Data from: Human variation impacting MCOLN2 restricts Salmonella Typhi replication by magnesium deprivation

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  • Human genetic diversity can reveal critical factors in host-pathogen interactions. This is especially useful for human-restricted pathogens like Salmonella enterica serovar Typhi (S. Typhi), the cause of Typhoid fever. One key dynamic during infection is competition for nutrients: host cells attempt to restrict intracellular replication by depriving bacteria of key nutrients or delivering toxic metabolites in a process called nutritional immunity. Here, a cellular genome-wide association study of intracellular replication by S. Typhi in nearly a thousand cell lines from around the world and extensive follow-up using intracellular S. Typhi transcriptomics and manipulation of magnesium concentrations demonstrates that the divalent cation channel mucolipin-2 (MCOLN2) restricts S. Typhi intracellular replication through magnesium deprivation. Our results reveal natural diversity in Mg2+ limitation as a key component of nutritional immunity against S. Typhi. ... [Read More]

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Data Citation
  • Ko, D., Gibbs, K., & Wang, L. (2022). Data from: Human variation impacting MCOLN2 restricts Salmonella Typhi replication by magnesium deprivation. Duke Research Data Repository. https://doi.org/10.7924/r4x92bd76
DOI
  • 10.7924/r4x92bd76
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  • ark:/87924/r4x92bd76
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  • Data from: Human variation impacting MCOLN2 restricts Salmonella Typhi replication by magnesium deprivation
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