SUMMARY
The aim of this review is to provide a comprehensive update on the current classification and identification of
Haemophilus
and
Aggregatibacter
species with exclusive or predominant host specificity for humans.
Haemophilus influenzae
and some of the other
Haemophilus
species are commonly encountered in the clinical microbiology laboratory and demonstrate a wide range of pathogenicity, from life-threatening invasive disease to respiratory infections to a nonpathogenic, commensal lifestyle. New species of
Haemophilus
have been described (
Haemophilus pittmaniae
and
Haemophilus sputorum
), and the new genus
Aggregatibacter
was created to accommodate some former
Haemophilus
and
Actinobacillus
species (
Aggregatibacter aphrophilus
,
Aggregatibacter segnis
, and
Aggregatibacter actinomycetemcomitans
).
Aggregatibacter
species are now a dominant etiology of infective endocarditis caused by fastidious organisms (HACEK endocarditis), and
A. aphrophilus
has emerged as an important cause of brain abscesses. Correct identification of
Haemophilus
and
Aggregatibacter
species based on phenotypic characterization can be challenging. It has become clear that 15 to 20% of presumptive
H. influenzae
isolates from the respiratory tracts of healthy individuals do not belong to this species but represent nonhemolytic variants of
Haemophilus haemolyticus
. Due to the limited pathogenicity of
H. haemolyticus
, the proportion of misidentified strains may be lower in clinical samples, but even among invasive strains, a misidentification rate of 0.5 to 2% can be found. Several methods have been investigated for differentiation of
H. influenzae
from its less pathogenic relatives, but a simple method for reliable discrimination is not available. With the implementation of identification by matrix-assisted laser desorption ionization–time of flight mass spectrometry, the more rarely encountered species of
Haemophilus
and
Aggregatibacter
will increasingly be identified in clinical microbiology practice. However, identification of some strains will still be problematic, necessitating DNA sequencing of multiple housekeeping gene fragments or full-length 16S rRNA genes.