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Published on: June 28, 2018
Acute otitis media otopathogens during 2008 to 2010 in Rochester, New York
Janet R Casey1, Ravinder Kaur2, Victoria C Friedel2
1Legacy Pediatrics, 1815 S. Clinton Avenue, Rochester NY 14618.
Insights
The distribution of bacteria causing acute otitis media (AOM) remained stable from 2008-2010. Nasopharyngeal swabs at AOM onset better identified otopathogens than swabs during healthy periods.
Area of Science:
- Pediatrics
- Infectious Diseases
- Microbiology
Background:
- The prevalence of otopathogens causing acute otitis media (AOM) is dynamic, influenced by vaccines like pneumococcal conjugate vaccine 7 (PCV7).
- Understanding pathogen distribution is crucial for managing AOM, especially with evolving vaccination strategies.
Purpose of the Study:
- To analyze the distribution and antibiotic susceptibility of otopathogens colonizing the nasopharynx (NP) and causing AOM.
- To compare NP isolates with middle ear fluid (MEF) isolates during AOM episodes.
Main Methods:
- Prospective follow-up of 277 children, collecting NP and MEF samples during AOM and NP samples during healthy visits.
- Utilizing multilocus sequence typing to speciate Streptococcus pneumoniae isolates.
- Monitoring vaccine status, including PCV7 and its substitution by PCV13.
Main Results:
- Otopathogen distribution in MEF was stable; PCV7 serotypes were rare.
- Streptococcus pneumoniae and nontypeable Haemophilus influenzae were the most frequent otopathogens.
- Penicillin non-susceptibility in S. pneumoniae remained stable; Moraxella catarrhalis and H. influenzae showed beta-lactamase production.
Conclusions:
- Otopathogen distribution, antibiotic susceptibility, and S. pneumoniae strain diversity were stable between 2008 and 2010.
- Nasopharyngeal isolates at AOM onset partially reflected MEF isolates, offering a better indicator than samples from healthy states.
Background:
The otopathogen distribution colonizing the nasopharynx (NP) and causing acute otitis media (AOM) is in flux following the introduction of pneumococcal conjugate vaccine 7 (PCV7) and will continue to change.
Methods:
Two hundred seventy-seven children were followed prospectively; tympanocentesis was performed during AOM and 208 NP samples were collected to compare with middle ear fluid (MEF) isolates. Eight hundred sixty-three NP samples were collected at 7 healthy visits between 6 and 30 months of age. All children received PCV7 until April 2010 when it was substituted by PCV13. Multilocus sequence typing was used to speciate Streptococcus pneumoniae.
Results:
The distribution of otopathogens in the MEF during the study time frame was stable. PCV7 serotypes of pneumococci were virtually absent. The frequency of isolation of S. pneumoniae was 26-36% compared with 28-34% for nontypeable Haemophilus influenzae. Moraxella catarrhalis isolation was less common, 7-18%. The proportion of S. pneumoniae that were penicillin nonsusceptible was stable during the 3 years, 40-52%. All M. catarrhalis and 34% of nontypeable H. influenzae were β-lactamase producing. NP isolates of otopathogens at onset of AOM included the isolate from the MEF and was dissimilar from the distribution at times of health. Sequence types 320 and 199 of S. pneumoniae expressing serotypes 19A and 15 most often caused AOM.
Conclusions:
The otopathogen distribution, antibiotic susceptibility and the diversity of strains within the S. pneumoniae species during 2008 through late 2010 were stable. NP isolation of otopathogens at onset of AOM better reflected, albeit incompletely, likely MEF isolates compared with NP isolates at times of health.
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