-
Je něco špatně v tomto záznamu ?
Ribosome-Mediated Attenuation of vga(A) Expression Is Shaped by the Antibiotic Resistance Specificity of Vga(A) Protein Variants
V. Vimberg, JP. Cavanagh, M. Novotna, J. Lenart, B. Nguyen Thi Ngoc, J. Vesela, M. Pain, M. Koberska, G. Balikova Novotna
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Free Medical Journals
od 1972 do Před 6 měsíci
Freely Accessible Science Journals
od 1995 do Před 6 měsíci
PubMed Central
od 1972 do Před 1 rokem
Europe PubMed Central
od 1972 do Před 6 měsíci
Open Access Digital Library
od 1972-01-01
Open Access Digital Library
od 1972-01-01
PubMed
32816732
DOI
10.1128/aac.00666-20
Knihovny.cz E-zdroje
- MeSH
- antibakteriální látky farmakologie MeSH
- bakteriální proteiny genetika MeSH
- linkosamidy MeSH
- makrolidy MeSH
- mnohočetná bakteriální léková rezistence * MeSH
- ribozomy genetika MeSH
- streptogramin A * MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Vga(A) protein variants confer different levels of resistance to lincosamides, streptogramin A, and pleuromutilins (LSAP) by displacing antibiotics from the ribosome. Here, we show that expression of vga(A) variants from Staphylococcus haemolyticus is regulated by cis-regulatory RNA in response to the LSAP antibiotics by the mechanism of ribosome-mediated attenuation. The specificity of induction depends on Vga(A)-mediated resistance rather than on the sequence of the riboregulator. Fine tuning between Vga(A) activity and its expression in response to the antibiotics may contribute to the selection of more potent Vga(A) variants because newly acquired mutation can be immediately phenotypically manifested.
Department of Clinical Medicine UiT The Arctic University of Norway Tromsø Norway
Department of Genetics and Microbiology Faculty of Science Charles University Prague Czech Republic
Department of Pediatrics University Hospital of North Norway Tromsø Norway
Institute of Microbiology of the Czech Academy of Sciences Vestec Czech Republic
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc21019969
- 003
- CZ-PrNML
- 005
- 20250923163117.0
- 007
- ta
- 008
- 210728s2020 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1128/AAC.00666-20 $2 doi
- 035 __
- $a (PubMed)32816732
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Vimberg, Vladimir $u Institute of Microbiology of the Czech Academy of Sciences, Vestec, Czech Republic
- 245 10
- $a Ribosome-Mediated Attenuation of vga(A) Expression Is Shaped by the Antibiotic Resistance Specificity of Vga(A) Protein Variants / $c V. Vimberg, JP. Cavanagh, M. Novotna, J. Lenart, B. Nguyen Thi Ngoc, J. Vesela, M. Pain, M. Koberska, G. Balikova Novotna
- 520 9_
- $a Vga(A) protein variants confer different levels of resistance to lincosamides, streptogramin A, and pleuromutilins (LSAP) by displacing antibiotics from the ribosome. Here, we show that expression of vga(A) variants from Staphylococcus haemolyticus is regulated by cis-regulatory RNA in response to the LSAP antibiotics by the mechanism of ribosome-mediated attenuation. The specificity of induction depends on Vga(A)-mediated resistance rather than on the sequence of the riboregulator. Fine tuning between Vga(A) activity and its expression in response to the antibiotics may contribute to the selection of more potent Vga(A) variants because newly acquired mutation can be immediately phenotypically manifested.
- 650 _2
- $a antibakteriální látky $x farmakologie $7 D000900
- 650 _2
- $a bakteriální proteiny $x genetika $7 D001426
- 650 12
- $a mnohočetná bakteriální léková rezistence $7 D024901
- 650 _2
- $a linkosamidy $7 D055231
- 650 _2
- $a makrolidy $7 D018942
- 650 _2
- $a ribozomy $x genetika $7 D012270
- 650 12
- $a streptogramin A $7 D025364
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Cavanagh, Jorunn Pauline $u Department of Pediatrics, University Hospital of North Norway, Tromsø, Norway $u Department of Clinical Medicine, UiT-The Arctic University of Norway, Tromsø, Norway
- 700 1_
- $a Novotna, Michaela $u Institute of Microbiology of the Czech Academy of Sciences, Vestec, Czech Republic
- 700 1_
- $a Lenart, Jakub $u Institute of Microbiology of the Czech Academy of Sciences, Vestec, Czech Republic $u Department of Genetics and Microbiology, Faculty of Science, Charles University, Prague, Czech Republic
- 700 1_
- $a Nguyen Thi Ngoc, Bich $u Institute of Microbiology of the Czech Academy of Sciences, Vestec, Czech Republic
- 700 1_
- $a Vesela, Jana $u Institute of Microbiology of the Czech Academy of Sciences, Vestec, Czech Republic
- 700 1_
- $a Pain, Maria $u Department of Clinical Medicine, UiT-The Arctic University of Norway, Tromsø, Norway
- 700 1_
- $a Koběrská, Markéta $u Institute of Microbiology of the Czech Academy of Sciences, Vestec, Czech Republic $7 xx0335030
- 700 1_
- $a Balikova Novotna, Gabriela $u Institute of Microbiology of the Czech Academy of Sciences, Vestec, Czech Republic gnovotna@biomed.cas.cz
- 773 0_
- $w MED00009215 $t Antimicrobial agents and chemotherapy $x 1098-6596 $g Roč. 64, č. 11 (2020)
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/32816732 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y p $z 0
- 990 __
- $a 20210728 $b ABA008
- 991 __
- $a 20250923163113 $b ABA008
- 999 __
- $a ok $b bmc $g 1690707 $s 1140415
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2020 $b 64 $c 11 $e 20201020 $i 1098-6596 $m Antimicrobial agents and chemotherapy $n Antimicrob Agents Chemother $x MED00009215
- LZP __
- $a Pubmed-20210728