Clonal distribution of invasive pneumococci, Czech Republic, 1996-2003.
In the Czech Republic, patients in follow-up care departments (i.e., <1% of the adult population), have been vaccinated with a 23-valent polysaccharide vaccine since 2001. PCV7 showed a reported 66% serotype coverage in children (8) and has been included in the routine childhood immunization program since January 2009.
Clones associated with IPD have been characterized by genotyping. Use of PCV7 exerts selective pressure against vaccine serotypes. Clonality data obtained before vaccine use will make it possible to demonstrate future changes in the genetic structure of pneumococci. Therefore, the purpose of our study was to identify IPD serotype distribution and clonality in adults in the Czech Republic before the use of PCV7.
Invasive pneumococcal isolates from adults [greater than or equal to] 18 years of age were obtained from blood (n = 460) and cerebrospinal fluid (CSF) (n = 229) during 1996-2003 by 54 laboratories serving [approximately equal to] 85% of the population in the Czech Republic. Isolates were serotyped by using the Quellung reaction (9). Antimicrobial drug susceptibility and MICs were determined by the broth microdilution method according to Clinical and Laboratory Standards Institute recommendations (10). Genotyping was performed by using pulsed-field gel electrophoresis (PFGE) (11) and multilocus sequence typing (MLST) (12). MLST results were identical between isolates of the same serotype within a PFGE subtype (13). Cluster analyses were based on allelic data that used the eBURST algorithm (14). Numerical trend was evaluated by regression analysis of the logarithm of the number of isolates by using SPSS for Windows version 14 (SPSS, Inc., Chicago, IL, USA). The [chi square] test for trend (Epi Info version 3.4; Centers for Disease Control and Prevention, Atlanta, GA, USA) was used to evaluate variations in proportions of different serotypes; p values <0.05 were considered significant.
During 1996-2003, a total of446 (64.7%) isolates were obtained from adults 18-64 years of age and 243 (35.3%) isolates were obtained from adults [greater than or equal to] 65 years of age. A progressive increase in recovery of isolates from blood was observed from 44 during 1996-1997 to 199 during 2002-2003 (p = 0.009) (Figure 1). Serotyping identified 48 serotypes; 10 of these serotypes included [greater than or equal to] 30 isolates. Half of all strains belonged to serotypes 3 (12.7%), 4 (8.6%), 8 (7%), 1 (5.8%), 19F (5.5%), 14 (5.5%), and 9V (5.2%) (Figure 2). Serotype coverage rates by PCV7, PCV10, PCV13, and 23-valent polysaccharide vaccine were 32.5%, 44.2%, 62.3%, and 82.1%, respectively, among adults 18-64 years of age and 35.4%, 42.8%, 61.3%, and 85.6%, respectively, among adults [greater than or equal to] 65 years of age.
Serotype distribution did not vary significantly with age group and type of isolate, except for serotype 1, which was more common (p = 0.037) among younger adults (18-64 years) and more prevalent in blood (p = 0.004). With the exception of 1998-1999, serotype 3 was most common identified. This serotype, which composed [approximately equal to] 11% of all isolates during 1996-2001, increased to 15% during 2002-2003 (p = 0.289). A change was also observed in the proportions of serotypes 1 and 4 (Figure 1). Serotype 1 increased from 6% during 1996-1997 to 17% during 1998-1999 (p = 0.027) and then decreased to 3% during 2002-2003 (p<0.001). Serotype 4 increased from 2% during 1996-1997 to 13% during 2002-2003 (p<0.001) (Figure 1).
Penicillin-resistant pneumococci were uncommon (range 1%-5%), and no isolate showed high resistance to penicillin (MIC >1 mg/L). Resistance to chloramphenicol decreased from 5% during 1996-1997 to 2% during 2002-2003 (p = 0.114). Tetracycline resistance also decreased from 8% during 1996-1997 to 6% during 2002-2003 (p = 0.732). Few ([less than or equal to] 9) isolates were resistant to erythromycin. Antimicrobial drug resistance was associated with certain serotypes. Eighteen of 23 penicillin-resistant pneumococci isolates belonged to serotype 9V. Resistance to chloram phenicol, usually observed with resistance to tetracycline, was seen most often in serotype 19F isolates.
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Of 347 isolates of the 7 most common serotypes, 335 were characterized by PFGE and 130 PFGE subtypes were analyzed by MLST (online Appendix Table, www.cdc.gov/ EID/content/16/2/287-appT.htm). Forty-six allelic profiles were identified, 18 of which carried new alleles (n = 11) or novel combinations of known alleles (n = 7). Of 10 new alleles, 5 belonged to serotype 4. The gdh128 allele was identified in serotype 4 and 9V isolates. Until recently, only gdh128 was found among isolates from other countries. At least 60% of isolates of serotypes 1, 3, 9V, 14, and 19F have been identified within clones in the Pneumococcal Molecular Epidemiology Network. In contrast, only 25% of serotype 4 and 8 isolates were identified in this network, and these serotypes consisted of larger clusters unrelated to global clones.
When we compared our results with those of a study from the United States (5), where 51% of IPD was among elderly persons before introduction of PCV7 and caused by pediatric serotypes (6B, 9V, 14, 19F, and 23F) (5), our data showed a low frequency (27.2%) of pediatric serotypes in older adults. The low frequency of penicillin-nonsusceptible pneumococci isolates of pediatric serotypes explains the observed predominance of drug-susceptible serotypes. Local differences in blood culture protocols could also bias the serotype distribution (7). Although the number of blood cultures performed in the Czech Republic is increasing, lower numbers of invasive pneumococci have been isolated than in other countries in Europe (www.rivm.nl/earss).
The observed predominance of serotype 3, previously reported as less invasive but associated with a high death rate (15), could be explained by sample collection primarily from the most severe IPD cases. In 1998, an increase in serotype 1 invasive disease was reported in Sweden. In our study, serotype 1 was the most common during the same period. Subsequently, the frequency of this serotype decreased but the frequency of bacteremia increased. The gradual increase in bacteremia and increased frequency of serotype 4, previously found to be moderately invasive (7), could be ascribed to the increase in blood cultures that facilitated detection of moderate disease caused by serotype 4 rather than dissemination of a specific invasive clone because the isolates showed high genotypic diversity. In our collection of invasive strains, the frequency of antimicrobial drug-resistant global clones, all previously found in the Czech Republic (13), varied between serotypes.
Our results support the need for IPD surveillance because differences in detection methods might modify the effect of the vaccine. Continued surveillance will be helpful in detecting any shift in the distribution of invasive serotypes and clones circulating in the Czech Republic and in monitoring the effect of PCV7 on serotype frequencies and the genetic structure of pneumococci.
We thank the regional microbiology laboratories for providing pneumococcal isolates.
This study was partly supported by contract LSHM-CT-2003-503413 (Pneumococcal Resistance Epidemicity and Virulence-an International Study) from the European Commission. This publication made use of the MLST website (www.mlst.net) at Imperial College London developed by David Aanensen and funded by the Wellcome Trust.
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Author affiliation: National Institute of Public Health, Prague, Czech Republic
Dr Zemlickova is head of the Czech National Collection of Type Cultures, National Institute of Public Health, Prague, Czech Republic. Her primary research interest is typing of gram-positive bacteria, particularly S. pneumoniae and methicillin-resistant Staphylococcus aureus.
Address for correspondence: Helena Zemlickova, National Institute of Public Health, Srobarova 48, 100 42 Prague 10, Czech Republic; email: firstname.lastname@example.org
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|Author:||Zemlickova, Helena; Urbaskova, Pavla; Jakubu, Vladislav; Motlova, Jitka; Musilek, Martin; Prochazka,|
|Publication:||Emerging Infectious Diseases|
|Date:||Feb 1, 2010|
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