Presence of Bordetella holmesii in an outbreak of pertussis in Chile

The incidence of whooping cough in Chile ranges from 4.1 and 7.5 per hundred thousand inhabitants. B. pertussis detection is performed by Real Time PCR (Q-PCR) directed to the insertion sequence IS481. However, this sequence is also found in the genome of B. bronchiseptica and B. holmesii. The latte...

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Veröffentlicht in:Revista chilena de infectología 2013-06, Vol.30 (3), p.237-243
Hauptverfasser: Miranda, Carolina, Wozniak, Aniela, Castillo, Claudia, Geoffroy, Enrique, Zumarán, Cecilia, Porte, Lorena, Román, Juan C, Potin, Marcela, García, Patricia
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container_issue 3
container_start_page 237
container_title Revista chilena de infectología
container_volume 30
creator Miranda, Carolina
Wozniak, Aniela
Castillo, Claudia
Geoffroy, Enrique
Zumarán, Cecilia
Porte, Lorena
Román, Juan C
Potin, Marcela
García, Patricia
description The incidence of whooping cough in Chile ranges from 4.1 and 7.5 per hundred thousand inhabitants. B. pertussis detection is performed by Real Time PCR (Q-PCR) directed to the insertion sequence IS481. However, this sequence is also found in the genome of B. bronchiseptica and B. holmesii. The latter is also a respiratory pathogen whose clinical features are similar to B. pertussis. However, it is important to differentiate between these species because in immunosuppressed patients B. holmesii is more likely to cause bacteremia and is less susceptible to erythromycin. The goal of this work is to measure prospectively and retrospectively the presence of B. holmesii in samples reported positive for B. pertussis in the period 2010-2011. During this period, 1994 nasopharyngeal specimens entered the laboratory for Bordetella sp. PCR, of which 224 were positive. The analysis by Q-PCR directed to the recA gene of B. holmesii of all 224 positive samples determined a prevalence of B. holmesii of 0.6% (12/1994). Because of its more aggressive behavior in immunosupressed patients and its different resistance pattern, routine screening of B. pertussis and B. holmesii is currently performed for all samples in which Bordetella sp PCR is initially detected.
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B. pertussis detection is performed by Real Time PCR (Q-PCR) directed to the insertion sequence IS481. However, this sequence is also found in the genome of B. bronchiseptica and B. holmesii. The latter is also a respiratory pathogen whose clinical features are similar to B. pertussis. However, it is important to differentiate between these species because in immunosuppressed patients B. holmesii is more likely to cause bacteremia and is less susceptible to erythromycin. The goal of this work is to measure prospectively and retrospectively the presence of B. holmesii in samples reported positive for B. pertussis in the period 2010-2011. During this period, 1994 nasopharyngeal specimens entered the laboratory for Bordetella sp. PCR, of which 224 were positive. The analysis by Q-PCR directed to the recA gene of B. holmesii of all 224 positive samples determined a prevalence of B. holmesii of 0.6% (12/1994). 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subjects Adolescent
Adult
Bordetella - genetics
Bordetella pertussis - genetics
Child
Child, Preschool
Chile - epidemiology
Disease Outbreaks
DNA, Bacterial - analysis
Epidemiologic Methods
Extinction, Biological
Female
Humans
Infant
Infant, Newborn
Male
Middle Aged
Real-Time Polymerase Chain Reaction
Seasons
Sequence Analysis, DNA
Whooping Cough - epidemiology
Whooping Cough - microbiology
Young Adult
title Presence of Bordetella holmesii in an outbreak of pertussis in Chile
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