Literature DB >> 26594376

Report on a transborder spread of carbapenemase-producing bacteria by a patient injured during Euromaidan, Ukraine.

J Hrabák1, V Študentová1, V Adámková2, L Šemberová2, P Kabelíková3, D Hedlová4, M Čurdová5, H Zemlickova6, C C Papagiannitsis1.   

Abstract

Spread of carbapenemase-producing bacteria has been described all over the world. This phenomenon may be accelerated by many factors, including wars and natural disasters. In this report, we described an NDM-1-producing Klebsiella pneumonia ST11 recovered from a patient injured during the Maidan revolution in Ukraine. To our knowledge, this is the first report of a carbapenemase-producing Enterobacteriaceae in Ukraine and one of several reports describing wound colonization/infection of humans injured during war.

Entities:  

Keywords:  Antibiotic resistance; Klebsiella pneumoniae; NDM-1; ST11; catastrophe; disaster; war

Year:  2015        PMID: 26594376      PMCID: PMC4610961          DOI: 10.1016/j.nmni.2015.09.005

Source DB:  PubMed          Journal:  New Microbes New Infect        ISSN: 2052-2975


Global spread of antibiotic resistance can be accelerated by many factors, including travelling and repatriation of patients. Additionally, antibiotic resistance can be spread by contaminated food as well as wild animals. Few studies describing spread of multiresistant bacteria after natural disasters (e.g. tsunami, earthquake) and repatriation of injured patients (soldiers, civilians) during war have been reported [1-4]. Here we report a case of transmission of NDM-1-producing Klebsiella pneumoniae sequence type 11 (ST11) recovered from a Ukrainian patient injured during the Maidan revolution, also known as the Euromaidan (Kiev, Ukraine). From February until March 2014, 27 Ukrainian patients injured in Maidan Nezalezhnosti square (Independence Square) during Euromaidan have been transferred to Czech hospitals. The patients were admitted to General University Hospital (Prague), Motol University Hospital (Prague) and Central Military Hospital (Prague). On the basis of the Czech National Guidelines for Control of Cases of Colonisation/Infection by Carbapenemase-Producing Enterobacteria (http://www.mzcr.cz/Legislativa/dokumenty/vestnik-c8/2012_6865_2510_11.html), preemptive isolation of the patients and active screening using a rectal swab were performed. Enterobacteriaceae isolates recovered from various screening materials (e.g. sputum, blood, swabs) from patients hospitalized in intensive care units were also subjected to susceptibility testing and detection of carbapenemases according to screening cutoffs [5]. All suspected isolates were sent for a confirmation of carbapenemase-production to the National Reference Laboratory of Antibiotics (National Institute of Public Health, Prague, Czech Republic) and Department of Microbiology, Faculty of Medicine, in Plzen (Charles University in Prague, Plzen, Czech Republic). In that period, all of the hospitals also participated on European Survey on Carbapenemase-Producing Enterobacteriaceae (EuSCAPE) [6,7]. At Motol University Hospital, a K. pneumoniae isolate with reduced susceptibility to carbapenems was recovered from a wound of a 51-year-old Ukrainian man on 24 March 2014. The patient was directly transferred from a hospital in Kiev. Using multilocus sequence typing [8], MALDI-TOF (matrix-assisted laser desorption/ionization time-of-flight mass spectrometry) hydrolysis assay [9] and PCR detection of carbapenemase genes followed by amplicon sequencing [5], the isolate was identified as an NDM-1 producer that was classified into ST11, which belongs to clonal complex 258. Minimum inhibitory concentrations (MICs) of the isolate were determined by the disk diffusion test and by Etest (bioMérieux, Prague, Czech Republic) and interpreted using European Committee on Antimicrobial Susceptibility Testing criteria (http://www.eucast.org). The isolate was nonsusceptible/resistant to ertapenem (MIC 12 mg/L), meropenem (MIC 24 mg/L) and imipenem (MIC 3 mg/L), amikacin, amoxicillin/clavulanic acid, ampicillin cefotaxime, ceftazidime, cefepime, ciprofloxacin, gentamicin, piperacillin/tazobactam, tobramycin and trimethoprim/sulfamethoxazole and was susceptible to aztreonam, colistin and tigecycline. No extended-spectrum β-lactamase was detected on the basis of the double-disk synergy test between aztreonam and amoxicillin/clavulanic acid [10]. Simultaneously, a carbapenem-hydrolyzing class D β-lactamase (CHDL)-producing Acinetobacter baumannii and a methicillin-resistant Staphylococcus aureus were isolated from the same clinical material. No other carbapenemase-producing Enterobacteriaceae was isolated from the rest of the 26 patients. As previously described by other groups, emergence of multidrug-resistant bacteria has been frequently observed among injured soldiers hospitalized in army medical centers [11-13]. Calhoun et al. [12] hypothesized that overuse of broad-spectrum antibiotics in military hospitals during war may play an important role in selection and spread of resistant bacteria. Interestingly, Acinetobacter baumannii has been recognized as the second most frequent bacterium causing bloodstream infection in U.S. soldiers with extremity wounds during the Vietnam War [14,15]. Spread of A. baumannii complex is probably caused by the presence of this bacterium in the hospital environment and hospital-acquired colonization of wounds. Primary colonization of the wound during injury does not probably play an important role [12]. In accordance with the hypotheses described above, isolation of a CHDL-producing isolate from the same clinical material may indicate nosocomial origin of the NDM-1 producer. To our knowledge, neither epidemiologic studies nor case reports describing multiresistant Gram-negative bacteria have been previously reported from Ukraine. However, a previous report from our group described the first NDM-1-producing K. pneumoniae (ST11) in the Czech Republic, which was probably imported from Slovakia [15]. Previously, we also reported an isolate of NDM-1-producing A. baumannii recovered from a patient repatriated from Egypt [16] and NDM-4-producing Enterobacter cloacae isolated from a patient previously hospitalized in Sri Lanka [17]. Such findings may indicate a hidden source of clinically important resistance determinants, such as blaNDM-1, in the specific geographical area. Further studies are needed to uncover the current epidemiologic situation in carbapenemase-producing Enterobacteriaceae in Ukraine and surrounding regions.

Conflict of Interest

None declared.
  17 in total

1.  Microbiological findings from the Haiti disaster.

Authors:  Alexandre Rodrigues Marra; Marines Dalla Valle Martino; Mauro Ricardo Ribas; Carlos Rodriguez-Taveras; Oscar Fernando Pavao Dos Santos
Journal:  Travel Med Infect Dis       Date:  2012-04-20       Impact factor: 6.211

2.  Emergence of multidrug resistance in bacteria and impact on antibiotic expenditure at a major army medical center caring for soldiers wounded in Iraq and Afghanistan.

Authors:  Michael J Zapor; Daniel Erwin; Goldina Erowele; Glenn Wortmann
Journal:  Infect Control Hosp Epidemiol       Date:  2008-07       Impact factor: 3.254

3.  Complete nucleotide sequences of two NDM-1-encoding plasmids from the same sequence type 11 Klebsiella pneumoniae strain.

Authors:  V Studentova; H Dobiasova; D Hedlova; M Dolejska; C C Papagiannitsis; J Hrabak
Journal:  Antimicrob Agents Chemother       Date:  2014-11-24       Impact factor: 5.191

Review 4.  Detection of carbapenemases in Enterobacteriaceae: a challenge for diagnostic microbiological laboratories.

Authors:  J Hrabák; E Chudáčková; C C Papagiannitsis
Journal:  Clin Microbiol Infect       Date:  2014-06-14       Impact factor: 8.067

5.  Multidrug-resistant bacterial colonization of combat-injured personnel at admission to medical centers after evacuation from Afghanistan and Iraq.

Authors:  Duane R Hospenthal; Helen K Crouch; Judith F English; Fluryanne Leach; Jane Pool; Nicholas G Conger; Timothy J Whitman; Glenn W Wortmann; Janelle L Robertson; Clinton K Murray
Journal:  J Trauma       Date:  2011-07

6.  Prevalence study on carbapenemase-producing Escherichia coli and Klebsiella pneumoniae isolates in Czech hospitals--results from Czech Part of European Survey on Carbapenemase--Producing Enterobacteriaceae (EuSCAPE).

Authors:  J Hrabák; V Študentová; V Jakubů; V Adámková; L Dvořáková; M Balejova; T Bergerová; E Chmelařová; P Ježek; P Kabelíková; M Kolář; P Paterová; R Tejkalová; C Papagiannitsis; H Žemličková
Journal:  Epidemiol Mikrobiol Imunol       Date:  2015-06       Impact factor: 0.444

Review 7.  Phenotypic detection of extended-spectrum beta-lactamase production in Enterobacteriaceae: review and bench guide.

Authors:  L Drieux; F Brossier; W Sougakoff; V Jarlier
Journal:  Clin Microbiol Infect       Date:  2008-01       Impact factor: 8.067

Review 8.  Multi-resistant infections in repatriated patients after natural disasters: lessons learned from the 2004 tsunami for hospital infection control.

Authors:  I Uçkay; H Sax; S Harbarth; L Bernard; D Pittet
Journal:  J Hosp Infect       Date:  2008-01       Impact factor: 3.926

9.  Detection of OXA-48-type carbapenemase-producing Enterobacteriaceae in diagnostic laboratories can be enhanced by addition of bicarbonates to cultivation media or reaction buffers.

Authors:  Vendula Studentova; Costas C Papagiannitsis; Radoslaw Izdebski; Yvonne Pfeifer; Eva Chudackova; Tamara Bergerova; Marek Gniadkowski; Jaroslav Hrabak
Journal:  Folia Microbiol (Praha)       Date:  2014-09-29       Impact factor: 2.099

10.  Multidrug-resistant Acinetobacter extremity infections in soldiers.

Authors:  Kepler A Davis; Kimberly A Moran; C Kenneth McAllister; Paula J Gray
Journal:  Emerg Infect Dis       Date:  2005-08       Impact factor: 6.883

View more
  2 in total

1.  Infection control and risk factors for acquisition of carbapenemase-producing enterobacteriaceae. A 5 year (2011-2016) case-control study.

Authors:  Luigi Segagni Lusignani; Elisabeth Presterl; Beata Zatorska; Miriam Van den Nest; Magda Diab-Elschahawi
Journal:  Antimicrob Resist Infect Control       Date:  2020-01-17       Impact factor: 4.887

Review 2.  Resistant Gram-Negative Bacteria and Diagnostic Point-of-Care Options for the Field Setting during Military Operations.

Authors:  Hagen Frickmann; Andreas Podbielski; Bernd Kreikemeyer
Journal:  Biomed Res Int       Date:  2018-06-12       Impact factor: 3.411

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.