Breakdown of plant virus resistance: can we predict and extend the durability of virus resistance?

Cultivars with introgressed natural resistance genes have been widely used for plant disease control, especially in the control of virus diseases, for which no effective chemical control agent is available. However, we often encounter virus mutants that break down or overcome the resistance. In this review, recent studies will be discussed with respect to breakdown of plant virus resistance.     

Effect of Cotton leaf curl virus infected plants on the biology of the whitefly,Bemisia tabaci (Hemiptera: Aleyrodidae): Vector–virus mutualism

Cotton leaf curl virus (CLCuV) (Geminiviridae : Begomovirus), the causative agent of leaf curl disease in cotton plants (Gossypium hirsutum), is exclusively transmitted by whitefly species Bemisia tabaci (Gennadius) (Hemiptera: Aleyrodidae). CLCuV transmission occurs in Sriganganagar (Rajasthan), an area endemic with cotton leaf curl disease. The relationships between plant viruses, their herbivore vectors and host plants can be beneficial, neutral, or antagonistic, depending on the species involved. To further understand these relationships, fecundity and life history parameters of an indigenous non- b (Asia II genetic group) biotype whitefly, B. tabaci, were compared on 10, 25, and 40 days post-inoculation (DPI), in CLCuV-infected and healthy cotton plants to determine the effect of virus on its vector. The development time of the immature stages of whiteflies was significantly reduced on CLCuV-infected plants. The development time of the immature stages did not change with severity of symptoms at 25 and 40 DPI (45- and 60-d-old plants). Cotton leaf curl virus infection increased percent egg viability of B. tabaci. Whiteflies deposited significantly fewer eggs on virus-infected plants than on healthy plants. Whiteflies had better egg viability on younger plants than older plants, whereas plant age did not affect the fecundity. Male and female whiteflies had shorter longevity on CLCuV-infected plants than on healthy plants.     

苹果潜隐病毒(Latent virus)研究Ⅰ.苹果衰退病毒研究

 1972年,辽宁金县大委家公社,在基砧为三叶海棠的国光品种树上,用红星和红冠二品种接穗进行高接换种之后,发生一种衰退病,共3000余株。通过病毒鉴定,初步明确病树中潜带褪绿叶斑病毒(CLSV)、茎痘病毒(SPV)和茎沟槽病毒(SGV)三种潜隐病毒。茎痘病毒是苹果衰退病的主要毒源。     

Nucleotide Sequence of the 3′ -terminal Region of Carnation vein mottle virus RNA

The 2326 nucleotides of the 3′-terminal region of Carnation vein mottle virus (CVMV) RNA, which included part of the nuclear inclusion b gene, the complete coat protein (CP) gene and the entire 3′-noncoding region (3′-NCR) were determined. The region encoding the CP gene is 843 nucleotides long and the deduced protein consists of 280 amino acids. A search of the EMBL and PIR databases showed that the amino acid sequence of CVMV CP most resembled that of Plum pox virus with a similarity of 67.9%. The 3′-NCR of CVMV RNA is 541 nucleotides long, second longest in the genus Potyvirus. These results indicate that CVMV is closely related to Plum pox virus but is a distinct species in the genus Potyvirus. Received 8 October 1999/ Accepted in revised form 9 January 2000     

Vertical transmission of granulosis virus of sugarcane shoot borer,Chilo infuscatellus Snell.†

Abstract

The granulosis virus (GV) of sugarcane shoot borer, Chilo infuscatellus Snelt., was found to be transmitted vertically when the fourth instar larvae were microfed with the virus at a sublethal dose of 1.1 x 10³ inclusion bodies/larva. The virus infection was found to alter the sex ratio in pupae in favour of male (1 : 5.70—♀ : ♂) from the normal 1 : 1 ratio. The per cent pupation and adult emergence were also significantly reduced. No adults emerged from abnormal pupae that lacked pigmentation on the ventral surface of the first abdominal segment. The GV was also found to be transmitted from the infected adult to the offspring through eggs and 50% of the larvae that hatched were found to die due to virosis.     

Grapevine virus A in Rheinland-Pfalz: Vorkommen und Bedeutung für den deutschen Weinbau

Grapevine virus A (GVA) is associated with Kober stem grooving disease which belongs to the Rugose wood complex. The virus is frequently found in grapevine affected by leafroll but is not strictly associated with this disease. Probably the virus has a worldwide distribution – but very little information is available about the occurrence of GVA in Rhineland-Palatinate. The detection of GVA was conducted with indexing procedures using Kober 5BB as indicator and serological methods (ELISA). Indexing trials with infected material did not show any symptoms of Kober stem grooving two years after wooden grafting and five years after green grafting. The most suitable tissue to detect GVA serologically was petioles from mature leaves or cortical scrapings from dormant canes. In all experiments the tests with petioles resulted in much higher extinction values compared to the blades. About 46.9% of the 209 samples tested had an infection of GVA, 87.8% in mixed infections together with GLRaV-1 and 5.1% together with GLRaV-3. Only 7.1% of the tested plants were exclusively infected by GVA, none of the other ampelo- and closteroviruses could be detected. None of the GVA positively tested plants showed any symptoms of Rugose wood. The results indicated that the importance of a GVA infection on vines in Germany seems to be extremely low.     

No detection of seed transmission of citrus tatter leaf virus in ‘Meyer’ lemon

Journal of Plant Diseases and Protection - Citrus tatter leaf virus (CTLV), a strain of apple stem grooving virus, is a virus of citrus that is of commercial importance for trifoliate orange...     

烟草脆裂病毒(Tobacco rattle virus)牡丹分离物-TRV-Pa的研究

 牡丹受一种病毒为害后,叶片呈现黄色花叶同时伴有少量的花药败育现象。经系统鉴定,此病毒被确认为烟草脆裂病毒的牡丹分离物(TRV-Pa)。该病毒人工接种时可侵染7个科的21种植物;其TDP为80℃,DEP为10^-3-10-4,L则为40天以上。TRV-Pa具有两种长度的杆状粒子,其大小分别为35-80×25nm和125-200×25nm。A 260/280为1.13,RNA含量为5.0%。经PAGE分析粒子有两条谱带,其Rf分别为0.25及0.26-0.28。迁移率分别是-1.57——1.6×10^-3及-1.71——1.75×10^-3cm²·Sec^-1·V^-1(BYDV的迁移率为-1.43——1.45×10^-3cm²·See^-1·V^-1)。两种核酸的分子量分别为RNA₁=2.45×10⁶,RNA₂=0.65×10⁶(标准核酸为TMV和雀麦花叶病毒的核酸分子)。外壳蛋白亚基是单一的,其分子量是2.11×10⁴(标准蛋白分别是牛血清清蛋白、胃蛋白酶,胰蛋白酶和细胞色素C)。并含有较多的天冬氨酸、谷氨酸,苏氨酸和丝氨酸,未明显测到酪氨酸和苯丙氨酸,缺少胱氨酸。对牡丹花药进行病理解剖学和血清学研究时,在花粉粒子中检测到病毒,被病毒侵染的花粉约有80%为空瘪。在牡丹的繁育中,应选用无毒繁殖材料防止TRV通过无性繁殖过程在牡丹上传播。     

Identification of ‘Ca. Phytoplasma asteris’, banana bunchy top virus and banana streak MY virus associated with Champa and Sabri banana cultivars in Tripura,a North Eastern state of India

European Journal of Plant Pathology - Symptoms of bunchy top, little leaf, leaf chlorosis with chlorotic streaks, leaf necrosis and stunted growth were noticed in two banana cultivars, Champa and...     

Lettuce ring necrosis,caused by a chytrid-borne agent distinct from lettuce big-vein ‘virus’

Ring necrosis is a serious disease of lettuce (Lactuca sativa) with often coalescing necrotic rings and ring-like patterns on middle leaves of plants or groups of plants in glasshouses during winter. Affected leaves may decay and plants rapidly become unmarketable. The disease was shown to be soil-borne and transmitted by the zoospores ofOlpidium brassicae. Symptoms in lettuce do not appear before seven weeks after inoculation via the soil. Additives to the inoculum and chilling of source leaves, inoculum buffer and utensils enabled mechanical transmission of a pathogenic agent toChenopodium quinoa, C. amaranticolor, Nicotiana benthamiana, N. clevelandii, N. hesperis, andN. occidentalis but not to lettuce. TheChenopodium spp. reacted with local lesions, infection was symptomless inN. clevelandii and mostly so inN. benthamiana, butN. hesperis andN. occidentalis reacted with leaf spotting and plant stunting. With zoospores of an originally pathogen-free fungus culture further cultivated on the roots of cuttings from sap-inoculated plants ofN. clevelandii andN. occidentalis, the agent could be transferred back to lettuce and the symptoms of ring necrosis be reproduced. The agent biologically resembles those of lettuce big-vein (LBV) and freesia leaf necrosis and the tobacco stunt virus. In lettuce it often occurs together with LBV virus but differs in longer incubation period, type of symptoms and symptom appearance only during winter. It could be separated from a mixture with LBV virus by serial transfer always selecting plants without LBV symptoms. So far cultural hygiene, including soil disinfection addressing the vector, is the main means of control.     

Is a helper factor necessary for infection of cowpea protoplasts with blackeye cowpea mosaic virus?

Samenvatting Bij inoculatie van mesofyl protoplasten van cowpea met een zeer infectieuze, gezuiverde suspensie van blackeye cowpea mosaic virus (BlCMV), een potyvirus, kon een infectie niet worden geconstateerd. Wanneer echter de bovenstaande vloeistof, verkregen na centrifugering bij laag toerental van sap van BlCMV-geînfecteerde planten, als inoculum werd gebruikt, dan kon vermeerdering van het virus in de protoplasten worden vastgesteld door middel van infectiositeitsproeven, immunofluorescentie en elektronenmicroscopie. Werd deze bovenstaande vloeistof, ontdaan van zijn infectiositeit, hetzij door bestraling met UV-licht, hetzij door centrifugering bij hoog toerental, en vervolgens gemengd met gezuiverd virus, dan trad er geen infectie van de protoplasten op.     

Historical virus isolate collections: An invaluable resource connecting plant virology’s pre-sequencing and post-sequencing eras

Many laboratories maintain historical collections of preserved plant virus isolates that store a wealth of untapped data, including original type isolates, studied in the pre-sequencing era. Currently, many recently recognized virus species exist with no supporting reference sequences. Also, many virus sequences appear new when compared to available sequences, but, on sequencing pre-sequencing era isolates, they may coincide. Such linkages allow access to data from previously determined biological and other parameters from pre-sequencing era studies. These linkages are increasingly being found using high-throughput sequencing, helping clarify virus taxonomy and improving understanding of virus ecology and evolution. Thus, mistakes can be avoided in naming viruses and in combining or separating them, as well as enabling identification of unknown viruses preserved long ago. With well-established viruses, success in dating and other evolutionary studies, and discovery of changes in regional virus populations, both depend upon comparisons between recent and old isolate sequences covering the greatest possible time periods. Such studies help reveal the extent that human activities have influenced virus evolution and changed virus populations on a global scale. Sequencing virus genomes from herbarium specimens, archaeological specimens, or living plant collections can provide complementary data. By bringing context to newly detected viruses and supporting plant pest risk analyses, linking new virus discoveries to previously generated disease symptom, host range, virus transmission, and geographical distribution data has important implications for plant health regulation. Also, historical isolates can provide an invaluable resource facilitating biosecurity investigations involving virus introductions, entry pathways, and baseline surveillance.     

Mathematical models of host plant infection by helper-dependent virus complexes: why are helper viruses always avirulent?

ABSTRACT Interactions between viruses in plants are common, and some viruses depend on such interactions for their survival. Frequently, a virus lacks some essential molecular function that another provides. In "helper-dependent" virus complexes, the helper virus is transmitted independently by a vector, whereas the dependent virus depends on molecular agents associated with the helper virus for transmission by a vector. A general mathematical model was developed of the dynamics of host plant infection by a helper-dependent virus complex. Four categories of host plants were considered: healthy, infected with helper virus alone, infected with dependent virus alone, and infected with both viruses. New planting of the host crop was constrained by a maximum abundance due to limitation of the cropping area. The ratio of infection rate to host loss rate due to infection is proposed as an important epidemiological quantity, A, that can be used as a measure of the mutual adaptation of the virus and host. A number of alternative equilibria of host infection could occur and were determined exclusively by parameter values; it was informative to display their distribution in the parameter plane: (1/A)(helper) versus (1/A)(dependent). A simple analysis of the distribution of the final equilibria illustrated that the dependent virus could affect the survival of the helper virus, so facilitation between the two can be reciprocal. The distribution of the final equilibria also indicated that a well-adapted helper virus increases the opportunity for a dependent virus to evolve and survive, and the model, therefore, explains why infection with a helper virus usually causes no or little damage to plants, whereas infection with a dependent virus or mixed infection with both often causes very severe damage.     

Sequence diversity in the coat protein and 3″-untranslated region of Chinese yam necrotic mosaic virus RNA

Sixteen isolates of Chinese yam necrotic mosaic virus (ChYNMV) were collected from nine sites in Japan and one site in Korea, and 1098 nucleotides of the 3-terminal of the genome were sequenced. Identity of the coat protein gene was 95.5%–99.7% among the isolates. Substitution in the deduced amino acids of the coat protein ranged from 0 to 7, mainly in the N-terminal region. The 3-untranslated region consisted of 231 nucleotides, which had 96.5%–100% nucleotide identity among the isolates. Sequence diversity was considerably less in ChYNMV than in Yam mosaic virus or Japanese yam mosaic virus.     

Distribution and phylogenetic analysis of the 3′UTR and coat protein gene of Iranian Beet black scorch virus

Journal of Plant Diseases and Protection - Beet black scorch virus (BBSV) was surveyed in major sugar beet cultivation areas in Iran in 2008–2013 growing seasons. A total of 148 out of 308...     

β-Aminobutyric acid-mediated enhancement of resistance in tobacco to tobacco mosaic virus depends on the accumulation of salicylic acid

A number of chemical and biological agents are known as inducers of systemic acquired resistance (SAR) to tobacco mosaic virus (TMV) in tobacco plants. In the present study, a local spray application of the non-protein amino acid DL-β-aminobutyric acid (BABA) was effective in enhancing resistance to TMV in tobacco plants containing the N gene. In contrast, the isomer α-aminobutyric acid (AABA) showed a much lower activity whereas γ-aminobutyric acid (GABA) was completely inactive, indicating a strong isomer specificity of aminobutyric acid in triggering enhanced virus resistance.Rapid cell death was detected in tobacco leaf tissues after foliar application of BABA, subsequently resulting in the development of macroscopically visible, necrotic lesions. BABA-induced cell death was associated with the rapid generation of superoxide and hydrogen peroxide. As further consequences, the occurrence of lipid peroxidation in treated tissues, a local and systemic increase of salicylic acid (SA) levels and the expression of PR-1a, a molecular marker of SAR in tobacco, could be observed. None of these responses was detectable after treatment with GABA.Enhancement of virus resistance by BABA was found to be strictly dependent on SA-mediated signal transduction since it could not be detected in salicylate hydroxylase (nahG) expressing transgenic tobacco plants. These findings suggest that in tobacco, primary processes triggered by foliar application of BABA, resemble those initiated by microbes during a hypersensitive response (HR) that result in SAR activation.     

Reverse transcription-duplex-polymerase chain reaction for simultaneous detection of Citrus tristeza virus and ‘Candidatus Liberibacter’ from citrus plants

Journal of Plant Diseases and Protection - Tristeza and Huanglongbing are the most important diseases of citrus caused by Citrus tristeza virus (CTV) and ‘Candidatus Liberibacter’...