Concurrent Bacteremia Due to Non-vaccine Serotype 24F Pneumococcus in Twins: A Rapid Increase in Serotype 24F-invasive Pneumococcal Disease and its High Invasive Potential.


Journal

The Pediatric infectious disease journal
ISSN: 1532-0987
Titre abrégé: Pediatr Infect Dis J
Pays: United States
ID NLM: 8701858

Informations de publication

Date de publication:
01 2020
Historique:
entrez: 10 12 2019
pubmed: 10 12 2019
medline: 22 9 2020
Statut: ppublish

Résumé

Although concurrent bacteremia in siblings is rare, serotype 24F Streptococcus pneumoniae was isolated from the blood of twin 1-year-old girls within a 3-day interval, supporting the high invasive potential of this serotype. As the prevalence of childhood serotype 24F-invasive pneumococcal diseases increases in Europe and the Western Pacific Region, investigation and surveillance of this serotype are necessary.

Identifiants

pubmed: 31815842
doi: 10.1097/INF.0000000000002508
pii: 00006454-202001000-00019
doi:

Types de publication

Case Reports Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

85-87

Références

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Suga S, Chang B, Asada K, et al. Nationwide population-based surveillance of invasive pneumococcal disease in Japanese children: effects of the seven-valent pneumococcal conjugate vaccine. Vaccine. 2015;33:6054–6060.
Hjuler T, Poulsen G, Wohlfahrt J, et al. Genetic susceptibility to severe infection in families with invasive pneumococcal disease. Am J Epidemiol. 2008;167:814–819.
Grazioli S, Hamilton SJ, McKinnon ML, et al. IRAK-4 deficiency as a cause for familial fatal invasive infection by Streptococcus pneumoniae. Clin Immunol. 2016;163:14–16.
Nakano S, Fujisawa T, Ito Y, et al. Serotypes, antimicrobial susceptibility, and molecular epidemiology of invasive and non-invasive Streptococcus pneumoniae isolates in paediatric patients after the introduction of 13-valent conjugate vaccine in a nationwide surveillance study conducted in Japan in 2012-2014. Vaccine. 2016;34:67–76.
Varon E, Cohen R, Béchet S, et al. Invasive disease potential of pneumococci before and after the 13-valent pneumococcal conjugate vaccine implementation in children. Vaccine. 2015;33:6178–6185.
Balsells E, Dagan R, Yildirim I, et al. The relative invasive disease potential of Streptococcus pneumoniae among children after PCV introduction: a systematic review and meta-analysis. J Infect. 2018;77:368–378.
Ouldali N, Levy C, Varon E, et al.; French Pediatric Meningitis Network. Incidence of paediatric pneumococcal meningitis and emergence of new serotypes: a time-series analysis of a 16-year French national survey. Lancet Infect Dis. 2018;18:983–991.
Balsells E, Guillot L, Nair H, et al. Serotype distribution of Streptococcus pneumoniae causing invasive disease in children in the post-PCV era: a systematic review and meta-analysis. PLoS One. 2017;12:e0177113.
Ubukata K, Takata M, Morozumi M, et al.; Invasive Pneumococcal Diseases Surveillance Study Group. Effects of pneumococcal conjugate vaccine on genotypic penicillin resistance and serotype changes, Japan, 2010-2017. Emerg Infect Dis. 2018;24:2010–2020.

Auteurs

Toshiaki Kawabata (T)

From the Department of Pediatrics, Kagoshima Seikyo Hospital, Kagoshima, Japan.

Yoichi Tenokuchi (Y)

From the Department of Pediatrics, Kagoshima Seikyo Hospital, Kagoshima, Japan.

Hiroki Yamakuchi (H)

Department of General Medicine, Kagoshima Seikyo Hospital, Kagoshima, Japan.

Hirotsugu Sameshima (H)

From the Department of Pediatrics, Kagoshima Seikyo Hospital, Kagoshima, Japan.

Hirosuke Katayama (H)

From the Department of Pediatrics, Kagoshima Seikyo Hospital, Kagoshima, Japan.

Takeshi Ota (T)

From the Department of Pediatrics, Kagoshima Seikyo Hospital, Kagoshima, Japan.

Masatomo Tokunaga (M)

From the Department of Pediatrics, Kagoshima Seikyo Hospital, Kagoshima, Japan.

Tomoko Takezaki (T)

From the Department of Pediatrics, Kagoshima Seikyo Hospital, Kagoshima, Japan.

Suehiro Tamae (S)

From the Department of Pediatrics, Kagoshima Seikyo Hospital, Kagoshima, Japan.

Toru Nakamura (T)

From the Department of Pediatrics, Kagoshima Seikyo Hospital, Kagoshima, Japan.

Bin Chang (B)

Department of Microbiology I, National Institute of Infectious Diseases, Tokyo, Japan.

Yuichi Kodama (Y)

Department of Pediatrics, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.

Naoko Imuta (N)

Department of Microbiology, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.

Tadasuke Ooka (T)

Department of Microbiology, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.

Yasuhiro Okamoto (Y)

Department of Pediatrics, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.

Shigeru Suga (S)

Infectious Disease Center and Department of Clinical Research, National Hospital Organization Mie Hospital, Mie, Japan.

Junichiro Nishi (J)

Department of Microbiology, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.

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