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Carbon monoxide releasing molecule-2 (CORM-2) inhibits growth of multidrug-resistant uropathogenic Escherichia coli in biofilm and following host cell colonization

Sahlberg Bang, Charlotte, 1967- (author)
Örebro universitet,Institutionen för medicinska vetenskaper,iRiSC - Inflammatory Responses and Infection Susceptibility Centre, Örebro University, Örebro, Sweden; iRiSC - Inflammatory Responses and Infection Susceptibility Centre, Örebro University Hospital, Örebro, Sweden
Kruse, Robert, 1972- (author)
Örebro universitet,Institutionen för medicinska vetenskaper,iRiSC - Inflammatory Responses and Infection Susceptibility Centre, Örebro University, Örebro, Sweden; iRiSC - Inflammatory Responses and Infection Susceptibility Centre, Örebro University Hospital, Örebro, Sweden
Johansson, Kjell, 1957- (author)
Örebro universitet,Institutionen för medicinska vetenskaper
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Persson, Katarina, 1962- (author)
Örebro universitet,Institutionen för medicinska vetenskaper,iRiSC - Inflammatory Responses and Infection Susceptibility Centre, Örebro University, Örebro, Sweden; iRiSC - Inflammatory Responses and Infection Susceptibility Centre, Örebro University Hospital, Örebro, Sweden
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 (creator_code:org_t)
2016-04-12
2016
English.
In: BMC Microbiology. - : BioMed Central. - 1471-2180. ; 16:1
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Increased resistance to antimicrobial agents is a characteristic of many bacteria growing in biofilms on for example indwelling urinary catheters or in intracellular bacterial reservoirs. Biofilm-related infections caused by multidrug-resistant bacteria, such as extended-spectrum β-lactamase (ESBL)-producing Enterobacteriaceae, are a major challenge. The aim of this study was to investigate if a carbon monoxide-releasing molecule (CORM-2) has antibacterial effects against ESBL-producing uropathogenic E. coli (UPEC) in the biofilm mode of growth and following colonization of host bladder epithelial cells.ResultsThe effect of CORM-2 was examined on bacteria grown within an established biofilm (biofilm formed for 24 h on plastic surface) by a live/dead viability staining assay. CORM-2 (500 μM) exposure for 24 h killed approximately 60 % of the ESBL-producing UPEC isolate. A non-ESBL-producing UPEC isolate and the E. coli K-12 strain TG1 were also sensitive to CORM-2 exposure when grown in biofilms. The antibacterial effect of CORM-2 on planktonic bacteria was reduced and delayed in the stationary growth phase compared to the exponential growth phase. In human bladder epithelial cell colonization experiments, CORM-2 exposure for 4 h significantly reduced the bacterial counts of an ESBL-producing UPEC isolate.ConclusionThis study shows that CORM-2 has antibacterial properties against multidrug-resistant UPEC under biofilm-like conditions and following host cell colonization, which motivate further studies of its therapeutic potential.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Andra medicinska och farmaceutiska grundvetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Other Basic Medicine (hsv//eng)
NATURVETENSKAP  -- Biologi -- Mikrobiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Microbiology (hsv//eng)

Keyword

Carbon monoxide releasing molecule
CORM-2
Extended-spectrum β-lactamase
Uropathogenic Escherichia coli
Biofilm

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Sahlberg Bang, C ...
Kruse, Robert, 1 ...
Johansson, Kjell ...
Persson, Katarin ...
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MEDICAL AND HEALTH SCIENCES
MEDICAL AND HEAL ...
and Basic Medicine
and Other Basic Medi ...
NATURAL SCIENCES
NATURAL SCIENCES
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and Microbiology
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BMC Microbiology
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Örebro University

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