Cargando…

Noninvasive Pneumococcal Pneumonia in Adults in Portugal (2012–2015): Resilience of Vaccine Serotypes and Emergence of Non-vaccine Serotypes

BACKGROUND: The 13-valent pneumococcal conjugate vaccine (PCV13) is available in Portugal through the private sector for children since 2010. In 2015 it was included in the national immunization program for children. With the aim of evaluating a possible herd effect, we monitored the serotypes and a...

Descripción completa

Detalles Bibliográficos
Autores principales: Horácio, Andreia N, Silva-Costa, Catarina, Lopes, Joana P, Ramirez, Mario, Melo-Cristino, Jose
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5631022/
http://dx.doi.org/10.1093/ofid/ofx163.1177
_version_ 1783269349971197952
author Horácio, Andreia N
Silva-Costa, Catarina
Lopes, Joana P
Ramirez, Mario
Melo-Cristino, Jose
author_facet Horácio, Andreia N
Silva-Costa, Catarina
Lopes, Joana P
Ramirez, Mario
Melo-Cristino, Jose
author_sort Horácio, Andreia N
collection PubMed
description BACKGROUND: The 13-valent pneumococcal conjugate vaccine (PCV13) is available in Portugal through the private sector for children since 2010. In 2015 it was included in the national immunization program for children. With the aim of evaluating a possible herd effect, we monitored the serotypes and antimicrobial resistance of isolates (2012–2015) causing noninvasive pneumococcal pneumonia (NIPP) in adults (≥18 yrs). METHODS: 1435 adult NIPP isolates were recovered, serotyped by the Quellung reaction and tested for susceptibility to antimicrobials by disk diffusion or Etest. RESULTS: There were 50 different serotypes among the 1435 isolates. The most common were serotypes 3 (14%), 11A (8%), 19F (6%), 23A (5%), 6C (5%), 19A (4%), 23B (4%) and 9N (4%). Non-typable isolates accounted for 4% of the collection. The overall proportion of PCV13 serotypes declined from 44% in 2010 to 30% in 2015 (P < 0.001) although it remained relatively stable in 2012–2015. Several serotypes exhibited strong fluctuations in 2007–2015, suggesting that adult NIPP was under the influence of both vaccine-related and non-vaccine-related pressures. PCV7 serotypes (12% in 2012–2015) and the serotypes exclusively found in the 23-valent polysaccharide vaccine (26% in 2012–2015) did not change significantly in 2007–2015, while non-vaccine types increased in proportion (from 27% in 2010 to 42% in 2015, P < 0.001). Penicillin non-susceptibility and erythromycin resistance was found in 18% and 22% of the isolates recovered in 2012–2015, with no significant changes seen since 2007. CONCLUSION: While a significant fraction of NIPP is still caused by vaccine serotypes, the availability of PCV13 in the national immunization program for children from 2015 onwards may further reduce their importance in NIPP, questioning the need for adult vaccination. DISCLOSURES: M. Ramirez, Pfizer: Speaker’s Bureau, Speaker honorarium; GSK: Consultant, Consulting fee; J. Melo-Cristino, Pfizer: Grant Investigator, Independent Contractor and Speaker’s Bureau, Grant recipient, Research grant and Speaker honorarium; GSK: Grant Investigator and Speaker’s Bureau, Grant recipient and Speaker honorarium; Bial: Speaker’s Bureau, Speaker honorarium; Novartis: Speaker’s Bureau, Speaker honorarium
format Online
Article
Text
id pubmed-5631022
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-56310222017-11-07 Noninvasive Pneumococcal Pneumonia in Adults in Portugal (2012–2015): Resilience of Vaccine Serotypes and Emergence of Non-vaccine Serotypes Horácio, Andreia N Silva-Costa, Catarina Lopes, Joana P Ramirez, Mario Melo-Cristino, Jose Open Forum Infect Dis Abstracts BACKGROUND: The 13-valent pneumococcal conjugate vaccine (PCV13) is available in Portugal through the private sector for children since 2010. In 2015 it was included in the national immunization program for children. With the aim of evaluating a possible herd effect, we monitored the serotypes and antimicrobial resistance of isolates (2012–2015) causing noninvasive pneumococcal pneumonia (NIPP) in adults (≥18 yrs). METHODS: 1435 adult NIPP isolates were recovered, serotyped by the Quellung reaction and tested for susceptibility to antimicrobials by disk diffusion or Etest. RESULTS: There were 50 different serotypes among the 1435 isolates. The most common were serotypes 3 (14%), 11A (8%), 19F (6%), 23A (5%), 6C (5%), 19A (4%), 23B (4%) and 9N (4%). Non-typable isolates accounted for 4% of the collection. The overall proportion of PCV13 serotypes declined from 44% in 2010 to 30% in 2015 (P < 0.001) although it remained relatively stable in 2012–2015. Several serotypes exhibited strong fluctuations in 2007–2015, suggesting that adult NIPP was under the influence of both vaccine-related and non-vaccine-related pressures. PCV7 serotypes (12% in 2012–2015) and the serotypes exclusively found in the 23-valent polysaccharide vaccine (26% in 2012–2015) did not change significantly in 2007–2015, while non-vaccine types increased in proportion (from 27% in 2010 to 42% in 2015, P < 0.001). Penicillin non-susceptibility and erythromycin resistance was found in 18% and 22% of the isolates recovered in 2012–2015, with no significant changes seen since 2007. CONCLUSION: While a significant fraction of NIPP is still caused by vaccine serotypes, the availability of PCV13 in the national immunization program for children from 2015 onwards may further reduce their importance in NIPP, questioning the need for adult vaccination. DISCLOSURES: M. Ramirez, Pfizer: Speaker’s Bureau, Speaker honorarium; GSK: Consultant, Consulting fee; J. Melo-Cristino, Pfizer: Grant Investigator, Independent Contractor and Speaker’s Bureau, Grant recipient, Research grant and Speaker honorarium; GSK: Grant Investigator and Speaker’s Bureau, Grant recipient and Speaker honorarium; Bial: Speaker’s Bureau, Speaker honorarium; Novartis: Speaker’s Bureau, Speaker honorarium Oxford University Press 2017-10-04 /pmc/articles/PMC5631022/ http://dx.doi.org/10.1093/ofid/ofx163.1177 Text en © The Author 2017. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Abstracts
Horácio, Andreia N
Silva-Costa, Catarina
Lopes, Joana P
Ramirez, Mario
Melo-Cristino, Jose
Noninvasive Pneumococcal Pneumonia in Adults in Portugal (2012–2015): Resilience of Vaccine Serotypes and Emergence of Non-vaccine Serotypes
title Noninvasive Pneumococcal Pneumonia in Adults in Portugal (2012–2015): Resilience of Vaccine Serotypes and Emergence of Non-vaccine Serotypes
title_full Noninvasive Pneumococcal Pneumonia in Adults in Portugal (2012–2015): Resilience of Vaccine Serotypes and Emergence of Non-vaccine Serotypes
title_fullStr Noninvasive Pneumococcal Pneumonia in Adults in Portugal (2012–2015): Resilience of Vaccine Serotypes and Emergence of Non-vaccine Serotypes
title_full_unstemmed Noninvasive Pneumococcal Pneumonia in Adults in Portugal (2012–2015): Resilience of Vaccine Serotypes and Emergence of Non-vaccine Serotypes
title_short Noninvasive Pneumococcal Pneumonia in Adults in Portugal (2012–2015): Resilience of Vaccine Serotypes and Emergence of Non-vaccine Serotypes
title_sort noninvasive pneumococcal pneumonia in adults in portugal (2012–2015): resilience of vaccine serotypes and emergence of non-vaccine serotypes
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5631022/
http://dx.doi.org/10.1093/ofid/ofx163.1177
work_keys_str_mv AT horacioandreian noninvasivepneumococcalpneumoniainadultsinportugal20122015resilienceofvaccineserotypesandemergenceofnonvaccineserotypes
AT silvacostacatarina noninvasivepneumococcalpneumoniainadultsinportugal20122015resilienceofvaccineserotypesandemergenceofnonvaccineserotypes
AT lopesjoanap noninvasivepneumococcalpneumoniainadultsinportugal20122015resilienceofvaccineserotypesandemergenceofnonvaccineserotypes
AT ramirezmario noninvasivepneumococcalpneumoniainadultsinportugal20122015resilienceofvaccineserotypesandemergenceofnonvaccineserotypes
AT melocristinojose noninvasivepneumococcalpneumoniainadultsinportugal20122015resilienceofvaccineserotypesandemergenceofnonvaccineserotypes
AT noninvasivepneumococcalpneumoniainadultsinportugal20122015resilienceofvaccineserotypesandemergenceofnonvaccineserotypes