دورية أكاديمية

Clinical Strains of Mycobacterium tuberculosis Representing Different Genotype Families Exhibit Distinct Propensities to Adopt the Differentially Culturable State.

التفاصيل البيبلوغرافية
العنوان: Clinical Strains of Mycobacterium tuberculosis Representing Different Genotype Families Exhibit Distinct Propensities to Adopt the Differentially Culturable State.
المؤلفون: Gordhan BG; Department of Science and Innovation and the National Research Foundation Centre of Excellence for Biomedical TB Research, School of Pathology, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg 2017, South Africa.; National Health Laboratory Service, Johannesburg 2000, South Africa., Padarath K; Department of Science and Innovation and the National Research Foundation Centre of Excellence for Biomedical TB Research, School of Pathology, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg 2017, South Africa.; National Health Laboratory Service, Johannesburg 2000, South Africa., Sewcharran A; Department of Science and Innovation and the National Research Foundation Centre of Excellence for Biomedical TB Research, School of Pathology, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg 2017, South Africa.; National Health Laboratory Service, Johannesburg 2000, South Africa., McIvor A; Department of Science and Innovation and the National Research Foundation Centre of Excellence for Biomedical TB Research, School of Pathology, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg 2017, South Africa.; National Health Laboratory Service, Johannesburg 2000, South Africa., VanNieuwenhze MS; Department of Chemistry, Indiana University Bloomington, Bloomington, IN 47405-7000, USA., Waja Z; Perinatal HIV Research Unit (PHRU), University of the Witwatersrand, Johannesburg 2017, South Africa., Martinson N; Perinatal HIV Research Unit (PHRU), University of the Witwatersrand, Johannesburg 2017, South Africa.; Center for TB Research, Johns Hopkins University, Baltimore, MD 21218, USA., Kana BD; Department of Science and Innovation and the National Research Foundation Centre of Excellence for Biomedical TB Research, School of Pathology, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg 2017, South Africa.; National Health Laboratory Service, Johannesburg 2000, South Africa.
المصدر: Pathogens (Basel, Switzerland) [Pathogens] 2024 Apr 12; Vol. 13 (4). Date of Electronic Publication: 2024 Apr 12.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: MDPI AG Country of Publication: Switzerland NLM ID: 101596317 Publication Model: Electronic Cited Medium: Print ISSN: 2076-0817 (Print) Linking ISSN: 20760817 NLM ISO Abbreviation: Pathogens Subsets: PubMed not MEDLINE
أسماء مطبوعة: Original Publication: Basel, Switzerland : MDPI AG, 2012-
مستخلص: Growing evidence points to the presence of differentially culturable tubercle bacteria (DCTB) in clinical specimens from individuals with active tuberculosis (TB) disease. These bacteria are unable to grow on solid media but can resuscitate in liquid media. Given the epidemiological success of certain clinical genotype families of Mycobacterium tuberculosis , we hypothesize that different strains may have distinct mechanisms of adaptation and tolerance. We used an in vitro carbon starvation model to determine the propensity of strains from lineages 2 and 4 that included the Beijing and LAM families respectively, to generate DCTB. Beijing strains were associated with a greater propensity to produce DCTB compared to LAM strains. Furthermore, LAM strains required culture filtrate (CF) for resuscitation whilst starved Beijing strains were not dependent on CF. Moreover, Beijing strains showed improved resuscitation with cognate CF, suggesting the presence of unique growth stimulatory molecules in this family. Analysis of starved Beijing and LAM strains showed longer cells, which with resuscitation were restored to a shorter length. Cell wall staining with fluorescent D-amino acids identified strain-specific incorporation patterns, indicating that cell surface remodeling during resuscitation was distinct between clinical strains. Collectively, our data demonstrate that M. tuberculosis clinical strains from different genotype lineages have differential propensities to generate DCTB, which may have implications for TB treatment success.
References: J Clin Microbiol. 2007 Feb;45(2):409-14. (PMID: 17166963)
Front Cell Infect Microbiol. 2023 Jan 12;12:1064148. (PMID: 36710965)
Proc Natl Acad Sci U S A. 2017 Jun 13;114(24):E4832-E4840. (PMID: 28559332)
Am J Respir Crit Care Med. 2020 May 1;201(9):1152-1155. (PMID: 31914319)
J Clin Microbiol. 2008 Apr;46(4):1363-8. (PMID: 18287322)
J Bacteriol. 2011 Jul;193(14):3446-52. (PMID: 21602344)
J Bacteriol. 2007 Apr;189(7):2583-9. (PMID: 17237171)
Infect Genet Evol. 2006 Nov;6(6):491-504. (PMID: 16632413)
J Bacteriol. 1933 Aug;26(2):167-200. (PMID: 16559650)
Am J Respir Crit Care Med. 2010 Jan 15;181(2):174-80. (PMID: 19875686)
Clin Infect Dis. 2008 Nov 15;47(10):1252-9. (PMID: 18834315)
Tuberculosis (Edinb). 2011 Mar;91(2):146-54. (PMID: 21262587)
Nat Rev Microbiol. 2014 Mar;12(3):159-67. (PMID: 24487820)
Adv Appl Microbiol. 2019;108:115-161. (PMID: 31495404)
Lancet. 2006 Nov 4;368(9547):1575-80. (PMID: 17084757)
Microbiol Spectr. 2017 Jan;5(1):. (PMID: 28233509)
Mol Microbiol. 2002 Feb;43(3):717-31. (PMID: 11929527)
J Clin Microbiol. 2010 Oct;48(10):3544-50. (PMID: 20702677)
BMC Biol. 2017 Dec 21;15(1):121. (PMID: 29262826)
mBio. 2018 Nov 20;9(6):. (PMID: 30459198)
Environ Microbiol. 2018 Jun;20(6):2038-2048. (PMID: 29457686)
FEMS Microbiol Rev. 2010 Jul;34(4):415-25. (PMID: 20059548)
Front Microbiol. 2019 Oct 23;10:2381. (PMID: 31749768)
Mol Microbiol. 2008 Jul;69(1):164-74. (PMID: 18466296)
mSystems. 2022 Jun 28;7(3):e0011022. (PMID: 35430871)
Lancet Infect Dis. 2010 Feb;10(2):103-11. (PMID: 20113979)
Infect Immun. 1996 Jun;64(6):2062-9. (PMID: 8675308)
Int J Tuberc Lung Dis. 2015 Jul;19(7):834-40. (PMID: 26056111)
Open Biol. 2014 Oct;4(10):. (PMID: 25320096)
Am J Respir Crit Care Med. 2016 Dec 15;194(12):1532-1540. (PMID: 27387272)
Tuberculosis (Edinb). 2021 Jul;129:102103. (PMID: 34144375)
Microbiology (Reading). 2002 May;148(Pt 5):1581-1591. (PMID: 11988533)
J Vis Exp. 2012 Feb 15;(60):. (PMID: 22371116)
J Infect Dis. 2008 Oct 1;198(7):1037-43. (PMID: 18702608)
J Exp Med. 2003 Sep 1;198(5):705-13. (PMID: 12953092)
Tuberculosis (Edinb). 2011 Nov;91(6):510-23. (PMID: 21835699)
Antimicrob Agents Chemother. 2016 Mar 25;60(4):2476-83. (PMID: 26883695)
Angew Chem Int Ed Engl. 2012 Dec 7;51(50):12519-23. (PMID: 23055266)
Emerg Infect Dis. 2009 Feb;15(2):335-9. (PMID: 19193289)
FEMS Immunol Med Microbiol. 2010 Feb;58(1):39-50. (PMID: 19799629)
Mol Microbiol. 2002 Nov;46(3):623-35. (PMID: 12410821)
Antimicrob Agents Chemother. 2021 Jul 16;65(8):e0060821. (PMID: 34060896)
Tuberculosis (Edinb). 2010 Sep;90(5):319-25. (PMID: 20832364)
Sci Rep. 2021 Mar 22;11(1):6493. (PMID: 33753820)
Front Cell Infect Microbiol. 2022 Sep 09;12:949370. (PMID: 36159642)
معلومات مُعتمدة: HHMI000 United States HHMI Howard Hughes Medical Institute
فهرسة مساهمة: Keywords: Beijing strains; LAM strains; Mycobacterium tuberculosis; differentially culturable tubercle bacteria; tuberculosis
تواريخ الأحداث: Date Created: 20240426 Latest Revision: 20240429
رمز التحديث: 20240429
مُعرف محوري في PubMed: PMC11054447
DOI: 10.3390/pathogens13040318
PMID: 38668273
قاعدة البيانات: MEDLINE
الوصف
تدمد:2076-0817
DOI:10.3390/pathogens13040318