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Have changing pneumococcal vaccination programmes impacted disease in Ontario?
Gillian H Lim1, Anne E Wormsbecker, Allison McGeer
1Immunization and Vaccine Preventable Diseases, Public Health Ontario, Toronto, ON, Canada. gillian.lim@oahpp.ca
Insights
Ontario’s infant pneumococcal conjugate vaccine (PCV) programs showed success, reducing invasive pneumococcal disease (IPD) rates. Early impacts of PCV10 were noted in infants, but older adults still face a significant IPD burden.
Area of Science:
- Infectious Diseases
- Vaccinology
- Public Health Surveillance
Background:
- Ontario introduced infant 7-valent pneumococcal conjugate vaccine (PCV7) in 2005, later replaced by PCV10 and PCV13.
- Adults aged 65+ have had universal access to the 23-valent polysaccharide vaccine (PPV23) since 1996.
- PCV13 became available for adults aged 50+ in 2012, prompting an examination of vaccination program impacts on invasive pneumococcal disease (IPD).
Purpose of the Study:
- To evaluate the effectiveness of publicly funded infant vaccination programs on invasive pneumococcal disease (IPD) incidence.
- To assess the impact of PCV7, PCV10, and PCV13 introduction on IPD serotype distribution and rates.
- To identify disease burden in different age groups, particularly among older adults eligible for PPV23 and PCV13.
Main Methods:
- Analysis of laboratory data from population-based IPD surveillance in Ontario, Canada.
- Inclusion of data from the Toronto Invasive Bacterial Disease Network and Public Health Ontario Laboratories.
- Study period: January 1, 2008, to December 31, 2010.
Main Results:
- Overall IPD incidence ranged from 7.4 to 9.3 per 100,000 population between 2008-2010.
- Adults aged 65+ exhibited the highest IPD incidence (21.5-25.6/100,000), with a significant increase during the study period.
- A 77% decrease in PCV7 serotype IPD was observed among vaccine-eligible children, with some impact also seen in non-eligible populations.
Conclusions:
- Ontario's PCV7 program demonstrated success through serotype-specific IPD reductions, indicating herd immunity effects.
- Early evidence suggests PCV10 introduction had a positive impact on infant IPD rates.
- A significant burden of invasive pneumococcal disease persists among older adult populations.
Background:
Publicly funded infant 7-valent pneumococcal conjugate vaccine (PCV7) was introduced in Ontario, Canada in 2005 and was replaced by 10- and 13-valent vaccines (PCV10, PCV13) in October 2009 and November 2010, respectively. Among adults ≥ 65 years, a 23-valent polysaccharide vaccine (PPV23) has been universally available since 1996. In January 2012, PCV13 was approved for adults ≥ 50 years. This study examines the impact of publicly funded vaccination programmes on invasive pneumococcal disease (IPD).
Methods:
Laboratory data from population-based surveillance for IPD conducted at the Toronto Invasive Bacterial Disease Network and from Public Health Ontario Laboratories between January 1, 2008 and December 31, 2010 were analyzed.
Results:
Between 2008 and 2010 there were 3259 cases of IPD; overall incidence was 7.4/9.3/8.3 per 100,000 in 2008/9/10, respectively. Incidence increased significantly among adults 65+ years during the period; this group had the highest incidence (21.5-25.6/100,000). The second highest incidence in 2008 and 2009 was in infants <1 year, whereas in 2010 it was in children 1-4 years. Among children <5 years, 68% and 19% of serotypes were covered by PCV13 and PCV10, respectively, between 2008 and 2010. In 2009, 6 cases with the 3 additional PCV10 serotypes were reported in infants compared with 2 in 2010. Among persons eligible for PCV7 (born≥2004), there was a 77% decrease in the rate of IPD due to PCV7 serotypes between 2008 and 2010 and a 60% decrease in PCV7 serotypes among persons not vaccine-eligible (born<2004). There was a 15% difference in serotype coverage between PCV13 and the 23-valent polysaccharide vaccine in adults≥50 years.
Conclusions:
During Ontario's PCV7 programme, serotype-specific decreases in IPD were observed, suggesting vaccine programme success, including herd immunity. Our results also suggest some early impact among infants from PCV10 introduction. A substantial burden of disease was also observed among older adults.
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