2020
DOI: 10.1128/cmr.00047-19
|View full text |Cite
|
Sign up to set email alerts
|

Epidemiology of β-Lactamase-Producing Pathogens

Abstract: SUMMARY β-Lactam antibiotics have been widely used as therapeutic agents for the past 70 years, resulting in emergence of an abundance of β-lactam-inactivating β-lactamases. Although penicillinases in Staphylococcus aureus challenged the initial uses of penicillin, β-lactamases are most important in Gram-negative bacteria, particularly in enteric and nonfermentative pathogens, where collectively they confer resistance to all β-lactam-containing antibiotics. Critical β-lactamases are those enzymes whose genes a… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

8
487
3
15

Year Published

2020
2020
2024
2024

Publication Types

Select...
9
1

Relationship

0
10

Authors

Journals

citations
Cited by 536 publications
(513 citation statements)
references
References 390 publications
(435 reference statements)
8
487
3
15
Order By: Relevance
“…This is a rapidly evolving class of β-lactamases, usually from bla TEM–1 , bla TEM–2 , or bla SHV–1 genes, which can hydrolyze third-generation cephalosporins and aztreonam and can be inhibited by clavulanic acid ( Paterson and Bonomo, 2005 ). Although new members of the ESBLs family are often found, the earlier bla CTX–M–14 and bla CTX–M–15 enzymes are prevalent in the world at large ( Bush and Fisher, 2011 ; Bush and Bradford, 2020 ), while bla CTX–M–3 enzymes are prevalent mainly in Europe ( Canton et al, 2008 ). Resistance to extended-spectrum cephalosporins such as ceftazidime, cefotaxime, and cefepime were often observed when ESBLs appeared in Klebsiella sp.…”
Section: Discussionmentioning
confidence: 99%
“…This is a rapidly evolving class of β-lactamases, usually from bla TEM–1 , bla TEM–2 , or bla SHV–1 genes, which can hydrolyze third-generation cephalosporins and aztreonam and can be inhibited by clavulanic acid ( Paterson and Bonomo, 2005 ). Although new members of the ESBLs family are often found, the earlier bla CTX–M–14 and bla CTX–M–15 enzymes are prevalent in the world at large ( Bush and Fisher, 2011 ; Bush and Bradford, 2020 ), while bla CTX–M–3 enzymes are prevalent mainly in Europe ( Canton et al, 2008 ). Resistance to extended-spectrum cephalosporins such as ceftazidime, cefotaxime, and cefepime were often observed when ESBLs appeared in Klebsiella sp.…”
Section: Discussionmentioning
confidence: 99%
“…The remaining isolates belonged to E. coli and K. pneumonia species. They do not constitutively express these types of enzyme because they lack the regulating genes, and their expression is produced by the acquisition of plasmids from the chromosomal β-lactamases of E. cloacae (ACT-1 and MIR-1), C. freundii (CMY), Hafnia alvei (ACC-1), and M. morganii (DHA-1) [ 25 ]. The observation of CMY-2 and DHA-1 in E. coli isolates and DHA-1 in K. pneumoniae isolates is very frequent [ 26 ].…”
Section: Discussionmentioning
confidence: 99%
“…CTX-M β-lactamases hydrolyze cefotaxime and ceftriaxone better than ceftazidime. However, the spectrum of hydrolysis varies by the enzyme, and there are CTX enzymes (CTX-M-15, CTXM-16 and CTX-M19) that exhibit enhanced catalytic efficiencies against ceftazidime [ 11 , 56 ].…”
Section: Classification Of Esblsmentioning
confidence: 99%