Name: تسليط الضوء على المؤلف: تسريع البحث حول فصل الحويصلات البكتيرية خارج الخلية وعدم التجانس
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تم دعم هذا العمل من قبل الصندوق الوطني للعلوم للعلماء الشباب المتميزين (82025024) ؛ المشروع الرئيسي للمؤسسة الوطنية للعلوم الطبيعية في الصين (82230080) ؛ البرنامج الوطني للبحث والتطوير الرئيسي في الصين (2021YFA1300604)؛ المؤسسة الوطنية للعلوم الطبيعية في الصين (81871735 و 82272438 و 82002245) ؛ صندوق قوانغدونغ للعلوم الطبيعية للعلماء الشباب المتميزين (2023B1515020058) ؛ مؤسسة العلوم الطبيعية بمقاطعة قوانغدونغ (2021A1515011639) ؛ برنامج تطوير البحوث الأساسية الرئيسي للدولة التابع لمؤسسة العلوم الطبيعية بمقاطعة شاندونغ في الصين (ZR2020ZD11) ؛ مؤسسة علوم ما بعد الدكتوراه (2022M720059) ؛ مخطط تنمية الشباب المتميز لمستشفى نانفانغ ، الجامعة الطبية الجنوبية (2022J001).

أقرت لجنة الأخلاقيات في مستشفى نانفانغ ، الجامعة الطبية الجنوبية ، هذه الدراسة ، التي أجريت بموافقة مستنيرة من المشاركين. التزمت جميع الطرق المستخدمة هنا بإرشادات التشغيل القياسية التي توفرها المعايير الدولية للميكروبيوم البشري (IHMS: http://www.microbiome-standards.org/). تم تكليف جميع إجراءات مناولة الس...

تعزيز عزل الحويصلات البكتيرية خارج الخلية للميكروبات متعددة الأوميكس

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الحويصلات البكتيرية خارج الخلية (BEVs) هي جسيمات نانوية ثنائية الطبقة تفرزها البكتيريا ، وتحمل ثروة من البروتينات والدهون والأحماض النووية وغيرها من الجزيئات النشطة بيولوجيا ، مما يساهم في التوسط في التأثيرات الوظيفية للبكتيريا20. تم التحقق من مشاركة BEVs المشتقة من الأمعاء في ت...

تعرف الأمعاء على نطاق واسع بأنها العضو الذي يؤوي المجتمعات الميكروبية الأكثر وفرة في جسم الإنسان ، حيث يشارك أكثر من 90٪ من البكتيريا في الاستعمار والتكاثر 1,2. أظهرت أدلة واسعة النطاق أن ميكروبيوتا الأمعاء تعدل البيئة الدقيقة للأمعاء وتتفاعل في نفس الوقت مع الخلل الوظيفي في الأعضاء البعيدة ، في المقام الأول من خلال ضعف الحاجز المعوي 3,4. تشير الأدلة المتزايدة إلى وجود علاقة بين اختلال توازن ميكروبيوتا الأمعاء وتطور مرض التهاب الأمعاء (IBD) 5,6 ، وكذلك الاضطرابات المعرفية من خلال محور الأمعاءوالدماغ 5،6،7،8. تلعب الحويصلات البكتيرية خارج الخلية (BEVs) التي تنتجها البكتيريا أدوارا مهمة في هذه العمليات المرضية.
BEVs هي جسيمات نانوية تغلف المشتقات البكتيرية ، بأقطار تتراوح من 20 إلى 400 نانومتر. لقد ثبت أنها تسهل التفاعلات بين البكتيريا والكائنات الحية المضيفةلها 9,10. على الرغم من عدم ظهورها ، فقد حظيت هذه الجسيمات باهتمام متزايد من الباحثين بسبب تطبيقاتها الواسعة المحتملة كمؤشرات حيوية تشخيصية وأهداف علاجية ومركبات توصيل الأدوية11. البراز البشري ، الذي يستخدم غالبا كعينات حيوية لدراسة BEVs ، والذي يتم الحصول عليه في الغالب من بكتيريا الأمعاء ، يحتوي على مزيج معقد من الماء والبكتيريا والدهون والبروتينات وبقايا الطعام غير المهضومة والخلايا الظهارية المقشرة وغيرها. يشكل تكوين البراز المعقد تحديات لعزل ونقاء BEVs ، مما يعيق إجراء تحليل شامل وموضوعي وواقعي ل BEVs. ومن ثم ، ظهرت استراتيجيات فعالة لتقليل التداخل من المكونات الملوثة وتعزيز إنتاجية BEVs كقضايا حاسمة تستحق الاهتمام الفوري.
تعتمد استراتيجيات العزل الحالية إلى حد كبير على تقنيات مثل الطرد المركزي فائق السرعة (UC) ، والطرد المركزي المتدرج الكثافة (DGC) ، وكروماتوغرافيا استبعاد الحجم (SEC) 12،13،14،15،16،17. حاليا ، تعد DGC واحدة من أكثر الطرق المطبقة على نطاق واسع في مجال فصل BEV ، وتشمل وضعين عائمين للترسيب ، "من أعلى إلى أسفل" و "من أسفل إلى أعلى" ، والتي يتم تحديدها من خلال موضع التحميل الأولي للعينة. تميز هذه المنهجيات الحويصلات خارج الخلية (EVs) عن المكونات الأخرى بناء على تفاوتات الحجم والكثافة ، مما ينتج عنه معدلات نقاء واسترداد متغيرة. أشارت الأبحاث السابقة إلى أن استراتيجيات النهج الواحد غير كافية لفصل EVs بشكل مناسب عن البروتينات القابلة للذوبان في عينات سوائل الجسم ، مثل البروتين الدهني في الدم18 وبروتين Tamm-Horsfall في البول19. بالإضافة إلى ذلك ، غالبا ما يتداخل توزيع حجم الحويصلات خارج الخلية حقيقية النواة (EEVs) مع توزيع BEVs ، مما يستلزم المزيد من التحسينات المنهجية لتحسين إنتاجية BEV. وبالتالي ، فإن النهوض بدراسة BEVs يتوقف على تطوير منهجيات فعالة للفصل والتنقية. والجدير بالذكر أن Tulkens etal 15 استخدم استراتيجية فيزيائية حيوية متعامدة لفصل BEVs البرازية عن EEVs ، حيث كان وقت الطرد المركزي لوضع DGC من أسفل إلى أعلى يصل إلى 18 ساعة. في المقابل ، خفضت هذه الدراسة إلى 7 ساعات ، مما أدى إلى توفير وقت الطرد المركزي الفائق التدرج بشكل كبير وتبسيط العملية.
في هذه الدراسة ، قمنا بعزل وتنقية BEVs البرازية باستخدام وضعين DGC في ظل ظروف عازلة محسنة ، بعد إثراء BEVs بمجموعة من سرعات الطرد المركزي التفاضلية ، من السرعة المنخفضة إلى السرعة العالية للغاية. أشارت التقييمات القائمة على التشكل وحجم الجسيمات والتركيز إلى أداء جدير بالثناء من خلال هذه الطريقة المعززة. يمكن أن تكون هذه الدراسة بمثابة أساس للبحث المستقبلي ، وتوسيع تطبيقاتها إلى مجال أوسع ، وتقديم رؤى حول عدم تجانس BEVs داخل جسم الإنسان. كما أنه يساهم في توحيد تقنيات فصل وتحليل BEV.

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>1 % (w/v) glutaraldehyde (prepared from 2.5 % stock solution in deionized water)</td>
			<td>ACMEC</td>
			<td>AP1126</td>
			<td>Morphological observation for BEVs using TEM at Step 8.3.3</td>
		</tr>
		<tr>
			<td>1 % (w/v) methylcellulose (prepared from original powder in deionized water)</td>
			<td>Sigma-Aldrich</td>
			<td>M7027</td>
			<td>Morphological observation for BEVs using TEM at Step 8.3.6</td>
		</tr>
		<tr>
			<td>1.5 % (w/v) uranyl acetate (prepared from original powder in deionized water)</td>
			<td>Polysciences</td>
			<td>21447-25</td>
			<td>Morphological observation for BEVs using TEM at Step 8.3.5</td>
		</tr>
		<tr>
			<td>1000 &#956;L, 200 &#956;L, 10 &#956;L Pipette</td>
			<td>KIRGEN</td>
			<td>KG1313, KG1212, KG1011</td>
			<td>Transfer the solution</td>
		</tr>
		<tr>
			<td>5 % (w/v) bovine serum albumin solution (prepared from the original powder in TBST buffer)</td>
			<td>Fdbio science</td>
			<td>FD0030</td>
			<td>Used in western blotting for blocking at Step 8.5.6</td>
		</tr>
		<tr>
			<td>5 &#215; loading buffer</td>
			<td>Fdbio science</td>
			<td>FD006</td>
			<td>Used in western blotting and Coomassie brilliant blue stain at Step 8.5.1</td>
		</tr>
		<tr>
			<td>75 % (v/v) alcohol</td>
			<td>LIRCON</td>
			<td>LIRCON-500 mL</td>
			<td>Surface disinfection</td>
		</tr>
		<tr>
			<td>96-well plate</td>
			<td>Rar</td>
			<td>A8096</td>
			<td>Measure the absorbance values&#160;</td>
		</tr>
		<tr>
			<td>Anti-Calnexin antibody</td>
			<td>Abcam</td>
			<td>ab92573</td>
			<td>Western blotting (Primary Antibody)</td>
		</tr>
		<tr>
			<td>Anti-CD63 antibody</td>
			<td>Abcam</td>
			<td>ab134045</td>
			<td>Western blotting (Primary Antibody)</td>
		</tr>
		<tr>
			<td>Anti-CD9 antibody</td>
			<td>Abcam</td>
			<td>ab236630</td>
			<td>Western blotting (Primary Antibody)</td>
		</tr>
		<tr>
			<td>Anti-Flagellin antibody</td>
			<td>Sino Biological</td>
			<td>40067-MM06</td>
			<td>Western blotting (Primary Antibody)</td>
		</tr>
		<tr>
			<td>Anti-Integrin beta 1 antibody</td>
			<td>Abcam</td>
			<td>ab30394</td>
			<td>Western blotting (Primary Antibody)</td>
		</tr>
		<tr>
			<td>Anti-LPS antibody</td>
			<td>Thermo Fisher</td>
			<td>MA1-83152</td>
			<td>Western blotting (Primary Antibody)</td>
		</tr>
		<tr>
			<td>Anti-LTA antibody</td>
			<td>Thermo Fisher&#160;</td>
			<td>MA1-7402</td>
			<td>Western blotting (Primary Antibody)</td>
		</tr>
		<tr>
			<td>Anti-OmpA antibody</td>
			<td>CUSABIO</td>
			<td>CSB-PA359226ZA01EOD, https://www.cusabio.com/</td>
			<td>Western blotting (Primary Antibody)</td>
		</tr>
		<tr>
			<td>Anti-Syntenin antibody</td>
			<td>Abcam</td>
			<td>ab133267</td>
			<td>Western blotting (Primary Antibody)</td>
		</tr>
		<tr>
			<td>Anti-TSG101 antibody</td>
			<td>Abcam</td>
			<td>ab125011</td>
			<td>Western blotting (Primary Antibody)</td>
		</tr>
		<tr>
			<td>Autoclave</td>
			<td>ZEALWAY</td>
			<td>GR110DP</td>
			<td>Sterilization for supplies and mediums used in the experiment</td>
		</tr>
		<tr>
			<td>Balance</td>
			<td>Mettler Toledo</td>
			<td>AL104</td>
			<td>Balance the tube sample-loaded with PBS</td>
		</tr>
		<tr>
			<td>Bicinchoninic acid assay&#160;</td>
			<td>Fdbio science</td>
			<td>FD2001</td>
			<td>Measure protein content of BEVs at Step 8.2</td>
		</tr>
		<tr>
			<td>BioRender</td>
			<td>BioRender</td>
			<td>https://app.biorender.com</td>
			<td>Make the schematic workflow of BEVs isolation and purification showed in Figure 1</td>
		</tr>
		<tr>
			<td>Biosafety cabinet</td>
			<td>Haier</td>
			<td>HR1200- II B2</td>
			<td>Peform the procedures about feces sample handling</td>
		</tr>
		<tr>
			<td>Centrifuge 5810 R; Rotor F-34-6-38</td>
			<td>Eppendorf</td>
			<td>5805000092; 5804727002, adapter: 5804774000</td>
			<td>Preprocess for BEVs (Step 3)</td>
		</tr>
		<tr>
			<td>Chemiluminescence Apparatus</td>
			<td>BIO-OI</td>
			<td>OI600SE-MF</td>
			<td>Used in western blotting for signal detection at Step 8.5.12</td>
		</tr>
		<tr>
			<td>Cytation 5</td>
			<td>BioTek</td>
			<td>F01</td>
			<td>Microplate detector for measuring the absorbance (Step 8.1) and fluorescence (Figure 6) values&#160;</td>
		</tr>
		<tr>
			<td>Dil-labled low density lipoprotein</td>
			<td>ACMEC</td>
			<td>AC12038</td>
			<td>Definition of distribution of interfering components&#160;</td>
		</tr>
		<tr>
			<td>Electrophoresis equipment</td>
			<td>Bio-rad</td>
			<td>1658033</td>
			<td>Used in western blotting for protein separation and transfer at Step 8.5.2, 8.5.3, 8.5.5</td>
		</tr>
		<tr>
			<td>Enhanced Chemiluminescence kit HRP&#160;</td>
			<td>Fdbio science</td>
			<td>FD8020</td>
			<td>Used in western blotting for signal detection at Step 8.5.12</td>
		</tr>
		<tr>
			<td>Escherichia coli&#160;</td>
			<td>American Type Culture Collection</td>
			<td>ATCC8739</td>
			<td>Isolate BEVs as a positive control. Protocol: Dissolve 25 g of the LB powder in 1 L deionized water, and autoclave. Transfer the 800 &#956;L of preserved Escherichia coli into the medium. Cultivate at 37 &#176;C in the incubator shaker. Then centrifuge at 3, 000 &#215; g for 20 min at 4 &#176;C, 12, 000 &#215; g for 30 min at 4 &#176;C, filter the supernatant through 0.22 &#956;m membrane, and perform ultra-speed centrifugation at 160, 000 &#215; g for 70 min at 4 &#176;C. Pellet defined as crude BEVs from Escherichia coli was suspended in 1.2 mL PBS (Step 3, 4).&#160;&#160;&#160;&#160;</td>
		</tr>
		<tr>
			<td>Falcon tubes 50 mL</td>
			<td>KIRGEN</td>
			<td>KG2811</td>
			<td>Preprocess for BEVs (Step 3)</td>
		</tr>
		<tr>
			<td>Feto Protein Staining Buffer</td>
			<td>Absci</td>
			<td>ab.001.50</td>
			<td>Coomassie brilliant blue staining at Step 8.5.4</td>
		</tr>
		<tr>
			<td>Filter paper</td>
			<td>Biosharp</td>
			<td>BS-TFP-070B</td>
			<td>Morphological observation for BEVs using TEM at Step 8.3 (Blotting the solution)</td>
		</tr>
		<tr>
			<td>Formvar/Carbon supported copper grids&#160;</td>
			<td>Sigma-Aldrich</td>
			<td>TEM-FCF200CU50</td>
			<td>Morphological observation for BEVs using TEM at Step 8.3</td>
		</tr>
		<tr>
			<td>HEPES powder</td>
			<td>Meilunbio</td>
			<td>MB6078</td>
			<td>Prepare iodixanol buffers with different concentrations for density gradient centrifugation</td>
		</tr>
		<tr>
			<td>HRP AffiniPure Goat Anti-Mouse IgG (H+L)</td>
			<td>Fdbio science</td>
			<td>FDM007</td>
			<td>Western blotting (Secondary Antibody)</td>
		</tr>
		<tr>
			<td>HRP AffiniPure Goat Anti-Rabbit IgG (H+L)</td>
			<td>Fdbio science</td>
			<td>FDR007</td>
			<td>Western blotting (Secondary Antibody)</td>
		</tr>
		<tr>
			<td>Incubator shaker</td>
			<td>Qiangwen</td>
			<td>DHZ-L</td>
			<td>Cultivate Escherichia coli&#160;</td>
		</tr>
		<tr>
			<td>Kimwipes&#8482; Delicate Task Wipes</td>
			<td>Kimtech Science</td>
			<td>34155</td>
			<td>Wipe the inner wall of the ultracentrifuge tube at Step 4.15</td>
		</tr>
		<tr>
			<td>LB broth</td>
			<td>Hopebio</td>
			<td>HB0128</td>
			<td>Cultivate Escherichia coli&#160;</td>
		</tr>
		<tr>
			<td>Low temperature freezer (-80 &#176;C)</td>
			<td>Haier</td>
			<td>DW-86L338J</td>
			<td>Store the samples</td>
		</tr>
		<tr>
			<td>Methanol</td>
			<td>Alalddin</td>
			<td>M116118</td>
			<td>Used in western blotting for activating PVDF membrane at Step 8.5.5</td>
		</tr>
		<tr>
			<td>Micro tubes 1.5 mL</td>
			<td>KIRGEN</td>
			<td>KG2211</td>
			<td>Recover fractions after density gradient centrifugation</td>
		</tr>
		<tr>
			<td>Micro tubes 2 mL</td>
			<td>KIRGEN</td>
			<td>KG2911</td>
			<td>Recover fractions after density gradient centrifugation</td>
		</tr>
		<tr>
			<td>Micro tubes 5 mL</td>
			<td>BBI</td>
			<td>F610888-0001</td>
			<td>Recover fractions after density gradient centrifugation</td>
		</tr>
		<tr>
			<td>Microplate reader&#160;</td>
			<td>Thermo Fisher&#160;</td>
			<td>Multiskan MK3</td>
			<td>Measure protein content of BEVs at Step 8.2</td>
		</tr>
		<tr>
			<td>Millipore filter 0.22 &#956;m</td>
			<td>Merck millipore</td>
			<td>SLGP033RB</td>
			<td>Filtration sterilization; Material: polyethersulfone, PES</td>
		</tr>
		<tr>
			<td>NaCl</td>
			<td>GHTECH</td>
			<td>1.01307.040</td>
			<td>Density gradient centrifugation solution</td>
		</tr>
		<tr>
			<td>NaOH</td>
			<td>GHTECH</td>
			<td>1.01394.068</td>
			<td>Density gradient centrifugation solution (pH adjustment)</td>
		</tr>
		<tr>
			<td>Optima&#8482; XPN-100</td>
			<td>Beckman Coulter</td>
			<td>A94469</td>
			<td>Ultracentrifugation for BEVs isolation at Step 4, 7</td>
		</tr>
		<tr>
			<td>OptiPrep&#8482;</td>
			<td>Serumwerk Bernburg AG</td>
			<td>1893</td>
			<td>Density gradient centrifugation stock solution</td>
		</tr>
		<tr>
			<td>Orbital Shaker</td>
			<td>Youning</td>
			<td>CS-100</td>
			<td>Dissolve feces at Step 2</td>
		</tr>
		<tr>
			<td>Phosphate buffered saline</td>
			<td>Procell</td>
			<td>PB180327</td>
			<td>Dissolve feces at Step 2</td>
		</tr>
		<tr>
			<td>Pipettor</td>
			<td>Eppendorf</td>
			<td>3120000267, 3120000259</td>
			<td>Transfer the solution</td>
		</tr>
		<tr>
			<td>Plastic pasteur pipette</td>
			<td>ABCbio</td>
			<td>ABC217003-4</td>
			<td>Remove supernatant in preprocessing at Step 3.4</td>
		</tr>
		<tr>
			<td>Polyvinylidene difluoride (PVDF) membranes</td>
			<td>Millipore</td>
			<td>ISEQ00010, IPVH00010</td>
			<td>Used in western blotting for protein transfer at Step 8.5.5</td>
		</tr>
		<tr>
			<td>Prefabricated polyacrylamide gel, 4&#8211;20% 15 Wells</td>
			<td>ACE</td>
			<td>F15420Gel</td>
			<td>Used in western blotting for protein separation at Step 8.5.2, 8.5.3</td>
		</tr>
		<tr>
			<td>Primary antibody diluent</td>
			<td>Fdbio science</td>
			<td>FD0040</td>
			<td>Used in western blotting at Step 8.5.8</td>
		</tr>
		<tr>
			<td>Protein ladder</td>
			<td>Fdbio science</td>
			<td>FD0672</td>
			<td>Used in western blotting and Coomassie brilliant blue stain at Step 8.5</td>
		</tr>
		<tr>
			<td>Rapid protein blotting solution</td>
			<td>UBIO</td>
			<td>UW0500</td>
			<td>Used in western blotting for protein transfer at Step 8.5.5</td>
		</tr>
		<tr>
			<td>Rotor SW 32 Ti Swinging-Bucket Rotor</td>
			<td>Beckman Coulter</td>
			<td>369650</td>
			<td>Ultracentrifugation for BEVs isolation at Step 4, 7</td>
		</tr>
		<tr>
			<td>Syringe 20 mL, 50 mL&#160;</td>
			<td>Jetway</td>
			<td>ZSQ-20ML, YCXWJZSQ-50 mL</td>
			<td>Transfer buffers amd remove supernatant in preprocessing</td>
		</tr>
		<tr>
			<td>TBS powder</td>
			<td>Fdbio science</td>
			<td>FD1021</td>
			<td>Used in western blotting at Step 8.5</td>
		</tr>
		<tr>
			<td>Transmission electron microscope (TEM)</td>
			<td>Hitachi&#160;</td>
			<td>H-7650</td>
			<td>Morphological observation for BEVs at Step 8.3</td>
		</tr>
		<tr>
			<td>Tween-20</td>
			<td>Fdbio science</td>
			<td>FD0020</td>
			<td>Used in western blotting at Step 8.5</td>
		</tr>
		<tr>
			<td>Ultracentrifuge tube</td>
			<td>Beckman</td>
			<td>326823, 355642</td>
			<td>Ultracentrifugation for BEVs isolation at Step 4, 7</td>
		</tr>
		<tr>
			<td>Ultra-clean bench</td>
			<td>AIRTECH</td>
			<td>SW-CJ-2FD</td>
			<td>Peform the procedures about liquid handling</td>
		</tr>
		<tr>
			<td>Water bath</td>
			<td>Bluepard</td>
			<td>CU600</td>
			<td>Used for measuring protein content of BEVs at Step 8.2.5</td>
		</tr>
		<tr>
			<td>ZetaView</td>
			<td>Particle Metrix</td>
			<td>S/N 21-734, Software ZetaView (version 8.05.14 SP7)</td>
			<td>Nanoparticle tracking analysis (NTA) for measuring the particle size and concentrarion of BEVs at Step 8.4</td>
		</tr>
	</tbody>
</table>

isolation and purification of bacterial extracellular vesicles from human feces using density gradient centrifugation

الحويصلات البكتيرية خارج الخلية (BEVs) هي حويصلات نانوية مشتقة من البكتيريا التي تلعب دورا نشطا في التواصل بين البكتيريا والبكتيريا والبكتيريا المضيفة ، حيث تنقل الجزيئات النشطة بيولوجيا مثل البروتينات والدهون والأحماض النووية الموروثة من البكتيريا الأم. BEVs المشتقة من ميكروبيوتا الأمعاء لها تأثيرات داخل الجهاز الهضمي ويمكن أن تصل إلى أعضاء بعيدة ، مما يؤدي إلى آثار كبيرة على علم وظائف الأعضاء وعلم الأمراض. تعد التحقيقات النظرية التي تستكشف أنواع وكميات وأدوار BEVs المشتقة من البراز البشري ضرورية لفهم إفراز ووظيفة BEVs من ميكروبات الأمعاء. تتطلب هذه التحقيقات أيضا تحسين الاستراتيجية الحالية لعزل وتنقية BEVs.
قامت هذه الدراسة بتحسين عملية عزل وتنقية BEVs من خلال إنشاء وضعين للطرد المركزي المتدرج الكثافة (DGC): من أعلى إلى أسفل ومن أسفل إلى أعلى. تم تحديد التوزيع المخصب للخلايا الكهربائية في الكسور من 6 إلى 8 (F6-F8). تم تقييم فعالية النهج بناء على مورفولوجيا الجسيمات والحجم والتركيز ومحتوى البروتين. تم حساب معدلات استرداد الجسيمات والبروتين ، وتم تحليل وجود علامات محددة لمقارنة استعادة ونقاء وضعي DGC. أشارت النتائج إلى أن وضع الطرد المركزي من أعلى إلى أسفل كان له مستويات تلوث أقل وحقق معدل استرداد ونقاء مماثل لمعدل الطرد من أسفل إلى أعلى. كان وقت الطرد المركزي البالغ 7 ساعات كافيا لتحقيق تركيز BEV برازي يبلغ 108 / ملغ.
بصرف النظر عن البراز ، يمكن تطبيق هذه الطريقة على أنواع سوائل الجسم الأخرى مع التعديل المناسب وفقا للاختلافات في المكونات واللزوجة. في الختام ، من شأن هذا البروتوكول المفصل والموثوق به أن يسهل عزل وتنقية BEVs الموحدة ، وبالتالي ، يضع أساسا لتحليل متعدد الأوميكس والتجارب الوظيفية اللاحقة.

The gut is widely recognized as the organ harboring the most abundant microbial communities in the human body, with over 90% of bacteria involved in colonization and multiplication1,2. Extensive evidence has demonstrated that the gut microbiota modulates the gut microenvironment and simultaneously interacts with dysfunction in distant organs, primarily through an impaired intestinal barrier3,4. Mounting evidence indicates a correlation between the imbalance of gut microbiota and the progression of inflammatory bowel disease (IBD)5,6, as well as cognitive disorders through the gut-brain axis5,6,7,8. Bacterial extracellular vesicles (BEVs) produced by bacteria play significant roles in these pathological processes.
BEVs are nanoscale particles encapsulating bacterial derivatives, with diameters ranging from 20 to 400 nm. They have been demonstrated to facilitate interactions between bacteria and their host organisms9,10. Despite their invisibility, these particles have garnered increasing attention from researchers due to their prospective broad applications as diagnostic biomarkers, therapeutic targets, and drug delivery vehicles11. Human feces, often used as biospecimens for studying BEVs, predominantly sourced from gut bacteria, contain a complex mixture of water, bacteria, lipids, proteins, undigested food residue, and exfoliated epithelial cells among others. The intricate fecal composition poses challenges to the isolation and purity of BEVs, thereby impeding a comprehensive, objective, and realistic analysis of BEVs. Hence, effective strategies to minimize interference from contaminating components and enhance the yield of BEVs have emerged as critical issues warranting immediate attention.
Existing isolation strategies largely rely on techniques such as ultra-high-speed centrifugation (UC), density gradient centrifugation (DGC), and size exclusion chromatography (SEC)12,13,14,15,16,17. Currently, DGC is one of the most widely applied methods in the field of BEV separation, encompassing two sedimentation-floating modes, &#34;Top-down&#34; and &#34;Bottom-up&#34;, which are determined by the initial loading position of the sample. These methodologies differentiate extracellular vesicles (EVs) from other components based on size and density disparities, yielding variable purity and recovery rates. Prior research has indicated that single-approach strategies are insufficient for adequately separating EVs from soluble proteins in body fluid samples, such as lipoprotein in blood18 and Tamm-Horsfall protein in urine19. Additionally, the size distribution of eukaryotic extracellular vesicles (EEVs) often overlaps with that of BEVs, thereby necessitating further methodological enhancements to optimize BEV yield. Consequently, advancing the study of BEVs hinges on the development of effective separation and purification methodologies. Notably, Tulkens et al15 employed an orthogonal biophysical strategy to separate fecal BEVs from EEVs, in which the centrifugation time of a Bottom-up DGC mode was up to 18 h. In contrast, this study reduced it to 7 h, greatly saving the gradient-ultracentrifugation time and simplifying the process.
In the present study, we isolated and purified fecal BEVs employing two DGC modes under optimized buffer conditions, after enriching BEVs with a range of differential centrifugation speeds, from low to extremely high velocity. Evaluations based on morphology, particle size, and concentration indicated a commendable performance by this enhanced method. This study could serve as the foundation for future research, extending its applications to a broader domain, and offering insights into the heterogeneity of BEVs within the human body. It also contributes to the standardization of BEV separation and analysis techniques.

تسليط الضوء على المؤلف: تسريع البحث حول فصل الحويصلات البكتيرية خارج الخلية وعدم التجانس 

عزل وتنقية الحويصلات البكتيرية خارج الخلية من البراز البشري باستخدام الطرد المركزي المتدرج الكثافة

Our study isolates, purifies, and characterize bacterial extracellular vesicles from physicists using density gradient centrifugation. We aim to address the separation of BEVs from contaminants and provide a reliable method for researchers. Our protocol reduces centrifugation time from 18 to 7 hours.Top down mode improves BEV separation and reduces contamination from liver proteins. Our method simplifies the separation of BEVs, setting a standard for future studies. It can be applied to other body fluids with appropriate modification, enhancing our understanding and facilitating the study of BEVs revealing their inherent heterogeneity within the human body.

تحديد توزيع الكسور المخصبة بالطاقة الكهربائية الهجينة لتحديد توزيع الحويصلات البكتيرية خارج الخلية (BEVs) - الكسور المخصبة ، تم إنشاء عنصر تحكم فارغ لقياس قيم الامتصاص عند OD 340 نانومتر ، وتم حساب كثافة كل جزء بناء على القياسات وإرشادات اليوديكسانول (الخطوة 8.1). يعرض الجدول 2</stro...

Watch this Scientific Journal Video about Accelerating Research on Bacterial Extracellular Vesicles Separation and Heterogeneity at JoVE.com

تصف هذه الدراسة طريقة لعزل وتنقية الحويصلات البكتيرية خارج الخلية (BEVs) المخصبة من البراز البشري عن طريق الطرد المركزي المتدرج الكثافة (DGC) ، وتحدد الخصائص الفيزيائية ل BEVs من التشكل وحجم الجسيمات والتركيز ، وتناقش التطبيقات المحتملة لنهج DGC في البحث السريري والعلمي.

Bacterial extracellular vesicles (BEVs) are nanovesicles derived from bacteria that play an active role in bacteria-bacteria and bacteria-host ...

تقوم دراستنا بعزل وتنقية وتوصيف الحويصلات البكتيرية خارج الخلية من الفيزيائيين باستخدام الطرد المركزي المتدرج الكثافة. نحن نهدف إلى معالجة فصل BEVs عن الملوثات وتوفير طريقة موثوقة للباحثين. يقلل بروتوكولنا من وقت الطرد المركزي من 18 إلى 7 ساعات.يعمل الوضع من أعلى إلى أسفل على تحسين فصل BEV وتقليل التلوث من بروتينات الكبد. تعمل طريقتنا على تبسيط فصل BEVs ، ووضع معيار للدراسات المستقبلية. يمكن تطبيقه على سوائل الجسم الأخرى مع التعديل المناسب ، مما يعزز فهمنا ويسهل دراسة BEVs التي تكشف عن عدم تجانسها المتأصل داخل جسم الإنسان.

isolation-purification-bacterial-extracellular-vesicles-from-human

Research

JoVE Journal

Biology

Isolation and Purification of Bacterial Extracellular Vesicles from Human Feces Using Density Gradient Centrifugation

Bacterial extracellular vesicles (BEVs) are nanovesicles derived from bacteria that play an active role in bacteria-bacteria and bacteria-host communication, transferring bioactive molecules such as proteins, lipids, and nucleic acids inherited from the parent bacteria. BEVs derived from the gut microbiota have effects within the gastrointestinal tract and can reach distant organs, resulting in significant implications for physiology and pathology. Theoretical investigations that explore the types, quantities, and roles of BEVs derived from human feces are crucial for understanding the secretion and function of BEVs from the gut microbiota. These investigations also necessitate an improvement in the current strategy for isolating and purifying BEVs.
This study optimized the isolation and purification process of BEVs by establishing two density gradient centrifugation (DGC) modes: Top-down and Bottom-up. The enriched distribution of BEVs was determined in fractions 6 to 8 (F6-F8). The effectiveness of the approach was evaluated based on particle morphology, size, concentration, and protein content. The particle and protein recovery rates were calculated, and the presence of specific markers was analyzed to compare the recovery and purity of the two DGC modes. The results indicated that the Top-down centrifugation mode had lower contamination levels and achieved a recovery rate and purity similar to that of the Bottom-up mode. A centrifugation time of 7 h was sufficient to achieve a fecal BEV concentration of 108/mg.
Apart from feces, this method could be applied to other body fluid types with proper modification according to the differences in components and viscosity. In conclusion, this detailed and reliable protocol would facilitate the standardized isolation and purification of BEVs and thus, lay a foundation for subsequent multi-omics analysis and functional experiments.

This study describes a method to isolate and purify bacterial extracellular vesicles (BEVs) enriched from human feces via density gradient centrifugation (DGC), identifies the physical characteristics of BEVs from morphology, particle size, and concentration, and discusses the potential applications of the DGC approach in clinical and scientific research.

Bacterial Extracellular Vesicles (BEVs) Enrichment from Human Faeces Using Differential Centrifugation Speeds

To begin, take the prepared human fecal samples. Cool the high speed refrigerated centrifuge to 4 degrees Celsius. Use PBS to adjust the weight of the sample tubes to 0.1 grams, and centrifuge them at 3, 000 G for 20 minutes at 4 degrees Celsius.Using a plastic pipette, transfer the supernatant into two 50 milliliter tubes, leaving 1 milliliter behind. Then, centrifuge the supernatant at 12, 000 G for 30 minutes at 4 degrees Celsius. Using a 20 milliliter syringe, aspirate the supernatant, and remove the needle from the syringe.Filter the liquid through 0.22 micrometer filters into 50 milliliter tubes. Next, wipe the bucket with 75%alcohol to eliminate any remaining contamination. Transfer approximately 30 milliliters of the filtered fecal supernatant into the ultracentrifuge tube.Fill the tube with approximately 8 milliliters of PBS, leaving a 3 millimeter gap from the tube's opening. Place the two ultracentrifuge tubes in opposing ultracentrifugation buckets, and equalize the weight of the two buckets using PBS. Load all buckets onto the rotor, irrespective of whether they are loaded with tubes.Place the samples in the centrifuge, initiate the vacuum and spin them at 160, 000 G for 70 minutes at 4 degrees Celsius. As soon as the centrifugation completes, release the chamber vacuum and open the door of the ultra centrifuge. Then, promptly remove the rotor.Transfer the buckets from the rotor to the rack, and pick up the tubes using a nipper. Discard the supernatant, and save the visible brown pellets. Add 1 milliliter of pre-chilled PBS to resuspend the pellets completely.Fill the tube with approximately 37 milliliters of PBS, leaving a 3 millimeter gap from the opening. After performing another round of ultracentrifugation, discard the supernatant and leave the tube inverted for 5 minutes. Remove any remaining solution on the inner wall with wipers.Using a 1, 000 microliter pipette, add 1.2 milliliters of pre-chilled PBS to resuspend pellets, and mix them by pipetting. Transfer 1.2 milliliters of the PBS BEV solution from one ultracentrifuge tube to a clean 1.5 milliliter micro tube.

إثراء الحويصلات البكتيرية خارج الخلية (BEVs) من البراز البشري باستخدام سرعات الطرد المركزي التفاضلية

Establishment of a Density Gradient Centrifugation System to Isolate and Purify Bacterial Extracellular Vesicles (BEVs) from Human Faeces

To begin, take 500 microliters of the prepared PBS/BEV solution. Combine it with three milliliters of PBS and mix gently using a 1, 000 microliter pipette. Place a 31 milliliter ultracentrifuge tube on a foam plate with holes, and label the tube with a downward arrow.Then hold a 1, 000 microliter pipette vertically and add three milliliters of the 50%iodixanol solution to the bottom of the tube. Place a tube holder slightly above the level of the foam plate below the tube opening, and tilt the tube to an angle of 70 degrees. Using a 1, 000 microliter pipette, add three milliliters of 40%iodixanol solution on top of the 50%iodixanol solution.Then layer three milliliters of 20%iodixanol solution on the 40%iodixanol solution. Using a 1, 000 microliter pipette, add three milliliters of a 10%iodixanol solution on top of the prepared 20%iodixanol solution. Next, add 3.5 milliliters of the PBS/BEV solution on top of the 10%iodixanol solution, and gently return the tubes to an upright position.Now, position a 31 milliliter ultracentrifuge tube on a foam plate with holes, and label it with an upward arrow. Using a 1, 000 microliter pipette, vertically add 2.5 milliliters of the 60%iodixanol stock solution into the bottom of the tube, and combine it with 500 microliters of PBS/BEV solution to get three milliliters of 50%iodixanol BEV solution. Mix the solution thoroughly by pipetting.Then after layering 40, 20 and 10%iodixanol solution in sequence, use a 1, 000 microliter pipette to add 3.5 milliliters of PBS on top of the 10%iodixanol solution. Adjust the weight of the two tubes with PBS to a total weight within plus minus 0.005 grams. Next, position the tubes in the buckets and centrifuge them at 160, 000 G for seven hours at four degrees Celsius.Using a pipetter, collect the fractions obtained from a gradient ultracentrifugation mode sequentially from top to bottom against the sidewall into 10 separate 38.5 milliliter ultracentrifuge tubes. Then ultracentrifuge the fractions at 160, 000 G for 70 minutes at four degrees Celsius. Remove the supernatant, and invert the ultracentrifuge tubes for five minutes.Next, resuspend the pellets in 200 microliters of pre-chilled PBS using a 200 microliter pipette. Transfer the PBS/BEV solution into a clean 1.5 milliliter microtube. Label the fractions from F1 to F10 as obtained from one gradient ultracentrifugation mode, and proceed for analysis.