ORIGINAL RESEARCH article
Volume 10 - 2019 | https://doi.org/10.3389/fmicb.2019.00431
Vector Competence of Thrips Species to Transmit Soybean Vein Necrosis Virus
- 1Department of Entomology and Plant Pathology, North Carolina State University, Raleigh, NC, United States
- 2Department of Bioagricultural Sciences and Pest Management, Colorado State University, Fort Collins, CO, United States
- 3Department of Anatomy and Cell Biology, Indiana University School of Medicine, Fort Wayne, IN, United States
Soybean vein necrosis virus (SVNV) is a newly discovered species of tospovirus infecting soybean plants that is transmitted by the primary vector, soybean thrips (Neohydatothrips variabilis), and two additional secondary vectors, tobacco thrips (Frankliniella fusca) and eastern flower thrips (F. tritici). This study was undertaken to elucidate the association between virus acquisition [6, 12, 24, and 48 h acquisition access period (AAP)] and transmission efficiency [12, 24, and 48 h inoculation access period (IAP)] in the primary vector, N. variabilis, and to examine the mechanisms of vector competence by analyzing the effect of AAP (6, 12, and 24 h) on virus infection in various tissues. In addition, we examined virus infection in tissues of the two secondary vectors. We found a significant effect of virus acquisition on transmission efficiency, transmission rate post 6 and 48 h AAP was significantly lower than 12 and 24 h AAP. Our analysis did not reveal a correlation between virus transmission rate and virus RNA in corresponding N. variabilis adults. On the contrary, N. variabilis adults harboring higher accumulation of the virus (>104) resulted in lower transmission rates. Analysis of SVNV infection in the tissues revealed the presence of the virus in the foregut, midgut (region 1, 2, and 3), tubular salivary glands and principal salivary glands (PSG) of adults of all three vector species, however, the frequency of infected tissues was highest in N. variabilis followed by F. fusca and F. tritici. The frequency of SVNV infection in individual tissues specifically the salivary glands was lowest after 6 h AAP compared to 12 and 24 h AAP. This finding is in agreement with the transmission assays, where significantly lower virus transmission rate was observed post 6 h AAP. In addition, N. variabilis adults with high PSG infection (12 and 24 h AAP) were likely to have high percentage of foregut and midgut region 2 infection. Overall, results from the transmission assays and immunolabeling experiments suggest that shorter AAP results in reduced virus infection in the various tissues especially PSG, which are important determinants of vector competence in SVNV-thrips interaction.
Soybean [Glycine max (L.) Merr.] is an important crop throughout the world due to its versatility as a food source along with applications in various industries such as textiles and biofuels. The United States is the global leader in soybean production with approximately 83 million acres planted and an estimated 117 million metric tons produced in 2017 (Soystats, 2017). There are several viral diseases that affect soybean crops in the United States. For instance, alfalfa mosaic virus, soybean mosaic virus and bean pod mottle virus cause significant yield reductions, decreased pod and seed set, reductions in oil content of seeds, and seed discoloration. Emergence of new viral diseases such as soybean dwarf virus, tobacco streak virus, and more recently soybean vein necrosis virus (SVNV) can further reduce yield. complicate the situation. Soybean vein necrosis virus is a species in the genus Orthotospovirus (Bunyavirales: Tospoviridae) and was first identified in Tennessee in 2008 (Tzanetakis et al., 2009). Since its discovery, SVNV has been documented in all the major soybean-growing in the United States and Ontario, Canada, including Arkansas, Illinois, Indiana, Iowa, Kentucky, Michigan, Minnesota, Ohio, Tennessee, Wisconsin (Bloomingdale et al., 2014). The symptoms begin with vein clearing followed by chlorosis or appearance of light-green to yellow blotchy patches near the main vein, followed by necrosis or dying of the leaf tissue at late stage of infection; hence, the name, SVNV.
Tospoviruses impact food and ornamental crops, encompassing hundreds of plant species, resulting in crop disease epidemics of economic significance worldwide (Pappu et al., 2009). Some members in this genus include, tomato spotted wilt virus (TSWV) and impatiens necrotic spot virus (INSV). As a member of the Orthotospovirus genus, SVNV is transmitted exclusively by thrips (Ullman et al., 1993). The thrips-Orthotospovirus relationship is unique since adult thrips are only able to transmit SVNV if acquisition occurs in the first instar and early second larval stages (Van De Wetering et al., 1996). This suggests that acquisition of the virus is an essential determinant of adult vector competency. Once virus is acquired by larval thrips, the virions enter the insect midgut (MG) epithelial cells, replicate and migrate to the muscle cells surrounding the midgut, and eventually reach and replicate in the salivary glands (Montero-Astúa et al., 2016). After infection of salivary glands, adults can release the virus into viable plant cells by the injection of viruliferous saliva during feeding. Infection of the principal salivary glands (PSG) is required for successful transmission (Kritzman et al., 2002), however, the route by which the virus reaches the salivary glands was not known. It was proposed that the virus may move from the MG to the salivary glands by direct contact between these tissues during early larval stages (Moritz et al., 2004); through the ligaments that connect each PSG to MG (Nagata et al., 1999; de Assis Filho et al., 2002); or the tubular salivary glands (TSG) that connect the MG directly to the PSG (Ullman et al., 1989). Recently, Montero-Astúa et al. (2016) showed that TSG and associated structures (e.g., Ligaments, efferent duct, filament-like structure) may serve as a channel for virus infection to progress from the MG to the PSG. The tospovirus membrane glycoproteins, GN and GC are involved in virus-binding and entry into thrips midgut epithelial cells (Bandla et al., 1998; Nagata et al., 2000; Whitfield et al., 2004). Presence of non-structural (NSs) protein in thrips is an indication of virus replication, whereas detection of nucleocapsid protein (NP) indicates presence or absence of virus in the insect tissues (Bandla et al., 1994). Tospoviruses are not transmitted transovarially (Wijkamp et al., 1996).
Currently there are 15 putative and 11 recognized tospovirus species with 15 thrips species in the family Thripidae that act as vectors (Rotenberg et al., 2015). There is considerable variation in thrips species ability to transmit tospoviruses (Jones, 2005). In a study, F. occidentalis, F. schultzei, Thrips tabaci, and T. palmi were evaluated for their competence to transmit four tospoviruses including, TSWV, tomato chlorotic spot virus (TCSV), groundnut ringspot virus (GRSV), and chrysanthemum stem necrosis virus (CSNV). Frankliniella occidentalis transmitted all four tospoviruses with different efficiencies. Frankliniella schultzei transmitted TCSV, GRSV, and CSNV, but T. tabaci and T. plami could not transmit any of the abovementioned viruses (Nagata et al., 2004). Srinivasan et al. (2012) showed that T. tabaci was a more efficient transmitter of IYSV compared to F. fusca (76.6 and 18.3% transmission rate, respectively). Transmission efficiencies can also vary within thrips populations or biotypes of the same species (Wijkamp et al., 1995; Chatzivassiliou et al., 2002; Nagata et al., 2004; Jacobson and Kennedy, 2013). For instance, the dark and pale forms of F. schultzei differ in their ability to transmit tospoviruses, with the dark form considered to be a more efficient vector (Wijkamp et al., 1995). These findings suggest that the transmission efficiency of a newly identified tospovirus in a specific area should be studied in the different populations of thrips species that live there.
Recently, soybean thrips, Neohydatothrips variabilis (Beach) was recognized as the primary vector of SVNV (Zhou and Tzanetakis, 2013; Keough et al., 2016). However, 2 years of thrips trapping in soybean fields in Indiana showed that there were as many as 8 different species including, N. variabilis, Frankliniella tritici, F. fusca, Frankliniella sp., Thrips tabaci, Phlaeothrips sp., Anaphothrips sp., and Echinothrips sp., Together, N. variabilis, F. tritici, and F. fusca account for nearly 75% of the thrips fauna found on soybean (Keough et al., 2018). Analysis of vector competence in the three thrips species revealed that tobacco thrips (F. fusca) and eastern flower thrips (F. tritici) are able to transmit SVNV albeit at a lower efficiency (36 and 6%, respectively) compared to the primary vector, soybean thrips (72%) (Keough et al., 2016). This was the first record of F. tritici as a vector of tospoviruses even though its vector competence to transmit other tospoviruses had been examined previously (Sakimura, 1953; de Assis Filho et al., 2005).
There has been progress in understanding various aspects of tospoviruses (Zhou et al., 2011; Khatabi et al., 2012; Zhou and Tzanetakis, 2013; Groves et al., 2016; Anderson et al., 2017), but many important details about virus acquisition, retention, and transmission by the vectors is are lacking. The aims of this study were to (1) elucidate the association virus acquisition [6, 12, 24, and 48 h acquisition access period (AAP)] and transmission efficiency [12, 24, and 48 h inoculation access period (IAP)] in the primary vector, N. variabilis, (2) understand mechanisms of vector competency by examining the effect of AAP (6, 12, and 24 h) on virus infection in the tissues of adult N. variabilis and (3) compare virus infection in the tissues all three vector species, N. variabilis, F. tritici, and F. fusca. Virus accumulation in adult insects was determined by absolute quantification method using Reverse Transcriptase-quantitative PCR (RT-qPCR) and transmission of virus to leaf tissues was determined by SVNV-specific double-antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA). Virus infection was determined by immunolabeling with antibody against SVNV-NP and imaged using confocal florescence microscopy.
Materials and Methods
Soybean variety Asgrow AG3334 (Monsanto, St. Louis, MO, United States) plants were grown in 15.24 cm pots at 25 ± 1°C with 60–70% relative humidity and a photoperiod of 16:8 (L:D) hours in an Environmental Control Room with IntellusUltra controller (Percival-Scientific, Perry, IA, United States). For plant maintenance, soybeans were fertilized weekly with Peters water-soluble fertilizer (14:14:14, N: P: K; Scotts-Sierra Horticultural Products, OH) at a rate of 3 g/l.
Populations of N. variabilis originally collected from several different soybean fields located in Purdue Agricultural Centers (PAC) throughout Indiana were maintained in 45.72 × 45.72 × 76.20 cm thrips-proof insect cages (Bioquip, CA, United States) on soybean varAG3334. Despite several attempts, we could not transmit SVNV by mechanical-inoculation from which acquisition assays could be conducted. Other studies reported having similar difficulty (Khatabi et al., 2012; Hajimorad et al., 2015), hence we maintained infected and non-infected vector colonies in separate rooms. Insects were grouped into SVNV-infected and non-infected populations were distinguished by setting up thrips lines, where a single adult female was allowed to infest on a detached leaf at V1 or vegetative stage 1 (14 days after planting) in separate modified Petri-dishes with lids fitted with thrips-proof mesh (Bioquip, CA, United States) for ventilation. Infested leaves were tested for presence or absence of SVNV using RT-PCR after 2 weeks of incubation (Keough et al., 2016). All the offspring from thrips lines that tested positive for SVNV were pooled together to start an SVNV-infected colony, whereas the offspring from leaves that tested negative for SVNV were combined to start SVNV non-infected colony. SVNV-infected and non-infected colonies were maintained in 45.72 × 45.72 × 76.20 cm thrips-proof insect cages in separate rooms. Colonies were tested monthly using Diagnostic DAS-ELISA and RT-PCR for the presence of SVNV in plants and insects, respectively. Two other thrips species, F. tritici and F. fusca, were also collected from PAC locations and maintained on red kidney bean leaves (Phaseolus vulgaris L) in modified 50 ml Falcon tubes with a water source at the bottom and lids fitted with thrips-proof mesh for ventilation. Both F. tritici and F. fusca had higher fecundity on red bean compared to soybean, hence we used red bean for routine colony maintenance to obtain sufficiently large population needed for molecular analysis and confocal microscopy experiments. However, previous research in our lab showed that F. tritici and F. fusca can feed and reproduce on soybean albeit not as successfully as N. variabilis (Keough et al., 2016). All thrips populations were reared under the similar condition at temperature of 25 ± 1°C and a photoperiod of 16:8 (L:D) hours.
SVNV was maintained in the greenhouse on soybean plants with continual transmission by N. variabilis at temperature of 25 ± 1°C and a photoperiod of 16:8 (L:D) hours. Disease-free, V3 stage of soybean plants were alternately added into SVNV-infected colony at 4–5 week intervals, allowing inoculation by viruliferous soybean thrips for 3–4 weeks in 45.72 × 45.72 × 76.20 cm thrips-proof cage at which time they were used as viral source in experiments. Plants were routinely checked for symptom development which typically took 3 weeks. Leaf tissues were harvested from symptomatic plants and infection was confirmed using SVNV-specific double-antibody sandwich enzyme-linked immunosorbent assay, DAS-ELISA kit (Agdia, Elkhart, IN, United States).
SVNV Acquisition and Transmission by N. variabilis in Leaf-Disk Assay
The experimental design was a 4 × 3 factorial with four AAP durations (6, 12, 24, and 48 h) and three IAP durations (24, 48, and 72 h). Given the logistics of performing a complete factorial, we focused each experiment on a specific AAP duration and the cohort of thrips post-AAP were divided into three subsamples for the three inoculation treatments: 24, 48, and 72 h IAP, respectively. Briefly, a cohort of 50 first instars of N. variabilis, up to 24 h old, were placed on detached SVNV-infected soybean leaves for either 6, 12, 24, or 4 8h of AAP in 15 cm diameter Petri-dishes with lids fitted with thrips-proof mesh for ventilation. The petioles of infected detached soybean leaf were inserted through a hole made in the Parafilm cover on the top of a 1.7 ml microcentrifuge tubes, this was done to keep the soybean leaves fresh during the acquisition assay. All systemically infected leaves used for AAP were confirmed to be positive with SVNV. After varying duration of AAP, the cohort of larvae were transferred to non-infected/healthy soybean leaves sealed in Petri-dishes and reared to adulthood. The transmission efficiencies of thrips were assessed by inoculating a single 1.5 cm-diameter healthy soybean leaf disk with an individual thrips, 24 h post-adult eclosion. The soybean leaf disk was placed on a piece of filter paper partially inserted in 1000 μl micropipette tip, which was sealed off at one end and filled with water. Insects were allowed 24, 48, and 72 h of IAP, after which time insects were collected in 1.7 ml microcentrifuge tubes and flash frozen in liquid nitrogen (Supplementary Figure 1). Virus level in each insect was quantified using RT-qPCR estimated by log10 copies of SVNV NP RNA as calculated from an external standard dilution series of the plasmid containing the NP-gene (Keough et al., 2016). Leaf disks after each IAP were incubated on water in a microtiter plate for 4 days to allow for virus replication before being tested for SVNV with DAS-ELISA. Three negative controls (healthy soybean leaves), two blank buffer controls and three positive controls were included in each ELISA plate. Absorbance values were measured at 405 nm in a photometer 1 h after substrate addition. Since each experiment/ELISA plate is considered independent in order to compare absorbance values between plates, we expressed absorbance as a ratio by dividing the absorbance value of each sample/well by the average absorbance of the negative control wells of the corresponding plate. Thus, the ratio indicates how many times higher or lower was the sample value with respect to the corresponding plate negative controls. Samples with an absorbance value higher than three times the average of the negative controls were considered SVNV positive. This experiment was repeated four times for a total of 272 insects and corresponding leaf disks for 12 AAP × IAP (4 AAP × 3 IAP) treatment combinations. A cohort of larvae exposed to healthy leaf tissues served as the control group. Assays were conducted under laboratory conditions mentioned previously.
Quantification of Virus in N. variabilis Adults Using Quantitative Real-Time-PCR
Total RNA was extracted from individual adult N. variabilis obtained from the acquisition and transmission assay described above using the Chelex 100 (Bio-Rad, Hercules, CA, United States) method (Boonham et al., 2002). A total of 11 μl of RNA was used for cDNA synthesis using the Verso cDNA® Synthesis Kit (Thermo Fisher Scientific, Pittsburgh, PA, United States). To quantify SVNV levels from samples, a standard curve was generated using a plasmid containing SVNV-NP gene at a known concentration as per Keough et al. (2016). Briefly, a 239 bp SVNV-NP fragment was amplified using RT-PCR with the designed primer pair (forward: 5′-GGAAGCTTACCCCTTCTGGC-3′ and reverse: 5′-ACTCCTCTCATTTGGGGTGC-3′). The cycling conditions as follows: 2 min incubation at 94°C followed by 40 cycles of 30 s denaturation at 94°C, 10 s annealing at 55°C, and 1 min extension at 72°C and a final 10 min incubation at 72°C. The amplicon was cloned into pCR8TM TA vector (2817 bp) using One Shot TOP10 chemically competent Escherichia coli (Thermo Fisher Scientific, Pittsburgh, PA, United States). Plasmid DNA was extracted using Qiagen Miniprep Kit following manufacturer’s protocol (Qiagen, Valencia, CA, United States) and sequenced. The nucleotide sequence was 100% identical to the target sequences deposited in GenBank (GU722322). The SVNV-NP sequence is deposited in NCBI GenBank under accession number MG190869. The concentration of the plasmid DNA containing the SVNV-NP gene was determined using a NanoDrop 1000 (Thermo Fisher Scientific, United States). The total plasmid size of 3056 bp was estimated by adding 239 bp of product size expected from the NP primers to 2817 bp of plasmid. The mass of the plasmid containing the NP gene was calculated using the following formula (Applied Biosystems, 2013), where m = mass and n = plasmid size (bp): m = (n) (1.096e-21g/bp). Ten-fold dilutions series, ranging from 7.54 × 108 copies/μl to 7.54 × 101 copies/μl, were prepared in RNase-free water for obtaining a standard curve. The qPCR Mastermix for SYBR Green® (BioRad, Berkeley, CA, United States) was used according to manufacturer’s instructions. Each reaction contained 5.0 μl of SYBR Green Taq, 0.5 μl of F primer, 0.5 μl of R primer, 2.0 μl of deionized water, and 2.0 μl of cDNA template. The qPCR was run on a CFX Connect® (BioRad, Berkeley, CA, United States) thermocycler, and the mean threshold cycles (Cq) values were calculated by the CFX ManagerTM Software Version 3.1. The cycling conditions used were: 95°C for 2 min; followed by 40 cycles of 95°C for 10 s, 55°C for 30 s, and then the final melt curve, starting at 65°C increasing to 95°C, in increments of 0.5°C every 5 s. Each reaction plate contained a negative and positive control and standard curve along with insect samples, which were performed in duplicate. The number of SVNV RNA molecule copies in each PCR reaction was estimated by interpolating the normalized NP Cq value against the standard curve. A normalization coefficient (Nc) was used for normalization of each NP Cq value, which was calculated from the internal control gene, Cytochrome C Oxidase Subunit I (COI), using the equation: Nc = 1 - (inCq - MinCq)/MinCq., where inCq is the Cq value of the internal control gene for a sample and MinCq is the mean inCq for all samples (Li et al., 2009). The primer pair for COI were 5′- GGATTTATTGTTTGAGCACACCAC-3′ and 5′-TCCTGTCAATCCTCCTAATGTGA-3′ (Harwood et al., 2007). The total copy number per thrips was calculated by multiplying the RNA dilution factor (9.1-fold) and then the cDNA template dilutions (40-fold). The amplification efficiency (E) was determined using the LinRegPCR software (Ruijter et al., 2009).
Dissecting and Immunolabeling of Thrips Guts and Salivary Glands
Cohorts of 50 first instars of N. variabilis fed on SVNV-infected leaves for 6, 12, or 24 h AAP were reared on healthy soybean leaves until adulthood as described previously. Fifty F. tritici and F. fusca first instar larvae were allowed a 24 h AAP on infected soybean tissues as results from acquisition assays with N. variablis found no difference in virus acquisition rate post 12 and 24 h AAP (Table 1). Thrips were then reared to adulthood on healthy tissues. Thrips, 48 h post-adult eclosion, were placed in the middle of a Petri-dish encircled by 7% sucrose for 3 h of gut clearing. Thrips dissection and immunolabeling method were modified based on previously published research (Montero-Astúa et al., 2016). Ice-cold live thrips were decapitated under stereo dissecting microscope by cutting between the first and second thorax segments with #15 sterile scalpel blades (Microscopes America, Cumming, GA, United States) on a glass slide coated with poly-L-lysine (Thermo Fisher Scientific, Waltham, MA, United States). A drop of ice-cold PBS (10 μl) was added on the decapitated thrips and the abdomen was gently pressed using a minute pin to help obtaining the gut and salivary glands. The gut and salivary glands were removed from the remaining thrips body by cutting at the mesothorax. The organs were kept in PBS (100 μl) for 20 min at 4°C. After processing of the guts, PBS was removed carefully by pipetting and a 1 cm-diameter of circular incubation chamber was made around the guts using a glue gun. Slide was placed on ice for 1 min to avoid overheating and then kept at room temperature to allow the glue to dry. The incubation chamber was filled with 200 μl of 4% paraformaldehyde in 50 mM sodium phosphate (pH 7.2) and incubated for 1 h at room temperature in a humid box wrapped with aluminum foil to protect from the light and desiccation throughout the immunolabeling procedure. The slide was washed once with PBS and left overnight in humid box at 4°C with 200 μl of PBS-1% Triton X-100. All the subsequent procedures were conducted at room temperature in dark surroundings. The slides were washed three times with PBS and incubated in blocking buffer [PBS-0.1% Triton X-100 and 10% normal goat serum (NGS)] for 1 h. After blocking, the guts and salivary glands were washed once with PBS and incubated with 200 μl of alkaline phosphatase conjugated antibody against SVNV-NP at 1:200 dilution in ECl buffer (Agdia, Elkhart, IN, United States) for 2 h. The slides were washed three times with PBS for 5 min and incubated with sheep polyclonal anti-alkaline phosphatase antibody conjugated with FITC (Abcam, Cambridge, MA, United States) at 5 μg/ml in PBS-0.1% Triton X-100 and 1% NGS for 2 h. The slides were washed once with PBS and incubated for 1 h with 100 μl of phalloidin conjugated to iFluor 594 (Abcam, Cambridge, MA, United States) at 1:1000 dilution in PBS and 100 μl of DAPI (4′, 6-diamidino-2-phenylindole, dihydrochloride) at 125 μg/ml (Invitrogen, Grand Island, NY, United States). The slides were washed five times with PBS, and then rinsed three times with distilled water. The slides were air dried for 1 min after removal of the incubation chamber with a razor blade. A cover slide was carefully covered on the guts where 30 μl of PBS-50% glycerol was applied. Slides were sealed with clear nail polish and kept at 4°C in a microscope slide box.
Table 1. Detection of SVNV-NP protein in soybean leaf tissues in leaf-disk assays and corresponding SVNV-NP log copies in viruliferous adults.
Confocal Fluorescent Microscopy
SVNV accumulation in guts and salivary glands were examined by Olympus Fluoview® FV10i Confocal Laser Scanning Microscopy (Olympus, Tokyo, Japan) using a B-2A filter and a 60X oil-immersion objective with variable scan zoom. Images were exported using Olympus FV10-ASW Version 3.1 and further processed with ImageJ Version 1.45. The pinhole aperture was fixed at ×2.0 μm for all three channels. The laser intensity and sensitivity of light absorption for specific wavelengths were set as follow: a 405 nm laser diode at 30% of sensitivity and 30% of laser intensity for detecting blue DAPI fluorescence; a 473 nm laser diode at 45% of sensitivity and 60% of laser intensity for detecting green FITC fluorescence; and a 559 nm laser diode at 45% of sensitivity and 55% of laser intensity for detecting red Alexa Fluor 594. Z-stacks were taken for every image for all three channels with an automatic calculated optimum of 1.00 μm per slide. The depth of each insect tissue for z-stack imaging was manually adjusted and set to the highest and lowest points of the observed feature, which were determined when one of the extremes was barely perceptible. Gain settings for green channel were fixed as mentioned above to compare the intensity of SVNV signal between images. Gain for the other two channels was adjusted accordingly to obtain the best detail of nuclei and actin in each image.
Quantitative Analysis of Fluorescence Signal in PSG
To quantify SVNV infection in the PSG, Image J software (Ansari et al., 2012) was used to analyze the FITC fluorescence signal. Images attained from green FITC fluorescence channel were used for measuring area, mean intensity and integral density (IntDen). Each image was converted to an 8-bit gray image after removal of the default scale. The area of interest in each image was confined with freehand selection tool for measurement. The regions with no fluorescence were also selected for obtaining readings for background. SVNV infection in PSG was evaluated by computing the mean intensity of fluorescence signal (MIS). MIS was calculated using the following formula: MIS = IntDen - (Area of selected tissue × Mean fluorescence of background readings).
Virus transmission (ELISA absorbance ratios) was treated as a binomial response (positive or negative), and differences were estimated by logistic regression analysis by using Proc GENMOD with logit link function in SAS 9.4 (SAS Institute, 2013) as per Srinivasan et al. (2012). Spearman’s rank correlation coefficients (rho) were calculated to determine correlation between virus transmission (binomial response) in the ELISA assays and SVNV log10 copies in corresponding insects. Analyses of percentage of SVNV-positive tissues by immunolabeling was performed using Chi-square test. A one-way ANOVA was performed to determine differences in the MIS in N. variabilis PSG after 6, 12, and 24 h AAP, and between MIS in F. fusca and F. tritici PSG. All statistical analyses were performed using Minitab® Version 16 (Minitab Stat College, PA, United States).
Acquisition and Transmission Efficiency of N. variabilis
There was a significant effect of AAP (χ2 = 24.85; df = 3; P < 0.0001), but not IAP (χ2 = 0.34; df = 2; P = 0.845) on virus transmission (binomial response -positive or negative) in leaf disks using ELISA (Table 1). The transmission rate was significantly different between 6 and 12 h AAP (P = 0.001), 6 and 24 h AAP (P = 0.001), 12 and 48 h AAP (P = 0.008), and 24 and 48 h AAP (P = 0.007). No difference in transmission rate was observed between 6 and 48 h AAP (P = 0.267) and 12 and 24 h AAP (P = 0.860). Interestingly, transmission rate was low at 6 and 48 h AAP despite the relatively high accumulation of virus in insect tissues (Table 1). No correlation was detected between virus transmission rate (binomial response -positive or negative) and SVNV-NP RNA levels in corresponding N. variabilis adults (rho = -0.21, P = 0.73). SVNV transmission occurred at varying levels of virus RNA accumulation in insect tissues ranging from > 102 to ≤ 106 (Figure 1). The highest transmission rate was observed at 103 copies of viral RNA per insect and transmission reduced in adults harboring higher accumulation of the virus (>104 to ≤ 106) (Figure 1).
Figure 1. Mean of soybean vein necrosis virus log copies in N. variabilis adults that exhibited successful virus transmission in leaf-disk assays. The number of SVNV-NP RNA in individual adults was categorized into each order from < 101 to 106. Numbers in parentheses above each bar represent the number of N. variabilis in each virus titer category. Transmission rate was calculated by dividing the number of individuals per category by total number of positive insects (n = 84).
Immunodetection of SVNV in N. variabilis Guts and Salivary Glands
The presence of SVNV virions in alimentary canal and salivary glands of adult N. variabilis after 6, 12, and 24 h AAP was detected using indirect immunofluorescence technique with primary antibody against SVNV-NP and FITC fluorophore-conjugated secondary antibody targeting the primary antibody and imaged using confocal fluorescent microscopy. Thrips fed on SVNV-free soybean leaves were used as negative control (Figures 2A–E). A total of 70 thrips were evaluated and 57 (81%) were considered SVNV-positive due to the detection of fluorescent signals in the various tissues. SVNV infection of each tissue from adult N. variabilis after varying AAP is summarized in Table 2. In adult N. variabilis, strong signals were detected in the foregut (FG), with high frequency of FG infection (>50%) at 12 and 24 h AAP. Foregut infection was only observed when MG1 was infected, indeed there was a significant association between FG and MG1 infection at 6-h AAP (χ2 = 11.045, df = 1, P = 0.001), but not at 12 and 24 h AAP (χ2 = 1.296, df = 1, P = 0.255 and χ2 = 1.279, df = 1, P = 0.258, respectively). Among three sections of midgut (MG1, MG2 and MG3), the highest percentage of infection was observed in MG1 followed by MG2 and MG3 (Table 2). Infection of the PSG was observed when the TSG were infected, however, the correlation was not statistically significant at either AAPs.
Figure 2. Immunodetection of SVNV in guts and salivary glands of N. variabilis adults. Localization of viral particles in the foregut (FG), midgut region 1 (MG1), midgut region 2 (MG2), principal salivary gland (PSG), and tubular salivary glands (TSG) was observed by confocal fluorescence microscopy with FITC conjugated secondary antibody against the primary antibody targeting SVNV-NP. The control for the labeling was SVNV-free or uninfected adult N. variabilis (A–E). SVNV infection in adults post 6 h AAP (F–J), post 12 h AAP (K–O), and post 24 h AAP (P–T). Green, blue and red fluorescences indicate presence of SVNV-NP, nuclei (DAPI) and actin (phalloidin conjugated to iFluor 594), respectively. Yellow arrows indicate intense fluorescent signal. White scale bar (50 μm) and yellow scale bar (20 μm).
Table 2. Immunodetection of SVNV in adult N. variabilis exposed to varying Acquisition access period (AAP) on SVNV-infected leaf tissues.
Frequency of SVNV infection in individual tissues including FG, MG1, MG2 and MG3, TSG, and PSG varied with AAP duration (Figures 2A–D,F–T and Table 2). At 6 h AAP, significantly lower virus infection was found in FG (χ2 = 5.847, df = 1, P = 0.016), MG2 (χ2 = 6.041, df = 1, P = 0.014), TSG (χ2 = 7.795, df = 1, P = 0.005) and PSG (χ2 = 7.052, df = 1, P = 0.008) compared to 12 h AAP (Table 2). Of the infection between 6 and 24 h AAP, significantly lower infection was found in MG2 (χ2 = 4.102, df = 1, P = 0.043) and PSG (χ2 = 4.248, df = 1, P = 0.039). The percentage of SVNV-infected tissues were similar between 12 and 24 h AAP (Table 2). Overall, the length of AAP did not affect virus infection in MG1, however, significantly lower infection was observed in FG, MG2, and PSG post 6 h AAP.
Given the significance of PSG infection in virus transmission, we quantified PSG infection indirectly by the MIS. We found significantly lower amount and extent of infection at 6 h AAP compared to 12 and 24 h AAP, but higher than SVNV-free control (Figure 3, P < 0.0001). It was not uncommon that SVNV infection was not detectable in PSG at 6 h AAP (Figure 2J). There was no significant difference of MIS in PSG between 12 and 24 h AAP (Figure 3). Overall, results of the confocal experiments mirror the transmission assay, in that lowest virus transmission was observed at 6 h AAP, which also had lowest frequency of SVNV infection in the various tissues. In addition, the frequency of infected tissues was largely similar between 12 and 24 h AAP and no significant difference in transmission rate was observed in the leaf-disk assay using ELISA (Tables 1, 2).
Figure 3. Mean intensity of fluorescence signal (MIS) in PSG of N. variabilis after varying time of AAP. Means that do not share a letter are significantly different.
Immunodetection of SVNV in F. tritici and F. fusca Guts and Salivary Glands
SVNV accumulation in adult F. fusca and F. tritici after 24 h AAP was investigated using the same immunolabeling procedure described for N. variabilis. A total of 22 F. fusca and 23 F. tritici were tested, among which 15 (68%) and 6 (26%) were considered SVNV-positive, respectively. The percentage of infection of each tissue for F. fusca and F. tritici is summarized in Table 3. Signals of virus infection was detected in all the examined tissues in F. fusca and F. tritici except for MG3 in F. tritici (Table 3 and Figure 4). The FG showed high frequency of infection in F. fusca but low infection in F. tritici (Table 3 and Figure 4). Consistent with the pattern observed in N. variabilis (Table 2), the MG1 showed the highest infection rate among the three regions of midgut in both F. fusca and F. tritici (Table 3). Unlike N. variabilis, where no significant association existed for SVNV infection between FG and MG1, we found a significant association between FG and MG1 in F. fusca and F. tritici (χ2 = 4.792, df = 1, P = 0.029 and χ2 = 3.972, df = 1, P = 0.046, respectively). The extremely low infection rate of PSG in F. tritici (9%) very likely contributed to their inefficiency for virus transmission. The MIS in PSG of F. tritici was lower than F. fusca after 24 h AAP but the difference was not significant (P = 0.822) (Figure 5).
Table 3. Immunodetection of SVNV in adult Frankliniella fusca and F. tritici exposed to 24 h Acquisition access period (AAP) on infected leaf tissues.
Figure 4. Immunodetection of SVNV in guts and salivary glands of F. fusca and F. tritici adults. Localization of viral particles in the foregut (FG), midgut region 1 (MG1), midgut region 2 (MG2), principal salivary gland (PSG) and tubular salivary glands (TSG) was observed by confocal fluorescence microscopy with FITC conjugated secondary antibody against the primary antibody targeting SVNV-NP. SVNV infection in adult F. fusca (A–D) and F. tritici (E–H) post 24 h AAP. The control for the labeling was SVNV-free or uninfected adult of each species (Data not shown). Green, blue and red fluorescences indicate presence of SVNV-NP, nuclei (DAPI) and actin (phalloidin conjugated to iFluor 594), respectively. Yellow arrows indicate intense fluorescent signal. Scale bar indicates 50 μm.
Figure 5. Mean intensity of fluorescence signal (MIS) in PSG of secondary vectors, F. fusca, and F. tritici after 24 h AAP. Means that do not share a letter are significantly different.
The viral load or number of virus RNA in transmitting adult thrips is considered a key determinant of virus transmission. For example, Nagata et al. (2002) found that adults of F. occidentalis that transmitted TSWV efficiently harbored higher titers of the virus compared to T. tabaci that failed to transmit the virus. Another study reported a positive correlation between transmission efficiency of thrips and TSWV titer in host plants (Okazaki et al., 2011). Rotenberg et al. (2009) found that not only was TSWV titer an important factor for vector competence, but virus titer was positively associated with frequency of transmission events. In contrast to the TSWV-thrips system, we did not detect a significant correlation between virus transmission rate (binomial response -positive or negative) measured by ELISA absorbance ratios and SVNV-NP RNA levels in corresponding N. variabilis adults. Indeed, some thrips having high virus titer (104–105) had similar transmission abilities like those harboring less virus titer (102). Similar result was reported for southern rice black-streaked dwarf virus accumulation in Sogatella furcifera adults (Matsukura et al., 2015). One possibility to explain this reduced transmission could be the failure of virus infection of the salivary glands or limited virus accumulation in these glands despite the vectors harboring high virus titer in their gut and other tissues. Also, extensive accumulation of viruses sometimes has negative impact on vector insects, such as lower feeding activity and reduced fitness (Robb, 1989; DeAngelis et al., 1993; Matsukura et al., 2015). Previously, we showed that fecundity of N. variabilis decreased with increasing viral titer (Keough et al., 2016). It is possible that excessive accumulation of SVNV might result in a lower virus transmission rate because of lower fecundity resulting from lower feeding activity of N. variabilis. Research is underway in our laboratory to determine the effect of viral load on probing activity of male and female thrips using the Electrical Penetration Graph (EPG) technique. Moreover, quantification of virus titer in salivary glands could be more informative because infection of the salivary glands is a requirement for virus transmission to occur. Nevertheless, knowledge of viral titer in the vector is a useful indicator to manage virus epidemics in the field.
Analysis of SVNV-NP protein revealed the presence of the virus in the foregut (FG), midgut (MG), tubular salivary gland (TSG) and principal salivary gland (PSG) of adult N. variabilis. We found that the MG had highest virus infection compared to other tissues. In adults that had high percentage of PSG infection (12 and 24 h AAP), the first region of the midgut (MG1) had slightly greater percentage of infection than that observed in the second and third regions of the midgut (MG2 and MG3, respectively). It has been reported that midgut regions have distinct morphological, histological, and genetic properties (Buchon et al., 2013; Marianes and Spradling, 2013; O’Brien Lucy, 2013), which may result in different regions being more or less competent to virus infection. We also observed a high frequency of FG infection at 12 and 24 h AAP (67 and 65%, respectively). In contrast, Montero-Astúa et al. (2016) reported ≤30% infection of FG in F. occidentalis adults post 18 h AAP on TSWV-infected tissues as first instars. It is believed that the infection first begins in the first larval instar by infecting MG1, followed by infection of midgut muscle cells, the TSG and the efferent duct that leads to the PSG. In adults, infection could spread from MG1 to the FG, MG2, and MG3 from previously infected tissues such as ligaments that connect at the junction of the FG and MG1, by cell-to-cell movement through midgut epithelial cells and/or midgut muscle cells (Nagata et al., 1999; Kritzman et al., 2002). Hence, the primary site of virus infection is shifted from MG1 and TSG in larvae to PSG in adults (Montero-Astúa et al., 2016). Our results reveal a high frequency of SVNV infection in FG and MG1 and MG2 of adult soybean thrips that showed consistent PSG infection. Since we did not analyze virus infection in larval stages, we cannot make conclusions about changes in tissue tropism from larvae to adults. Nevertheless, the importance of secondary amplification of the virus in other organs outside the MG before reaching the PSG needs further investigation. Analysis of N. variabilis adults where the PSG and TSG were intact showed co-occurrence of virus infection in the two tissues albeit not statistically significant. This confirms previous reports that TSG serve as conduit for virus movement from MG1 to the PSG in adult thrips (Ullman et al., 1992; Nagata et al., 1999; Montero-Astúa et al., 2016). Overall, there appears to be similarities and differences between the TSWV-F. occidentalis system and SVNV- N. variabilis system. Viral proteins were detected in similar organs in F. occidentalis and N. variabilis, and adults with consistent PSG infection are likely to have corresponding TSG infected. N. variabilis adults that had high PSG infection also had high percentage of FG and MG2 infection, whereas FG and MG2 infection was low in F. occidentalis adults. This suggest greater lateral cell migration of virions in N. variabilis compared to F. occidentalis adults. Lastly, both MG1 and PSG were heavily infected in N. variabilis adults, whereas PSG appear to be primary site of virus infection in adult F. occidentalis.
Based on our previous results from acquisition and transmission assays, we wanted to investigate the effect of AAP on SVNV accumulation in alimentary canal and salivary glands of N. variabilis. Our analysis revealed that most N. variabilis adults became infected after AAP of 6, 12, or 24 h with the infection found in all organs being studied. Interestingly, the length of AAP did not affect virus infection in MG1, however, significantly lower infection was observed in FG, MG2, and PSG post 6 h AAP. In a previous study, there was no effect of AAP on MG infection in adult F. occidentalis, however, the percentage of infected vesicular muscles cells was lower in thrips fed on infected plants for 3 h than those which had fed for 16 h AAP (Nagata et al., 1999). The percentage of PSG infection was significantly lower for N. variabilis adults that acquired the virus as larvae after 6 h AAP than 12 and 24 h AAP, where infection rates of PSG were nearly 2.5 and 1.7 times higher, respectively. This suggests that there are significant differences in development of infection in larval tissues when given shorter time of virus acquisition. Since transmission efficiency is highly dependent on the degree of infection of PSG, the partial and/or weak infection of PSG at 6 h AAP could result in much lower transmission rate than the actual infection rate of PSG (Nagata et al., 1999). Overall, results from the transmission assays and immunolabeling experiments suggest that shorter AAP results in reduced virus infection in the various tissues especially in the PSG which could be due to the restriction of virus to the midgut and/or failure to disseminate from the midgut to PSG, which subsequently results in reduced transmission efficiency.
Two secondary vector species, F. fusca and F. tritici that fed on SVNV-infected tissue for 24 h as first instar larvae were able to acquire and transmit the virus as indicated by detection of viral proteins (N) in individual thrips using confocal fluorescence microcopy. However, the frequency of infected tissues was lower in F. fusca and F. tritici compared to the primary vector, N. variabilis. These results are in concordance with our previously published work where we found presence of non-structural NSs proteins in adult F. fusca and F. tritici after feeding on virus-infected material, which confirmed virus replication in these insects (Keough et al., 2016). The pattern of virus accumulation in N. variabilis, F. fusca, and F. tritici was similar except for lack of virus infection in MG3 of F. tritici. SVNV was also detected in TSG and PSG of both secondary vectors, which supports the theory that TSG serve as potential route for tospoviruses to infest PSG in thrips vectors. Our data showed that SVNV is able to infect PSG of F. tritici after 24 h AAP on virus-infected material. A previous study did not detect TSWV-NSs protein in PSG, ligaments, TSG, and hindgut of F. tritici (de Assis Filho et al., 2005). Unlike TSWV, it appears that SVNV has evolved the ability to be acquired and transmitted by a previous non-vector of tospovirus, F. tritici. Overall, results of our study identified similarities and differences in virus transmission mechanisms compared to the well-studied TSWV-F. occidentalis system. There appears to be distinct associations between thrips species and their ability to transmit tospoviruses (Jones, 2005), hence it is important to assess vector competence in each thrips species. Future research should be aimed at tissue-specific analysis of thrips-encoded proteins that mediate virus replication which would greatly improve our knowledge of molecular interaction between the virus and vector and identify novel targets for development of transgenic technologies to limit the ability of insect vectors to transmit plant pathogens.
PN conceived and designed the experiments, analyzed the data, and wrote the manuscript. JH performed the experiments, analyzed the data, and wrote a draft of the manuscript. VN analyzed the data and revised the manuscript. I-CY provided training for use of the confocal microscope. All authors read and approved the final manuscript.
This research was funded by grants from the Indiana Soybean Alliance and USDA National Institute of Food and Agriculture-Agriculture and Food Research Initiative (USDA NIFA-AFRI) Grant No. 2014-67014-21719.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
We would like to thank Agdia Inc., Elkhart, Indiana for providing SVNV-NP antibody. We also acknowledge Dr. Mauricio Montero Astúa for helpful comments on an earlier version of the manuscript. We thank the editor and reviewers for their helpful comments and suggestions.
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmicb.2019.00431/full#supplementary-material
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Keywords: soybean vein necrosis virus, thrips, vector competence, immunolabeling, confocal microscopy
Citation: Han J, Nalam VJ, Yu I-C and Nachappa P (2019) Vector Competence of Thrips Species to Transmit Soybean Vein Necrosis Virus. Front. Microbiol. 10:431. doi: 10.3389/fmicb.2019.00431
Received: 27 November 2018; Accepted: 19 February 2019;
Published: 19 March 2019.
Edited by:Nobuhiro Suzuki, Okayama University, Japan
Reviewed by:Taiyun Wei, Fujian Agriculture and Forestry University, China
Massimo Turina, Italian National Research Council (CNR), Italy
Copyright © 2019 Han, Nalam, Yu and Nachappa. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Punya Nachappa, email@example.com