Whole genome sequencing and prediction of antimicrobial susceptibilities in non-tuberculous mycobacteria
Non-tuberculous mycobacteria (NTM) are opportunistic pathogens commonly causing chronic, pulmonary disease which is notoriously hard to treat. Current treatment for NTM infections involves at least three active drugs (including one macrolide: clarithromycin or azithromycin) over 12 months or longer....
Saved in:
Published in | Frontiers in microbiology Vol. 13; p. 1044515 |
---|---|
Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media S.A
29.11.2022
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Non-tuberculous mycobacteria (NTM) are opportunistic pathogens commonly causing chronic, pulmonary disease which is notoriously hard to treat. Current treatment for NTM infections involves at least three active drugs (including one macrolide: clarithromycin or azithromycin) over 12 months or longer. At present there are limited phenotypic
in vitro
drug susceptibility testing options for NTM which are standardised globally. As seen with tuberculosis, whole genome sequencing has the potential to transform drug susceptibility testing in NTM, by utilising a genotypic approach. The Comprehensive Resistance Prediction for Tuberculosis is a database used to predict
Mycobacterium tuberculosis
resistance: at present there are no similar databases available to accurately predict NTM resistance. Recent studies have shown concordance between phenotypic and genotypic NTM resistance results. To benefit from the advantages of whole genome sequencing, further advances in resistance prediction need to take place, as well as there being better information on novel drug mutations and an understanding of the impact of whole genome sequencing on NTM treatment outcomes. |
---|---|
AbstractList | Non-tuberculous mycobacteria (NTM) are opportunistic pathogens commonly causing chronic, pulmonary disease which is notoriously hard to treat. Current treatment for NTM infections involves at least three active drugs (including one macrolide: clarithromycin or azithromycin) over 12 months or longer. At present there are limited phenotypic in vitro drug susceptibility testing options for NTM which are standardised globally. As seen with tuberculosis, whole genome sequencing has the potential to transform drug susceptibility testing in NTM, by utilising a genotypic approach. The Comprehensive Resistance Prediction for Tuberculosis is a database used to predict Mycobacterium tuberculosis resistance: at present there are no similar databases available to accurately predict NTM resistance. Recent studies have shown concordance between phenotypic and genotypic NTM resistance results. To benefit from the advantages of whole genome sequencing, further advances in resistance prediction need to take place, as well as there being better information on novel drug mutations and an understanding of the impact of whole genome sequencing on NTM treatment outcomes.Non-tuberculous mycobacteria (NTM) are opportunistic pathogens commonly causing chronic, pulmonary disease which is notoriously hard to treat. Current treatment for NTM infections involves at least three active drugs (including one macrolide: clarithromycin or azithromycin) over 12 months or longer. At present there are limited phenotypic in vitro drug susceptibility testing options for NTM which are standardised globally. As seen with tuberculosis, whole genome sequencing has the potential to transform drug susceptibility testing in NTM, by utilising a genotypic approach. The Comprehensive Resistance Prediction for Tuberculosis is a database used to predict Mycobacterium tuberculosis resistance: at present there are no similar databases available to accurately predict NTM resistance. Recent studies have shown concordance between phenotypic and genotypic NTM resistance results. To benefit from the advantages of whole genome sequencing, further advances in resistance prediction need to take place, as well as there being better information on novel drug mutations and an understanding of the impact of whole genome sequencing on NTM treatment outcomes. Non-tuberculous mycobacteria (NTM) are opportunistic pathogens commonly causing chronic, pulmonary disease which is notoriously hard to treat. Current treatment for NTM infections involves at least three active drugs (including one macrolide: clarithromycin or azithromycin) over 12 months or longer. At present there are limited phenotypic drug susceptibility testing options for NTM which are standardised globally. As seen with tuberculosis, whole genome sequencing has the potential to transform drug susceptibility testing in NTM, by utilising a genotypic approach. The Comprehensive Resistance Prediction for Tuberculosis is a database used to predict resistance: at present there are no similar databases available to accurately predict NTM resistance. Recent studies have shown concordance between phenotypic and genotypic NTM resistance results. To benefit from the advantages of whole genome sequencing, further advances in resistance prediction need to take place, as well as there being better information on novel drug mutations and an understanding of the impact of whole genome sequencing on NTM treatment outcomes. Non-tuberculous mycobacteria (NTM) are opportunistic pathogens commonly causing chronic, pulmonary disease which is notoriously hard to treat. Current treatment for NTM infections involves at least three active drugs (including one macrolide: clarithromycin or azithromycin) over 12 months or longer. At present there are limited phenotypic in vitro drug susceptibility testing options for NTM which are standardised globally. As seen with tuberculosis, whole genome sequencing has the potential to transform drug susceptibility testing in NTM, by utilising a genotypic approach. The Comprehensive Resistance Prediction for Tuberculosis is a database used to predict Mycobacterium tuberculosis resistance: at present there are no similar databases available to accurately predict NTM resistance. Recent studies have shown concordance between phenotypic and genotypic NTM resistance results. To benefit from the advantages of whole genome sequencing, further advances in resistance prediction need to take place, as well as there being better information on novel drug mutations and an understanding of the impact of whole genome sequencing on NTM treatment outcomes. Non-tuberculous mycobacteria (NTM) are opportunistic pathogens commonly causing chronic, pulmonary disease which is notoriously hard to treat. Current treatment for NTM infections involves at least three active drugs (including one macrolide: clarithromycin or azithromycin) over 12 months or longer. At present there are limited phenotypic in vitro drug susceptibility testing options for NTM which are standardised globally. As seen with tuberculosis, whole genome sequencing has the potential to transform drug susceptibility testing in NTM, by utilising a genotypic approach. The Comprehensive Resistance Prediction for Tuberculosis is a database used to predict Mycobacterium tuberculosis resistance: at present there are no similar databases available to accurately predict NTM resistance. Recent studies have shown concordance between phenotypic and genotypic NTM resistance results. To benefit from the advantages of whole genome sequencing, further advances in resistance prediction need to take place, as well as there being better information on novel drug mutations and an understanding of the impact of whole genome sequencing on NTM treatment outcomes. |
Author | Solanki, Priya Satta, Giovanni McHugh, Timothy D. Lipman, Marc |
AuthorAffiliation | 1 UCL-TB and UCL Centre for Clinical Microbiology, University College London , London , United Kingdom 2 UCL-TB and UCL Respiratory, University College London , London , United Kingdom 3 Royal Free London NHS Foundation Trust , London , United Kingdom |
AuthorAffiliation_xml | – name: 2 UCL-TB and UCL Respiratory, University College London , London , United Kingdom – name: 3 Royal Free London NHS Foundation Trust , London , United Kingdom – name: 1 UCL-TB and UCL Centre for Clinical Microbiology, University College London , London , United Kingdom |
Author_xml | – sequence: 1 givenname: Priya surname: Solanki fullname: Solanki, Priya – sequence: 2 givenname: Marc surname: Lipman fullname: Lipman, Marc – sequence: 3 givenname: Timothy D. surname: McHugh fullname: McHugh, Timothy D. – sequence: 4 givenname: Giovanni surname: Satta fullname: Satta, Giovanni |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/36523832$$D View this record in MEDLINE/PubMed |
BookMark | eNp9Uk1vVCEUJabG1to_4MK8pZs38vGANxsT02jbpIkbje4IXHgzNDwYgWfSfy_TmZrWhSyAXO45h9xzXqOTmKJD6C3BK8bG9Ydp9mBWFFO6IngYOOEv0BkRYugZpj9PntxP0UUpd7itAdO2v0KnTHDKRkbP0PbHNgXXbVxMs-uK-7W4CD5uOh1tt8vOeqg-xS5NrVJ9E83JeB26shRwu-qND756Vzofu_bFvi7GZVhCWko330MyGqrLXr9BLycdirs4nufo-5fP3y6v-9uvVzeXn257GMRY-1FyOZo1cAlEgwBm7WQHYsnIrBETMwZLy6jDVltqqMYMyARmGtYgGKGGnaObA69N-k7tsp91vldJe_VQSHmjdK4eglMYiOXCjcRKPgjguglSMJiAdHRk68b18cC1W8zsLLhYsw7PSJ-_RL9Vm_RbrWUzhPJG8P5IkFObbKlq9m1sIejo2oAUlZxzKQkVrfXdU62_Io9WtYbx0NAcKCW7SYGvem9Ok_ZBEaz2wVAPwVD7YKhjMBqU_gN9ZP8P6A-uQMCG |
CitedBy_id | crossref_primary_10_1016_j_clinme_2024_100017 crossref_primary_10_1016_j_cll_2024_10_002 crossref_primary_10_1080_14737159_2024_2362165 |
Cites_doi | 10.3389/fimmu.2020.00303 10.3390/biology10020096 10.1128/JCM.00834-19 10.1016/j.jmoldx.2021.07.023 10.1016/j.jfma.2020.05.002 10.1093/nar/gkz935 10.1128/AAC.39.12.2625 10.1093/jac/dkr209 10.1016/s0732-8893(98)00013-3 10.3390/microorganisms9112237 10.1128/AAC.38.2.381 10.1016/S2213-2600(15)00466-X 10.1093/jac/dky526 10.1093/nar/gkz943 10.3389/fmed.2017.00027 10.1074/jbc.M113.538959 10.1128/AAC.45.1.1-12.2001 10.3390/pathogens9080641 10.1128/AAC.42.5.1295 10.1128/AAC.01000-19 10.1093/jac/dkx476 10.1016/s1473-3099(21)00586-7 10.1128/AAC.02440-16 10.1038/s41598-020-57844-8 10.3389/fmicb.2019.01977 10.1007/s13318-021-00687-z 10.1093/cid/cix517 10.1016/j.ijid.2021.03.033 10.1086/515328 10.1371/journal.pone.0140166 10.1183/13993003.01483-2019 10.1186/s12879-022-07329-y 10.1093/bioinformatics/btab681 10.1586/14787210.2013.830413 10.3390/antibiotics10121515 10.1016/j.drudis.2018.04.001 10.1128/AAC.02615-15 10.3389/fcimb.2021.659997 10.4103/ijmr.IJMR_902_20 10.1371/journal.pone.0239146 10.1128/JCM.02087-16 10.1016/S2666-5247(20)30031-8 10.1038/s41579-020-0331-1 10.1128/AAC.40.7.1676 10.1136/bmjresp-2020-000591 10.1007/s10096-018-3315-6 10.1016/j.cmi.2017.10.030 10.1016/S2666-5247(21)00128-2 10.1164/rccm.200604-571ST 10.1128/AAC.01704-21 10.1093/cid/ciab796 10.1038/s41598-018-37350-8 10.1128/AAC.00943-16 10.1046/j.1365-2958.1997.5811946.x 10.1093/jac/dkt410 10.1038/s41380-021-01418-1 10.1093/cid/ciaa241 10.1016/j.jfma.2020.05.028 10.3389/fmicb.2022.775030 10.1038/sdata.2016.18 10.3390/ijms20235868 |
ContentType | Journal Article |
Copyright | Copyright © 2022 Solanki, Lipman, McHugh and Satta. Copyright © 2022 Solanki, Lipman, McHugh and Satta. 2022 Solanki, Lipman, McHugh and Satta |
Copyright_xml | – notice: Copyright © 2022 Solanki, Lipman, McHugh and Satta. – notice: Copyright © 2022 Solanki, Lipman, McHugh and Satta. 2022 Solanki, Lipman, McHugh and Satta |
DBID | AAYXX CITATION NPM 7X8 5PM DOA |
DOI | 10.3389/fmicb.2022.1044515 |
DatabaseName | CrossRef PubMed MEDLINE - Academic PubMed Central (Full Participant titles) DOAJ Directory of Open Access Journals |
DatabaseTitle | CrossRef PubMed MEDLINE - Academic |
DatabaseTitleList | MEDLINE - Academic PubMed CrossRef |
Database_xml | – sequence: 1 dbid: DOA name: DOAJ Directory of Open Access Journals url: https://www.doaj.org/ sourceTypes: Open Website – sequence: 2 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Biology |
EISSN | 1664-302X |
ExternalDocumentID | oai_doaj_org_article_0c1d56e81d7546c5aac62cb01c7e2839 PMC9745125 36523832 10_3389_fmicb_2022_1044515 |
Genre | Journal Article Review |
GrantInformation_xml | – fundername: Medical Research Council grantid: MR/T023686/1 – fundername: Medical Research Council grantid: MR/T023686/2 |
GroupedDBID | 53G 5VS 9T4 AAFWJ AAKDD AAYXX ACGFO ACGFS ACXDI ADBBV ADRAZ AENEX AFPKN ALMA_UNASSIGNED_HOLDINGS AOIJS BAWUL BCNDV CITATION DIK ECGQY GROUPED_DOAJ GX1 HYE KQ8 M48 M~E O5R O5S OK1 PGMZT RNS RPM IPNFZ NPM RIG 7X8 5PM |
ID | FETCH-LOGICAL-c468t-87578b9c57c1ac6c3ddfd41d183db6f3bb07d32e0dad2b2a03c1fcbf49c6312b3 |
IEDL.DBID | M48 |
ISSN | 1664-302X |
IngestDate | Wed Aug 27 01:15:59 EDT 2025 Thu Aug 21 18:39:26 EDT 2025 Fri Jul 11 13:32:43 EDT 2025 Sat May 31 02:11:02 EDT 2025 Tue Jul 01 00:57:53 EDT 2025 Thu Apr 24 23:01:20 EDT 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Keywords | Mycobacterium non-tuberculous mycobacteria mutations resistance sequencing |
Language | English |
License | Copyright © 2022 Solanki, Lipman, McHugh and Satta. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c468t-87578b9c57c1ac6c3ddfd41d183db6f3bb07d32e0dad2b2a03c1fcbf49c6312b3 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 ObjectType-Review-3 content type line 23 This article was submitted to Infectious Agents and Disease, a section of the journal Frontiers in Microbiology Edited by: Abdolrazagh Hashemi Shahraki, University of Florida, United States Reviewed by: Daria Bottai, University of Pisa, Italy; Abu Sayed Chowdhury, National Marrow Donor Program, United States |
OpenAccessLink | https://doaj.org/article/0c1d56e81d7546c5aac62cb01c7e2839 |
PMID | 36523832 |
PQID | 2755577126 |
PQPubID | 23479 |
ParticipantIDs | doaj_primary_oai_doaj_org_article_0c1d56e81d7546c5aac62cb01c7e2839 pubmedcentral_primary_oai_pubmedcentral_nih_gov_9745125 proquest_miscellaneous_2755577126 pubmed_primary_36523832 crossref_citationtrail_10_3389_fmicb_2022_1044515 crossref_primary_10_3389_fmicb_2022_1044515 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2022-11-29 |
PublicationDateYYYYMMDD | 2022-11-29 |
PublicationDate_xml | – month: 11 year: 2022 text: 2022-11-29 day: 29 |
PublicationDecade | 2020 |
PublicationPlace | Switzerland |
PublicationPlace_xml | – name: Switzerland |
PublicationTitle | Frontiers in microbiology |
PublicationTitleAlternate | Front Microbiol |
PublicationYear | 2022 |
Publisher | Frontiers Media S.A |
Publisher_xml | – name: Frontiers Media S.A |
References | Nimmo (B36) 2020; 1 Dohál (B14) 2021; 9 Liu (B28) 2022; 27 Ratnatunga (B44) 2020; 11 Alexander (B3) 2017; 55 Axson (B4) 2018; 37 Satta (B51) 2018; 24 Wallace (B60) 1996; 40 Lange (B24) 2022; 22 Vester (B58) 2001; 45 (B56) 2022 de Carvalho (B12) 2018; 73 Wu (B64) 2018; 23 Chen (B8) 2019; 10 Lam (B23) 2021; 113 Gutiérrez (B18) 2019; 63 Victoria (B59) 2021; 11 Huang (B19) 2020; 119 van Ingen (B57) 2013; 11 Davis (B11) 2020; 48 Daley (B10) 2020; 71 Ren (B46) 2022; 38 Burman (B7) 1998; 31 Dookie (B15) 2022; 13 Nicklas (B35) 2022; 66 Degiacomi (B13) 2019; 20 Kekre (B21) 2021; 73 Lipman (B26) 2020; 7 Pankhurst (B39) 2016; 4 Weng (B61) 2020; 119 Wilkinson (B62) 2016; 3 Kwak (B22) 2017; 65 Saxena (B52) 2021; 10 Alangaden (B1) 1998; 42 Lipworth (B27) 2021; 2 Nessar (B34) 2011; 66 Prammananan (B41) 1998; 177 Oren (B38) 2019; 54 Radhakrishnan (B42) 2014; 289 Rampacci (B43) 2020; 9 (B9) 2011 Brown-Elliott (B6) 2019; 57 Schiff (B53) 2019; 9 Bouzinbi (B5) 2020; 15 Ruth (B49) 2019; 74 Sharma (B54) 2020; 152 Nishiuchi (B37) 2017; 4 Realegeno (B45) 2021; 23 Soroka (B55) 2014; 69 Johansen (B20) 2020; 18 Meier (B31) 1994; 38 Park (B40) 2022; 22 (B63) 2018 Mougari (B32) 2017; 61 Rubino (B47) 2021; 46 Sander (B50) 1997; 26 Alcock (B2) 2020; 48 Lopeman (B29) 2020; 27 Nash (B33) 1995; 39 Maitra (B30) 2021; 10 Lefebvre (B25) 2017; 61 Griffith (B17) 2007; 175 Rubio (B48) 2015; 10 Ferro (B16) 2016; 60 |
References_xml | – volume: 11 year: 2020 ident: B44 article-title: The rise of non-tuberculosis mycobacterial lung disease. publication-title: Front. Immunol. doi: 10.3389/fimmu.2020.00303 – volume: 10 start-page: 1 year: 2021 ident: B52 article-title: Drug resistance in nontuberculous mycobacteria: mechanisms and models. publication-title: Biology doi: 10.3390/biology10020096 – volume: 57 year: 2019 ident: B6 article-title: Antimycobacterial susceptibility testing of nontuberculous mycobacteria. publication-title: J. Clin. Microbiol. doi: 10.1128/JCM.00834-19 – volume: 23 start-page: 1460 year: 2021 ident: B45 article-title: Clinical whole genome sequencing for clarithromycin and amikacin resistance prediction and subspecies identification of Mycobacterium abscessus. publication-title: J. Mol. Diagn. doi: 10.1016/j.jmoldx.2021.07.023 – volume: 119 start-page: S32 year: 2020 ident: B19 article-title: Identification and drug susceptibility testing for nontuberculous mycobacteria. publication-title: J. Formos. Med. Assoc. doi: 10.1016/j.jfma.2020.05.002 – volume: 48 start-page: D517 year: 2020 ident: B2 article-title: CARD 2020: antibiotic resistome surveillance with the comprehensive antibiotic resistance database. publication-title: Nucleic Acids Res. doi: 10.1093/nar/gkz935 – volume: 39 start-page: 2625 year: 1995 ident: B33 article-title: Genetic basis of macrolide resistance in Mycobacterium avium isolated from patients with disseminated disease. publication-title: Antimicrob. Agents Chemother. doi: 10.1128/AAC.39.12.2625 – volume: 66 start-page: 1719 year: 2011 ident: B34 article-title: Genetic analysis of new 16s rRNA mutations conferring aminoglycoside resistance in Mycobacterium abscessus. publication-title: J. Antimicrob. Chemother. doi: 10.1093/jac/dkr209 – volume: 31 start-page: 369 year: 1998 ident: B7 article-title: AIDS-related Mycobacterium kansasii infection with initial resistance to clarithromycin. publication-title: Diagn. Microbiol. Infect. Dis. doi: 10.1016/s0732-8893(98)00013-3 – volume: 9 year: 2021 ident: B14 article-title: Whole genome sequencing in the management of non-tuberculous mycobacterial infections. publication-title: Microorganisms doi: 10.3390/microorganisms9112237 – volume: 38 start-page: 381 year: 1994 ident: B31 article-title: Identification of mutations in 23S rRNA gene of clarithromycin-resistant Mycobacterium intracellulare. publication-title: Antimicrob. Agents Chemother. doi: 10.1128/AAC.38.2.381 – volume: 4 start-page: 49 year: 2016 ident: B39 article-title: Rapid, comprehensive, and affordable mycobacterial diagnosis with whole-genome sequencing: a prospective study. publication-title: Lancet Respir. Med. doi: 10.1016/S2213-2600(15)00466-X – volume: 74 start-page: 935 year: 2019 ident: B49 article-title: A bedaquiline/clofazimine combination regimen might add activity to the treatment of clinically relevant non-tuberculous mycobacteria. publication-title: J. Antimicrob. Chemother. doi: 10.1093/jac/dky526 – volume: 48 start-page: D606 year: 2020 ident: B11 article-title: The PATRIC bioinformatics resource center: expanding data and analysis capabilities. publication-title: Nucleic Acids Res. doi: 10.1093/nar/gkz943 – volume: 4 year: 2017 ident: B37 article-title: Infection sources of a common non-tuberculous mycobacterial pathogen, Mycobacterium avium complex. publication-title: Front. Med. doi: 10.3389/fmed.2017.00027 – volume: 289 start-page: 16526 year: 2014 ident: B42 article-title: Crystal structure of the transcriptional regulator Rv0678 of Mycobacterium tuberculosis. publication-title: J. Biol. Chem. doi: 10.1074/jbc.M113.538959 – volume: 45 start-page: 1 year: 2001 ident: B58 article-title: Macrolide resistance conferred by base substitutions in 23S rRNA. publication-title: Antimicrob. Agents Chemother. doi: 10.1128/AAC.45.1.1-12.2001 – year: 2018 ident: B63 publication-title: The use of next-generation sequencing technologies for the detection of mutations associated with drug resistance in Mycobacterium tuberculosis complex: technical guide 2018. – volume: 9 start-page: 1 year: 2020 ident: B43 article-title: Preclinical models of nontuberculous mycobacteria infection for early drug discovery and vaccine research. publication-title: Pathogens doi: 10.3390/pathogens9080641 – year: 2022 ident: B56 publication-title: Comprehensive resistance prediction for tuberculosis: an international consortium (CRyPTIC). – volume: 42 start-page: 1295 year: 1998 ident: B1 article-title: Mechanism of resistance to amikacin and kanamycin in Mycobacterium tuberculosis. publication-title: Antimicrob. Agents Chemother. doi: 10.1128/AAC.42.5.1295 – volume: 63 start-page: e1000 year: 2019 ident: B18 article-title: The TetR family transcription factor MAB_2299c regulates the expression of two distinct MmpS-MmpL efflux pumps involved in cross-resistance to clofazimine and bedaquiline in Mycobacterium abscessus. publication-title: Antimicrob. Agents Chemother. doi: 10.1128/AAC.01000-19 – volume: 73 start-page: 862 year: 2018 ident: B12 article-title: Genetic correlates of clarithromycin susceptibility among isolates of the Mycobacterium abscessus group and the potential clinical applicability of a PCR-based analysis of erm(41). publication-title: J. Antimicrob. Chemother. doi: 10.1093/jac/dkx476 – volume: 22 start-page: e178 year: 2022 ident: B24 article-title: Consensus management recommendations for less common non-tuberculous mycobacterial pulmonary diseases. publication-title: Lancet Infect. Dis. doi: 10.1016/s1473-3099(21)00586-7 – volume: 61 start-page: e2440 year: 2017 ident: B25 article-title: Inhibition of the β-lactamase BlaMab by avibactam improves the in vitro and in vivo efficacy of imipenem against Mycobacterium abscessus. publication-title: Antimicrob. Agents Chemother. doi: 10.1128/AAC.02440-16 – volume: 27 start-page: 1469 year: 2020 ident: B29 article-title: Effect of amoxicillin in combination with imipenem-relebactam against Mycobacterium abscessus. publication-title: Sci. Rep. doi: 10.1038/s41598-020-57844-8 – volume: 10 year: 2019 ident: B8 article-title: Clinical efficacy and adverse effects of antibiotics used to treat Mycobacterium abscessus pulmonary disease. publication-title: Front. Microbiol. doi: 10.3389/fmicb.2019.01977 – volume: 46 start-page: 573 year: 2021 ident: B47 article-title: Correction to: population pharmacokinetic evaluation of amikacin liposome inhalation suspension in patients with treatment-refractory nontuberculous mycobacterial lung disease. publication-title: Eur. J. Drug Metab. Pharmacokinet. doi: 10.1007/s13318-021-00687-z – volume: 65 start-page: 1077 year: 2017 ident: B22 article-title: Treatment outcomes of mycobacterium avium complex lung disease: a systematic review and meta-analysis. publication-title: Clin. Infect. Dis. doi: 10.1093/cid/cix517 – volume: 113 start-page: S48 year: 2021 ident: B23 article-title: Value of routine whole genome sequencing for Mycobacterium tuberculosis drug resistance detection. publication-title: Int. J. Infect. Dis. doi: 10.1016/j.ijid.2021.03.033 – volume: 177 start-page: 1573 year: 1998 ident: B41 article-title: A single 16S ribosomal RNA substitution is responsible for resistance to amikacin and other 2-deoxystreptamine aminoglycosides in Mycobacterium abscessus and Mycobacterium chelonae. publication-title: J. Infect. Dis. doi: 10.1086/515328 – volume: 10 year: 2015 ident: B48 article-title: Inducible and acquired clarithromycin resistance in the Mycobacterium abscessus complex. publication-title: PLoS One doi: 10.1371/journal.pone.0140166 – volume: 54 year: 2019 ident: B38 article-title: On the valid publication of names of mycobacteria. publication-title: Eur. Respir. J. doi: 10.1183/13993003.01483-2019 – volume: 22 year: 2022 ident: B40 article-title: Evaluating the clinical impact of routine whole genome sequencing in tuberculosis treatment decisions and the issue of isoniazid mono-resistance. publication-title: BMC Infect. Dis. doi: 10.1186/s12879-022-07329-y – volume: 38 start-page: 325 year: 2022 ident: B46 article-title: Prediction of antimicrobial resistance based on whole-genome sequencing and machine learning. publication-title: Bioinformatics doi: 10.1093/bioinformatics/btab681 – volume: 11 start-page: 1065 year: 2013 ident: B57 article-title: Drug treatment of pulmonary nontuberculous mycobacterial disease in HIV-negative patients: the evidence. publication-title: Expert Rev. Anti Infective Therapy doi: 10.1586/14787210.2013.830413 – volume: 10 year: 2021 ident: B30 article-title: Improving the drug development pipeline for mycobacteria: modelling antibiotic exposure in the hollow fibre infection model. publication-title: Antibiotics doi: 10.3390/antibiotics10121515 – volume: 23 start-page: 1502 year: 2018 ident: B64 article-title: NTM drug discovery: status, gaps and the way forward. publication-title: Drug Discov. Today doi: 10.1016/j.drudis.2018.04.001 – volume: 60 start-page: 1097 year: 2016 ident: B16 article-title: Clofazimine prevents the regrowth of Mycobacterium abscessus and Mycobacterium avium type strains exposed to Amikacin and clarithromycin. publication-title: Antimicrob. Agents Chemother. doi: 10.1128/AAC.02615-15 – volume: 11 year: 2021 ident: B59 article-title: Mycobacterium abscessus complex: a review of recent developments in an emerging pathogen. publication-title: Front. Cell. Infect. Microbiol. doi: 10.3389/fcimb.2021.659997 – volume: 152 start-page: 185 year: 2020 ident: B54 article-title: Epidemiology, diagnosis & treatment of non-tuberculous mycobacterial diseases. publication-title: Indian J. Med. Res. doi: 10.4103/ijmr.IJMR_902_20 – volume: 15 year: 2020 ident: B5 article-title: Evaluation of the GenoType NTM-DR assay performance for the identification and molecular detection of antibiotic resistance in Mycobacterium abscessus complex. publication-title: PLoS One doi: 10.1371/journal.pone.0239146 – volume: 55 start-page: 574 year: 2017 ident: B3 article-title: Emergence of mmpT5 variants during bedaquiline treatment of mycobacterium intracellulare lung disease. publication-title: J. Clin. Microbiol. doi: 10.1128/JCM.02087-16 – volume: 1 start-page: e165 year: 2020 ident: B36 article-title: Population-level emergence of bedaquiline and clofazimine resistance-associated variants among patients with drug-resistant tuberculosis in southern Africa: a phenotypic and phylogenetic analysis. publication-title: Lancet Microbe doi: 10.1016/S2666-5247(20)30031-8 – volume: 18 start-page: 392 year: 2020 ident: B20 article-title: Non-tuberculous mycobacteria and the rise of Mycobacterium abscessus. publication-title: Nat. Rev. Microbiol. doi: 10.1038/s41579-020-0331-1 – volume: 40 start-page: 1676 year: 1996 ident: B60 article-title: Genetic basis for clarithromycin resistance among isolates of Mycobacterium chelonae and Mycobacterium abscessus. publication-title: Antimicrob. Agents Chemother. doi: 10.1128/AAC.40.7.1676 – volume: 7 year: 2020 ident: B26 article-title: Current and future management of non-tuberculous mycobacterial pulmonary disease (NTM-PD) in the UK. publication-title: BMJ Open Respir. Res. doi: 10.1136/bmjresp-2020-000591 – volume: 37 start-page: 1795 year: 2018 ident: B4 article-title: Nontuberculous mycobacterial disease managed within UK primary care, 2006–2016. publication-title: Eur. J. Clin. Microbiol. Infect. Dis. doi: 10.1007/s10096-018-3315-6 – year: 2011 ident: B9 publication-title: Susceptibility testing of mycobacteria, nocardiae, and other aerobic actinomycetes. Approved standard-second edition. – volume: 24 start-page: 604 year: 2018 ident: B51 article-title: Mycobacterium tuberculosis and whole-genome sequencing: how close are we to unleashing its full potential? publication-title: Clin. Microbiol. Infect. doi: 10.1016/j.cmi.2017.10.030 – volume: 2 start-page: e498 year: 2021 ident: B27 article-title: Epidemiology of Mycobacterium abscessus in England: an observational study. publication-title: Lancet Microbe doi: 10.1016/S2666-5247(21)00128-2 – volume: 175 start-page: 367 year: 2007 ident: B17 article-title: An official ATS/IDSA statement: diagnosis, treatment, and prevention of nontuberculous mycobacterial diseases. publication-title: Am. J. Respir. Crit. Care Med. doi: 10.1164/rccm.200604-571ST – volume: 66 year: 2022 ident: B35 article-title: Potency of omadacycline against Mycobacteroides abscessus clinical isolates in vitro and in a mouse model of pulmonary infection. publication-title: Antimicrob. Agents Chemother. doi: 10.1128/AAC.01704-21 – volume: 73 start-page: S258 year: 2021 ident: B21 article-title: Integrating scalable genome sequencing into microbiology laboratories for routine antimicrobial resistance surveillance. publication-title: Clin. Infect. Dis. doi: 10.1093/cid/ciab796 – volume: 9 year: 2019 ident: B53 article-title: Clinical relevance of non-tuberculous mycobacteria isolated from respiratory specimens: seven year experience in a UK hospital. publication-title: Sci. Rep. doi: 10.1038/s41598-018-37350-8 – volume: 61 start-page: e943 year: 2017 ident: B32 article-title: Selection of resistance to clarithromycin in Mycobacterium abscessus subspecies. publication-title: Antimicrob. Agents Chemother. doi: 10.1128/AAC.00943-16 – volume: 26 start-page: 469 year: 1997 ident: B50 article-title: The role of ribosomal RNAs in macrolide resistance. publication-title: Mol. Microbiol. doi: 10.1046/j.1365-2958.1997.5811946.x – volume: 69 start-page: 691 year: 2014 ident: B55 article-title: Characterization of broad-spectrum Mycobacterium abscessus class A β-lactamase. publication-title: J. Antimicrob. Chemother. doi: 10.1093/jac/dkt410 – volume: 27 start-page: 1469 year: 2022 ident: B28 article-title: Application of deep learning algorithm on whole genome sequencing data uncovers structural variants associated with multiple mental disorders in African American patients. publication-title: Mol. Psychiatry doi: 10.1038/s41380-021-01418-1 – volume: 71 start-page: E1 year: 2020 ident: B10 article-title: Treatment of nontuberculous mycobacterial pulmonary disease: an official ats/ers/escmid/idsa clinical practice guideline. publication-title: Clin. Infect. Dis. doi: 10.1093/cid/ciaa241 – volume: 119 start-page: S58 year: 2020 ident: B61 article-title: Treatment for Mycobacterium abscessus complex–lung disease. publication-title: J. Formos. Med. Assoc. doi: 10.1016/j.jfma.2020.05.028 – volume: 13 year: 2022 ident: B15 article-title: Application of next generation sequencing for diagnosis and clinical management of drug-resistant tuberculosis: updates on recent developments in the field. publication-title: Front. Microbiol. doi: 10.3389/fmicb.2022.775030 – volume: 3 year: 2016 ident: B62 article-title: The FAIR guiding principles for scientific data management and stewardship. publication-title: Sci. Data doi: 10.1038/sdata.2016.18 – volume: 20 year: 2019 ident: B13 article-title: Mycobacterium abscessus, an emerging and worrisome pathogen among cystic fibrosis patients. publication-title: Int. J. Mol. Sci. doi: 10.3390/ijms20235868 |
SSID | ssj0000402000 |
Score | 2.3676436 |
SecondaryResourceType | review_article |
Snippet | Non-tuberculous mycobacteria (NTM) are opportunistic pathogens commonly causing chronic, pulmonary disease which is notoriously hard to treat. Current... |
SourceID | doaj pubmedcentral proquest pubmed crossref |
SourceType | Open Website Open Access Repository Aggregation Database Index Database Enrichment Source |
StartPage | 1044515 |
SubjectTerms | Microbiology mutations Mycobacterium non-tuberculous mycobacteria resistance sequencing |
SummonAdditionalLinks | – databaseName: DOAJ Directory of Open Access Journals dbid: DOA link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1La9wwEBYlEOgl9JGm7iOokFswtWRLso5tSQiF9tSQ3IQ1kokh6w279iH_vjOys-yWklxytWVLzGg086GZbxg70TFo42vIRVAIUKyMuY3SouEFPJEFQCuoOPnXb31xWf28Vtdbrb4oJ2yiB54E97UA_IuOGFYZVWlQTQNagi8EmIiuMZXuoc_bAlPpDCZYVBRTlQyiMItq6sAjHpSSrjUrRX1wtzxRIuz_X5T5b7Lklvc5f8UO5rCRf5uW-5q9iP0btj81krx_y26uqM0tJ8LVReRzejQ6Jd70gd-t6DKGFMCXLT4ZukWX6Jfwh-txnfJaUoosgmbe9bxf9vkw-riC8XY5rvniHtDoE6lzc8guz8_-_LjI5x4KOVS6HvLEV-8tKAMCJQdlCG2oREBLpgK80vvChFLGIjRBetkUJYgWfFtZ0KWQvnzH9nDa-J7xwhL8CnUQJRBxWAMq1B5krLUl1vqMiQd5OpgJxqnPxa1DoEE6cEkHjnTgZh1k7HTzzd1Er_Ho6O-kps1IosZOD3DDuHnDuKc2TMa-PCjZoSnR_UjTRxSnk0YpZYyQOmNHk9I3U5UaETuefhkzO9thZy27b_ruJtF1I2LDqEp9eI7Ff2QvSSBUDCntJ7Y3rMb4GaOiwR8nA_gLqt0ONw priority: 102 providerName: Directory of Open Access Journals |
Title | Whole genome sequencing and prediction of antimicrobial susceptibilities in non-tuberculous mycobacteria |
URI | https://www.ncbi.nlm.nih.gov/pubmed/36523832 https://www.proquest.com/docview/2755577126 https://pubmed.ncbi.nlm.nih.gov/PMC9745125 https://doaj.org/article/0c1d56e81d7546c5aac62cb01c7e2839 |
Volume | 13 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV3fa9swEBalY7CXsd_zuhYN9jY8LNmS7Icy2rGuDLqnheXNWCd5NSRO59iw_Pe9k52wjG6wl0Acx7L16XT3WbrvGHurvdPG5hALp5CgFNLHhZcFGp7DGVkA1IKSk6--6stZ9mWu5gdsW-5o6sD1ndSO6knNusX7Xz83H9DgT4lxor9FBBqwSPWkpBXLTFHO-T30TIYM9WoK98PMTGQpZKUIrWlBQM7HPJq_XGbPVwVJ_7vi0D-3U_7mny4esYdTYMnPxpHwmB349gm7P5aa3Dxl19-pEC4nSdal59MGanRbvGodv-louYYg4qsaj_TNsgkCTXjB9bAOO1_CJlqk1bxpebtq436wvoNhsRrWfLkBnBaC7HP1jM0uPn37eBlPVRZiyHTex0HR3hagDIgKNKTO1S4TDm2dUvRSaxPjUukTVzlpZZWkIGqwdVaAToW06XN2iM36l4wnBRE0lzuRAkmLVaBcbkH6XBekax8xse3PEiYJcqqEsSiRihAGZcCgJAzKCYOIvdv952YU4Pjn2ecE0-5MEs8OB1bdj3KyxTIBHJjaY6RuVKZBVfjYEmwiwHiMtoqIvdmCXKKx0QpK1XrszlIapZQxQuqIvRhB3zWVauT0OD9GzOwNh7172f-lba6DoDdyOoy71Kv_etQj9oC-Ul6kLF6zw74b_DEGSL09CS8W8PPzXJwEC7gFb7AR3A |
linkProvider | Scholars Portal |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Whole+genome+sequencing+and+prediction+of+antimicrobial+susceptibilities+in+non-tuberculous+mycobacteria&rft.jtitle=Frontiers+in+microbiology&rft.au=Solanki%2C+Priya&rft.au=Lipman%2C+Marc&rft.au=McHugh%2C+Timothy+D.&rft.au=Satta%2C+Giovanni&rft.date=2022-11-29&rft.issn=1664-302X&rft.eissn=1664-302X&rft.volume=13&rft_id=info:doi/10.3389%2Ffmicb.2022.1044515&rft.externalDBID=n%2Fa&rft.externalDocID=10_3389_fmicb_2022_1044515 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1664-302X&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1664-302X&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1664-302X&client=summon |