Botryosphaeria stevensii (Botryosphaeria disease, grapevine)
Identity
- Preferred Scientific Name
- Botryosphaeria stevensii Shoemaker
- Preferred Common Name
- Botryosphaeria disease, grapevine
- Other Scientific Names
- Diplodia mutila (Fr.) Mont.
- Diplodia quercina Westend.
- Diplodia quercus Fuckel
- Diplodia samararum Sacc.
- Physalospora mutila (Fr.) N.E. Stevens
- Sphaeria mutila Fr.
- Sphaeropsis malorum (Berk.) Berk.
- International Common Names
- EnglishBotryosphaeria cankerDecline syndrome, grapevine
- Frenchdead-arm noir de la vigne
- Local Common Names
- Hungaryblack dead arm, grapevine
- EPPO code
- BOTSST (Botryosphaeria stevensii)
Pictures
Distribution
Host Plants and Other Plants Affected
Symptoms
Symptoms do not vary substantially on the main tree hosts. On oak, B. stevensii was first reported as pathogenic on Quercus prinus in the USA by Schmidt and Fergus (1965) and on Q. petraea in Europe (Hungary) by Vajna (1986). Infections produce bark necroses and cankers on twigs with a diameter of 2-6 cm, especially on apical twigs, and are often characterized by mucilaginous exudates. When a necrotic lesion girdles the stem, the upper portion is immediately affected by wilting and subsequent dieback. Leaves become chlorotic and finally wilt, often remaining attached to the dying stems. During the vegetative growing season, erumpent pycnidia, which look like black pustules, may be observed on necrotic areas after weeks or months. The necrotic bark can be easily removed, revealing black phloem, cambium and outer sapwood. Single infections are not able to kill an adult tree, but repeated attacks over consecutive years may compromise large sections of the crown and impair its tolerance to environmental stresses. However, symptoms caused by B. stevensii often merge with those of the syndrome known as oak decline or, more recently, oak puzzle disease; these syndromes are triggered by various soil and environmental factors.
On other broadleaved trees, B. stevensii induces quite similar symptoms: for example, on young shoots of Fraxinus excelsior, dark-brown, necrotic lesions of the bark are sometimes associated with brownish discoloration and wilting of leaves (Przybyl, 2002). 5-7-year-old suckers and stems of adult trees of Fraxinus ornus in Sicily, Italy, were found to be infected by B. stevensii, and suffered necrotic areas that subsequently split, epicormic shoots under the cankers, and crown dieback (Sidoti and Granata, 2004).
On juniper (Juniperus spp.), infections cause elongated cankers at the base of shoots, associated with sudden yellowing and browning of large portions of the crown.
External symptoms on grapevine are not substantially different from those previously described for tree hosts. In Hungary, where the attacks by B. stevensii have been known since 1974, the syndrome is known as 'black dead arm disease' and consists of leaf chlorosis and wilting, browning and subsequent drying of the berries. The xylem of the trunk is streaked black under areas of necrotic bark tissue (Lehoczky, 1974).
On other broadleaved trees, B. stevensii induces quite similar symptoms: for example, on young shoots of Fraxinus excelsior, dark-brown, necrotic lesions of the bark are sometimes associated with brownish discoloration and wilting of leaves (Przybyl, 2002). 5-7-year-old suckers and stems of adult trees of Fraxinus ornus in Sicily, Italy, were found to be infected by B. stevensii, and suffered necrotic areas that subsequently split, epicormic shoots under the cankers, and crown dieback (Sidoti and Granata, 2004).
On juniper (Juniperus spp.), infections cause elongated cankers at the base of shoots, associated with sudden yellowing and browning of large portions of the crown.
External symptoms on grapevine are not substantially different from those previously described for tree hosts. In Hungary, where the attacks by B. stevensii have been known since 1974, the syndrome is known as 'black dead arm disease' and consists of leaf chlorosis and wilting, browning and subsequent drying of the berries. The xylem of the trunk is streaked black under areas of necrotic bark tissue (Lehoczky, 1974).
List of Symptoms/Signs
Symptom or sign | Life stages | Sign or diagnosis |
---|---|---|
Plants/Leaves/wilting | ||
Plants/Leaves/wilting | ||
Plants/Leaves/yellowed or dead | ||
Plants/Leaves/yellowed or dead | ||
Plants/Stems/canker on woody stem | ||
Plants/Stems/canker on woody stem | ||
Plants/Stems/dieback | ||
Plants/Stems/dieback | ||
Plants/Stems/necrosis | ||
Plants/Stems/necrosis | ||
Plants/Stems/wilt | ||
Plants/Stems/wilt |
Prevention and Control
Cultural Control and Sanitary Methods
Cultural control of attacks by B. stevensii is only possible for isolated trees, as it is not feasible to perform systematic sanitary prunings in the forest. Infected twigs must be cut at least 15 cm under the visible lower edge of infection and carried out the forest to reduce the inoculum potential. In the nursery, plants must be grown in optimal conditions, especially with regard to water supply, to avoid stress conditions that promote attack by the pathogen.
Host-Plant Resistance
Studies for resistance of oaks to B. stevensii are still at an early stage. Trials performed on several cultivars of Quercus suber have shown the existence of resistant genotypes in all tested Mediterranean countries of origin (Bakry et al., 1999).
Biological Control
Possible attempts of biological control must be based on antagonistic or hyperparasitic organisms already found in nature (see Notes on Natural Enemies), because they have to find a suitable environment for growing and reproduction when introduced to the natural habitat of B. stevensii.
Worthy of further studies is the activity of some species of Pseudomonas (P. fluorescens, P. corrugata, P. tolaasii) isolated from Tuber borchii (an ascomycete often living in natural oak forests), which have been found to produce in vitro biocontrol substances with a weak effect against some pathogenic fungi, including B. stevensii (Bedini et al., 1999).
Cultural control of attacks by B. stevensii is only possible for isolated trees, as it is not feasible to perform systematic sanitary prunings in the forest. Infected twigs must be cut at least 15 cm under the visible lower edge of infection and carried out the forest to reduce the inoculum potential. In the nursery, plants must be grown in optimal conditions, especially with regard to water supply, to avoid stress conditions that promote attack by the pathogen.
Host-Plant Resistance
Studies for resistance of oaks to B. stevensii are still at an early stage. Trials performed on several cultivars of Quercus suber have shown the existence of resistant genotypes in all tested Mediterranean countries of origin (Bakry et al., 1999).
Biological Control
Possible attempts of biological control must be based on antagonistic or hyperparasitic organisms already found in nature (see Notes on Natural Enemies), because they have to find a suitable environment for growing and reproduction when introduced to the natural habitat of B. stevensii.
Worthy of further studies is the activity of some species of Pseudomonas (P. fluorescens, P. corrugata, P. tolaasii) isolated from Tuber borchii (an ascomycete often living in natural oak forests), which have been found to produce in vitro biocontrol substances with a weak effect against some pathogenic fungi, including B. stevensii (Bedini et al., 1999).
Chemical Control
Due to the variable regulations around (de-)registration of pesticides, we are for the moment not including any specific chemical control recommendations. For further information, we recommend you visit the following resources:
•
EU pesticides database (http://ec.europa.eu/food/plant/pesticides/eu-pesticides-database/)
•
PAN pesticide database (www.pesticideinfo.org)
•
Your national pesticide guide
Impact
Attacks by B. stevensii have an economic impact in oak forests, reducing the annual increment of wood as a consequence of the wilting and the death of large sections of crown. Unfortunately, quantitative valuations of damage are lacking and, the specific damage caused by this pathogen often merges with the heavier damage as a result of "oak puzzle disease". As regards the grapevine, except for the case of "black dead arm disease" which is geographically restricted, the role of B. stevensii in the context of various decline syndromes is too controversial and/or uncertain to ascribe to it a specific damage.
Information & Authors
Information
Published In
Copyright
Copyright © CABI. CABI is a registered EU trademark. This article is published under a Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)
History
Published online: 9 October 2023
Language
English
Authors
Metrics & Citations
Metrics
SCITE_
Citations
Export citation
Select the format you want to export the citations of this publication.
EXPORT CITATIONSExport Citation
View Options
View options
Get Access
Login Options
Check if you access through your login credentials or your institution to get full access on this article.