Cargando…

Comparative genomic analysis identifies X-factor (haemin)-independent Haemophilus haemolyticus: a formal re-classification of 'Haemophilus intermedius'

The heterogeneous and highly recombinogenic genus Haemophilus comprises several species, some of which are pathogenic to humans. All share an absolute requirement for blood-derived factors during growth. Certain species, such as the pathogen Haemophilus influenzae and the commensal Haemophilus haemo...

Descripción completa

Detalles Bibliográficos
Autores principales: Harris, Tegan M., Price, Erin P., Sarovich, Derek S., Nørskov-Lauritsen, Niels, Beissbarth, Jemima, Chang, Anne B., Smith-Vaughan, Heidi C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Microbiology Society 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7067038/
https://www.ncbi.nlm.nih.gov/pubmed/31860436
http://dx.doi.org/10.1099/mgen.0.000303
_version_ 1783505346558427136
author Harris, Tegan M.
Price, Erin P.
Sarovich, Derek S.
Nørskov-Lauritsen, Niels
Beissbarth, Jemima
Chang, Anne B.
Smith-Vaughan, Heidi C.
author_facet Harris, Tegan M.
Price, Erin P.
Sarovich, Derek S.
Nørskov-Lauritsen, Niels
Beissbarth, Jemima
Chang, Anne B.
Smith-Vaughan, Heidi C.
author_sort Harris, Tegan M.
collection PubMed
description The heterogeneous and highly recombinogenic genus Haemophilus comprises several species, some of which are pathogenic to humans. All share an absolute requirement for blood-derived factors during growth. Certain species, such as the pathogen Haemophilus influenzae and the commensal Haemophilus haemolyticus , are thought to require both haemin (X-factor) and nicotinamide adenine dinucleotide (NAD, V-factor), whereas others, such as the informally classified ‘Haemophilus intermedius subsp. intermedius’, and Haemophilus parainfluenzae , only require V-factor. These differing growth requirements are commonly used for species differentiation, although a number of studies are now revealing issues with this approach. Here, we perform large-scale phylogenomics of 240 Haemophilus spp. genomes, including five ‘H. intermedius’ genomes generated in the current study, to reveal that strains of the ‘H. intermedius’ group are in fact haemin-independent H. haemolyticus (hiHh). Closer examination of these hiHh strains revealed that they encode an intact haemin biosynthesis pathway, unlike haemin-dependent H. haemolyticus and H. influenzae , which lack most haemin biosynthesis genes. Our results suggest that the common ancestor of modern-day H. haemolyticus and H. influenzae lost key haemin biosynthesis loci, likely as a consequence of specialized adaptation to otorhinolaryngeal and respiratory niches during their divergence from H. parainfluenzae . Genetic similarity analysis demonstrated that the haemin biosynthesis loci acquired in the hiHh lineage were likely laterally transferred from a H. parainfluenzae ancestor, and that this event probably occurred only once in hiHh. This study further challenges the validity of phenotypic methods for differentiating among Haemophilus species, and highlights the need for whole-genome sequencing for accurate characterization of species within this taxonomically challenging genus.
format Online
Article
Text
id pubmed-7067038
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Microbiology Society
record_format MEDLINE/PubMed
spelling pubmed-70670382020-03-17 Comparative genomic analysis identifies X-factor (haemin)-independent Haemophilus haemolyticus: a formal re-classification of 'Haemophilus intermedius' Harris, Tegan M. Price, Erin P. Sarovich, Derek S. Nørskov-Lauritsen, Niels Beissbarth, Jemima Chang, Anne B. Smith-Vaughan, Heidi C. Microb Genom Research Article The heterogeneous and highly recombinogenic genus Haemophilus comprises several species, some of which are pathogenic to humans. All share an absolute requirement for blood-derived factors during growth. Certain species, such as the pathogen Haemophilus influenzae and the commensal Haemophilus haemolyticus , are thought to require both haemin (X-factor) and nicotinamide adenine dinucleotide (NAD, V-factor), whereas others, such as the informally classified ‘Haemophilus intermedius subsp. intermedius’, and Haemophilus parainfluenzae , only require V-factor. These differing growth requirements are commonly used for species differentiation, although a number of studies are now revealing issues with this approach. Here, we perform large-scale phylogenomics of 240 Haemophilus spp. genomes, including five ‘H. intermedius’ genomes generated in the current study, to reveal that strains of the ‘H. intermedius’ group are in fact haemin-independent H. haemolyticus (hiHh). Closer examination of these hiHh strains revealed that they encode an intact haemin biosynthesis pathway, unlike haemin-dependent H. haemolyticus and H. influenzae , which lack most haemin biosynthesis genes. Our results suggest that the common ancestor of modern-day H. haemolyticus and H. influenzae lost key haemin biosynthesis loci, likely as a consequence of specialized adaptation to otorhinolaryngeal and respiratory niches during their divergence from H. parainfluenzae . Genetic similarity analysis demonstrated that the haemin biosynthesis loci acquired in the hiHh lineage were likely laterally transferred from a H. parainfluenzae ancestor, and that this event probably occurred only once in hiHh. This study further challenges the validity of phenotypic methods for differentiating among Haemophilus species, and highlights the need for whole-genome sequencing for accurate characterization of species within this taxonomically challenging genus. Microbiology Society 2019-12-20 /pmc/articles/PMC7067038/ /pubmed/31860436 http://dx.doi.org/10.1099/mgen.0.000303 Text en © 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License.
spellingShingle Research Article
Harris, Tegan M.
Price, Erin P.
Sarovich, Derek S.
Nørskov-Lauritsen, Niels
Beissbarth, Jemima
Chang, Anne B.
Smith-Vaughan, Heidi C.
Comparative genomic analysis identifies X-factor (haemin)-independent Haemophilus haemolyticus: a formal re-classification of 'Haemophilus intermedius'
title Comparative genomic analysis identifies X-factor (haemin)-independent Haemophilus haemolyticus: a formal re-classification of 'Haemophilus intermedius'
title_full Comparative genomic analysis identifies X-factor (haemin)-independent Haemophilus haemolyticus: a formal re-classification of 'Haemophilus intermedius'
title_fullStr Comparative genomic analysis identifies X-factor (haemin)-independent Haemophilus haemolyticus: a formal re-classification of 'Haemophilus intermedius'
title_full_unstemmed Comparative genomic analysis identifies X-factor (haemin)-independent Haemophilus haemolyticus: a formal re-classification of 'Haemophilus intermedius'
title_short Comparative genomic analysis identifies X-factor (haemin)-independent Haemophilus haemolyticus: a formal re-classification of 'Haemophilus intermedius'
title_sort comparative genomic analysis identifies x-factor (haemin)-independent haemophilus haemolyticus: a formal re-classification of 'haemophilus intermedius'
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7067038/
https://www.ncbi.nlm.nih.gov/pubmed/31860436
http://dx.doi.org/10.1099/mgen.0.000303
work_keys_str_mv AT harristeganm comparativegenomicanalysisidentifiesxfactorhaeminindependenthaemophilushaemolyticusaformalreclassificationofhaemophilusintermedius
AT priceerinp comparativegenomicanalysisidentifiesxfactorhaeminindependenthaemophilushaemolyticusaformalreclassificationofhaemophilusintermedius
AT sarovichdereks comparativegenomicanalysisidentifiesxfactorhaeminindependenthaemophilushaemolyticusaformalreclassificationofhaemophilusintermedius
AT nørskovlauritsenniels comparativegenomicanalysisidentifiesxfactorhaeminindependenthaemophilushaemolyticusaformalreclassificationofhaemophilusintermedius
AT beissbarthjemima comparativegenomicanalysisidentifiesxfactorhaeminindependenthaemophilushaemolyticusaformalreclassificationofhaemophilusintermedius
AT changanneb comparativegenomicanalysisidentifiesxfactorhaeminindependenthaemophilushaemolyticusaformalreclassificationofhaemophilusintermedius
AT smithvaughanheidic comparativegenomicanalysisidentifiesxfactorhaeminindependenthaemophilushaemolyticusaformalreclassificationofhaemophilusintermedius