Moraxella catarrhalis

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'''Moraxella catarrhalis'''
'''Moraxella catarrhalis'''
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It is a Gram-negative, aerobic, oxidase-positive diplococcus that may both colonize and cause respiratory tract-associated infection in humans.
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{| border="1" style="text-align: left;"
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|+ '''Scientific classification'''
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!Kingdom || Bacteria
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|-
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! Phylum || Proteobacteria
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|-
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! Class || Gammaproteobacteria
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|-
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! Order || Pseudomonadales
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|-
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! Family || Moraxellaceae
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|-
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! Genus || Moraxella
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|-
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! Species || '''''M. catarrhalis'''''
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|-
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! Binomial || ''Moraxella catarrhalis''
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|}
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==Surface Characteristics==
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The LOS consists of an oligosaccharide and lipid A and is similar to the lipopolysaccharide (LPS) of gramnegative enteric pathogens, but it lacks the O-antigenic side chain of repeating units characteristic of classical LPS. The oligosaccharide part consists of the following residues : α-D-Galp-(1-->4)-β-D-Galp-(1-->4)-α-D-Glcp-(1-->2)-β-D-Glcp-(1-->6)-α-D-Glcp [branched to α-D-GlcpNAc-(1-->2)-β-D-Glcp-(1-->4)] and [branched to β-D-Glcp-(1-->3)] -(1-->5)-Kdo[ branched to Kdop-(2-?)]
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==Pathogenic Activity==
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These bacteria are known to cause otitis media, bronchitis, sinusitis, and laryngitis. Elderly patients and long-term heavy smokers with chronic pulmonary disease should be aware that M. catarrhalis is associated with bronchopneumonia, as well as exacerbations of existing chronic obstructive pulmonary disease (COPD).
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==Virulence==
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Lipooligosaccharide is considered one possible virulence factor. The great majority of clinical isolates of this organism produce beta-lactamases and are resistant to penicillin. Resistance to trimethoprim, trimethoprim-sulfamethoxazole (TMP-SMX) and tetracycline have been reported. It is susceptible to fluoroquinolones, most second and third generation cephalosporins, erythromycin and amoxicillin-clavulanate.
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==References==
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[http://en.wikipedia.org/wiki/Moraxella_catarrhalis Wikipedia]
[[category: CarboDB]]
[[category: CarboDB]]

Revision as of 06:09, 10 July 2010

Moraxella catarrhalis

It is a Gram-negative, aerobic, oxidase-positive diplococcus that may both colonize and cause respiratory tract-associated infection in humans.


Scientific classification
Kingdom Bacteria
Phylum Proteobacteria
Class Gammaproteobacteria
Order Pseudomonadales
Family Moraxellaceae
Genus Moraxella
Species M. catarrhalis
Binomial Moraxella catarrhalis


Contents

Surface Characteristics

The LOS consists of an oligosaccharide and lipid A and is similar to the lipopolysaccharide (LPS) of gramnegative enteric pathogens, but it lacks the O-antigenic side chain of repeating units characteristic of classical LPS. The oligosaccharide part consists of the following residues : α-D-Galp-(1-->4)-β-D-Galp-(1-->4)-α-D-Glcp-(1-->2)-β-D-Glcp-(1-->6)-α-D-Glcp [branched to α-D-GlcpNAc-(1-->2)-β-D-Glcp-(1-->4)] and [branched to β-D-Glcp-(1-->3)] -(1-->5)-Kdo[ branched to Kdop-(2-?)]

Pathogenic Activity

These bacteria are known to cause otitis media, bronchitis, sinusitis, and laryngitis. Elderly patients and long-term heavy smokers with chronic pulmonary disease should be aware that M. catarrhalis is associated with bronchopneumonia, as well as exacerbations of existing chronic obstructive pulmonary disease (COPD).

Virulence

Lipooligosaccharide is considered one possible virulence factor. The great majority of clinical isolates of this organism produce beta-lactamases and are resistant to penicillin. Resistance to trimethoprim, trimethoprim-sulfamethoxazole (TMP-SMX) and tetracycline have been reported. It is susceptible to fluoroquinolones, most second and third generation cephalosporins, erythromycin and amoxicillin-clavulanate.

References

Wikipedia