Background: Magnetotactic bacteria (MTB) are a unique group of prokaryotes that have a potentially high impact on global geochemical cycling of significant primary elements because of their metabolic plasticity and the ability to biomineralize iron-rich magnetic particles called magnetosomes. Understanding the genetic composition of the few cultivated MTB along with the unique morphological features of this group of bacteria may provide an important framework for discerning their potential biogeochemical roles in natural environments.
Results: Genomic and ultrastructural analyses were combined to characterize the cultivated magnetotactic coccus Magnetofaba australis strain IT-1. Cells of this species synthesize a single chain of elongated, cuboctahedral magnetite (FeO) magnetosomes that cause them to align along magnetic field lines while they swim being propelled by two bundles of flagella at velocities up to 300 μm s. High-speed microscopy imaging showed the cells move in a straight line rather than in the helical trajectory described for other magnetotactic cocci. Specific genes within the genome of Mf. australis strain IT-1 suggest the strain is capable of nitrogen fixation, sulfur reduction and oxidation, synthesis of intracellular polyphosphate granules and transporting iron with low and high affinity. Mf. australis strain IT-1 and Magnetococcus marinus strain MC-1 are closely related phylogenetically although similarity values between their homologous proteins are not very high.
Conclusion: Mf. australis strain IT-1 inhabits a constantly changing environment and its complete genome sequence reveals a great metabolic plasticity to deal with these changes. Aside from its chemoautotrophic and chemoheterotrophic metabolism, genomic data indicate the cells are capable of nitrogen fixation, possess high and low affinity iron transporters, and might be capable of reducing and oxidizing a number of sulfur compounds. The relatively large number of genes encoding transporters as well as chemotaxis receptors in the genome of Mf. australis strain IT-1 combined with its rapid swimming velocities, indicate that cells respond rapidly to environmental changes.
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http://dx.doi.org/10.1186/s12864-016-3064-9 | DOI Listing |
Trop Med Infect Dis
November 2024
Istituto Zooprofilattico Sperimentale delle Venezie (IZSVe), Viale dell'Università 10, 35020 Legnaro, Italy.
Leptospirosis is a widespread disease throughout the world, presenting in severe clinical forms in dogs. The pathogenicity of the different serovars in field infections is not fully documented, and clinical diagnosis is often limited to a combination of serological tests and molecular analyses. The latter, although a fundamental tool, cannot identify the infecting strain without further analysis.
View Article and Find Full Text PDFVaccines (Basel)
September 2024
Boehringer Ingelheim, Lyon Porte des Alpes, 99 rue de l'Aviation, 69800 Saint-Priest, France.
Background: Australis is one of the most prevalent strains infecting dogs, leading, in natural conditions, to severe life-threatening cases.
Objective: The objective was to evaluate the onset and duration of immunity (OOI and DOI) induced by a new licensed quadrivalent antileptospiral vaccine (EURICAN L4) including four components (Canicola, Icterohaemorrhagiae, Grippotyphosa and Australis) against Australis. To this end, a severe Australis challenge model was developed, using a canine strain recently isolated from the field.
Microorganisms
September 2024
Boehringer Ingelheim Animal Health, Global Innovation, 813 Cours du Troisième Millénaire, 69800 Saint-Priest, France.
Leptospirosis is a widespread zoonosis caused by spirochaetes belonging to the pathogenic species of , which are classified into more than 25 serogroups and 250 serovars. Vaccination can prevent the disease in dogs but offers incomplete efficacy because of a lack of cross-protection between serogroups. The aim of this study was to validate a robust recruitment and sampling process, with the objectives of isolating and typing circulating pathogenic strains and then selecting those of proven virulence and pathogenicity for vaccine development.
View Article and Find Full Text PDFSci Rep
October 2024
Division of Microbiology and Biotechnology, Yenepoya (Deemed to be University), Yenepoya Research Centre, University Road, Deralakatte, Mangalore, 575018, India.
Harmful Algae
September 2024
Laboratoire des Sciences de l'Environnement Marin, UMR 6539 LEMAR (UBO/CNRS/IRD/Ifremer). Institut Universitaire Européen de la Mer, Rue Dumont d'Urville, Technopộle Brest-Iroise, Plouzané 29280, France. Electronic address:
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