Genome-Wide Identification of the PR-1 Gene Family in Pyrus betulaefolia Bunge and Its Expression Analysis Under Fire Blight Stress

Fire blight, caused by <i>Erwinia amylovora</i>, is a devastating bacterial disease threatening apple, pear, and other Rosaceae species. In our prior study, transcriptome analysis identified a fire blight-resistant variety, Duli (<i>Pyrus betulifolia</i> Bunge), and highlighted the PR1 gene as a key resistance factor. Using Duli's genomic data, we systematically identified and characterized the <i>Pb-PR-1</i> gene family through bioinformatics analysis. A total of 31 <i>Pb-PR-1</i> genes were found, encoding proteins of 123-341 amino acids. Phylogenetic analysis grouped these genes into four subfamilies, with 27 genes distributed across seven chromosomes, all contain a conserved CAP superfamily domain. Their promoter regions were enriched in hormone and stress-responsive elements. After inoculation with <i>E. amylovora</i>, susceptible Duli showed lesion development by day 2, with rapid disease progression, while resistant plants exhibited slower disease advancement and smaller lesions. Enzyme activity assays revealed that in resistant plants, PPO (polyphenol oxidase) and CAT (catalase) activities peaked on day 6, showing a 2.4-fold and 3.81-fold increase compared to susceptible Duli. At the same time, MDA (malondialdehyde) content decreased by 16.6%. The activities of SOD (superoxide dismutase) and PAL (phenylalanine ammonia-lyase) peaked on day 4, with increments of 34.32% and 47.1% over susceptible Duli. qRT-PCR showed significant differences in <i>Pb-PR-1</i> gene family expression between resistant and susceptible plants post-inoculation. Notably, <i>Pb-PR-1-11</i>, <i>Pb-PR-1-21</i>, and <i>Pb-PR-1-26</i> expression increased with infection duration, aligning with PPO and CAT activity trends. Other genes showed high early infection expression but declined by day 6. <i>Pb-PR-1-3</i>, <i>Pb-PR-1-6</i>, <i>Pb-PR-1-8</i>, <i>Pb-PR-1-16</i>, and <i>Pb-PR-1-30</i> were upregulated 13.17-fold on average by day 2. In summary, the <i>Pb-PR-1</i> family exhibited elevated expression during early infection and enhanced defense-related enzyme activities, improving plant resistance. This study provides a foundation for understanding the <i>PR-1</i> family's role in Duli and advancing fire blight resistance in Pyrus species.

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Publication Details

Journal
International Journal of Molecular Sciences
Published
2025-05-24
DOI
https://doi.org/10.3390/ijms26115074
Citations
2
Primary Topic
Plant-Microbe Interactions and Immunity
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article
Field-Weighted Citation Impact
3.50
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article

Genome-Wide Identification of the PR-1 Gene Family in Pyrus betulaefolia Bunge and Its Expression Analysis Under Fire Blight Stress

Jingyi Sai, Li Xu, Yue Wen, Chen Chen et al.
2 citations
International Journal of Molecular Sciences
Plant-Microbe Interactions and Immunity
3.50
article

Genome-Wide Identification of the PR-1 Gene Family in Pyrus betulaefolia Bunge and Its Expression Analysis Under Fire Blight Stress

Jingyi Sai, Li Xu, Yue Wen, Chen Chen, Lei Wang, Jia Tian, Abudusufuer Wufuerjiang
article en
2 citations

Abstract

Fire blight, caused by <i>Erwinia amylovora</i>, is a devastating bacterial disease threatening apple, pear, and other Rosaceae species. In our prior study, transcriptome analysis identified a fire blight-resistant variety, Duli (<i>Pyrus betulifolia</i> Bunge), and highlighted the PR1 gene as a key resistance factor. Using Duli's genomic data, we systematically identified and characterized the <i>Pb-PR-1</i> gene family through bioinformatics analysis. A total of 31 <i>Pb-PR-1</i> genes were found, encoding proteins of 123-341 amino acids. Phylogenetic analysis grouped these genes into four subfamilies, with 27 genes distributed across seven chromosomes, all contain a conserved CAP superfamily domain. Their promoter regions were enriched in hormone and stress-responsive elements. After inoculation with <i>E. amylovora</i>, susceptible Duli showed lesion development by day 2, with rapid disease progression, while resistant plants exhibited slower disease advancement and smaller lesions. Enzyme activity assays revealed that in resistant plants, PPO (polyphenol oxidase) and CAT (catalase) activities peaked on day 6, showing a 2.4-fold and 3.81-fold increase compared to susceptible Duli. At the same time, MDA (malondialdehyde) content decreased by 16.6%. The activities of SOD (superoxide dismutase) and PAL (phenylalanine ammonia-lyase) peaked on day 4, with increments of 34.32% and 47.1% over susceptible Duli. qRT-PCR showed significant differences in <i>Pb-PR-1</i> gene family expression between resistant and susceptible plants post-inoculation. Notably, <i>Pb-PR-1-11</i>, <i>Pb-PR-1-21</i>, and <i>Pb-PR-1-26</i> expression increased with infection duration, aligning with PPO and CAT activity trends. Other genes showed high early infection expression but declined by day 6. <i>Pb-PR-1-3</i>, <i>Pb-PR-1-6</i>, <i>Pb-PR-1-8</i>, <i>Pb-PR-1-16</i>, and <i>Pb-PR-1-30</i> were upregulated 13.17-fold on average by day 2. In summary, the <i>Pb-PR-1</i> family exhibited elevated expression during early infection and enhanced defense-related enzyme activities, improving plant resistance. This study provides a foundation for understanding the <i>PR-1</i> family's role in Duli and advancing fire blight resistance in Pyrus species.

International Journal of Molecular SciencesVol. 26(11)
Xinjiang Agricultural University (CN)
Life in Land
Openalex Percentile: Top 8%
Plant-Microbe Interactions and Immunity
3.50
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