Global proteomic profiling of salmonella infection by a Giant phage

Susan E Weintraub, Nurul Humaira Mohd Redzuan, Melissa K. Barton, Nur Amira Md Amin, Maxim I. Desmond, Lily E. Adams, Bazla Ali, Sammy Pardo, Dana Molleur, Weimin Wu, William W. Newcomb, Michael V. Osier, Lindsay W. Black, Alasdair C. Steven, Julie A. Thomas

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

The 240-kb Salmonella phage SPN3US genome encodes 264 gene products, many of which are functionally uncharacterized. We have previously used mass spectrometry to define the proteomes of wild-type and mutant forms of the SPN3US virion. In this study, we sought to determine whether this technique was suitable for the characterization of the SPN3US proteome during liquid infection. Mass spectrometry of SPN3US-infected cells identified 232 SPN3US and 1,994 Salmonella proteins. SPN3US proteins with related functions, such as proteins with roles in DNA replication, transcription, and virion formation, were coordinately expressed in a temporal manner. Mass spectral counts showed the four most abundant SPN3US proteins to be the major capsid protein, two head ejection proteins, and the functionally unassigned protein gp22. This high abundance of gp22 in infected bacteria contrasted with its absence from mature virions, suggesting that it might be the scaffold protein, an essential head morphogenesis protein yet to be identified in giant phages. We identified homologs to SPN3US gp22 in 45 related giant phages, including KZ, whose counterpart is also abundant in infected bacteria but absent in the virion. We determined the KZ counterpart to be cleaved in vitro by its prohead protease, an event that has been observed to promote head maturation of some other phages. Our findings are consistent with a scaffold protein assignment for SPN3US gp22, although direct evidence is required for its confirmation. These studies demonstrate the power of mass spectral analyses for facilitating the acquisition of new knowledge into the molecular events of viral infection. IMPORTANCE “Giant” phages with genomes 200 kb are being isolated in increasing numbers from a range of environments. With hosts such as Salmonella enterica, Pseudomonas aeruginosa, and Erwinia amylovora, these phages are of interest for phage therapy of multidrug-resistant pathogens. However, our understanding of how these complex phages interact with their hosts is impeded by the proportion (80%) of their gene products that are functionally uncharacterized. To develop the repertoire of techniques for analysis of phages, we analyzed a liquid infection of Salmonella phage SPN3US (240-kb genome) using third-generation mass spectrometry. We observed the temporal production of phage proteins whose genes collectively represent 96% of the SPN3US genome. These findings demonstrate the sensitivity of mass spectrometry for global proteomic profiling of virus-infected cells, and the identification of a candidate for a major head morphogenesis protein will facilitate further studies into giant phage head assembly.

Original languageEnglish (US)
Article number01833-18
JournalJournal of Virology
Volume93
Issue number5
DOIs
StatePublished - Mar 1 2019

Fingerprint

Salmonella Infections
salmonellosis
bacteriophages
Proteomics
proteomics
Bacteriophages
Proteins
virion
Virion
proteins
Mass Spectrometry
Salmonella Phages
Head
mass spectrometry
scaffolding proteins
Genome
genome
Proteome
proteome
Morphogenesis

Keywords

  • Bacteriophage assembly
  • Giant phage
  • Mass spectrometry
  • Salmonella

ASJC Scopus subject areas

  • Microbiology
  • Immunology
  • Insect Science
  • Virology

Cite this

Weintraub, S. E., Redzuan, N. H. M., Barton, M. K., Amin, N. A. M., Desmond, M. I., Adams, L. E., ... Thomas, J. A. (2019). Global proteomic profiling of salmonella infection by a Giant phage. Journal of Virology, 93(5), [01833-18]. https://doi.org/10.1128/JVI.01833-18

Global proteomic profiling of salmonella infection by a Giant phage. / Weintraub, Susan E; Redzuan, Nurul Humaira Mohd; Barton, Melissa K.; Amin, Nur Amira Md; Desmond, Maxim I.; Adams, Lily E.; Ali, Bazla; Pardo, Sammy; Molleur, Dana; Wu, Weimin; Newcomb, William W.; Osier, Michael V.; Black, Lindsay W.; Steven, Alasdair C.; Thomas, Julie A.

In: Journal of Virology, Vol. 93, No. 5, 01833-18, 01.03.2019.

Research output: Contribution to journalArticle

Weintraub, SE, Redzuan, NHM, Barton, MK, Amin, NAM, Desmond, MI, Adams, LE, Ali, B, Pardo, S, Molleur, D, Wu, W, Newcomb, WW, Osier, MV, Black, LW, Steven, AC & Thomas, JA 2019, 'Global proteomic profiling of salmonella infection by a Giant phage', Journal of Virology, vol. 93, no. 5, 01833-18. https://doi.org/10.1128/JVI.01833-18
Weintraub SE, Redzuan NHM, Barton MK, Amin NAM, Desmond MI, Adams LE et al. Global proteomic profiling of salmonella infection by a Giant phage. Journal of Virology. 2019 Mar 1;93(5). 01833-18. https://doi.org/10.1128/JVI.01833-18
Weintraub, Susan E ; Redzuan, Nurul Humaira Mohd ; Barton, Melissa K. ; Amin, Nur Amira Md ; Desmond, Maxim I. ; Adams, Lily E. ; Ali, Bazla ; Pardo, Sammy ; Molleur, Dana ; Wu, Weimin ; Newcomb, William W. ; Osier, Michael V. ; Black, Lindsay W. ; Steven, Alasdair C. ; Thomas, Julie A. / Global proteomic profiling of salmonella infection by a Giant phage. In: Journal of Virology. 2019 ; Vol. 93, No. 5.
@article{5e2bffb5e9274dd399b4a1bc0406fb07,
title = "Global proteomic profiling of salmonella infection by a Giant phage",
abstract = "The 240-kb Salmonella phage SPN3US genome encodes 264 gene products, many of which are functionally uncharacterized. We have previously used mass spectrometry to define the proteomes of wild-type and mutant forms of the SPN3US virion. In this study, we sought to determine whether this technique was suitable for the characterization of the SPN3US proteome during liquid infection. Mass spectrometry of SPN3US-infected cells identified 232 SPN3US and 1,994 Salmonella proteins. SPN3US proteins with related functions, such as proteins with roles in DNA replication, transcription, and virion formation, were coordinately expressed in a temporal manner. Mass spectral counts showed the four most abundant SPN3US proteins to be the major capsid protein, two head ejection proteins, and the functionally unassigned protein gp22. This high abundance of gp22 in infected bacteria contrasted with its absence from mature virions, suggesting that it might be the scaffold protein, an essential head morphogenesis protein yet to be identified in giant phages. We identified homologs to SPN3US gp22 in 45 related giant phages, including KZ, whose counterpart is also abundant in infected bacteria but absent in the virion. We determined the KZ counterpart to be cleaved in vitro by its prohead protease, an event that has been observed to promote head maturation of some other phages. Our findings are consistent with a scaffold protein assignment for SPN3US gp22, although direct evidence is required for its confirmation. These studies demonstrate the power of mass spectral analyses for facilitating the acquisition of new knowledge into the molecular events of viral infection. IMPORTANCE “Giant” phages with genomes 200 kb are being isolated in increasing numbers from a range of environments. With hosts such as Salmonella enterica, Pseudomonas aeruginosa, and Erwinia amylovora, these phages are of interest for phage therapy of multidrug-resistant pathogens. However, our understanding of how these complex phages interact with their hosts is impeded by the proportion (80{\%}) of their gene products that are functionally uncharacterized. To develop the repertoire of techniques for analysis of phages, we analyzed a liquid infection of Salmonella phage SPN3US (240-kb genome) using third-generation mass spectrometry. We observed the temporal production of phage proteins whose genes collectively represent 96{\%} of the SPN3US genome. These findings demonstrate the sensitivity of mass spectrometry for global proteomic profiling of virus-infected cells, and the identification of a candidate for a major head morphogenesis protein will facilitate further studies into giant phage head assembly.",
keywords = "Bacteriophage assembly, Giant phage, Mass spectrometry, Salmonella",
author = "Weintraub, {Susan E} and Redzuan, {Nurul Humaira Mohd} and Barton, {Melissa K.} and Amin, {Nur Amira Md} and Desmond, {Maxim I.} and Adams, {Lily E.} and Bazla Ali and Sammy Pardo and Dana Molleur and Weimin Wu and Newcomb, {William W.} and Osier, {Michael V.} and Black, {Lindsay W.} and Steven, {Alasdair C.} and Thomas, {Julie A.}",
year = "2019",
month = "3",
day = "1",
doi = "10.1128/JVI.01833-18",
language = "English (US)",
volume = "93",
journal = "Journal of Virology",
issn = "0022-538X",
publisher = "American Society for Microbiology",
number = "5",

}

TY - JOUR

T1 - Global proteomic profiling of salmonella infection by a Giant phage

AU - Weintraub, Susan E

AU - Redzuan, Nurul Humaira Mohd

AU - Barton, Melissa K.

AU - Amin, Nur Amira Md

AU - Desmond, Maxim I.

AU - Adams, Lily E.

AU - Ali, Bazla

AU - Pardo, Sammy

AU - Molleur, Dana

AU - Wu, Weimin

AU - Newcomb, William W.

AU - Osier, Michael V.

AU - Black, Lindsay W.

AU - Steven, Alasdair C.

AU - Thomas, Julie A.

PY - 2019/3/1

Y1 - 2019/3/1

N2 - The 240-kb Salmonella phage SPN3US genome encodes 264 gene products, many of which are functionally uncharacterized. We have previously used mass spectrometry to define the proteomes of wild-type and mutant forms of the SPN3US virion. In this study, we sought to determine whether this technique was suitable for the characterization of the SPN3US proteome during liquid infection. Mass spectrometry of SPN3US-infected cells identified 232 SPN3US and 1,994 Salmonella proteins. SPN3US proteins with related functions, such as proteins with roles in DNA replication, transcription, and virion formation, were coordinately expressed in a temporal manner. Mass spectral counts showed the four most abundant SPN3US proteins to be the major capsid protein, two head ejection proteins, and the functionally unassigned protein gp22. This high abundance of gp22 in infected bacteria contrasted with its absence from mature virions, suggesting that it might be the scaffold protein, an essential head morphogenesis protein yet to be identified in giant phages. We identified homologs to SPN3US gp22 in 45 related giant phages, including KZ, whose counterpart is also abundant in infected bacteria but absent in the virion. We determined the KZ counterpart to be cleaved in vitro by its prohead protease, an event that has been observed to promote head maturation of some other phages. Our findings are consistent with a scaffold protein assignment for SPN3US gp22, although direct evidence is required for its confirmation. These studies demonstrate the power of mass spectral analyses for facilitating the acquisition of new knowledge into the molecular events of viral infection. IMPORTANCE “Giant” phages with genomes 200 kb are being isolated in increasing numbers from a range of environments. With hosts such as Salmonella enterica, Pseudomonas aeruginosa, and Erwinia amylovora, these phages are of interest for phage therapy of multidrug-resistant pathogens. However, our understanding of how these complex phages interact with their hosts is impeded by the proportion (80%) of their gene products that are functionally uncharacterized. To develop the repertoire of techniques for analysis of phages, we analyzed a liquid infection of Salmonella phage SPN3US (240-kb genome) using third-generation mass spectrometry. We observed the temporal production of phage proteins whose genes collectively represent 96% of the SPN3US genome. These findings demonstrate the sensitivity of mass spectrometry for global proteomic profiling of virus-infected cells, and the identification of a candidate for a major head morphogenesis protein will facilitate further studies into giant phage head assembly.

AB - The 240-kb Salmonella phage SPN3US genome encodes 264 gene products, many of which are functionally uncharacterized. We have previously used mass spectrometry to define the proteomes of wild-type and mutant forms of the SPN3US virion. In this study, we sought to determine whether this technique was suitable for the characterization of the SPN3US proteome during liquid infection. Mass spectrometry of SPN3US-infected cells identified 232 SPN3US and 1,994 Salmonella proteins. SPN3US proteins with related functions, such as proteins with roles in DNA replication, transcription, and virion formation, were coordinately expressed in a temporal manner. Mass spectral counts showed the four most abundant SPN3US proteins to be the major capsid protein, two head ejection proteins, and the functionally unassigned protein gp22. This high abundance of gp22 in infected bacteria contrasted with its absence from mature virions, suggesting that it might be the scaffold protein, an essential head morphogenesis protein yet to be identified in giant phages. We identified homologs to SPN3US gp22 in 45 related giant phages, including KZ, whose counterpart is also abundant in infected bacteria but absent in the virion. We determined the KZ counterpart to be cleaved in vitro by its prohead protease, an event that has been observed to promote head maturation of some other phages. Our findings are consistent with a scaffold protein assignment for SPN3US gp22, although direct evidence is required for its confirmation. These studies demonstrate the power of mass spectral analyses for facilitating the acquisition of new knowledge into the molecular events of viral infection. IMPORTANCE “Giant” phages with genomes 200 kb are being isolated in increasing numbers from a range of environments. With hosts such as Salmonella enterica, Pseudomonas aeruginosa, and Erwinia amylovora, these phages are of interest for phage therapy of multidrug-resistant pathogens. However, our understanding of how these complex phages interact with their hosts is impeded by the proportion (80%) of their gene products that are functionally uncharacterized. To develop the repertoire of techniques for analysis of phages, we analyzed a liquid infection of Salmonella phage SPN3US (240-kb genome) using third-generation mass spectrometry. We observed the temporal production of phage proteins whose genes collectively represent 96% of the SPN3US genome. These findings demonstrate the sensitivity of mass spectrometry for global proteomic profiling of virus-infected cells, and the identification of a candidate for a major head morphogenesis protein will facilitate further studies into giant phage head assembly.

KW - Bacteriophage assembly

KW - Giant phage

KW - Mass spectrometry

KW - Salmonella

UR - http://www.scopus.com/inward/record.url?scp=85061874556&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=85061874556&partnerID=8YFLogxK

U2 - 10.1128/JVI.01833-18

DO - 10.1128/JVI.01833-18

M3 - Article

VL - 93

JO - Journal of Virology

JF - Journal of Virology

SN - 0022-538X

IS - 5

M1 - 01833-18

ER -