TY - JOUR
T1 - Evidence of tailocin persistence and resistance in pseudomonas
AU - Kandel, P. P.
AU - Baltrus, David A.
AU - Hockett, Kevin L.
N1 - Publisher Copyright:
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY 4.0 International license.
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2019/7/30
Y1 - 2019/7/30
N2 - Tailocins are bacterially-produced, phage tail-like bacteriocins that have been proposed as therapeutics for treatment of bacterial infections. However, we have a limited understanding of how target populations survive tailocin exposure. In this paper, we demonstrate that cells of a target population of Pseudomonas syringae are able to survive lethal doses of a tailocin through both physiological and genetic mechanisms with stationary phase cells predominantly surviving using a physiological mechanism. Regardless of growth phase, a significant fraction of cells that survived tailocin exposure did not exhibit any increased resistance to subsequent exposure, indicating that these cells survive by persistence rather than resistance mechanism. Of those cells that did gain a detectable increase in tailocin resistance, there was a range from insensitive (complete resistance) to partially sensitive. We also recovered a mutant exhibiting a high-persistence like phenotype that showed significantly increased survival to transient exposure but no detectable growth after prolonged tailocin treatment. By sequencing the genome of multiple types of mutants, we identified several genes linked to lipopolysaccharide (LPS) biogenesis and implicated in tailocin tolerance and resistance. In particular, we found a specific genomic region that, when mutated, gave rise to the various classes of resistance and the high persistence phenotypes. Furthermore, we showed that a hypothetical gene involved in the high persistence phenotype is transcriptionally fused with the LPS biosynthetic region and contains a signal peptide and several trans-membrane domains. While the complete resistant mutants had lost their LPS O-antigen, incomplete resistant mutants contained minor to significant changes in their O-antigen. This work demonstrates that Gram-negative bacteria can survive tailocin exposure through multiple strategies, including the first description of a persistence-like mechanism for tolerating tailocin exposure.
AB - Tailocins are bacterially-produced, phage tail-like bacteriocins that have been proposed as therapeutics for treatment of bacterial infections. However, we have a limited understanding of how target populations survive tailocin exposure. In this paper, we demonstrate that cells of a target population of Pseudomonas syringae are able to survive lethal doses of a tailocin through both physiological and genetic mechanisms with stationary phase cells predominantly surviving using a physiological mechanism. Regardless of growth phase, a significant fraction of cells that survived tailocin exposure did not exhibit any increased resistance to subsequent exposure, indicating that these cells survive by persistence rather than resistance mechanism. Of those cells that did gain a detectable increase in tailocin resistance, there was a range from insensitive (complete resistance) to partially sensitive. We also recovered a mutant exhibiting a high-persistence like phenotype that showed significantly increased survival to transient exposure but no detectable growth after prolonged tailocin treatment. By sequencing the genome of multiple types of mutants, we identified several genes linked to lipopolysaccharide (LPS) biogenesis and implicated in tailocin tolerance and resistance. In particular, we found a specific genomic region that, when mutated, gave rise to the various classes of resistance and the high persistence phenotypes. Furthermore, we showed that a hypothetical gene involved in the high persistence phenotype is transcriptionally fused with the LPS biosynthetic region and contains a signal peptide and several trans-membrane domains. While the complete resistant mutants had lost their LPS O-antigen, incomplete resistant mutants contained minor to significant changes in their O-antigen. This work demonstrates that Gram-negative bacteria can survive tailocin exposure through multiple strategies, including the first description of a persistence-like mechanism for tolerating tailocin exposure.
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U2 - 10.1101/719799
DO - 10.1101/719799
M3 - Article
AN - SCOPUS:85094413957
JO - Nuclear Physics A
JF - Nuclear Physics A
SN - 0375-9474
ER -