scholarly journals Causal Role of Xylella fastidiosa in Oleander Leaf Scorch Disease

1999 ◽  
Vol 89 (1) ◽  
pp. 53-58 ◽  
Author(s):  
A. H. Purcell ◽  
S. R. Saunders ◽  
M. Hendson ◽  
M. E. Grebus ◽  
M. J. Henry

A lethal leaf scorch disease of oleander (Nerium oleander) appeared in southern California in 1993. A bacterium, Xylella fastidiosa, was detected by culturing, enzyme-linked immunoassay, and polymerase chain reaction in most symptomatic plants but not in symptomless plants or negative controls. Inoculating oleanders mechanically with X. fastidiosa cultures from diseased oleanders caused oleander leaf scorch (OLS) disease. The bacterium was reisolated from inoculated plants that became diseased. Three species of xylem sap-feeding leafhoppers transmitted the bacterium from oleander to oleander. The bacterium multiplied, moved systemically, and caused wilting in Madagascar periwinkle (Catharanthus rosea) and leaf scorch in periwinkle (Vinca major) in a greenhouse after inoculation with needle puncture. No bacterium was reisolated from grapevine (Vitis vinifera), peach (Prunus persica), olive (Olea europaea), California blackberry (Rubus ursinus), or valley oak (Quercus lobata) mechanically inoculated with OLS strains of X. fastidiosa. A 500-bp sequence of the 16S-23S ribosomal intergenic region of oleander strains showed 99.2% identity with Pierce's disease strains, 98.4% identity with oak leaf scorch strains, and 98.6% identity with phony peach, plum leaf scald, and almond leaf scorch strains.

Insects ◽  
2019 ◽  
Vol 10 (10) ◽  
pp. 324 ◽  
Author(s):  
Vincenzo Cavalieri ◽  
Giuseppe Altamura ◽  
Giulio Fumarola ◽  
Michele di Carolo ◽  
Maria Saponari ◽  
...  

Diseases associated with Xylella fastidiosa have been described mostly in North and South America. However, during the last five years, widespread X. fastidiosa infections have been reported in a constrained area of the Apulia region (southern Italy), in olives trees suffering a severe disease, denoted as Olive Quick Decline Syndrome (OQDS). Because many xylem sap-feeding insects can function as vectors for the transmission of this exotic pathogen in EU, several research programs are ongoing to assess the role of candidate vectors in the spread of the infections. Initial investigations identified Philaenus spumarius (L.) as the predominant vector species in the olive orchards affected by the OQDS. Additional experiments have been carried out during 2016 and 2017 to assess the role of other species. More specifically, adults of the spittlebugs Philaenus italosignus Drosopolous and Remane, Neophilaenus campestris (Fallen) and of the planthopper Latilica tunetana (Matsumura) (Issidae) have been tested in transmission experiments to assess their ability to acquire the bacterium from infected olives and to infect different susceptible hosts (olives, almond, myrtle –leaf milkwort, periwinkle). Acquisition rates determined by testing individual insects in quantitative PCR assays, ranging from 5.6% in N. campestris to 22.2% in P. italosignus, whereas no acquisition was recorded for L. tunetana. Successful transmissions were detected in the recipient plants exposed to P. italosignus and N. campestris, whereas no trasmissions occurred with L. tunetana. The known vector Philaenus spumarius has been included in all the experiments for validation. The systematic surveys conducted in 2016 and 2017 provided further evidence on the population dynamics and seasonal abundance of the spittlebug populations in the olive groves.


Plant Disease ◽  
1998 ◽  
Vol 82 (5) ◽  
pp. 569-572 ◽  
Author(s):  
E. L. Barnard ◽  
E. C. Ash ◽  
D. L. Hopkins ◽  
R. J. McGovern

A survey of more than 200 trees has documented the widespread occurrence of Xylella fastidiosa in Florida oak populations. The pathogen was detected readily via enzyme-linked immunosorbent assay in oaks exhibiting decline or leaf scorch symptoms and was infrequently detected in asymptomatic trees. It was also associated with reduced growth in Quercus laevis as measured by current-year shoot length. The occurrence of X. fastidiosa in Q. laevis and the evidence for its occurrence in Q. incana represent first reports for these oak hosts. The role of X. fastidiosa in oak decline scenarios deserves further attention.


HortScience ◽  
2009 ◽  
Vol 44 (7) ◽  
pp. 1928-1931 ◽  
Author(s):  
Craig A. Ledbetter ◽  
Elizabeth E. Rogers

Seedling peach (Prunus persica Batsch) and clonal peach–almond hybrids are popular rootstock choices for commercial almond growers in California. In this study, clonal replicates of peach and almond [P. dulcis (Mill.) D.A. Webb] rootstock germplasm and a first-generation peach–almond hybrid created from them were challenged with Xylella fastidiosa isolate M23. Clonal replicates were needle-inoculated with M23 and maintained in a greenhouse environment for a growing season. Typical almond leaf scorch disease symptoms began to develop on M23-inoculated almonds 11 weeks after inoculation. No leaf scorch symptoms were observed on M23-inoculated peach or peach–almond hybrids. Quantitative real-time polymerase chain reaction revealed consistent levels of X. fastidiosa DNA among inoculated almond replicates, whereas X. fastidiosa DNA was undetectable in replicates of peach–almond hybrids. A trace level of X. fastidiosa DNA was detected in a single peach replicate, and statistical analysis demonstrated that this level differed significantly (P < 0.001) from that detected in almond replicates. Selected almonds were further sampled sequentially along their meristematic axes to examine bacterial titer throughout the trees. Selected almond trees differed significantly (P = 0.036) in bacterial titer, but no significant differences were noted in levels of X. fastidiosa from different vertical sections of the main growth axes. The results suggest that peach and peach–almond hybrid rootstock germplasm used by commercial almond tree nurseries in California are not primary inoculum sources for X. fastidiosa-induced diseases.


Microbiology ◽  
2021 ◽  
Vol 167 (10) ◽  
Author(s):  
Lindsey P. Burbank ◽  
M. Caroline Roper

Xylella fastidiosa is a vector-borne plant vascular pathogen that has caused devastating disease outbreaks in diverse agricultural crops worldwide. A major global quarantine pathogen, X. fastidiosa can infect hundreds of plant species and can be transmitted by many different xylem sap-feeding insects. Several decades of research have revealed a complex lifestyle dependent on adaptation to the xylem and insect environments and interactions with host plant tissues.


Plant Disease ◽  
2000 ◽  
Vol 84 (2) ◽  
pp. 198-198 ◽  
Author(s):  
R. L. Wichman ◽  
D. L. Hopkins ◽  
T. A. Wichman

During the spring of 1998, mature oleanders (Nerium oleander L.), pruned to form a 2-m-high hedge along an interstate highway in Orlando, FL, were observed declining and dying. Numerous plants along a 200-m section of highway were in various stages of decline. Symptoms began as chlorotic mottling along the edges of leaves and as the disease progressed, mottling became more severe and leaf margins became necrotic. Scorched leaves died, and symptoms spread throughout the plants, resulting in defoliation. New growth from the base of affected plants was stunted and severely mottled. Petioles and leaf midribs were taken from leaves with mottling symptoms and assayed for the presence of Xylella fastidiosa by polymerase chain reaction (PCR) and culturing on periwinkle wilt agar medium. For PCR assay, infected tissue from three plants was extracted by grinding in SCP buffer (1.0 g of trisodium citrate and 1.0 g of disodium succinate per liter, in 0.015 M phosphate buffer, pH 7.0) containing 0.02 M sodium ascorbate and 5% acid-washed polyvinylpyrrolidone. Amplification was performed with primers RST31 and RST33, as previously described, for specific detection of X. fastidiosa strains (1). A X. fastidiosa-specific amplification product was produced from all three extracts. For culturing, petioles and leaf midribs were cut into 0.5-cm sections, and sap was extracted from the tissue by squeezing with a forceps. Sap was blotted directly onto the medium and incubated at 28°C. Colonies typical of X. fastidiosa were observed after 10 to 14 days of incubation, and single colonies were transferred to fresh periwinkle wilt agar. The colonies were confirmed as X. fastidiosa by PCR assay. Two of the oleander strains were used to inoculate three red and three white 18-month-old oleanders by needle-puncture of the stem through a cloudy drop of bacterium in SCP buffer (108 CFU/ml). For controls, three red and three white oleanders were inoculated with SCP buffer alone. After 9 weeks in a screenhouse, marginal leaf mottling was observed in both the red and white oleanders inoculated with X. fastidiosa, and the bacterium was reisolated from leaves as described above, completing Koch's postulates. Control plants remained symptomless. Oleander leaf scorch caused by X. fastidiosa has been described previously in California and Texas (2). This is the first report of oleander leaf scorch in Florida and the eastern United States. References: (1) G. V. Minsavage et al. Phytopathology 84:456, 1994. (2) A. H. Purcell et al. Phytopathology 89:53, 1999.


Plant Disease ◽  
2009 ◽  
Vol 93 (11) ◽  
pp. 1131-1138 ◽  
Author(s):  
R. Hernandez-Martinez ◽  
D. A. Cooksey ◽  
F. P. Wong

Sweetgum dieback and leaf scorch of purple-leafed plum are two new diseases of southern California landscape ornamentals. Samplings were conducted in 2003 and 2004 and 28 of 105 sweetgum (Liquidambar styraciflua) and 38 of 62 purple-leafed plum (Prunus cerasifera) plants tested positive for Xylella fastidiosa by enzyme linked immunosorbent assay. In all, 3 strains of X. fastidiosa were isolated from sweetgum and 13 from purple-leafed plum. All sweetgum strains and some purple-leafed plum strains grew on PW but not PD3 media. Strain PC045 from purple-leafed plum and strain LS022 from sweetgum were inoculated into their original hosts in addition to almond, oleander, and grapevine plants. Sweetgum plants also were inoculated with strains causing Pierce's disease, almond leaf scorch, and oleander leaf scorch. Strain PC045 caused symptoms in purple-leafed plum and almond plants within 6 months, and the pathogen was recovered from 93 and 100% of inoculated plants, respectively. Inoculation of grapevine and oleander plants with PC045 did not result in disease or recovery of the pathogen. In all, 5 of 25 sweetgum plants inoculated with LS022 showed symptoms after 9 months, and the pathogen was recovered from 3 of these plants. Inoculation of grapevine, oleander, and almond with LS022 resulted in no disease or recovery of the pathogen from the plants. A strain of Pierce's disease, a strain of oleander leaf scorch, and two strains from almond did not cause disease in sweetgum. These results confirm the role of X. fastidiosa strains as pathogens of purple-leafed plum and sweetgum, and that strains from sweetgum are unique in their host range.


Plant Disease ◽  
2010 ◽  
Vol 94 (2) ◽  
pp. 274-274 ◽  
Author(s):  
R. Singh ◽  
D. M. Ferrin ◽  
Q. Huang

Oleander (Nerium oleander L.) is an evergreen shrub native to the Mediterranean Region and Southeast Asia. Despite being poisonous, it is a popular ornamental plant for use in landscapes, gardens, parks, roadsides, and highway medians. During the fall of 2008, several oleander plants with leaf scorch symptoms were observed at Arsenal Park in Baton Rouge, LA. Symptomatic oleander samples were also received from a commercial nursery in Baton Rouge, LA and a homeowner in Thibodeaux, LA. Symptoms resembled leaf scorch caused by Xylella fastidiosa Wells et al. and included chlorotic mottling of the leaves that started from the tips and margins and progressed toward the midribs. As disease developed, leaf tips and margins became necrotic. Severely infected plants defoliated and died. Leaf petioles from 13 samples (8 from Arsenal Park, 3 from the commercial nursery, and 2 from the homeowner) from symptomatic plants gave positive reactions for X. fastidiosa by ELISA (Agdia, Inc., Elkhart, IN). Leaf petioles from six healthy oleander plants gave a negative reaction for X. fastidiosa by ELISA. Isolation of X. fastidiosa was attempted from eight ELISA-positive and six ELISA-negative oleander samples. Leaf petioles weighing 0.05 g from each sample were used for isolation. The petioles were surface sterilized in 70% ethanol for 1.5 min and then in 2% sodium hypochlorite for 1.5 min, followed by three 1-min washes in sterile water. The petioles were chopped into small pieces under aseptic conditions and soaked in 500 μl sterile water for 30 min. One hundred microliters of the suspension were spread onto periwinkle wilt (PW) plates and incubated in the dark at 28°C. After incubation for 7 days, bacterial colonies typical of X. fastidiosa appeared on five of eight ELISA-positive sample plates. No colonies were observed on six ELISA-negative sample plates. Single colonies were transferred to fresh PW plates to obtain pure cultures. Bacterial colonies from five pure cultures were suspended in nuclease-free water and boiled for 10 min to obtain DNA. DNA from eight symptomatic and six healthy oleander plants was extracted with a DNeasy Plant Mini kit (Qiagen Inc., Valencia, CA) according to the manufacturer's guidelines. Primers (QHOLS-08 and QHOLS-05) (1) specific to the oleander strain of X. fastidiosa amplified a 274-bp portion of DNA from both symptomatic oleander tissues and pure culture of X. fastidiosa isolated from symptomatic tissue. No such amplification was observed in healthy tissue. These primers amplify a portion of DNA encoding a hypothetical protein of unknown function that has been shown to be unique to oleander strains of X. fastidiosa. The PCR product was sequenced and compared with the whole genome shotgun sequence of the oleander strain Ann-1 of X. fastidiosa (GenBank Accession No. AAAM03000099), which resulted in 100% identity with nucleotides 11343 to 11616 in contig 228. X. fastidiosa has been previously reported to cause oleander leaf scorch in California (3), Florida (4), and Texas (2). To our knowledge, this is the first report of X. fastidiosa associated with oleander leaf scorch in Louisiana, extending the geographic range of this important bacterial disease. References: (1) Q. Huang. Curr. Microbiol. 58:393, 2009. (2) Q. Huang et al. Plant Dis. 88:1049, 2004. (3) A. H. Purcell et al. Phytopathology 89:53, 1999. (4) R. L. Wichman et al. Plant Dis. 84:198, 2000.


2020 ◽  
Vol 120 ◽  
pp. 103995 ◽  
Author(s):  
Emanuele Ranieri ◽  
Gianluca Zitti ◽  
Paola Riolo ◽  
Nunzio Isidoro ◽  
Sara Ruschioni ◽  
...  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Despoina Ev. Kapantaidaki ◽  
Spyridon Antonatos ◽  
Vasiliki Evangelou ◽  
Dimitrios P. Papachristos ◽  
Panagiotis Milonas

AbstractThe plant-pathogenic bacterium Xylella fastidiosa which causes significant diseases to various plant species worldwide, is exclusively transmitted by xylem sap-feeding insects. Given the fact that X. fastidiosa poses a serious potential threat for olive cultivation in Greece, the main aim of this study was to investigate the genetic variation of Greek populations of three spittlebug species (Philaenus spumarius, P. signatus and Neophilaenus campestris), by examining the molecular markers Cytochrome Oxidase I, cytochrome b and Internal Transcribed Spacer. Moreover, the infection status of the secondary endosymbionts Wolbachia, Arsenophonus, Hamiltonella, Cardinium and Rickettsia, among these populations, was determined. According to the results, the ITS2 region was the less polymorphic, while the analyzed fragments of COI and cytb genes, displayed high genetic diversity. The phylogenetic analysis placed the Greek populations of P. spumarius into the previously obtained Southwest clade in Europe. The analysis of the bacterial diversity revealed a diverse infection status. Rickettsia was the most predominant endosymbiont while Cardinium was totally absent from all examined populations. Philaenus spumarius harbored Rickettsia, Arsenophonus, Hamiltonella and Wolbachia, N. campestris carried Rickettsia, Hamiltonella and Wolbachia while P. signatus was infected only by Rickettsia. The results of this study will provide an important knowledge resource for understanding the population dynamics of vectors of X. fastidiosa with a view to formulate effective management strategies towards the bacterium.


2006 ◽  
Vol 8 (4) ◽  
pp. 747-754 ◽  
Author(s):  
Jorge L. M. Rodrigues ◽  
Maria E. Silva-Stenico ◽  
Adriane N. de Souza ◽  
Joao R. S. Lopes ◽  
Siu M. Tsai

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