TY - JOUR
T1 - Genetic diversity and clonal patterns among antibiotic-susceptible and -resistant Streptococcus pneumoniae colonizing children
T2 - Day care centers as autonomous epidemiological units
AU - Sá-Leão, Raquel
AU - Tomasz, Alexander
AU - Santos Sanches, Ilda
AU - Nunes, Sónia
AU - Alves, C. Rute
AU - Brito-Avô, António
AU - Saldanha, Joana
AU - Kristinsson, Karl G.
AU - de Lencastre, Herminia
PY - 2000
Y1 - 2000
N2 - Characterization by antibiotype of the 1,096Streptococcuspneumoniaerecovered from 2,111 nasopharyngeal samples ofchildrenattending 16daycarecenters(DCCs) in Lisbon, Portugal, and molecular typing of 413 drug-resistantpneumococci (DRPn) and 89 fully drug-susceptible pneumococci (DSPn) has allowed several conclusions. (i) There was an increase in the frequency of DRPncolonizingchildrenin DCCs from 40% in 1996 to 45% in 1997 to 50% in 1998. (ii) Drug resistance spread by cross-transmission of DRPn clones. A few (8 out of 57) DRPn clones were repeatedly isolated from a large number ofchildrenin several DCCs and during each period of surveillance, suggesting the epidemic nature of these clones, which included lineages representing internationally spread S.pneumoniaeclones. (iii) Dissemination of resistance determinants among pneumococcicolonizingthe nasopharynx occurred. Association of identical pulsed-field gel electrophoresispatternswith diverse antibiotypes among pneumococcicolonizingchildrensuggests that the high prevalence of DRPn involves not only cross-transmission ofresistantstrains but also dispersal of resistance genes through recombinational mechanisms. (iv) DCCs areautonomousepidemiologicalunits. Among the 413 DRPn, 57 different lineages were detected; these lineages were dispersed among the 16 DCCs to produce unique microbiological profiles for each of the DCCs. Highergeneticdiversityand less sharing ofclonaltypes were observed among the DSPn.
AB - Characterization by antibiotype of the 1,096Streptococcuspneumoniaerecovered from 2,111 nasopharyngeal samples ofchildrenattending 16daycarecenters(DCCs) in Lisbon, Portugal, and molecular typing of 413 drug-resistantpneumococci (DRPn) and 89 fully drug-susceptible pneumococci (DSPn) has allowed several conclusions. (i) There was an increase in the frequency of DRPncolonizingchildrenin DCCs from 40% in 1996 to 45% in 1997 to 50% in 1998. (ii) Drug resistance spread by cross-transmission of DRPn clones. A few (8 out of 57) DRPn clones were repeatedly isolated from a large number ofchildrenin several DCCs and during each period of surveillance, suggesting the epidemic nature of these clones, which included lineages representing internationally spread S.pneumoniaeclones. (iii) Dissemination of resistance determinants among pneumococcicolonizingthe nasopharynx occurred. Association of identical pulsed-field gel electrophoresispatternswith diverse antibiotypes among pneumococcicolonizingchildrensuggests that the high prevalence of DRPn involves not only cross-transmission ofresistantstrains but also dispersal of resistance genes through recombinational mechanisms. (iv) DCCs areautonomousepidemiologicalunits. Among the 413 DRPn, 57 different lineages were detected; these lineages were dispersed among the 16 DCCs to produce unique microbiological profiles for each of the DCCs. Highergeneticdiversityand less sharing ofclonaltypes were observed among the DSPn.
UR - http://www.scopus.com/inward/record.url?scp=0034458699&partnerID=8YFLogxK
U2 - 10.1128/jcm.38.11.4137-4144.2000
DO - 10.1128/jcm.38.11.4137-4144.2000
M3 - Article
C2 - 11060081
SN - 0095-1137
VL - 38
SP - 4137
EP - 4144
JO - Journal Of Clinical Microbiology
JF - Journal Of Clinical Microbiology
IS - 11
ER -