Genomic analysis of bacteria in the Acute Oak Decline pathobiome

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Genomic analysis of bacteria in the Acute Oak Decline pathobiome. / Doonan, James; Denman, Sandra; Pachebat, Justin A.; McDonald, James E.

In: Microbial genomics, Vol. 5, No. 1, 240, 2019.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Doonan, J, Denman, S, Pachebat, JA & McDonald, JE 2019, 'Genomic analysis of bacteria in the Acute Oak Decline pathobiome', Microbial genomics, vol. 5, no. 1, 240. https://doi.org/10.1099/mgen.0.000240

APA

Doonan, J., Denman, S., Pachebat, J. A., & McDonald, J. E. (2019). Genomic analysis of bacteria in the Acute Oak Decline pathobiome. Microbial genomics, 5(1), [240]. https://doi.org/10.1099/mgen.0.000240

Vancouver

Doonan J, Denman S, Pachebat JA, McDonald JE. Genomic analysis of bacteria in the Acute Oak Decline pathobiome. Microbial genomics. 2019;5(1). 240. https://doi.org/10.1099/mgen.0.000240

Author

Doonan, James ; Denman, Sandra ; Pachebat, Justin A. ; McDonald, James E. / Genomic analysis of bacteria in the Acute Oak Decline pathobiome. In: Microbial genomics. 2019 ; Vol. 5, No. 1.

Bibtex

@article{6333f8df882344dca8cc3bada066c837,
title = "Genomic analysis of bacteria in the Acute Oak Decline pathobiome",
abstract = "The UK{\textquoteright}s native oak is under serious threat from Acute Oak Decline (AOD). Stem tissue necrosis is a primary symptom of AOD and several bacteria are associated with necrotic lesions. Two members of the lesion pathobiome, Brenneria goodwinii and Gibbsiella quercinecans, have been identified as causative agents of tissue necrosis. However, additional bacteria including Lonsdalea britannica and Rahnella species have been detected in the lesion microbiome, but their role in tissue degradation is unclear. Consequently, information on potential genome-encoded mechanisms for tissue necrosis is critical to understand the role and mechanisms used by bacterial members of the lesion pathobiome in the aetiology of AOD. Here, the whole genomes of bacteria isolated from AOD-affected trees were sequenced, annotated and compared against canonical bacterial phytopathogens and non-pathogenic symbionts. Using orthologous gene inference methods, shared virulence genes that retain the same function were identified. Furthermore, functional annotation of phytopathogenic virulence genes demonstrated that all studied members of the AOD lesion microbiota possessed genes associated with phytopathogens. However, the genome of B. goodwinii was the most characteristic of a necrogenic phytopathogen, corroborating previous pathological and metatranscriptomic studies that implicate it as the key causal agent of AOD lesions. Furthermore, we investigated the genome sequences of other AOD lesion microbiota to understand the potential ability of microbes to cause disease or contribute to pathogenic potential of organisms isolated from this complex pathobiome. The role of these members remains uncertain but some such as G. quercinecans may contribute to tissue necrosis through the release of necrotizing enzymes and may help more dangerous pathogens activate and realize their pathogenic potential or they may contribute as secondary/opportunistic pathogens with the potential to act as accessory species for B. goodwinii. We demonstrate that in combination with ecological data, whole genome sequencing provides key insights into the pathogenic potential of bacterial species whether they be phytopathogens, part-contributors or stimulators of the pathobiome.",
author = "James Doonan and Sandra Denman and Pachebat, {Justin A.} and McDonald, {James E.}",
year = "2019",
doi = "10.1099/mgen.0.000240",
language = "English",
volume = "5",
journal = "Microbial genomics",
issn = "2057-5858",
publisher = "Microbiology Society",
number = "1",

}

RIS

TY - JOUR

T1 - Genomic analysis of bacteria in the Acute Oak Decline pathobiome

AU - Doonan, James

AU - Denman, Sandra

AU - Pachebat, Justin A.

AU - McDonald, James E.

PY - 2019

Y1 - 2019

N2 - The UK’s native oak is under serious threat from Acute Oak Decline (AOD). Stem tissue necrosis is a primary symptom of AOD and several bacteria are associated with necrotic lesions. Two members of the lesion pathobiome, Brenneria goodwinii and Gibbsiella quercinecans, have been identified as causative agents of tissue necrosis. However, additional bacteria including Lonsdalea britannica and Rahnella species have been detected in the lesion microbiome, but their role in tissue degradation is unclear. Consequently, information on potential genome-encoded mechanisms for tissue necrosis is critical to understand the role and mechanisms used by bacterial members of the lesion pathobiome in the aetiology of AOD. Here, the whole genomes of bacteria isolated from AOD-affected trees were sequenced, annotated and compared against canonical bacterial phytopathogens and non-pathogenic symbionts. Using orthologous gene inference methods, shared virulence genes that retain the same function were identified. Furthermore, functional annotation of phytopathogenic virulence genes demonstrated that all studied members of the AOD lesion microbiota possessed genes associated with phytopathogens. However, the genome of B. goodwinii was the most characteristic of a necrogenic phytopathogen, corroborating previous pathological and metatranscriptomic studies that implicate it as the key causal agent of AOD lesions. Furthermore, we investigated the genome sequences of other AOD lesion microbiota to understand the potential ability of microbes to cause disease or contribute to pathogenic potential of organisms isolated from this complex pathobiome. The role of these members remains uncertain but some such as G. quercinecans may contribute to tissue necrosis through the release of necrotizing enzymes and may help more dangerous pathogens activate and realize their pathogenic potential or they may contribute as secondary/opportunistic pathogens with the potential to act as accessory species for B. goodwinii. We demonstrate that in combination with ecological data, whole genome sequencing provides key insights into the pathogenic potential of bacterial species whether they be phytopathogens, part-contributors or stimulators of the pathobiome.

AB - The UK’s native oak is under serious threat from Acute Oak Decline (AOD). Stem tissue necrosis is a primary symptom of AOD and several bacteria are associated with necrotic lesions. Two members of the lesion pathobiome, Brenneria goodwinii and Gibbsiella quercinecans, have been identified as causative agents of tissue necrosis. However, additional bacteria including Lonsdalea britannica and Rahnella species have been detected in the lesion microbiome, but their role in tissue degradation is unclear. Consequently, information on potential genome-encoded mechanisms for tissue necrosis is critical to understand the role and mechanisms used by bacterial members of the lesion pathobiome in the aetiology of AOD. Here, the whole genomes of bacteria isolated from AOD-affected trees were sequenced, annotated and compared against canonical bacterial phytopathogens and non-pathogenic symbionts. Using orthologous gene inference methods, shared virulence genes that retain the same function were identified. Furthermore, functional annotation of phytopathogenic virulence genes demonstrated that all studied members of the AOD lesion microbiota possessed genes associated with phytopathogens. However, the genome of B. goodwinii was the most characteristic of a necrogenic phytopathogen, corroborating previous pathological and metatranscriptomic studies that implicate it as the key causal agent of AOD lesions. Furthermore, we investigated the genome sequences of other AOD lesion microbiota to understand the potential ability of microbes to cause disease or contribute to pathogenic potential of organisms isolated from this complex pathobiome. The role of these members remains uncertain but some such as G. quercinecans may contribute to tissue necrosis through the release of necrotizing enzymes and may help more dangerous pathogens activate and realize their pathogenic potential or they may contribute as secondary/opportunistic pathogens with the potential to act as accessory species for B. goodwinii. We demonstrate that in combination with ecological data, whole genome sequencing provides key insights into the pathogenic potential of bacterial species whether they be phytopathogens, part-contributors or stimulators of the pathobiome.

U2 - 10.1099/mgen.0.000240

DO - 10.1099/mgen.0.000240

M3 - Journal article

VL - 5

JO - Microbial genomics

JF - Microbial genomics

SN - 2057-5858

IS - 1

M1 - 240

ER -

ID: 340122721