Danila Zimenkov

ORCID: 0000-0002-2040-0904
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About
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Research Areas
  • Tuberculosis Research and Epidemiology
  • Mycobacterium research and diagnosis
  • Bacteriophages and microbial interactions
  • Cancer therapeutics and mechanisms
  • Diagnosis and treatment of tuberculosis
  • Bacterial Genetics and Biotechnology
  • Infectious Diseases and Mycology
  • CRISPR and Genetic Engineering
  • Cancer Research and Treatments
  • Innovative Microfluidic and Catalytic Techniques Innovation
  • Infectious Diseases and Tuberculosis
  • Pneumonia and Respiratory Infections
  • Advanced Biosensing Techniques and Applications
  • Microfluidic and Capillary Electrophoresis Applications
  • Monoclonal and Polyclonal Antibodies Research
  • Microbial Metabolic Engineering and Bioproduction
  • Chronic Myeloid Leukemia Treatments
  • Microbial infections and disease research
  • Biochemical and Molecular Research
  • DNA Repair Mechanisms
  • Biosensors and Analytical Detection
  • Neutrophil, Myeloperoxidase and Oxidative Mechanisms
  • Animal Genetics and Reproduction
  • interferon and immune responses
  • Bacterial biofilms and quorum sensing

Engelhardt Institute of Molecular Biology
2015-2025

Genetic Technologies (Australia)
2025

Russian Academy of Sciences
2011-2015

Ajinomoto (United States)
2009

Ajinomoto (Russia)
2005-2008

Genetika
2005-2008

Timothy M. Walker Paolo Miotto Claudio U. Köser P. W. Fowler Jeff Knaggs and 95 more Zamin Iqbal Martin Hunt Leonid Chindelevitch Maha Farhat Daniela María Cirillo Iñaki Comas James E. Posey Shaheed Vally Omar Tim Peto Anita Suresh Swapna Uplekar Sacha Laurent Rebecca E. Colman Carl‐Michael Nathanson Matteo Zignol Ann Sarah Walker Derrick W. Crook Nazir Ismail Timothy C. Rodwell Timothy M. Walker Adrie J. C. Steyn Ajit Lalvani Alain R. Baulard Alan Christoffels Alberto Mendoza‐Ticona Alberto Trovato Alena Skrahina Alexander S. Lachapelle Alice Brankin Amy S. Piatek Ana Gibertoni Cruz Anastasia Koch Andrea Maurizio Cabibbe Andrea Spitaleri Angela Pires Brandão Angkana Chaiprasert Anita Suresh A. I. Barbova Annelies Van Rie Arash Ghodousi Arnold Bainomugisa Ayan Mandal Aysha Roohi Babak Javid Baoli Zhu Brice Letcher Camilla Rodrigues Camus Nimmo Carl‐Michael Nathanson Carla Duncan Christopher Coulter Christian Utpatel Chunfa Liu Clara Grazian Clare Kong Claudio U. Köser Daniel J. Wilson Daniela María Cirillo Daniela Matias Danielle Jorgensen Danila Zimenkov Darren Chetty David Moore David A. Clifton Derrick W. Crook Dick van Soolingen Dongxin Liu Donna Kohlerschmidt Dráurio Barreira Dumisani Ngcamu David Santos-Lázaro Ellis Kelly Emanuele Borroni Emma Roycroft Emmanuel André Erik C. Böttger Esther Robinson Fabrizio Menardo Flavia F Mendes Frances Jamieson Francesc Coll George F. Gao George William Kasule Gian María Rossolini Gillian Rodger E. Grace Smith Graeme Meintjes Guy Thwaites Harald Hoffmann Heidi Albert Helen Cox Ian F. Laurenson Iñaki Comas Irena Arandjelović Ivan Barilar

Molecular diagnostics are considered the most promising route to achieving rapid, universal drug susceptibility testing for

10.1016/s2666-5247(21)00301-3 article EN cc-by The Lancet Microbe 2022-03-08

To study the isolates with acquired resistance to bedaquiline and linezolid that were obtained from patients enrolled in a clinical of novel therapy regimen for drug-resistant TB Moscow, Russia.Linezolid was detected using MGIT 960 critical concentration 1 mg/L. The MIC determined proportion method. identify genetic determinants resistance, sequencing mmpR ( Rv0678 ), atpE , atpC pepQ Rv1979c rrl rplC rplD loci performed.A total 85 27 reduced susceptibility (MIC ≥0.06 mg/L) tested. Most...

10.1093/jac/dkx094 article EN Journal of Antimicrobial Chemotherapy 2017-03-06

Ethionamide and prothionamide are now included in group C of the WHO recommended drugs for treatment tuberculosis resistant to rifampicin multidrug-resistant tuberculosis. The clinical relevance ethionamide has increased with wide spread tuberculosis.We retrospectively analyzed 349 isolates obtained between 2016 2020. susceptibility was tested using both BactecTM MGITTM 960 system SensititreTM MYCOTB plate.The MIC increases total resistance a row from susceptible XDR strains. A significant...

10.3390/antibiotics11020133 article EN cc-by Antibiotics 2022-01-20

Bedaquiline is a cornerstone drug for treating drug-resistant tuberculosis. We analyzed 11 isolates from 9 patients who were treated with bedaquiline-based regimen and remained culture-positive long after treatment start. In 4 of 8 resistant isolates, we found substitutions in AtpE, which encodes subunit c the Mycobacterium tuberculosis ATP synthase rarely identified clinical isolates. Ile66Met Glu61Asp 2 cases each. Additional mutations mmpL5, mmpL4, atpB genes could affect susceptibility...

10.3201/eid3103.241488 article EN Emerging infectious diseases 2025-02-21

Aim. To study the susceptibility of clinical strains M. tuberculosis complex (MTB) to delamanid using automated Bactec MGIT system. Material and methods. We studied 79 isolates from 78 TB patients treated in 2017-2023. 39 MTB were susceptibile 40 had different drug resistance profiles anti-tubercular drugs. Minimum inhibitory concentrations (MIC) Middlebrook 7H9 liquid medium determined system, results assessed critical concentration 0.06 μg/ml recommended by WHO. Whole genome sequencing was...

10.54921/2413-0346-2024-12-4-25-35 article EN cc-by Tuberkulez i socialʹno značimye zabolevaniâ 2025-03-01

The development of modern producer strains with metabolically engineered pathways poses special problems that often require manipulating many genes and expressing them individually at different levels or under separate regulatory controls. construction plasmid-less marker-less has advantages for the further practical exploitation these bacteria in industry. Such are usually constructed by sequential chromosome modifications including deletions integration genetic material. For purposes...

10.1186/1472-6750-8-63 article EN cc-by BMC Biotechnology 2008-01-01

The steady rise in the spread of multidrug-resistant tuberculosis (MDR-TB) and extensively drug-resistant (XDR-TB) requires rapid reliable methods to identify resistant strains. current molecular detect MTB resistance second-line drugs either do not cover an extended spectrum mutations be identified or are easily implemented clinical laboratories. A technique for detection M. has been developed using hybridisation analysis on microarrays. method allows identification within gyrA gyrB genes...

10.1186/1471-2334-13-240 article EN cc-by BMC Infectious Diseases 2013-05-24

Immobilization of molecular probes in 3D hydrogel elements provides some essential advantages compared with conventional flat surfaces. In this article, an integrated technology based on the use low-density microarrays comprised hemispherical gel elements, developed at Engelhardt Institute Molecular Biology (Moscow, Russia) for various applications will be reviewed. The structure can adapted immobilization virtually any biological molecules a natural hydrophilic environment. discrimination...

10.1586/erm.11.73 article EN Expert Review of Molecular Diagnostics 2011-10-24

Nucleic acid amplification tests are widely used in TB diagnostics. Priority tasks their development consist of increasing the specificity and sensitivity detection resistance to a wide spectrum anti-TB drugs. We developed multiplexed assay allowing 116 drug resistance-determining mutations rpoB, katG, inhA, ahpC, gyrA, gyrB, rrs, eis embB genes Mycobacterium tuberculosis complex genome six SNPs identify main lineages circulating Russia. The is based on 17 fragments using universal primer...

10.1093/jac/dkw015 article EN Journal of Antimicrobial Chemotherapy 2016-02-29

In addition to the obligatory pathogenic species of Mycobacterium tuberculosis complex and leprae, genus also includes conditionally that in rare cases can lead development nontuberculous mycobacterial diseases. Because mycobacteriosis have similar clinical signs, accurate identification causative agent a microbiology laboratory is important for diagnostic verification appropriate treatment. This report describes low-density hydrogel-based microarray containing oligonucleotide probes based...

10.1128/jcm.02579-14 article EN Journal of Clinical Microbiology 2015-01-22

The pentose-phosphate pathway (PPP) is an important part of central metabolism in many organisms. A pgl(-) mutation that decreases the efficiency second stage PPP has been described and mapped at approx. 17.2 min Escherichia coli chromosome more than 30 years ago. Although it recently shown deletion ORF ybhE leads to earlier detected Pgl(-) phenotype for E. mutant strain, 6-phosphogluconolactonase from this organism not characterized. In present, independent investigation we show DeltaybhE...

10.1016/j.femsle.2005.01.050 article EN FEMS Microbiology Letters 2005-02-10

Background The goal of this study was to compare the consistency three assays for determination drug resistance Mycobacterium tuberculosis (MTB) strains with various profiles isolated from Moscow region. Methods A total 144 MTB clinical isolates a strong bias toward were examined using Bactec MGIT 960, Sensititre MycoTB, and microarray-based molecular assay TB-TEST detect substitutions in rpoB, katG, inhA, ahpC, gyrA, gyrB, rrs, eis, embB genes that are associated rifampin, isoniazid,...

10.1371/journal.pone.0167093 article EN cc-by PLoS ONE 2016-11-30

We investigated the rise of nontuberculous mycobacteria (NTM) infections in Bulgaria, focusing on species identification and distribution from 2018 to 2022. Utilizing advanced diagnostic tools, including Hain Mycobacterium CM/AS method, Myco-biochip assay, whole-genome sequencing, study identifies characterizes a diverse range clinical samples. While M. avium, gordonae, fortuitum, chelonae were dominating, number rare also found. They include such as marseillense celatum. Moreover,...

10.3390/ijms251910434 article EN International Journal of Molecular Sciences 2024-09-27

Background: Linezolid, bedaquiline, and newer fluoroquinolones are currently placed as priority Group A drugs for the treatment of drug-resistant tuberculosis. The number reported linezolid-resistant clinical strains is still low, correlation molecular determinants with phenotype not perfect. Methods: We determined linezolid MICs isolates from Moscow region identified mutations in rplC rrl genes. Results: All 16 had previously or loci, 13 them bore a RplC C154R substitution. Detection this...

10.3390/antibiotics10101243 article EN cc-by Antibiotics 2021-10-13
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