Increase in serotype 19A prevalence and amoxicillin non-susceptibility among paediatric Streptococcus pneumoniae isolates from middle ear fluid in a passive laboratory-based surveillance in Spain, 1997-2009
© Fenoll et al; licensee BioMed Central Ltd. 2011
Received: 25 November 2010
Accepted: 12 September 2011
Published: 12 September 2011
Conjugate vaccines, such as the 7-valent conjugate vaccine (PCV7), alter serotype nasopharyngeal carriage, potentially increasing cases of otitis media by non-vaccine serotypes.
All paediatric middle ear fluid (MEF) isolates received in the Spanish Reference Laboratory for Pneumococci through a passive, laboratory-based surveillance system from January 1997 to June 2009 were analysed. Data from 1997 to 2000 were pooled as pre-vaccination period. Trends over time were explored by linear regression analysis.
A total of 2,077 isolates were analysed: 855 belonging to PCV7 serotypes, 466 to serotype 19A, 215 to serotype 3, 89 to serotype 6A and 452 to other serotypes (< 40 isolates each). Over time, there has been a decreasing trend for PCV7 serotypes (R2 = 0.944; p < 0.001, with significant decreasing trends for serotypes 19F, 14, 23F and 9V), and increasing trends for serotype 19A (R2 = 0.901; p < 0.001), serotype 3 (R2 = 0.463; p = 0.030) and other non-PCV7 serotypes (R2 = 0.877; p < 0.001), but not for serotype 6A (R2 = 0.311; p = 0.094). Considering all isolates, amoxicillin non-susceptibility showed an increasing trend (R2 = 0.528; p = 0.017). Regarding serotype 19A, increasing trends in non-susceptibility to penicillin (R2 = 0.726; p = 0.001), amoxicillin (R2 = 0.804; p < 0.001), cefotaxime (R2 = 0.546; p = 0.005) and erythromycin (R2 = 0.546; p = 0.009) were found, with amoxicillin non-susceptibility firstly detected in 2003 (7.4%) and increasing up to 38.0% in 2009. In PCV7 serotypes (which prevalence decreased from 70.7% during 1997-2000 to 10.6% in 2009) amoxicillin non-susceptibility rates showed an increasing trend (R2 = 0.702; p = 0.002). However, overall, amoxicillin non-susceptibility (≈25% in 2008-9) could be mainly attributed to serotype 19A (> 35% isolates) since PCV7 strains represented < 11% of total clinical isolates.
In contrast to reports on invasive pneumococcal strains, in MEF isolates the reduction in the prevalence of PCV7 serotypes was not associated with decreases in penicillin/erythromycin non-susceptibility. The high prevalence of serotype 19A among paediatric MEF isolates and the amoxicillin non-susceptibility found in this serotype are worrisome since amoxicillin is the most common antibiotic used in the treatment of acute otitis media. These data suggest that non-PCV7 serotypes (mainly serotype 19A followed by serotypes 3 and 6A) are important etiological agents of acute otitis media and support the added value of the broader coverage of the new 13-valent conjugate vaccine.
KeywordsSusceptibility serotype 19A middle ear isolates non-susceptibility time trends surveillance
Acute otitis media (AOM) is the most common infection in children following pneumococcal colonization of the upper respiratory tract , and the most common reason for which antibiotics are prescribed in children . Streptococcus pneumoniae is worldwide identified in 30-60% cases of AOM [3, 4]. In recent decades the emergence of pneumococcal strains exhibiting non-susceptibility to penicillin, especially in middle ear fluid isolates [5–7], has evolved into a global problem because non-susceptibility to penicillin is associated with decreases in the intrinsic activity of other oral β-lactams.
Among the 93 pneumococcal serotypes , the seven most commonly found in the US causing invasive disease in children are targeted by the 7-valent pneumococcal conjugate vaccine (PCV7) . PCV7 is available in Spain (approx. 45 million inhabitants) since October 2001, but only in the private market for children under 2 years of age, with a vaccination schedule of 2-, 4-, 6-month primary series plus a fourth dose at 15-18 months. Although the vaccine use increased from 2002 onwards, the reported vaccine coverage in 2006 was below 50% (assuming complete vaccination schedules) . In October 2006, the Autonomous Region of Madrid (approx. 6 million inhabitants) approved its inclusion in the childhood vaccination calendar with the vaccination schedule stated above. Despite the irregular regional PCV7 uptake in Spain, vaccination has resulted in a decrease in PCV7 serotypes among invasive isolates from children and adults (due to herd effect). This reduction has been associated with a decrease in the proportion of isolates non-susceptible to penicillin [11–13]. However, as in other countries, these changes were associated with an increase in the prevalence of non-PCV7 serotypes causing invasive disease .
Conjugate vaccines protect against nasopharyngeal carriage of serotypes included in the vaccine . This ecological niche can then be filled by other serotypes , with subsequent potential increases in otitis media by non-vaccine serotypes [14, 16].
This study focuses on pneumococcal isolates from middle ear fluid received in the Spanish Reference Laboratory for Pneumococci (SRLP) from hospitals located all over Spain, and analyses changes in serotype distribution and antibiotic susceptibility in the period 1997-2009.
All paediatric (≤ 14 years of age) S. pneumoniae isolates from middle ear fluid received in the SRLP from hospitals located all over the 17 Autonomous Regions in Spain from January 1997 to June 2009 were analysed. Isolates had been sent on a voluntary basis through a passive, laboratory-based surveillance system. All MEF isolates in global and the subgroups of PCV7 and 19A isolates were distributed per age group (< 2 years, 2-4 years and 5-14 years). Data from 1997 to 2000 were pooled as pre-vaccination period. Isolates were serotyped by Quellung reaction  and/or Dot blot assay . Susceptibility to penicillin, amoxicillin, cefotaxime and erythromycin was determined by agar dilution using Mueller-Hinton agar (Difco Laboratories, Detroit, MI, USA) supplemented with 5% sheep blood (Biomedics, Madrid, Spain) as culture media. Plates were incubated under 5% CO2 atmosphere as recommended by the Clinical and Laboratory Standards Institute . S. pneumoniae ATCC 6303 and S. pneumoniae ATCC 49619 plus six clinical isolates were used as quality controls . Current non-susceptibility breakpoints for oral penicillin (MIC ≥ 0.12 μg/ml), amoxicillin (MIC ≥ 4 μg/ml), cefotaxime (MIC ≥ 2 μg/ml; non-meningitis) and erythromycin (MIC ≥ 0.5 μg/ml)  were considered.
Trends along time (1997-2000 to 2009) of serotype prevalence and non-susceptibility rates were explored by regression analysis (SPSS v14 programme, SPSS Inc, Chicago IL) with time as independent variable. Linear regression analysis was used, based on highest goodness of fit.
Annual total number of paediatric isolates (invasive + non-invasive) received by the SRLP, total no. (%) of paediatric middle ear fluid isolates (MEF), and among them, no. (%) of PCV7 and 19A isolates.
MEF [n (%)]
< 2 yrs.
PCV-7 [n (%)]*
< 2 yrs.
19A [n (%)]*
< 2 yrs.
Regarding non-susceptibility, only PCV7 serotypes (as a group) and serotypes 19A and 3 had more than 10 isolates per year and could be analysed in separate. Serotype 3 was fully susceptible to penicillin, amoxicillin and cefotaxime over the study period, with non-susceptibility rates to erythromycin < 10% from 2005 on.
Number of paediatric middle ear fluid isolates (MEF), and among them, number of PCV-7 and 19A isolates, with per-group percentages of non-susceptibility to penicillin (PEN), amoxicillin (AMX), cefotaxime (CTX), and erythromycin (ERY)
For serotype 19A (for which the prevalence increased over the study period), increasing trends were found for non-susceptibility to penicillin (R2 = 0.726; β = 0.870; p = 0.001), amoxicillin (R2 = 0.804; β = 0.909; p < 0.001), cefotaxime (R2 = 0.546; β = 0.772; p = 0.005) and erythromycin (R2 = 0.546; β = 0.772; p = 0.009). Non-susceptibility rates to penicillin and erythromycin were around 80% in 2008-2009. Non-susceptibility to amoxicillin was first detected in 2003 and increased up to 38.0% in 2009. Non-susceptibility to cefotaxime was found in a single strain in 1999 whereas in the period 2001-2009 was firstly detected in 2004 and increased up to 20.0% in 2009.
When analyzing non-susceptibility rates in PCV7 serotypes (for which the prevalence decreased over the study period), no trends were found for penicillin (R2 = 0.106; β = -0.130; p = 0.721) with non-susceptibility rates of ≥ 67.5%, neither for erythromycin (R2 = 0.283; β = -0.602; p = 0.065) with non-susceptibility rates of ≥ 36.4%, nor for cefotaxime (R2 = 0.120; β = 0.067; p = 0.854) with non-susceptibility rates of ≤ 12.5% over the studied period. In contrast, there was a significant increasing trend for non-susceptibility to amoxicillin (R2 = 0.702; β = 0.858; p = 0.002), with rates around 50% in 2008-9. The individual analysis of PCV7 serotypes to determine serotype(s) responsible(s) for this increasing trend, showed that there was a non-susceptibility increasing trend for serotypes 19F (332 isolates; R2 = 0.517; β = 0.755; p = 0.012), 6B (138 isolates; R2 = 0.690; β = 0.851; p = 0.002), and 9V (49 isolates; R2 = 0.379; β = 0.669; p = 0.034), but not for serotypes 14 (203 isolates), 23F (93 isolates) and 4 (9 isolates). Isolates belonging to serotype 18C (31 isolates) were fully susceptible to amoxicillin.
Considering multiple resistance as a concomitant non-susceptibility event to β-lactams (using cefotaxime as marker) and erythromycin in a single isolate, the percentage of isolates exhibiting multiple resistance was > 10% in serotype 19A, with rates ranging from 11.7% to 20.0% in the 2007-2009 period.
Data from the United States at the time of PCV7 licensure showed that the vaccine (including the most common invasive and often drug-resistant serotypes causing disease in children) provided 89.1% protective efficacy against invasive disease caused by all serotypes . In a post-introduction surveillance study the percentage of reduction in invasive disease caused by PCV7 serotypes was 78%, with 50% reduction in invasive disease caused by vaccine-related serotypes . However, serotype replacement has been reported in surveillances (laboratory-based surveillance system) analyzing invasive isolates along the current decade in Spain [11–13], USA  and several European countries . In addition, several studies have shown that PCV7 vaccination also reduces the nasopharyngeal carriage of vaccine serotypes and increases carriage of non-vaccine types, with an overall rate of pneumococcal colonization unchanged in most cases [25–28]. AOM is the most common infection following pneumococcal colonization. Since PCV7 introduction, 57%-66.7% reduction in otitis media episodes caused by PCV7 serotypes has been reported with an increase in cases caused by non-vaccine serotypes, both in clinical trials [21, 29] and post-introduction surveillances [30, 31]. However the possible decrease in PCV7 serotypes among middle ear fluid isolates after the introduction of the PCV7 in Spain, remained to be explored.
The present study showed that serotype replacement has occurred among middle ear isolates from children in Spain as demonstrated by the decrease in PCV7 serotypes (from 62.9% in 2001 to 10.6% in 2009) and the increase in the prevalence of serotype 19A (from 6.7% in 1997-00 to > 35% from 2007 on) and to a lesser extent of serotype 3 (already described as an emergent serotype due to replacement ).
In a previous study analysing invasive isolates from children, one important fact of the significant decrease in the prevalence of PCV7 serotypes (from 62.4% in 2000 to 14.6% in 2007) was that the reduction was followed by a significant decrease in non-susceptibility to penicillin and erythromycin (from 51.4% and 39.5%, respectively, to around 20% for both antibiotics in 2007) . In contrast to this, the main finding of the present study is that in middle ear fluid isolates from children the significant decrease in PCV7 serotypes after PCV7 introduction was not associated with a decrease in non-susceptibility to penicillin or erythromycin among middle ear fluid isolates. High non-susceptibility rates (≈40-50%) to these two antibiotic markers were found all over the study period among all middle ear fluid isolates. Even more, a significant increase in amoxicillin non-susceptibility (from 8.1% in 2001 to ≈25% in 2008 and 2009) was found. By analysing the two major subgroups (serotype 19A and non-PCV7 serotypes), it can be deduced that this increase was mainly attributed to the significant increase in the prevalence of serotype 19A. In this serotype, it is important to remark that the first middle ear isolates non-susceptible to amoxicillin were detected in 2003, and proportions increased up to ≈38% in the period 2007-9, as occurred with non-susceptibility to cefotaxime that in the present decade was first detected in 2004 and reached 20% in 2009. Non-susceptibility to these two β-lactams and to erythromycin (multiple resistance) was found in > 10% of 19A isolates in the last years of the decade. This multiresistance pattern, challenging common therapeutic options, has also been described after vaccine introduction in USA in serotype 19A middle ear fluid isolates from children .
However, in our study, amoxicillin non-susceptibility cannot be entirely attributed to serotype 19A or other non-PCV7 serotypes since the significant decrease in PCV7 serotypes was associated with a significant increase in amoxicillin non-susceptibility among them, clustered in PCV7 serotypes 19F, 6B and 9V. The fact that these serotypes exhibited a significant decreasing trend over the study period suggests that these serotypes (and thus non-susceptibility to amoxicillin) will further decrease as vaccination rates increase. Nevertheless, the contribution of PCV7 serotypes to the prevalence of amoxicillin non-susceptibility among all middle ear isolates is relatively low since, although amoxicillin non-susceptibility in PCV7 isolates was ≈50% in 2008-9, all PCV7 isolates represented only ≈10% of all middle ear isolates received in the SRLP. The high antibiotic consumption for the treatment of AOM (the most common infection for which antibiotics are prescribed in children in the community ) represents the major pressure for resistance selection . This antibiotic pressure over the selectable residual occurrence of PCV7 serotypes (probably due to low vaccine coverage) may be a reason for the lack of reduction in resistance in parallel to the reduction in the prevalence of PCV7 serotypes (in contrast to invasive isolates). In this sense a previous study showed that S. pneumoniae is more often resistant to antibiotics in otitis prone children , and consumption of aminopenicillins is by far greater than consumption of macrolides in Spain .
As stated, data of this study came from a passive laboratory-based surveillance system with strains sent on a voluntary basis from hospitals all over the Spanish geography. Although the high number of isolates analysed over the large study period and its geographic diversity strengthen conclusions about serotypes involved in otitis in Spain, three main limitations of the study may be identified: 1) isolates were sent by microbiology departments in hospitals, and the SRLP does not have clinical information on the type of otitis or on how samples were collected, 2) isolates came from hospitals, thus they are not necessarily representative of pneumococci causing otitis in children attending primary care centres and 3) multilocus sequence typing was not performed, thus specific sequence types responsible for the increase in 19A cannot be identified, as was done for paediatric invasive isolates in a previous study highlighting the outstanding role of sequence types 320 and 878 (first detected in 2003 and 2007, respectively) .
The high prevalence of serotype 19A among paediatric middle ear isolates and the high rates of amoxicillin non-susceptibility found in this serotype are of great concern since amoxicillin is the most common antibiotic used in the treatment of AOM. These data suggest that non-PCV7 serotypes (mainly serotype 19A followed by serotypes 3 and 6A) are important etiological agents of AOM and support the added value of the broader coverage of the new 13-valent conjugate vaccine. Reducing nasopharyngeal carriage (and subsequently preventing AOM) of vaccine serotypes may be an added value in a context where it has been postulated that the reduction in drug-resistant S. pneumoniae will require a combination of conjugate vaccine and reductions in antibiotic use .
Acute otitis media
Middle ear fluid
7-valent pneumococcal conjugate vaccine
Spanish reference laboratory for pneumococci.
The authors are in debt with J. Yuste and C. Mendez for their critical review of the manuscript.
Part of this study was presented at the 28th Annual Meeting of the European Society for Paediatric Infectious Diseases, Nice, France, May 4-8, 2010, Abstract no. 424.
This study was supported in part by an unrestricted grant from Pfizer S.A., Madrid, Spain and PRISM-AG, Madrid, Spain. O.R. belongs to the Spanish Network for the Research in Infectious Diseases (REIPI).
- Hanage WP, Auranen K, Syrjänen R, Herva E, Mäkelä PH, Kilpi T, Spratt BG: Ability of pneumococcal serotypes and clones to cause acute otitis media: implications for the prevention of otitis media by conjugate vaccines. Infect Immun. 2004, 72: 76-81. 10.1128/IAI.72.1.76-81.2004.View ArticlePubMedPubMed CentralGoogle Scholar
- American Academy of Pediatrics Subcommittee on Management of Acute Otitis Media: Diagnosis and management of acute otitis media. Pediatrics. 2004, 113: 1451-1465.View ArticleGoogle Scholar
- Rodgers GL, Arguedas A, Cohen R, Dagan R: Global serotype distribution among Streptococcus pneumoniae isolates causing otitis media in children: potential implications for pneumococcal conjugate vaccines. Vaccine. 2009, 27: 3802-3810. 10.1016/j.vaccine.2009.04.021.View ArticlePubMedGoogle Scholar
- Dupont D, Mahjoub-Messai F, François M, Doit C, Mariani-Kurkdjian P, Bidet P, Bonacorsi S, Carol A, Bingen E: Evolving microbiology of complicated acute otitis media before and after introduction of the pneumococcal conjugate vaccine in France. Diagn Microbiol Infect Dis. 2010, 68: 89-92. 10.1016/j.diagmicrobio.2010.04.012.View ArticlePubMedGoogle Scholar
- Hotomi M, Billal DS, Kamide Y, Kanesada K, Uno Y, Kudo F, Ito M, Kakehata S, Sugita R, Ogami M, Yamanaka N, Advanced Treatment for Otitis Media Study Group (ATOMS): Serotype distribution and penicillin resistance of Streptococcus pneumoniae isolates from middle ear fluids of pediatric patients with acute otitis media in Japan. J Clin Microbiol. 2008, 46: 3808-3810. 10.1128/JCM.01782-08.View ArticlePubMedPubMed CentralGoogle Scholar
- Onwubiko C, Shires C, Quin LR, Swiatlo E, McDaniel LS: Characterization of Streptococcus pneumoniae isolated from children with otitis media. FEMS Immunol Med Microbiol. 2007, 50: 119-125. 10.1111/j.1574-695X.2007.00245.x.View ArticlePubMedGoogle Scholar
- Fenoll A, Aguilar L, Robledo O, Giménez MJ, Tarragó D, Granizo JJ, Gimeno M, Coronel P: Influence of the beta-lactam resistance phenotype on the cefuroxime versus cefditoren susceptibility of Streptococcus pneumoniae and Haemophilus influenzae recovered from children with acute otitis media. J Antimicrob Chemother. 2007, 60: 323-327. 10.1093/jac/dkm209.View ArticlePubMedGoogle Scholar
- Thomas JC, Figueira M, Fennie KP, Laufer AS, Kong Y, Pichicheiro ME, Pelton SI, Pettigrew MM: Streptococcus pneumoniae clonal complex 199: genetic diversity and tissue-specific virulence. PLoS One. 2011, 6: e18649-10.1371/journal.pone.0018649.View ArticlePubMedPubMed CentralGoogle Scholar
- Gruber MF, Pratt D, Haase M: Licensing of pneumococcal conjugate vaccines for children and adults: regulatory perspective from the European Medicines Agency and the U.S. Food and Drug Administration. Pneumoccal Vaccines. Edited by: Siber GR, Klugman KP, Mäkelä PH. 2008, Washington DC: ASM Press, 183-196. 1View ArticleGoogle Scholar
- Grupo de Trabajo de la Ponencia de Registro y Programa de Vacunas: Enfermedad invasora por Streptococcus pneumoniae. Implicación de la vacunación con la vacuna conjugada heptavalente. Ministerio de Sanidad y Consumo. 2006, Madrid, SpainGoogle Scholar
- Fenoll A, Granizo JJ, Aguilar L, Giménez MJ, Aragoneses-Fenoll L, Hanquet G, Casal J, Tarragó D: Temporal trends of invasive Streptococcus pneumoniae serotypes and antimicrobial resistance patterns in Spain from 1979 to 2007. J Clin Microbiol. 2009, 47: 1012-1020. 10.1128/JCM.01454-08.View ArticlePubMedPubMed CentralGoogle Scholar
- Fenoll A, Aguilar L, Granizo JJ, Giménez MJ, Aragoneses-Fenoll L, Mendez C, Tarragó D: Has the licensing of respiratory quinolones for adults and the 7-valent pneumococcal conjugate vaccine (PCV-7) for children had herd effects with respect to antimicrobial non-susceptibility in invasive Streptococcus pneumoniae?. J Antimicrob Chemother. 2008, 62: 1430-1433. 10.1093/jac/dkn413.View ArticlePubMedGoogle Scholar
- Fenoll A, Giménez MJ, Vicioso MD, Granizo JJ, Robledo O, Aguilar L: Susceptibility of pneumococci causing meningitis in Spain and prevalence among such isolates of serotypes contained in the 7-valent pneumococcal conjugate vaccine. J Antimicrob Chemother. 2009, 64: 1338-1340. 10.1093/jac/dkp376.View ArticlePubMedGoogle Scholar
- Millar EV, O'Brien KL, Watt JP, Bronsdon MA, Dallas J, Whitney CG, Reid R, Santosham M: Effect of community-wide conjugate pneumococcal vaccine use in infancy on nasopharyngeal carriage through 3 years of age: a cross-sectional study in a high-risk population. Clin Infect Dis. 2006, 43: 8-15. 10.1086/504802.View ArticlePubMedGoogle Scholar
- Spratt BG, Greenwood BM: Prevention of pneumococcal disease by vaccination: does serotype replacement matter?. Lancet. 2000, 356: 1210-1211. 10.1016/S0140-6736(00)02779-3.View ArticlePubMedGoogle Scholar
- Ghaffar F, Barton T, Lozano J, Muniz LS, Hicks P, Gan V, Ahmad N, McCracken GH: Effect of the 7-valent pneumococcal conjugate vaccine on nasopharyngeal colonization by Streptococcus pneumoniae in the first 2 years of life. Clin Infect Dis. 2004, 39: 930-938. 10.1086/423379.View ArticlePubMedGoogle Scholar
- Lund E, Henrichsen J: Laboratory diagnosis, serology and epidemiology of Streptococcus pneumoniae. Methods Microbiol. 1978, 12: 241-262.View ArticleGoogle Scholar
- Fenoll A, Jado I, Vicioso D, Casal J: Dot blot assay for the serotyping of pneumococci. J Clin Microbiol. 1997, 35: 764-766.PubMedPubMed CentralGoogle Scholar
- Clinical and Laboratory Standards Institute/NCCLS: Performance Standards for Antimicrobial Susceptibility Testing: Nineteenth Informational Supplement M100-S19. CLSI. 2009, Wayne, PA, USAGoogle Scholar
- Fenoll A, Aguilar L, Robledo O, Giménez MJ, Granizo JJ, Biek D, Tarragó D: In vitro activity of ceftaroline against Streptococcus pneumoniae isolates exhibiting resistance to penicillin, amoxicillin, and cefotaxime. Antimicrob Agents Chemother. 2008, 52: 4209-4210. 10.1128/AAC.00712-08.View ArticlePubMedPubMed CentralGoogle Scholar
- Black S, Shinefield H, Fireman B, Lewis E, Ray P, Hansen JR, Elvin L, Ensor KM, Hackell J, Siber G, Malinoski F, Madore D, Chang I, Kohberger R, Watson W, Austrian R, Edwards K: Efficacy, safety and immunogenicity of heptavalent pneumococcal conjugate vaccine in children. Northern California Kaiser Permanente Vaccine Study Center Group. Pediatr Infect Dis J. 2000, 19: 187-195. 10.1097/00006454-200003000-00003.View ArticlePubMedGoogle Scholar
- Whitney CG, Farley MM, Hadler J, Harrison LH, Bennett NM, Lynfield R, Reingold A, Cieslak PR, Pilishvili T, Jackson D, Facklam RR, Jorgensen JH, Schuchat A, Active Bacterial Core Surveillance of the Emerging Infections Program Network: Decline in invasive pneumococcal disease after the introduction of protein-polysaccharide conjugate vaccine. N Engl J Med. 2003, 348: 1737-1746. 10.1056/NEJMoa022823.View ArticlePubMedGoogle Scholar
- Kyaw MH, Lynfield R, Schaffner W, Craig AS, Hadler J, Reingold A, Thomas AR, Harrison LH, Bennett NM, Farley MM, Facklam RR, Jorgensen JH, Besser J, Zell ER, Schuchat A, Whitney CG, Active Bacterial Core Surveillance of the Emerging Infections Program Network: Effect of introduction of the pneumococcal conjugate vaccine on drug-resistant Streptococcus pneumoniae. N Engl J Med. 2006, 354: 1455-1463. 10.1056/NEJMoa051642.View ArticlePubMedGoogle Scholar
- Isaacman DJ, McIntosh ED, Reinert RR: Burden of invasive pneumococcal disease and serotype distribution among Streptococcus pneumoniae isolates in young children in Europe: impact of the 7-valent pneumococcal conjugate vaccine and considerations for future conjugate vaccines. Int J Infect Dis. 2010, 14: e197-209.View ArticlePubMedGoogle Scholar
- Hennessy TW, Singleton RJ, Bulkow LR, Bruden DL, Hurlburt DA, Parks D, Moore M, Parkinson AJ, Schuchat A, Butler JC: Impact of heptavalent pneumococcal conjugate vaccine on invasive disease, antimicrobial resistance and colonization in Alaska Natives: progress towards elimination of a health disparity. Vaccine. 2005, 23: 5464-5473. 10.1016/j.vaccine.2005.08.100.View ArticlePubMedGoogle Scholar
- Frazão N, Brito-Avô A, Simas C, Saldanha J, Mato R, Nunes S, Sousa NG, Carriço JA, Almeida JS, Santos-Sanches I, de Lencastre H: Effect of the seven-valent conjugate pneumococcal vaccine on carriage and drug resistance of Streptococcus pneumoniae in healthy children attending day-care centers in Lisbon. Pediatr Infect Dis J. 2005, 24: 243-252. 10.1097/01.inf.0000154326.77617.3e.View ArticlePubMedGoogle Scholar
- Revai K, McCormick DP, Patel J, Grady JJ, Saeed K, Chonmaitree T: Effect of pneumococcal conjugate vaccine on nasopharyngeal bacterial colonization during acute otitis media. Pediatrics. 2006, 117: 1823-1829. 10.1542/peds.2005-1983.View ArticlePubMedGoogle Scholar
- McGee L: The coming of age of niche vaccines? Effect of vaccines on resistance profiles in Streptococcus pneumoniae. Curr Opin Microbiol. 2007, 10: 473-478. 10.1016/j.mib.2007.08.008.View ArticlePubMedGoogle Scholar
- Eskola J, Kilpi T, Palmu A, Jokinen J, Haapakoski J, Herva E, Takala A, Käyhty H, Karma P, Kohberger R, Siber G, Mäkelä PH, Finnish Otitis Media Study Group: Efficacy of a pneumococcal conjugate vaccine against acute otitis media. N Engl J Med. 2001, 344: 403-409. 10.1056/NEJM200102083440602.View ArticlePubMedGoogle Scholar
- Jacobs MR, Good CE, Beall B, Bajaksouzian S, Windau AR, Whitney CG: Changes in serotypes and antimicrobial susceptibility of invasive Streptococcus pneumoniae strains in Cleveland: a quarter century of experience. J Clin Microbiol. 2008, 46: 982-990. 10.1128/JCM.02321-07.View ArticlePubMedPubMed CentralGoogle Scholar
- Casey JR, Adlowitz DG, Pichichero ME: New patterns in the otopathogens causing acute otitis media six to eight years after introduction of pneumococcal conjugate vaccine. Pediatr Infect Dis J. 2010, 29: 304-309.PubMedPubMed CentralGoogle Scholar
- Abdelnour A, Soley C, Guevara S, Porat N, Dagan R, Arguedas A: Streptococcus pneumoniae serotype 3 among Costa Rican children with otitis media: clinical, epidemiological characteristics and antimicrobial resistance patterns. BMC Pediatr. 2009, 9: 52-10.1186/1471-2431-9-52.View ArticlePubMedPubMed CentralGoogle Scholar
- Pichichero ME, Casey JR: Emergence of a multiresistant serotype 19A pneumococcal strain not included in the 7-valent conjugate vaccine as an otopathogen in children. JAMA. 2007, 298: 1772-1778. 10.1001/jama.298.15.1772.View ArticlePubMedGoogle Scholar
- Tarragó D, Aguilar L, García R, Gimenez MJ, Granizo JJ, Fenoll A: Evolution of Clonal and Susceptibility Profiles of Serotype 19A Streptococcus pneumoniae among Invasive Isolates from Children in Spain, 1990 to 2008. Antimicrob Agents Chemother. 2011, 55: 2297-2302. 10.1128/AAC.01494-10.View ArticlePubMedPubMed CentralGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2334/11/239/prepub
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