Serotype distribution and antimicrobial resistance of invasiveStreptococcus pneumoniaeisolates in Bulgaria before the introduction of pneumococcal conjugate vaccine

2012 ◽  
Vol 24 (1) ◽  
pp. 12-17 ◽  
Author(s):  
L P Setchanova ◽  
A Alexandrova ◽  
I Mitov ◽  
D Nashev ◽  
T Kantardjiev ◽  
...  
Vaccine ◽  
2011 ◽  
Vol 29 (6) ◽  
pp. 1139-1144 ◽  
Author(s):  
Ana Paula de O. Menezes ◽  
Leila C. Campos ◽  
Milena S. dos Santos ◽  
Jailton Azevedo ◽  
Renan C.N. dos Santos ◽  
...  

2021 ◽  
Vol 9 (7) ◽  
pp. 1428
Author(s):  
Catarina Silva-Costa ◽  
Joana Gomes-Silva ◽  
Lúcia Prados ◽  
Mário Ramirez ◽  
José Melo-Cristino ◽  
...  

The introduction of pneumococcal conjugate vaccines PCV7 and PCV13 led to decreases in incidence of pediatric invasive pneumococcal disease (pIPD) and changes in serotype distribution. We evaluated the consequences of higher vaccine uptake after the introduction of PCV13 in the National Immunization Plan (NIP) in 2015. Besides culture and conventional serotyping, the use of molecular methods to detect and serotype pneumococci in both pleural and cerebrospinal fluid samples contributed to 30% of all pIPD (n = 232) in 2015–2018. The most frequently detected serotypes were: 3 (n = 59, 26%), 10A (n = 17, 8%), 8 (n = 16, 7%) and 19A (n = 10, 4%). PCV13 serotypes still accounted for 46% of pIPD cases. Serotypes not included in any currently available conjugate vaccine (NVT) are becoming important causes of pIPD, with the increases in serotypes 8 and 33F being of particular concern given the importance of serotype 8 in adult IPD and the antimicrobial resistance of serotype 33F isolates. This study highlights the importance of using molecular methods in pIPD surveillance since these allowed a better case ascertainment and the identification of serotype 3 as the leading cause of pIPD. Even in a situation of vaccine uptake >95% for 3 years, PCV13 serotypes remain important causes of pIPD.


2013 ◽  
Vol 13 (1) ◽  
Author(s):  
Felipe Piedade Gonçalves Neves ◽  
Tatiana Castro Abreu Pinto ◽  
Mariane Alves Corrêa ◽  
Roberta dos Anjos Barreto ◽  
Laís de Souza Gouveia Moreira ◽  
...  

2021 ◽  
Vol 8 ◽  
Author(s):  
Markus A. Rose ◽  
Maren Laurenz ◽  
Ralf Sprenger ◽  
Matthias Imöhl ◽  
Mark van der Linden

Epidemiological data on nasopharyngeal (NP) bacterial carriage in children in Germany are scarce. We prospectively characterized NP colonization to evaluate the impact of pneumococcal immunization. We longitudinally collected NP swabs from 2-month-old infants (visit 1; V1) at eight representative pediatric offices 10/2008-06/2009. The second swabs were taken at age 9–12 months (V2); the third swab was taken 3–6 months after the booster vaccination at age 17–19 months (V3), and the fourth swab (V4) at age 59–61 months. Samples were broth enriched, cultured for bacteria, and isolates were serotyped. Demographic risk factors for colonization were evaluated. Among 242 vaccinees, bacterial NP carriage increased with age [from 27.2% (V1) to 70.1% (V4)]; leading isolates were S. pneumoniae, H. influenzae, M. catarrhalis, and S. pyogenes. Overall pneumococcal carriage increased [14.7% (V1), 31.5% (V2), 34.8% (V3), 42.2% (V4)], being even greater among day-care attendees. Serotype distribution changed during the study period, with vaccine serotypes declining. At visit 4, 10-valent pneumococcal conjugate vaccine (PCV10) serotypes were no longer among the NP flora, while some serotypes unique to 13-valent pneumococcal conjugate vaccine (PCV13; 3 and 19A) were found. In Germany, universal infant PCV immunization was associated with an almost complete eradication of PCV-serotypes and concomitant increase of non-PCV-serotypes, mainly 11A, 22F, and 23A.


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