Literature DB >> 6978350

In vitro evaluation of pyridine-2-azo-p-dimethylaniline cephalosporin, a new diagnostic chromogenic reagent, and comparison with nitrocefin, cephacetrile, and other beta-lactam compounds.

R N Jones, H W Wilson, W J Novick.   

Abstract

Pyridine-2-azo-p-dimethylanaline cephalosporin (PADAC), a chromogenic reagent which is purple and changes to yellow upon cleavage of its beta-lactam ring, was evaluated in comparison with other chromogenic cephalosporins. PADAC exhibited little antimicrobial activity against gram-negative bacteria, but did have good activity (minimum inhibitory concentration, 0.12 to 0.5 microgram/ml) against Staphylococcus aureus, a quality comparable to nitrocefin. Nitrocefin, however, demonstrated an unexpected and uniquely potent activity against Streptococcus faecalis (minimum inhibitory concentration, less than or equal to 0.06 to 0.12 microgram/ml) The relative hydrolysis rate of PADAC when subjected to six different beta-lactamases was substantially greater than that of cephacetrile, but less than that of nitrocefin. The relative hydrolysis rates of PADAC and nitrocefin were comparable with type IIIa beta lactamase and the derived from Bacillus cereus. The inhibition of beta-lactamase hydrolysis of the chromogenic cephalosporin substrates by six enzyme-stable inhibitors was generally greater with PADAC than with nitrocefin. Unlike nitrocefin, PADAC mixed with 50% human serum or various broth culture media showed no evidence of color change or degradation over several hours. The subsequent enzyme hydrolysis rates of such mixtures were the same as in phosphate buffer. Beta-lactamase-containing bacterial suspensions and clinical specimens containing such bacteria produced positive visual and spectrophotometric color changes when mixed with PADAC or nitrocefin. Although color changes occurred more slowly with PADAC than with nitrocefin, PADAC was not adversely influenced (non-enzyme-related color change) by the protein content of specimens. PADAC appears to be a promising alternative for beta-lactamase diagnostic testing in the clinical and research microbiology laboratory.

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Year:  1982        PMID: 6978350      PMCID: PMC272166          DOI: 10.1128/jcm.15.4.677-683.1982

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  16 in total

1.  Partial characterization of a beta-lactamase from Vibrio parahaemolyticus by a new automated microiodometric technique.

Authors:  R M DeBell; T M Hickey; D E Uddin
Journal:  Antimicrob Agents Chemother       Date:  1978-02       Impact factor: 5.191

Review 2.  The beta-lactamases of gram-negative bacteria and their possible physiological role.

Authors:  M H Richmond; R B Sykes
Journal:  Adv Microb Physiol       Date:  1973       Impact factor: 3.517

3.  Letter: Ampicillin-resistant Haemophilus influenzae meningitis.

Authors:  W J Thomas; J W McReynolds; C R Mock; D W Bailey
Journal:  Lancet       Date:  1974-02-23       Impact factor: 79.321

4.  Rapid capillary tube method for detecting penicillin resistance in Staphylococcus aureus.

Authors:  I G Rosen; J Jacobson; R Rudderman
Journal:  Appl Microbiol       Date:  1972-03

5.  Penicillinase-producing Gonococci in Liverpool.

Authors:  A Percival; J Rowlands; J E Corkill; C D Alergant; O P Arya; E Rees; E H Annels
Journal:  Lancet       Date:  1976-12-25       Impact factor: 79.321

6.  Rapid penicillinase paper strip test for detection of beta-lactamase-producing Haemophilus influenzae and Neisseria gonorrhoeae.

Authors:  J H Jorgensen; J C Lee; G A Alexander
Journal:  Antimicrob Agents Chemother       Date:  1977-06       Impact factor: 5.191

7.  Interaction of a new cephalosporin, 7-cyanacetamidocephalosporanic acid, with some gram-negative and gram-positive beta-lactamase-producing bacteria.

Authors:  A D Russel
Journal:  Antimicrob Agents Chemother       Date:  1972-10       Impact factor: 5.191

8.  Iodometric detection of Haemophilus influenzae beta-lactamase: rapid presumptive test for ampicillin resistance.

Authors:  B W Catlin
Journal:  Antimicrob Agents Chemother       Date:  1975-03       Impact factor: 5.191

9.  Novel method for detection of beta-lactamases by using a chromogenic cephalosporin substrate.

Authors:  C H O'Callaghan; A Morris; S M Kirby; A H Shingler
Journal:  Antimicrob Agents Chemother       Date:  1972-04       Impact factor: 5.191

10.  Ampicillin-resistant Haemophilus paraphrophilus laryngo-epiglottitis.

Authors:  R N Jones; J Slepack; J Bigelow
Journal:  J Clin Microbiol       Date:  1976-11       Impact factor: 5.948

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  20 in total

1.  Components of the protein-excretion apparatus of Pseudomonas aeruginosa are processed by the type IV prepilin peptidase.

Authors:  D N Nunn; S Lory
Journal:  Proc Natl Acad Sci U S A       Date:  1992-01-01       Impact factor: 11.205

2.  Autogenous regulation of the Escherichia coli ksgA gene at the level of translation.

Authors:  B van Gemen; J Twisk; P H van Knippenberg
Journal:  J Bacteriol       Date:  1989-07       Impact factor: 3.490

3.  Evaluation of a method for rapid detection of penicillinase-producing Neisseria gonorrhoeae in urethral exudates.

Authors:  V M Herve; A J Georges; M Massanga; P M Martin
Journal:  J Clin Microbiol       Date:  1989-01       Impact factor: 5.948

4.  In vitro effects of beta-lactams combined with beta-lactamase inhibitors against methicillin-resistant Staphylococcus aureus.

Authors:  S Kobayashi; S Arai; S Hayashi; T Sakaguchi
Journal:  Antimicrob Agents Chemother       Date:  1989-03       Impact factor: 5.191

5.  A promoter probe vector (pJAC4) that utilizes the ampC beta-lactamase gene of Escherichia coli.

Authors:  B Jaurin
Journal:  Nucleic Acids Res       Date:  1987-10-26       Impact factor: 16.971

6.  In vitro evaluation of CENTA, a new beta-lactamase-susceptible chromogenic cephalosporin reagent.

Authors:  R N Jones; H W Wilson; W J Novick; A L Barry; C Thornsberry
Journal:  J Clin Microbiol       Date:  1982-05       Impact factor: 5.948

7.  Simple assay of beta-lactamase with agar medium containing a chromogenic cephalosporin, pyridinium-2-azo-p-dimethylaniline chromophore (PADAC).

Authors:  S Kobayashi; S Arai; S Hayashi; T Sakaguchi
Journal:  Antimicrob Agents Chemother       Date:  1988-07       Impact factor: 5.191

8.  Mutations in the consensus ATP-binding sites of XcpR and PilB eliminate extracellular protein secretion and pilus biogenesis in Pseudomonas aeruginosa.

Authors:  L R Turner; J C Lara; D N Nunn; S Lory
Journal:  J Bacteriol       Date:  1993-08       Impact factor: 3.490

9.  Comparative beta-lactamase hydrolysis of and inhibition by 7-aminothiazolyl alpha-methoxyimino cephalosporins.

Authors:  R N Jones; H W Wilson
Journal:  Infection       Date:  1982 Sep-Oct       Impact factor: 3.553

10.  Cefotetan, a new cephamycin: comparison of in vitro antimicrobial activity with other cephems, beta-lactamase stability, and preliminary recommendations for disk diffusion testing.

Authors:  L W Ayers; R N Jones; A L Barry; C Thornsberry; P C Fuchs; T L Gavan; E H Gerlach; H M Sommers
Journal:  Antimicrob Agents Chemother       Date:  1982-11       Impact factor: 5.191

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