Mechanisms of resistance in cotton to whitefly (<Emphasis Type="Italic">Bemisia tabaci</Emphasis>): antixenosis

Screenhouse experiments were conducted under free-choice conditions to determine the mechanism of resistance operating in cotton against whitefly, Bemisia tabaci (Gennadius) (Homoptera: Aleyrodidae). Twelve cotton genotypes belonging to Gossypium hirsutum and G. arboreum were assessed for oviposition preference by whitefly. The trichome density and length, distance from lower leaf surface to nearest vascular bundles, leaf lamina thickness and compactness of vascular bundles were estimated for each genotype and correlations with number of eggs laid were determined. The genotypes RS2098, CNH911, and PA183 were non-preferred for oviposition and exhibited an antixenosis mechanism of resistance. NHH44, LK861, Supriya, RS2013 and LD694 were categorized as moderately resistant while IS-376/4/1/20/72 and F846 were categorized as susceptible. Greater leaf lamina thickness and more compact vascular bundles were correlated with egg laying by whitefly.     

Elucidating resistance in cotton genotypes to whitefly, <Emphasis Type="Italic">Bemisia tabaci,</Emphasis> by population buildup studies

Plant resistance has become an important component of integrated pest management (IPM) for management of whitefly, Bemisia tabaci (Gennadius) (Homoptera: Aleyrodidae), an important pest of cotton in India. The present studies were undertaken to standardize the plant stage and identify resistant cotton genotypes against whitefly. Nine plant stages of F846, a susceptible cotton genotype, were exposed to whitefly for 25 days under no-choice conditions. The population buildup (eggs, nymphs, pupae and adults) was recorded. The 12-, 14- and 16-leaf stages were suitable for plant resistance studies against whitefly, and the 14-leaf stage was taken for further studies. Ten cotton genotypes of Gossypium hirsutum and two of G. arboreum were covered with split cages in which five pairs of B. tabaci (F₁) were released. The population buildup was recorded to categorize genotypes as resistant, moderately resistant, moderately susceptible or susceptible. The experiment was repeated with F₂ and F₃ generation whiteflies. Based on overall average score of three experiments, LD694 was rated as resistant; LK861, Supriya, RS2013, CNH911 and PA183 as moderately resistant; IS-376/4/1/20/72, NHH44, TxMaroon2-78, Bt 6304 and RS2098 as moderately susceptible; and F846 as susceptible. LD694 was found to be resistant in three consecutive generations of whitefly.     

Morphological Basis of Resistance in Cotton to the WhiteflyBemisia Tabaci

The morphological basis of resistance to the whiteflyBemisia tabaci Genn. (Aleyrodidae: Hemiptera) was studied. The plant characters examined were leaf area, thickness of leaf lamina, hair density, hair length, angle of insertion of leaf hair, and density of gossypol glands. Hair density and leaf thickness were positively correlated with the population ofB. tabaci, and a positive correlation was obtained between the adult whitefly population and gossypol glands on stem internodes. Cotton genotype USA-22 (sparsely hairy) was found to be more tolerant toB. tabaci than was genotype USA-13 (velvety hairy). The use of thinner and glabrous leaved cotton varieties is suggested to minimize the whitefly menace in cotton.     

Comparison of Resistance to Tomato Leaf Curl Virus (India) and Tomato Yellow Leaf Curl Virus (Israel) among Lycopersicon Wild Species, Breeding Lines and Hybrids

The objective of this study was to screen wild and domesticated tomatoes for resistance to Tomato yellow leaf curl virus, Israel (TYLCV-Is) and Tomato leaf curl virus from Bangalore isolate 4, India (ToLCV-[Ban4]) to find sources of resistance to both viruses. A total of 34 tomato genotypes resistant/tolerant to TYLCV-Is were screened for resistance to ToLCV-[Ban4] under glasshouse and field conditions at the University of Agricultural Sciences, Bangalore, India. Resistance was assessed by criteria like disease incidence, symptom severity and squash-blot hybridization. All the tomato genotypes inoculated with ToLCV-[Ban4] by the whitefly vector Bemisia tabaci (Gennadius) produced disease symptoms. In some plants of the lines 902 and 910, however, the virus was not detected by hybridization. The tomato genotypes susceptible to ToLCV-[Ban4] by whitefly-mediated inoculation were also found susceptible to the virus under field conditions. However, there were substantial differences between genotypes in disease incidence, spread, symptom severity and crop yield. Despite early disease incidence, many genotypes produced substantially higher yields than the local hybrid, Avinash-2. Sixteen tomato genotypes from India resistant/tolerant to ToLCV-[Ban4] were also tested for TYLCV-Is resistance at the Hebrew University of Jerusalem, Rehovot, Israel. Accessions of wild species, Lycopersicon hirsutum LA 1777 and PI 390659 were the best sources of resistance to both viruses. Lines 902 and 910, which were, resistant to TYLCV-Is were only tolerant to ToLCV-[Ban4] and accession Lycopersicon peruvianum CMV Sel. INRA, resistant to ToLCV-[Ban4], was only tolerant to TYLCV-Is. Implications of using the resistant lines in breeding programme is discussed.     

Epidemiological studies of the tomato yellow leaf curl virus (TYLCV) in the Jordan Valley,Israel

The spread of tomato yellow leaf curl virus (TYLCV) is significantly correlated with the population size of its vector,Bemisia tabaci Genn. The perennial weedCynanchum acutum L. and the annual weedMalva parviflora L. were found to be natural hosts of TYLCV in the Jordan Valley.C. acutum is not a preferred host forB. tabaci, but the whitefly feeds on it sufficiently long to acquire the virus. Whiteflies marked with fluorescent dust while feeding naturally onC. acutum along the banks of the Jordan River, were subsequently trapped within the main tomato-production area 7 km away. An increase in theB. tabaci population and in TYLCV infectivity was found in plots surrounded by windbreaks. The epidemiological cycle of TYLCV is described and cultural control measures are suggested.     

Tomato yellow leaf curl virus accumulates in vesicle-like structures in descending and ascending midgut epithelial cells of the vector whitefly, Bemisia tabaci, but not in those of nonvector whitefly Trialeurodes vaporariorum

Begomoviruses are transmitted by a single species of vector insect, the whitefly Bemisia tabaci, in a circulative manner. However, the mechanisms of this strict vector specificity have not been clarified. By immunoelectron microscopy, we showed that a begomovirus, Tomato yellow leaf curl virus (TYLCV), can enter midgut epithelial cells of the vector whitefly B. tabaci but not those of a nonvector whitefly, Trialeurodes vaporariorum, belonging to the same family. In midgut epithelial cells of viruliferous B. tabaci, the virus was localized in vesicle-like structures, suggesting endocytosis as an entry mechanism. These structures were also observed in midgut cells of nonviruliferous B. tabaci that had fed on healthy plants and in those of the nonvector T. vaporariorum that had fed on virus-infected plants. Vesicles containing TYLCV particles were observed most frequently in cells in the anterior part of the descending midgut, suggesting that this is the major entry site. These results clearly demonstrated that the virus-containing vector and nonvector whiteflies differ in the cellular localization of the virus and strongly suggest that a critical step in determining the vector insect specificity of begomoviruses is the entry of the viruses into midgut epithelial cells.     

Biochemical determination of acetylcholinesterase genotypes conferring resistance to the organophosphate insecticide chlorpyriphos in field populations of Bemisia tabaci from Benin, West Africa

Resistance to chlorpyriphos insecticide in Bemisia tabaci from a field population collected in Benin, West Africa was suggested with bioassay showing the presence of two sub-populations. Patterns of acetylcholinesterase (AChE) inhibition by the organophosphate chlorpyriphos-oxon were analyzed to estimate the number of possible genotypes with different sensitivity expected in three B. tabaci field populations collected in Benin. The analysis of inhibition patterns in these populations compared with four laboratory strains of B. tabaci using chlorpyriphos-oxon allowed the differentiation of three possible genotypes. In the reference strain SUD-S we detected two different acetylcholinesterases with different sensitivity to chlorpyriphos oxon suggesting the presence of two genes ace 1 and ace 2. The proportion of the insensitive enzyme (ace 2) was estimated to be 31%. In field populations we can detect two alleles at the same gene locus ace 1: one susceptible ace1S and one resistant ace1R. Both strains called Arizona University and Mexico-S2 have lost sensitive ace1S but the field populations from Benin clearly contained at least three genotypes confirming heterogeneous populations not completely resistant.     

Two cytochrome P450 genes are involved in imidacloprid resistance in field populations of the whitefly, Bemisia tabaci, in China

The sweet potato whitefly, Bemisia tabaci (Gennadius) (Hemiptera:Aleyrodidae), is an invasive and damaging pest of field crops worldwide. The neonicotinoid insecticide imidacloprid has been widely used to control this pest. We assessed the species composition (B vs. Q), imidacloprid resistance, and association between imidacloprid resistance and the expression of five P450 genes for 14–17 B. tabaci populations in 12 provinces in China. Fifteen of 17 populations contained only B. tabaci Q, and two populations contained both B and Q. Seven of 17 populations exhibited moderate to high resistance to imidacloprid, and eight populations exhibited low resistance to imidacloprid, compared with the most susceptible field WHHB population. In a study of 14 of the populations, resistance level was correlated with the expression of the P450 genes CYP6CM1 and CYP4C64 but not with the expression of CYP6CX1, CYP6CX4, or CYP6DZ7. This study indicates that B. tabaci Q has a wider distribution in China than previously reported. Resistance to imidacloprid in field populations of B. tabaci is associated with the increased expression of two cytochrome P450 genes (CYP6CM1 and CYP4C64).     

Screening tomato genotypes for resistance and tolerance to Tomato chlorosis virus

Tomato chlorosis virus (ToCV) is an emerging crinivirus in Brazil that causes an economically important disease in tomato (Solanum lycopersicum) and other solanaceous species. ToCV is transmitted predominantly by the whitefly Bemisia tabaci Middle East‐Asia Minor 1 (MEAM1, formerly biotype B), in a semipersistent manner. As all cultivated tomato varieties and hybrids are susceptible to this crinivirus, the main alternatives for the control of the disease are the use of healthy seedlings for transplanting and the chemical control of the insect vector. The objective of this work was to evaluate the responses of tomato genotypes to infection with this crinivirus and their tolerance to the disease in order to support the development of other alternatives for disease control. Resistance to infection was evaluated by ToCV inoculation with viruliferous B. tabaciMEAM1 followed by virus detection by RT‐PCR and RT‐qPCR. To measure tolerance to the disease, plant development and fruit yield of ToCV‐infected and healthy plants were compared. Among 56 genotypes, only the lineage IAC‐CN‐RT (S. lycopersicum ‘Angela Gigante’ × S. peruvianum ‘LA 444‐1’) was highly resistant to infection with ToCV. Tolerance to the disease over two trials with different genotypes showed variable results. The effect of ToCV on plant development varied from 2.9% to 71.9% reduction, while yield loss varied from 0.2% to 51.8%. The highly ToCV‐resistant lineage IAC‐CN‐RT, which is also resistant to a Spanish isolate of ToCV, might be useful for tomato breeding programmes.     

Effect of Host Plant Resistance to Tomato yellow leaf curl virus (TYLCV) on Virus Acquisition and Transmission by Its Whitefly Vector

ABSTRACT The effect that Tomato yellow leaf curl virus (TYLCV)-infected resistant tomato plants may have on virus epidemiology was studied. Four tomato genotypes that exhibit different levels of viral resistance, ranging from fully susceptible to highly resistant, served as TYLCV-infected source plants. Viral acquisition and transmission rates by white-flies following feeding on the different source plants were evaluated. TYLCV transmission rate by whiteflies that had fed on infected source plants 21 days postinoculation (DPI), shortly after the appearance of TYLCV symptoms, was negatively correlated with the level of resistance displayed by the source plant. Therefore, the higher the resistance, the lower the transmission rate. In addition, TYLCV DNA accumulation was shown to be lower in the resistant source plants compared with the susceptible plants. Whitefly survival rate, following feeding on source plants 21 DPI, was similar for all the cultivars tested. Significant differences in whitefly survival were found, however, following feeding on the infected source plants at 35 DPI; here, whitefly survival rate increased with higher levels of resistance displayed by the source plant. At 35 DPI, the susceptible plants had developed severe TYLCV disease symptoms, and transmission rates from these plants were the lowest, presumably due to the poor condition of these plants. Transmission rates from source plants displaying a medium level of resistance level were highest, with rates declining following feeding on source plants displaying higher levels of TYLCV resistance. TYLCV DNA accumulation in whiteflies following feeding on infected source plants at both 21 and 35 DPI was directly correlated with viral DNA accumulation in source plants. Results show that, in essence, the higher the resistance expressed, the less suitable the plant was as a viral source. Consequently, following acquisition from a highly resistant plant, TYLCV transmission by whiteflies will be less efficient.     

Insecticide resistance in field populations of Bemisia tabaci (Hemiptera: Aleyrodidae) in West Africa

BACKGROUND: The tobacco whitefly, Bemisia tabaci Gennadius (Hemiptera: Aleyrodidae), has developed a high degree of resistance to several chemical classes of insecticides throughout the world. To evaluate the resistance status in West Africa, eight insecticides from different chemical families were tested using the leaf‐dip method on four field populations collected from cotton in Benin, Togo and Burkina Faso. RESULTS: Some field populations showed a significant loss of susceptibility to pyrethroids such as deltamethrin [resistance ratio (RR) 3–5] and bifenthrin (RR 4–36), to organophosphates (OPs) such as dimethoate (RR 8–15) and chlorpyrifos (RR 5–7) and to neonicotinoids such as acetamiprid (RR 7–8) and thiamethoxam (RR 3–7). Bemisia tabaci was also resistant to pymetrozine (RR 3–18) and to endosulfan (RR 14–30). CONCLUSION: The resistance of B. tabaci to pyrethroids and OPs is certainly due to their systematic use in cotton treatments for more than 30 years. Acetamiprid has been recently introduced for the control of whiteflies. Unfortunately, B. tabaci populations from Burkina Faso seem to be already resistant. Because cross‐resistance between these compounds has never been observed elsewhere, resistance to neonicotinoids could be due to the presence of an invasive B. tabaci biotype recently detected in the region. Copyright © 2010 Society of Chemical Industry     

Identification of mutations in the para sodium channel of Bemisia tabaci from Crete, associated with resistance to pyrethroids

We investigated the mechanisms of resistance to α-cypermethrin in a Q biotype, highly resistant Bemisia tabaci strain (GRMAL-RP) isolated from Crete. Cytochrome P450-dependent monoxygenase activity with the substrate ethoxycoumarin, and carboxylesterase activity with the substrates α-naphthyl-acetate, β-naphthyl-acetate, and para-nitrophenol acetate were substantially elevated in the GRMAL-RP, compared to the susceptible SUD-S strain, while glutathione-S-transferase activity with the substrate 1-chloro-2,4-dinitrobenzene was not different. The metabolic inhibitors piperonyl butoxide and S,S,S-tributyl phosphorotrithioate synergised cypermethrin toxicity in the GRMAL-RP strain, however, mortality was still lower than that of the susceptible strain, indicating the presence of an additional resistance mechanism. Analysis of the sequence of the IIS4-IIS6 region of the para sodium channel gene of the GRMAL-RP strain revealed two amino acid replacements compared to that of the SUD-S susceptible strain. One is the leucine to isoleucine substitution at position 925 (L925I) previously implicated in B. tabaci pyrethroid resistance and the other is a novel kdr resistant mutation for B. tabaci, a threonine to valine substitution at position 929 (T929V). Genotype analysis showed that the L925I and T929V were present in all GRMAL-RP males tested, at an approximately 1:1 frequency, but never in combination in the same haplotype.     

Race-specific elicitors from the Peronospora parasitica / Arabidopsis thaliana pathosystem

Intercellular washing fluids (IWFs) were isolated from compatible interactions ofPeronospora parasitica with Arabidopsis. IWFs were filter-sterilized then infiltrated into leaves of resistant and susceptible Arabidopsis genotypes. P. parasitica isolates WELA (virulent on Landsberg erecta (La-er) and Weiningen (Wei-0) but avirulent on Columbia (Col-0) and RLD) and NOCO (virulent on Col-0 and RLD but avirulent on La-er) were used. A “reciprocal check” pattern of necrosis-induction was observed in which IWFs from a compatible interaction caused necrosis in leaves of the Arabidopsis genotypes resistant to the “parent” fungal isolate but not in those genotypes susceptible to it. Analysis of variance showed that the interaction between fungal isolate and necrosis in host genotypes was highly significant. The necrosis-inducing activity was significantly correlated with a high degree of asexual sporulation in the compatible interaction from which the IWF was isolated. However, the necrosis-inducing activity was not correlated with the protein content of the IWF.     

Note: First report of the Q biotype of<Emphasis Type="Italic">Bemisia tabaci</Emphasis> in Southern Sonora,Mexico

Bemisia tabaci (Gennadius) adults were collected from poinsettia plants (Euphorbia pulcherrima) in retail nurseries in Cd. Obregon and Navojoa, Sonora, Mexico. A single field sample was collected from broccoli plants in Obregon, Sonora. Both adult whitefly and immature instars were observed on infested leaves. Whiteflies were identified asB. tabaci using morphological characters of the pupae to distinguish them from the greenhouse whitefly; and to specific biotype, by molecular analysis using the mitochondrial cytochrome oxidase I (mtCOI) sequence. Phylogenetic analysis of mtCOI sequences indicated that poinsettias were colonized both by the Q and the B biotype. The Q biotype was found only on poinsettia plants, and one poinsettia sample was infested with both the Q and the B biotype. The B biotype alone was associated with the field-collected broccoli sample analyzed in the study. A more extensive survey is required to determine the extent of the distribution of the Q biotype in Mexico, particularly where ornamental plants are transported from central to northern Mexico. Such plants could serve as the source of the Q biotype, which has been reported to be highly resistant to insecticides including the neo-nicotinoids that are widely used to control the B biotype in much of Mexico. This is the first report of the Q biotype in Mexico. http://www.phytoparasitica.org posting May 2, 2007.     

Structural changes of homogalacturonan,rhamnogalacturonan I and arabinogalactan protein in xylem cell walls of tomato genotypes in reaction to Ralstonia solanacearum

Healthy and Ralstonia solanacearum-inoculated tomato genotypes susceptible or resistant to bacterial wilt including recombinant inbred lines (RILs) deriving from a cross between the resistant genotype Hawaii7996 and the susceptible Wva700 were compared for symptom and bacterial population development, and for the composition and structure of pectic polysaccharides and arabinogalactan proteins (AGPs) of xylem cell walls by immunological staining of tissue prints. Constitutive differences were observed between resistant and susceptible RILs, with a higher degree of methyl-esterification of homogalacturonan (HG) detected by antibody JIM7 in the resistant plants. After inoculation, decreased methyl-esterification of HG indicated by stronger labeling with antibody JIM5 was observed in all susceptible genotypes and in five of eleven resistant genotypes, with a clear increase in the non-blockwise de-esterification pattern of HG (LM7) only in the susceptible lines, indicating the mode of action of the pectinmethylesterase of R. solanacearum. In the susceptible lines infection generally leads to increased branching of rhamnogalacturonan I indicated by the detection of arabinan (LM6) and galactan (LM5) side chains, and of arabinogalactan protein (LM2), while only few of the resistant genotypes reacted with changes in these epitopes. All the resistant, symptomless genotypes contained relatively high pathogen populations in stems. A clear relation between cell wall composition and degree of latent infection of resistant genotypes was not found.     

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.     

First record of the Q Biotype of the sweetpotato whitefly, Bemisia tabaci, intercepted in the UK

For the UK, Bemisia tabaci poses a threat primarily to protected vegetable crops due to the transmission of several plant-pathogenic viruses. There are at least 24 different biotypes of B. tabaci that cannot be differentiated through morphological traits. The B (Middle East-Asia Minor 1 species) and Q (Mediterranean species) biotypes are widely considered to be the most important and, as such, the ability to rapidly and precisely biotype B. tabaci interceptions is vital when developing effective control strategies. Intercepted adult/pupal B. tabaci received from the UK Plant Health and Seeds Inspectorate (PHSI) during 2002–2003 (n?=?60) and 2010–2011 (n?=?42) were both biotyped and tested for the presence of Tomato yellow leaf curl virus (TYLCV) and Tomato yellow leaf curl Sardinia virus (TYLCSV) using a real-time PCR assay based on TaqMan? chemistry. The positive results indicated that during 2002–2003 the Q biotype comprised 68.3?% of the interceptions whilst in 2010–2011 it comprised 66.7?% of the B. tabaci samples intercepted. Only three of the B biotypes collected during 2002–2003 were positive for TYLCSV, two originating from Israel and the other of unknown origin. The implications in regards to pest management of the insect are discussed.     

Mechanisms of resistance in cotton to whitefly (<Emphasis Type="Italic">Bemisia tabaci</Emphasis>): Tolerance

Screen house experiments were conducted under no choice conditions, to determine the tolerance, a mechanism of resistance, in cotton under a population pressure of 150 and 300 pairs of whiteflies Bemisia tabaci (Gennadius) (Homoptera: Aleyrodidae). Twelve cotton genotypes, viz., four resistant (NHH 44, Supriya, LD694 and PA 183), four susceptible (F 846, IS-376/4/1/20/72, LK 861 and RS 2013) and four with moderate reaction (T x Maroon 2-78, MRC 6304Bt, RS 2098 and CNH 911) to B. tabaci were assessed in terms of decrease in plant height, number of nodes and chlorophyll content (a, b and total) from control. The study revealed that all three characters are important to identify tolerance. A strong tolerance mechanism is operating in NHH 44. The genotypes LD 694 and PA 183 were rated as moderately tolerant, however, IS 376/4/1/20/72, Tx Maroon 2-78, MRC 6304Bt, F 846 and CNH 911 exhibited no tolerance mechanism and were categorized as the most susceptible genotypes.     

The ovicidal properties of the juvenile hormone mimic sumitomo S-31183 (SK-591) to insects

S-31183 was assayed against preimaginal stages of the tobacco whitefly,Bemisia tabaci (Genn.), and eggs of the Egyptian cotton leafworm,Spodoptera littoralis (Boisd.). The compound was found to be an ovicide forB. tabaci eggs in both preinfestation and postinfestation treatments. FreshS. littoralis eggs were very susceptible to the compound at 0.05 ppm a.i., response was much poorer with 1-2-day-old eggs and 2-3-day-old eggs were not affected even by 100 ppm. Publication of the Agricultural Research Organization. No. 2271-E, 1988 series.