The authors would like to thank Mant Acon for the plants used in this study. The funding was provided by the U.S. Department of Agriculture (USDA) CRIS project 8062-22410-007-000-D and USDA NIFA grant 2020-70029-33176.

1. Production of citrus plants for experimental compound injection
<ol>
	<li>Propagate small potted citrus trees from either rooted vegetative cuttings or seeds. Grow the potted citrus lines under a 16 h/8 h light/dark day length and at 28 &#176;C.</li>
	<li>Select citrus plants of the appropriate size for the experiment. The described applications required the plants to be between 12 cm and 100 cm in height with trunk diameters of 4-14 mm. If new flush growth is required, cut back the plants prior to the experiment.</li>
</ol>
2. Three-dimensional printing of the DPI device and mold components
<ol>
	<li>Apply a thin layer of polyvinyl acetate-based glue to the print bed.</li>
	<li>Load nylon filament into the 3D printer, and prepare the printer according to the manufacturer&#39;s instructions. Import the desired .STL file (Supplementary File 1, Supplementary File 2, Supplementary File 3, Supplementary File 4, Supplementary File 5, Supplementary File 6, Supplementary File 7, Supplementary File 8, Supplementary File 9, Supplementary File 10, Supplementary File 11, Supplementary File 12, Supplementary File 13, and Supplementary File 14), set up, and start printing.</li>
	<li>Remove the piece from the print bed. Rinse the polyvinyl acetate-based glue from the base of the printed component with water, and remove any support structures.</li>
	<li>Spray the DPI component with two coats of clear gloss spray paint.</li>
</ol>
3. Fabrication of the plastisol ring mold
<ol>
	<li>Assemble a mold form large enough to hold the pattern pieces by building a rectangular enclosure using snap-together plastic blocks on a base (Supplementary Figure S1A).</li>
	<li>Mix the RTV silicone monomer and the catalyst together at a 10:1 ratio, and stir without introducing bubbles for 1 min. Color by adding food coloring (3 drops/25 mL of silicone mixture) and hand soap (1 mL of soap/25 mL of silicone mixture) (Supplementary Figure S1B).</li>
	<li>Pour a thin layer of silicone into the mold form that is sufficient to completely cover the bottom. Tamp to flatten the surface, and wait 24 h for the silicone to set (Supplementary Figure S1C).</li>
	<li>Pour a second layer of silicone, as described above, that is deep enough to cover the center hole core print on the pattern (visible at the top of the pattern in Supplementary Figure S1D). Insert the pattern into the liquid silicone with the center hole core print facing down. Ensure that no bubbles are trapped and that the patterns are well separated and not touching (Supplementary Figure S1E).</li>
	<li>Secure the patterns with either a heavy object and/or tape to prevent them from floating out of the silicone while it sets. Wait 24 h for the newly poured layer to set (Supplementary Figure S1F).</li>
	<li>Pour additional layers of silicone until the level is flush with the top of the pattern. Wait 24 h to cure (Supplementary Figure S1G).</li>
	<li>Disassemble the snap-together plastic blocks to release the mold. Remove the patterns (Supplementary Figure S1H). Inspect the mold for tears or deformities (Supplementary Figure S1I).</li>
</ol>
4. Casting of the plastisol rings
<ol>
	<li>Coat the interior of the mold, all the core components, and the O-rings with cooking oil (Supplementary Figure S2A, B). Place an O-ring around the notch in the middle of the center post core, and place the core in the center hole of the plastisol ring mold (Supplementary Figure S2C).</li>
	<li>Insert the delivery channel core into the hole on the side of the plastisol ring mold. Orient the V-shaped tip at the end of the delivery channel core to align with the O-ring on the center post core (Supplementary Figure S2D,E).</li>
	<li>Heat plastisol in the microwave for short 10 s bursts (Supplementary Figure S2F, G). Stir plastisol gently to avoid bubbles (Supplementary Figure S2H). Repeat the heating and stirring until the solution reaches a temperature between 160 &#176;C and 170 &#176;C (Supplementary Figure S2I). 
	CAUTION: Overheating of the plastisol can lead to the release of toxic fumes. Perform the procedure in a well-ventilated area or fume hood. Do not heat the plastisol over 170 &#176;C.</li>
	<li>Pour the molten plastisol into the plastisol ring mold near the outside edge of the mold without introducing bubbles (Supplementary Figure S2J). Wait 1 h for the plastisol rings to cool (Supplementary Figure S2K). Remove the rings from the mold. Ensure proper fit with the DPI device before use in experimental assays (Supplementary Figure S2L).</li>
</ol>
5. Attachment of the DPI device to the plant
<ol>
	<li>Find a smooth, healthy site on the trunk for the device attachment. Avoid any bumps or knots, as these can contribute to device leakage.</li>
	<li>Use a 2 mm diameter drill bit to drill a hole horizontally through the center of the stem at a 90&#176; angle with the trunk surface (Supplementary Figure S3A). Run the drill bit through the hole several times to clean and smooth it to create an unobstructed hole (Supplementary Figure S3B).</li>
	<li>Create a vertical slice in the plastisol ring on the opposite side of the compound delivery channel (Supplementary Figure S3C). Fit the ring around the plant, and line the delivery channel up with the previously drilled hole (Supplementary Figure S3D). 
	NOTE: The ring must fit snugly around the trunk to avoid leakages; core assemblies with various diameters can be used to make plastisol rings for different-sized plant stems.</li>
	<li>Add the DPI device to the plastisol ring, ensuring they fit snugly together. Align the DPI device spout with the plastisol ring delivery channel and drilled hole (Supplementary Figure S3E). 
	NOTE: Using a drill bit to line up the hole and the DPI device spout can be helpful.</li>
	<li>Wrap tightly with silicone tape to hold the apparatus in place (Supplementary Figure S3F). Inspect the fully assembled and attached device to ensure proper alignment and orientation on the plant.</li>
</ol>
6. Applying the compound of interest using the DPI device
<ol>
	<li>Use a syringe or pipette to fill the DPI device with the solution of interest (Supplementary Figure S3G). Use a syringe to penetrate the silicone tape and plastisol ring on the opposite side of the DPI device to pull air out of the interior channel and avoid the introduction of air bubbles into the plant vasculature (Supplementary Figure S3H). Replace any extracted compound back into the DPI device.</li>
	<li>Add an additional small patch of silicone tape over the hole created by the syringe to reinforce the area and prevent tears. Inspect the apparatus for visible leakages at the attachment point, and inspect the device reservoir for a stable liquid level. 
	NOTE: Water can be used initially to test for leaks to avoid waste of test solution.</li>
	<li>Cover the open end of the DPI device with wax sealing film, and pull down to form a seal and reduce the evaporation of the experimental compound. Poke a single hole in the wax film with a syringe tip to prevent the development of a vacuum, and subsequently refill the device (Supplementary Figure S3I).</li>
	<li>Check the apparatus daily to ensure proper alignment of the components (Supplementary Figure S3J), and top off the liquid using a syringe to avoid the reservoir running dry. Repeat this process until the desired amount of experimental solution has been introduced. 
	NOTE: Compounds can be successfully introduced from a given device for up to 1 month. Solution uptake durations that exceed this time frame should be tested empirically before the experimental setup.</li>
</ol>
7. Using CFDA to observe vascular movement with citrus plants
<ol>
	<li>Attach the DPI device to 25 cm tall citron (Citrus medica L.) plants, apply a single 2.0 mL treatment of either 20% DMSO in H2O control or CFDA to the DPI device, and allow it to uptake for 24 h. To follow this protocol, prepare the working CFDA solution by adding 1.6 mL of H2O to 400 &#181;L of CFDA stock solution (the stock solution contains 10 mM CFDA dissolved in 100% dimethyl sulfoxide [DMSO]) to generate a final CFDA concentration of 2 mM and 20% DMSO.</li>
	<li>Make cross-sections of various tissues of the plant, and use a stereoscope or compound microscope with a fluorescent filter that includes the 498 nm wavelength to visualize the CFDA in the plant tissues. Compare the images to the 20% DMSO in H2O controls to account for autofluorescence in the tissue.</li>
</ol>
8. Measuring changes in the CLas titer in leaf samples following streptomycin treatment
<ol>
	<li>Using 0.75 m tall greenhouse-grown CLas-infected Valencia (Citrus sinensis (L.) Osbeck &#34;Valencia&#34;) plants, collect the petiole and midrib of two HLB symptomatic leaves from each plant, chop them into small sections, pool each tissue type, and store them separately in 2 mL impact-resistant sample tubes containing a steel ball of 6.35 mm in diameter.</li>
	<li>Grind the sample using a homogenizer programmed for two 15 s cycles at 3.4 m/s. Extract the total nucleic acid as described previously19.</li>
	<li>Perform qPCR on the CLas-infected leaf samples using the qPCR mix defined in Table 1 and the reaction conditions defined in Table 2. Use plants showing robust CLas infections (robust infection is generally defined as qPCR-based Ct values &#60; 30 for the CLas 16S LasLong (LL) primer set) for further analysis. 
	NOTE: The bacterial titer is estimated using CLas 16S Las Long (LL) and citrus dehydrin DNA primers to estimate the relative genome equivalents, as described previously20.</li>
	<li>Outfit the citrus plants that meet the minimum infection titer outlined above with DPI devices, and subject them to a one-time treatment of 2.0 mL of either H2O solution or streptomycin solution at the desired concentration. To follow this study, use a single 2.0 mL treatment of 9.5 mg/mL (19 mg in total) streptomycin dissolved in H2O.</li>
	<li>Collect leaf samples at 7 days, 14 days, and 28 days post treatment. Assay the sampled leaves for the CLas titer using the same protocol as described above.</li>
	<li>At 60 days post treatment, obtain photographs of the plants treated with H2O or streptomycin. Use visual observations of the CLas infection to score the infection severity. Look for &#60;50% of leaves showing interveinal chlorosis and vein corking along with leaf flush growth as signs of mild infection and greater than 50% of leaves with interveinal chlorosis and vein corking as well as leaf abscission and stunting of the plant growth as signs of more severe infections.</li>
</ol>
9. Measuring the mortality of&#160; D. citri following imidacloprid treatment
<ol>
	<li>Prune 0.5 m tall citron (Citrus medica L.) plants to a height of 12 cm to encourage the growth of new flush. 
	NOTE: The speed of flush growth can be dependent upon the plant health and time of year; so, take this into account during experimental design.</li>
	<li>After &#62;6 flush, 1-2 cm in length, have developed, introduce the plants into cages containing adult D. citri. Leave the plants in the cages for 24 h to allow for the deposition of eggs.</li>
	<li>Conduct representative egg counts on three flush shoots 1-2 days after laying, and subsequently apply the DPI devices. Fill these devices with 2.0 mL of either a water control or the desired concentration of imidacloprid (21.8% active ingredient). To follow this protocol, use 528 &#181;L/L, 52.8 &#181;L/L, and 5.28 &#181;L/L of imidacloprid. 
	NOTE: Egg counts are a destructive measure, so the counts at this stage are used to estimate the number of eggs on the uncounted flush of the same plant and help provide a baseline for the subsequent nymph emergence counts that are conducted at the end of the experiment.</li>
	<li>Collect the D. citri emergence rate on at least three of the remaining flush shoots. Acquire representative plant photographs 7 days after compound introduction.</li>
</ol>

Molecule Delivery in Plants Using a Direct Infusion Device

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The authors have no conflicts of interest. The use of trade, firm, or corporation names in this publication is for the information and convenience of the reader. Such use does not constitute an official endorsement or approval by the United States Department of Agriculture or the Agricultural Research Service of any product or service to the exclusion of others that may be suitable. The U.S. Department of Agriculture (USDA) prohibits discrimination in all its programs and activities on the basis of race, color, national origin, age, disability, and where applicable, sex, marital status, familial status, parental status, religion, sexual orientation, genetic information, political beliefs, reprisal, or because all or part of an individual's income is derived from any public assistance program. Not all prohibited bases apply to all programs. Persons with disabilities who require alternative means for communication of program information (Braille, large print, audiotape, etc.) should contact USDA's TARGET Center at (202) 720-2600 (voice and TDD). To file a complaint of discrimination, write to USDA, Director, Office of Civil Rights, 1400 Independence Avenue, S.W., Washington, D.C. 20250-9410, or call (800) 795-3272 (voice) or (202) 720-6382 (TDD). USDA is an equal opportunity provider and employer.

For the DPI device to be considered a viable method for exogenous compound delivery into plants, it must contribute to robust and consistent compound uptake into a variety of tissue types. The experiment utilizing CFDA clearly showed both acropetal and basipetal compound movement, as well as in both the vascular system and mesophyll cells of the leaf. Additionally, and presumably because the bored hole used in this DPI device provides a large amount of surface area for compound uptake, the CFDA was present in relatively equal amounts in all sections of the stem, not just in a small subset of the vasculature adjacent to the device, as has been seen in previous dye uptake studies in plants using trunk injection6. Additionally, the delivery of green fluorescent protein and floral dye was tested using the DPI device, and a distribution of these compounds similar to CFDA was observed (data not shown). These data suggest that the device can be used to systemically deliver a variety of compounds that vary in size and molecular structure. However, it is worth noting that there were differences in the compound uptake based on the leaf development stage, with younger developing leaves taking up more compound than older established leaves. This may be due to the changes in the vasculature properties present in sink versus source tissue and should be optimized for a given experiment. 
The DPI device showed sufficient compound uptake for the visualization of CFDA, GFP, and floral dye, and it also took up enough to show the antibacterial and insecticidal effects of streptomycin and imidacloprid, respectively. Both these compounds resulted in changes in the target organism viability 1 week after a single 2.0 mL treatment. These data suggest that the DPI device could be used in whole-plant assays to test the viability of a wide variety of compounds for the control of microbial and insect pests. Moreover, due to its direct contact with the vascular system, this device may even provide an opportunity to test compounds that are not efficiently taken up by the roots or epidermal cells. Of particular interest would be RNA interference (RNAi), as this could be used to modulate the gene expression within the host plant, pathogen, or pathogen vector. Previous research that introduced hairpin RNA through a drilled hole in the trunk of apple and grape plants showed that the RNA molecules were restricted to the xylem tissue, suggesting that these molecules may only be effective against chewing and xylem sap-feeding organisms22. Given that the DPI device uses a similar drilled-hole delivery system, it stands to reason that hairpin RNA delivered with this device may also be restricted to the xylem tissue. However, the observed decrease in the titer of the phloem-limited CLas after streptomycin treatment from the DPI device strongly suggests that this antibiotic was present in the phloem. Therefore, it is likely that the vascular distribution of the compounds delivered using the DPI device is dependent on their size and chemistry, and each molecule should be evaluated on an individual basis.
Although there are a number of commercially available DPI devices available on the market, the device described here can be manufactured in-house and is modifiable. In this way, improvements and changes in size may be made based on the plant species and experimental design being used, and it is not reliant on commercial products. In addition, the device is semi-permanently attached to the plant, meaning that multiple treatments of a given compound can be performed concurrently without having to reinjure the plant with multiple compound injections. On a cautionary note, the device can leak if not installed properly. As a result, the compound is lost to the environment instead of being delivered to the plant. Therefore, care should be taken to inspect the device for any signs of leakage during setup and the first few days afterward. Although drilling a hole in the tree is potentially harmful, this method was chosen to ensure robust and consistent compound uptake. Additionally, no adverse effects on plant health were seen from the attachment of the DPI device in these experiments. However, extra plants should be included in the experimental design to replace those that may lose vigor throughout the course of a given experiment. Lastly, since this device uses passive flow to introduce compounds, it can be difficult to predict the rate of uptake across different plant species or developmental stages of the same species. This may complicate experiments if the speed of compound uptake is a limiting factor. For the best results, experiments should be planned so that sufficient time is provided for the plant to fully absorb the 2.5 mL of compound, which can take up to 1 week. In conclusion, this DPI device is an effective tool for the rapid evaluation of the in planta activity of antimicrobial or insecticidal compounds against CLas and its vector, D. citri, thus providing more information on the systemic effectiveness and influence on plant performance than the previously presented detached leaf assay23. Undoubtedly, the variety of applications for this system reaches well beyond the specific uses described in this study.

The management of plants in commercial and landscape settings often requires the use of chemical compounds to optimize the plant growth and health. How these molecules are delivered depends on the type of molecule, the function of the molecule, the type of plant, and the management system in place. Foliar and soil applications are the easiest delivery strategies, but limitations in the uptake of some molecules necessitate direct delivery. An example of these molecules is therapeutic molecules that function best when they move systemically within the plant but cannot be effectively delivered by simple topical applications1. This is the case with Huanglongbing (HLB), also called citrus greening disease. HLB is a disease associated with a phloem-limited bacterium, Candidatus Liberibacter asiaticus (CLas), which cannot be cultured outside of the plant, or its insect vector, Diaphorina citri Kuwayama (D. citri)2.
If the putative therapeutic molecules are gene products, they can be tested by creating transgenic plants expressing these compounds. However, transgenic plant production can be time- and resource-intensive, is highly genotype-dependent, and can be inhibited by gene silencing3. In addition, even if these transgenics show promising results, regulatory and public perception constraints reduce the likelihood of their commercial acceptance4,5. The exogenous application of compounds, however, simplifies the testing of biological and synthetic molecules because it does not require the production of stable or transiently expressing transgenic plants, which reduces the time and resources for testing a molecule&#39;s effects. A method for the effective and efficient systemic plant delivery of exogenous compounds could be used for a wide variety of research and screening purposes.
One of these applications is the analysis of systemic molecule movement within a plant&#39;s vascular system, which can be done using trackable markers, whether they are fluorescent, visible, or unique chemical isotopes6,7,8,9. One commonly used fluorescent marker is 5,6-carboxyfluorescein-diacetate (CFDA), which is a membrane-permeable dye that is degraded by intracellular esterases into 5,6-carboxyfluorescein (CF) and, subsequently, becomes fluorescent and membrane-impermeable10. CFDA has been extensively used to monitor phloem transport, sink and source relationships, and vasculature patterning in plant tissue11,12.
In addition to these markers, certain compounds may directly alter the plant&#39;s physiology to increase the productivity or kill the plant in the case of herbicides. Both insecticides and antimicrobial compounds are a means of increasing plant productivity, especially in the presence of HLB. An example of an antimicrobial molecule that is used to control CLas is streptomycin. Streptomycin is an aminoglycoside antibiotic that was originally isolated from Streptomyces griseus and has been shown to inhibit bacterial growth through the inhibition of protein biosynthesis13. In terms of insecticides, the main target for HLB research is D. citri, which transmits CLas from tree to tree14. For this purpose, neonicotinoids, such as imidacloprid, are commonly utilized, as they are the gold standard for controlling insect pests15. All these varied uses are important aspects of current plant management strategies, and the development of novel products is dependent on efficient screening assays.
One method that is used for the introduction of compounds into woody plants is direct injection into the trunk. A variety of systems have been designed that vary in their needs for predrilled injection sites, and these systems utilize either pressure-based injection or passive flow16. Although pressure-based systems allow for the quick introduction of a given compound, the potential physical damage caused by forcing liquid through blocked or embolized vasculature needs to be considered17. Although the foliar or drench application of compounds is less time-intensive to implement, direct plant injection reduces waste of the compound of interest due to losses to the air or soil and can also lengthen the time that compounds are in an active state by reducing the exposure to the outside environment18. Both these aspects are important for preserving expensive reagents and ensuring consistency among replicates in research settings.
This study describes the design, construction, and use of an innovative direct plant infusion (DPI) device, which can be used to assess how compounds of interest affect a host plant. A standard 3D printer was used to manufacture both the device itself and several components associated with its construction. This in-house construction method allows researchers to modify the device and device components based on their specific experimental needs and reduces the reliance on commercially available plant injection devices. The device setup is simple and efficient, and all the auxiliary components are readily available and inexpensive. Although the system was designed for use with a variety of plant species, the examples presented here pertain to potted citrus plants. Additionally, this study demonstrates that this device is capable of efficiently delivering multiple types of compounds systemically to young citrus plants without causing lethality. The compounds tested included CFDA, which was used to assess the compound distribution in the plant, and streptomycin and imidacloprid, which were used to verify that the antimicrobial and insecticidal effects of these compounds were observed when delivered via DPI.

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>0.5 cm Diameter Steel Balls</td>
			<td>Ballistic Products Inc.</td>
			<td>#SHT #T</td>
			<td></td>
		</tr>
		<tr>
			<td>10 mL Luer-Lok Syringe</td>
			<td>Becton Dickinson</td>
			<td>382903029952</td>
			<td></td>
		</tr>
		<tr>
			<td>20 G 1 Syringe Needle</td>
			<td>Becton Dickinson</td>
			<td>305175</td>
			<td></td>
		</tr>
		<tr>
			<td>2 mL Screw Cap Tubes</td>
			<td>USA Scientific</td>
			<td>1420-9710</td>
			<td></td>
		</tr>
		<tr>
			<td>3/32nd Inch Black Oxide Drill Bit</td>
			<td>Sears</td>
			<td>964077</td>
			<td></td>
		</tr>
		<tr>
			<td>3D Printer</td>
			<td>Markforged</td>
			<td>F-PR-2027</td>
			<td></td>
		</tr>
		<tr>
			<td>3D Printing Software</td>
			<td>Markforged</td>
			<td>F-SW-FDVX</td>
			<td></td>
		</tr>
		<tr>
			<td>3D Printing Software</td>
			<td>Markforged</td>
			<td>S-FW-OEVX</td>
			<td></td>
		</tr>
		<tr>
			<td>5(6)-CFDA (5-(and-6)-Carboxyfluorescein Diacetate)</td>
			<td>Invitrogen</td>
			<td>C195</td>
			<td></td>
		</tr>
		<tr>
			<td>5/64th Inch Black Oxide Drill Bit</td>
			<td>Sears</td>
			<td>964502</td>
			<td></td>
		</tr>
		<tr>
			<td>96 Well qPCR Machine</td>
			<td>Roche</td>
			<td>5815916001</td>
			<td></td>
		</tr>
		<tr>
			<td>Centrifuge</td>
			<td>Eppendorf</td>
			<td>22621408</td>
			<td></td>
		</tr>
		<tr>
			<td>Fluorescent Microscope</td>
			<td>Olympus</td>
			<td>SP-BX43-BI</td>
			<td></td>
		</tr>
		<tr>
			<td>Fluorescent Microscope Filter</td>
			<td>Chroma</td>
			<td>69401-ET</td>
			<td></td>
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			<td>Gloss Clear Spray Paint</td>
			<td>Rustoleum</td>
			<td>249117</td>
			<td></td>
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			<td>Grey Lego Baseplate</td>
			<td>Lego</td>
			<td>11024</td>
			<td></td>
		</tr>
		<tr>
			<td>Handheld Cordless Drill</td>
			<td>Makita</td>
			<td>6349D</td>
			<td></td>
		</tr>
		<tr>
			<td>Homogenizer</td>
			<td>Fisher Scientific</td>
			<td>15-340-163</td>
			<td></td>
		</tr>
		<tr>
			<td>Imidacloprid 2F</td>
			<td>Quali-Pro</td>
			<td>83080133</td>
			<td></td>
		</tr>
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			<td>Liquid Plastisol Medium Hardness</td>
			<td>Fusion X Fishing Lures</td>
			<td>XSOL-505</td>
			<td></td>
		</tr>
		<tr>
			<td>Red Silicone 70 Shore A O-Ring</td>
			<td>Grainger</td>
			<td>Varies by Size</td>
			<td></td>
		</tr>
		<tr>
			<td>Non-Stick Cooking Spray</td>
			<td>PAM</td>
			<td>64144030217</td>
			<td></td>
		</tr>
		<tr>
			<td>NucleoSpin Plant II</td>
			<td>Macherey-Nagel</td>
			<td>740770.5</td>
			<td></td>
		</tr>
		<tr>
			<td>Parafilm</td>
			<td>Bemis</td>
			<td>HS234526A</td>
			<td></td>
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			<td>Poly Viyl Acetate Based Glue</td>
			<td>Elmers</td>
			<td>E301</td>
			<td></td>
		</tr>
		<tr>
			<td>qPCR Master Mix</td>
			<td>Promega</td>
			<td>A6001</td>
			<td></td>
		</tr>
		<tr>
			<td>qPCR Primers</td>
			<td>Integrated DNA Technologies</td>
			<td>Varies by DNA sequence</td>
			<td></td>
		</tr>
		<tr>
			<td>Reverse Transcriptase</td>
			<td>Promega</td>
			<td>A5003</td>
			<td></td>
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			<td>Single Edge Razor Blade</td>
			<td>Garvey</td>
			<td>40475</td>
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			<td>Translucent Silicone RTV Rubber</td>
			<td>Aero Marine Products</td>
			<td>AM 115T</td>
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			<td>Transparent Silicone Tape</td>
			<td>Maxwell</td>
			<td>KE30S</td>
			<td></td>
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			<td>Truncated Oncocin 112</td>
			<td>Genscript</td>
			<td>Varies by peptide sequence</td>
			<td></td>
		</tr>
		<tr>
			<td>White 1 x 6 Lego Piece</td>
			<td>Lego</td>
			<td>300901</td>
			<td></td>
		</tr>
		<tr>
			<td>White Nylon</td>
			<td>Markforged</td>
			<td>F-MF-0003</td>
			<td></td>
		</tr>
	</tbody>
</table>

direct infusion device for molecule delivery in plants

Testing the function of therapeutic compounds in plants is an important component of agricultural research. Foliar and soil-drench methods are routine but have drawbacks, including variable uptake and the environmental breakdown of tested molecules. Trunk injection of trees is well-established, but most methods for this require expensive, proprietary equipment. To screen various treatments for Huanglongbing, a simple, low-cost method to deliver these compounds to the vascular tissue of small greenhouse-grown citrus trees infected with the phloem-limited bacterium Candidatus Liberibacter asiaticus (CLas) or infested with the phloem-feeding CLas insect vector Diaphorina citri Kuwayama (D. citri) is needed.
To meet these screening requirements, a direct plant infusion (DPI) device was designed that connects to the plant&#39;s trunk. The device is made using a nylon-based 3D-printing system and easily obtainable auxiliary components. The compound uptake efficacy of this device was tested in citrus plants using the fluorescent marker 5,6-carboxyfluorescein-diacetate. Uniform compound distribution of the marker throughout the plants was routinely observed.
Furthermore, this device was used to deliver antimicrobial and insecticidal molecules to determine their effects on CLas and D. citri respectively. The aminoglycoside antibiotic streptomycin was delivered into CLas-infected citrus plants using the device, which resulted in a reduction in the CLas titer from 2 weeks to 4 weeks post treatment. Delivering the neonicotinoid insecticide imidacloprid into D. citri-infested citrus plants resulted in a significant increase in psyllid mortality after 7 days. These results suggest that this DPI device represents a useful system for delivering molecules into plants for&#160;testing and facilitate research and screening purposes.

Watch this Scientific Journal Video about Direct Infusion Device for Molecule Delivery in Plants at JoVE.com

Author Spotlight: Direct Infusion Device for Molecule Delivery in Plants  

This manuscript describes a novel direct plant infusion device for screening the effectiveness of molecules against the bacteria (Candidatus Liberibacter asiaticus) or its insect vector (Diaphorina citri, Kuwayama) that, in combination, are associated with Huanglongbing citrus disease.

Direct Infusion Device for Molecule Delivery in Plants

Testing the function of therapeutic compounds in plants is an important component of agricultural research. Foliar and soil-drench methods are routine but ...

direct-infusion-device-for-molecule-delivery-in-plants

Nanyang Technological University

Research

JoVE Journal

Biology

2.1K Views.  United States Department of Agriculture Agricultural Research Service U.S. Horticultural Research Laboratory. This manuscript describes a novel direct plant infusion device for screening the effectiveness of molecules against the bacteria (Candidatus Liberibacter asiaticus) or its insect vector (Diaphorina citri, Kuwayama) that, in combination, are associated with Huanglongbing citrus disease.

Video: Author Spotlight: Direct Infusion Device for Molecule Delivery in Plants  

Preparing E18 Cortical Rat Neurons for Compartmentalization in a Microfluidic Device

In this video, we demonstrate the preparation of E18 cortical rat neurons. E18 cortical rat neurons are obtained from E18 fetal rat cortex previously dissected and prepared. The E18 cortex is, upon dissection, immediately dissociated into individual neurons. It is possible to store E18 cortex in Hibernate E buffer containing B27 at 4&deg;C for up to a week before the dissociation is performed. However, there will be a drop in cell viability. Typically we obtain our E18 Cortex fresh. It is transported to the lab in ice cold Calcium free Magnesium free dissection buffer (CMFM). Upon arrival, trypsin is added to the cortex to a final concentration of 0.125%. The cortex is then incubated at 37&deg;C for 8 minutes. DMEM containing 10% FBS is added to the cortex to stop the reaction. The cortex is then centrifuged at 2500 rpm for 2 minutes. The supernatant is removed and 2 ml of Neural Basal Media (NBM) containing 2% B27 (vol/vol) and 0.25% Glutamax (vol/vol) is added to the cortex which is then re-suspended by pipetting up and down. Next, the cortex is triturated with previously fire polished glass pipettes, each with a successive smaller opening. After triturating, the cortex is once again centrifuged at 2500 rpm for 2 minutes. The supernatant is then removed and the cortex pellet re-suspended with 2 ml of NBM containing B27 and Glutamax. The cell suspension is then passed through a 40 um nylon cell strainer. Next the cells are counted. The neurons are now ready for loading into the neuron microfluidic device.

In this video we demonstrate the preparation of E18 Cortical Rat Neurons.

In this video, we demonstrate the preparation of E18 cortical rat neurons. E18 cortical rat neurons are obtained from E18 fetal rat cortex previously ...

Single Molecule Methods for Monitoring Changes in Bilayer Elastic Properties

Membrane protein function is regulated by the cell membrane lipid composition.  This regulation is due to a combination of specific lipid-protein interactions and more general lipid bilayer-protein interactions. These interactions are particularly important in pharmacological research, as many current pharmaceuticals on the market can alter the lipid bilayer material properties, which can lead to altered membrane protein function.   The formation of gramicidin channels are dependent on conformational changes in gramicidin subunits which are in turn dependent on the properties of the lipid.  Hence the gramicidin channel  current is a reporter of altered properties of the bilayer due to certain compounds.  

Membrane protein function is regulated by the cell membrane lipid composition. This video-article details how to form a patch using bilayer patch electrodes, as well as how to use gramicidin channels as reporters of altered membrane properties.

Membrane protein function is regulated by the cell membrane lipid composition.  This regulation is due to a combination of specific lipid-protein ...

Direct Observation of Enzymes Replicating DNA Using a Single-molecule DNA Stretching Assay

We describe a method for observing real time replication of individual DNA molecules mediated by proteins of the bacteriophage replication system. Linearized &lambda; DNA is modified to have a biotin on the end of one strand, and a digoxigenin moiety on the other end of the same strand. The biotinylated end is attached to a functionalized glass coverslip and the digoxigeninated end to a small bead. The assembly of these DNA-bead tethers on the surface of a flow cell allows a laminar flow to be applied to exert a drag force on the bead. As a result, the DNA is stretched close to and parallel to the surface of the coverslip at a force that is determined by the flow rate (Figure 1). The length of the DNA is measured by monitoring the position of the bead. Length differences between single- and double-stranded DNA are utilized to obtain real-time information on the activity of the replication proteins at the fork. Measuring the position of the bead allows precise determination of the rates and processivities of DNA unwinding and polymerization (Figure 2).

We describe a method for observing real time replication of individual DNA molecules mediated by proteins of the bacteriophage replication system.

We describe a method for observing real time replication of individual DNA molecules mediated by proteins of the bacteriophage replication system. ...

Generation of Composite Plants in Medicago truncatula used for Nodulation Assays

Similar to Agrobacterium tumerfaciens, Agrobacterium rhizogenes can transfer foreign DNAs into plant cells based on the autonomous root-inducing (Ri) plasmid. A. rhizogenes can cause hairy root formation on plant tissues and form composite plants after transformation. On these composite plants, some of the regenerated roots are transgenic, carrying the wild type T-DNA and the engineered binary vector; while the shoots are still non-transgenic, serving to provide energy and growth support. These hairy root composite plants will not produce transgenic seeds, but there are a number of important features that make these composite plants very useful in plant research. First, with a broad host range,A. rhizogenes can transform many plant species, especially dicots, allowing genetic engineering in a variety of species. Second, A. rhizogenes infect tissues and explants directly; no tissue cultures prior to transformation is necessary to obtain composite plants, making them ideal for transforming recalcitrant plant species. Moreover, transgenic root tissues can be generated in a matter of weeks. For Medicago truncatula, we can obtain transgenic roots in as short as three weeks, faster than normal floral dip Arabidopsis transformation. Overall, the hairy root composite plant technology is a versatile and useful tool to study gene functions and root related-phenotypes. Here we demonstrate how hairy root composite plants can be used to study plant-rhizobium interactions and nodulation in the difficult-to-transform species M. truncatula.

Generation of Composite Plants in Medicago truncatula used for Nodulation Assays

We demonstrate how hairy root composite plants can be used to study plant-rhizobium interactions and nodulation in the difficult-to-transform species Medicago truncatula.

Similar to Agrobacterium tumerfaciens, Agrobacterium rhizogenes can transfer foreign DNAs into plant cells based on the autonomous root-inducing (Ri) ...

In Situ Hybridization for the Precise Localization of Transcripts in Plants

With the advances in genomics research of the past decade, plant biology has seen numerous studies presenting large-scale quantitative analyses of gene expression. Microarray and next generation sequencing approaches are being used to investigate developmental, physiological and stress response processes, dissect epigenetic and small RNA pathways, and build large gene regulatory networks1-3. While these techniques facilitate the simultaneous analysis of large gene sets, they typically provide a very limited spatiotemporal resolution of gene expression changes. This limitation can be partially overcome by using either profiling method in conjunction with lasermicrodissection or fluorescence-activated cell sorting4-7. However, to fully understand the biological role of a gene, knowledge of its spatiotemporal pattern of expression at a cellular resolution is essential. Particularly, when studying development or the effects of environmental stimuli and mutants can the detailed analysis of a gene's expression pattern become essential. For instance, subtle quantitative differences in the expression levels of key regulatory genes can lead to dramatic phenotypes when associated with the loss or gain of expression in specific cell types. 
Several methods are routinely used for the detailed examination of gene expression patterns. One is through analysis of transgenic reporter lines. Such analysis can, however, become time-consuming when analyzing multiple genes or working in plants recalcitrant to transformation. Moreover, an independent validation to ensure that the transgene expression pattern mimics that of the endogenous gene is typically required. Immunohistochemical protein localization or mRNA in situ hybridization present relatively fast alternatives for the direct visualization of gene expression within cells and tissues. The latter has the distinct advantage that it can be readily used on any gene of interest. In situ hybridization allows detection of target mRNAs in cells by hybridization with a labeled anti-sense RNA probe obtained by in vitro transcription of the gene of interest. 
Here we outline a protocol for the in situ localization of gene expression in plants that is highly sensitivity and specific. It is optimized for use with paraformaldehyde fixed, paraffin-embedded sections, which give excellent preservation of histology, and DIG-labeled probes that are visualized by immuno-detection and alkaline-phosphatase colorimetric reaction. This protocol has been successfully applied to a number of tissues from a wide range of plant species, and can be used to analyze expression of mRNAs as well as small RNAs8-14.

In Situ Hybridization for the Precise Localization of Transcripts in Plants

The in situ hybridization protocol described here allows a direct localization of mRNA and small RNA expression at the cellular level with high sensitivity and specificity. The procedure is optimized for paraffin-embedded plant tissue sections, is applicable to a wide range of plants and tissues, and can be completed within ten days.

With the advances in genomics research of the past decade, plant biology has seen numerous studies presenting large-scale quantitative analyses of gene ...

Do-It-Yourself Device for Recovery of Cryopreserved Samples Accidentally Dropped into Cryogenic Storage Tanks

Liquid nitrogen is colorless, odorless, extremely cold (-196 &deg;C) liquid kept under pressure. It is commonly used as a cryogenic fluid for long term storage of biological materials such as blood, cells and tissues 1,2. The cryogenic nature of liquid nitrogen, while ideal for sample preservation, can cause rapid freezing of live tissues on contact - known as 'cryogenic burn'2, which may lead to severe frostbite in persons closely involved in storage and retrieval of samples from Dewars. Additionally, as liquid nitrogen evaporates it reduces the oxygen concentration in the air and might cause asphyxia, especially in confined spaces2.
In laboratories, biological samples are often stored in cryovials or cryoboxes stacked in stainless steel racks within the Dewar tanks1. These storage racks are provided with a long shaft to prevent boxes from slipping out from the racks and into the bottom of Dewars during routine handling. All too often, however, boxes or vials with precious samples slip out and sink to the bottom of liquid nitrogen filled tank. In such cases, samples could be tediously retrieved after transferring the liquid nitrogen into a spare container or discarding it. The boxes and vials can then be relatively safely recovered from emptied Dewar. However, the cryogenic nature of liquid nitrogen and its expansion rate makes sunken sample retrieval hazardous. It is commonly recommended by Safety Offices that sample retrieval be never carried out by a single person. Another alternative is to use commercially available cool grabbers or tongs to pull out the vials3. However, limited visibility within the dark liquid filled Dewars poses a major limitation in their use.
In this article, we describe the construction of a Cryotolerant DIY retrieval device, which makes sample retrieval from Dewar containing cryogenic fluids both safe and easy.

Here we present a low cost, durable cryotolerant device for sample retrieval from Dewar tanks filled with liquid nitrogen. The ease of construction and modular design of the device makes the process of sample retrieval from cryogenic tanks safe and easy.

Liquid nitrogen is colorless, odorless, extremely cold (-196 &deg;C) liquid kept under pressure. It is commonly used as a cryogenic fluid for long term ...

Measuring Spatial and Temporal Ca2+ Signals in Arabidopsis Plants

Developmental and environmental cues induce Ca2+ fluctuations in plant cells. Stimulus-specific spatial-temporal Ca2+ patterns are sensed by cellular Ca2+ binding proteins that initiate Ca2+ signaling cascades. However, we still know little about how stimulus specific Ca2+ signals are generated. The specificity of a Ca2+ signal may be attributed to the sophisticated regulation of the activities of Ca2+ channels and/or transporters in response to a given stimulus. To identify these cellular components and understand their functions, it is crucial to use systems that allow a sensitive and robust recording of Ca2+ signals at both the tissue and cellular levels. Genetically encoded Ca2+ indicators that are targeted to different cellular compartments have provided a platform for live cell confocal imaging of cellular Ca2+ signals. Here we describe instructions for the use of two Ca2+ detection systems: aequorin based FAS (film adhesive seedlings) luminescence Ca2+ imaging and case12 based live cell confocal fluorescence Ca2+ imaging. Luminescence imaging using the FAS system provides a simple, robust and sensitive detection of spatial and temporal Ca2+ signals at the tissue level, while live cell confocal imaging using Case12 provides simultaneous detection of cytosolic and nuclear Ca2+ signals at a high resolution.

Measuring Spatial and Temporal Ca2+ Signals in Arabidopsis Plants

Ca2+ signaling regulates diverse biological processes in plants. Here we present approaches for monitoring abiotic stress induced spatial and temporal Ca2+ signals in Arabidopsis cells and tissues using the genetically encoded Ca2+ indicators Aequorin or Case12.

Developmental and environmental cues induce Ca2+ fluctuations in plant cells. Stimulus-specific spatial-temporal Ca2+ patterns are sensed by cellular Ca2+ ...

Direct Protein Delivery to Mammalian Cells Using Cell-permeable Cys2-His2 Zinc-finger Domains

Due to their modularity and ability to be reprogrammed to recognize a wide range of DNA sequences, Cys2-His2 zinc-finger DNA-binding domains have emerged as useful tools for targeted genome engineering. Like many other DNA-binding proteins, zinc-fingers also possess the innate ability to cross cell membranes. We recently demonstrated that this intrinsic cell-permeability could be leveraged for intracellular protein delivery. Genetic fusion of zinc-finger motifs leads to efficient transport of protein and enzyme cargo into a broad range of mammalian cell types. Unlike other protein transduction technologies, delivery via zinc-finger domains does not inhibit enzyme activity and leads to high levels of cytosolic delivery. Here a detailed step-by-step protocol is presented for the implementation of zinc-finger technology for protein delivery into mammalian cells. Key steps for achieving high levels of intracellular zinc-finger-mediated delivery are highlighted and strategies for maximizing the performance of this system are discussed.

Direct Protein Delivery to Mammalian Cells Using Cell-permeable Cys2-His2 Zinc-finger Domains

Zinc-finger domains are intrinsically cell-permeable and capable of mediating protein delivery into a broad range of mammalian cell types. Here, a detailed step-by-step protocol for implementing zinc-finger technology for intracellular protein delivery is presented.

Due to their modularity and ability to be reprogrammed to recognize a wide range of DNA sequences, Cys2-His2 zinc-finger DNA-binding domains have emerged ...

A Fast Air-dry Dropping Chromosome Preparation Method Suitable for FISH in Plants

Preparation of chromosome spreads is a prerequisite for the successful performance of fluorescence in situ hybridization (FISH). Preparation of high quality plant chromosome spreads is challenging due to the rigid cell wall. One of the approved methods for the preparation of plant chromosomes is a so-called drop preparation, also known as drop-spreading or air-drying technique. Here, we present a protocol for the fast preparation of mitotic chromosome spreads suitable for the FISH detection of single and high copy DNA probes. This method is an improved variant of the air-dry drop method performed under a relative humidity of 50%-55%. This protocol comprises a reduced number of washing steps making its application easy, efficient and reproducible. Obvious benefits of this approach are well-spread, undamaged and numerous metaphase chromosomes serving as a perfect prerequisite for successful FISH analysis. Using this protocol we obtained high-quality chromosome spreads and reproducible FISH results for Hordeum vulgare, H. bulbosum, H. marinum, H. murinum, H. pubiflorum and Secale cereale.

A protocol is described for the preparation of high-quality mitotic plant chromosome spreads by a fast air-dry dropping method suitable for the FISH detection of single and high copy DNA probes.

Preparation of chromosome spreads is a prerequisite for the successful performance of fluorescence in situ hybridization (FISH). Preparation of high ...

Laser-Capture Microdissection RNA-Sequencing for Spatial and Temporal Tissue-Specific Gene Expression Analysis in Plants

The development of a complex multicellular organism is governed by distinct cell types that have different transcriptional profiles. To identify transcriptional regulatory networks that govern developmental processes it is necessary to measure the spatial and temporal gene expression profiles of these individual cell types. Therefore, insight into the spatio-temporal control of gene expression is essential to gain understanding of how biological and developmental processes are regulated. Here, we describe a laser-capture microdissection (LCM) method to isolate small number of cells from three barley embryo organs over a time-course during germination followed by transcript profiling. The method consists of tissue fixation, tissue processing, paraffin embedding, sectioning, LCM and RNA extraction followed by real-time PCR or RNA-seq. This method has enabled us to obtain spatial and temporal profiles of seed organ transcriptomes from varying numbers of cells (tens to hundreds), providing much greater tissue-specificity than typical bulk-tissue analyses. From these data we were able to define and compare transcriptional regulatory networks as well as predict candidate regulatory transcription factors for individual tissues. The method should be applicable to other plant tissues with minimal optimization.

Presented here is a protocol for laser-capture microdissection (LCM) of plant tissues. LCM is a microscopic technique for isolating areas of tissue in a contamination-free manner. The procedure includes tissue fixation, paraffin embedding, sectioning, LCM and RNA extraction. RNA is used in the downstream tissue-specific, temporally resolved analysis of transcriptomes.

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Laser-Capture Microdissection RNA-Sequencing for Spatial and Temporal Tissue-Specific Gene Expression Analysis in Plants