treatment, (iii) Linezolid, (iv) PEG-AgNPs (1X), (v) PEG-AgNPs (2X), (vi) Plant leaves extract, (vii) AgNPs (1X), (viii) AgNPs (2X), (ix) AgNO 3 , and (x) Triton X-100. Linezolid and Triton X-100 were taken as positive controls. In each quadrant, Q 1 and Q 3 depict the percentage of live cells whereas Q 2 and Q 4 depict the percentage of dead cells. (d) Bar diagram representing the percentage of dead cells of Mycobacterium species treated with test compounds.
Article Snippet: The chemicals used for the culture of
Techniques: Inhibition, Activity Assay, Positive Control, Membrane, Staining
Journal: Heliyon
Article Title: Facile green synthesis of silver nanoparticles derived from the medicinal plant Clerodendrum serratum and its biological activity against Mycobacterium species
doi: 10.1016/j.heliyon.2024.e31116
Figure Lengend Snippet: Zone of inhibition and the MIC values of PEG-AgNPs, AgNPs, and PLE against Mycobacterium species.
Article Snippet: The chemicals used for the culture of
Techniques: Inhibition, Concentration Assay
Journal: Heliyon
Article Title: Facile green synthesis of silver nanoparticles derived from the medicinal plant Clerodendrum serratum and its biological activity against Mycobacterium species
doi: 10.1016/j.heliyon.2024.e31116
Figure Lengend Snippet: Topographic statistics of biofilm surfaces analyzed through AFM.
Article Snippet: The chemicals used for the culture of
Techniques: