» Articles » PMID: 36616252

Citrus Canker Pathogen, Its Mechanism of Infection, Eradication, and Impacts

Overview
Journal Plants (Basel)
Date 2023 Jan 8
PMID 36616252
Authors
Affiliations
Soon will be listed here.
Abstract

Citrus canker is a ravaging bacterial disease threatening citrus crops. Its major types are Asiatic Canker, Cancrosis B, and Cancrosis C, caused by pv. (Xcc), pv. pathotype-B (XauB), and pathotype-C (XauC), respectively. The bacterium enters its host through stomata and wounds, from which it invades the intercellular spaces in the apoplast. It produces erumpent corky necrotic lesions often surrounded by a chlorotic halo on the leaves, young stems, and fruits, which causes dark spots, defoliation, reduced photosynthetic rate, rupture of leaf epidermis, dieback, and premature fruit drop in severe cases. Its main pathogenicity determinant gene is , whose variants are present in all citrus canker-causing pathogens. Countries where citrus canker is not endemic adopt different methods to prevent the introduction of the pathogen into the region, eradicate the pathogen, and minimize its dissemination, whereas endemic regions require an integrated management program to control the disease. The main aim of the present manuscript is to shed light on the pathogen profile, its mechanism of infection, and fruitful strategies for disease management. Although an adequate method to completely eradicate citrus canker has not been introduced so far, many new methods are under research to abate the disease.

Citing Articles

Two TAL effectors of Xanthomonas citri promote pustule formation by directly repressing the expression of GRAS transcription factor in citrus.

Yan Y, Tang X, Zhu Z, Yin K, Zhang Y, Xu Z Mol Hortic. 2025; 5(1):30.

PMID: 40083016 PMC: 11907795. DOI: 10.1186/s43897-024-00131-1.


Xanthomonas citri subsp. citri requires a polyketide cyclase to activate the type III secretion system for virulence.

Zhu S, Wu S, Liu Y, Zhang Z, Zou H BMC Microbiol. 2025; 25(1):59.

PMID: 39893476 PMC: 11786466. DOI: 10.1186/s12866-025-03749-3.


Evolution and spread of subsp. in the São Paulo, Brazil, citrus belt inferred from 758 novel genomes.

Zamuner C, Carhuaricra-Huaman D, Ragupathy R, Redfern J, Rodriguez-Cueva C, Behlau F Microb Genom. 2025; 11(1.

PMID: 39817540 PMC: 11736806. DOI: 10.1099/mgen.0.001338.


Transcriptomic analysis reveals differential transcriptional regulation underlying Citrus Bacterial Canker (CBC) tolerance in Citrus sinensis.

Ouyang Z, Wang X, Peng X, Zhong L, Zeng W, Huang T BMC Genomics. 2024; 25(1):1136.

PMID: 39587469 PMC: 11587780. DOI: 10.1186/s12864-024-11070-y.


Loop-Mediated Isothermal Amplification Assay for the Detection of Citrus Canker Causing Bacterial Variant, pv. A Strain.

Sidireddi S, Park J, Gonzalez M, Setamou M, Kunta M Int J Mol Sci. 2024; 25(21).

PMID: 39519140 PMC: 11546398. DOI: 10.3390/ijms252111590.


References
1.
Patane J, Martins Jr J, Rangel L, Belasque J, Digiampietri L, Facincani A . Origin and diversification of Xanthomonas citri subsp. citri pathotypes revealed by inclusive phylogenomic, dating, and biogeographic analyses. BMC Genomics. 2019; 20(1):700. PMC: 6734499. DOI: 10.1186/s12864-019-6007-4. View

2.
Bui T, Verniere C, Jarne P, Brisse S, Guerin F, Boutry S . From local surveys to global surveillance: three high-throughput genotyping methods for epidemiological monitoring of Xanthomonas citri pv. citri pathotypes. Appl Environ Microbiol. 2008; 75(4):1173-84. PMC: 2643580. DOI: 10.1128/AEM.02245-08. View

3.
Cavalca L, Zamuner C, Saldanha L, Polaquini C, Regasini L, Behlau F . Hexyl gallate for the control of citrus canker caused by Xanthomonas citri subsp citri. Microbiologyopen. 2020; 9(9):e1104. PMC: 7520989. DOI: 10.1002/mbo3.1104. View

4.
Zhang Y, Jalan N, Zhou X, Goss E, Jones J, Setubal J . Positive selection is the main driving force for evolution of citrus canker-causing Xanthomonas. ISME J. 2015; 9(10):2128-38. PMC: 4579464. DOI: 10.1038/ismej.2015.15. View

5.
Yoda H, Fujimura K, Takahashi H, Munemura I, Uchimiya H, Sano H . Polyamines as a common source of hydrogen peroxide in host- and nonhost hypersensitive response during pathogen infection. Plant Mol Biol. 2009; 70(1-2):103-12. DOI: 10.1007/s11103-009-9459-0. View