Traditionally, cephalosporins are divided into first-generation, second-generation, third-generation, fourth-generation and fifth-generation, according to their antibacterial activity (Table 1). They differ in their antimicrobial spectrum, β-lactamase stability, absorption, metabolism, stability and side-effects. First-generation members have narrowed or limited activity when compared with third-generation, fourth-generation or fifth-generation broader spectrum cephalosporins. The structure–activity features responsible for the various properties in the penicillins (oral activity, β-lactamase stability, etc.) are similar with the cephalosporins .
First-generation cephalosporins are very active against Gram-positive cocci, except enterococci and methicillin-resistant staphylococci, and moderately active against some Gram-negative rods primarily Escherichia coli, Proteus, and Klebsiella. Anaerobic cocci are often sensitive, but Bacteroides fragilis is not.
Cephalexin, cephradine and cefadroxil are absorbed from the gut to a variable extent and can be used to treat urinary and respiratory tract infections. Other first-generation cephalosporins must be injected to give adequate levels in blood and tissues. Cefazolin is a choice for surgical prophylaxis because it gives the highest (90–120 μg/ml) levels with every 8-h dosing. Cephalothin and cephapirin in the same dose give lower levels. None of the first-generation drugs penetrate the central nervous system, and they are not drugs of first choice for any infection .
The second-generation cephalosporins are a heterogeneous group. All are active against organisms covered by first-generation drugs, but have extended coverage against Gram-negative rods, including Klebsiella and Proteus, and not against Pseudomonas aeruginosa. Some (not all) oral second-generation cephalosporins can be used to treat sinusitis and otitis caused by Haemophilus influenzae, including β-lactamase-producing strains.
Cefoxitin and cefotetan are not cephalosporins but cephamycins. Often, cephamycins are considered as second-generation cephlosporins for its clinical utility. They are particularly active against B. fragilis and, thus, are used in mixed anaerobic infections, including peritonitis or pelvic inflammatory disease .
Third-generation cephalosporins have decreased activity against Gram-positive cocci, and enterococci often produce super-infections during their use. Most third-generation cephalosporins are active against staphylococci, but ceftazidime is only weakly active . A major advantage of third-generation drugs is their enhanced activity against Gram-negative rods . Whereas second-generation drugs tend to fail against P. aeruginosa, ceftazidime or cefoperazone may succeed. Thus, third-generation drugs are very useful in the management of hospital-acquired Gram-negative bacteremia. In immunocompromised patients, these drugs are often combined with an aminoglycoside. Ceftazidime may also be lifesaving in severe melioidosis (Pseudomonas pseudomallei) infection.
Another important distinguishing feature of several third-generation drugs is the ability to reach the central nervous system and to appear in the spinal fluid in sufficient concentrations to treat meningitis caused by Gram-negative rods. Cefotaxime, ceftriaxone or ceftizoxime given intravenously is normally the choice for management of Gram-negative bacteria sepsis and meningitis .
Cefepime and cefpirome are the only fourth-generation cephalosporins in the market. They have enhanced activity against Enterobacter and Citrobacter species that are resistant to third-generation cephalosporins. Cefepime has activity comparable with that of ceftazidime against P. aeruginosa. The activity against streptococci and methicillin-susceptible staphylococci is greater than that of ceftazidime and comparable with that of the other third-generation compounds .
Fifth-generation cephalosporins were developed in the laboratory to specifically target against resistant strains of bacteria. Particularly, ceftobiprole is effective against methicillin-resistant S. aureus (MRSA). Until this drug was introduced, this strain of Staphylococcus was impossible to contain. Other drugs in this class include cefotetan and cefoxitin, used against anaerobic Gram-negative bacilli. This class of drugs is ineffective against enterococci bacteria. Ceftaroline is a new oxyimino-cefalosporine that is also effective against MRSA , but ineffective against extended-spectrum β-lactamase (ESBL) producers or active AmpCs. However, ceftaroline has showed to be effective against broader spectrum β-lactamases (ESBLs and AmpCs) in synergism with amikacin .
Monobactams have a monocyclic β-lactam ring and are resistant to β-lactamases. They are active against Gram-negative rods, but not against Gram-positive bacteria or anaerobes. The first drug to become available was aztreonam . Patients with immunoglobulin-E-mediated penicillin allergy can tolerate it without reaction and, apart from skin rashes and minor aminotransferase disturbances, no major toxicity has been reported. Super-infections with staphylococci and enterococci can occur .
These drugs are structurally related to β-lactam antibiotics. Imipenem, the first drug of this type, has good activity against many Gram-negative rods, Gram-positive organisms and anaerobes. It is resistant to some β-lactamases, but is inactivated by dihydropeptidases in renal tubules. Consequently, it is administered together with a peptidase inhibitor such as cilastatin .
Imipenem (Fig. 4) penetrates the body tissues and fluids well, including cerebrospinal fluid. Imipenem may be indicated for infections caused by microorganisms resistant to other drugs. Nevertheless, Pseudomonas species rapidly develop resistance to this drug, and the concomitant use of an aminoglycoside is, therefore, required. However, this procedure may not delay the development of resistance .
Meropenem (Fig. 4) is similar to imipenem in pharmacology and antimicrobial spectrum of activity. However, it is not inactivated by dipeptidases and is less likely to cause seizures than imipenem .
Antimicrobial resistance to β-lactam
Since the discovery of the first antibiotic, penicillin, by Alexander Flemming in 1928, until now enormous changes in this field have occurred. First of all, the use of antibiotic was a medical revolution like no other in the treatment of infectious diseases . Nevertheless, a rapid appearance of a great number of bacteria presenting acquired resistance was observed, thus resulting in therapeutic failures. Six years after the introduction of benzylpenicillin in the market, for example, the frequency of staphylococci resistance in British hospitals increased from less than 10% up to 60% and today is over 90% at world level .
Antibiotic mode of action and resistance
β-Lactams are a group of antibiotics that have specificity for bacteria. Bacteria are prokaryotic and, hence, offer numerous structural and metabolic effects that differ from those of the eukaryotic cells such as the animal or human host. There are several possible targets for antibiotics [27,28]. Generally speaking, we can group the mechanisms of action of antibiotics into five categories (Fig. 5): inhibition of cell wall synthesis; impairment cytoplasmic membrane; inhibition of nucleic acid synthesis; inhibition of protein synthesis; and metabolic antagonist action. In general, there are four basic mechanisms (Fig. 5) by which resistance to drug may occur in bacteria: alteration of the antimicrobial target that can be due to the complete loss of affinity or simple reduction of it; reduction in the amount of the antimicrobial that reaches the target by entrance reduction caused by a decrease permeability due to porin mutation or by an exit increase caused by the pumping out by an efflux transporter; the presence of an enzymatic mechanism that totally or partially destroys the antimicrobial molecules; and the development of an alternative metabolic pathway involving precursors [28–30].
The most widespread mode of clinical resistance development to β-lactam antibiotics is the expression of β-lactamases that hydrolyze the antibiotic. It is estimated that $30 billion is the annual economic loss to the US population from disease caused by β-lactamase-producing resistant bacteria .
β-Lactamases hydrolyze the four-membered β-lactam ring in both penicillin and cephalosporin classes of antibiotics as well as the carbapenem series. They thereby destroy the antibacterial activity by deactivating the chemical properties of the drug molecule, which is the chemically reactive acylating group for modifying the active site serine side-chains in the PBPs. β-Lactamase activity was detected a few years before clinical use of penicillins in humans, indicating its presence in soil bacteria that combat the natural product penicillins .
There are many different types of β-lactamases and several different systems have been proposed to classify them. The functional classification was first attempted by Bush and collaborators  in 1989 and then improved in 1995. The structural classification proposed by Ambler  in 1980 suggests four distinct molecular classes: A, B, C and D based on the amino acid sequencing.
Ambler β-lactamases molecular classes A, C and D are active site serine enzymes, with architectural and mechanistic similarities to the PBPs, suggesting evolution from PBPs. In the A, C and D classes of β-lactamases, the same type of penicilloyl-O-Ser enzyme covalent intermediates are formed as in the catalytic cycle of PBPs, which attack and open the β-lactam ring and become self-acylated. There is no such covalent penicilloyl enzyme intermediate in the catalytic site of the zinc-dependent, class B β-lactamases, which enables the failure of class B β-lactamases to be inhibited by certain drugs .
It has been argued that PBPs may have evolved into β-lactamases independently to generate the different orientations of the active site residues in the class A, C and D β-lactamases .
The first plasmid-mediated β-lactamase in Gram-negative bacteria, TEM-1, was described in the early 1960s. The TEM-1 enzyme was originally found in a single strain of E. coli isolated from a blood culture from a patient named Temoniera in Greece, hence the designation TEM. Being plasmid-mediated and transposon-mediated, the spread of TEM-1 was facilitated to other species of bacteria. Within a few years after its first isolation, the TEM-1 β-lactamase spread worldwide and is now found in many different species of members of the family Enterobacteriaceae, P. aeruginosa, H. influenzae and Neisseria gonorrhoeae. The TEM-1 and related TEM-2 β-lactamases, prevalent in Gram-negative bacteria such as E. coli and Klebsiella pneumoniae, are encoded on transposable elements and move rapidly through these populations .
Extended-spectrum cephalosporins such as ceftazidime and cefotaxime were developed to combat resistance provided by TEM-1 and related β-lactamases. In turn, subsequent widespread cephalosporin use is thought to have selected for sequential mutants in the TEM β-lactamases, producing hydrolytic enzymes that have improved affinity for these lactam scaffolds and consequent extended-spectrum β-lactam resistance. Many variants of TEM β-lactamases have been isolated and sequenced. Another common plasmid-mediated β-lactamase found in K. pneumoniae and E. coli is SHV-1 (for sulphydryl variable). SHV-1 β-lactamase is chromosomally encoded in the majority of isolates of K. pneumoniae, but is usually plasmid mediated in E. coli.
The class A plasmid-encoded, broad-spectrum β-lactamases, TEM-1, TEM-2 and SHV-1, of Gram-negative bacilli hydrolyze penicillins and narrow-spectrum cephalosporins, but not extended-spectrum cephalosporins, aztreonam (the monobactam) and the carbapenems, imipenem and meropenem. However, variants of these enzymes are capable to destroy the four-member β-lactam ring of the extended-spectrum cephalosporins, that is, third-generation cephalosporins, and thus called extended-spectrum cephalosporinases or ESBLs .
By definition, ESBLs are plasmid-encoded β-lactamases that not only hydrolyze the third-generation cephalosporins but also penicillins and narrow-spectrum cephalosporins, but not the cephamycins (e.g. cefoxitin and cefotetan) and carbapenems (e.g. imipenem, meropenem and ertapenem), which are inhibited by clavulanic acid .
Although ESBLs are inhibited by clavulanate, sulbactam and tazobactam, hyperproduction of these enzymes can result in resistance to β-lactam/β-lactamase combinations as well. The only β-lactam antibiotics that are reliably stable to the ESBLs are the carbapenems imipenem and meropenem . Organisms carrying ESBLs are frequently resistant to other classes of antimicrobial drugs, such as aminoglycosides, trimethoprim/sulfamethoxazole and tetracyclines, as a consequence of additional resistance genes linked to the ESBL bla genes. In addition, these isolates are also commonly resistant to the fluoroquinolones .
ESBLs were first reported in the early 1980s in Europe. Since that time, ESBLs have been identified worldwide. The number of different types of ESBLs has steadily increased, and also their prevalence. Another fast-growing group of non-TEM and non-SHV was first reported in a E. coli strain isolated from the fecal flora of a laboratory dog that was being used for pharmacologic tests in 1986 in Japan and another strain was then isolated in 1986 in Germany from a clinical isolate and was called CTX-M-1 due to its particular affinity to cefotaxime .
The β-lactam resistance emergence began even before the first β-lactam penicillin was developed. These enzymes are numerous, and they mutate continuously in response to the heavy pressure of antibiotic use, leading to the development of ESBLs. Examples are the mutated TEM, SHV and CTX-M genes, mainly found in strains of E. coli and K. pneumonia, respectively .
The difference between TEM and SHV and CTX-M enzymes is their affinity for ceftazidime and cefotaxime. TEM and SHV have more affinity and lower catalytic constant (kcat) to cefatazidime than to cefotaxime, both third-generation cefalosporins. CTX-M enzyme in opposition presents higher catalytic efficiency to cefotaxime than to ceftazidime .
CTX-M enzymes have become the most prevalent type of cefotaximases found during the past 5 years among ESBL-producing bacteria isolated in certain European and South American countries . The CTX-M β-lactamases, now described in more than 50 different types, can be divided into five groups based on their amino acid identities: CTX-M1, CTX-M2, CTX-M8, CTX-M9 and CTX-M25 .
The CTX-M enzymes originated from the Kluyvera spp. of environmental bacteria, usually having higher activity against cefotaxime than ceftazidime (although certain types also inactivate ceftazidime), and are associated with mobile elements such as ISEcp1 . The epidemiology of organisms producing CTX-M enzymes is very different from those that produce TEM-derived and SHV-derived ESBLs. CTX-M enzymes are not limited to nosocomial infections caused by Klebsiella spp., and their potential ability to spread beyond the hospital environment serves to exacerbate public health concerns. E. coli is most often responsible for producing CTX-M β-lactamases and seems to be a true community ESBL pathogen .
The two types of β-lactamases that are causing most of the increasing multidrug resistance (MDR) seen in Gram-negative bacillary pathogens are class A ESBL and the class C enzymes, namely the chromosomal-encoded AmpC β-lactamases . AmpC β-lactamases are widely well distributed and are expressed constitutively at very low levels. These enzymes generally do not contribute to β-lactam resistance, but in some organisms (Serratia marcescens, Citrobacter freundii, Morganella morganii, Providencia stuartii, Acinetobacter calcoaceticus and especially Enterobacter cloacae) they can be induced under certain circumstances such as the presence of a β-lactam or mutations on regulatory genes ampR, ampD and ampG involved in the expression of AmpC β-lactamases .
β-Lactamases of class B have a binuclear zinc cluster in the active site, but are commonly known as metallo-β-lactamases or MBLs. Unlike the class A, C and D β-lactamases, which open the β-lactam ring via covalent acyl enzyme intermediates, described above, the class B β-lactamases use zinc to activate a water molecule and catalyze its direct addition to the β-lactam ring (Fig. 6).
The MBLs of type B are thought to be the major subclass of hydrolases that destroy the carbapenem antibiotics such as imipenem (thienamycin) and mer-openem. The widespread use of carbapenems in Japan has probably been instrumental in selecting the IMP-1 version of the zinc β-lactamase first seen in Ser. marcescens and P. aeruginosa. The carbapenemases have been described as a clinical concerning issue for pseudomonal infections, but the more acute carbapenem resistance problems in P. aeruginosa are efflux mechanisms .
β-Lactams’ target alteration
The most important example of target alteration to β-lactams is the case of MRSA. By definition, the presence of mecA gene is responsible for methicillin resistance phenotype in staphylococci . Originally, S. aureus has four PBPs (PBP 1, 2, 3 and 4). The mecA gene encodes a modified PBP of 78 kDa, designated PBP2a or PBP2’, which is a peptidoglycan transpeptidase, which differs from S. aureus endogenous PBP. This peptidoglycan transpeptidase PBP2a retains its normal enzymatic activity. However, the PBP2a differs because it has the recognition site for β-lactam modified. Thus, when the PBPs are linked to β-lactams and become inactive, except that PBP2a by being insensitive to various β-lactams, including methicillin. Therefore, despite being linked to methicillin, the PBP2a can also promote cell wall synthesis .
The regulation of expression of mecA and the consequent production of PBP2a that confers resistance to methicillin in MRSA is processed and mediated by an operon. Thus, the complex regulator of mecA gene consists of three genes, mecR1, mecA and mecI. The exterior domain of the protein is also a MecR1 PBP. So when the β-lactam binds covalently to the PBP domain, in this case the fragment MecR1, transmembrane signaling is initiated, resulting in the release of a cytoplasmic fragment with MecR2 in the interior domain. This fragment of MecR2 will subsequently cleave the protein into two fragments with intact MecI relieving, thus, the repression of the mecA gene, resulting in the synthesis of PBP2a .
Permeability changes to β-lactams
One of the mechanisms of resistance to β-lactam is the permeability change in outer membrane. This alteration on permeability can be due to the presence of efflux proteins or to the alteration or loss of porins. The presence of efflux proteins in the cell wall of both Gram-negative and Gram-positive has been known as one of the causes of the pumping of some unrelated agents such as antibiotics, organic solvents, dyes and detergents. Generally, a wide range of structurally dissimilar compounds have also been identified, and these have become known as MDR exporters or MDR efflux pumps .
There are two major types of efflux pumps, ATP-dependent transporters and those that are secondary transports driven by proton motive force (PMF). Among PMF transporters, there are presently four main families: resistance nodulation division (RND), the major facilitator superfamily, the small MDR family and the MDR and toxic compound extrusion (MATE) family .
Both the proton and sodium ion gradients have been identified as the energy source for substrate transport for MATE family transporters . Another important group of MDR pumps is the ATP-binding cassette (ABC) family that is not driven by PMF but is ATP-dependent. The ABC transporters are more important for clinical resistance in eukaryotic cells such as the resistance to chemotherapy presented by tumor cells , parasites  and some opportunistic fungi .
The RND-type pump is the one most thoroughly studied in Gram-negative bacteria. It is located in the cytoplasmic membrane of the bacteria, working together with a membrane fusion protein (MFP) that spans through the periplasmatic space and an outer membrane efflux protein (OEP). These three proteins (RND–MFP–OEP) form a complex that can move a substrate (e.g. an antibiotic) from the interior of the bacterium to the exterior. The best characterized of those complexes in E. coli is the AcrAB–TolC complex in which AcrB is the RND, AcrA is the MFP and TolC is the OEP .
It has been described that increased levels of multiple antibiotic resistance (mar) locus expression in relation to the presence of some efflux pumps, such as AcrB  and porin losses . Thus, genetic regulation of AcrAB–TolC system seems to be complex and, besides mar locus, it seems to be involving the oxidative stress machinery, such as superoxide dismutase (soxSlocus) and Rob-binding proteins acting as transcriptional regulator, SdiA, and AcrR among others .
AcrAB–TolC system has also been found in some clinical important issues involving Gram-negative bacilli. In Salmonella enterica, it has been recently reported that the system AcrAB–TolC may have some importance in pathogenesis. There is also recent evidence that AcrAB may system be involved in the cell basic metabolism, as it participates in the intracellular regulation of the levels of coenzyme A in E. coli.
Regarding antibiotics in E. coli strains and other Enterobacteriaceae, mutation of either TolC or AcrA/B proteins, display hypersensitivity to quinolones, tetracyclines, tigecycline, eritromycin, novobiocin, among others . Also, it has been demonstrated in P. aeruginosa that a similar pump (MexEF-OprN) has as substrates some β-lactamase inhibitors (clavulanate, cloxacillin and BRL42715) . However, few evidence until now has shown little involvement of AcrAB–TolC or other efflux systems in E. coli as a mechanism of resistance to β-lactams. A pilot study was published by Källman et al.  suggesting an efflux mechanism to cefuroxime resistance. More studies are needed to enlighten this issue.
In the last decades, antimicrobial resistance has gone from being an interesting scientific observation to a reality of great medical importance. There are no new antibiotics being developed by the pharmaceutical industry and for some pathogens fifth-generation cephalosporins are the ultimate drug. Massive usage of antibiotics in clinical practice resulted in resistance of bacteria to antimicrobial agents.
The introduction of the β-lactam antibiotics was met with the emergence of altered targets, such as PBP2a, resulting MRSA and antibiotic inactivating by β-lactamases. Some of these new β-lactamases, such as ESBLs and AmpCs, result from simple point mutations in existing β-lactamase genes that lead to a changed substrate profile. Also, these resistance genes have been borrowed from the chromosomally encoded genes that occur naturally in some species to conjugative plasmids increasing their spreading ability among other species, becoming an emerging public health concern.
Better understanding of the chemical structure for new drug development, of the mechanisms of antibiotic resistance and their expression would allow us to develop therapeutic, screening and control strategies that are needed to reduce the spread of resistant bacteria and their evolution.
Conflicts of interest
There are no conflicts of interest.
1. Bryskier A. Antibiotics and antibacterial agents: classification and structure–activity relationship.
In: Bryskier A, editor. Antimicrobial agents, antibacterial and antifungals
. Washington, District of Columbia: ASM Press; 2005. pp. 13–39.
2. Davies J. Are antibiotics naturally antibiotics? J Ind Microbiol Biotech
3. Yim G, Wang HH, Davies J. The truth about antibiotics. Int J Med Microbiol
4. Fleming A. On the antibacterial action of cultures of a penicillium, with special reference to their use in the isolation of B. Influenzae
. Br J Exp Pathol
5. Crowfoot D, Bunn C, Rogers-Low B, Turner-Jones. A X-ray crystallographic investigation of the structure of penicillin.
In: Clarke HT, Johnson JR, Robinson SR, editors. The chemistry of penicillin.
Princeton, New Jersey: Princeton University Press; 1949. pp. 310–367.
6. Long AJ, Clifton IJ, Roach PL, Baldwin JE, Rutledge PJ, Schofield CJ. Structural studies on the reaction of isopenicillin N synthase with the truncated substrate analogues delta-(L-alpha-aminoadipoyl)-L-cysteinyl-glycine and delta-(L-alpha-aminoadipoyl)-L-cysteinyl-D-alanine. Biochemistry
7. Bialy-Golan A, Brenner S. Penicillamine-induced bullous dermatoses. J Am Acad Dermatol
8. Bradford PA. Extended-spectrum β-lactamases in the 21st century: characterization, epidemiology, and detection of this important resistance threat. Clin Microbiol Rev
9. Sheehan JC. The chemistry of synthetic and semisynthetic penicillins. Ann N Y Acad Sci
10. Maiti SN, Phillips OA, Micetich RG, Livermore DM. β-Lactamase inhibitors: agents to overcome bacterial resistance. Curr Med Chem
11. Bousquet PJ, Pipet A, Bousquet-Rouanet L, Demoly P. Oral challenges are needed in the diagnosis of β-lactam hypersensitivity. Clin Exp Allergy
12. Dalhoff A, Thomson CJ. The art of fusion: from penams and cephems to penems. Chemotherapy
13. Pedregal C. Inibidores enzimáticos que interfieren con la biosínteses de las paredes celulares.
In: Avedaño C, editor. Introducción a la química farmacéutica
ed. Madrid, Spain: McGraw-Hill Interamericana; 2001. pp. 251–274.
14. Newton GG, Abraham EP. Cephalosporin C, a new antibiotic containing sulphur and D-alpha-aminoadipic acid. Nature
15. Velasco J, Adrio LJ, Angel Moreno M, Díez B, Soler G, Barredo JL. Environmentally safe production of 7-aminodeacetoxycephalosporanic acid (7-ADCA) using recombinant strains of Acremonium chrysogenum
. Nat Biotechnol
16. Baldo BA, Zhao Z, Pham NH. Antibiotic allergy: immunochemical and clinical considerations. Curr Allergy Asthma Rep
17. Page MG. Emerging cephalosporins. Expert Opin Emerg Drugs
18. Fung-Tomc JC, Huczko E, Stickle T, Minassian B, Kolek B, Denbleyker K, et al. Antibacterial activities of cefprozil compared with those of 13 oral cephems and 3 macrolides. Antimicrob Agents Chemother
19. Bennett PN, Brown MJ. Clinical pharmacology
. 9th ed. Toronto, Ontario: Churchill Livingston; 2009.
20. Paladino JA, Sunderlin JL, Singer ME, Adelman MH, Schentag JJ. Influence of extended-spectrum β-lactams
on Gram-negative bacterial resistance. Am J Health Syst Pharm
21. O’Neill E, Humphreys H, Phillips J, Smyth EG. Third-generation cephalosporin resistance among Gram-negative bacilli causing meningitis in neurosurgical patients: significant challenges in ensuring effective antibiotic therapy. J Antimicrob Chemother
22. Fritsche TR, Sader HS, Jones RN. Antimicrobial activity of ceftobiprole, a novel antimethicillin-resistant Staphylococcus aureus cephalosporin, tested against contemporary pathogens: results from the SENTRY Antimicrobial Surveillance Program (2005–2006). Diagn Microbiol Infect Dis
23. Gould IM, David MZ, Esposito S, Garau J, Lina G, Mazzei T, Peters G. New insights into meticillin-resistant Staphylococcus aureus
(MRSA) pathogenesis, treatment and resistance. Int J Antimicrob Agents
24. Vidaillac C, Leonard SN, Sader HS, Jones RN, Rybak MJ. In vitro activity of ceftaroline alone and in combination against clinical isolates of resistant gram-negative pathogens, including β-lactamase-producing Enterobacteriaceae and Pseudomonas aeruginosa
. Antimicrob Agents Chemother
25. Singh GS. β-Lactams
in the new millennium. Part-I: Monobactams and carbapenems. Mini Rev Med Chem
26. Moellering RC Jr. Meeting the challenges of β-lactamases. J Antimicrob Chemother
1993; 31 (Suppl A):1–8.
27. Walsh C. Antibiotics, action, origins and resistance
. Washington, District of Columbia: ASM Press; 2003.
28. Walsh C. Molecular mechanisms that confer antibacterial drug resistance. Nature
29. Livermore DM. β-Lactamases in laboratory and clinical resistance. Clin Microbiol Rev
30. Harbottle H, Thakur S, Zhao S, White DG. Genetics of antimicrobial resistance. Anim Biotechnol
31. Livermore DM, Woodford N. Carbapenemases: a problem in waiting? Curr Opin Microbiol
32. Bush K, Jacoby G, Medeiros A. A functional classification scheme for β-lactamases and its correlation with molecular structure. Antimicrob Agents Chemother
33. Ambler RP. The structure of β-lactamases. Philos Trans R Soc London Ser B
34. Galleni M, Lamotte-Brasseur J, Raquet X, Dubus A, Monnaie D, Knox JR, Frère JM. The enigmatic catalytic mechanism of active-site serine β-lactamases. Biochem Pharmacol
35. Amyes SGB. Magic bullets, lost horizons: the rise and fall of antibiotics
. New York, New York: Taylor and Francis; 2001
36. Heritage J, M’Zali FH, Gascoyne-Binzi D, Hawkey P. Evolution and spread of SHV extended-spectrum β-lactamases in Gram-negative bacteria. J Antimicrob Chemother
37. Samaha-Kfoury JN, Araj GF. Recent developments in β-lactamases and extended-spectrum β-lactamases. BMJ
38. Colodner R. Extended-spectrum β-lactamases: a challenge for clinical microbiologists and infection control specialists. Am J Infect Control
39. Bonnet R. Growing group of extended-spectrum β-lactamases: the CTX-M enzymes. Antimicrob Agents Chemother
40. Cantón R, Coque TM. The CTX-M β-lactamase pandemic. Curr Opin Microbiol
41. Walther-Rasmussen J, Hoiby N. Cefotaximases (CTX-M-ases), an expanding family of extended-spectrum β-lactamases. Can J Microbiol
42. Pitout JD, Nordmann P, Laupland KB, Poirel L. Emergence of Enterobacteriaceae producing extended-spectrum β-lactamases (ESBLs) in the community. J Antimicrob Chemother
43. Alvarez M, Tran JH, Chow N, Jacoby GA. Epidemiology of conjugative plasmid-mediated AmpC β-lactamases in the United States. Antimicrob Agents Chemother
44. Jacobs C, Frere JM, Normark S. Cytosolic intermediates for cell wall biosynthesis and degradation control inducible β-lactam resistance in Gram-negative bacteria. Cell
45. Kurokawa H, Yagi T, Shibata N, Shibayama K, Arakawa Y. Worldwide proliferation of carbapenem-resistant Gram-negative bacteria. Lancet
46. Boyle-Vavra S, Daum RS. Community-acquired methicillin-resistant Staphylococcus aureus
: the role of Panton–Valentine leukocidin. Lab Invest
47. Gordon RJ, Lowy FD. Pathogenesis of methicillin-resistant Staphylococcus aureus infection. Clin Infect Dis
48. Lewis K. Multidrug resistance pumps in bacteria: variations on a theme. Trends Biochem Sci
49. Brown MH, Paulsen IT, Skurray RA. The multidrug efflux protein NorM is a prototype of a new family of transporters. Mol Microbiol
50. He G-X, Kuroda T, Mima T, Morita Y, Mizushima T, Tsuchiya T. An H+
-coupled multidrug efflux pump, PmpM, a member of the MATE family of transporters, from Pseudomonas aeruginosa
. J Bacteriol
51. Ambudkar SV, Kimchi-Sarfaty C, Sauna ZE, Gottesman MM. P-glycoprotein: from genomics to mechanism. Oncogene
52. Perez-Victoria JM, Di Pietro A, Barron D, Ravelo AG, Castanys S, Gamarro F. Multidrug resistance phenotype mediated by the P-glycoprotein-like transporter in Leishmania
: a search for reversal agents. Curr Drug Targets
53. Okusu H, Ma D, Nikaido H. AcrAB efflux pump plays a major role in the antibiotic resistance phenotype of Escherichia coli
multiple-antibiotic-resistance (Mar) mutants. J Bacteriol
54. Zgurskaya HI, Nikaido H. Multidrug resistance mechanisms: drug efflux across two membranes. Mol Microbiol
55. Cohen SP, McMurry LM, Levy SB. marA locus causes decreased expression of OmpF porin in multiple-antibiotic-resistant (Mar) mutants of Escherichia coli
. J Bacteriol
56. Nikaido E, Yamaguchi A, Nishino K. AcrAB multidrug efflux pump regulation in Salmonella enterica
serovar Typhimurium by RamA in response to environmental signals. J Biol Chem
57. Potrykus J, Wegrzyn G. The acrAB locus is involved in modulating intracellular acetyl coenzyme A levels in a strain of Escherichia coli
CM2555 expressing the chloramphenicol acetyltransferase (cat) gene. Arch Microbiol
58. Keeney D, Ruzin A, McAleese F, Murphy E, Bradford PA. MarA-mediated overexpression of the AcrAB efflux pump results in decreased susceptibility to tigecycline in Escherichia coli. J Antimicrob Chemother
59. Li XZ, Zhang L, Srikumar R, Poole K. β-Lactamase inhibitors are substrates for the multidrug efflux pumps of Pseudomonas aeruginosa
. Antimicrob Agents Chemother
60. Källman O, Fendukly F, Karlsson I, Kronvall G. Contribution of efflux to cefuroxime resistance in clinical isolates of Escherichia coli
. Scand J Infect Dis
Keywords:© 2013 Wolters Kluwer Health | Lippincott Williams & Wilkins
β-lactams; chemical structure; mechanisms of resistance; mode of action