Mycobacterium ulcerans liflandii

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Mycobacterium liflandii
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M. ulcerans liflandii
Binomial name
Mycobacterium ulcerans liflandii

Mycobacterium ulcerans liflandii has been isolated from Xenopus tropicalis and Xenopus laevis in a laboratory in the US and causes a Mycobacterium ulcerans-like disease in anurans. [1] [2] The strain was unofficially titled under its own species name until it was renamed to be an ecovariation of Mycobacterium ulcerans . [3]

<i>Mycobacterium ulcerans</i> species of bacterium

Mycobacterium ulcerans is a slow-growing mycobacterium that classically infects the skin and subcutaneous tissues, giving rise to indolent nonulcerated and ulcerated lesions. After tuberculosis and leprosy, Buruli ulcer is the third most common mycobacteriosis of humans. M. ulcerans grows optimally on routine mycobacteriologic media at 33 °C and elaborates a necrotizing immunosuppressive cytotoxin (mycolactone). The bacteria are considered microaerophilic. Large ulcers almost certainly caused by M. ulcerans were first observed by Cook in Uganda in 1897; however, the etiologic agent was not isolated and characterized until 1948 in Australia by MacCallum and associates.

Contents

The strain of M. liflandii that has been isolated from anuran sources at the University of California, Berkeley, has been designated KT1. KT1 is characterized and differentiated from its closest relatives, Mycobacterium ulcerans and Mycobacterium marinum , by the following molecular and physical traits.

Mycobacterium marinum is a free-living bacterium, which causes opportunistic infections in humans. M. marinum sometimes causes a rare disease known as aquarium granuloma, which typically affects individuals who work with fish or keep home aquariums.

Genomic results

Restriction Fragment Length Polymorphism (RFLP) assay KT1 has a three base-pair difference from M. ulcerans and M. marinum in its Internal Transcribed Spacer (ITS) that results in a lack of a Fok1 restriction enzyme site that is present in M. ulcerans and M. marinum. Amplification of ITS [1] followed by Fok1 digestion results in an RFLP with a major product of 213 base-pairs for both M. ulcerans and M. marinum, and a product band of 266 base-pairs for M. liflandii.

Sequence analysis

The following additional comparative differences were also used to identify M. liflandii KT1. [1] 1) KT1 is identical to M. ulcerans in the 5' signature region of RNA Polymerase subunit B (rpoB) and one base-pair off from M. ulcerans in the 3' region. It is three base-pairs different from M. marinum in the 5' region of rpoB and identical to M. marinum in the 3' region of rpoB. 2) KT1 is positive for both M. ulcerans-specific Insertion Sequences, IS2404 and IS2606. 3) KT1 is identical to the M. marinum heat shock protein 65 (hsp65) and 3 base-pairs different from M. ulcerans. 4) KT1 is 2 base-pairs different from the 16s ribosomal RNA gene (16sRNA) of M. marinum and 3 base-pairs different from M. ulcerans.

Physical characteristics

KT1 is a non-photochromogenic acid-fast mycobacterium. On Middlebrook 7H11 media supplemented with OADC, colonies are non-pigmented and slightly buff-colored, with rough morphology. KT1 has an optimal growth temperature of 28 °C with no growth seen at 35 °C. Growth rate on Lowenstein-Jensen is 30–35 days.

Information taken from https://web.archive.org/web/20060906181604/http://tropicalis.berkeley.edu/home/husbandry/disease_files/M-liflandii.html

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Buruli ulcer tropical disease

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Mycolactone chemical compound

Mycolactone is a polyketide-derived macrolide produced and secreted by a group of very closely related pathogenic Mycobacteria species that have been assigned a variety of names including, M. ulcerans, M. liflandii, M. pseudoshottsii, and some strains of M. marinum. These mycobacteria are collectively referred to as mycolactone-producing mycobacteria or MPM.

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DsrA RNA

DsrA RNA is a non-coding RNA that regulates both transcription, by overcoming transcriptional silencing by the nucleoid-associated H-NS protein, and translation, by promoting efficient translation of the stress sigma factor, RpoS. These two activities of DsrA can be separated by mutation: the first of three stem-loops of the 85 nucleotide RNA is necessary for RpoS translation but not for anti-H-NS action, while the second stem-loop is essential for antisilencing and less critical for RpoS translation. The third stem-loop, which behaves as a transcription terminator, can be substituted by the trp transcription terminator without loss of either DsrA function. The sequence of the first stem-loop of DsrA is complementary with the upstream leader portion of RpoS messenger RNA, suggesting that pairing of DsrA with the RpoS message might be important for translational regulation. The structures of DsrA and DsrA/rpoS complex were studied by NMR. The study concluded that the sRNA contains a dynamic conformational equilibrium for its second stem–loop which might be an important mechanism for DsrA to regulate the translations of its multiple target mRNAs.

Bacterial small RNAs (sRNA) are small RNAs produced by bacteria; they are 50- to 500-nucleotide non-coding RNA molecules, highly structured and containing several stem-loops. Numerous sRNAs have been identified using both computational analysis and laboratory-based techniques such as Northern blotting, microarrays and RNA-Seq in a number of bacterial species including Escherichia coli, the model pathogen Salmonella, the nitrogen-fixing alphaproteobacterium Sinorhizobium meliloti, marine cyanobacteria, Francisella tularensis, Streptococcus pyogenes, the pathogen Staphylococcus aureus, and the plant pathogen Xanthomonas oryzae pathovar oryzae. Bacterial sRNAs affect how genes are expressed within bacterial cells via interaction with mRNA or protein, and thus can affect a variety of bacterial functions like metabolism, virulence, environmental stress response, and structure.

References

  1. 1 2 3 Trott KA, Stacy BA, Lifland BD, et al. (June 2004). "Characterization of a Mycobacterium ulcerans-like infection in a colony of African tropical clawed frogs (Xenopus tropicalis)". Comp. Med. 54 (3): 309–17. PMID   15253278.
  2. Mve-Obiang A, Lee RE, Umstot ES, et al. (June 2005). "A newly discovered mycobacterial pathogen isolated from laboratory colonies of Xenopus species with lethal infections produces a novel form of mycolactone, the Mycobacterium ulcerans macrolide toxin". Infect. Immun. 73 (6): 3307–12. doi:10.1128/IAI.73.6.3307-3312.2005. PMC   1111873 . PMID   15908356.
  3. Nicholas J. Tobias; Kenneth D. Doig; Marnix H. Medema; Honglei Chen; Volker Haring; Robert Moore; Torsten Seemann; Timothy P. Stinear (30 November 2012). "Complete Genome Sequence of the Frog Pathogen Mycobacterium ulcerans ecovar Liflandii" (PDF). Journal of Bacteriology. 195 (3): 556–564. doi:10.1128/JB.02132-12. PMC   3554023 . PMID   23204453. Archived (PDF) from the original on 12 December 2016. Retrieved 12 December 2016.