scholarly journals Chromosomally Encodedhok-sokToxin-Antitoxin System in the Fire Blight PathogenErwinia amylovora: Identification and Functional Characterization

2019 ◽  
Vol 85 (15) ◽  
Author(s):  
Jingyu Peng ◽  
Lindsay R. Triplett ◽  
Jeffrey K. Schachterle ◽  
George W. Sundin
Keyword(s):  
Noncoding Rna ◽  
Pathogenic Bacteria ◽  
Fire Blight ◽  
Erwinia Amylovora ◽  
Functional Characterization ◽  
Pathogenic Bacterium ◽  
Type I ◽  
Plant Pathogenic Bacterium ◽  
Content Type ◽  
Protein Toxin

ABSTRACTToxin-antitoxin (TA) systems are genetic elements composed of a protein toxin and a counteracting antitoxin that is either a noncoding RNA or protein. In type I TA systems, the antitoxin is a noncoding small RNA (sRNA) that base pairs with the cognate toxin mRNA interfering with its translation. Although type I TA systems have been extensively studied inEscherichia coliand a few human or animal bacterial pathogens, they have not been characterized in plant-pathogenic bacteria. In this study, we characterized a chromosomal locus in the plant pathogenErwinia amylovoraEa1189 that is homologous to thehok-soktype I TA system previously identified in theEnterobacteriaceae-restricted plasmid R1. Phylogenetic analysis indicated that the chromosomal location of thehok-soklocus is, thus far, unique toE. amylovora. We demonstrated that ectopic overexpression ofhokis highly toxic toE. amylovoraand that the sRNAsokreversed the toxicity ofhokthroughmok, a reading frame presumably translationally coupled withhok. We also identified the region that is essential for maintenance of the main toxicity of Hok. Through ahok-sokdeletion mutant (Ea1189Δhok-sok), we determined the contribution of thehok-soklocus to cellular growth, micromorphology, and catalase activity. Combined, our findings indicate that thehok-sokTA system, besides being potentially self-toxic, provides fitness advantages toE. amylovora.IMPORTANCEBacterial toxin-antitoxin systems have received great attention because of their potential as targets for antimicrobial development and as tools for biotechnology.Erwinia amylovora, the causal agent of fire blight disease on pome fruit trees, is a major plant-pathogenic bacterium. In this study, we identified and functionally characterized a unique chromosomally encodedhok-soktoxin-antitoxin system inE. amylovorathat resembles the plasmid-encoded copies of this system in otherEnterobacteriaceae. This study of a type I toxin-antitoxin system in a plant-pathogenic bacterium provides the basis to further understand the involvement of toxin-antitoxin systems during infection by a plant-pathogenic bacterium. The new linkage between thehok-soktoxin-antitoxin system and the catalase-mediated oxidative stress response leads to additional considerations of targeting this system for antimicrobial development.

scholarly journals Whole-Genome Sequence of Pseudomonas fluorescens EK007-RG4, a Promising Biocontrol Agent against a Broad Range of Bacteria, Including the Fire Blight Bacterium Erwinia amylovora

2017 ◽  
Vol 5 (13) ◽  
Author(s):  
Roghayeh Habibi ◽  
Saeed Tarighi ◽  
Javad Behravan ◽  
Parissa Taheri ◽  
Annelise Helene Kjøller ◽  
...  
Keyword(s):  
Pseudomonas Fluorescens ◽  
Genome Sequence ◽  
Pathogenic Bacteria ◽  
Fire Blight ◽  
Erwinia Amylovora ◽  
Whole Genome Sequence ◽  
Whole Genome ◽  
Content Type ◽  
Pear Tree ◽  
Blight Disease

ABSTRACT Here, we report the first draft whole-genome sequence of Pseudomonas fluorescens strain EK007-RG4, which was isolated from the phylloplane of a pear tree. P. fluorescens EK007-RG4 displays strong antagonism against Erwinia amylovora, the causal agent for fire blight disease, in addition to several other pathogenic and non-pathogenic bacteria.

Isolation and characterization of Hena1 – a novel Erwinia amylovora bacteriophage

2020 ◽  
Vol 367 (9) ◽  
Author(s):  
Natalya V Besarab ◽  
Artur E Akhremchuk ◽  
Maryna A Zlatohurska ◽  
Liudmyla V Romaniuk ◽  
Leonid N Valentovich ◽  
...  
Keyword(s):  
Pathogenic Bacteria ◽  
Fire Blight ◽  
Antimicrobial Agents ◽  
Erwinia Amylovora ◽  
Gc Content ◽  
Control Measures ◽  
Effective Control ◽  
Lytic Phage ◽  
Trna Genes ◽  
Isolation And Characterization

ABSTRACT Fire blight, caused by plant pathogenic bacterium Erwinia amylovora, is one of the most important diseases of Rosaceae plants. Due to the lack of effective control measures, fire blight infections pose a recurrent threat on agricultural production worldwide. Recently, bacterial viruses, or bacteriophages, have been proposed as environmentally friendly natural antimicrobial agents for fire blight control. Here, we isolated a novel bacteriophage Hena1 with activity against E. amylovora. Further analysis revealed that Hena1 is a narrow-host-range lytic phage belonging to Myoviridae family. Its genome consists of a linear 148,842 bp dsDNA (48.42% GC content) encoding 240 ORFs and 23 tRNA genes. Based on virion structure and genomic composition, Hena1 was classified as a new species of bacteriophage subfamily Vequintavirinae. The comprehensive analysis of Hena1 genome may provide further insights into evolution of bacteriophages infecting plant pathogenic bacteria.

scholarly journals Bacterial Enzymes Catalyzing the Synthesis of 1,8-Dihydroxynaphthalene, a Key Precursor of Dihydroxynaphthalene Melanin, fromSorangium cellulosum

2018 ◽  
Vol 84 (9) ◽  
Author(s):  
Yusuke Sone ◽  
Shuto Nakamura ◽  
Makoto Sasaki ◽  
Fumihito Hasebe ◽  
Seung-Young Kim ◽  
...  
Keyword(s):  
Pathogenic Bacteria ◽  
Optical Purity ◽  
Brown Pigment ◽  
Type I ◽  
Enzymatic System ◽  
Type Iii Polyketide Synthase ◽  
Content Type ◽  
Type Iii ◽  
Bacterial Origin

ABSTRACT1,8-Dihydroxynaphthalene (1,8-DHN) is a key intermediate in the biosynthesis of DHN melanin, which is specific to fungi. In this study, we characterized the enzymatic properties of the gene products of an operon consisting ofsoceCHS1,bdsA, andbdsBfrom the Gram-negative bacteriumSorangium cellulosum. Heterologous expression ofsoceCHS1,bdsA, andbdsBinStreptomyces coelicolorcaused secretion of a dark-brown pigment into the broth. High-performance liquid chromatography (HPLC) analysis of the broth revealed that the recombinant strain produced 1,8-DHN, indicating that the operon encoded a novel enzymatic system for the synthesis of 1,8-DHN. Simultaneous incubation of the recombinant SoceCHS1, BdsA, and BdsB with malonyl-coenzyme A (malonyl-CoA) and NADPH resulted in the synthesis of 1,8-DHN. SoceCHS1, a type III polyketide synthase (PKS), catalyzed the synthesis of 1,3,6,8-tetrahydroxynaphthalene (T4HN)in vitro. T4HN was in turn converted to 1,8-DHN by successive steps of reduction and dehydration, which were catalyzed by BdsA and BdsB. BdsA, which is a member of the aldo-keto reductase (AKR) superfamily, catalyzed the reduction of T4HN and 1,3,8-tetrahydroxynaphthalene (T3HN) to scytalone and vermelone, respectively. The stereoselectivity of T4HN reduction by BdsA occurred on thesi-face to give (R)-scytalone with more than 99% optical purity. BdsB, a SnoaL2-like protein, catalyzed the dehydration of scytalone and vermelone to T3HN and 1,8-DHN, respectively. The fungal pathway for the synthesis of 1,8-DHN is composed of a type I PKS, naphthol reductases of the short-chain dehydrogenase/reductase (SDR) superfamily, and scytalone dehydratase (SD). These findings demonstrated 1,8-DHN synthesis by novel enzymes of bacterial origin.IMPORTANCEAlthough the DHN biosynthetic pathway was thought to be specific to fungi, we discovered novel DHN synthesis enzymes of bacterial origin. The biosynthesis of bacterial DHN utilized a type III PKS for polyketide synthesis, an AKR superfamily for reduction, and a SnoaL2-like NTF2 superfamily for dehydration, whereas the biosynthesis of fungal DHN utilized a type I PKS, SDR superfamily enzyme, and SD-like NTF2 superfamily. Surprisingly, the enzyme systems comprising the pathway were significantly different from each other, suggesting independent, parallel evolution leading to the same biosynthesis. DHN melanin plays roles in host invasion and adaptation to stress in pathogenic fungi and is therefore important to study. However, it is unclear whether DHN biosynthesis occurs in bacteria. Importantly, we did find that bacterial DHN biosynthetic enzymes were conserved among pathogenic bacteria.

scholarly journals Structural and functional characterization of proteins from the fire blight pathogen Erwinia amylovora. A review on the state of the art

2020 ◽  
Author(s):  
Stefano Benini
Keyword(s):  
Fire Blight ◽  
Erwinia Amylovora ◽  
Functional Characterization ◽  
Data Bank ◽  
Knock Out ◽  
X Ray ◽  
X Ray Crystallography ◽  
Starting Point ◽  
Good Starting Point

Abstract Together with genome analysis and knock-out mutants, structural and functional characterization of proteins provide valuable hints on the biology of the organism under investigation. Structural characterization can be achieved by techniques such as X-ray crystallography, NMR, Cryo-EM. The information derived from the structure are a good starting point to comprehend the details of the proteins molecular function for a better understanding of their biological role. This review aims at describing the progress in the structural and functional characterization of proteins from the plant pathogen Erwinia amylovora obtained by structural biology and currently deposited in the Protein Data Bank.

scholarly journals Effects of Exposure Time and Biological State on Acquisition and Accumulation of Erwinia amylovora by Drosophila melanogaster

2019 ◽  
Vol 85 (15) ◽  
Author(s):  
Matthew Boucher ◽  
Rowan Collins ◽  
Kerik Cox ◽  
Greg Loeb
Keyword(s):  
Drosophila Melanogaster ◽  
Exposure Time ◽  
Fire Blight ◽  
Erwinia Amylovora ◽  
Current Knowledge ◽  
Selective Medium ◽  
Nutritional State ◽  
Biological Factors ◽  
Content Type ◽  
Disease Cycle

ABSTRACT Fire blight, caused by the bacterium Erwinia amylovora, is a disease devastating the production of rosaceous crops, primarily apple and pear, with worldwide distribution. Fire blight begins in the spring when primary inoculum is produced as ooze, which consists of plant sap, E. amylovora, and exopolysaccharides. Ooze is believed to be transferred to healthy tissues by wind, rain, and insects. However, the mechanisms by which insects locate and transmit ooze are largely undocumented. The goals of this study were to investigate the biological factors affecting acquisition of E. amylovora from ooze by a model dipteran, Drosophila melanogaster, and to determine whether flies are able to mechanically transfer this bacterium after acquisition. We found that the percentage of positive flies increased as exposure time increased, but nutritional state, mating status, and sex did not significantly alter the number of positive individuals. Bacterial abundance was highly variable at all exposure times, suggesting that other biological factors play a role in acquisition. Nutritional state had a significant effect on E. amylovora abundance, and food-deprived flies had higher E. amylovora counts than satiated flies. We also demonstrated that D. melanogaster transmits E. amylovora to a selective medium surface and hypothesize that the same is possible for plant surfaces, where bacteria can persist until an opportunity to colonize the host arises. Collectively, these data suggest a more significant role for flies than previously thought in transmission of fire blight and contribute to a shift in our understanding of the E. amylovora disease cycle. IMPORTANCE A recent hypothesis proposed that dissemination of Erwinia amylovora from ooze by flies to native rosaceous trees was likely key to the life cycle of the bacterium during its evolution. Our study validates an important component of this hypothesis by showing that flies are capable of acquiring and transmitting this bacterium from ooze under various biotic conditions. Understanding how dipterans interact with ooze advances our current knowledge of its epidemiological function and provides strong evidence for an underappreciated role of flies in the disease cycle. These findings may be especially important as they pertain to shoot blight, because this stage of the disease is poorly understood and may involve a significant amount of insect activity. Broadly, this study underscores a need to consider the depth, breadth, and origin of interactions between flies and E. amylovora to better understand its epidemiology.

scholarly journals Draft Genome Sequences of Four Streptomycin-Sensitive Erwinia amylovora Strains Isolated from Commercial Apple Orchards in Ohio

2021 ◽  
Vol 10 (50) ◽  
Author(s):  
A. M. Jimenez Madrid ◽  
T. Klass ◽  
V. Roman-Reyna ◽  
J. Jacobs ◽  
M. L. Lewis Ivey
Keyword(s):  
Causative Agent ◽  
Fire Blight ◽  
Erwinia Amylovora ◽  
Draft Genome ◽  
Apple Orchards ◽  
Genome Sequences ◽  
Apple Trees ◽  
Content Type

Erwinia amylovora is the causative agent of fire blight, a devastating disease of apples and pears worldwide. Here, we report draft genome sequences of four streptomycin-sensitive strains of E. amylovora that were isolated from diseased apple trees in Ohio.

scholarly journals First Report of Fire Blight Caused by Erwinia amylovora on Meadowsweet (Spirea prunifolia) in Turkey

Plant Disease ◽  
2014 ◽  
Vol 98 (1) ◽  
pp. 153-153 ◽  
Author(s):  
K. K. Bastas ◽  
F. Sahin
Keyword(s):  
Pathogenic Bacteria ◽  
Fire Blight ◽  
Erwinia Amylovora ◽  
Natural Infection ◽  
Hypodermic Needle ◽  
Identification System ◽  
Bacterial Strains ◽  
First Report ◽  
Molecular Tests ◽  
Initial Symptoms

Fire blight, caused by Erwinia amylovora (Burr.) Winslow et al., affects plants in the Rosaceae family, which includes trees and shrubs in orchards, nurseries, and landscape plantations. During the springs and summers of 2008 and 2010, dying branches, necrotic leaves attached to shoots, and blighted twigs of meadowsweet (Spirea prunifolia) were observed at three different locations of landscape areas in Konya Province, Turkey. Disease incidence was approximately 1% on the plants during the surveys. Initial symptoms of reddish to brownish streaks on the shoots of infected plants were observed in spring. Nine representative bacterial strains were isolated from the lesions on shoots of seven meadowsweet plants on nutrient sucrose agar (NSA) medium and identified as E. amylovora on basis of biochemical, physiological (2,3) and molecular tests (1). Bacteria were gram-negative, rod shaped, aerobic, fermentative, yellow-orange on Miller and Scroth medium (2), positive for levan formation and acetoin production, did not grow at 36°C, positive for gelatin hydrolysis, and negative for esculin hydrolysis, indole, urease, catalase, oxidase, arginine dehydrolase, reduction of nitrate, acid production from lactose, and inositol. All strains were hypersensitive response-positive on tobacco (Nicotiana tabacum var. White Burley) plants. All strains were identified as E. amylovora using the species-specific primers set, A/B (1), by PCR assay, and by fatty acid methyl ester (FAME) profiles determined by Sherlock Microbial Identification System software (TSBA 6 v. 6.00; Microbial ID, Newark, DE) with similarity indices ranging from of 79 to 99%. Pathogenicity was tested by injecting of petioles and actively growing three shoot tips of 2-year-old S. prunifolia seedlings cv. number 29 using a 0.46 mm-diameter hypodermic needle with bacterial suspensions containing 108 CFU mL–1 in sterile distilled water (SDW) Plants were inoculated with each of the nine bacterial strains and two references strains, Ea29 and NCPPB 2791 (Selcuk University, Department of Plant Protection, Konya, Turkey). Symptoms resembling those associated with natural infection appeared on the inoculated plants 7 days after inoculation. Plants inoculated with SDW served as a negative control treatment, and no symptoms were observed on these plants. All tests were repeated three times with the same results. Bacterial re-isolations were attempted from the control plants as well as shoots and leaves inoculated with the two reference strains and the nine bacteria identified as E. amylovora. Bacteria isolated from inoculated plants were identified as E. amylovora using the biochemical, physiological, and molecular tests described above, but this bacterium was not isolated from the control plants. Phytosanitary measures must be taken to avoid spread of the pathogen to ornamentals in new landscape areas in Turkey. This report is important because infected Spirea spp. can be a potential inoculum source for other rosaceous ornamentals. To our knowledge, this is the first report of the occurrence of fire blight on meadowsweet in Turkey. References: (1) S. Bereswill et al. Appl. Environ. Microbiol. 58:3522, 1992. (2) A. L. Jones and K. Geider. Laboratory Guide for Identification of Plant Pathogenic Bacteria, pp. 40-55. American Phytopathological Society, St. Paul, MN, 2001. (3) R. A. Lelliott and D. E. Stead. Methods for Diagnosis of Bacterial Diseases of Plants (Methods in Plant Pathology). Oxford, UK, 1987.

scholarly journals Draft Genome Sequences of Seven Strains of Dickeya dadantii, a Quick Decline-Causing Pathogen in Fruit Trees, Isolated in Japan

2020 ◽  
Vol 9 (28) ◽  
Author(s):  
Takashi Fujikawa ◽  
Hiroe Hatomi ◽  
Nobuyoshi Ota
Keyword(s):  
Draft Genome ◽  
Fruit Trees ◽  
Pathogenic Bacterium ◽  
Japanese Pear ◽  
Plant Pathogenic Bacterium ◽  
Genome Sequences ◽  
Dickeya Dadantii ◽  
Content Type

ABSTRACT The plant-pathogenic bacterium Dickeya dadantii causes quick decline in fruit trees (e.g., apple, Japanese pear, and peach). In this study, we report on the draft genome sequences of seven strains of D. dadantii that were isolated from fruit trees with typical quick decline symptoms in Japan.

scholarly journals Intergenerational Pathogen-Induced Diapause in Caenorhabditis elegans Is Modulated by mir-243

mBio ◽  
2020 ◽  
Vol 11 (5) ◽  
Author(s):  
Carolaing Gabaldón ◽  
Marcela Legüe ◽  
M. Fernanda Palominos ◽  
Lidia Verdugo ◽  
Florence Gutzwiller ◽  
...  
Keyword(s):  
Caenorhabditis Elegans ◽  
Noncoding Rna ◽  
Pathogenic Bacteria ◽  
Developmental Change ◽  
Differential Expression Analysis ◽  
Phenotypic Analysis ◽  
Content Type ◽  
C Elegans ◽  
Two Generations ◽  
Dauer Formation

ABSTRACT The interaction and communication between bacteria and their hosts modulate many aspects of animal physiology and behavior. Dauer entry as a response to chronic exposure to pathogenic bacteria in Caenorhabditis elegans is an example of a dramatic survival response. This response is dependent on the RNA interference (RNAi) machinery, suggesting the involvement of small RNAs (sRNAs) as effectors. Interestingly, dauer formation occurs after two generations of interaction with two unrelated moderately pathogenic bacteria. Therefore, we sought to discover the identity of C. elegans RNAs involved in pathogen-induced diapause. Using transcriptomics and differential expression analysis of coding and long and small noncoding RNAs, we found that mir-243-3p (the mature form of mir-243) is the only transcript continuously upregulated in animals exposed to both Pseudomonas aeruginosa and Salmonella enterica for two generations. Phenotypic analysis of mutants showed that mir-243 is required for dauer formation under pathogenesis but not under starvation. Moreover, DAF-16, a master regulator of defensive responses in the animal and required for dauer formation was found to be necessary for mir-243 expression. This work highlights the role of a small noncoding RNA in the intergenerational defensive response against pathogenic bacteria and interkingdom communication. IMPORTANCE Persistent infection of the bacterivore nematode C. elegans with bacteria such as P. aeruginosa and S. enterica makes the worm diapause or hibernate. By doing this, the worm closes its mouth, avoiding infection. This response takes two generations to be implemented. In this work, we looked for genes expressed upon infection that could mediate the worm diapause triggered by pathogens. We identify mir-243-3p as the only transcript commonly upregulated when animals feed on P. aeruginosa and S. enterica for two consecutive generations. Moreover, we demonstrate that mir-243-3p is required for pathogen-induced dauer formation, a new function that has not been previously described for this microRNA (miRNA). We also find that the transcriptional activators DAF-16, PQM-1, and CRH-2 are necessary for the expression of mir-243 under pathogenesis. Here we establish a relationship between a small RNA and a developmental change that ensures the survival of a percentage of the progeny.

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