Novel plasmid pCM3 harboring the aph(3) gene confers phosphorylation-driven streptomycin resistance in Clavibacter michiganensis

Xiaoli Xu , Cen Qian , Zhigang Hao , Meng Xie , Na Jiang , Jianqiang Li , Laixin Luo

mLife ›› 2026, Vol. 5 ›› Issue (3) : 383 -387.

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mLife ›› 2026, Vol. 5 ›› Issue (3) :383 -387. DOI: 10.1002/mlf2.70091
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Novel plasmid pCM3 harboring the aph(3) gene confers phosphorylation-driven streptomycin resistance in Clavibacter michiganensis
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Abstract

Antibiotic resistance in plant pathogens threatens sustainable crop protection, and yet, its molecular basis remains incompletely understood. We report that streptomycin resistance in Clavibacter michiganensis strain TX-0702 is mediated by a plasmid-borne aminoglycoside phosphotransferase, APH(3), encoded on an uncharacterized plasmid, pCM3. Functional and biochemical analyses demonstrate that APH(3) inactivates streptomycin through phosphorylation, establishing a phosphorylation-driven resistance mechanism in Gram-positive plant pathogens. Sequence analyses reveal that pCM3 carries mobile genetic elements, suggesting environmental dissemination of resistance genes in plant-associated microbes. These findings expand understanding of phytopathogen antibiotic resistance and plant microbiomes as potential resistance gene sources for agricultural, food, and human health safety.

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Xiaoli Xu, Cen Qian, Zhigang Hao, Meng Xie, Na Jiang, Jianqiang Li, Laixin Luo. Novel plasmid pCM3 harboring the aph(3) gene confers phosphorylation-driven streptomycin resistance in Clavibacter michiganensis. mLife, 2026, 5 (3) : 383-387 DOI:10.1002/mlf2.70091

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References

[1]

Gleason ML. Survival and dissemination of Clavibacter michiganensis subsp. michiganensis in tomatoes. Phytopathology. 1991; 81: 1519–1523.

[2]

Fatmi M, Schaad NW. Survival of Clavibacter michiganensis ssp. michiganensis in infected tomato stems under natural field conditions in California, Ohio and Morocco. Plant Pathol. 2002; 51: 149–154.

[3]

Hausbeck MK, Bell J, Medina-Mora C, Podolsky R, Fulbright DW. Effect of bactericides on population sizes and spread of Clavibacter michiganensis subsp. michiganensis on tomatoes in the greenhouse and on disease development and crop yield in the field. Phytopathology. 2000; 90: 38–44.

[4]

Demirci H, Murphy F, Murphy E, Gregory ST, Dahlberg AE, Jogl G. A structural basis for streptomycin-induced misreading of the genetic code. Nat Commun. 2013; 4: 1355.

[5]

Finken M, Kirschner P, Meier A, Wrede A, Böttger EC. Molecular basis of streptomycin resistance in Mycobacterium tuberculosis: alterations of the ribosomal protein S12 gene and point mutations within a functional 16S ribosomal RNA pseudoknot. Mol Microbiol. 1993; 9: 1239–1246.

[6]

Okamoto S, Tamaru A, Nakajima C, Nishimura K, Tanaka Y, Tokuyama S, et al. Loss of a conserved 7-methylguanosine modification in 16S rRNA confers low-level streptomycin resistance in bacteria. Mol Microbiol. 2007; 63: 1096–1106.

[7]

de Lima Procópio RE, da Silva IR, Martins MK, de Azevedo JL, de Araújo JM. Antibiotics produced by Streptomyces. Braz J Infect Dis. 2012; 16: 466–471.

[8]

Sundin GW, Bender CL. Dissemination of the strA-strB streptomycin-resistance genes among commensal and pathogenic bacteria from humans, animals, and plants. Mol Ecol. 1996; 5: 133–143.

[9]

McGhee GC, Guasco J, Bellomo LM, Blumer-Schuette SE, Shane WW, Irish-Brown A, et al. Genetic analysis of streptomycin-resistant (Sm(R)) strains of Erwinia amylovora suggests that dissemination of two genotypes is responsible for the current distribution of Sm(R) E. amylovora in Michigan. Phytopathology. 2011; 101: 182–191.

[10]

Valenzuela M, Méndez V, Montenegro I, Besoain X, Seeger M. Streptomycin resistance in Clavibacter michiganensis subsp. michiganensis strains from Chile is related to an rpsL gene mutation. Plant Pathol. 2019; 68: 426–433.

[11]

Lyu Q, Bai K, Kan Y, Jiang N, Thapa SP, Coaker G, et al. Variation in streptomycin resistance mechanisms in Clavibacter michiganensis. Phytopathology. 2019; 109: 1849–1858.

[12]

Kirchner O, Gartemann KH, Zellermann EM, Eichenlaub R, Burger A. A highly efficient transposon mutagenesis system for the tomato pathogen Clavibacter michiganensis subsp. michiganensis. Mol Plant Microbe Interact. 2001; 14: 1312–1318.

[13]

Del Solar G, Espinosa M. Plasmid copy number control: an ever-growing story. Mol Microbiol. 2000; 37: 492–500.

[14]

Siregar JJ, Miroshnikov K, Mobashery S. Purification, characterization, and investigation of the mechanism of aminoglycoside 3′-phosphotransferase type Ia. Biochemistry. 1995; 34: 12681–12688.

[15]

Hwang IS, Lee HM, Oh EJ, Lee S, Heu S, Oh CS. Plasmid composition and the chpG gene determine the virulence level of Clavibacter capsici natural isolates in pepper. Mol Plant Pathol. 2020; 21: 808–819.

[16]

Feng Y, Lu X, Zhao J, Li H, Xu J, Li Z, et al. Regional antimicrobial resistance gene flow among the One Health sectors in China. Microbiome. 2025; 13: 3.

[17]

Rizzo L, Manaia C, Merlin C, Schwartz T, Dagot C, Ploy MC, et al. Urban wastewater treatment plants as hotspots for antibiotic resistant bacteria and genes spread into the environment: a review. Sci Total Environ. 2013; 447: 345–360.

[18]

Cheng D, Liu Y, Shehata E, Feng Y, Lin H, Xue J, et al. In-feed antibiotic use changed the behaviors of oxytetracycline, sulfamerazine, and ciprofloxacin and related antibiotic resistance genes during swine manure composting. J Hazard Mater. 2021; 402:123710.

[19]

Funke G, Aravena-Roman M, Frodl R. First description of Curtobacterium spp. isolated from human clinical specimens. J Clin Microbiol. 2005; 43: 1032–1036.

[20]

Tauch A, Krieft S, Kalinowski J, Pühler A. The 51,409-bp R-plasmid pTP10 from the multiresistant clinical isolate Corynebacterium striatum M82B is composed of DNA segments initially identified in soil bacteria and in plant, animal, and human pathogens. Mol Gen Genet. 2000; 263: 1–11.

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2026 The Author(s). mLife published by John Wiley & Sons Australia, Ltd on behalf of Institute of Microbiology, Chinese Academy of Sciences.

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