Bordetella pertussis: Difference between revisions

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==Cell structure and metabolism==
==Cell structure and metabolism==


''Bordetella pertussis'' is an aerobe and thus utilizes aerobic respiration as its metabolism. ''Bordetella pertussis'' is also a Gram negative bacterium so its cell structure would consist of an outer membrane, an inner membrane and a periplasmic space with a thin peptidoglycan layer in between. On its outer membrane, ''Bordetella pertussis'' has unusual lipoopolysaccharides (LPS), endotoxins that are unlike other Gram-negative bacterium.
It is different in that it contains two forms differing in its phosphate composition of the lipid portion of the LPS. This form is designated Lipid X, instead of the usual Lipid A form. The role of the unusual LPS is not fully understood in the pathogenesis of pertussis.
[8]


==Ecology==
==Ecology==

Revision as of 09:59, 4 June 2007

A Microbial Biorealm page on the genus Bordetella pertussis

Classification

Higher order taxa

Kingdom: Bacteria

Phylum: Proteobacteria

Class: Betaproteobacteria

Order: Burkholderiales

Family: Alcaligenaceae

Genus: Bordetella

Species: B. pertussis


Species

Bordetella pertussis

Other Names: “Haemophilus pertussis” (Pribram 1933) “Bacterium tussis-convulsivae” (Lehmann and Neumann 1927) "Hemophilus pertussis" (Bergey et al. 1923), and "Microbe de la coqueluche" Bordet and Gengou 1906. [10]

NCBI: Taxonomy

Description and significance

Bordetella pertussis is a small, Gram-negative, coccoid bacterium about the size of 0.8 µm by 0.4 µm. It is an encapsulated immotile aerobe that does not make spores. Bordetella pertussis produces a number of virulence factors, including pertussis toxin, adenylate cyclase toxin, filamentous hemagglutinin, and hemolysin. It cannot survive in the environment; it must reside in a host either in small groups or singly. It grows at an optimal temperature of 35-37ºC. [1]

Bordetella pertussis is a strict human pathogen that is the causative agent of pertussis (whooping cough). Its natural habitat is in the human respiratory mucosa. Whooping Cough, or pertussis, is a respiratory infection in which a “whooping” sound is produced when the sufferer breathes. Pertussis kills an estimated 300,000 children annually, most of which occur in developing countries. [6]

Genome structure

Bordetella pertussis strain Tohama I has its complete genome sequenced. The genome consists of 1 circular chromosome with 4,086,189 nucleotides (3867 genes). Approximately 67% of the genome is GC rich and its coding density is 82% (1056 bp/gene). [10]

The IncP-1 beta plasmid pBP136 from Bordetella pertussis is also sequenced. It contains 41,268 bp nucleotides and carries 46 ORFs. Two of the ORFs have similar genes with unknown function to a plant pathogen called “Xylella fastidiosa”. pBP136 plasmid do not contain any accessory genes that code for antibiotics, mercury resistance, or xenobiotic degradation. Its role in the bacteria is unclear and is still under investigation. [9]

Cell structure and metabolism

Bordetella pertussis is an aerobe and thus utilizes aerobic respiration as its metabolism. Bordetella pertussis is also a Gram negative bacterium so its cell structure would consist of an outer membrane, an inner membrane and a periplasmic space with a thin peptidoglycan layer in between. On its outer membrane, Bordetella pertussis has unusual lipoopolysaccharides (LPS), endotoxins that are unlike other Gram-negative bacterium. It is different in that it contains two forms differing in its phosphate composition of the lipid portion of the LPS. This form is designated Lipid X, instead of the usual Lipid A form. The role of the unusual LPS is not fully understood in the pathogenesis of pertussis. [8]

Ecology

Pathology

Application to Biotechnology

Current Research

References

Edited by Linda Wang a student of Rachel Larsen and Kit Pogliano