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Nat Commun ; 11(1): 3363, 2020 07 03.
Article in English | MEDLINE | ID: mdl-32620750

ABSTRACT

Studying emerging or neglected pathogens is often challenging due to insufficient information and absence of genetic tools. Dual RNA-seq provides insights into host-pathogen interactions, and is particularly informative for intracellular organisms. Here we apply dual RNA-seq to Orientia tsutsugamushi (Ot), an obligate intracellular bacterium that causes the vector-borne human disease scrub typhus. Half the Ot genome is composed of repetitive DNA, and there is minimal collinearity in gene order between strains. Integrating RNA-seq, comparative genomics, proteomics, and machine learning to study the transcriptional architecture of Ot, we find evidence for wide-spread post-transcriptional antisense regulation. Comparing the host response to two clinical isolates, we identify distinct immune response networks for each strain, leading to predictions of relative virulence that are validated in a mouse infection model. Thus, dual RNA-seq can provide insight into the biology and host-pathogen interactions of a poorly characterized and genetically intractable organism such as Ot.


Subject(s)
Gene Expression Regulation, Bacterial/immunology , Host-Pathogen Interactions/immunology , Neglected Diseases/immunology , Orientia tsutsugamushi/genetics , Scrub Typhus/immunology , Animals , Bacterial Proteins/genetics , Bacterial Proteins/immunology , Bacterial Proteins/metabolism , Cell Line , Disease Models, Animal , Feasibility Studies , Female , Genome, Bacterial , Human Umbilical Vein Endothelial Cells , Humans , Interferon Type I/immunology , Interferon Type I/metabolism , Interspersed Repetitive Sequences/genetics , Mice , Neglected Diseases/microbiology , Orientia tsutsugamushi/immunology , Orientia tsutsugamushi/pathogenicity , Proteomics , RNA, Bacterial/genetics , RNA, Bacterial/isolation & purification , RNA, Bacterial/metabolism , RNA, Untranslated/genetics , RNA, Untranslated/metabolism , RNA-Seq , Scrub Typhus/microbiology , Transcription, Genetic , Exome Sequencing
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