In vitro study on the antimicrobial activity of various antibiotics against clinical isolates of Streptococcus pneumoniae from Belgium collected during winter 1998-1999

Citation
R. Vanhoof et al., In vitro study on the antimicrobial activity of various antibiotics against clinical isolates of Streptococcus pneumoniae from Belgium collected during winter 1998-1999, ACT CLIN B, 55(6), 2000, pp. 312-322
Citations number
31
Categorie Soggetti
General & Internal Medicine
Journal title
ACTA CLINICA BELGICA
ISSN journal
00015512 → ACNP
Volume
55
Issue
6
Year of publication
2000
Pages
312 - 322
Database
ISI
SICI code
0001-5512(200011/12)55:6<312:IVSOTA>2.0.ZU;2-F
Abstract
A total of 205 isolates of Streptococcus pneumoniae obtained from 10 differ ent centres were included in this study. The susceptibilities to penicillin ampicillin, amoxicillin, amoxicillin/clavulanic acid, cefaclor, cefuroxime , cefotaxime, imipenem, ciprofloxacin, gemifloxacin, grepafloxacin, levoflo xacin, trovafloxacin, erythromycin, clarithromycin, miocamycin, clindamycin and tetracycline were determined by a microdilution technique following NC CLS recommendations. Decreased susceptibility to penicillin was 16.1% [6.8% intermediate (0.12 - 1 mug/mL) and 9.3% high-level (greater than or equal to2 mug/mL)], cefotaxime insusceptibility (greater than or equal to1 mug/mL ) 12.7 %, ciprofloxacine insusceptibilty (greater than or equal to2 mug/mL) 15.6 % with 1.5 % of high level resistance (greater than or equal to4 mug/ mL), erythromycin insusceptibility (greater than or equal to0.5 mug/mL) 36. 1 % and tetracycline insusceptibility (greater than or equal to4 mug/mL) 22 .9 %. Decreased susceptibility to cefotaxime was found in 78.8 % of the pen icillin-insusceptible isolates. No decreased susceptibility was found for g emifloxacin (greater than or equal to0.5 mug/mL) and trovafloxacin (greater than or equal to1 mug/mL). Compared to the 1996-1997 surveillance, penicil lin, cefotaxime and erythromycin insusceptibility rose by 3.8 %, 5.2 % and 5.0 % respectively, while tetracycline insusceptibility decreased with 8.2 %. MICs of all beta -lactams rose with those of penicillin for penicillin-i nsusceptible isolates. Amoxicillin +/- cravulanate, cefotaxime and imipenem were generally 1, 1 and 5 doubling dilutions respectively more potent than penicillin on these isolates. Penicillin, ampicillin and cefuroxime were e qually active while cefaclor was generally 5 dilutions less potent. Most pe nicillin-insusceptible isolates remained fully susceptible to amoxicillin /- clavulanate and imipenem. The penicillin-insusceptible isolates were 36. 4 %, 27.3 % and 3.0 % co-insusceptible to erythromycin, erythromycin plus t etracycline and tetracycline respectively. A subpopulation of 52 isolates o btained from children aged less than or equal to 3 years was also studied. Compared to the other isolates we found a statistically significant increas e in insusceptibility for penicillin, cefaclor, cefuroxime, erythromycin, c larithromycin and tetracycline while a significant decrease was found for c iprofloxacin.