In Silico Analysis of Extended-Spectrum beta-Lactamases in Bacteria
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15110%2F21%3A73610972" target="_blank" >RIV/61989592:15110/21:73610972 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/61989592:15310/21:73610972
Výsledek na webu
<a href="https://www.mdpi.com/2079-6382/10/7/812" target="_blank" >https://www.mdpi.com/2079-6382/10/7/812</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.3390/antibiotics10070812" target="_blank" >10.3390/antibiotics10070812</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
In Silico Analysis of Extended-Spectrum beta-Lactamases in Bacteria
Popis výsledku v původním jazyce
The growing bacterial resistance to available beta-lactam antibiotics is a very serious public health problem, especially due to the production of a wide range of beta-lactamases. At present, clinically important bacteria are increasingly acquiring new elements of resistance to carbapenems and polymyxins, including extended-spectrum beta-lactamases (ESBLs), carbapenemases and phosphoethanolamine transferases of the MCR type. These bacterial enzymes limit therapeutic options in human and veterinary medicine. It must be emphasized that there is a real risk of losing the ability to treat serious and life-threatening infections. The present study aimed to design specific oligonucleotides for rapid PCR detection of ESBL-encoding genes and in silico analysis of selected ESBL enzymes. A total of 58 primers were designed to detect 49 types of different ESBL genes. After comparing the amino acid sequences of ESBLs (CTX-M, SHV and TEM), phylogenetic trees were created based on the presence of conserved amino acids and homologous motifs. This study indicates that the proposed primers should be able to specifically detect more than 99.8% of all described ESBL enzymes. The results suggest that the in silico tested primers could be used for PCR to detect the presence of ESBL genes in various bacteria, as well as to monitor their spread.
Název v anglickém jazyce
In Silico Analysis of Extended-Spectrum beta-Lactamases in Bacteria
Popis výsledku anglicky
The growing bacterial resistance to available beta-lactam antibiotics is a very serious public health problem, especially due to the production of a wide range of beta-lactamases. At present, clinically important bacteria are increasingly acquiring new elements of resistance to carbapenems and polymyxins, including extended-spectrum beta-lactamases (ESBLs), carbapenemases and phosphoethanolamine transferases of the MCR type. These bacterial enzymes limit therapeutic options in human and veterinary medicine. It must be emphasized that there is a real risk of losing the ability to treat serious and life-threatening infections. The present study aimed to design specific oligonucleotides for rapid PCR detection of ESBL-encoding genes and in silico analysis of selected ESBL enzymes. A total of 58 primers were designed to detect 49 types of different ESBL genes. After comparing the amino acid sequences of ESBLs (CTX-M, SHV and TEM), phylogenetic trees were created based on the presence of conserved amino acids and homologous motifs. This study indicates that the proposed primers should be able to specifically detect more than 99.8% of all described ESBL enzymes. The results suggest that the in silico tested primers could be used for PCR to detect the presence of ESBL genes in various bacteria, as well as to monitor their spread.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10606 - Microbiology
Návaznosti výsledku
Projekt
—
Návaznosti
S - Specificky vyzkum na vysokych skolach<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2021
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Antibiotics-Basel
ISSN
2079-6382
e-ISSN
—
Svazek periodika
7
Číslo periodika v rámci svazku
10
Stát vydavatele periodika
CH - Švýcarská konfederace
Počet stran výsledku
21
Strana od-do
"nestránkováno"
Kód UT WoS článku
000678883200001
EID výsledku v databázi Scopus
2-s2.0-85110723258