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Characteristics of the strain VNIIKR-B-0035 Erwinia rhapontici isolated from common barley (Hordeum vulgare L.)

https://doi.org/10.69536/FKR.2025.46.28.005

Abstract

Erwinia rhapontici (Millard 1924) Burkholder 1948 is a phytopathogenic bacterium that causes pink grain of cereals and legumes, as well as various types of rot and other symptoms in a wide range of valuable agricultural plants, and to fully understand the pathogenic potential of this bacterium, it is necessary to study in detail as many strains as possible. The aim of this work is to create a comprehensive characterization of the bacterial strain VNIIKR-B-0035 E. rhapontici, isolated from common winter barley (Hordeum vulgare L.), origin – Republic of Crimea. The paper presents its morphology studied using cell microscopy, as well as photographs of bacterial colonies cultured on R2A nutrient medium. The cells of this strain are rod-shaped, measuring 0.8–1.5 μm long and 0.2–0.4 μm wide. Bacterial colonies of strain VNIIKR-B-0035 on R2A medium are whitish, slimy, and uniform. They have a round, convex shape, a smooth, shiny surface, and are opaque. They do not produce water-soluble pigments. Biochemical characteristics were studied using the API 20E kit for the identification of Enterobacteriaceae and physiologically similar bacteria (Biomerieux, France). Bacteria of this strain are capable of fermenting many types of sugars, reduce nitrites, do not produce arginine dihydrolase, lysine decarboxylase, ornithine decarboxylase, urease, indole, acetoin, gelatinase and H2S, and are also unable to utilize citrates. Molecular genetic characterization was conducted using four PCR tests for various genes specific to this phytopathogenic bacterium. Strain VNIIKR-B-0035 was identified using PCR tests with primers TSU01/TSU02, ERH-1A/ERH-1B, and isoRF/isoRR, as well as by sequencing a portion of the rpoD gene. This is the first molecular genetic identification of E. rhapontici in Russia. This study confirmed that common barley (Hordeum vulgare L.) can serve as a source of E. rhapontici isolation.

About the Authors

O. Yu. Slovareva
All-Russian Plant Quarantine Center (FGBU “VNIIKR”); Peoples' Friendship University of Russia (RUDN University)
Russian Federation

Olga Slovareva, Senior Researcher – Head of Research and Methodology Department of Bacteriology; Associate Professor of the Basic Department of Phytosanitary Biology and Ecosystem Safety

Bykovo, Ramwnskoye, Moscow Oblast, 140150



I. S. Avdeev
All-Russian Plant Quarantine Center (FGBU “VNIIKR”); Peoples' Friendship University of Russia (RUDN University)
Russian Federation

Ivan Avdeev, Junior Researcher, Research and Methodology Department of Bacteriology; student at the Institute of Ecology

Bykovo, Ramwnskoye, Moscow Oblast, 140150



A. B. Yaremko
All-Russian Plant Quarantine Center (FGBU “VNIIKR”)
Russian Federation

Anastasia Yaremko, Junior Researcher, Center for Collective Use "Molecular Genetics"

Bykovo, Ramwnskoye, Moscow Oblast, 140150



K. V. Panchenko
All-Russian Plant Quarantine Center (FGBU “VNIIKR”)
Russian Federation

Ksenia Panchenko, Junior Rese archer, Research and Methodology Department of Bacteriology

Bykovo, Ramwnskoye, Moscow Oblast, 140150



References

1. Belkin D.L., Bondarenko G.N., Yaremko A.B., Uvarova D.A. Sequencing method in species identification of quarantine pests [Metod sekvenirovaniya v vidovoy identifikatsii karantinnykh vrednykh organizmov] // Plant Health. Research and Practice. 2019; 28 (2): 31–34.

2. Mazurin E.S., Kopina M.B., Sherokolava N.A. Control of the reliability of the results of phytosanitary examination using molecular diagnostic methods [Kontrol dostovernosti rezultatov fitosanitarnoy ekspertizy pri ispolzovanii molekulyarnykh metodov diagnostiki] // Bulletin of RUDN. Series: Agronomy and Animal Husbandry. 2012; 3: 31–37. (In Russ.)

3. Nikitinsky D.A., Nikitinskaya E.V. Molecular genetic methods used for detection of quarantine objects. Innovations, challenges and prospects. Plant He a l th and Q uarantine. 20 2 5; ( 3 ): 85 –107. https://doi.org/10.69536/FKR.2025.67.86.006.

4. Dutrecq A., Debras P., Stevaux J., Klaessens D. Estimation of bacterial flora on scalded wheat heads // Parasitica. 1990. T. 2-3. No. 46. P. 69–84.

5. Gehring I., Geider K. Identification of Erwinia species isolated from apples and pears by differential PCR. // Journal of Microbiological Methods. 2012. Vol. 89. No. 1. P. 57-62. doi: 10.1016/j.mimet.2012.01.018.

6. Genebank project, NARO. Details of microorganism genetic resources. Details of MAFF 150529. URL: https://www.gene.affrc.go.jp/databasesmicro_search_detail_en.php?maff=150529.

7. Huang H. C., Erickson R. S., Hsieh T. F. Lack of host specificity of strains of Erwinia rhapontici, causal agent of pink seed of pulse and cereal crops // Botanical Studies. 2007. Vol. 48. No. 2. P. 181–186.

8. Kahala M., Blasco L., Joutsjoki V. Molecular characterization of spoilage bacteria as a means to observe the microbiological quality of carrot // Journal of Food Protection. 2012. Vol. 75. No. 3. P. 523-532. doi: 10.4315/0362-028X.JFP-11-185.

9. Kotan R., Sahin F., Ala A. Identification and pathogenicity of bacteria isolated from pome fruit trees in the Eastern Anatolia region of Turkey // Journal of Plant Diseases and Protection. 2006. Vol. 113. No. 1. P. 8–13.

10. Muvingi M., Slovareva O.Y., Yaremko A.B., Zargar M., Lyashko, M., Pakina E., Vvedenskiy V. Variations of the Bacterial Community in Wheat (Triticum aestivum), Oats (Avena sativa L.), Barley (Hordeum vulgare L.) and Triticale (Triticosecale) from Three Regions of the Republic of Crimea // Preprints. 2023. doi: 10.20944/preprints202307.1559.v1.

11. Naas T., Aubert D., Vimont S., Nordmann P. Identification of a chromosome-borne class C betalactamase from Erwinia rhapontici // Journal of Antimicrobial Chemotherapy. 2004. Vol. 54. No. 5. P. 932–935. doi: 10.1093/jac/dkh446.

12. Ramírez-Rojas S., Osuna-Canizalez F.J., García-Pérez F., Canul-Ku J., Palacios-Talavera A., Hernández-Romano J., Ornelas-Ocampo K., Landa-Salgado P. Molecular identification of bacteria associated to ornamental plants obtained in vitro // Revista Mexicana de Fitopatología. 2016. Vol. 34. No. 2. P. 173–183. doi: 10.18781/R.MEX.FIT.1511-3.

13. Reasoner D.J., Geldreich E.E., 1985. A new medium for the enumeration and subculture of bacteria from potable water. Applied and Environmental Microbiology. 1985. Vol. 49. No. 1. P. 1–7. doi: 10.1128/aem.49.1.1-7.1985.

14. Schober I., Koblitz J., Carbasse J.S., Ebeling C., Schmidt M.L., Podstawka A., Gupta R., Ilangovan V., Chamanara J., Overmann J., Reimer L.C., BacDive in 2025: the core database for prokaryotic strain data, Nucleic Acids Research, 2025. Vol. 53. Issue D1. P. D748–D756. doi: 10.1093/nar/gkae959.

15. Thapa S. P. Cho S. Y., Hur J. H., Lim C. K. Phenotypic and genetic characterization of Erwinia rhapontici isolated from diseased Asian pear fruit trees // Phytoparasitica. 2012. Vol. 40. No. 5. P. 507-514. doi: 10.1007/s12600-012-0251-3.

16. Tharreau D., Gaignard J. L., Luisetti J., Gibbon C. B. Presence d'une microflore bacterienne abondante et variee a la surface de trois plantes aromatiques et medicinales. Herba Gallica., 1992. No. 2. 79–89.

17. Tsuji M., Kadota I., Takikawa Y. Genetic and phenotypic characterization of bacterial strains isolated in Japan that resemble Erwinia rhapontici and E. persicinus // Journal of General Plant Pathoogy. 2020. Vol. 86. No. 1. P. 24–33. doi: 10.1007/s10327-019-00873-7.


Review

For citations:


Slovareva O.Yu., Avdeev I.S., Yaremko A.B., Panchenko K.V. Characteristics of the strain VNIIKR-B-0035 Erwinia rhapontici isolated from common barley (Hordeum vulgare L.). Plant Health and Quarantine. 2025;(4):44-53. (In Russ.) https://doi.org/10.69536/FKR.2025.46.28.005

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