Host tropism and host-pathogen interplay of typhoidal Salmonella enterica
Résumé
The species Salmonella enterica is one of the most prevalent human and animal pathogens, it includes
Non Typhoïdal Salmonella (NTS) serovars like Typhimurium and Enteridis, that are generalist pathogens
with broad host specificity and Typhoïdal Salmonella (TS) serovars, like Typhi and Paratyphi A, that are
specialized pathogens strictly adapted to the human host and the cause of an invasive, dangerous disease
known as enteric (typhoid) fever [1,2,3].
The SalHostTrop project aims at identifying, characterizing and understanding the human-restricted
tropism of Typhoidal Salmonella (TS) using comparative dual-RNAseq sequencing and other
complementary approaches.
We combine state of the art genome and transcriptome sequencing methods to decipher the molecular
basis of host-tropism in clinical strains. We contrast the comparative genomics and differential expression
analyses to explore and assess the variability and plasticity of pathogenesis routes among and between
typhoidal and non-typhoidal serovars.
We present our on-going work including the Pacbio long-read genomic sequencing, assembly and
annotation [4] of a new S. Typhi strain (120130191) and the dual RNAseq data analysis of a pilot experiment
of S. Typhimurium and S. Paratyphi A during human epithelial cells infection. The new S. Typhi strain
includes one circularized complete chromosome and one plasmid of about 4.78 Mb with 4638 coding genes
and 106.7 kb with 128 coding genes, respectively. The dual RNAseq pilot first analyses demonstrate the
feasibility of the protocol to target both pathogen and host transcripts simultaneously during infection. We
also built a S. enterica subsp. enterica reference phylogenetic tree from the super-alignment of Salmonella
core genes in 214 complete genomes of various serotypes that is in agreement with previous studies and will
be used to explore pseudogene content of serotypes according to their evolutionary history
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