BACKGROUND: Multi-locus sequence typing (MLST) of pneumococcal isolates collected during an efficacy trial of the 7-valent pneumococcal conjugate vaccine (PCV7) among Navajo and White Mountain Apache children from 1998 to 2000 showed a non-differential expansion of pre-existing sequence types (STs) and only one capsule-switching event in the PCV7-randomized communities. PCV7 was introduced as a routine infant vaccine in October 2000. We assessed variability in PCV7 effectiveness and mechanisms of ST replacement after prolonged routine PCV7 use. METHODS: We applied MLST to 267 non-vaccine type pneumococcal carriage and invasive disease isolates from Navajo and White Mountain Apache children from 2006 to 2008, and compared them to those from 1998 to 2000. Microarray was used to confirm capsule switching events. RESULTS: The primary mechanism of ST replacement among Navajo and White Mountain Apache children was expansion of existing STs, although introduction of new STs was an important secondary mechanism. ST199, a majority being serotype 19A, was the most common ST in both eras. Only ST193 (serotype 21) was preferentially expanding in the PCV7 era. Three examples of capsule switching were identified. No variability in vaccine effectiveness by ST was observed. CONCLUSION: We did not observe an influence of ST on PCV7 serotype-specific effectiveness, although some STs may be favored in replacement. Copyright Â
BACKGROUND: Multi-locus sequence typing (MLST) of pneumococcal isolates collected during an efficacy trial of the 7-valent pneumococcal conjugate vaccine (PCV7) among Navajo and White Mountain Apache children from 1998 to 2000 showed a non-differential expansion of pre-existing sequence types (STs) and only one capsule-switching event in the PCV7-randomized communities. PCV7 was introduced as a routine infant vaccine in October 2000. We assessed variability in PCV7 effectiveness and mechanisms of ST replacement after prolonged routine PCV7 use. METHODS: We applied MLST to 267 non-vaccine type pneumococcal carriage and invasive disease isolates from Navajo and White Mountain Apache children from 2006 to 2008, and compared them to those from 1998 to 2000. Microarray was used to confirm capsule switching events. RESULTS: The primary mechanism of ST replacement among Navajo and White Mountain Apache children was expansion of existing STs, although introduction of new STs was an important secondary mechanism. ST199, a majority being serotype 19A, was the most common ST in both eras. Only ST193 (serotype 21) was preferentially expanding in the PCV7 era. Three examples of capsule switching were identified. No variability in vaccine effectiveness by ST was observed. CONCLUSION: We did not observe an influence of ST on PCV7 serotype-specific effectiveness, although some STs may be favored in replacement. Copyright Â
Authors: Jennifer R Scott; Jason Hinds; Katherine A Gould; Eugene V Millar; Raymond Reid; Mathuram Santosham; Katherine L O'Brien; William P Hanage Journal: J Infect Dis Date: 2012-04-25 Impact factor: 5.226
Authors: Gabriela Echániz-Aviles; Soraia I Guerreiro; Catarina Silva-Costa; Catarina I Mendes; João André Carriço; María Noemí Carnalla-Barajas; Araceli Soto-Noguerón; Maria Elena Velazquez-Meza; José Melo-Cristino; Antonio Luévanos-Velazquez; Lucía Martínez-Medina; María Del Rosario Vázquez-Larios; Mário Ramirez Journal: J Clin Microbiol Date: 2019-01-02 Impact factor: 5.948
Authors: K Aaron Geno; Gwendolyn L Gilbert; Joon Young Song; Ian C Skovsted; Keith P Klugman; Christopher Jones; Helle B Konradsen; Moon H Nahm Journal: Clin Microbiol Rev Date: 2015-07 Impact factor: 26.132
Authors: Rene L Begay; Nanibaa' A Garrison; Franklin Sage; Mark Bauer; Ursula Knoki-Wilson; David H Begay; Beverly Becenti-Pigman; Katrina G Claw Journal: Hum Biol Date: 2020-07-09 Impact factor: 0.553
Authors: Karen Rudolph; M G Bruce; L Bulkow; T Zulz; A Reasonover; M Harker-Jones; D Hurlburt; T W Hennessy Journal: Int J Circumpolar Health Date: 2013-08-05 Impact factor: 1.228
Authors: Paul Adamiak; Otto G Vanderkooi; James D Kellner; Anthony B Schryvers; Julie A Bettinger; Joenel Alcantara Journal: BMC Microbiol Date: 2014-06-03 Impact factor: 3.605