scholarly journals Tomato Chlorosis Virus Infection Facilitates Bemisia tabaci MED Reproduction by Elevating Vitellogenin Expression

Insects ◽  
2021 ◽  
Vol 12 (2) ◽  
pp. 101
Author(s):  
Liping Huang ◽  
Xiaobin Shi ◽  
Jizhe Shi ◽  
Zhuo Zhang ◽  
Yong Fang ◽  
...  
Keyword(s):  
Bemisia Tabaci ◽  
Plant Virus ◽  
Ovarian Development ◽  
Insect Vectors ◽  
Tomato Plants ◽  
Pathogenic Viruses ◽  
Infected Tomato ◽  
Tomato Chlorosis Virus ◽  
Q Biotype

Transmission of plant pathogenic viruses mostly relies on insect vectors. Plant virus could enhance its transmission by modulating the vector. Previously, we showed that feeding on virus infected plants can promote the reproduction of the sweet potato whitefly, Bemisia tabaci MED (Q biotype). In this study, using a whitefly-Tomato chlorosis virus (ToCV)-tomato system, we investigated how ToCV modulates B. tabaci MED reproduction to facilitate its spread. Here, we hypothesized that ToCV-infected tomato plants would increase B. tabaci MED fecundity via elevated vitellogenin (Vg) gene expression. As a result, fecundity and the relative expression of B. tabaci MED Vg was measured on ToCV-infected and uninfected tomato plants on days 4, 8, 12, 16, 20 and 24. The role of Vg on B. tabaci MED reproduction was examined in the presence and absence of ToCV using dietary RNAi. ToCV infection significantly increased B. tabaci MED fecundity on days 12, 16 and 20, and elevated Vg expression on days 8, 12 and 16. Both ovarian development and fecundity of B. tabaci MED were suppressed when Vg was silenced with or without ToCV infection. These combined results suggest that ToCV infection increases B. tabaci MED fecundity via elevated Vg expression.

scholarly journals Expanding Knowledge of the Host Range of Tomato chlorosis virus and Host Plant Preference of Bemisia tabaci MEAM1

Plant Disease ◽  
2019 ◽  
Vol 103 (6) ◽  
pp. 1132-1137 ◽  
Author(s):  
Arnaldo E. Fariña ◽  
Jorge A. M. Rezende ◽  
William M. Wintermantel
Keyword(s):  
Host Range ◽  
Bemisia Tabaci ◽  
Chenopodium Quinoa ◽  
Virus Transmission ◽  
Tomato Plants ◽  
Virus Acquisition ◽  
Infected Tomato ◽  
Primary Vector ◽  
Tomato Chlorosis Virus ◽  
Whitefly Vector

The crinivirus Tomato chlorosis virus (ToCV) is often found infecting tomato crops in Brazil, with variable incidence, but associated with prevalence of its primary vector, Bemisia tabaci MEAM1. ToCV control is difficult because there are no resistant commercial tomato varieties or hybrids available and chemical spray for control of the whitefly vector has not been effective. The present study evaluated the partial host range of a Brazilian isolate of ToCV and the preference of B. tabaci MEAM1 for oviposition on those species identified as susceptible to the virus. Subsequently, transmission tests were performed using plants of each ToCV host species as sources of inoculum to elucidate the epidemiological importance of nontomato sources of inoculum for infection of tomato. Among 80 species experimentally inoculated, 25 were susceptible, including 6 previously not known to be hosts (Jaltomata procumbens, Physalis pruinosa, Solanum aculeatissimum, S. viarum, Beta vulgaris var. cicla, and Chenopodium quinoa). Preference of whitefly for oviposition and infection by ToCV under free-choice transmission tests varied among the susceptible species. When ToCV-infected tomato, eggplant, and C. quinoa were used separately as sources of inoculum for virus transmission to tomato plants, mean percentages of infected plants were 76.6, 3, and 0%, respectively. Average oviposition of Bemisia tabaci on these three hosts were 2.7, 10.6, and 0.0 eggs/cm2, respectively. Additional studies will be necessary to evaluate the importance of ToCV host plants under field conditions and their efficiency as sources of inoculum for virus acquisition and transmission to tomato crops.

scholarly journals Rate of Tomato yellow leaf curl virus Translocation in the Circulative Transmission Pathway of its Vector, the Whitefly Bemisia tabaci

2001 ◽  
Vol 91 (2) ◽  
pp. 188-196 ◽  
Author(s):  
Murad Ghanim ◽  
Shai Morin ◽  
Henryk Czosnek
Keyword(s):  
Salivary Glands ◽  
Bemisia Tabaci ◽  
Virus Genome ◽  
Tomato Yellow Leaf ◽  
Yellow Leaf ◽  
Tomato Plants ◽  
Hemolymph Sample ◽  
Infected Tomato ◽  
Leaf Curl Virus ◽  
Leaf Curl

Whiteflies (Bemisia tabaci, biotype B) were able to transmit Tomato yellow leaf curl virus (TYLCV) 8 h after they were caged with infected tomato plants. The spread of TYLCV during this latent period was followed in organs thought to be involved in the translocation of the virus in B. tabaci. After increasing acquisition access periods (AAPs) on infected tomato plants, the stylets, the head, the midgut, a hemolymph sample, and the salivary glands dissected from individual insects were subjected to polymerase chain reaction (PCR) without any treatment; the presence of TYLCV was assessed with virus-specific primers. TYLCV DNA was first detected in the head of B. tabaci after a 10-min AAP. The virus was present in the midgut after 40 min and was first detected in the hemolymph after 90 min. TYLCV was found in the salivary glands 5.5 h after it was first detected in the hemolymph. Subjecting the insect organs to immunocapture-PCR showed that the virus capsid protein was in the insect organs at the same time as the virus genome, suggesting that at least some TYLCV translocates as virions. Although females are more efficient as vectors than males, TYLCV was detected in the salivary glands of males and of females after approximately the same AAP.

scholarly journals Kinetics of Systemic Invasion and Latent and Incubation Periods of Tomato severe rugose virus and Tomato chlorosis virus in Single and Co-Infections in Tomato Plants

2019 ◽  
Vol 109 (3) ◽  
pp. 480-487 ◽  
Author(s):  
Gabriel Madoglio Favara ◽  
Daiana Bampi ◽  
Juan Pablo Edwards Molina ◽  
Jorge Alberto Marques Rezende
Keyword(s):  
Middle East ◽  
East Asia ◽  
Latent Period ◽  
Asia Minor ◽  
Tomato Plants ◽  
Incubation Periods ◽  
Infected Tomato ◽  
The Mean ◽  
Tomato Chlorosis Virus ◽  
Kinetics Of

Tomato severe rugose virus (ToSRV) and Tomato chlorosis virus (ToCV) are among the major viruses that affect tomato (Solanum lycopersicum) development and yield in Brazil. ToSRV and ToCV are transmitted in a persistent circulative and semipersistent manner, respectively, by the whitefly Bemisia tabaci Middle East-Asia Minor 1, considered the main vector of these viruses. In this study, the kinetics of systemic invasion and the latent and incubation periods of ToSRV and ToCV were evaluated in singly and doubly infected tomato plants. Both viruses moved systemically into tomato plants as early as 1 day after inoculation. The mean ToCV latent periods in single infections and co-infections with ToSRV were 13 and 11 days, respectively, while incubation periods in single and co-infections were, on average, 30 and 31 days, respectively. For ToSRV, the mean latent period was 7 days in single infections and 6 days in co-infections with ToCV. Incubation periods were, on average, 18 and 17 days in single and co-infections, respectively. Because latent periods for both viruses were shorter than their respective incubation periods, field-infected tomato plants may act as sources of inocula soon after infection and before onset of symptoms.

scholarly journals Severe Yellowing Outbreaks in Tomato in Spain Associated with Infections of Tomato chlorosis virus

Plant Disease ◽  
2000 ◽  
Vol 84 (8) ◽  
pp. 835-837 ◽  
Author(s):  
J. Navas-Castillo ◽  
R. Camero ◽  
M. Bueno ◽  
E. Moriones
Keyword(s):  
Lycopersicon Esculentum ◽  
Bemisia Tabaci ◽  
Disease Outbreaks ◽  
Fruit Growth ◽  
Southern Spain ◽  
Tomato Plants ◽  
First Report ◽  
Yellowing Disease ◽  
Disease Agent ◽  
Tomato Chlorosis Virus

Since 1997, yellowing disease outbreaks have occurred in tomato (Lycopersicon esculentum) crops in southern Spain. The outbreaks were associated with high populations of the whitefly Bemisia tabaci. Symptoms consisted mainly of interveinal yellowing that developed initially on lower leaves and then progressed to the upper part of the plant. Affected plants were less vigorous and yielded less due to reduced fruit growth and delayed ripening. During 1998 and 1999, the yellowing disease was widespread and occurred at high incidences in the Málaga province. The disease agent was readily transmissible from tomato to tomato by B. tabaci biotype Q. Samples from symptomatic tomato plants were analyzed and shown to be infected with Tomato chlorosis virus (ToCV) (genus Crinivirus, family Closteroviridae). This is the first report of ToCV epidemics in Europe.

scholarly journals Sub-Lethal Effects of Partially Purified Protein Extracted from Beauveria bassiana (Balsamo) and Its Presumptive Role in Tomato (Lycopersicon esculentum L.) Defense against Whitefly (Bemisia tabaci Genn.)

Insects ◽  
2020 ◽  
Vol 11 (9) ◽  
pp. 574
Author(s):  
Azhar Uddin Keerio ◽  
Talha Nazir ◽  
Tauqir Anwar ◽  
Muhammad Zeeshan Majeed ◽  
Yusuf Ali Abdulle ◽  
...  
Keyword(s):  
Lycopersicon Esculentum ◽  
Beauveria Bassiana ◽  
Bemisia Tabaci ◽  
Defense Mechanisms ◽  
Tomato Plants ◽  
Fungal Protein ◽  
Fecundity Rate ◽  
Survival Percentage ◽  
Putative Role

Plants rely on various physiological and molecular defense mechanisms against biotic stresses such as herbivore insects. Many entomopathogenic fungi synthesize protein molecules that can trigger these plant defenses. This laboratory study characterized the bioactivity of a partially purified protein derived from Beauveria bassiana (ARSEF 2860) against whitefly, Bemisia tabaci (Hemiptera: Aleyrodidae), which is an economically important pest of agricultural and horticultural crops worldwide. Different concentrations (i.e., 0.021, 0.042 and 0.063 μM) of fungal protein were bioassayed to determine their sub-lethal effect on the survival percentage and fecundity rate of B. tabaci on tomato (Lycopersicon esculentum) plants. In addition, the putative role of this partially purified B. bassiana protein in the defense mechanisms of plant was assessed through the expression analyses of important genes related to salicylic acid (SA)—and jasmonic acid (JA)—associated pathways using RT-qPCR. Results revealed a significant suppression of the survival percentage and fecundity rate of B. tabaci by the fungal protein. Lowest survival (41%) was recorded for the highest concentration of protein (0.063 μM), whereas mean survival for the other two protein concentrations (0.042 and 0.021 μM) were 62 and 71%, respectively. Likewise, the highest and lowest mean fecundity rates were observed for the control and the highest protein concentration (i.e., 3.3 and 1.8 eggs day−1 female−1, respectively). Furthermore, the exogenous application of B. bassiana-derived protein on tomato plants strongly up-regulated the SA-related genes (PAL, PR1, BGL2 and EDS1) and slightly up-regulated the JA-related genes (AOC, AOS, OPR3 and LOX) as compared to the control plants. These findings demonstrate the putative role of this partially purified B. bassiana protein fraction in inducing systemic resistance in the tomato plants against B. tabaci, suggesting its further purification and characterization to be used as novel biological pest control tool against B. tabaci and other sap-sucking insect pests.

scholarly journals Impacts of cucurbit chlorotic yellows virus (CCYV) on biological characteristics of its vector Bemisia tabaci

2021 ◽  
Author(s):  
Haifang He ◽  
Jingjing Li ◽  
Zelong Zhang ◽  
Xuefei Tang ◽  
Danyang Song ◽  
...  
Keyword(s):  
Bemisia Tabaci ◽  
Plant Virus ◽  
Host Plants ◽  
Plant Viruses ◽  
The Body ◽  
Biological Characteristics ◽  
Adult Longevity ◽  
Male Adult ◽  
Q Biotype ◽  
Cucurbit Chlorotic Yellows Virus

Abstract It is known that plant viruses, to facilitate their transmission, can change the phenotypes and defense pathways of the host plants and the performance of their vectors. Cucurbit chlorotic yellows virus (CCYV), a newly reported virus occurring on cucurbit plants and many other plant species, is transmitted specifically by Middle East-Minor Asia 1 (B biotype) and Mediterranean (Q biotype) cryptic species of whitefly, Bemisia tabaci (Gennadius), in a semipersistent manner. This study evaluated the direct and indirect effects of CCYV on B. tabaci biology to better understand the plant-virus-vector interaction. By using CCYV-B. tabaci-cucumber as the model, we investigated whether or how a semipersistent plant virus impacts the biology of its whitefly vectors. CCYV mRNA were detectable in nymphs from 1st to 4th instars and adults of B. tabaci with different titers. Female nymph duration and female adult longevity greatly extended on CCYV-infected plants, but male nymph duration and male adult longevity were not significantly influenced. In addition, on CCYV-infected plants, the body length and oviposition of adult B. tabaci increased, but the hatching rates of eggs and survival rates of different stages were not affected. Most interestingly, the sex ratio (male:female) significantly reduced to 0.506:1 in whitefly populations on CCYV-infected plants, while the ratio remained about 0.979:1 on healthy plants. These results indicated that CCYV can significantly impact the biological characteristics of its vector B. tabaci through the host plants. It is speculated that CCYV and B. tabaci have established a typical mutualist relationship mediated by host plants.

scholarly journals Identification of Plant Virus Receptor Candidates in the Stylets of Their Aphid Vectors

2018 ◽  
Vol 92 (14) ◽  
Author(s):  
Craig G. Webster ◽  
Elodie Pichon ◽  
Manuella van Munster ◽  
Baptiste Monsion ◽  
Maëlle Deshoux ◽  
...  
Keyword(s):  
Mosaic Virus ◽  
Myzus Persicae ◽  
Plant Virus ◽  
Plant Viruses ◽  
Cauliflower Mosaic Virus ◽  
Insect Vectors ◽  
Virus Receptor ◽  
Content Type ◽  
Cuticular Proteins

ABSTRACTPlant viruses transmitted by insects cause tremendous losses in most important crops around the world. The identification of receptors of plant viruses within their insect vectors is a key challenge to understanding the mechanisms of transmission and offers an avenue for future alternative control strategies to limit viral spread. We here report the identification of two cuticular proteins within aphid mouthparts, and we provide experimental support for the role of one of them in the transmission of a noncirculative virus. These two proteins, named Stylin-01 and Stylin-02, belong to the RR-1 cuticular protein subfamily and are highly conserved among aphid species. Using an immunolabeling approach, they were localized in the maxillary stylets of the pea aphidAcyrthosiphon pisumand the green peach aphidMyzus persicae, in the acrostyle, an organ earlier shown to harbor receptors of a noncirculative virus. A peptide motif present at the C termini of both Stylin-01 and Stylin-02 is readily accessible all over the surface of the acrostyle. Competition forin vitrobinding to the acrostyle was observed between an antibody targeting this peptide and the helper component protein P2 ofCauliflower mosaic virus. Furthermore, silencing thestylin-01but notstylin-02gene through RNA interference decreased the efficiency ofCauliflower mosaic virustransmission byMyzus persicae. These results identify the first cuticular proteins ever reported within arthropod mouthparts and distinguish Stylin-01 as the best candidate receptor for the aphid transmission of noncirculative plant viruses.IMPORTANCEMost noncirculative plant viruses transmitted by insect vectors bind to their mouthparts. They are acquired and inoculated within seconds when insects hop from plant to plant. The receptors involved remain totally elusive due to a long-standing technical bottleneck in working with insect cuticle. Here we characterize the role of the two first cuticular proteins ever identified in arthropod mouthparts. A domain of these proteins is directly accessible at the surface of the cuticle of the acrostyle, an organ at the tip of aphid stylets. The acrostyle has been shown to bind a plant virus, and we consistently demonstrated that one of the identified proteins is involved in viral transmission. Our findings provide an approach to identify proteins in insect mouthparts and point at an unprecedented gene candidate for a plant virus receptor.

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