Publications

4479

Objetivo. Informe sobre especies de garrapatas que parasitan a los humanos en un área del bioma semiárido de Caatinga, noreste de Brasil, con nota de infección por rickettsias. Materiales y métodos. Todas las garrapatas se identificaron morfológicamente con estereomicroscopio. Algunas de las garrapatas recolectadas se analizaron molecularmente para detectar la presencia de ADN de bacterias del género Rickettsia. Las garrapatas se sometieron individualmente a la extracción de ADN (gen de la citrato sintasa [gltA] y gen de la proteína de la membrana externa [ompA]). Resultados. Se recolectaron un total de 78 garrapatas en humanos, identificadas como adultos de Amblyomma parvum (62 hembras y 16 machos). De estas, 15 mujeres fueron infectadas por ‘Candidatus Rickettsia andeanae’. Conclusiones. El presente estudio confirma una zona más de riesgo humano de picaduras de garrapatas en Brasil, también de la rickettsia no patógena 'Ca. Rickettsia andeanae'

AbstractMembers of the bacterial genusRickettsiawere originally identified as causative agents of vector-borne diseases in mammals. However, manyRickettsiaspecies are arthropod symbionts and close relatives of ‘CandidatusMegaira’, which are symbiotic associates of microeukaryotes. Here, we clarify the evolutionary relationships between these organisms by assembling 26 genomes ofRickettsiaspecies from understudied groups, including the Torix group, and two genomes of ‘Ca. Megaira’ from various insects and microeukaryotes. Our analyses of the new genomes, in comparison with previously described ones, indicate that the accessory genome diversity and broad host range of TorixRickettsiaare comparable to those of all otherRickettsiacombined. Therefore, the Torix clade may play unrecognized roles in invertebrate biology and physiology. We argue this clade should be given its own genus status, for which we propose the name ‘CandidatusTisiphia’.

Abstract Microbes are the most abundant form of life on Earth and play crucial roles in carbon and nutrient cycling. Despite their crucial role, our understanding of microbial diversity and physiology on the ocean floor is limited. To address this gap in knowledge, we obtained 55 novel bacterial metagenome-assembled genomes (MAGs) from coastal and deep sea sediments. Phylogenomic analyses revealed they belong to four new and one poorly described bacterial phyla. Comparison of their rRNA genes with public databases revealed they are all globally distributed. These novel bacteria are capable of the anaerobic degradation of polysaccharides and proteins, and the respiration of sulfur and nitrogen. These genomes code for an unusually high proportion (~ 9, and up to 20% per genome) of protein families lacking representatives in public databases. Hundreds of these protein families are predicted to be co-localized with genes for sulfur reduction, nitrogen cycling, energy conservation, and the degradation of organic compounds. These findings expand our understanding of microbial diversity and link previously overlooked gene families with key metabolic processes in the oceans.