Culture enriched molecular profiling of the cystic fibrosis airway microbiome

Autor: Margot E. Grinwis, Michael D. Parkins, Monica Martins Pereira Faria, Scot E. Dowd, Christopher D. Sibley, Christina S. Eshaghurshan, Tyler R. Field, Michael G. Surette, Harvey R. Rabin
Jazyk: angličtina
Rok vydání: 2011
Předmět:
Bacterial Diseases
Cystic Fibrosis
Pulmonology
Respiratory System
lcsh:Medicine
Biology
medicine.disease_cause
Microbiology
Deep sequencing
Microbial Ecology
03 medical and health sciences
Autosomal Recessive
RNA
Ribosomal
16S

Genetics
medicine
DNA Barcoding
Taxonomic

Humans
Microbiome
lcsh:Science
030304 developmental biology
Clinical Genetics
0303 health sciences
Multidisciplinary
Bacteria
030306 microbiology
Pseudomonas aeruginosa
lcsh:R
Sputum
Bacterial taxonomy
Obligate anaerobe
Human Genetics
Bacteriology
Genomics
Bacteria Present
Bacterial Pathogens
Lower Respiratory Tract Infections
Infectious Diseases
Medical Microbiology
Respiratory Infections
Metagenome
Medicine
lcsh:Q
Metagenomics
Anaerobic bacteria
Restriction fragment length polymorphism
Polymorphism
Restriction Fragment Length

Research Article
Zdroj: PLoS ONE, Vol 6, Iss 7, p e22702 (2011)
PLoS ONE
ISSN: 1932-6203
Popis: The microbiome of the respiratory tract, including the nasopharyngeal and oropharyngeal microbiota, is a dynamic community of microorganisms that is highly diverse. The cystic fibrosis (CF) airway microbiome refers to the polymicrobial communities present in the lower airways of CF patients. It is comprised of chronic opportunistic pathogens (such as Pseudomonas aeruginosa) and a variety of organisms derived mostly from the normal microbiota of the upper respiratory tract. The complexity of these communities has been inferred primarily from culture independent molecular profiling. As with most microbial communities it is generally assumed that most of the organisms present are not readily cultured. Our culture collection generated using more extensive cultivation approaches, reveals a more complex microbial community than that obtained by conventional CF culture methods. To directly evaluate the cultivability of the airway microbiome, we examined six samples in depth using culture-enriched molecular profiling which combines culture-based methods with the molecular profiling methods of terminal restriction fragment length polymorphisms and 16S rRNA gene sequencing. We demonstrate that combining culture-dependent and culture-independent approaches enhances the sensitivity of either approach alone. Our techniques were able to cultivate 43 of the 48 families detected by deep sequencing; the five families recovered solely by culture-independent approaches were all present at very low abundance (
Databáze: OpenAIRE