This Project was funded by Funda&#231;&#227;o para a Ci&#234;ncia e a Tecnologia (FCT)/ Minist&#233;rio da Ci&#234;ncia, Tecnologia e Ensino Superior (MCTES) through Fundos do Or&#231;amento de Estado (ref.: ID/BIM/50005/2019). LMF is an Investigator of the Funda&#231;&#227;o para a Ci&#234;ncia e Tecnologia (IF/01050/2014) and the laboratory is funded by ERC (FatTryp, ref.771714). Publication of this work was also funded UID/BIM/50005/2019&#160; project funded&#160; by Funda&#231;&#227;o para a Ci&#234;ncia e a Tecnologia (FCT)/ Minist&#233;rio da Ci&#234;ncia, Tecnologia e Ensino Superior (MCTES) through Fundos do Or&#231;amento de Estado. We thank Andreia Pinto from the Histology and Comparative Pathology Laboratory of the iMM for expert Electron Microscopy assistance, and Sandra Trindade, Tiago Rebelo and Henrique Machado (iMM) for sharing tissues from infected mice.

All animal experiments in this protocol were performed according to EU regulations and approved by the Animal Ethics Committee of Instituto de Medicina Molecular (iMM), (AEC_2011_006_LF_TBrucei_IMM). The animal facility of iMM complies with the Portuguese law for the use of laboratory animals (Decree-Law 113/2013) and follows the European Directive 2010/63/EU and the FELASA (Federation of European Laboratory Animal Science Associations) guidelines and recommendations concerning laboratory animal welfare.
1. Aspiration of Parasites from the External Male Reproductive Organs of the Mouse
NOTE: Fine needle aspiration (FNA) was performed in wild-type male C57BL/6J mice, 6 to&#160;10 weeks old, infected with T. brucei through intraperitoneal injection of 200 &#181;L of saline with 2,000 parasites as described previously16.
<ol>
	<li>For FNA of the external male reproductive organs, place the mouse in a laminar flow hood, anesthetize the animal with an intraperitoneal injection of 200 &#181;L of a mixture of 75 mg/kg Ketamine + 1 mg/kg Medetomidine in saline.
	<ol>
		<li>Confirm anesthetization with the toe pinch method. When the reflex of the retraction of the leg is absent, position mouse in dorsal recumbency (Figure 2A).</li>
		<li>Carefully palpate the testis, assessing size and distance from the overlying skin. Restrain the organ between the index and middle finger or between the index finger and thumb. Stretch the overlying skin tightly across the mass to further immobilize the target. Clean the surface with alcohol wipes (Figure 2A).</li>
		<li>Hold the assembled 22 G needle and 5 mL syringe and insert the needle tip into the target, always with the plunger in the rest state (Figure 2B-C).</li>
		<li>Apply suction by retracting the syringe plunger to the 4 mL to 5 mL mark 2-3 times. Redirect the needle within the organ either in a straight line or along several different tangents to increase the probability of a representative sample and of targeting smaller structures like the epididymis. Make sure that this procedure is gentle, to minimize the tissue damage (Figure 2C-D).</li>
		<li>Release the suction and then withdraw the needle. Do not redraw the needle with the retracted plunger as this will lead to the suction of the aspirate into the barrel of the syringe and impede its recovery (Figure 2E). After the withdrawal of the needle, control any bleeding by applying pressure with a sterilized&#160;gauze sponge at the puncture site.</li>
		<li>Disconnect the syringe from the needle, fill it with air, reconnect the needle and gently eject the contents of the needle onto a slide. Place the tip of the needle very close or even on the slide to avoid splattering (Figure 2F-I).</li>
		<li>Perform at least one additional aspiration per organ/animal to ensure replicate sampling.</li>
		<li>Revert anesthesia with a subcutaneous injection of 200 &#181;L of 1 mg/kg Atipamezole in saline and return animals to their home cage for recovery and observe until full recovery.&#160;</li>
	</ol>
	</li>
</ol>
2. Smear Preparation from the Aspirated Material
NOTE: Use gloves throughout the procedure and ensure safe disposal of needles and syringes.
<ol>
	<li>Two steps pull method
	<ol>
		<li>Pick up the slide that has the drop of the aspirate using the nondominant hand, and pinch the frosted end between the thumb and index finger (Figure 3A).</li>
		<li>Pick up a second clean slide, the spreader slide, with the dominant hand and bring it across the first slide with the drop of the aspirate. Place the smooth clean edge of the slide on the specimen slide just on the top of the drop at an angle of approximately 30&#176; (Figure 3B).</li>
		<li>Glide the slide forward with one light, continuous and steady movement to obtain a thin film (Figure 3C).</li>
		<li>Rest the slide and allow for the complete and fast air drying of the material (Figure 3D). Do not heat-fix. Label the frosted edge of the slide with a pencil. 
		NOTE: The protocol can be paused at this step and smears can be stored indefinitely until ready to be stained.</li>
	</ol>
	</li>
</ol>
3. Staining of the Smears
NOTE: Use gloves throughout the procedure and ensure that steps 3.1.4 and 3.2.9 are performed inside a fume hood.
<ol>
	<li>Giemsa staining protocol
	<ol>
		<li>Fix air-dried smears by immersing the slides into a Coplin jar containing 100% methanol for 5 min (Figure 3E).</li>
		<li>Transfer the slide into a Coplin jar containing 20% Giemsa solution (diluted to 1/5 in distilled water) for 30 min, or 10% Giemsa for 10 min (Figure 3F).</li>
		<li>Rinse off in tap water and dry thoroughly using tissue paper to dab.</li>
		<li>Hold the slide horizontally and apply one drop of the non-aqueous mounting medium onto the smear. Place the edge of a cover-glass onto the slide, lower it and press gently to remove any air bubbles.</li>
	</ol>
	</li>
	<li>Immunocytochemistry in FNA smears
	<ol>
		<li>Fix air-dried smears in 100% methanol at room temperature for 10 min.</li>
		<li>Wash the slide for 5 min in a Coplin jar with 1x phosphate buffer (PBS), repeating this step 3 times using fresh 1x PBS every time.</li>
		<li>Remove the slide from Coplin jar, wipe excess buffer without touching the smear and draw a circle around the smear with a water repellent pen (Table of Materials).</li>
		<li>Hold the slide horizontally and apply 150 &#956;L of diluted primary antibody solution to each smear and incubate for 1 h at room temperature. 
		NOTE: Primary antibody used here is a non-purified rabbit serum anti-T. brucei VSG13 antigen (cross-reactive with many T. brucei VSGs, produced in-house), diluted in 1x PBS at 1:50,000. Perform negative controls by replacing the appropriate primary antibody with preimmune serum (Table of Materials) to allow for the assessment of the non-specific binding of the secondary antibody.</li>
		<li>Wash the slide for 5 min in a Coplin jar with 1x PBS, repeating this step 3 times using fresh 1x PBS every time.</li>
		<li>Hold the slide horizontally and apply 150 &#956;L of commercially available horseradish peroxidase/DAB visualization system to each smear. Incubate for 30 min at room temperature (Table of Materials).</li>
		<li>Wash for 3x for 5 min in 1x PBS.</li>
		<li>Counterstain by immersing the slides into a Coplin jar containing Harris hematoxylin. Rinse off in tap water and dry thoroughly using paper to dab.</li>
		<li>Hold the slide horizontally and apply one drop of the non-aqueous mounting medium onto the smear. Place the edge of a cover-glass onto the slide, lower it and press gently to remove any air bubbles.</li>
	</ol>
	</li>
</ol>

<ol>
	<li>Leopold, G., Koss, M. R. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> Koss&#8217; Diagnostic cytology and it&#8217;s histologic bases. , (2006).</li><li>Raskin, R. E., Meyer, D. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> Canine and Feline Cytology: a Color Atlas and Interpretation Guide. Canine and Feline Cytology. , (2016).</li><li>Hopper, K. D., Abendroth, C. S., Sturtz, K. W., Matthews, Y. L., Shirk, S. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Fine-needle+aspiration+biopsy+for+cytopathologic+analysis:+Utility+of+syringe+handles,+automated+guns,+and+the+nonsuction+method.">Fine-needle aspiration biopsy for cytopathologic analysis: Utility of syringe handles, automated guns, and the nonsuction method.</a> Radiology. 185 (3), 819-824 (1992).</li><li>Saliba, A. E., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Microfluidic+sorting+and+multimodal+typing+of+cancer+cells+in+self-assembled+magnetic+arrays.">Microfluidic sorting and multimodal typing of cancer cells in self-assembled magnetic arrays.</a> Proceedings of the National Academy of Sciences, U.S.A. 107 (33), 14524-14529 (2010).</li><li>Guzera, M., Cian, F., Leo, C., Winnicka, A., Archer, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+use+of+flow+cytometry+for+immunophenotyping+lymphoproliferative+disorders+in+cats:+a+retrospective+study+of+19+cases.">The use of flow cytometry for immunophenotyping lymphoproliferative disorders in cats: a retrospective study of 19 cases.</a> Veterinary and Comparative Oncology. 14, 40-51 (2016).</li><li>Young, N. A., Al-Saleem, T. I., Ehya, H., Smith, M. R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Utilization+of+fine-needle+aspiration+cytology+and+flow+cytometry+in+the+diagnosis+and+subclassification+of+primary+and+recurrent+lymphoma.">Utilization of fine-needle aspiration cytology and flow cytometry in the diagnosis and subclassification of primary and recurrent lymphoma.</a> Cancer. 40 (4), 307-319 (1998).</li><li>Carroll, C. S. E., Altin, J. G., Neeman, T., Fahrer, A. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Repeated+fine-needle+aspiration+of+solid+tumours+in+mice+allows+the+identification+of+multiple+infiltrating+immune+cell+types.">Repeated fine-needle aspiration of solid tumours in mice allows the identification of multiple infiltrating immune cell types.</a> Journal of Immunological Methods. 425, 102-107 (2015).</li><li>Araujo, R. W., Paiva, V., Gartner, F., Amendoeira, I., Martinez Oliveira, J., Schmitt, F. C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Fine+needle+aspiration+as+a+tool+to+establish+primary+human+breast+cancer+cultures+in+vitro.">Fine needle aspiration as a tool to establish primary human breast cancer cultures in vitro.</a> Acta Cytologica. 43 (6), 985-990 (1999).</li><li>Craft, I., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Percutaneous+epididymal+sperm+aspiration+and+intracytoplasmic+sperm+injection+in+the+management+of+infertility+due+to+obstructive+azoospermia.">Percutaneous epididymal sperm aspiration and intracytoplasmic sperm injection in the management of infertility due to obstructive azoospermia.</a> Fertility and Sterility. 63 (5), 1038-1042 (1995).</li><li>Powers, C. N. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Diagnosis+of+infectious+diseases:+A+cytopathologist&#8217;s+perspective.">Diagnosis of infectious diseases: A cytopathologist&#8217;s perspective.</a> Clinical Microbiology Reviews. 120 (3), 351-367 (1998).</li><li>Diamantis, A., Magiorkinis, E., Koutselini, H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Fine-needle+aspiration+(FNA)+biopsy:+Historical+aspects.">Fine-needle aspiration (FNA) biopsy: Historical aspects.</a> Folia Histochemica et Cytobiologica. 47 (2), 191-197 (2009).</li><li>Greig, E. D. W., Gray, A. C. H. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Note+on+the+lymphatic+glands+in+sleeping+sickness.">Note on the lymphatic glands in sleeping sickness.</a> British Medical Journal. 1 (2265), 1252 (1904).</li><li>Robson, J., Ashkar, T. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Trypanosomiasis+in+domestic+livestock+in+the+Lambwe+Valley+area+and+a+field+evaluation+of+various+diagnostic+techniques.">Trypanosomiasis in domestic livestock in the Lambwe Valley area and a field evaluation of various diagnostic techniques.</a> Bulletin of the World Health Organization. 47 (6), 727-734 (1972).</li><li>Disease, T. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=African+Animal+Trypanosomiasis.">African Animal Trypanosomiasis.</a> In Vitro. , 1-15 (2009).</li><li>Kennedy, P. G. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Clinical+features,+diagnosis,+and+treatment+of+human+African+trypanosomiasis+(sleeping+sickness).">Clinical features, diagnosis, and treatment of human African trypanosomiasis (sleeping sickness).</a> Lancet Neurology. 12 (2), 186-194 (2012).</li><li>Trindade, S., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Trypanosoma+brucei+parasites+occupy+and+functionally+adapt+to+the+adipose+tissue+in+mice.">Trypanosoma brucei parasites occupy and functionally adapt to the adipose tissue in mice.</a> Cell Host and Microbe. 19 (6), 837-848 (2016).</li><li>Carvalho, T., Trindade, S., Pimenta, S., Santos, A. B., Rijo-Ferreira, F., Figueiredo, L. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Trypanosoma+bruceitriggers+a+marked+immune+response+in+male+reproductive+organs.">Trypanosoma bruceitriggers a marked immune response in male reproductive organs.</a> PLoS Neglected Tropical Diseases. 12 (8), 1-15 (2018).</li><li>Sundberg, R. D., Hodgson, R. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Aspiration+of+bone+marrow+in+laboratory+animals.">Aspiration of bone marrow in laboratory animals.</a> Blood. 4 (5), 557-561 (2013).</li><li>Sottnik, J. L., Guth, A. M., Mitchell, L. A., Dow, S. W. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Minimally+invasive+assessment+of+tumor+angiogenesis+by+fine+needle+aspiration+and+flow+cytometry.">Minimally invasive assessment of tumor angiogenesis by fine needle aspiration and flow cytometry.</a> Angiogenesis. 13 (3), 251-258 (2010).</li><li>Betka, J., Hovorka, O., Boucek, J., Ulbrich, K., Etrych, T., Rihova, B. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Fine+needle+aspiration+biopsy+proves+increased+T-lymphocyte+proliferation+in+tumor+and+decreased+metastatic+infiltration+after+treatment+with+doxorubicin+bound+to+PHPMA+copolymer+carrier.">Fine needle aspiration biopsy proves increased T-lymphocyte proliferation in tumor and decreased metastatic infiltration after treatment with doxorubicin bound to PHPMA copolymer carrier.</a> Journal of Drug Targeting. 21 (7), 648-661 (2013).</li></ol>

The authors have nothing to disclose.

Fine Needle Aspiration (FNA) is a method widely used to diagnose disease in human and domestic animals. The technique has been standardized over many years1,2, which makes use of a small-bore needle to aspirate cells or fluid from a palpable mass or organ1,3. The aspirate is then typically smeared on a glass slide and stained for microscopic observation to achieve a diagnosis, but the technique can also be used to retrieve cells for other purposes4,5,6,7,8,9.
The procedure is quick (&#60;5 min per mouse, for an experienced researcher) and the risk of complications is minimal, similar to the risk incurred when undergoing simple venous puncture. For this reason, for FNA of palpable masses, anesthesia is only required for sensitive anatomic locations or when a good immobilization of the animal and stabilization of the organ or mass to be aspirated is extremely crucial for optimum results. This is frequent for small laboratory animals, as safe and effective restraint of a small rodent with one hand while ensuring the best access to the area for aspiration with the other hand, is hard to achieve without anesthesia. Short-term anesthesia is in most instances sufficient, nonetheless necessary, for a good FNA in the mouse. A good immobilization maximizes the chances of obtaining an aspirate that is representative of the cellular components of the lesion and also minimizes the chances of externalizing the tip of the needle while negative pressure is applied.
Although the procedure itself is very simple, coordinated application and release of vacuum are the most critical steps. After insertion of the needle, the plunger of the syringe is retracted to achieve a controlled vacuum (suction), and the needle can only be removed from the mass after releasing the negative pressure by letting go of the plunger (Figure 2); otherwise the aspirate is sucked into the barrel of the syringe and is then very hard to recover. Another very important step is the preparation of high-quality smears. There are various methods to make a smear but regardless of the method, smears should be prepared immediately after the material has been placed onto the glass. The biological material should be spread out gently to avoid cell-crush artifacts. Use of a coverslip as spreader can help prevent these artifacts. However, the application of too much force while making the smear will break the coverslip. A good quality smear typically has most of the cell population distributed as monolayer so that they can easily transmit light. Cellular material should not be excessively trapped in the blood clot.
The goal of an FNA is to collect cells from a mass, tissue or organ. The use of larger bore needles is helpful to increase the cellularity, but can be associated with excessive blood contamination, while sampling with smaller needles yields higher quality, though less abundant material. In our case, percutaneous aspiration of the external male reproductive structures in mice experimentally infected with T. brucei, was performed with 22-gauge needles coupled to a 5 mL syringe. Mice were anesthetized, the testis was stabilized with one hand and puncture and aspiration guided and performed with the other hand. We retrieved numerous trypanosomes admixed with germ cells, spermatozoa, epithelial cells and stromal cells, which were smeared and immunostained for the parasites&#8217; surface proteins (VSG) (Figure 4).
There is always the potential sampling error in aspirates yielding negative results because although multiple areas of a given lesion can be sampled multiple times, this is a blind aspiration where we do not visualize the needle tip and target organ or mass. This is extremely relevant in a clinical setting, where a negative FNA of a suspicious lesion does not obviate further investigations, but it&#8217;s not so relevant in animal models of disease. Thus, general limitations include mainly false negative results, and less frequently false positive results (e.g., from blood contamination), but the most important limitation in the setting of animal experimentation is the lack of information on tissue architecture17, like we have with histopathology, e.g. distribution pattern of parasites, of immune cells, and cell-cell interaction features. Nonetheless, advantages are that FNA is a non-terminal procedure allowing for the repeated sampling in the same animal over-time and always allows for better preserved cellular morphology (Figure 5). Alternatives to FNA for harvesting host cells, immune cells or microorganisms from a mouse always rely on euthanizing the mouse to collect the mass or organs of interest.
To our knowledge, there are only a few reports on the use of FNA in small laboratory animals, one from 1949 corresponding to the aspiration of bone marrow with 22 G needle for studying hematopoiesis18, and all other in combination with flow cytometry to quantify either tumor-associated inflammatory cells or endothelial cells7,19,20. Our work shows that this technique can be extended to the diagnosis and study of infectious disease models and can combine cytology with techniques like immunocytochemistry or electron microscopy. Two of the major advantages of the method in experimental animals are: (1) this procedure is not terminal, i.e., can be performed in live mice; and (2) due to its mild severity it allows for serial aspirations in the same animal. Hence fewer mice are required for each study, and the correlation between progression of clinical disease and evolution of the cellular and molecular features of a disease and/or microorganism can be easily performed, thus enabling longitudinal studies.
Perhaps the first report on the use of FNA for diagnosing an infectious diseases is a study by Grieg and Gray in 1904 that reports needle aspirations of lymph nodes from patients with sleeping sickness, which revealed motile trypanosomes12. If our findings in laboratory mice find translation to cattle, i.e., that if Trypanosoma can be easily sampled by FNA from the external male reproductive structures, one can expect that this technique will be useful to veterinarians for diagnosing animal trypanosomiasis in-farm, in livestock.

Fine Needle Aspiration (FNA) is widely used in the diagnosis of cancer and non-neoplastic diseases, both in human and domestic animals. The technique has been standardized over the years and is described in numerous textbooks1,2.
It largely consists of the percutaneous aspiration of palpable masses, organs or effusions with a thin needle fitted onto an empty syringe, using the negative pressure to withdraw cells or fluid from the mass1,3. Needles are typically 22 to 25 G (gauge corresponding to the needle inner diameter), and the use of a larger bore needle (large diameter, e.g., 21 G) is helpful to increase the cellularity, although this can produce excessive blood contamination. Needle length will depend on the depth of the mass but 1 or 1&#189; inch is commonly used for superficial masses. Syringes are typically 5 to 10 mL, with larger syringes achieving higher vacuum, which in turn increases aspirate yield. Non-palpable deep-seated masses can also be aspirated, with longer needles and under image guidance (ultrasonography). The retrieved aspirate can then be smeared, air dried, wet-fixed, stained and observed under a microscope to achieve a diagnosis3 (Figure 1).
This is a simple, inexpensive, painless and minimally invasive technique mainly used in the preoperative setting to achieve a diagnosis on palpable masses and also for organs, like lymph nodes, thyroid, prostate or even the external male reproductive structures1. In addition to being a diagnostic tool, this technique can be used for the collection of cells for other purposes as well, namely cytogenetics, electron microscopy (Figure 1D), flow cytometric characterization4,5,6,7, establishment of cell cultures8. A&#160;common example in clinical practice is sperm retrieval for in vitro fertilization9.
Aspiration can be repeated several times in the same mass to obtain multiple smears. In case of a heterogeneous lesion, e.g., a solid area and a cystic space, it is important that cells are aspirated from each region. The material collected by FNA is in general highly cellular, which in most cases allows for the diagnosis of diseases without the need for a tissue biopsy. Special stains, immunofluorescence. immunocytochemistry&#160;(Figure 1D), and molecular techniques may also be performed in smears obtained through FNA, e.g., for the identification of infectious agents when not recognizable by morphology alone10. A brief overview of the general applications and of the equipment and supplies needed for FNA are summarized in Tables 1 and 2, respectively.
The first report on the use of the needle puncture for diagnostic purposes is described in early writings of Arab medicine, but it&#8217;s in the early 20th century that modern needle aspiration techniques were implemented11. Notably, perhaps the first report that suggests the use of FNA for the diagnosis of infectious diseases was a study in 1904, where Grieg and Gray reported needle aspirations of lymph nodes from patients with sleeping sickness revealed motile trypanosomes12. The authors reported the presence of trypanosomes in both early and advanced cases, and at a higher density than that seen in blood smears, where these are often rare events12.
Current diagnosis of Trypanosomiasis in cattle relies on the direct observation of parasites in the blood, lymph or in immunodiagnostic techniques13,14,15. We have previously shown that in experimental Trypanosoma infections in the mouse, Trypanosoma brucei (T. brucei) has a remarkable tropism to adipose tissue16 and also to some of the external male reproductive structures, namely epididymis17. Parasites accumulate in the stroma of these tissues in large numbers16.
The protocol depicted below describes a detailed step-by-step technical procedure for FNA in live mice, aimed at the aspiration of trypanosomes present in the external male reproductive structures (testis, epididymis, and epididymal fat), followed by conventional cytology and immunostaining for specific parasite proteins (VSG)16,17. Aspiration was performed 6 days after the infection and safety procedures that apply are those commonly established for routine handling of experimental animals. Additional measures are required for animals that have immune deficiencies (wearing a steam-sterilized gown, mask, hair bonnet, sterile gloves, and ensuring aseptic technique at all times) to mitigate accidental exposure to opportunistic pathogens.

<table>
<tbody>
<tr>
<td>Atipamezole (ANTISEDAN 10 mL)</td>
<td>Bio 2</td>
<td>7418046</td>
<td>Anesthesia reversal</td>
</tr>
<tr>
<td>Cover slips (24 x 60 No.1)</td>
<td>VWR</td>
<td>631-0664</td>
<td>Smear making</td>
</tr>
<tr>
<td>DAB</td>
<td>Dako</td>
<td>K3468</td>
<td>Immunocytochemistry</td>
</tr>
<tr>
<td>Entellan (500 mL)</td>
<td>VWR</td>
<td>1.07961.0500</td>
<td>Mounting media</td>
</tr>
<tr>
<td>Envision Flex antibody diluent </td>
<td>Dako</td>
<td>8006</td>
<td>Immunocytochemistry</td>
</tr>
<tr>
<td>EnVision Flex conjugated w/ HRP (anti-rabbit)</td>
<td>Dako</td>
<td>K4010</td>
<td>Immunocytochemistry</td>
</tr>
<tr>
<td>Envision Flex Wash Buffer </td>
<td>Dako</td>
<td>K8007</td>
<td>Immunocytochemistry</td>
</tr>
<tr>
<td>Giemsa stain </td>
<td>Atom Scientific Ltd</td>
<td>RRSPSS-A</td>
<td>Smear staining</td>
</tr>
<tr>
<td>Glass slides (Superfrost Plus)</td>
<td>VWR</td>
<td>631-9483</td>
<td>Smear making</td>
</tr>
<tr>
<td>Harris Haematoxylin </td>
<td>Bio-optica</td>
<td>05-06004E</td>
<td>Immunocytochemistry</td>
</tr>
<tr>
<td>Hydrogen Peroxidase solution </td>
<td>Sigma</td>
<td>H1009-500ML</td>
<td>Immunocytochemistry</td>
</tr>
<tr>
<td>Hypodermic needles Microlance 3 (23G) </td>
<td>Henry Schein</td>
<td>902-8001</td>
<td>Aspiration technique</td>
</tr>
<tr>
<td>Ketamin (IMALGENE 1000 - 10 mL)</td>
<td>Bio 2</td>
<td>7410928</td>
<td>Anesthesia </td>
</tr>
<tr>
<td>Medetomidine (DOMITOR 10 mL) </td>
<td>Bio 2</td>
<td>7418335</td>
<td>Anesthesia </td>
</tr>
<tr>
<td>Methanol</td>
<td>Merck</td>
<td>1.06009.2511</td>
<td>Smear fixative</td>
</tr>
<tr>
<td>Pap pen </td>
<td>Merck</td>
<td>Z377821-1EA</td>
<td>Immunocytochemistry</td>
</tr>
<tr>
<td>Protein Block Serum free </td>
<td>Dako</td>
<td>X0909</td>
<td>Immunocytochemistry</td>
</tr>
<tr>
<td>Syringes (5 mL, 10 mL)</td>
<td>Henry Schein</td>
<td>900-3311, 900-3304</td>
<td>Aspiration technique</td>
</tr>
</tbody>
</table>

detection of extravascular trypanosoma parasites by fine needle aspiration

Fine Needle Aspiration (FNA) is a routine diagnostic procedure essential to both medical and veterinary practices. It consists of the percutaneous aspiration of cells and/or microorganisms from palpable masses, organs or effusions (fluid accumulation in a body cavity) using a thin needle similar to the regular needle used for the venous puncture. The material collected by FNA is in general highly cellular, and the retrieved aspirate is then smeared, air dried, wet-fixed, stained and observed under a microscope. In the clinical context, FNA is an important diagnostic tool that serves as a guide to the appropriate therapeutic management. Because it is simple, fast, minimally invasive and requires limited investment in the laboratory and human resources, it is extensively used by veterinary practitioners, mostly in domestic, but also in farm animals. In studies using animal models, FNA has the advantage that it can be performed repeatedly in the same animal, enabling longitudinal studies through the collection of cells from tumors and organs/tissues over the course of the disease. In addition to routine microscopy, retrieved material can also be used for immunocytochemistry, electron microscopy, biochemical analysis, flow cytometry, molecular biology or in vitro assays. FNA has been used to identify the protozoan parasite Trypanosoma brucei in the gonads of infected mice, opening the possibility for a future diagnosis in cattle.

FNA was performed in the external male reproductive organs of mice infected with T. brucei using a 22 G needle coupled to a 5 mL syringe, and glass slides for the smear preparation (Figure 1A-C). The method is simple but optimal results rely on critical steps: perfect immobilization of the mouse achieved through general anesthesia, and stabilization of the organs throughout the whole procedure (Figure 2A-B). Suction was applied 2-3 times and needle redirected 1-2 times to allow for representative sampling of the smaller organs and tissues: epididymis and epididymal fat. Negative pressure was released prior to externalizing the needle. The aspirate&#160;contained in the lumen and hub of the needle (approximately 20 &#181;L), was used to produce 2 smears (Figure 3A-C). In cases where the needle was withdrawn without the release of the suction, the material was sucked into the syringe and was not recoverable. The process was successfully repeated twice, one for each paired organ. After drying, smears were wet-fixed and immunocytochemistry for the trypanosome surface proteins was performed.
A good quality smear (Figure 4A-C) was characterized by a monolayer of cells with good cellular density, in which host cells show preserved morphological features, allowing for the identification of their tissue of origin and relative proportion between one another. Parasites were efficiently immuno-stained, identifiable and countable (Figure 4B). One case of an FNA of a peritoneal effusion in an infected mouse, stained with Giemsa for direct observation and diagnosis, is also shown (Figure 3D-F and Figure 4C).
A poor or negative FNA result may be due to different reasons: (1) too little FNA material is expressed onto the slide and is under-representative of the sample; (2) too much FNA material is expressed onto a single slide, making overly thick smears and impairing cytological evaluation; (3) too much force is applied when making the smear, and cells are disrupted, resulting in a lot of naked nuclei and DNA streaks (crush artifact); or (4) not enough force is applied when making the smear and cells do not disaggregate, resulting in a stratified layer that impedes evaluation of the morphological features of the cells (Figure 5).
When we compare FNA cytopathology with histopathology, i.e., the analysis of cells versus tissues, the fist has the advantage that cellular morphology is better preserved and relative proportions and counting of cells can be better assessed (Figure 6). Furthermore, immunocytochemistry is simpler, faster and easier to optimize than immunohistochemistry, which is typically performed in formalin-fixed and paraffin-embedded tissue.
<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>Target</td>
			<td>Applications</td>
			<td>Advantages</td>
			<td>Limitations</td>
		</tr>
		<tr>
			<td>Palpable mass</td>
			<td>Routine microscopy, diagnosis</td>
			<td>Simple, quick</td>
			<td>No tissue architecture</td>
		</tr>
		<tr>
			<td>Organ</td>
			<td>Immunohistochemistry</td>
			<td>Low cost</td>
			<td rowspan="4">Blind aspiration (needle may miss target tangentially; aspiration may target necrotic, cystic or hemorrhagic areas)</td>
		</tr>
		<tr>
			<td>Effusions</td>
			<td>Flow cytometry</td>
			<td>Sampling from multiple sites</td>
		</tr>
		<tr>
			<td></td>
			<td>Cytogenetics</td>
			<td>Well-preserved cellular morphology</td>
		</tr>
		<tr>
			<td></td>
			<td>Electron microscopy</td>
			<td>Free of complications</td>
		</tr>
		<tr>
			<td></td>
			<td>PCR, other molecular techniques</td>
			<td>High diagnostic accuracy</td>
			<td></td>
		</tr>
		<tr>
			<td></td>
			<td>Biochemical analysis</td>
			<td>Anesthesia (for immobilization)</td>
			<td></td>
		</tr>
		<tr>
			<td></td>
			<td>In vitro assays, cell culture</td>
			<td>Non-terminal procedure</td>
			<td></td>
		</tr>
	</tbody>
</table>
Table 1: Target, general applications, advantages and limitation of fine needle aspiration.
<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>FNA Kit</td>
			<td>Archetype of an aspiration needle and syringe</td>
		</tr>
		<tr>
			<td>Aspiration:</td>
			<td>Needle parts:</td>
		</tr>
		<tr>
			<td>1. Disposable plastic syringes (5 or 10 mL) (Figure 1B)</td>
			<td>Bevel. Tip of the needle shaft is slanted to form a point, the slant being the bevel. Only beveled needles are suitable for percutaneous aspirations.</td>
		</tr>
		<tr>
			<td>3.&#160;Needles of 22 to 25-gauge (diameter); 0.75, 1.0, 1.5 inches long, with standard beveled needle tip edge (Figure 1A)</td>
			<td>Shaft. Hollow tubular portion of the needle whose length may be adjusted according to the depth of the mass. The gauge of the needle corresponds to the diameter of its bore, which is the diameter of the inside of the shaft (smaller needles have higher gauge). The use of larger bore needles (less than 22 G) is helpful to increase the cellularity, although this can produce excessive iatrogenic blood contamination.</td>
		</tr>
		<tr>
			<td>1. Anesthesia (if necessary). Pain associated with FNA is similar to that of a venous puncture, however, good aspiration requires good immobilization of the subject, specially important in small-sized animals and/or for small, fluctuant lesions and organs. Rats and mice subject to FNA should be appropriately passively restrained, or, when necessary, sedated or be under light general anesthesia.</td>
			<td>Hub. Plastic portion of the needle that is attached to the syringe; should be transparent to allow for the visualization of the aspirated material. The aspirate material obtained during FNA should be collected in the needle shaft and the aspiration stopped when material is seen entering the hub.</td>
		</tr>
		<tr>
			<td>FNA smear making and interpretation:</td>
			<td>Syringe parts:</td>
		</tr>
		<tr>
			<td>1. Frosted end glass microscope slides (Figure 1C)</td>
			<td>Barrel/cylinder. Hollow portion of the syringe. Unless dealing with cystic lesions or effusions, material that is aspirated to the barrel generally cannot be recovered. Ideal volume of aspirate for FNA cytology is approximately 5 &#956;L, corresponding to the average volume of aspirate that occupies the shaft and hub of the needle.</td>
		</tr>
		<tr>
			<td>2. Romanowsky type stains (e.g. Diff-Quik, Giemsa)</td>
			<td>Tip. End of the barrel to which the needle hub is attached.</td>
		</tr>
		<tr>
			<td>3. Microscope (bright-field)</td>
			<td>Plunger. Movable portion of the syringe that has a flat disk or lip at one end and a rubber seal at the other end. Fits into the barrel and provides the pressure to draw the cells, fluid into the needle. A perfectly sealed plunger that creates good negative pressure is obligatory to obtain a good aspirate yield.</td>
		</tr>
	</tbody>
</table>
Table 2: Equipment and supplies needed for fine needle aspiration.
<img alt="Figure 1" class="xfigimg" src="/files/ftp_upload/59798/59798fig01v4.jpg" /> 
Figure 1: Tools and results for fine needle aspiration.&#160;(A) Ideal diameter of the needle for FNA is from 22 to 25 G. (B) Ideal syringe volume to obtain a good aspirate yield is of 5 to 10 mL. (C) Clean, dry, free of grease glass slide with frosted marking area for writing with pencil and pre-coated (if for immunohistochemistry). (D) Example of Trypanosomes observed with Giemsa staining (black arrowhead), immunostained for the VSG surface proteins (white arrowhead) and under transmission electron microscopy (block arrow). <a href="https://www.jove.com/files/ftp_upload/59798/59798fig01v4large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 2" class="xfigimg" src="/files/ftp_upload/59798/59798fig02v4.jpg" /> 
Figure 2: Schematics showing fine needle aspiration (FNA) of the external male reproductive organs (testis, epididymis, and epididymal fat) in mice.&#160;(A) Once the animal is secured, the previously assembled aspiration instrument is picked up. (B-C) Insert the needle tip into the target organ. (D) Apply the suction by retracting the syringe plunger to the 1 mL to 2 mL mark, repeatedly 3-4 times. Needle tip can also be moved back and forth within the target while applying suction, to collect sufficient material. (E) Release the suction and only then withdraw the needle. (F) Remove the needle from the syringe and (G) Pull the plunger back. (H) Reattach the needle. (I) Expel the material onto a glass slide by pushing the plunger swiftly through the syringe. In order to avoid splattering, ensure that the tip of the needle rest very close or even on the slide. The drop of aspirate is placed approximately 1 cm from the edge of the frosted marking area. <a href="https://www.jove.com/files/ftp_upload/59798/59798fig02v4large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 3" class="xfigimg" src="/files/ftp_upload/59798/59798fig03v2.jpg" /> 
Figure 3: Smear preparation and staining.&#160;(A) Hold one end of the slide (frosted area) between the thumb and index finger. (B) Place the smooth clean edge of a second slide (spreader) on the specimen slide just in front of the drop of material. (C) Slide the spread forward once with moderate speed to obtain a thin film. (D) Allow the slide to air dry and label the frosted edge of the slide with a pencil. (E) After complete drying fix with methanol for 5 min. (F) Stain with 20% Giemsa solution for 30 min (or 10% Giemsa for 10 min). Lightly rinse with water, dry completely, dip in xylene, and mounted with a water-insoluble mounting agent.&#160;<a href="https://www.jove.com/files/ftp_upload/59798/59798fig03large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 4" class="xfigimg" src="/files/ftp_upload/59798/59798fig04v4.jpg" /> 
Figure 4: Microphotographs of smears obtained from FNA of external male reproductive structures in mice infected with T. brucei.&#160;(A) Gross appearance of a good quality direct smear: the material was expressed onto the slide approximately 1 cm away from the frosted edge (black dot), smeared and stopped 0.5 cm before the edge of the slide (parallel lines). (B) Immunocytochemistry for the surface proteins of the parasite (VSG) was performed for smears obtained from FNA of the external male reproductive organs on the day 6 of infection. Numerous parasites (arrowhead) were detected admixed with mouse germ cells (arrow). DAB counterstained with Harris hematoxylin. Original magnification: 40x (Scale bar = 50 &#956;m). (C) Giemsa-staining of the smear obtained after FNA of a peritoneal effusion on day 21 of the infection, showed numerous parasites (arrowhead) admixed with host (mouse) cells, in this case inflammatory cells, macrophages (arrow) and lymphocytes. Original magnification: 40x (Scale bar = 50 &#956;m). <a href="https://www.jove.com/files/ftp_upload/59798/59798fig04v4large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 5" class="xfigimg" src="/files/ftp_upload/59798/59798fig05v4.jpg" /> 
Figure 5: Poor quality FNA smears.&#160;(A) Poorly cellular smear, under-representative of the mass or organ. (B) Very thick smear. (C) Crushed artifact, with disrupted cells, naked nuclei and DNA streaks. (D) Aggregates and stratified layers of cells. DAB counterstained with Harris hematoxylin. Original magnification: 20x (Scale bar = 100 &#956;m). <a href="https://www.jove.com/files/ftp_upload/59798/59798fig05v4large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 6" class="xfigimg" src="/files/ftp_upload/59798/59798fig06v4.jpg" /> 
Figure 6: Comparison of epididymal cytology and histology in mice infected with T. brucei.&#160;(A) Microphotographs corresponding to an FNA smear and (B) a 4 &#956;m paraffin section, at the same magnification (20x original magnification, Scale bar = 100 &#956;m), both immunostained for the surface proteins of the parasite (VSG). The smear showed large numbers of parasites (arrowhead) with well-preserved cellular morphology, admixed with moderate numbers of germ cells and few spermatozoa (arrow). The histological section showed a well-preserved tissue architecture, composed of epididymal ducts with intra-luminal spermatozoa (arrow), and the presence of large numbers of parasites expanding the epididymal stroma (arrowhead). DAB counterstained with Harris hematoxylin. Original magnification: 20x (Scale bar = 100 &#956;m). <a href="https://www.jove.com/files/ftp_upload/59798/59798fig06v4large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>

Watch this Scientific Journal Video about Detection of Extravascular Trypanosoma Parasites by Fine Needle Aspiration at JoVE.com

Detection of Extravascular Trypanosoma Parasites by Fine Needle Aspiration

Fine Needle Aspiration is a technique, whereby cells are obtained from a lesion or organ using a thin needle. Aspirated material is smeared, stained and examined under a microscope for diagnosis or used for molecular biology, cytometry or in vitro analysis. It is cheap, simple, quick and causes minimal trauma.

Detection of Extravascular Trypanosoma Parasites by Fine Needle Aspiration

Fine Needle Aspiration (FNA) is a routine diagnostic procedure essential to both medical and veterinary practices. It consists of the percutaneous ...

detection-extravascular-trypanosoma-parasites-fine-needle

Research

JoVE Journal

Immunology and Infection

8.9K Views.  Instituto de Medicina Molecular – Faculdade de Medicina de Lisboa. Fine Needle Aspiration is a technique, whereby cells are obtained from a lesion or organ using a thin needle. Aspirated material is smeared, stained and examined under a microscope for diagnosis or used for molecular biology, cytometry or in vitro analysis. It is cheap, simple, quick and causes minimal trauma.

Video: Detection of Extravascular Trypanosoma Parasites by Fine Needle Aspiration

Examination of the Telomere G-overhang Structure in Trypanosoma brucei

The telomere G-overhang structure has been identified in many eukaryotes including yeast, vertebrates, and Trypanosoma brucei. It serves as the substrate for telomerase for de novo telomere DNA synthesis and is therefore important for telomere maintenance. T. brucei is a protozoan parasite that causes sleeping sickness in humans and nagana in cattle. Once infected mammalian host, T. brucei cell regularly switches its surface antigen to evade the host's immune attack. We have recently demonstrated that the T. brucei telomere structure plays an essential role in regulation of surface antigen gene expression, which is critical for T. brucei pathogenesis. However, T. brucei telomere structure has not been extensively studied due to the limitation of methods for analysis of this specialized structure. We have now successfully adopted the native in-gel hybridization and ligation-mediated primer extension methods for examination of the telomere G-overhang structure and an adaptor ligation method for determination of the telomere terminal nucleotide in T. brucei cells. Here, we will describe the protocols in detail and compare their different advantages and limitations.

Examination of the Telomere G-overhang Structure in Trypanosoma brucei

Telomeres are essential for chromosome stability and the telomere G-overhang structure is essential for telomerase-mediated telomere maintenance. We have recently adopted two methods for detecting the telomere G-overhang structure in Trypanosoma brucei, which are native in-gel hybridization and ligation-mediated primer extension, which will be described.

The telomere G-overhang structure has been identified in many eukaryotes including yeast, vertebrates, and Trypanosoma brucei. It serves as the substrate ...

Combination of Adhesive-tape-based Sampling and Fluorescence in situ Hybridization for Rapid Detection of Salmonella on Fresh Produce

This protocol describes a simple approach for adhesive-tape-based sampling of tomato and other fresh produce surfaces, followed by on-tape fluorescence in situ hybridization (FISH) for rapid culture-independent detection of Salmonella spp. Cell-charged tapes can also be placed face-down on selective agar for solid-phase enrichment prior to detection. Alternatively, low-volume liquid enrichments (liquid surface miniculture) can be performed on the surface of the tape in non-selective broth, followed by FISH and analysis via flow cytometry. To begin, sterile adhesive tape is brought into contact with fresh produce, gentle pressure is applied, and the tape is removed, physically extracting microbes present on these surfaces. Tapes are mounted sticky-side up onto glass microscope slides and the sampled cells are fixed with 10% formalin (30 min) and dehydrated using a graded ethanol series (50, 80, and 95%; 3 min each concentration). Next, cell-charged tapes are spotted with buffer containing a Salmonella-targeted DNA probe cocktail and hybridized for 15 - 30 min at 55&deg;C, followed by a brief rinse in a washing buffer to remove unbound probe. Adherent, FISH-labeled cells are then counterstained with the DNA dye 4',6-diamidino-2-phenylindole (DAPI) and results are viewed using fluorescence microscopy. For solid-phase enrichment, cell-charged tapes are placed face-down on a suitable selective agar surface and incubated to allow in situ growth of Salmonella microcolonies, followed by FISH and microscopy as described above. For liquid surface miniculture, cell-charged tapes are placed sticky side up and a silicone perfusion chamber is applied so that the tape and microscope slide form the bottom of a water-tight chamber into which a small volume (&le; 500 &mu;L) of Trypticase Soy Broth (TSB) is introduced. The inlet ports are sealed and the chambers are incubated at 35 - 37&deg;C, allowing growth-based amplification of tape-extracted microbes. Following incubation, inlet ports are unsealed, cells are detached and mixed with vigorous back and forth pipetting, harvested via centrifugation and fixed in 10% neutral buffered formalin. Finally, samples are hybridized and examined via flow cytometry to reveal the presence of Salmonella spp. As described here, our "tape-FISH" approach can provide simple and rapid sampling and detection of Salmonella on tomato surfaces. We have also used this approach for sampling other types of fresh produce, including spinach and jalape&ntilde;o peppers.

Combination of Adhesive-tape-based Sampling and Fluorescence in situ Hybridization for Rapid Detection of Salmonella on Fresh Produce

This protocol describes a simple adhesive-tape-based approach for sampling of tomato and other fresh produce surfaces, followed by rapid whole cell detection of Salmonella using fluorescence in situ hybridization (FISH).

This protocol describes a simple approach for adhesive-tape-based sampling of tomato and other fresh produce surfaces, followed by on-tape fluorescence in ...

Protocol for Production of a Genetic Cross of the Rodent Malaria Parasites

Variation in response to antimalarial drugs and in pathogenicity of malaria parasites is of biologic and medical importance. Linkage mapping has led to successful identification of genes or loci underlying various traits in malaria parasites of rodents1-3 and humans4-6. The malaria parasite Plasmodium yoelii is one of many malaria species isolated from wild African rodents and has been adapted to grow in laboratories. This species reproduces many of the biologic characteristics of the human malaria parasites; genetic markers such as microsatellite and amplified fragment length polymorphism (AFLP) markers have also been developed for the parasite7-9. Thus, genetic studies in rodent malaria parasites can be performed to complement research on Plasmodium falciparum. Here, we demonstrate the techniques for producing a genetic cross in P. yoelii that were first pioneered by Drs. David Walliker, Richard Carter, and colleagues at the University of Edinburgh10.

Genetic crosses in P. yoelii and other rodent malaria parasites are conducted by infecting mice Mus musculus with an inoculum containing gametocytes of two genetically distinct clones that differ in phenotypes of interest and by allowing mosquitoes to feed on the infected mice 4 days after infection. The presence of male and female gametocytes in the mouse blood is microscopically confirmed before feeding. Within 48 hrs after feeding, in the midgut of the mosquito, the haploid gametocytes differentiate into male and female gametes, fertilize, and form a diploid zygote (Fig. 1). During development of a zygote into an ookinete, meiosis appears to occur11. If the zygote is derived through cross-fertilization between gametes of the two genetically distinct parasites, genetic exchanges (chromosomal reassortment and cross-overs between the non-sister chromatids of a pair of homologous chromosomes; Fig. 2) may occur, resulting in recombination of genetic material at homologous loci. Each zygote undergoes two successive nuclear divisions, leading to four haploid nuclei. An ookinete further develops into an oocyst. Once the oocyst matures, thousands of sporozoites (the progeny of the cross) are formed and released into mosquito hemoceal. Sporozoites are harvested from the salivary glands and injected into a new murine host, where pre-erythrocytic and erythrocytic stage development takes place. Erythrocytic forms are cloned and classified with regard to the characters distinguishing the parental lines prior to genetic linkage mapping. Control infections of individual parental clones are performed in the same way as the production of a genetic cross.

Genetic crosses of rodent malaria parasites are performed by feeding two genetically distinct parasites to mosquitoes. Recombinant progeny are cloned from mouse blood after allowing mosquitoes to bite infected mice. This video shows how to produce genetic crosses of Plasmodium yoelii and is applicable to other rodent malaria parasites.

Variation in response to antimalarial drugs and in pathogenicity of malaria parasites is of biologic and medical importance. Linkage mapping has led to ...

Detection of Infectious Virus from Field-collected Mosquitoes by Vero Cell Culture Assay

Mosquitoes transmit a number of distinct viruses including important human pathogens such as West Nile virus, dengue virus, and chickungunya virus. Many of these viruses have intensified in their endemic ranges and expanded to new territories, necessitating effective surveillance and control programs to respond to these threats. One strategy to monitor virus activity involves collecting large numbers of mosquitoes from endemic sites and testing them for viral infection. In this article, we describe how to handle, process, and screen field-collected mosquitoes for infectious virus by Vero cell culture assay. Mosquitoes are sorted by trap location and species, and grouped into pools containing &le;50 individuals. Pooled specimens are homogenized in buffered saline using a mixer-mill and the aqueous phase is inoculated onto confluent Vero cell cultures (Clone E6). Cell cultures are monitored for cytopathic effect from days 3-7 post-inoculation and any viruses grown in cell culture are identified by the appropriate diagnostic assays. By utilizing this approach, we have isolated 9 different viruses from mosquitoes collected in Connecticut, USA, and among these, 5 are known to cause human disease. Three of these viruses (West Nile virus, Potosi virus, and La Crosse virus) represent new records for North America or the New England region since 1999. The ability to detect a wide diversity of viruses is critical to monitoring both established and newly emerging viruses in the mosquito population.

We describe a method to process and screen field-collected mosquitoes for a diversity of viruses by Vero cell culture assay. By employing this technique, we have detected 9 different viruses from 4 taxonomic families in mosquitoes collected in Connecticut.

Mosquitoes transmit a number of distinct viruses including important human pathogens such as West Nile virus, dengue virus, and chickungunya virus. Many ...

Microwave Assisted Rapid Diagnosis of Plant Virus Diseases by Transmission Electron Microscopy

Investigations of ultrastructural changes induced by viruses are often necessary to clearly identify viral diseases in plants. With conventional sample preparation for transmission electron microscopy (TEM) such investigations can take several days1,2 and are therefore not suited for a rapid diagnosis of plant virus diseases. Microwave fixation can be used to drastically reduce sample preparation time for TEM investigations with similar ultrastructural results as observed after conventionally sample preparation3-5. Many different custom made microwave devices are currently available which can be used for the successful fixation and embedding of biological samples for TEM investigations5-8. In this study we demonstrate on Tobacco Mosaic Virus (TMV) infected Nicotiana tabacum plants that it is possible to diagnose ultrastructural alterations in leaves in about half a day by using microwave assisted sample preparation for TEM. We have chosen to perform this study with a commercially available microwave device as it performs sample preparation almost fully automatically5 in contrast to the other available devices where many steps still have to be performed manually6-8 and are therefore more time and labor consuming. As sample preparation is performed fully automatically negative staining of viral particles in the sap of the remaining TMV-infected leaves and the following examination of ultrastructure and size can be performed during fixation and embedding.

This study describes a method that allows the rapid and clear diagnosis of plant virus diseases in about half a day by using a combination of microwave assisted plant sample preparation for transmission electron microscopy and negative staining methods.

Investigations of ultrastructural changes induced by viruses are often necessary to clearly identify viral diseases in plants. With conventional sample ...

Detection of Toxin Translocation into the Host Cytosol by Surface Plasmon Resonance

AB toxins consist of an enzymatic A subunit and a cell-binding B subunit1. These toxins are secreted into the extracellular milieu, but they act upon targets within the eukaryotic cytosol. Some AB toxins travel by vesicle carriers from the cell surface to the endoplasmic reticulum (ER) before entering the cytosol2-4. In the ER, the catalytic A chain dissociates from the rest of the toxin and moves through a protein-conducting channel to reach its cytosolic target5. The translocated, cytosolic A chain is difficult to detect because toxin trafficking to the ER is an extremely inefficient process: most internalized toxin is routed to the lysosomes for degradation, so only a small fraction of surface-bound toxin reaches the Golgi apparatus and ER6-12.

To monitor toxin translocation from the ER to the cytosol in cultured cells, we combined a subcellular fractionation protocol with the highly sensitive detection method of surface plasmon resonance (SPR)13-15. The plasma membrane of toxin-treated cells is selectively permeabilized with digitonin, allowing collection of a cytosolic fraction which is subsequently perfused over an SPR sensor coated with an anti-toxin A chain antibody. The antibody-coated sensor can capture and detect pg/mL quantities of cytosolic toxin. With this protocol, it is possible to follow the kinetics of toxin entry into the cytosol and to characterize inhibitory effects on the translocation event. The concentration of cytosolic toxin can also be calculated from a standard curve generated with known quantities of A chain standards that have been perfused over the sensor. Our method represents a rapid, sensitive, and quantitative detection system that does not require radiolabeling or other modifications to the target toxin.

In this report, we describe how surface plasmon resonance is used to detect toxin entry into the host cytosol. This highly sensitive method can provide quantitative data on the amount of cytosolic toxin, and it can be applied to a range of toxins.

AB toxins consist of an enzymatic A subunit and a cell-binding B subunit1.  These toxins are secreted into the extracellular milieu, but they act upon ...

High-throughput Gene Tagging in Trypanosoma brucei

Improvements in mass spectrometry, sequencing and bioinformatics have generated large datasets of potentially interesting genes. Tagging these proteins can give insights into their function by determining their localization within the cell and enabling interaction partner identification. We recently published a fast and scalable method to generate Trypanosoma brucei cell lines that express a tagged protein from the endogenous locus. The method was based on a plasmid we generated that, when coupled with long primer PCR, can be used to modify a gene to encode a protein tagged at either terminus. This allows the tagging of dozens of trypanosome proteins in parallel, facilitating the large-scale validation of candidate genes of interest. This system can be used to tag proteins for localization (using a fluorescent protein, epitope tag or electron microscopy tag) or biochemistry (using tags for purification, such as the TAP (tandem affinity purification) tag). Here, we describe a protocol to perform the long primer PCR and the electroporation in 96-well plates, with the recovery and selection of transgenic trypanosomes occurring in 24-well plates. With this workflow, hundreds of proteins can be tagged in parallel; this is an order of magnitude improvement to our previous protocol and genome scale tagging is now possible.

High-throughput Gene Tagging in Trypanosoma brucei

Addition of a tag to a protein is a powerful way of gaining insight into its function. Here, we describe a protocol to endogenously tag hundreds of Trypanosoma brucei proteins in parallel such that genome scale tagging is achievable.

Improvements in mass spectrometry, sequencing and bioinformatics have generated large datasets of potentially interesting genes. Tagging these proteins ...

Detection of Trypanosoma brucei Variant Surface Glycoprotein Switching by Magnetic Activated Cell Sorting and Flow Cytometry

Trypanosoma brucei, a protozoan parasite that causes both Human and Animal African Trypanosomiasis (known as sleeping sickness and nagana, respectively) cycles between a tsetse vector and a mammalian host. It evades the mammalian host immune system by periodically switching the dense, variant surface glycoprotein (VSG) that covers its surface. The detection of antigenic variation in Trypanosoma brucei can be both cumbersome and labor intensive. Here, we present a method for quantifying the number of parasites that have 'switched' to express a new VSG in a given population. The parasites are first stained with an antibody against the starting VSG, and then stained with a secondary antibody attached to a magnetic bead. Parasites expressing the starting VSG are then separated from the rest of the population by running the parasites over a column attached to a magnet. Parasites expressing the dominant, starting VSG are retained on the column, while the flow-through contains parasites that express a new VSG as well as some contaminants expressing the starting VSG. This flow-through population is stained again with a fluorescently labeled antibody against the starting VSG to label contaminants, and propidium iodide (PI), which labels dead cells. A known number of absolute counting beads that are visible by flow cytometry are added to the flow-through population. The ratio of beads to number of cells collected can then be used to extrapolate the number of cells in the entire sample. Flow cytometry is used to quantify the population of switchers by counting the number of PI negative cells that do not stain positively for the starting, dominant VSG. The proportion of switchers in the population can then be calculated using the flow cytometry data.

Detection of Trypanosoma brucei Variant Surface Glycoprotein Switching by Magnetic Activated Cell Sorting and Flow Cytometry

African trypanosomes grown in vitro undergo antigenic variation at a low rate, such that populations are made up of parasites expressing a dominant variant surface glycoprotein (VSG) type and a small population of "switched" variants. This protocol describes a fast method for detecting and quantifying these populations.

Trypanosoma brucei, a protozoan parasite that causes both Human and Animal African Trypanosomiasis (known as sleeping sickness and nagana, respectively) ...

High-throughput Detection of Respiratory Pathogens in Animal Specimens by Nanoscale PCR

Nanoliter scale real-time PCR uses spatial multiplexing to allow multiple assays to be run in parallel on a single plate without the typical drawbacks of combining reactions together. We designed and evaluated a panel based on this principle to rapidly identify the presence of common disease agents in dogs and horses with acute respiratory illness. This manuscript describes a nanoscale diagnostic PCR workflow for sample preparation, amplification, and analysis of target pathogen sequences, focusing on procedures that are different from microliter scale reactions. In the respiratory panel presented, 18 assays were each set up in triplicate, accommodating up to 48 samples per plate. A universal extraction and pre-amplification workflow was optimized for high-throughput sample preparation to accommodate multiple matrices and DNA and RNA based pathogens. Representative data are presented for one RNA target (influenza A matrix) and one DNA target (equine herpesvirus 1). The ability to quickly and accurately test for a comprehensive, syndrome-based group of pathogens is a valuable tool for improving efficiency and ergonomics of diagnostic testing and for acute respiratory disease diagnosis and management.

High-throughput testing of DNA and RNA based pathogens by nanoscale PCR is described using a syndromic canine and equine respiratory PCR panel.

Nanoliter scale real-time PCR uses spatial multiplexing to allow multiple assays to be run in parallel on a single plate without the typical drawbacks of ...

Ultrasensitive Detection of Biomarkers by Using a Molecular Imprinting Based Capacitive Biosensor

The ability to detect and quantitate biomolecules in complex solutions has always been highly sought-after within natural science; being used for the detection of biomarkers, contaminants, and other molecules of interest. A commonly used technique for this purpose is the Enzyme-linked Immunosorbent Assay (ELISA), where often one antibody is directed towards a specific target molecule, and a second labeled antibody is used for the detection of the primary antibody, allowing for the absolute quantification of the biomolecule under study. However, the usage of antibodies as recognition elements limits the robustness of the method; as does the need of using labeled molecules. To overcome these limitations, molecular imprinting has been implemented, creating artificial recognition sites complementary to the template molecule, and obsoleting the necessity of using antibodies for initial binding. Further, for even higher sensitivity, the secondary labeled antibody can be replaced by biosensors relying on the capacitance for the quantification of the target molecule. In this protocol, we describe a method to rapidly and label-free detect and quantitate low-abundant biomolecules (proteins and viruses) in complex samples, with a sensitivity that is significantly better than commonly used detection systems such as the ELISA. This is all mediated by molecular imprinting in combination with a capacitance biosensor.

Here, we present a protocol for the detection and quantification of low abundant molecules in complex solutions using molecular imprinting in combination with a capacitance biosensor.

The ability to detect and quantitate biomolecules in complex solutions has always been highly sought-after within natural science; being used for the ...

Detection of Extravascular Trypanosoma Parasites by Fine Needle Aspiration

Summary

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Chapters in this video

Examination of the Telomere G-overhang Structure in Trypanosoma brucei

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Protocol for Production of a Genetic Cross of the Rodent Malaria Parasites

Detection of Infectious Virus from Field-collected Mosquitoes by Vero Cell Culture Assay

Microwave Assisted Rapid Diagnosis of Plant Virus Diseases by Transmission Electron Microscopy

Detection of Toxin Translocation into the Host Cytosol by Surface Plasmon Resonance

High-throughput Gene Tagging in Trypanosoma brucei

Detection of Trypanosoma brucei Variant Surface Glycoprotein Switching by Magnetic Activated Cell Sorting and Flow Cytometry

High-throughput Detection of Respiratory Pathogens in Animal Specimens by Nanoscale PCR

Ultrasensitive Detection of Biomarkers by Using a Molecular Imprinting Based Capacitive Biosensor