-
Je něco špatně v tomto záznamu ?
Selective growth-inhibitory effect of 8-hydroxyquinoline towards Clostridium difficile and Bifidobacterium longum subsp. longum in co-culture analysed by flow cytometry
J. Novakova, M. Džunková, S. Musilova, E. Vlkova, L. Kokoska, A. Moya, G. D'Auria,
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
25298160
DOI
10.1099/jmm.0.080796-0
Knihovny.cz E-zdroje
- MeSH
- antibakteriální látky farmakologie MeSH
- Bifidobacterium účinky léků růst a vývoj MeSH
- Clostridioides difficile účinky léků růst a vývoj MeSH
- hybridizace in situ fluorescenční MeSH
- mikrobiální interakce MeSH
- oxychinolin farmakologie MeSH
- průtoková cytometrie MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
The major risk factor for Clostridium difficile infection (CDI) is the use of antibiotics owing to the disruption of the equilibrium of the host gut microbiota. To preserve the beneficial resident probiotic bacteria during infection treatment, the use of molecules with selective antibacterial activity enhances the efficacy by selectively removing C. difficile. One of them is the plant alkaloid 8-hydroxyquinoline (8HQ), which has been shown to selectively inhibit clostridia without repressing bifidobacteria. Selective antimicrobial activity is generally tested by culture techniques of individual bacterial strains. However, the main limitation of these techniques is the inability to describe differential growth dynamics of more bacterial strains in co-culture within the same experiment. In the present study, we combined fluorescent in situ hybridization and flow cytometry to describe the changes in active and non-active cells of a mixed culture formed by the opportunistic pathogen C. difficile CECT 531 and the beneficial Bifidobacterium longum subsp. longum CCMDMND BL1 after exposure to 8HQ. It was observed that without 8HQ, the proportion of both strains was almost equal, oscillating between 22.7 and 77.9 % during a time lapse of 12 h, whereas with 8HQ the proportion of active C. difficile decreased after 4 h, and persisted only between 8.8 and 17.5 %. In contrast, bifidobacterial growth was not disturbed by 8HQ. The results of this study showed the selective inhibitory effect of 8HQ on clostridial and bifidobacterial growth dynamics, and the potential of this compound for the development of selective agents to control CDIs.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc15014029
- 003
- CZ-PrNML
- 005
- 20150428101134.0
- 007
- ta
- 008
- 150420s2014 enk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1099/jmm.0.080796-0 $2 doi
- 035 __
- $a (PubMed)25298160
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a enk
- 100 1_
- $a Novakova, Jitka $u Department of Crop Sciences and Agroforestry, Faculty of Tropical AgriSciences, Czech University of Life Sciences Prague, Kamycka 129, 165 21 Prague 6-Suchdol, Czech Republic.
- 245 10
- $a Selective growth-inhibitory effect of 8-hydroxyquinoline towards Clostridium difficile and Bifidobacterium longum subsp. longum in co-culture analysed by flow cytometry / $c J. Novakova, M. Džunková, S. Musilova, E. Vlkova, L. Kokoska, A. Moya, G. D'Auria,
- 520 9_
- $a The major risk factor for Clostridium difficile infection (CDI) is the use of antibiotics owing to the disruption of the equilibrium of the host gut microbiota. To preserve the beneficial resident probiotic bacteria during infection treatment, the use of molecules with selective antibacterial activity enhances the efficacy by selectively removing C. difficile. One of them is the plant alkaloid 8-hydroxyquinoline (8HQ), which has been shown to selectively inhibit clostridia without repressing bifidobacteria. Selective antimicrobial activity is generally tested by culture techniques of individual bacterial strains. However, the main limitation of these techniques is the inability to describe differential growth dynamics of more bacterial strains in co-culture within the same experiment. In the present study, we combined fluorescent in situ hybridization and flow cytometry to describe the changes in active and non-active cells of a mixed culture formed by the opportunistic pathogen C. difficile CECT 531 and the beneficial Bifidobacterium longum subsp. longum CCMDMND BL1 after exposure to 8HQ. It was observed that without 8HQ, the proportion of both strains was almost equal, oscillating between 22.7 and 77.9 % during a time lapse of 12 h, whereas with 8HQ the proportion of active C. difficile decreased after 4 h, and persisted only between 8.8 and 17.5 %. In contrast, bifidobacterial growth was not disturbed by 8HQ. The results of this study showed the selective inhibitory effect of 8HQ on clostridial and bifidobacterial growth dynamics, and the potential of this compound for the development of selective agents to control CDIs.
- 650 _2
- $a antibakteriální látky $x farmakologie $7 D000900
- 650 _2
- $a Bifidobacterium $x účinky léků $x růst a vývoj $7 D001644
- 650 _2
- $a Clostridioides difficile $x účinky léků $x růst a vývoj $7 D016360
- 650 _2
- $a průtoková cytometrie $7 D005434
- 650 _2
- $a hybridizace in situ fluorescenční $7 D017404
- 650 _2
- $a mikrobiální interakce $7 D056265
- 650 _2
- $a oxychinolin $x farmakologie $7 D015125
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Džunková, Mária $u Joint Unit of Research in Genomics and Health, Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunidad Valenciana (FISABIO)-Salud Pública, Avenida de Catalunya 21, Valencia 46020, Spain Instituto Cavanilles de Biodiversidad y Biología Evolutiva, University of Valencia, c/Catedrático José Beltrán 2, 46980 Paterna, Valencia, Spain Centro de Investigación en Red en Epidemiología y Salud Pública (CIBEResp), Melchor Fernández Almagro 3-5, 28029 Madrid, Spain.
- 700 1_
- $a Musilova, Sarka $u Department of Microbiology, Nutrition and Dietetics, Faculty of Agrobiology, Food and Natural Resources, Czech University of Life Sciences Prague, Kamycka 129, 165 21 Prague 6-Suchdol, Czech Republic.
- 700 1_
- $a Vlkova, Eva $u Department of Microbiology, Nutrition and Dietetics, Faculty of Agrobiology, Food and Natural Resources, Czech University of Life Sciences Prague, Kamycka 129, 165 21 Prague 6-Suchdol, Czech Republic.
- 700 1_
- $a Kokoska, Ladislav $u Department of Crop Sciences and Agroforestry, Faculty of Tropical AgriSciences, Czech University of Life Sciences Prague, Kamycka 129, 165 21 Prague 6-Suchdol, Czech Republic.
- 700 1_
- $a Moya, Andrés $u Joint Unit of Research in Genomics and Health, Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunidad Valenciana (FISABIO)-Salud Pública, Avenida de Catalunya 21, Valencia 46020, Spain Instituto Cavanilles de Biodiversidad y Biología Evolutiva, University of Valencia, c/Catedrático José Beltrán 2, 46980 Paterna, Valencia, Spain Centro de Investigación en Red en Epidemiología y Salud Pública (CIBEResp), Melchor Fernández Almagro 3-5, 28029 Madrid, Spain.
- 700 1_
- $a D'Auria, Giuseppe $u Joint Unit of Research in Genomics and Health, Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunidad Valenciana (FISABIO)-Salud Pública, Avenida de Catalunya 21, Valencia 46020, Spain Instituto Cavanilles de Biodiversidad y Biología Evolutiva, University of Valencia, c/Catedrático José Beltrán 2, 46980 Paterna, Valencia, Spain Centro de Investigación en Red en Epidemiología y Salud Pública (CIBEResp), Melchor Fernández Almagro 3-5, 28029 Madrid, Spain dauria_giu@gva.es.
- 773 0_
- $w MED00002792 $t Journal of medical microbiology $x 1473-5644 $g Roč. 63, č. Pt 12 (2014), s. 1663-9
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/25298160 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20150420 $b ABA008
- 991 __
- $a 20150428101437 $b ABA008
- 999 __
- $a ok $b bmc $g 1071610 $s 896907
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2014 $b 63 $c Pt 12 $d 1663-9 $i 1473-5644 $m Journal of Medical Microbiology $n J Med Microbiol $x MED00002792
- LZP __
- $a Pubmed-20150420