Everything about Beta-lactamase totally explained
Beta-lactamases are
enzymes produced by some bacteria and are responsible for their
resistance to
beta-lactam antibiotics like
penicillins,
cephalosporins,
cephamycins and
carbapenems. These
antibiotics have a common element in their molecular structure: a four-atom ring known as a
beta-lactam. The lactamase enzyme breaks that ring open, deactivating the molecule's antibacterial properties.
Beta-lactam antibiotics are typically used to treat a broad spectrum of gram positive and gram-negative bacteria. Beta-lactamases produced by gram-positive organisms are usually secreted.
Beta-lactamase may be clinically beneficial when orally administered to preserve the natural intestinal flora during the
parenteral administration of anti-biotics. "This could provide protection against a broad range of nosocomial pathogens," per Dr. Usha Stiefel at the 47th annual Interscience Conference of Antimicrobial Agents and Chemotherapy.
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The structure of a
Streptomyces β lactamase is given by .
Penicillinase
Penicillinase is a specific type of β lactamase, showing specificity for
penicillins, again by
hydrolysing the
beta-lactam ring. Molecular weights of the various penicillinases tend to cluster near 50,000.
Penicillinase was the first β-lactamase to be identified: it was first isolated by Abraham and Chain in 1940 from gram-negative
E. coli even before penicillin entered clinical use but penicillinase production quickly spread to bacteria that previously didn't produce it or only produced it rarely. Penicillinase-resistant β lactams such as
methicillin were developed, but there's now widespread
resistance to even these (for example,
MRSA).
Classification of Beta Lactamase
Functional Classification
Group 1
CEPHALOSPORINASE, Molecular Class C
(not inhibited by clavulanic acid)
Group 1 are cephalosporinases not inhibited by
clavulanic acid, belonging to the molecular class C
Group 2
Group 2 are penicillinases, cephalosporinases, or both inhibited by clavulanic acid, corresponding to the molecular classes A and D reflecting the original TEM and SHV genes. However, because of the increasing number of TEM and SHV derived lactamases need
zinc for their action
"Penicillinase" was discovered in 1940 and re-named Beta-lactamase when the structure of the Beta-lactam ring was finally elucidated.
Resistance in gram negative bacteria
Among gram-negative bacteria, the emergence of resistance to expanded-spectrum cephalosporins has been a major concern. It appeared initially in a limited number of bacterial species (
E. cloacae,
C. freundii,
S. marcescens, and
P. aeruginosa ) that could mutate to hyperproduce their chromosomal class C β-lactamase. A few years later, resistance appeared in bacterial species not naturally producing AmpC enzymes (
K. pneumoniae,
Salmonella spp.,
P. mirabilis) due to the production of TEM- or SHV-type ESBLs. Characteristically, such resistance has included oxyimino- (for example
ceftizoxime,
cefotaxime,
ceftriaxone, and
ceftazidime, as well as the oxyimino-monobactam
aztreonam )but not 7-alpha-methoxy-cephalosporins (
cephamycins) or in other words (
cefoxitin and
cefotetan ), has been blocked by inhibitors such as
clavulanate,
sulbactam, or
tazobactam, and didn't involve
carbapenems. Plasmid-mediated AmpC β-lactamases represent a new threat since they confer resistance to 7-alpha-methoxy-cephalosporins (
cephamycins) such as
cefoxitin or
cefotetan, are not affected by commercially available β-lactamase inhibitors, and can, in strains with loss of outer membrane porins, provide resistance to carbapenems..
Extended spectrum beta lactamase (ESBL)
Members of the family
Enterobacteriaceae commonly express plasmid-encoded β-lactamases (for example, TEM-1, TEM-2, and SHV-1) which confer resistance to penicillins but not to expanded-spectrum cephalosporins . In the mid-1980s a new group of enzymes, the extended-spectrum b-lactamases (ESBLs), was detected. (first detected in Germany in 1983). ESBLs are beta-lactamases that hydrolyze extended-spectrum cephalosporins with an oxyimino side chain. These cephalosporins include
cefotaxime,
ceftriaxone, and
ceftazidime, as well as the oxyimino-monobactam
aztreonam. ESBLs confer resistance to expanded-spectrum cephalosporins (for example
ceftriaxone,
cefotaxime,and
ceftazidime ),
aztreonam, and related oxyimino-beta lactams. Typically, they derive from genes for TEM-1, TEM-2, or SHV-1 by mutations that alter the amino acid configuration around the active site of these β-lactamases. This extends the spectrum of β-lactam antibiotics susceptible to hydrolysis by these enzymes. An increasing number of ESBLs not of TEM or SHV lineage have recently been described.. The ESBLs are frequently plasmid encoded. Plasmids responsible for ESBL production frequently carry genes encoding resistance to other drug classes (for example, aminoglycosides). Therefore, antibiotic options in the treatment of ESBL-producing organisms are extremely limited. Carbapenems are the treatment of choice for serious infections due to ESBL-producing organisms, yet carbapenem-resistant isolates have recently been reported. ESBL-producing organisms may appear susceptible to some extended-spectrum cephalosporins. However, treatment with such antibiotics has been associated with high failure rates.
Types
TEM beta-lactamases (class A)
TEM-1 is the most commonly encountered beta-lactamase in
gram-negative bacteria. Up to 90% of ampicillin resistance in
E. coli is due to the production of TEM-1. Also responsible for the ampicillin and penicillin resistance that's seen in
H. influenzae and
N. gonorrhoeae in increasing numbers. Although TEM-type beta-lactamases are most often found in
E. coli and
K. pneumoniae, they're also found in other species of gram-negative bacteria with increasing frequency. The amino acid substitutions responsible for the ESBL phenotype cluster around the active site of the enzyme and change its configuration, allowing access to oxyimino-beta-lactam substrates. Opening the active site to beta-lactam substrates also typically enhances the susceptibility of the enzyme to b-lactamase inhibitors, such as clavulanic acid. Single amino acid substitutions at positions 104, 164, 238, and 240 produce the ESBL phenotype, but ESBLs with the broadest spectrum usually have more than a single amino acid substitution. Based upon different combinations of changes, currently 140 TEM-type enzymes have been described. TEM-10, TEM-12, and TEM-26 are among the most common in the United States.
SHV beta-lactamases (class A)
SHV-1 shares 68 percent of its amino acids with TEM-1 and has a similar overall structure. The SHV-1 beta-lactamase is most commonly found in
K. pneumoniae and is responsible for up to 20% of the plasmid-mediated ampicillin resistance in this species. ESBLs in this family also have amino acid changes around the active site, most commonly at positions 238 or 238 and 240. More than 60 SHV varieties are known. They are the predominant ESBL type in Europe and the United States and are found worldwide. SHV-5 and SHV-12 are among the most common.
CTX-M beta-lactamases (class A)
These enzymes were named for their greater activity against
cefotaxime than other oxyimino-beta-lactam substrates (eg,
ceftazidime,
ceftriaxone, or
cefepime). Rather than arising by mutation, they represent examples of plasmid acquisition of beta-lactamase genes normally found on the chromosome of
Kluyvera species, a group of rarely pathogenic commensal organisms. These enzymes are not very closely related to TEM or SHV beta-lactamases in that they show only approximately 40% identity with these two commonly isolated beta-lactamases. More than 40 CTX-M enzymes are currently known. Despite their name, a few are more active on
ceftazidime than
cefotaxime. They have mainly been found in strains of
Salmonella enterica serovar
Typhimurium and
E. coli, but have also been described in other species of
Enterobacteriaceae and are the predominant ESBL type in parts of South America. (They are also seen in eastern Europe) CTX-M-14, CTX-M-3, and CTX-M-2 are the most widespread. CTX-M-15 is currently (2006) the most widespread type in
E. coli the UK and is widely prevalent in the community.
OXA beta-lactamases (class D)
OXA beta-lactamases were long recognized as a less common but also plasmid-mediated beta-lactamase variety that could hydrolyze
oxacillin and related anti-staphylococcal penicillins. These beta-lactamases differ from the TEM and SHV enzymes in that they belong to molecular class D and functional group 2d . The OXA-type beta-lactamases confer resistance to
ampicillin and
cephalothin and are characterized by their high hydrolytic activity against
oxacillin and
cloxacillin and the fact that they're poorly inhibited by
clavulanic acid. Amino acid substitutions in OXA enzymes can also give the ESBL phenotype. While most ESBLs have been found in
E. coli,
K. pneumoniae, and other
Enterobacteriaceae, the OXA-type ESBLs have been found mainly in
P. aeruginosa. OXA-type ESBLs have been found mainly in
Pseudomonas aeruginosa isolates from Turkey and France. The OXA beta-lactamase family was originally created as a phenotypic rather than a genotypic group for a few beta-lactamases that had a specific hydrolysis profile. Therefore, there's as little as 20% sequence homology among some of the members of this family. However, recent additions to this family show some degree of homology to one or more of the existing members of the OXA beta-lactamase family. Some confer resistance predominantly to ceftazidime, but OXA-17 confers greater resistance to cefotaxime and cefepime than it does resistance to ceftazidime.
Others
Other plasmid-mediated ESBLs, such as PER, VEB, GES, and IBC beta-lactamases, have been described but are uncommon and have been found mainly in
P. aeruginosa and at a limited number of geographic sites. PER-1 in isolates in Turkey, France, and Italy; VEB-1 and VEB-2 in strains from Southeast Asia; and GES-1, GES-2, and IBC-2 in isolates from South Africa, France, and Greece. PER-1 is also common in multiresistant acinetobacter species in Korea and Turkey. Some of these enzymes are found in Enterobacteriaceae as well, whereas other uncommon ESBLs (such as BES-1, IBC-1, SFO-1, and TLA-1) have been found only in Enterobacteriaceae.
Treatment
While ESBL-producing organisms were previously associated with hospitals and institutional care, these organisms are now increasingly found in the community. CTX-M-15 positive
E. coli are a cause of community-acquired
urinary infections in the UK, and tend to be resistant to all oral β-lactam antibiotics, as well as
quinolones and
sulfonamides. Treatment options may include
nitrofurantoin,
fosfomycin,
mecillinam and
chloramphenicol. In desperation, once-daily
ertapenem or
gentamicin injections may also be used.
Inhibitor resistant β-lactamases
Although the inhibitor-resistant β-lactamases are not ESBLs, they're often discussed with ESBLs because they're also derivatives of the classical TEM- or SHV-type enzymes. These enzymes were at first given the designation IRT for inhibitor-resistant TEM β-lactamase; however, all have subsequently been renamed with numerical TEM designations. There are at least 19 distinct inhibitor-resistant TEM β-lactamases. Inhibitor-resistant TEM β-lactamases have been found mainly in clinical isolates of
E. coli, but also some strains of
K. pneumoniae,
Klebsiella oxytoca,
P. mirabilis, and
Citrobacter freundii .Although the inhibitor-resistant TEM variants are resistant to inhibition by
clavulanic acid and
sulbactam, thereby showing clinical resistance to the beta-lactam--lactamase inhibitor combinations of
amoxicillin-
clavulanate (
Co-amoxiclav),
ticarcillin-
clavulanate, and
ampicillin/sulbactam, they remain susceptible to inhibition by
tazobactam and subsequently the combination of
piperacillin/tazobactam. To date, these beta-lactamases have primarily been detected in France and a few other locations within Europe..
AmpC type β-lactamases(Class C)
AmpC type β-lactamases are commonly isolated from extended-spectrum cephalosporin-resistant Gram-negative bacteria. AmpC β-lactamases (also termed class C or group 1) are typically encoded on the chromosome of many Gram-negative bacteria including
Citrobacter,
Serratia and
Enterobacter species where its expression is usually inducible; it may also occur on
Escherichia coli but isn't usually inducible, although it can be hyperexpressed. AmpC type β-lactamases may also be carried on plasmids. AmpC β-lactamases, in contrast to ESBLs, hydrolyse broad and extended-spectrum cephalosporins (cephamycins as well as to oxyimino-β-lactams) but are not inhibited by β-lactamase inhibitors such as
clavulanic acid.
Carbapenemases
Carbapenems are famously stable to AmpC β-lactamases and extended-spectrum-β-lactamases. Carbapenemases are a diverse group of b-lactamases that are active not only against the oxyimino-cephalosporins and cephamycins but also against the carbapenems. Aztreonam is stable to the metallo-β-lactamases
but many IMP and VIM producers are resistant, owing to other mechanisms. Carbapenemases were formerly believed to derive only from classes A, B, and D, but a class C carbapenemase has been described.
IMP-type carbapenemases (one of the metallo-b-lactamases)
Plasmidmediated IMP-type carbapenemases, 17 varieties of which are currently known, became established in Japan in the 1990s in both enteric gram-negative organisms and in
Pseudomonas and
Acinetobacter species. IMP enzymes spread slowly to other countries in the Far East, were reported from Europe in 1997, and have been found in Canada and Brazil.
VIM (Verona integron-encoded metallo-b-lactamase)
A second growing family of carbapenemases, the VIM family, was reported from Italy in 1999 and now includes 10 members, which have a wide geographic distribution in Europe, South America, and the Far East and have been found in the United States. VIM-1 was discovered in P. aeruginosa in Italy in 1996; subsequently, VIM-2 -now the predominant variant- was found repeatedly in Europe and the Far East; VIM-3 and -4 are minor variants of VIM-2 and -1, respectively. VIM enzymes mostly occur in P. aeruginosa, also P. putidaand, very rarely, Enterobacteriaceae
Amino acid sequence diversity is up to 10% in the VIM family, 15% in the IMP family, and 70% between VIM and IMP. Enzymes of both the families nevertheless are similar.1 Both are integron-associated, sometimes within plasmids. Both hydrolyse all β-lactams except monobactams, and evade all β-lactam inhibitors.
OXA (oxacillinase) group of β-lactamases (Class D)
The OXA group of β-lactamases mainly occur in Acinetobacter species and are divided into two clusters. OXA carbapenemases hydrolyse carbapenems very slowly
in vitro, and the high MICs seen for some Acinetobacter hosts (>64 mg/L) may reflect secondary mechanisms. They are sometimes augmented in clinical isolates by additional resistance mechanisms, such as impermeability or efflux.
KPC (K. pneumoniae carbapenemase) (Class A)
A few class A enzymes, notably the plasmid-mediated KPC enzymes, are effective carbapenemases as well. Three variants are known, distinguished by one or two amino-acid substitutions. KPC-1 was found in North Carolina, KPC-2 in Baltimore and KPC-3 in New York. They have only 45% homology with SME and NMC/IMI enzymes and, unlike them, can be encoded by self-transmissible plasmids.
CMY (Class C)
The first class C carbapenemase was described in 2006 and was isolated from a virulent strain of
Enterobacter aerogenes. It is carried on a plasmid, pYMG-1, and is therefore transmissible to other bacterial strains.
SME, IMI, NMC and CcrA
generally of little clinical significance.
CcrA (CfiA). Its gene occurs in c. 1-3% of B. fragilis isolates, but fewer produce the enzyme since expression demands appropriate migration of an insertion sequence. CcrA was known before imipenem was introduced, and producers have shown little subsequent increase.
Treatment of ESBL/AmpC/carbapenemases
General Overview
Generally, an isolate is suspected to be an ESBL producer when it shows
in vitro susceptibility to the second generation cephalosporins (cefoxitin, cefotetan) but resistance to the third generation cephalosporins and to aztreonam. Moreover, one should suspect these strains when treatment with these agents for Gram negative infections fails despite reported
in vitro susceptibility. Once an ESBL producing strain is detected, the laboratory should report it as “resistant” to all penicillins, cephalosporins, and aztreonam, even if they test as susceptible. Associated resistance to
aminoglycosides and
trimethoprim-
sulfamethoxazole as well as high frequency of co-existence of
fluoroquinolone resistance creates problems. Beta-lactamase inhibitors such as
clavulanate,
sulbactam or
tazobactam in vitro inhibit most ESBLs, but the clinical effectiveness of beta-lactam/beta-lactamase inhibitor combinations can't be relied on consistently for therapy. Although
cephamycins (
cefoxitin and
cefotetan) are not hydrolyzed by majority of ESBLs but are hydrolyzed by associated AmpC-type β-lactamase. similarly β-lactam/β-lactamase inhibitor combinations may not be effective against organisms that produce AmpC-type β-lactamase. Also sometimes these strains decrease the expression of outer membrane proteins, rendering them resistant to cephamycins.
In vivo studies have yielded mixed results against ESBL-producing
K. pneumoniae. (
Cefepime, a fourth-generation cephalosporin, has demonstrated
in vitro stability in the presence of many ESBL/AmpC strains.) Currently,
carbapenems are generally regarded as the preferred agent for treatment of infections due to ESBL-producing organisms. Carbapenems are resistant to ESBL-mediated hydrolysis and exhibit excellent
in vitro activity against strains of
Enterobacteriaceae expressing ESBLs.
According to genes
ESBLs
Strains producing only ESBLs are susceptible to
cephamycins and
carbapenems in vitro and show little if any inoculum effect with these agents.
For organisms producing
TEM and
SHV type ESBLs, apparent
in vitro sensitivity to
cefepime and to
piperacillin/tazobactam is common, but both drugs show an inoculum effect, with diminished susceptibility as the size of the inoculum is increased from 100000 to 10000000 organisms.
Strains with some
CTX-M–type and
OXA-type ESBLs are resistant to
cefepime on testing, despite the use of a standard inoculum.
Inhibitor-Resistant β-Lactamases
Although the inhibitor-resistant TEM variants are resistant to inhibition by
clavulanic acid and
sulbactam, thereby showing clinical resistance to the beta-lactam--lactamase inhibitor combinations of
amoxicillin-
clavulanate (
Co-amoxiclav),
ticarcillin-
clavulanate, and
ampicillin/sulbactam, they remain susceptible to inhibition by
tazobactam and subsequently the combination of
piperacillin/tazobactam.
AmpC
AmpC-producing strains are typically resistant to
oxyimino-beta lactams and to
cephamycins and are susceptible to
carbapenems; however, diminished porin expression can make such a strain carbapenem-resistant as well.
Carbapenemases
Strains with
IMP-, VIM-, and OXA-type carbapenemases usually remain susceptible to
aztreonam. Resistance to non–b-lactam antibiotics is common in strains making any of these enzymes, such that alternative options for non–b-lactam therapy need to be determined by direct susceptibility testing. Resistance to
fluoroquinolones and
aminoglycosides is especially high.
According to Species
E. coli or klebsiella
For infections caused by ESBL-producing
E. coli or
klebsiella species, treatment with
imipenem or
meropenem has been associated with the best outcomes in terms of survival and bacteriologic clearance.
Cefepime and
piperacillin/tazobactam have been less successful.
Ceftriaxone,
cefotaxime, and
ceftazidime have failed even more often, despite the organism’s susceptibility to the antibiotic
in vitro. Several reports have documented failure of
cephamycin therapy as a result of resistance due to porin loss. Some patients have responded to
aminoglycoside or
quinolone therapy, but in a recent comparison of
ciprofloxacin and
imipenem for bacteremia involving an ESBL-producing
K. pneumoniae,
imipenem produced the better outcome.
P. aeruginosa
There have been few clinical studies to define the optimal therapy for infections caused by ESBL producing
P. aeruginosa strains.
Further Information
Get more info on 'Beta-lactamase'.
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