Differential Expression of Resistant and Efflux Pump Genes in MDR-TB Isolates

被引:15
作者
AlMatar, Manaf [1 ]
Var, Isil [2 ]
Kayar, Begum [3 ]
Koksal, Fatih [3 ]
机构
[1] Cukurova Univ, Inst Nat & Appl Sci, Dept Biotechnol, Fen Bilimleri Enstitusu, Adana, Turkey
[2] Cukurova Univ, Agr Fac, Dept Food Engn, Adana, Turkey
[3] Cukurova Univ, Fac Med, Dept Med Microbiol, Adana, Turkey
关键词
Mycobacterium tuberculosis; antituberculosis agents; efflux pumps; gene expression; RT-qPCR; drug resistance; CATALASE-PEROXIDASE GENE; LEVEL ISONIAZID RESISTANCE; OXIDATIVE STRESS RESPONSES; INTRINSIC DRUG-RESISTANCE; MYCOBACTERIUM-TUBERCULOSIS; MOLECULAR CHARACTERIZATION; RIFAMPIN RESISTANCE; ENZYMATIC CHARACTERIZATION; COMPENSATORY MUTATIONS; ANTIBIOTIC-RESISTANCE;
D O I
10.2174/1871530319666191009153834
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Numerous investigations demonstrate efflux as a worldwide bacterial mode of action which contributes to the resistance of drugs. The activity of antibiotics, which subjects to efflux, can be improved by the combined usage of efflux inhibitors. However, the efflux role to the overall levels of antibiotic resistance of clinical M. tuberculosis isolates is inadequately comprehended and is still disregarded by many. Methods: Here, we assessed the contribution of resistant genes associated with isoniazid (INH) and rifampin (R) resistance to the levels of drug resistance in the (27) clinical isolates of MDR-TB. Additionally, the role of the resistance for six putative drug efflux pump genes to the antibiotics was investigated. The level of katG expression was down-regulated in 24/27 (88.88%) of MDR-TB isolates. Of the 27 MDR-TB isolates, inhA, oxyR-ahpC, and rpoB showed either overexpression or up-regulation in 8 (29.62%), 4 (14.81 %), and 24 (88.88%), respectively. Moreover, the efflux pump genes drrA, drrB, efpA, Rv2459, Rv1634, and Rv1250 were overexpressed under INH/RIF plus fresh pomegranate juice (FPJ) stress signifying the efflux pumps contribution to the overall levels of the resistance of MDR-TB isolates. Conclusion: These results displayed that the levels of drug resistance of MDR-TB clinical isolates are due to combination among drug efflux pump and the presence of mutations in target genes, a truth which is often ignored by the specialists of tuberculosis in favour of the almost undoubted significance of drug target-gene mutations for the resistance in M. tuberculosis.
引用
收藏
页码:271 / 287
页数:17
相关论文
共 134 条
[1]   lsoniazid and rifampicin resistance mutations and their effect on second-line anti-tuberculosis treatment [J].
Abate, D. ;
Tedla, Y. ;
Meressa, D. ;
Ameni, G. .
INTERNATIONAL JOURNAL OF TUBERCULOSIS AND LUNG DISEASE, 2014, 18 (08) :946-951
[2]   Modified protocol for drug susceptibility testing of MGIT cultures of Mycobacterium tuberculosis by the MGIT 960 [J].
Adami, Aline Gois ;
Gallo, Juliana Failde ;
Watanabe Pinhata, Juliana Maira ;
Martins, Maria Conceicao ;
Saraiva Giampaglia, Carmen Maria ;
de Oliveira, Rosangela Siqueira .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2017, 87 (02) :108-111
[3]   Contribution of AGC to ACC and other mutations at codon 315 of the katG gene in isoniazid-resistant Mycobacterium tuberculosis isolates from the Middle East [J].
Ahmad, S ;
Mokaddas, E .
INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2004, 23 (05) :473-479
[4]  
AlMatar M., 2017, PHARM REP
[5]   Evaluation of Polyphenolic Profile and Antibacterial Activity of Pome-granate Juice in Combination with Rifampin (R) against MDR-TB Clinical Isolates [J].
AlMatar, Manaf ;
Var, Isil ;
Kayar, Begum ;
Eker, Emel ;
Kafkas, Ebru ;
Zarifikhosroshahi, Mozhgan ;
Koksal, Fatih .
CURRENT PHARMACEUTICAL BIOTECHNOLOGY, 2019, 20 (04) :317-326
[6]   Antimicrobial peptides as an alternative to anti-tuberculosis drugs [J].
AlMatar, Manaf ;
Makky, Essam A. ;
Yakici, Gulfer ;
Var, Isil ;
Kayar, Begum ;
Koksal, Fatih .
PHARMACOLOGICAL RESEARCH, 2018, 128 :288-305
[7]   New drugs for the treatment of Mycobacterium tuberculosis infection [J].
AlMatar, Manaf ;
AlMandeal, Husam ;
Var, Isil ;
Kayar, Begum ;
Koksal, Fatih .
BIOMEDICINE & PHARMACOTHERAPY, 2017, 91 :546-558
[8]   Downregulation of katG expression is associated with isoniazid resistance in Mycobacterium tuberculosis [J].
Ando, Hiroki ;
Kitao, Tomoe ;
Miyoshi-Akiyama, Tohru ;
Kato, Seiya ;
Mori, Toru ;
Kirikae, Teruo .
MOLECULAR MICROBIOLOGY, 2011, 79 (06) :1615-1628
[9]   Identification of katG Mutations Associated with High-Level Isoniazid Resistance in Mycobacterium tuberculosis [J].
Ando, Hiroki ;
Kondo, Yuji ;
Suetake, Toshinori ;
Toyota, Emiko ;
Kato, Seiya ;
Mori, Toru ;
Kirikae, Teruo .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2010, 54 (05) :1793-1799
[10]   Sequence-Based Analysis Uncovers an Abundance of Non-Coding RNA in the Total Transcriptome of Mycobacterium tuberculosis [J].
Arnvig, Kristine B. ;
Comas, Inaki ;
Thomson, Nicholas R. ;
Houghton, Joanna ;
Boshoff, Helena I. ;
Croucher, Nicholas J. ;
Rose, Graham ;
Perkins, Timothy T. ;
Parkhill, Julian ;
Dougan, Gordon ;
Young, Douglas B. .
PLOS PATHOGENS, 2011, 7 (11)