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      Exploring the mechanisms of endophytic bacteria for suppressing early blight disease in tomato ( Solanum lycopersicum L.)

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          Abstract

          Controlling early blight of tomatoes using endophytic bacteria is an eco-friendly and sustainable approach to manage this common fungal disease caused by Alternaria solani, Alternaria alternata, and Curvularia lunata. Endophytic bacteria are microorganisms that live inside plant tissues without causing harm and can help protect the host plant from pathogens. In this work, twenty endophytic bacterial isolates from tomato healthy plants were tested against pathogenic fungal isolates that caused early blight disease in vitro. Out of the 20 tested isolates, three (B4, B7, and B17) were considered effective isolates against the growth of fungal pathogens. The three isolates were recognized as Enterobacter cloacae HS-6 (B4), Pseudomonas gessardii HS-5 (B 7), and Pseudomonas mediterranea HS-4 (B17) using 16s-rDNA sequencing. Different concentrations of bacterial cultural diltrates at 20, 40, and 60% were tested for their antagonistic effects on the development of pathogenic fungi in vitro. The lowest dry weights of pathogenic isolates in all bacterial culture filtrates were discovered at 60%. In all culture filtrates, phenolic compounds showed the largest peak area. Under greenhouse conditions, the least disease severity of tomato early blight was found for E. cloacae and its culture filtrate compared to other treatments. Real-time PCR was used to examine the expression pattern of the defense response gene β-1.3 glucanase gene in infected tomato plants with pathogenic fungi (control) as well as its relations with efficient biocontrol agent ( E. cloacae). The expression of the gene increased substantially and significantly after three days from the inoculation-infected plants with C. lunata and E. cloacae while it reached the maximum after five days from the inoculation with A. alternata, A. solani and E. cloacae. Our study concluded that the endophytic bacterial isolate E. cloacae can be considered a promising biocontrol agent for preventing tomato early blight.

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          16S ribosomal DNA amplification for phylogenetic study.

          A set of oligonucleotide primers capable of initiating enzymatic amplification (polymerase chain reaction) on a phylogenetically and taxonomically wide range of bacteria is described along with methods for their use and examples. One pair of primers is capable of amplifying nearly full-length 16S ribosomal DNA (rDNA) from many bacterial genera; the additional primers are useful for various exceptional sequences. Methods for purification of amplified material, direct sequencing, cloning, sequencing, and transcription are outlined. An obligate intracellular parasite of bovine erythrocytes, Anaplasma marginale, is used as an example; its 16S rDNA was amplified, cloned, sequenced, and phylogenetically placed. Anaplasmas are related to the genera Rickettsia and Ehrlichia. In addition, 16S rDNAs from several species were readily amplified from material found in lyophilized ampoules from the American Type Culture Collection. By use of this method, the phylogenetic study of extremely fastidious or highly pathogenic bacterial species can be carried out without the need to culture them. In theory, any gene segment for which polymerase chain reaction primer design is possible can be derived from a readily obtainable lyophilized bacterial culture.
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            Control of blackleg and tuber soft rot of potato caused by Pectobacterium and Dickeya species: a review

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              The effect of Bacillus spp. bacteria used as probiotics on digestive enzyme activity, survival and growth in the Indian white shrimp Fenneropenaeus indicus

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                Author and article information

                Contributors
                Journal
                Front Microbiol
                Front Microbiol
                Front. Microbiol.
                Frontiers in Microbiology
                Frontiers Media S.A.
                1664-302X
                21 September 2023
                2023
                : 14
                : 1184343
                Affiliations
                [1] 1Department of Plant Pathology, Faculty of Agriculture, Assiut University , Assiut, Egypt
                [2] 2Department of Genetics, Faculty of Agriculture, Assiut University , Assiut, Egypt
                [3] 3Department of Arid Land Agriculture, Faculty of Meteorology, Environment and Arid Land Agriculture, King Abdulaziz University , Jeddah, Saudi Arabia
                [4] 4Department of Entomology and Plant Pathology, Auburn University , Auburn, AL, United States
                [5] 5Department Genebank, Leibniz Institute of Plant Genetics and Crop Plant Research (IPK) , Gatersleben, Germany
                Author notes

                Edited by: Giancarlo Perrone, National Research Council (CNR), Italy

                Reviewed by: Khamis Youssef, Agricultural Research Center, Egypt; Malkhan Singh Gurjar, Indian Agricultural Research Institute (ICAR), India

                *Correspondence: Nashwa M. A. Sallam, nashwasallam@ 123456aun.edu.eg
                Article
                10.3389/fmicb.2023.1184343
                10551630
                37808317
                d75b242c-c866-4ead-8f55-eb368ab5ac63
                Copyright © 2023 Sallam, AbdElfatah, Khalil Bagy, Elfarash, Abo-Elyousr, Sikora and Sallam.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 11 March 2023
                : 24 August 2023
                Page count
                Figures: 7, Tables: 1, Equations: 0, References: 62, Pages: 11, Words: 8189
                Categories
                Microbiology
                Original Research
                Custom metadata
                Food Microbiology

                Microbiology & Virology
                biocontrol agents,16s-rdna,gene expression,gc-ms analysis,alternaria solani

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