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The Staphylococcus aureus CidA and LrgA Proteins Are Functional Holins Involved in the Transport of By-Products of Carbohydrate Metabolism

The Staphylococcus aureus cidABC and lrgAB operons encode members of a well-conserved family of proteins thought to be involved in programmed cell death (PCD). Based on the structural similarities that CidA and LrgA share with bacteriophage holins, we have hypothesized that these proteins function b...

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Autores principales: Endres, Jennifer L., Chaudhari, Sujata S., Zhang, Xinyan, Prahlad, Janani, Wang, Shu-Qi, Foley, Lily A., Luca, Sorin, Bose, Jeffrey L., Thomas, Vinai C., Bayles, Kenneth W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8805020/
https://www.ncbi.nlm.nih.gov/pubmed/35100878
http://dx.doi.org/10.1128/mbio.02827-21
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author Endres, Jennifer L.
Chaudhari, Sujata S.
Zhang, Xinyan
Prahlad, Janani
Wang, Shu-Qi
Foley, Lily A.
Luca, Sorin
Bose, Jeffrey L.
Thomas, Vinai C.
Bayles, Kenneth W.
author_facet Endres, Jennifer L.
Chaudhari, Sujata S.
Zhang, Xinyan
Prahlad, Janani
Wang, Shu-Qi
Foley, Lily A.
Luca, Sorin
Bose, Jeffrey L.
Thomas, Vinai C.
Bayles, Kenneth W.
author_sort Endres, Jennifer L.
collection PubMed
description The Staphylococcus aureus cidABC and lrgAB operons encode members of a well-conserved family of proteins thought to be involved in programmed cell death (PCD). Based on the structural similarities that CidA and LrgA share with bacteriophage holins, we have hypothesized that these proteins function by forming pores within the cytoplasmic membrane. To test this, we utilized a “lysis cassette” system that demonstrated the abilities of the cidA and lrgA genes to support bacteriophage endolysin-induced cell lysis. Typical of holins, CidA- and LrgA-induced lysis was dependent on the coexpression of endolysin, consistent with the proposed holin-like functions of these proteins. In addition, the CidA and LrgA proteins were shown to localize to the surface of membrane vesicles and cause leakage of small molecules, providing direct evidence of their hole-forming potential. Consistent with recent reports demonstrating a role for the lrgAB homologues in other bacterial and plant species in the transport of by-products of carbohydrate metabolism, we also show that lrgAB is important for S. aureus to utilize pyruvate during microaerobic and anaerobic growth, by promoting the uptake of pyruvate under these conditions. Combined, these data reveal that the CidA and LrgA membrane proteins possess holin-like properties that play an important role in the transport of small by-products of carbohydrate metabolism.
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spelling pubmed-88050202022-02-07 The Staphylococcus aureus CidA and LrgA Proteins Are Functional Holins Involved in the Transport of By-Products of Carbohydrate Metabolism Endres, Jennifer L. Chaudhari, Sujata S. Zhang, Xinyan Prahlad, Janani Wang, Shu-Qi Foley, Lily A. Luca, Sorin Bose, Jeffrey L. Thomas, Vinai C. Bayles, Kenneth W. mBio Research Article The Staphylococcus aureus cidABC and lrgAB operons encode members of a well-conserved family of proteins thought to be involved in programmed cell death (PCD). Based on the structural similarities that CidA and LrgA share with bacteriophage holins, we have hypothesized that these proteins function by forming pores within the cytoplasmic membrane. To test this, we utilized a “lysis cassette” system that demonstrated the abilities of the cidA and lrgA genes to support bacteriophage endolysin-induced cell lysis. Typical of holins, CidA- and LrgA-induced lysis was dependent on the coexpression of endolysin, consistent with the proposed holin-like functions of these proteins. In addition, the CidA and LrgA proteins were shown to localize to the surface of membrane vesicles and cause leakage of small molecules, providing direct evidence of their hole-forming potential. Consistent with recent reports demonstrating a role for the lrgAB homologues in other bacterial and plant species in the transport of by-products of carbohydrate metabolism, we also show that lrgAB is important for S. aureus to utilize pyruvate during microaerobic and anaerobic growth, by promoting the uptake of pyruvate under these conditions. Combined, these data reveal that the CidA and LrgA membrane proteins possess holin-like properties that play an important role in the transport of small by-products of carbohydrate metabolism. American Society for Microbiology 2022-02-01 /pmc/articles/PMC8805020/ /pubmed/35100878 http://dx.doi.org/10.1128/mbio.02827-21 Text en Copyright © 2022 Endres et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Endres, Jennifer L.
Chaudhari, Sujata S.
Zhang, Xinyan
Prahlad, Janani
Wang, Shu-Qi
Foley, Lily A.
Luca, Sorin
Bose, Jeffrey L.
Thomas, Vinai C.
Bayles, Kenneth W.
The Staphylococcus aureus CidA and LrgA Proteins Are Functional Holins Involved in the Transport of By-Products of Carbohydrate Metabolism
title The Staphylococcus aureus CidA and LrgA Proteins Are Functional Holins Involved in the Transport of By-Products of Carbohydrate Metabolism
title_full The Staphylococcus aureus CidA and LrgA Proteins Are Functional Holins Involved in the Transport of By-Products of Carbohydrate Metabolism
title_fullStr The Staphylococcus aureus CidA and LrgA Proteins Are Functional Holins Involved in the Transport of By-Products of Carbohydrate Metabolism
title_full_unstemmed The Staphylococcus aureus CidA and LrgA Proteins Are Functional Holins Involved in the Transport of By-Products of Carbohydrate Metabolism
title_short The Staphylococcus aureus CidA and LrgA Proteins Are Functional Holins Involved in the Transport of By-Products of Carbohydrate Metabolism
title_sort staphylococcus aureus cida and lrga proteins are functional holins involved in the transport of by-products of carbohydrate metabolism
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8805020/
https://www.ncbi.nlm.nih.gov/pubmed/35100878
http://dx.doi.org/10.1128/mbio.02827-21
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