Haemophilus influenzae

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Haemophilus influenzae

Scientific classification

Kingdom:	Bacteria
Phylum:	Proteobacteria
Class:	Gamma Proteobacteria
Order:	Pasteurellales
Family:	Pasteurellaceae
Genus:	Haemophilus
Species:	H. influenzae

Binomial name

Haemophilus influenzae
Lehmann & Neumann, 1896

Haemophilus influenzae, formerly called Pfeiffer's bacillus, is a non-motile Gram-negative coccobacillus first described in 1892 by Dr. Robert Pfeiffer during the influenza pandemic. It is generally aerobic, but can grow as a facultative anaerobe. Haemophilus influenzae was mistakenly considered to be the cause of the common flu until 1933, when the viral etiology of the flu became apparent. Still, Haemophilus influenzae is responsible for a wide range of clinical diseases. Because of its small genome, Haemophilus influenzae became the first free-living organism with its entire genome sequenced. Its genome consists of 1,830,140 base pairs of DNA and contains 1740 genes. The sequencing project, completed and published in Science in 1995, was conducted at The Institute for Genomic Research under the direction of Dr. Robert Fleischmann.

1 Serotypes
2 Diseases
3 Interaction with Streptococcus pneumoniae
4 References
5 External links

Serotypes

In 1930, 2 major categories of H. influenzae were defined: the unencapsulated strains and the encapsulated strains. The pathogenesis of H. influenzae infections is not completely understood, although the presence of the encapsulated type b (HiB) is known to be the major factor in virulence. Their capsule allows them to resist phagocytosis and complement-mediated lysis in the non-immune host. Unencapsulated strains are less invasive, but they are able to induce an inflammatory response that causes disease. Vaccination with Hib conjugate vaccines is effective in preventing infection, and several vaccines are now available for routine use.

Diseases

Most strains of H. influenzae are opportunistic pathogens - that is, they usually live in their host without causing disease, but cause problems only when other factors (such as a viral infection or reduced immune function) create an opportunity.

Naturally-acquired disease caused by H. influenzae seems to occur in humans only. In infants and young children, H. influenzae type B causes bacteremia and acute bacterial meningitis. Occasionally, it causes obstructive laryngitis, cellulitis, osteomyelitis and joint infections. Unencapsulated H. influenzae causes ear infections and sinusitis in children and is associated with pneumonia.

Interaction with Streptococcus pneumoniae

Both H. influenzae and S. pneumoniae can be found in the upper respiratory system of humans. A study of competition in a laboratory revealed that, in a petrì dish, S. pneumoniae always overpowered H. influenzae by attacking it with a hydrogen peroxide and stripping off the surface molecules H. influenzae needs for survival.

When both bacteria are placed together into a nasal cavity, within 2 weeks, only H. influenzae survives. When both are placed separately into a nasal cavity, each one survives. Upon examining the upper respiratory tissue from mice exposed to both bacteria species, an extraordinaririly large number of neutrophils immune cells were found. In mice exposed to only one bacteria, the cells were not present.

Lab tests showed that neutrophils exposed to dead H. influenzae were more aggressive in attacking S. pneumoniae that unexposed neutrophils. Exposure to dead H. influenzae had no effect on live H. influenzae.

Two scenarios may be responsible for this response:

When H. influenzae is attacked by S. pneumoniae, it signals the immune system to attack the S. pneumoniae
The combination of the two species together triggers an immune system response that is not set off by either species individually.

It is unclear why H. influenzae is not affected by the immune response. (Lysenko, et al., 2005)

References

Lysenko, E.S., A.J. Ratner, A.L. Nelson, and J.N. Weiser. In press. The role of innate immune responses in the outcome of interspecies competition for colonization of mucosal surfaces. PLoS Pathogens.