Literature DB >> 20847012

Colonization of healthy children by Moraxella catarrhalis is characterized by genotype heterogeneity, virulence gene diversity and co-colonization with Haemophilus influenzae.

Suzanne J C Verhaegh1,2, Martine L Snippe2, Foster Levy3, Henri A Verbrugh2, Vincent W V Jaddoe4,5,1, Albert Hofman4,1, Henriëtte A Moll5, Alex van Belkum2, John P Hays2.   

Abstract

The colonization dynamics of Moraxella catarrhalis were studied in a population comprising 1079 healthy children living in Rotterdam, The Netherlands (the Generation R Focus cohort). A total of 2751 nasal swabs were obtained during four clinic visits timed to take place at 1.5, 6, 14 and 24 months of age, yielding a total of 709 M. catarrhalis and 621 Haemophilus influenzae isolates. Between January 2004 and December 2006, approximate but regular 6-monthly cycles of colonization were observed, with peak colonization incidences occurring in the autumn/winter for M. catarrhalis, and winter/spring for H. influenzae. Co-colonization was significantly more likely than single-species colonization with either M. catarrhalis or H. influenzae, with genotypic analysis revealing no clonality for co-colonizing or single colonizers of either bacterial species. This finding is especially relevant considering the recent discovery of the importance of H. influenzae-M. catarrhalis quorum sensing in biofilm formation and host clearance. Bacterial genotype heterogeneity was maintained over the 3-year period of the study, even within this relatively localized geographical region, and there was no association of genotypes with either season or year of isolation. Furthermore, chronological and genotypic diversity in three immunologically important M. catarrhalis virulence genes (uspA1, uspA2 and hag/mid) was also observed. This study indicates that genotypic variation is a key factor contributing to the success of M. catarrhalis colonization of healthy children in the first years of life. Furthermore, variation in immunologically relevant virulence genes within colonizing populations, and even within genotypically identical M. catarrhalis isolates, may be a result of immune evasion by this pathogen. Finally, the factors facilitating M. catarrhalis and H. influenzae co-colonization need to be further investigated.

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Year:  2010        PMID: 20847012     DOI: 10.1099/mic.0.042929-0

Source DB:  PubMed          Journal:  Microbiology        ISSN: 1350-0872            Impact factor:   2.777


  27 in total

1.  The Generation R Study: Biobank update 2015.

Authors:  Claudia J Kruithof; Marjolein N Kooijman; Cornelia M van Duijn; Oscar H Franco; Johan C de Jongste; Caroline C W Klaver; Johan P Mackenbach; Henriëtte A Moll; Hein Raat; Edmond H H M Rings; Fernando Rivadeneira; Eric A P Steegers; Henning Tiemeier; Andre G Uitterlinden; Frank C Verhulst; Eppo B Wolvius; Albert Hofman; Vincent W V Jaddoe
Journal:  Eur J Epidemiol       Date:  2014-12-21       Impact factor: 8.082

Review 2.  Panel 5: Microbiology and immunology panel.

Authors:  Timothy F Murphy; Tasnee Chonmaitree; Stephen Barenkamp; Jennelle Kyd; Johanna Nokso-Koivisto; Janak A Patel; Terho Heikkinen; Noboru Yamanaka; Pearay Ogra; W Edward Swords; Tania Sih; Melinda M Pettigrew
Journal:  Otolaryngol Head Neck Surg       Date:  2013-04       Impact factor: 3.497

3.  The Moraxella catarrhalis nitric oxide reductase is essential for nitric oxide detoxification.

Authors:  Wei Wang; Traci Kinkel; Willm Martens-Habbena; David A Stahl; Ferric C Fang; Eric J Hansen
Journal:  J Bacteriol       Date:  2011-03-25       Impact factor: 3.490

4.  Use of the chinchilla model for nasopharyngeal colonization to study gene expression by Moraxella catarrhalis.

Authors:  Todd C Hoopman; Wei Liu; Stephanie N Joslin; Christine Pybus; Jennifer L Sedillo; Maria Labandeira-Rey; Cassie A Laurence; Wei Wang; James A Richardson; Lauren O Bakaletz; Eric J Hansen
Journal:  Infect Immun       Date:  2011-12-19       Impact factor: 3.441

5.  RbsB (NTHI_0632) mediates quorum signal uptake in nontypeable Haemophilus influenzae strain 86-028NP.

Authors:  Chelsie E Armbruster; Bing Pang; Kyle Murrah; Richard A Juneau; Antonia C Perez; Kristin E D Weimer; W Edward Swords
Journal:  Mol Microbiol       Date:  2011-10-20       Impact factor: 3.501

6.  Microbiological Features of Upper Respiratory Tract Infections in Bulgarian Children for the Period 1998-2014.

Authors:  Raina Tzvetanova Gergova; Guergana Petrova; Stefan Gergov; Petko Minchev; Ivan Mitov; Tanya Strateva
Journal:  Balkan Med J       Date:  2016-11-01       Impact factor: 2.021

7.  Effect of pneumococcal vaccination on nasopharyngeal carriage of Streptococcus pneumoniae, Haemophilus influenzae, Moraxella catarrhalis, and Staphylococcus aureus in Fijian children.

Authors:  Eileen M Dunne; Jayne Manning; Fiona M Russell; Roy M Robins-Browne; E Kim Mulholland; Catherine Satzke
Journal:  J Clin Microbiol       Date:  2011-12-14       Impact factor: 5.948

8.  Substrate binding protein SBP2 of a putative ABC transporter as a novel vaccine antigen of Moraxella catarrhalis.

Authors:  Taketo Otsuka; Charmaine Kirkham; Antoinette Johnson; Megan M Jones; Timothy F Murphy
Journal:  Infect Immun       Date:  2014-06-09       Impact factor: 3.441

9.  Identification of an outer membrane lipoprotein involved in nasopharyngeal colonization by Moraxella catarrhalis in an animal model.

Authors:  Wei Wang; Stephanie N Joslin; Christine Pybus; Amanda S Evans; Flora Lichaa; Chad A Brautigam; Eric J Hansen
Journal:  Infect Immun       Date:  2014-03-18       Impact factor: 3.441

Review 10.  Quorum signaling and sensing by nontypeable Haemophilus influenzae.

Authors:  W Edward Swords
Journal:  Front Cell Infect Microbiol       Date:  2012-07-19       Impact factor: 5.293

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