Mycobacterium marinum M
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Names | Mycobacterium marinum M |
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Accession numbers | NC_010604, NC_010612 |
Background | Mycobacterium marinum, a ubiquitous pathogen of fish and amphibia, is a near relative of Mycobacterium tuberculosis, the etiologic agent of tuberculosis in humans. It is Gram-positive, rod-shaped, facultative anaerobic bacterium commonly found in various aquatic environments around the world, including swimming pools and drinking water. In 1926, Joseph D. Aronson isolated a Mycobacterium from tubercles observed predominantly in the spleen and liver of diseased fish that had died in the Philadelphia Aquarium and named it M. marinum. It was subsequently shown to also be a human pathogen when it was isolated again much later in a swimming pool-associated outbreak of human granulomatous skin lesions, although in this report the Mycobacterium was mistakenly given a new species name, Mycobacterium balnei, a name that is no longer used. This bacterium causes a tuberculosis-like disease in frogs, fish and other poikilothermic animals, and a peripheral granulomatous disease in humans. M. marinum infection of humans, called fish tank or aquarium tank granuloma, typically occurs when M. marinum is inoculated through the skin by cuts and scratches following direct contact with an infected fish or contaminated aquatic environments. The ensuing granulomatous infection generally limited to the skin and soft tissues extremities is pathologically indistinguishable from M. tuberculosis dermal disease. Its optimal growth temperature is 35 degrees Celsius (in Middlebrook 7H9 medium). Its lower optimal growth temperature likely explains its causing systemic disease in poikilotherms animals and a superficial disease, restricted cooler extremities of the body, in warm-blooded animals. In contrast to M. tuberculosis, it is unable to reduce nitrate and produces characteristic bright yellow carotenoid pigments when exposed to light. These photochromogenic pigments protect it from UV damage in incident sunlight by reducing singlet oxygen species. It can form biofilms. (EBI Integr8) |
Taxonomy | |
Kingdom: | Bacteria |
Phylum: | Actinobacteria |
Class: | Actinobacteria |
Order: | Actinomycetales |
Family: | Mycobacteriaceae |
Genus: | Mycobacterium |
Species: | marinum |
Strain | M |
Complete | Yes |
Sequencing centre | (09-AUG-2007) Pathogen Sequencing Unit, Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge (19-APR-2008) National Center for Biotechnology Information, NIH, Bethesda, MD 20894, USA |
Sequencing quality | Level 6: Finished |
Sequencing depth | NA |
Sequencing method | Sanger |
Isolation site | "Human patient isolate from Moffett Hospital, University of California, San Francisco in 1992" |
Isolation country | USA |
Number of replicons | 2 |
Gram staining properties | Positive |
Shape | Bacilli |
Mobility | No |
Flagellar presence | No |
Number of membranes | 1 |
Oxygen requirements | Aerobic |
Optimal temperature | 32.0 |
Temperature range | Mesophilic |
Habitat | Multiple |
Biotic relationship | Free living |
Host name | Homo sapiens |
Cell arrangement | Singles |
Sporulation | Nonsporulating |
Metabolism | NA |
Energy source | Chemoorganotroph |
Diseases | Tuberculosis-like infection in fish, Skin infection, arthritis in human |
Pathogenicity | Yes |
Glycolysis / Gluconeogenesis
Citrate cycle (TCA cycle)
Pentose phosphate pathway
Fatty acid metabolism
Synthesis and degradation of ketone bodies
Purine metabolism
Pyrimidine metabolism
Alanine, aspartate and glutamate metabolism
Glycine, serine and threonine metabolism
Cysteine and methionine metabolism
Valine, leucine and isoleucine degradation
Geraniol degradation
Valine, leucine and isoleucine biosynthesis
Lysine biosynthesis
Arginine and proline metabolism
Histidine metabolism
Phenylalanine metabolism
Bisphenol degradation
Phenylalanine, tyrosine and tryptophan biosynthesis
beta-Alanine metabolism
Taurine and hypotaurine metabolism
Selenocompound metabolism
D-Glutamine and D-glutamate metabolism
D-Arginine and D-ornithine metabolism
D-Alanine metabolism
Streptomycin biosynthesis
Peptidoglycan biosynthesis
Pyruvate metabolism
Chloroalkane and chloroalkene degradation
Nitrotoluene degradation
Propanoate metabolism
Butanoate metabolism
C5-Branched dibasic acid metabolism
One carbon pool by folate
Thiamine metabolism
Riboflavin metabolism
Vitamin B6 metabolism
Nicotinate and nicotinamide metabolism
Pantothenate and CoA biosynthesis
Biotin metabolism
Lipoic acid metabolism
Folate biosynthesis
Porphyrin and chlorophyll metabolism
Terpenoid backbone biosynthesis
Limonene and pinene degradation
Sulfur metabolism
Caprolactam degradation
Aminoacyl-tRNA biosynthesis
Citrate cycle (TCA cycle)
Pentose phosphate pathway
Fatty acid metabolism
Synthesis and degradation of ketone bodies
Purine metabolism
Pyrimidine metabolism
Alanine, aspartate and glutamate metabolism
Glycine, serine and threonine metabolism
Cysteine and methionine metabolism
Valine, leucine and isoleucine degradation
Geraniol degradation
Valine, leucine and isoleucine biosynthesis
Lysine biosynthesis
Arginine and proline metabolism
Histidine metabolism
Phenylalanine metabolism
Bisphenol degradation
Phenylalanine, tyrosine and tryptophan biosynthesis
beta-Alanine metabolism
Taurine and hypotaurine metabolism
Selenocompound metabolism
D-Glutamine and D-glutamate metabolism
D-Arginine and D-ornithine metabolism
D-Alanine metabolism
Streptomycin biosynthesis
Peptidoglycan biosynthesis
Pyruvate metabolism
Chloroalkane and chloroalkene degradation
Nitrotoluene degradation
Propanoate metabolism
Butanoate metabolism
C5-Branched dibasic acid metabolism
One carbon pool by folate
Thiamine metabolism
Riboflavin metabolism
Vitamin B6 metabolism
Nicotinate and nicotinamide metabolism
Pantothenate and CoA biosynthesis
Biotin metabolism
Lipoic acid metabolism
Folate biosynthesis
Porphyrin and chlorophyll metabolism
Terpenoid backbone biosynthesis
Limonene and pinene degradation
Sulfur metabolism
Caprolactam degradation
Aminoacyl-tRNA biosynthesis