Nontypeable Haemophilus influenzae genetic islands associated with chronic pulmonary infection.

<h4>Background</h4>Haemophilus influenzae (Hi) colonizes the human respiratory tract and is an important pathogen associated with chronic obstructive pulmonary disease (COPD). Bacterial factors that interact with the human host may be important in the pathogenesis of COPD. These factors,...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Lixin Zhang, Jingping Xie, Mayuri Patel, Arsala Bakhtyar, Garth D Ehrlich, Azad Ahmed, Josh Earl, Carl F Marrs, Daniel Clemans, Timothy F Murphy, Janet R Gilsdorf
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2012
Materias:
R
Q
Acceso en línea:https://doaj.org/article/86e36140375842389a45b4a3ba0d2ad5
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:86e36140375842389a45b4a3ba0d2ad5
record_format dspace
spelling oai:doaj.org-article:86e36140375842389a45b4a3ba0d2ad52021-11-18T07:06:19ZNontypeable Haemophilus influenzae genetic islands associated with chronic pulmonary infection.1932-620310.1371/journal.pone.0044730https://doaj.org/article/86e36140375842389a45b4a3ba0d2ad52012-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22970300/pdf/?tool=EBIhttps://doaj.org/toc/1932-6203<h4>Background</h4>Haemophilus influenzae (Hi) colonizes the human respiratory tract and is an important pathogen associated with chronic obstructive pulmonary disease (COPD). Bacterial factors that interact with the human host may be important in the pathogenesis of COPD. These factors, however, have not been well defined. The overall goal of this study was to identify bacterial genetic elements with increased prevalence among H. influenzae strains isolated from patients with COPD compared to those isolated from the pharynges of healthy individuals.<h4>Methodology/principal findings</h4>Four nontypeable H. influenzae (NTHi) strains, two isolated from the airways of patients with COPD and two from a healthy individual, were subjected to whole genome sequencing using 454 FLX Titanium technology. COPD strain-specific genetic islands greater than 500 bp in size were identified by in silico subtraction. Open reading frames residing within these islands include known Hi virulence genes such as lic2b, hgbA, iga, hmw1 and hmw2, as well as genes encoding urease and other enzymes involving metabolic pathways. The distributions of seven selected genetic islands were assessed among a panel of 421 NTHi strains of both disease and commensal origins using a Library-on-a-Slide high throughput dot blot DNA hybridization procedure. Four of the seven islands screened, containing genes that encode a methyltransferase, a dehydrogenase, a urease synthesis enzyme, and a set of unknown short ORFs, respectively, were more prevalent in COPD strains than in colonizing strains with prevalence ratios ranging from 1.21 to 2.85 (p ≤ 0.0002). Surprisingly, none of these sequences show increased prevalence among NTHi isolated from the airways of patients with cystic fibrosis.<h4>Conclusions/significance</h4>Our data suggest that specific bacterial genes, many involved in metabolic functions, are associated with the ability of NTHi strains to survive in the lower airways of patients with COPD.Lixin ZhangJingping XieMayuri PatelArsala BakhtyarGarth D EhrlichAzad AhmedJosh EarlCarl F MarrsDaniel ClemansTimothy F MurphyJanet R GilsdorfPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 7, Iss 9, p e44730 (2012)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Lixin Zhang
Jingping Xie
Mayuri Patel
Arsala Bakhtyar
Garth D Ehrlich
Azad Ahmed
Josh Earl
Carl F Marrs
Daniel Clemans
Timothy F Murphy
Janet R Gilsdorf
Nontypeable Haemophilus influenzae genetic islands associated with chronic pulmonary infection.
description <h4>Background</h4>Haemophilus influenzae (Hi) colonizes the human respiratory tract and is an important pathogen associated with chronic obstructive pulmonary disease (COPD). Bacterial factors that interact with the human host may be important in the pathogenesis of COPD. These factors, however, have not been well defined. The overall goal of this study was to identify bacterial genetic elements with increased prevalence among H. influenzae strains isolated from patients with COPD compared to those isolated from the pharynges of healthy individuals.<h4>Methodology/principal findings</h4>Four nontypeable H. influenzae (NTHi) strains, two isolated from the airways of patients with COPD and two from a healthy individual, were subjected to whole genome sequencing using 454 FLX Titanium technology. COPD strain-specific genetic islands greater than 500 bp in size were identified by in silico subtraction. Open reading frames residing within these islands include known Hi virulence genes such as lic2b, hgbA, iga, hmw1 and hmw2, as well as genes encoding urease and other enzymes involving metabolic pathways. The distributions of seven selected genetic islands were assessed among a panel of 421 NTHi strains of both disease and commensal origins using a Library-on-a-Slide high throughput dot blot DNA hybridization procedure. Four of the seven islands screened, containing genes that encode a methyltransferase, a dehydrogenase, a urease synthesis enzyme, and a set of unknown short ORFs, respectively, were more prevalent in COPD strains than in colonizing strains with prevalence ratios ranging from 1.21 to 2.85 (p ≤ 0.0002). Surprisingly, none of these sequences show increased prevalence among NTHi isolated from the airways of patients with cystic fibrosis.<h4>Conclusions/significance</h4>Our data suggest that specific bacterial genes, many involved in metabolic functions, are associated with the ability of NTHi strains to survive in the lower airways of patients with COPD.
format article
author Lixin Zhang
Jingping Xie
Mayuri Patel
Arsala Bakhtyar
Garth D Ehrlich
Azad Ahmed
Josh Earl
Carl F Marrs
Daniel Clemans
Timothy F Murphy
Janet R Gilsdorf
author_facet Lixin Zhang
Jingping Xie
Mayuri Patel
Arsala Bakhtyar
Garth D Ehrlich
Azad Ahmed
Josh Earl
Carl F Marrs
Daniel Clemans
Timothy F Murphy
Janet R Gilsdorf
author_sort Lixin Zhang
title Nontypeable Haemophilus influenzae genetic islands associated with chronic pulmonary infection.
title_short Nontypeable Haemophilus influenzae genetic islands associated with chronic pulmonary infection.
title_full Nontypeable Haemophilus influenzae genetic islands associated with chronic pulmonary infection.
title_fullStr Nontypeable Haemophilus influenzae genetic islands associated with chronic pulmonary infection.
title_full_unstemmed Nontypeable Haemophilus influenzae genetic islands associated with chronic pulmonary infection.
title_sort nontypeable haemophilus influenzae genetic islands associated with chronic pulmonary infection.
publisher Public Library of Science (PLoS)
publishDate 2012
url https://doaj.org/article/86e36140375842389a45b4a3ba0d2ad5
work_keys_str_mv AT lixinzhang nontypeablehaemophilusinfluenzaegeneticislandsassociatedwithchronicpulmonaryinfection
AT jingpingxie nontypeablehaemophilusinfluenzaegeneticislandsassociatedwithchronicpulmonaryinfection
AT mayuripatel nontypeablehaemophilusinfluenzaegeneticislandsassociatedwithchronicpulmonaryinfection
AT arsalabakhtyar nontypeablehaemophilusinfluenzaegeneticislandsassociatedwithchronicpulmonaryinfection
AT garthdehrlich nontypeablehaemophilusinfluenzaegeneticislandsassociatedwithchronicpulmonaryinfection
AT azadahmed nontypeablehaemophilusinfluenzaegeneticislandsassociatedwithchronicpulmonaryinfection
AT joshearl nontypeablehaemophilusinfluenzaegeneticislandsassociatedwithchronicpulmonaryinfection
AT carlfmarrs nontypeablehaemophilusinfluenzaegeneticislandsassociatedwithchronicpulmonaryinfection
AT danielclemans nontypeablehaemophilusinfluenzaegeneticislandsassociatedwithchronicpulmonaryinfection
AT timothyfmurphy nontypeablehaemophilusinfluenzaegeneticislandsassociatedwithchronicpulmonaryinfection
AT janetrgilsdorf nontypeablehaemophilusinfluenzaegeneticislandsassociatedwithchronicpulmonaryinfection
_version_ 1718423926341632000