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1.
Viruses ; 13(5)2021 04 21.
Article in English | MEDLINE | ID: mdl-33919362

ABSTRACT

Xylella fastidiosa (Xf) is a plant pathogen causing significant losses in agriculture worldwide. Originating from America, this bacterium caused recent epidemics in southern Europe and is thus considered an emerging pathogen. As the European regulations do not authorize antibiotic treatment in plants, alternative treatments are urgently needed to control the spread of the pathogen and eventually to cure infected crops. One such alternative is the use of phage therapy, developed more than 100 years ago to cure human dysentery and nowadays adapted to agriculture. The first step towards phage therapy is the isolation of the appropriate bacteriophages. With this goal, we searched for phages able to infect Xf strains that are endemic in the Mediterranean area. However, as Xf is truly a fastidious organism, we chose the phylogenetically closest and relatively fast-growing organism X. albineans as a surrogate host for the isolation step. Our results showed the isolation from various sources and preliminary characterization of several phages active on different Xf strains, namely, from the fastidiosa (Xff), multiplex (Xfm), and pauca (Xfp) subspecies, as well as on X. albilineans. We sequenced their genomes, described their genomic features, and provided a phylogeny analysis that allowed us to propose new taxonomic elements. Among the 14 genomes sequenced, we could identify two new phage species, belonging to two new genera of the Caudoviricetes order, namely, Usmevirus (Podoviridae family) and Subavirus (Siphoviridae family). Interestingly, no specific phages could be isolated from infected plant samples, whereas one was isolated from vector insects captured in a contaminated area, and several from surface and sewage waters from the Marseille area.


Subject(s)
Bacteriophages/physiology , Plants/microbiology , Xanthomonas/virology , Xylella/virology , Bacteriophages/classification , Bacteriophages/isolation & purification , Bacteriophages/ultrastructure , DNA, Viral , Host Specificity , Phylogeny , Plant Diseases/microbiology , Viral Tropism , Virulence , Xanthomonas/isolation & purification , Xylella/isolation & purification
2.
PLoS One ; 10(6): e0128902, 2015.
Article in English | MEDLINE | ID: mdl-26107261

ABSTRACT

Pierce's Disease (PD) of grapevines, caused by Xylella fastidiosa subsp. fastidiosa (Xf), is a limiting factor in the cultivation of grapevines in the US. There are presently no effective control methods to prevent or treat PD. The therapeutic and prophylactic efficacy of a phage cocktail composed of four virulent (lytic) phages was evaluated for control of PD. Xf levels in grapevines were significantly reduced in therapeutically or prophylactically treated grapevines. PD symptoms ceased to progress one week post-therapeutic treatment and symptoms were not observed in prophylactically treated grapevines. Cocktail phage levels increased in grapevines in the presence of the host. No in planta phage-resistant Xf isolates were obtained. Moreover, Xf mutants selected for phage resistance in vitro did not cause PD symptoms. Our results indicate that phages have great potential for biocontrol of PD and other economically important diseases caused by Xylella.


Subject(s)
Bacteriophages/physiology , Biological Control Agents , Plant Diseases/microbiology , Vitis/microbiology , Xylella/virology , Colony Count, Microbial , Lysogeny , Mutation , Xylella/growth & development , Xylella/pathogenicity
3.
J Bacteriol ; 196(2): 459-71, 2014 Jan.
Article in English | MEDLINE | ID: mdl-24214944

ABSTRACT

The xylem-limited bacterium Xylella fastidiosa is the causal agent of several plant diseases, most notably Pierce's disease of grape and citrus variegated chlorosis. We report the isolation and characterization of the first virulent phages for X. fastidiosa, siphophages Sano and Salvo and podophages Prado and Paz, with a host range that includes Xanthomonas spp. Phages propagated on homologous hosts had observed adsorption rate constants of ~4 × 10(-12) ml cell(-1) min(-1) for X. fastidiosa strain Temecula 1 and ~5 × 10(-10) to 7 × 10(-10) ml cell(-1) min(-1) for Xanthomonas strain EC-12. Sano and Salvo exhibit >80% nucleotide identity to each other in aligned regions and are syntenic to phage BcepNazgul. We propose that phage BcepNazgul is the founding member of a novel phage type, to which Sano and Salvo belong. The lysis genes of the Nazgul-like phage type include a gene that encodes an outer membrane lipoprotein endolysin and also spanin gene families that provide insight into the evolution of the lysis pathway for phages of Gram-negative hosts. Prado and Paz, although exhibiting no significant DNA homology to each other, are new members of the phiKMV-like phage type, based on the position of the single-subunit RNA polymerase gene. The four phages are type IV pilus dependent for infection of both X. fastidiosa and Xanthomonas. The phages may be useful as agents for an effective and environmentally responsible strategy for the control of diseases caused by X. fastidiosa.


Subject(s)
Bacteriophages/isolation & purification , Bacteriophages/physiology , Xanthomonas/virology , Xylella/virology , Bacteriophages/genetics , Bacteriophages/ultrastructure , DNA, Viral/chemistry , DNA, Viral/genetics , Genes, Viral , Genome, Viral , Host Specificity , Microscopy, Electron, Transmission , Molecular Sequence Data , Podoviridae/genetics , Podoviridae/isolation & purification , Podoviridae/physiology , Podoviridae/ultrastructure , Sequence Analysis, DNA , Siphoviridae/genetics , Siphoviridae/isolation & purification , Siphoviridae/physiology , Siphoviridae/ultrastructure , Synteny , Virus Attachment
4.
J Bacteriol ; 192(1): 179-90, 2010 Jan.
Article in English | MEDLINE | ID: mdl-19897657

ABSTRACT

We report the plaque propagation and genomic analysis of Xfas53, a temperate phage of Xylella fastidiosa. Xfas53 was isolated from supernatants of X. fastidiosa strain 53 and forms plaques on the sequenced strain Temecula. Xfas53 forms short-tailed virions, morphologically similar to podophage P22. The 36.7-kb genome is predicted to encode 45 proteins. The Xfas53 terminase and structural genes are related at a protein and gene order level to P22. The left arm of the Xfas53 genome has over 90% nucleotide identity to multiple prophage elements of the sequenced X. fastidiosa strains. This arm encodes proteins involved in DNA metabolism, integration, and lysogenic control. In contrast to Xfas53, each of these prophages encodes head and DNA packaging proteins related to the siphophage lambda and tail morphogenesis proteins related to those of myophage P2. Therefore, it appears that Xfas53 was formed by recombination between a widespread family of X. fastidiosa P2-related prophage elements and a podophage distantly related to phage P22. The lysis cassette of Xfas53 is predicted to encode a pinholin, a signal anchor and release (SAR) endolysin, and Rz and Rz1 equivalents. The holin gene encodes a pinholin and appears to be subject to an unprecedented degree of negative regulation at both the level of expression, with rho-independent transcriptional termination and RNA structure-dependent translational repression, and the level of holin function, with two upstream translational starts predicted to encode antiholin products. A notable feature of Xfas53 and related prophages is the presence of 220- to 390-nucleotide degenerate tandem direct repeats encoding putative DNA binding proteins. Additionally, each phage encodes at least two BroN domain-containing proteins possibly involved in lysogenic control. Xfas53 exhibits unusually slow adsorption kinetics, possibly an adaptation to the confined niche of its slow-growing host.


Subject(s)
Bacteriophages/genetics , Genome, Viral/genetics , Prophages/genetics , Xylella/virology , Bacteriophages/growth & development , Bacteriophages/ultrastructure , DNA, Viral/genetics , Microscopy, Electron, Transmission , Models, Genetic , Prophages/growth & development , Prophages/ultrastructure , Virus Replication/genetics , Virus Replication/physiology , Xylella/cytology
5.
Virol J ; 5: 75, 2008 Jun 06.
Article in English | MEDLINE | ID: mdl-18538030

ABSTRACT

Presumptive phage particles associated with Xylella fastidiosa strain Temecula-1 grown in PW broth were observed by transmission electron microscopy (TEM) in ultrathin sections of bacterial cell-containing low speed centrifugation pellets and in partially purified preparations from CsCl equilibrium centrifugation density gradients. Ultrathin-sectioned cell pellets contained icosahedral particles of about 45 nm in diameter. Samples collected from CsCl density gradients revealed mostly non-tailed icosahedral but also tailed particles. The icosahedral particles could be divided into two types: a large type (about 45 nm) and a small type (about 30 nm). Filamentous phage-like particles (17 x 120 to 6,300 nm) were also observed. The presence of different types of phage-like particles resembling to those in several bacteriophage families provides new physical evidence, in addition to X. fastidiosa genomic information, that X. fastidiosa possesses active phages. This is the first report of phage particles released in X. fastidiosa cultures.


Subject(s)
Bacteriophages/isolation & purification , Xylella/virology , Bacteriophages/ultrastructure , Centrifugation, Density Gradient , Microscopy, Electron, Transmission , Virion/ultrastructure
6.
J Virol Methods ; 133(2): 130-6, 2006 May.
Article in English | MEDLINE | ID: mdl-16337281

ABSTRACT

An extraction technique for reverse transcription-PCR (RT-PCR) detection of plant pathogens including viruses, bacteria and phytoplasma is described. The total nucleic acid of these plant pathogens was obtained by direct spotting of crude sap derived from infected leaf, petiole or cambial tissue onto two different types of membranes, positively charged Hybond N(+) Nylon and FTA membranes, and processed for use in PCR. Thirteen different plant viruses, Xylella fastidiosa (causal agent of Pierce's disease) and phytoplasmas were included in the experiment. A thermal treatment (95 degrees C for 10 min) of the Hybond N(+) Nylon discs in a buffered solution improved the detection, but for FTA membrane discs the thermal treatment was not required and the discs were directly placed in the PCR reaction cocktail. Specific amplification of genomic or ribosomal RNA fragments of these pathogens was obtained by one-step RT-PCR except for X. fastidiosa in which a fragment of the genomic DNA was used for amplification. The same sample preparation methods also worked well for real-time RT-PCR (TaqMan). The sample preparation techniques reported here could be used to store samples for future PCR test or for long distance shipment to a detection laboratory.


Subject(s)
Plant Viruses/isolation & purification , Plant Viruses/pathogenicity , Polymerase Chain Reaction/methods , Reverse Transcriptase Polymerase Chain Reaction/methods , Trees/virology , Edetic Acid/pharmacology , Electrophoresis, Agar Gel , Evaluation Studies as Topic , Membranes, Artificial , Octoxynol/pharmacology , Phytoplasma/genetics , Phytoplasma/isolation & purification , Phytoplasma/virology , Plant Viruses/genetics , Xylella/genetics , Xylella/isolation & purification , Xylella/virology
7.
OMICS ; 9(2): 146-59, 2005.
Article in English | MEDLINE | ID: mdl-15969647

ABSTRACT

The gamma-proteobacterium Xanthomonadales groups two closely related genera of plant pathogens, Xanthomonas and Xylella. Whole genome sequencing and comparative analyses disclosed a high degree of identity and co-linearity of the chromosome backbone between species and strains. Differences observed are usually clustered into genomic islands, most of which are delimited by genetic mobile elements. Focus is given in this paper to describe which groups of mobile elements are found and what is the relative contribution of these elements to Xanthomonas and Xylella genomes. Insertion sequence (IS) elements have invaded the Xanthomonas genome several times, whereas Xylella is rich in phage-related regions. Also, different plasmids are found inhabiting the bacterial cells studied here. Altogether, these results suggest that the integrative elements such as phages and transposable elements as well as the episomal plasmids are important drivers of the genome evolution of this important group of plant pathogens.


Subject(s)
Retroelements , Xanthomonas/genetics , Xylella/genetics , Amino Acid Sequence , Bacteriophages/genetics , Base Sequence , DNA Transposable Elements/genetics , DNA, Bacterial/genetics , Genome, Bacterial , Molecular Sequence Data , Phylogeny , Plasmids/genetics , Prophages/genetics , Species Specificity , Xanthomonas/classification , Xanthomonas/virology , Xylella/classification , Xylella/virology
8.
Curr Microbiol ; 50(2): 78-83, 2005 Feb.
Article in English | MEDLINE | ID: mdl-15723179

ABSTRACT

Xylella fastidiosa causes many important plant diseases including Pierce's disease (PD) in grape and almond leaf scorch disease (ALSD). DNA-based methodologies, such as randomly amplified polymorphic DNA (RAPD) analysis, have been playing key roles in genetic information collection of the bacterium. This study further analyzed the nucleotide sequences of selected RAPDs from X. fastidiosa strains in conjunction with the available genome sequence databases and unveiled several previously unknown novel genetic traits. These include a sequence highly similar to those in the phage family of Podoviridae. Genome comparisons among X. fastidiosa strains suggested that the "phage" is currently active. Two other RAPDs were also related to horizontal gene transfer: one was part of a broadly distributed cryptic plasmid and the other was associated with conjugal transfer. One RAPD inferred a genomic rearrangement event among X. fastidiosa PD strains and another identified a single nucleotide polymorphism of evolutionary value.


Subject(s)
DNA, Bacterial/genetics , Xylella/genetics , Bacteriophages/genetics , Bacteriophages/isolation & purification , Base Sequence , Conjugation, Genetic , Evolution, Molecular , Gene Rearrangement , Genes, Bacterial , Genome, Bacterial , Molecular Sequence Data , Plant Diseases/microbiology , Plasmids/genetics , Podoviridae/genetics , Podoviridae/isolation & purification , Polymorphism, Single Nucleotide , Random Amplified Polymorphic DNA Technique , Xylella/pathogenicity , Xylella/virology
9.
BMC Bioinformatics ; 5: 90, 2004 Jul 07.
Article in English | MEDLINE | ID: mdl-15239845

ABSTRACT

BACKGROUND: Oligonucleotide frequencies were shown to be conserved signatures for bacterial genomes, however, the underlying constraints have yet not been resolved in detail. In this paper we analyzed oligonucleotide usage (OU) biases in a comprehensive collection of 155 completely sequenced bacterial chromosomes, 316 plasmids and 104 phages. RESULTS: Two global features were analyzed: pattern skew (PS) and variance of OU deviations normalized by mononucleotide content of the sequence (OUV). OUV reflects the strength of OU biases and taxonomic signals. PS denotes asymmetry of OU in direct and reverse DNA strands. A trend towards minimal PS was observed for almost all complete sequences of bacterial chromosomes and plasmids, however, PS was substantially higher in separate genomic loci and several types of plasmids and phages characterized by long stretches of non-coding DNA and/or asymmetric gene distribution on the two DNA strands. Five of the 155 bacterial chromosomes have anomalously high PS, of which the chromosomes of Xylella fastidiosa 9a5c and Prochlorococcus marinus MIT9313 exhibit extreme PS values suggesting an intermediate unstable state of these two genomes. CONCLUSIONS: Strand symmetry as indicated by minimal PS is a universally conserved feature of complete bacterial genomes that results from the matching mutual compensation of local OU biases on both replichors while OUV is more a taxon specific feature. Local events such as inversions or the incorporation of genome islands are balanced by global changes in genome organization to minimize PS that may represent one of the leading evolutionary forces driving bacterial genome diversification.


Subject(s)
Bacteriophages/genetics , Chromosomes, Bacterial/genetics , Oligonucleotides/genetics , Plasmids/genetics , Base Composition/genetics , Cyanobacteria/genetics , Cyanobacteria/virology , DNA, Bacterial/genetics , DNA, Viral/genetics , Genetic Variation/genetics , Genome, Bacterial , Nucleic Acid Conformation , Xylella/genetics , Xylella/virology
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