Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2024 Nov;30(11):1777-1793.
doi: 10.1007/s12298-024-01523-9. Epub 2024 Nov 2.

Changes in soluble sugars and the expression of sugar transporter protein genes in strawberry crowns responding to Colletotrichum fructicola infection

Affiliations

Changes in soluble sugars and the expression of sugar transporter protein genes in strawberry crowns responding to Colletotrichum fructicola infection

Si-Yu Chen et al. Physiol Mol Biol Plants. 2024 Nov.

Abstract

Strawberry (Fragaria × ananassa) production has been greatly hampered by anthracnose crown rot caused by Colletotrichum fructicola. Crown, the modified stem of strawberry, is a sink organ involved in sugar allocation. Some Sugar Transport Proteins (STPs) are involved in competition for sugars between pathogen and host. However, the chemical nature and involvement of strawberry STPs (FaSTPs) in crown rot development is largely elusive. To reveal how strawberry alters soluble sugars and upregulates STPs in responses to C. fructicola, high performance liquid chromatograph and FaSTP expression analysis were performed in the crowns of three strawberry varieties, following a genome-wide identification of FaSTPs. Both C. fructicola and mock treatment/control changed glucose, fructose and sucrose accumulation in strawberry crowns. With increasing infection duration, the hexose/sucrose ratio increased in all varieties; no such trend was clearly visible in mock-treated plants. A total of 56 FaSTP loci scattered across four subgenomes were identified in octoploid strawberry, and most of the protein products of these genes had a preferential location on plasma membrane. Putative fungal elicitor responsive cis-elements were identified in the promoters of more than half FaSTPs. At least eight members were upregulated in strawberry crowns during C. fructicola invasion. Of them, FaSTP8 expression was markedly enhanced in three varieties at all time points except for 3 dpi in 'Jiuxiang'. RNAseq data retrieval further validated the expression responses of FaSTPs to Colletotrichum spp. In summary, this work identified several FaSTP candidate genes responsive to Colletotrichum fructicola invasion, demonstrated changes in soluble sugar levels in strawberry crowns as a result of infection, and laid the groundwork for future efforts to engineer strawberry resistance to Colletotrichum spp.

Supplementary information: The online version contains supplementary material available at 10.1007/s12298-024-01523-9.

Keywords: Anthracnose crown rot (ACR); Colletotrichum fructicola; Fragaria × ananassa; Soluble sugar; Sugar transport protein (STP).

PubMed Disclaimer

Conflict of interest statement

Conflict of interestThe authors declare that they have no conflict of interest.

Similar articles

References

    1. Amil-Ruiz F, Garrido-Gala J, Blanco-Portales R et al (2013) Identification and validation of reference genes for transcript normalization in strawberry (Fragaria × ananassa) defense responses. PLoS ONE 8(8):e70603–e70603 - PMC - PubMed
    1. Bailey TL, Johnson J, Grant CE et al (2015) The MEME suite. Nucleic Acids Res 43(W1):W39-49 - PMC - PubMed
    1. Berger S, Papadopoulos M, Schreiber U et al (2004) Complex regulation of gene expression, photosynthesis and sugar levels by pathogen infection in tomato. Physiol Plant 122:419–428
    1. Bezrutczyk M, Yang J, Eom JS et al (2018) Sugar flux and signaling in plant-microbe interactions. Plant J 93(4):675–685 - PubMed
    1. Bolouri Moghaddam MR, Van den Ende W (2012) Sugars and plant innate immunity. J Exp Bot 63(11):3989–3998 - PubMed

LinkOut - more resources