Yazarlar, Johns Hopkins Sıtma Araştırma Enstitüsü'ne (JHMRI) finansal destek için Bloomberg Hayırseverlerine teşekkür ediyor. JHMRI böcek ve parazitoloji çekirdek tesisleri tarafından sağlanan uzmanlık olmasaydı bu çalışma mümkün olmazdı.

<ol>
	<li>World Health Organization. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=World+Malaria+Report.">World Malaria Report.</a> World Health Organization. , (2018).</li><li>Sinden, R. E., Smalley, M. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Gametocytogenesis+of+Plasmodium+falciparum+in+vitro:+The+cell-cycle.">Gametocytogenesis of Plasmodium falciparum in vitro: The cell-cycle.</a> Parasitology. 79 (2), 277-296 (1979).</li><li>Sinden, 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=Sexual+Development+of+Malarial+Parasites.">Sexual Development of Malarial Parasites.</a> Advances in Parasitology. 22, 153-216 (1983).</li><li>Joice, R., 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=Plasmodium+falciparum+transmission+stages+accumulate+in+the+human+bone+marrow.">Plasmodium falciparum transmission stages accumulate in the human bone marrow.</a> Science Translational Medicine. 6 (244), 5 (2014).</li><li>Abdulsalam, A. H., Sabeeh, N., Bain, B. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Immature+Plasmodium+falciparum+gametocytes+in+bone+marrow.">Immature Plasmodium falciparum gametocytes in bone marrow.</a> American Journal of Hematology. 85 (12), 943 (2010).</li><li>Ghosh, A. K., Jacobs-Lorena, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Plasmodium+sporozoite+invasion+of+the+mosquito+salivary+gland.">Plasmodium sporozoite invasion of the mosquito salivary gland.</a> Current Opinion in Microbiology. 12 (4), 394-400 (2009).</li><li>Bennink, S., Kiesow, M. J., Pradel, G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+development+of+malaria+parasites+in+the+mosquito+midgut.">The development of malaria parasites in the mosquito midgut.</a> Cellular Microbiology. 18 (7), 905-918 (2016).</li><li>Trager, W., Jenson, J. B. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Cultivation+of+malarial+parasites.">Cultivation of malarial parasites.</a> Nature. 273 (5664), 621-622 (1978).</li><li>Duffy, S., Loganathan, S., Holleran, J. P., Avery, V. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Large-scale+production+of+Plasmodium+falciparum+gametocytes+for+malaria+drug+discovery.">Large-scale production of Plasmodium falciparum gametocytes for malaria drug discovery.</a> Nature Protocols. 11 (5), 976-992 (2016).</li><li>Delves, M. J., 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=Routine+in+vitro+culture+of+P.+Falciparum+gametocytes+to+evaluate+novel+transmission-blocking+interventions.">Routine in vitro culture of P. Falciparum gametocytes to evaluate novel transmission-blocking interventions.</a> Nature Protocols. 11 (9), 1668-1680 (2016).</li><li>Habtewold, T., 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=Streamlined+SMFA+and+mosquito+dark-feeding+regime+significantly+improve+malaria+transmission-blocking+assay+robustness+and+sensitivity.">Streamlined SMFA and mosquito dark-feeding regime significantly improve malaria transmission-blocking assay robustness and sensitivity.</a> Malaria Journal. 18 (1), 24 (2019).</li><li>Demanga, C. G., 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=The+development+of+sexual+stage+malaria+gametocytes+in+a+Wave+Bioreactor.">The development of sexual stage malaria gametocytes in a Wave Bioreactor.</a> Parasites and Vectors. 10 (1), 216 (2017).</li><li>Brockelman, C. R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Conditions+favoring+gametocytogenesis+in+the+continuous+culture+of+Plasmodium+falciparum.">Conditions favoring gametocytogenesis in the continuous culture of Plasmodium falciparum.</a> Journal of Eukaryotic Microbiology. 29, 454-458 (1982).</li><li>Meibalan, E., Marti, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Biology+of+malaria+transmission.">Biology of malaria transmission.</a> Cold Spring Harbor Perspectives in Medicine. 7, (2017).</li><li>Essuman, 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=A+novel+gametocyte+biomarker+for+superior+molecular+detection+of+the+plasmodium+falciparum+infectious+reservoirs.">A novel gametocyte biomarker for superior molecular detection of the plasmodium falciparum infectious reservoirs.</a> Journal of Infectious Diseases. 216 (10), 1264-1272 (2017).</li><li>Sim&#245;es, M. L., Mlambo, G., Tripathi, A., Dong, Y., Dimopoulos, G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Immune+regulation+of+plasmodium+is+anopheles+species+specific+and+infection+intensity+dependent.">Immune regulation of plasmodium is anopheles species specific and infection intensity dependent.</a> mBio. 8 (5), 01631 (2017).</li><li>Oakley, M. 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=Transcriptome+analysis+based+detection+of+Plasmodium+falciparum+development+in+Anopheles+stephensi+mosquitoes.">Transcriptome analysis based detection of Plasmodium falciparum development in Anopheles stephensi mosquitoes.</a> Scientific Reports. 8, 11568 (2018).</li><li>Saraiva, R. G., 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=Chromobacterium+spp.+mediate+their+anti-Plasmodium+activity+through+secretion+of+the+histone+deacetylase+inhibitor+romidepsin.">Chromobacterium spp. mediate their anti-Plasmodium activity through secretion of the histone deacetylase inhibitor romidepsin.</a> Scientific Reports. 8, 6176 (2018).</li><li>Tao, D., 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=Sex-partitioning+of+the+Plasmodium+falciparum+stage+V+gametocyte+proteome+provides+insight+into+falciparum-specific+cell+biology.">Sex-partitioning of the Plasmodium falciparum stage V gametocyte proteome provides insight into falciparum-specific cell biology.</a> Molecular and Cellular Proteomics. 13 (10), 2705-2724 (2014).</li><li>Grabias, B., Zheng, H., Mlambo, G., Tripathi, A. K., Kumar, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+sensitive+enhanced+chemiluminescent-ELISA+for+the+detection+of+Plasmodium+falciparum+circumsporozoite+antigen+in+midguts+of+Anopheles+stephensi+mosquitoes.">A sensitive enhanced chemiluminescent-ELISA for the detection of Plasmodium falciparum circumsporozoite antigen in midguts of Anopheles stephensi mosquitoes.</a> Journal of Microbiological Methods. 108, 19-24 (2015).</li><li>Ferrer, P., Vega-Rodriguez, J., Tripathi, A. K., Jacobs-Lorena, M., Sullivan, 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=Antimalarial+iron+chelator+FBS0701+blocks+transmission+by+Plasmodium+falciparum+gametocyte+activation+inhibition.">Antimalarial iron chelator FBS0701 blocks transmission by Plasmodium falciparum gametocyte activation inhibition.</a> Antimicrobial Agents and Chemotherapy. 59 (3), 1418-1426 (2015).</li><li>Sanders, N. G., Sullivan, D. J., Mlambo, G., Dimopoulos, G., Tripathi, A. K. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Gametocytocidal+screen+identifies+novel+chemical+classes+with+Plasmodium+falciparum+transmission+blocking+activity.">Gametocytocidal screen identifies novel chemical classes with Plasmodium falciparum transmission blocking activity.</a> PLoS One. 9 (8), 105817 (2014).</li><li>Lindner, S. 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=Transcriptomics+and+proteomics+reveal+two+waves+of+translational+repression+during+the+maturation+of+malaria+parasite+sporozoites.">Transcriptomics and proteomics reveal two waves of translational repression during the maturation of malaria parasite sporozoites.</a> Nature Communications. 10, 4964 (2019).</li><li>McLean, K. J., 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=Generation+of+Transmission-Competent+Human+Malaria+Parasites+with+Chromosomally-Integrated+Fluorescent+Reporters.">Generation of Transmission-Competent Human Malaria Parasites with Chromosomally-Integrated Fluorescent Reporters.</a> Scientific Reports. 9, 13131 (2019).</li><li>Espinosa, D. A., 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=Proteolytic+Cleavage+of+the+Plasmodium+falciparum+Circumsporozoite+Protein+Is+a+Target+of+Protective+Antibodies.">Proteolytic Cleavage of the Plasmodium falciparum Circumsporozoite Protein Is a Target of Protective Antibodies.</a> Journal of Infectious Diseases. 212 (7), 1111-1119 (2015).</li><li>Swearingen, K. 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=Interrogating+the+Plasmodium+Sporozoite+Surface:+Identification+of+Surface-Exposed+Proteins+and+Demonstration+of+Glycosylation+on+CSP+and+TRAP+by+Mass+Spectrometry-Based+Proteomics.">Interrogating the Plasmodium Sporozoite Surface: Identification of Surface-Exposed Proteins and Demonstration of Glycosylation on CSP and TRAP by Mass Spectrometry-Based Proteomics.</a> PLoS Pathogens. 12 (4), 1005606 (2016).</li><li>Ifediba, T., Vanderberg, J. P. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Complete+in+vitro+maturation+of+Plasmodium+falciparum+gametocytes.">Complete in vitro maturation of Plasmodium falciparum gametocytes.</a> Nature. 294 (5839), 364-366 (1981).</li><li>Miura, K., 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=An+inter-laboratory+comparison+of+standard+membrane-feeding+assays+for+evaluation+of+malaria+transmission-blocking+vaccines.">An inter-laboratory comparison of standard membrane-feeding assays for evaluation of malaria transmission-blocking vaccines.</a> Malaria Journal. 15, 463 (2016).</li><li>Miura, K., 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=Qualification+of+Standard+Membrane-Feeding+Assay+with+Plasmodium+falciparum+Malaria+and+Potential+Improvements+for+Future+Assays.">Qualification of Standard Membrane-Feeding Assay with Plasmodium falciparum Malaria and Potential Improvements for Future Assays.</a> PLoS One. 8 (3), 57909 (2013).</li></ol>

Yazarların açıklayacak bir şeyi yok.

Burada açıklanan yöntemler Johns Hopkins Sıtma Araştırma Enstitüsü'nde 10 yıldan fazla bir süredir başarıyla kullanılmaktadır15,16,17,18,19,20,21,22. Bu protokol kullanılarak üretilen gametositler, yüksek verimli gametositocidal tahliller<s...

Sıtma Plazmodium parazitlerinden kaynaklanır ve omurgalı konaklarına dişi Anopheles sivrisineklerinin bulaşıcı ısırması yoluyla bulaşır. Dünya Sağlık Örgütü'nün (WHO) 2019 raporuna göre, toplam 228 milyon sıtma vakasından tahmini 405.000 ölümoldu 1. Sıtmaya bağlı ölümlerin çoğu, özellikle beş yaşın altındaki çocuklar arasında Afrika bölgesinde yoğunlaşmıştır. Sıtmanın genel görülme oranı 2010 yılından itibaren küresel olarak azalırken, son yıllarda düşüş platolanmıştır ve hastalığı ortadan kaldırmak için acilen ek kontrol stratejilerine ihtiyaç vardır.
Sıtma parazitlerinin döngüsel aseksüel kan evreleri hastalık patogenezine neden olur ve bunların küçük bir alt kümesi kadın ve erkek gametositlerine ayrılır. Plazmodium falciparum gametositler, morfolojik olarak farklı beş aşamadan geçerek 7-10 gün sürdükleri için doğada benzersizdir. Aşama I'den IV'e olgunlaşmamış gametositler kemik iliği parankiminde inzdidadır ve büyük ölçüde periferik dolaşımda yoktur2,3,4,5. Olgun evre V gametositlerle enfekte olmuş eritrositler kan dolaşımında serbest bırakılır ve sivrisinekler tarafından alınmak üzere serbestçe dolaşır. Sivrisinek midgut içine girdikten sonra, gametositler, sıcaklıktaki bir değişiklik ve midgut ortamına maruz kalma yoluyla aktive edilir, dişi ve erkek gametlere dönüşür ve sivrisinek tükürük bezlerindeki sporozoitlerin enfektif aşamaları ile sonuçlanan sivrisinek aşamalarının geliştirilmesine başlar6,7.
Trager ve Jenson8 P. falciparumkültürü için standartlaştırılmış bir yöntem tanımladığından, aseksüel kan aşamaları üzerine çalışmalar büyük ölçüde ilerlemiştir. Bununla birlikte, cinsel aşamalar için güvenilir bir kültür sisteminin olmaması, P. falciparum gametositlerini, iletim biyolojisini ve sivrisinek aşamalarını incelemeyi zorlaştırmıştır. Son yıllarda, gametosit kültürlerinin kurulmasında laboratuvarlara yardımcı olan çeşitli yöntemler yayınlanmıştır9,10,11,12. Bu makale, sıtma araştırma topluluğu için değerli bir kaynağı temsil edebilecek P. falciparum gametositleri kültürü için standartlaştırılmış ve güvenilir protokolü açıklar. Bu yöntem, standartlaştırılmış bir sivrisinek besleme protokolü ile birlikte son derece güvenilir sivrisinek enfeksiyözitesi ile sonuçlanan olgun ve bulaşıcı gametositlerin sağlam üretimini sağlar. Bu yöntemler, gametositlerin ve sivrisinek evresi parazitlerinin kesintisiz tedarikini sağlamak için kurulmuştur. Bu yazıda, kapsamlı bir gametosit kültür protokolü (Şekil 1), cam membran besleyicilerin hazırlanması ve bu membran besleyiciler kullanılarak sivrisineklerin enfeksiyonu (Şekil 2), midgut diseksiyonu (Şekil 3) ve sivrisineklerin tükürük bezi (Şekil 4) ve midgut ve tükürük bezi diseksiyonu sonrası sivrisinekte enfeksiyonun nicelleştirilmesi.

<table>
	<tbody>
		<tr>
			<td>10% Sugar solution</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>10ml serological pipet</td>
			<td>Falcon</td>
			<td>357551</td>
			<td></td>
		</tr>
		<tr>
			<td>15 ml conical tube</td>
			<td>Falcon</td>
			<td>352096</td>
			<td></td>
		</tr>
		<tr>
			<td>1ml serological pipet</td>
			<td>Falcon</td>
			<td>357521</td>
			<td></td>
		</tr>
		<tr>
			<td>25 ml serological pipet</td>
			<td>Falcon</td>
			<td>357535</td>
			<td></td>
		</tr>
		<tr>
			<td>37&#176;C Incubator</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>50 ml conical tube</td>
			<td>Falcon</td>
			<td>352070</td>
			<td></td>
		</tr>
		<tr>
			<td>5ml serological pipet</td>
			<td>Falcon</td>
			<td>357543</td>
			<td></td>
		</tr>
		<tr>
			<td>6 well tissue culture plates</td>
			<td>Falcon</td>
			<td>353046</td>
			<td></td>
		</tr>
		<tr>
			<td>70% Ethanol</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>9&#34; glass pipet</td>
			<td>Fisherbrand</td>
			<td>13-678-6B</td>
			<td></td>
		</tr>
		<tr>
			<td>Anopheles Mosquitoes</td>
			<td>JHMRI, Insectary core</td>
			<td></td>
			<td>We use A. stephensi or A. gambiae (keele)</td>
		</tr>
		<tr>
			<td>cell counter</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Circulating water bath</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>fine tip forceps</td>
			<td>Fisherbrand</td>
			<td>12-000-122</td>
			<td></td>
		</tr>
		<tr>
			<td>Geimsa stain</td>
			<td>Sigma</td>
			<td>GS1L</td>
			<td></td>
		</tr>
		<tr>
			<td>Glass desiccator</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Glass membrane feeder</td>
			<td>Chemglass Life Sciences</td>
			<td>CG183570</td>
			<td></td>
		</tr>
		<tr>
			<td>Glass slides</td>
			<td>Fisherbrand</td>
			<td>12-552-3</td>
			<td></td>
		</tr>
		<tr>
			<td>HBSS</td>
			<td>Sigma</td>
			<td>H6648</td>
			<td></td>
		</tr>
		<tr>
			<td>Human Blood O+</td>
			<td>JHU</td>
			<td></td>
			<td>Wash RBCs three times with RPMI and refrigerate at 50% heamatocrit</td>
		</tr>
		<tr>
			<td>Human Serum O+</td>
			<td>Interstate blood bank</td>
			<td></td>
			<td>Pool at-least 6 units of serum from different donors and freeze down aliquots at -20&#176;C.</td>
		</tr>
		<tr>
			<td>Hypoxanthine</td>
			<td>Sigma</td>
			<td>H9337</td>
			<td>Make 500x stock in 1M NaOH</td>
		</tr>
		<tr>
			<td>Mercurochrome</td>
			<td>Sigma</td>
			<td>M7011</td>
			<td>Prepare 1% stock solution in PBS that can be diluted to 0.1% when needed</td>
		</tr>
		<tr>
			<td>Micro Pipette</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Microscope</td>
			<td>Olympus</td>
			<td></td>
			<td>Any microscope with 10x, 40x and 100x objective will work.</td>
		</tr>
		<tr>
			<td>Mosquito cups</td>
			<td>Neptune cups</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>N-acetylglucosamine</td>
			<td>Sigma</td>
			<td>A3286</td>
			<td>Optional and needed only when pure gametocytes are required.</td>
		</tr>
		<tr>
			<td>Netting</td>
			<td></td>
			<td></td>
			<td>Make sure it can contain mosquitoes and allow blood feeding</td>
		</tr>
		<tr>
			<td>Parafilm</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>PBS</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Petri dish</td>
			<td>Thermo Scientific</td>
			<td>249964</td>
			<td></td>
		</tr>
		<tr>
			<td>Pipet tips</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Pipetman</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Plasmodium falciparum NF54</td>
			<td>BEI Resources</td>
			<td>MRA-1000</td>
			<td>Freeze down large numbers of early passage culture to make sure you have a constant supply</td>
		</tr>
		<tr>
			<td>RPMI 1640</td>
			<td>Corning</td>
			<td>CV-041-CV</td>
			<td>Media contains glutamine and HEPES</td>
		</tr>
		<tr>
			<td>Slide warmer</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Sodium bicarbonate</td>
			<td>Sigma</td>
			<td>S6297</td>
			<td>Optional for media, add only when using malaria gas mix during culture incubation</td>
		</tr>
		<tr>
			<td>water bath</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Xanthurenic Acid</td>
			<td>Sigma</td>
			<td>D120804</td>
			<td>For flagellation media</td>
		</tr>
	</tbody>
</table>

plasmodium falciparum gametocyte culture and mosquito infection through artificial membrane feeding

Sıtma, önemli morbidite ve mortaliteye neden olan en önemli halk sağlığı sorunlarından biri olmaya devam etmektedir. Sıtma, dişi Anopheles sivrisineklerinden bulaşıcı bir ısırık yoluyla bulaşan sivrisinek kaynaklı bir hastalıktır. Sıtma kontrolü sonunda sivrisineklere, sivrisineklere ve sivrisineklerden bulaşmayı engellemenin yollarını içeren çok sayıda yaklaşıma dayanacaktır. Laboratuvarda sıtma parazitlerinin sivrisinek aşamalarını incelemek için, insan konakçıdan sivrisinek vektörüne bulaşmak için gerekli bir parazit aşaması olan son derece bulaşıcı Plasmodium falciparum gametositlerini kültüre etmek için bir protokol optimize ettik. P. falciparum gametositleri yaklaşık 1-2 hafta süren morfolojik olarak farklı beş adımla olgunlaşır. Bu protokolde açıklanan gametosit kültürü 15 günde tamamlanır ve 15-18. günlerden itibaren sivrisineklere bulaşıcıdır. Bu protokoller, sürekli bir enfeksiyon yetkin gametosit döngüsünü sürdürmek ve parazitin sivrisinek aşamalarının kesintisiz tedarikini sağlamak için geliştirilmiştir. Burada, gametosit kültürünün metodolojisini ve cam membran besleyiciler kullanarak sivrisineklerin bu parazitlerle nasıl enfekte olduğunu açıklıyoruz.

Burada, yukarıdaki protokol kullanılarak oluşturulan P. falciparum NF54 gametocyte kültürleri kullanılarak bir dizi membran beslemesinden elde edilen sonuçları sunuyoruz (bkz. Gametosit kültürü, 0. günde yaklaşık %0.5 karışık evre aseksüel kültürle başlatıldı ve bu kültür 4. Bu yüksek parazitmide Şekil 5A'da gösterildiği gibi, parazitler strese girer ve aseksüel sahne kültürü çökür. Bununla birlikte, bu stres birlikte...

Watch this Scientific Journal Video about Plasmodium falciparum Gametocyte Culture and Mosquito Infection Through Artificial Membrane Feeding at JoVE.com

Plasmodium falciparum Gametocyte Culture and Mosquito Infection Through Artificial Membrane Feeding

Sıtma parazitlerinin sivrisinek aşamaları üzerinde ayrıntılı araştırmalar, etkili bulaşma engelleme stratejileri tasarlamak için kritik öneme sahiptir. Bu protokol, enfeksiyöz gametositlerin etkili bir şekilde nasıl kültüreılacağını ve daha sonra bu gametositlerin sivrisineklere nasıl beslendiğini gösterir P. falciparumsivrisinek aşamaları .

Plazmodium falciparum Yapay Membran Besleme Yoluyla Gametosit Kültürü ve Sivrisinek Enfeksiyonu

Malaria remains one of the most important public health problems, causing significant morbidity and mortality. Malaria is a mosquito borne disease ...

plasmodium-falciparum-gametocyte-culture-mosquito-infection-through

Research

JoVE Journal

Biology

Plasmodium falciparum Gametocyte Culture and Mosquito Infection Through Artificial Membrane Feeding

7.3K Görüntüleme.  Johns Hopkins University. Sıtma parazitlerinin sivrisinek aşamaları üzerinde ayrıntılı araştırmalar, etkili bulaşma engelleme stratejileri tasarlamak için kritik öneme sahiptir. Bu protokol, enfeksiyöz gametositlerin etkili bir şekilde nasıl kültüreılacağını ve daha sonra bu gametositlerin sivrisineklere nasıl beslendiğini gösterir P. falciparumsivrisinek aşamaları .

Video: Plasmodium falciparum Gametocyte Culture and Mosquito Infection Through Artificial Membrane Feeding

Harvesting Sperm and Artificial Insemination of Mice

Rodents of the genus Peromyscus (deer mice) are the most prevalent native North American mammals. Peromyscus species are used in a wide range of research including toxicology, epidemiology, ecology, behavioral, and genetic studies. Here they provide a useful model for demonstrations of artificial insemination. 

Methods similar to those displayed here have previously been used in several deer mouse studies, yet no detailed protocol has been published. Here we demonstrate the basic method of artificial insemination. This method entails extracting the testes from the rodent, then isolating the sperm from the epididymis and vas deferens. The mature sperm, now in a milk mixture, are placed in the female&#x2019;s reproductive tract at the time of ovulation. Fertilization is counted as day 0 for timing of embryo development. Embryos can then be retrieved at the desired time-point and manipulated.

Artificial insemination can be used in a variety of rodent species where exact embryo timing is crucial or hard to obtain. This technique is vital for species or strains (including most Peromyscus) which may not mate immediately and/or where mating is hard to assess. In addition, artificial insemination provides exact timing for embryo development either in mapping developmental progress and/or transgenic work. Reduced numbers of animals can be used since fertilization is guaranteed. This method has been vital to furthering the Peromyscus system, and will hopefully benefit others as well.

This protocol demonstrates methods for extracting sperm from the testes of males and then inseminating female mice. This procedure is useful when precise time is needed in developmental studies as well as transgenic work.

Farelerin Hasat Sperm ve Suni Tohumlama

Rodents of the genus Peromyscus (deer mice) are the most prevalent native North American mammals.  Peromyscus species are used in a wide range of research ...

Biyoloji

Protocol for Plasmodium falciparum Infections in Mosquitoes and Infection Phenotype Determination

Once a gene is identified as potentially refractory for malaria, it must be evaluated for its role in preventing Plasmodium infections within the mosquito.    This protocol illustrates how the extent of plasmodium infections of mosquitoes can be assayed.  The techniques for preparing the gametocyte culture, membrane feeding mosquitoes human blood, and assaying viral titers in the mosquito midgut are demonstrated.

Once a gene is identified as potentially refractory for malaria, it must be evaluated for its role in preventing Plasmodium infections within the mosquito. This protocol illustrates how the extent of plasmodium infections of mosquitoes can be assayed. The techniques for preparing the gametocyte culture, membrane feeding mosquitoes human blood, and assaying viral titers in the mosquito midgut are demonstrated.

Sivrisinekler ve Enfeksiyon Fenotip belirlenmesi Plasmodium falciparum Enfeksiyonlar Protokol

Once a gene is identified as potentially refractory for malaria, it must be evaluated for its role in preventing Plasmodium infections within the ...

Crystallizing Membrane Proteins for Structure Determination using Lipidic Mesophases

A detailed protocol for crystallizing membrane proteins by using lipidic mesophases is described. This method has variously been referred to as the lipidic cubic phase or in meso method. The method has been shown to be quite versatile in that it has been used to solve X-ray crystallographic structures of prokaryotic and eukaryotic proteins, proteins that are monomeric, homo- and hetero-multimeric, chromophore-containing and chromophore-free, and alpha-helical and beta-barrel proteins. Recent successes using in meso crystallization are the human engineered beta2-adrenergic and adenosine A2a G protein-coupled receptors. Protocols are presented for reconstituting the membrane protein into the monoolein-based mesophase, and for setting up crystallizations in the manual mode. Additional steps in the overall process, such as crystal harvesting, are to be addressed in future video articles. The time required to prepare the protein-loaded mesophase and to set up a crystallization plate manually is about one hour.

Herein is described the procedure implemented in the Caffrey Membrane Structural and Functional Biology Group to set up manually crystallization trials of membrane proteins in lipidic mesophases.

Lipidik Mesophases kullanarak Yapı Tayini için Membran Proteinleri Kristalize

A detailed protocol for crystallizing membrane proteins by using lipidic mesophases is described. This method has variously been referred to as the ...

Use of a Robot for High-throughput Crystallization of Membrane Proteins in Lipidic Mesophases

Structure-function studies of membrane proteins greatly benefit from having available high-resolution 3-D structures of the type provided through macromolecular X-ray crystallography (MX). An essential ingredient of MX is a steady supply of ideally diffraction-quality crystals. The in meso or lipidic cubic phase (LCP) method for crystallizing membrane proteins is one of several methods available for crystallizing membrane proteins. It makes use of a bicontinuous mesophase in which to grow crystals. As a method, it has had some spectacular successes of late and has attracted much attention with many research groups now interested in using it. One of the challenges associated with the method is that the hosting mesophase is extremely viscous and sticky, reminiscent of a thick toothpaste. Thus, dispensing it manually in a reproducible manner in small volumes into crystallization wells requires skill, patience and a steady hand. A protocol for doing just that was developed in the Membrane Structural &amp; Functional Biology (MS&amp;FB) Group1-3. JoVE video articles describing the method are available1,4. 
The manual approach for setting up in meso trials has distinct advantages with specialty applications, such as crystal optimization and derivatization. It does however suffer from being a low throughput method. Here, we demonstrate a protocol for performing in meso crystallization trials robotically. A robot offers the advantages of speed, accuracy, precision, miniaturization and being able to work continuously for extended periods under what could be regarded as hostile conditions such as in the dark, in a reducing atmosphere or at low or high temperatures. An in meso robot, when used properly, can greatly improve the productivity of membrane protein structure and function research by facilitating crystallization which is one of the slow steps in the overall structure determination pipeline. 
In this video article, we demonstrate the use of three commercially available robots that can dispense the viscous and sticky mesophase integral to in meso crystallogenesis. The first robot was developed in the MS&amp;FB Group5,6. The other two have recently become available and are included here for completeness.	
An overview of the protocol covered in this article is presented in Figure 1. All manipulations were performed at room temperature (~20 &deg;C) under ambient conditions.

Herein is described a robotic approach to high-throughput crystallization of membrane proteins in lipidic mesophases for use in structure determination using macromolecular X-ray crystallography. Three robots capable of handling the viscous and sticky protein-laden mesophase integral to the method are introduced.

Lipidik Mesophases Membran Proteinleri Yüksek throughput Kristalizasyon için bir robot kullanımı

Structure-function studies of membrane proteins greatly benefit from having available high-resolution 3-D structures of the type provided through ...

Harvesting and Cryo-cooling Crystals of Membrane Proteins Grown in Lipidic Mesophases for Structure Determination by Macromolecular Crystallography

An important route to understanding how proteins function at a mechanistic level is to have the structure of the target protein available, ideally at atomic resolution. Presently, there is only one way to capture such information as applied to integral membrane proteins (Figure 1), and the complexes they form, and that method is macromolecular X-ray crystallography (MX). To do MX diffraction quality crystals are needed which, in the case of membrane proteins, do not form readily. A method for crystallizing membrane proteins that involves the use of lipidic mesophases, specifically the cubic and sponge phases1-5, has gained considerable attention of late due to the successes it has had in the G protein-coupled receptor field6-21 (<a href="http://www.mpdb.tcd.ie" target="_blank">www.mpdb.tcd.ie</a>). However, the method, henceforth referred to as the in meso or lipidic cubic phase method, comes with its own technical challenges. These arise, in part, due to the generally viscous and sticky nature of the lipidic mesophase in which the crystals, which are often micro-crystals, grow. Manipulating crystals becomes difficult as a result and particularly so during harvesting22,23. Problems arise too at the step that precedes harvesting which requires that the glass sandwich plates in which the crystals grow (Figure 2)24,25 are opened to expose the mesophase bolus, and the crystals therein, for harvesting, cryo-cooling and eventual X-ray diffraction data collection.
The cubic and sponge mesophase variants (Figure 3) from which crystals must be harvested have profoundly different rheologies4,26. The cubic phase is viscous and sticky akin to a thick toothpaste. By contrast, the sponge phase is more fluid with a distinct tendency to flow. Accordingly, different approaches for opening crystallization wells containing crystals growing in the cubic and the sponge phase are called for as indeed different methods are required for harvesting crystals from the two mesophase types. Protocols for doing just that have been refined and implemented in the Membrane Structural and Functional Biology (MS&amp;FB) Group, and are described in detail in this JoVE article (Figure 4). Examples are given of situations where crystals are successfully harvested and cryo-cooled. We also provide examples of cases where problems arise that lead to the irretrievable loss of crystals and describe how these problems can be avoided. In this article the Viewer is provided with step-by-step instructions for opening glass sandwich crystallization wells, for harvesting and for cryo-cooling crystals of membrane proteins growing in cubic and in sponge phases.

Herein is described procedures implemented in the Caffrey Membrane Structural and Functional Biology Group to harvest and cryo-cool membrane protein crystals grown in lipidic cubic and sponge phases for use in structure determination using macromolecular X-ray crystallography.

Makromoleküler Kristalografi tarafından Yapı Tayini için lipidik Mesophases Yetiştirilen Membran Proteinlerinin Hasat ve Cryo-soğutma Kristaller

An important route to understanding how proteins function at a mechanistic level is to have the structure of the target protein available, ideally at ...

Measuring Glutathione-induced Feeding Response in Hydra

Hydra is among the most primitive organisms possessing a nervous system and chemosensation for detecting reduced glutathione (GSH) for capturing the prey. The movement of prey organisms causes mechanosensory discharge of the stinging cells called nematocysts from hydra, which are inserted into the prey. The feeding response in hydra, which includes curling of the tentacles to bring the prey towards the mouth, opening of the mouth and consequent engulfing of the prey, is triggered by GSH present in the fluid released from the injured prey. To be able to identify the molecular mechanism of the feeding response in hydra which is unknown to date, it is necessary to establish an assay to measure the feeding response. Here, we describe a simple method for the quantitation of the feeding response in which the distance between the apical end of the tentacle and mouth of hydra is measured and the ratio of such distance before and after the addition of GSH is determined. The ratio, called the relative tentacle spread, was found to give a measure of the feeding response. This assay was validated using a starvation model in which starved hydra show an enhanced feeding response in comparison with daily fed hydra.

Here we describe a simple assay for the quantification of the feeding response in hydra induced by the reduced form of glutathione. This assay relies on measuring the distance between the apical end of the tentacle and mouth of hydra.

Hydra Glutatyon kaynaklı Besleme Tepki Ölçüm

Hydra is among the most primitive organisms possessing a nervous system and chemosensation for detecting reduced glutathione (GSH) for capturing the prey. ...

High-fat Feeding Paradigm for Larval Zebrafish: Feeding, Live Imaging, and Quantification of Food Intake

Zebrafish are emerging as a model of dietary lipid processing and metabolic disease. This protocol describes how to feed larval zebrafish a lipid-rich meal, which consists of an emulsion of chicken egg yolk liposomes created by sonicating egg yolk in embryo media. Detailed instructions are provided to screen larvae for egg yolk consumption so that larvae that fail to feed will not confound experimental results. The chicken egg yolk liposomes can be spiked with fluorescent lipid analogs, including fatty acids and cholesterol, enabling both systemic and subcellular visualization of dietary lipid processing. Several methods are described to mount larvae that are conducive to short- and long-term live imaging with both upright and inverted objectives at high and low magnification. Additionally presented is an assay to quantify larval food intake by extracting the lipids of larvae fed fluorescent lipid analogs, spotting the lipids on a thin layer chromatography plate, and quantifying the fluorescence. Finally, critical aspects of the procedures, important controls, options for modifying the protocols to address specific experimental questions, and potential limitations are discussed. These techniques can be applied not only to focused, hypothesis driven inquiries, but also to a variety of screens and live imaging techniques to study dietary lipid metabolism and the control of food intake.

Zebrafish are emerging as a valuable model of dietary lipid processing and metabolic disease. Described are protocols of lipid-rich larval feeds, live imaging of dietary fluorescent lipid analogs, and quantification of food intake. These techniques can be applied to a variety of screening, imaging, and hypothesis driven inquiry techniques.

Larva Zebra balığı için Paradigma Besleme Yüksek yağlı: Besleme, Canlı Görüntüleme ve Gıda Alımı miktarının belirlenmesi

Zebrafish are emerging as a model of dietary lipid processing and metabolic disease. This protocol describes how to feed larval zebrafish a lipid-rich ...

Ground State Depletion Super-resolution Imaging in Mammalian Cells

Advances in fluorescent microscopy and cell biology are intimately correlated, with the enhanced ability to visualize cellular events often leading to dramatic leaps in our understanding of how cells function. The development and availability of super-resolution microscopy has considerably extended the limits of optical resolution from ~250-20 nm. Biologists are no longer limited to describing molecular interactions in terms of colocalization within a diffraction limited area, rather it is now possible to visualize the dynamic interactions of individual molecules. Here, we outline a protocol for the visualization and quantification of cellular proteins by ground-state depletion microscopy&#160;for fixed cell imaging. We provide examples from two different membrane proteins, an element of the endoplasmic reticulum translocon, sec61&#946;, and a plasma membrane-localized voltage-gated L-type Ca2+ channel (CaV1.2). Discussed are the specific microscope parameters, fixation methods, photo-switching buffer formulation, and pitfalls and challenges of image processing.

This article outlines a protocol for the detection of one or more plasma and/or intracellular membrane proteins using Ground State Depletion (GSD) super-resolution microscopy in mammalian cells. Here, we discuss the benefits and considerations of using such approaches for the visualization and quantification of cellular proteins.

Memeli hücrelerinde devlet tükenmesi süper kararlılık düşsel yer

Advances in fluorescent microscopy and cell biology are intimately correlated, with the enhanced ability to visualize cellular events often leading to ...

Isolation and Culture of Human Mature Adipocytes Using Membrane Mature Adipocyte Aggregate Cultures (MAAC)

White adipose tissue (WAT) dysregulation plays a central role in development of insulin resistance and type 2 diabetes (T2D). To develop new treatments for T2D, more physiologically relevant in vitro adipocyte models are required. This study describes a new technique to isolate and culture mature human adipocytes. This method is entitled MAAC (membrane mature adipocyte aggregate culture), and compared to other adipocyte in vitro models, MAAC possesses an adipogenic gene signature that is the closest to freshly isolated mature adipocytes. Using MAAC, adipocytes can be cultured from lean and obese patients, different adipose depots, co-cultured with different cell types, and importantly, can be kept in culture for 2 weeks. Functional experiments can also be performed on MAAC including glucose uptake, lipogenesis, and lipolysis. Moreover, MAAC responds robustly to diverse pharmacological agonism and can be used to study adipocyte phenotypic changes, including the transdifferentiation of white adipocytes into brown-like fat cells.

Isolation and Culture of Human Mature Adipocytes Using Membrane Mature Adipocyte Aggregate Cultures MAAC

Membrane mature adipocyte aggregate culture (MAAC) is a new method to culture mature human adipocytes. Here we detail how to isolate adipocytes from human adipose and how to set up MAAC.

Membran Olgun Adiposit Agrega Kültürleri (MAAC) Kullanarak İnsan Olgun Adipositlerin İzolasyon ve Kültürü

White adipose tissue (WAT) dysregulation plays a central role in development of insulin resistance and type 2 diabetes (T2D). To develop new treatments ...

Large-Scale Preparation of Synovial Fluid Mesenchymal Stem Cell-Derived Exosomes by 3D Bioreactor Culture

Exosomes secreted by mesenchymal stem cells (MSCs) have been suggested as promising candidates for cartilage injuries and osteoarthritis treatment. Exosomes for clinical application require large-scale production. To this aim, human synovial fluid MSCs (hSF-MSCs) were grown on microcarrier beads, and then cultured in a dynamic three-dimension (3D) culture system. Through utilizing 3D dynamic culture, this protocol successfully obtained large-scale exosomes from SF-MSC culture supernatants. Exosomes were harvested by ultracentrifugation and verified by a transmission electron microscope, nanoparticle transmission assay, and western blotting. Also, the microbiological safety of exosomes was detected. Results of exosome detection suggest that this approach can produce a large number of good manufacturing practices (GMP)-grade exosomes. These exosomes could be utilized in exosome biology research and clinical osteoarthritis treatment.

Here, we present a protocol to produce a large number of GMP-grade exosomes from synovial fluid mesenchymal stem cells using a 3D bioreactor.

Sinovyal Sıvı Mezenkimal Kök Hücre Kaynaklı Eksozomların 3D Biyoreaktör Kültürü ile Büyük Ölçekli Hazırlanması

Exosomes secreted by mesenchymal stem cells (MSCs) have been suggested as promising candidates for cartilage injuries and osteoarthritis treatment. ...