המחברים מבקשים להודות לחוסה לואיס ראמוס-בלדראס על תמיכתו הטכנית. עבודה זו נתמכה על ידי המענק הבא ל- PLL מ- CONACYT (FORDECYT-PRONACE-303027). OM-P ו-EO-M קיבלו מלגה מ-CONACYT (736162 ו-481437, בהתאמה). MCM-M קיבל מלגה מ- CONACYT (Estancias Posdoctorales por México 2022 (3)).

<ol>
	<li>Centers for Disease Control and Prevention. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> Parasites - Hookworm. , (2022).</li><li>Camberis, M., Le Gros, G., Urban, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Animal+model+of+Nippostrongylus+brasiliensis+and+Heligmosomoides+polygyrus.">Animal model of Nippostrongylus brasiliensis and Heligmosomoides polygyrus.</a> Current Protocols in Immunology. , (2003).</li><li>Mearns, H., 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=Interleukin-4-promoted+T+helper+2+responses+enhance+Nippostrongylus+brasiliensis-induced+pulmonary+pathology.">Interleukin-4-promoted T helper 2 responses enhance Nippostrongylus brasiliensis-induced pulmonary pathology.</a> Infection and Immunity. 76 (12), 5535-5542 (2008).</li><li>Licona-Limon, P., 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=Th9+cells+drive+host+immunity+against+gastrointestinal+worm+infection.">Th9 cells drive host immunity against gastrointestinal worm infection.</a> Immunity. 39 (4), 744-757 (2013).</li><li>Ferrer-Font, L., 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=High-dimensional+analysis+of+intestinal+immune+cells+during+helminth+infection.">High-dimensional analysis of intestinal immune cells during helminth infection.</a> Elife. 9, 51678 (2020).</li><li>Kharwadkar, 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=Expression+efficiency+of+multiple+IL9+reporter+alleles+Is+determined+by+cell+lineage.">Expression efficiency of multiple IL9 reporter alleles Is determined by cell lineage.</a> Immunohorizons. 4 (5), 282-291 (2020).</li><li>Wilhelm, C., 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+IL-9+fate+reporter+demonstrates+the+induction+of+an+innate+IL-9+response+in+lung+inflammation.">An IL-9 fate reporter demonstrates the induction of an innate IL-9 response in lung inflammation.</a> Nature Immunology. 12 (11), 1071-1077 (2011).</li><li>Gerlach, 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=TH9+cells+that+express+the+transcription+factor+PU.1+drive+T+cell-mediated+colitis+via+IL-9+receptor+signaling+in+intestinal+epithelial+cells.">TH9 cells that express the transcription factor PU.1 drive T cell-mediated colitis via IL-9 receptor signaling in intestinal epithelial cells.</a> Nature Immunology. 15 (7), 676-686 (2014).</li><li>Olson, M. 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=Paracrine+IL-2+is+required+for+optimal+type+2+effector+cytokine+production.">Paracrine IL-2 is required for optimal type 2 effector cytokine production.</a> Journal of Immunology. 198 (11), 4352-4359 (2017).</li><li>Cold Spring Harbor Protocols. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Phosphate-buffered+saline+(PBS).">Phosphate-buffered saline (PBS).</a> Cold Spring Harbor Protocols. , (2006).</li><li>Pinto, M. E. S., Licona-Limon, P. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Th9+cells+and+parasitic+inflammation:+Use+of+Nippostrongylus+and+Schistosoma+models.">Th9 cells and parasitic inflammation: Use of Nippostrongylus and Schistosoma models.</a> Methods in Molecular Biology. 1585, 223-245 (2017).</li><li>Lawrance, C. C., Lucas, E. A., Clarke, S. L., Smith, B. J., Kuvibidila, S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Differential+effects+of+isoflurane+and+CO2+inhalation+on+plasma+levels+of+inflammatory+markers+associated+with+collagen-induced+arthritis+in+DBA+mice.">Differential effects of isoflurane and CO2 inhalation on plasma levels of inflammatory markers associated with collagen-induced arthritis in DBA mice.</a> International Immunopharmacology. 9 (7-8), 807-809 (2009).</li><li>Boivin, G. P., Bottomley, M. A., Schiml, P. A., Goss, L., Grobe, N. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Physiologic,+behavioral,+and+histologic+responses+to+various+euthanasia+methods+in+C57BL/6Ntac+male+mice.">Physiologic, behavioral, and histologic responses to various euthanasia methods in C57BL/6Ntac male mice.</a> Journal of the American Association for Laboratory Animal Science. 56 (1), 69-78 (2017).</li><li>old Spring Harbor Protocols. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Hank's+balanced+salt+solution+(HBSS)+without+phenol+red.">Hank's balanced salt solution (HBSS) without phenol red.</a> Cold Spring Harbor Protocols. , (2006).</li><li>Bielecki, P., 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=Skin-resident+innate+lymphoid+cells+converge+on+a+pathogenic+effector+state.">Skin-resident innate lymphoid cells converge on a pathogenic effector state.</a> Nature. 592 (7852), 128-132 (2021).</li><li>Sanjabi, S., Mosaheb, M. M., Flavell, R. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Opposing+effects+of+TGF-beta+and+IL-15+cytokines+control+the+number+of+short-lived+effector+CD8++T+cells.">Opposing effects of TGF-beta and IL-15 cytokines control the number of short-lived effector CD8+ T cells.</a> Immunity. 31 (1), 131-144 (2009).</li><li>Liu, H., Li, M., Wang, Y., Piper, J., Jiang, L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Improving+single-cell+encapsulation+efficiency+and+reliability+through+neutral+buoyancy+of+suspension.">Improving single-cell encapsulation efficiency and reliability through neutral buoyancy of suspension.</a> Micromachines. 11 (1), 94 (2020).</li><li>Huang, Y., 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=IL-25-responsive,+lineage-negative+KLRG1(hi)+cells+are+multipotential+'inflammatory'+type+2+innate+lymphoid+cells.">IL-25-responsive, lineage-negative KLRG1(hi) cells are multipotential 'inflammatory' type 2 innate lymphoid cells.</a> Nature Immunology. 16 (2), 161-169 (2015).</li><li>Huang, Y., 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=S1P-dependent+interorgan+trafficking+of+group+2+innate+lymphoid+cells+supports+host+defense.">S1P-dependent interorgan trafficking of group 2 innate lymphoid cells supports host defense.</a> Science. 359 (6371), 114-119 (2018).</li><li>Flamar, A. L., 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=Interleukin-33+induces+the+enzyme+Tryptophan+hydroxylase+1+to+promote+inflammatory+group+2+innate+lymphoid+cell-mediated+immunity.">Interleukin-33 induces the enzyme Tryptophan hydroxylase 1 to promote inflammatory group 2 innate lymphoid cell-mediated immunity.</a> Immunity. 52 (4), 606-619 (2020).</li><li>Olgu&#237;n-Mart&#237;nez, 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=IL-33+and+the+PKA+pathway+regulate+ILC2+populations+expressing+IL-9+and+ST2.">IL-33 and the PKA pathway regulate ILC2 populations expressing IL-9 and ST2.</a> Frontiers in Immunology. 13, 787713 (2022).</li><li>Olguin-Martinez, E., Ruiz-Medina, B. E., Licona-Limon, P. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Tissue-specific+molecular+markers+and+heterogeneity+in+type+2+innate+lymphoid+cells.">Tissue-specific molecular markers and heterogeneity in type 2 innate lymphoid cells.</a> Frontiers in Immunology. 12, 757967 (2021).</li><li>Noelle, R. J., Nowark, E. C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Cellular+sources+and+immune+functions+of+interleukin-9.">Cellular sources and immune functions of interleukin-9.</a> Nature Reviews. Immunology. 10 (10), 683-687 (2010).</li></ol>

למחברים אין מה לחשוף.

הבנה מלאה של אינטראקציות טפיל-מארח במעי ותגובות חיסוניות לזיהום הלמינת'ס דורשת זיהוי וניתוח של אוכלוסיות התאים השונות ומולקולות ההשפעה שהן המפתח להשראת עיצוב מחדש של רקמות וסילוק תולעים. זיהומי הלמינת'ס המועברים בקרקע מהווים בעיה גדולה במדינות מתפתחות ברחבי העולם. עם זאת, עד לאחרונה, פרוטוקול שאיפשר ניתוח של אוכלוסיות תאים נדירים הנמצאים במעי הדק, האיבר העיקרי המושפע מזיהום זה, לא היה זמין5. פרוטוקול זה מכסה שיטות שתוארו בעבר המאפשרות ניתוח ציטומטרי זרימה של תאי לימפה המבטאים IL-9 בריאה, בבלוטות הלימפה המדיאסטינליות והמזנטריות במהלך זיהום N. brasiliensis , עם יתרון נוסף של זיהוי אוכלוסייה זו לראשונה במעי הדק.
הצלחתו של פרוטוקול זה תלויה מאוד בזמני עיבוד הרקמות. זה הכרחי לעבד מקסימום של שש דגימות המעי הדק, לאדם, בבת אחת. אם רוצים לעבד איברים שונים, אנו ממליצים לעשות זאת במקביל על ידי אדם אחר. על ידי שימוש בעומס טפיל נמוך יחסית (200 זחלי L3), פרוטוקול זה מאפשר בידוד של תאי לימפה מהמעי הנגוע ב- N. brasiliensis, תוך שמירה על היכולת לבודד תאים אלה מאיברים אחרים. השימוש בעומסי טפילים גבוהים יותר מסכן את האיכות והכמות של התאים המבודדים מהמעי הדק (הנתונים אינם מוצגים); עם זאת, זה יכול לגרום לעלייה משמעותית של תאי לימפה המבטאים IL-9 באיברים אחרים4. בעת עיבוד המעי ובלוטות הלימפה המזנטריות, חיוני להסיר את רקמת השומן הדבוקה, שכן כישלון בכך גורם למוות מוגבר של תאים. הנתונים תומכים בתצפית כי מהלך הזיהום הטבעי משפיע לרעה על המספר האבסולוטי של תאי הלימפה שהתאוששו מהמעי הדק. במחקרים המתוארים כאן, התדרים של תאי IL-9+ ILC2 נשארים עקביים, בעוד מספרים מוחלטים מראים שונות גבוהה בכל ניסוי עצמאי. לפיכך, מסקנות הנובעות ממספרים מוחלטים עלולות להיות לא מדויקות ויש להימנע מהן. בנוסף, בהתחשב בתדירות הנמוכה של תאי T המבטאים IL-9 ברקמות, מומלץ לרכוש ולהכתים את מספר התאים הגבוה ביותר האפשרי.
מגבלה של ניתוח ILC2 זה היא השימוש בשילוב בדיד של סמנים כדי להגדיר אוכלוסייה זו. בהתאם לרקמת העניין ולשלב הזיהום, סמנים נוספים, כגון CD25, Klrg1 ו- ST2 בין היתר, יכולים לשמש לאפיון פנוטיפי מפורט יותר של תאי ILC222. אנו מכירים בכך שהפרוטוקול המוצג כאן מבוסס על זן העכברINFER reporter 4, ועשוי להוות יתרון לזיהוי תאים המבטאים IL-9. עם זאת, אנו מצפים כי התוצאות שנמצאו כאן ניתן להשיג באמצעות אסטרטגיות חלופיות, כולל שימוש בזנים אחרים של עכבר מדווח וצביעת IL-9 תוך תאית 6,7,8,9. חשוב לציין ששימוש בעכברים רגילים וביצוע צביעה תוך-תאית של IL-9 בתאים תוך-אפיתליאליים ולמינה פרופריה עלולים לגרום לאיבוד כל אות שניתן לזיהוי ולסכן את הנתונים המתקבלים (איור משלים 7). זה יכול להיות בגלל מניפולציה ארוכת טווח הנדרשת כדי להכתים תת-קבוצה שכבר קשה לבודד ולשמור על ex vivo. לכן, אנו ממליצים על שימוש בזני עכברים מדווחים כדי לקצר את זמני העיבוד ולהבטיח ניתוח אמין של ביטוי IL-9 in vivo. אנו גם מכירים בעובדה שתאי Th9 אינם תאי T היחידים המבטאים IL-923; עם זאת, במודל טפילי זה, לא היינו מצפים מתתי-קבוצות אחרות לבטא אותו. עם זאת, כדי לשלול את נוכחותן של תת-קבוצות אחרות המבטאות IL-9 בהקשר המתואר, אפיון מלא של ציטוקינים מסוג 2 יחד עם שימוש בסמני שעתוק אפשרי.
בעבר דווח על כימות תאי לימפה המבטאים IL-9 לפני היום החמישי שלאחר ההדבקה; עם זאת, התוצאה היא תדרי תאים נמוכים מאוד4. הפרוטוקול במחקר זה מכסה חלק גדול מהקינטיקה של זיהום N. brasiliensis עד תחילת פינוי הטפיל2. עם זאת, שמנו לב שחלק מאוכלוסיות התאים במחקר זה לא חזרו לרמות הבסיס במסגרת הזמן שנותחה, מה שמרמז על כך שהמחקר יכול להפיק תועלת מנקודות זמן ממושכות כדי לקבל פרספקטיבה מלאה על ההתנהגות של תאים אלה בשלב מתקדם יותר של זיהום in vivo. בכל מקרה, אנו מאמינים כי העבודה המוצגת כאן יכולה לשמש מדריך עזר לחוקרים המעוניינים לחקור תאי לימפה המבטאים IL-9 במודלים של זיהום טפילים, ולאפשר להם לבחור את השלב האידיאלי של זיהום לזיהוי סוגי תאים ספציפיים מרקמות מעניינות. בסך הכל, השיטות המתוארות כאן יהיו שימושיות כדי להעריך את הפנוטיפ והתפקוד של לימפוציטים מסוג T ותאי ILC2 המבטאים IL-9 במהלך מודל רלוונטי מבחינה פיזיולוגית של זיהום טפילים, מה שמרחיב את הידע שלנו על תאים אלה ועשוי לשפר את הבנתנו אותם במצבים פתולוגיים אחרים.

תולעי קרס הן טפילי מעיים המדביקים כ-700 מיליון בני אדם ברחבי העולם, בעיקר באזורים טרופיים במדינות לא מפותחות. זיהומים בעוצמה גבוהה עם Ancylostoma duodenale ו - Necator americanus, טפילי תולעי הקרס הנפוצים ביותר בבני אדם, גורמים לאנמיה ומחסור בחלבון שעלולים לגרום לעיכוב בגדילה ובהתפתחות הנפשית1. N. americanus וטפיל המכרסם Nippostrongylus brasiliensis גורמים לתגובה חיסונית טיפוסית מסוג 2 אצל הפונדקאי שלהם וחולקים קווי דמיון במחזור החיים שלהם. לפיכך, זיהום של עכברים עם N. brasiliensis הוא המודל הנפוץ ביותר עבור זיהומים תולעי קרס אנושיים. שלב 3 (L3) זחלים זיהומיים N. brasiliensis עוברים מהעור לריאה בשעות הראשונות שלאחר ההדבקה. ברגע שהם בריאה, הם הופכים ל-L4 ונודדים במעלה קנה הנשימה כדי להיבלע, לעבור דרך הקיבה ולהגיע למעיים כדי להפוך למבוגרים (L5) תוך 4-5 ימים. במעיים, תולעי L5 מטילות ביצים המופרשות בצואה כדי להפעיל מחדש את מחזור החיים של הטפיל2.
התגובה החיסונית הנגרמת על ידי N. brasiliensis מאופיינת על ידי עלייה במספר ציטוקינים מסוג 2, כולל IL-4, IL-5, IL-9, IL-10 ו- IL-13, יחד עם אאוזינופיליה, בזופיליה, היפרפלזיה של גביע ותאי פיטום, וייצור מוגבר של IgG1 ו- IgE. רוב המחקרים המנסים לזהות ולהגדיר את התגובות החיסוניות המתעוררות על זיהום N. brasiliensis מתמקדים בתפקיד של IL-4 או IL-13 במודל זה3. עם זאת, הזיהוי והאפיון של תאים המבטאים IL-9 ותפקודו של ציטוקין זה התעלמו במידה רבה, עד שליקונה-לימון ועמיתיו פרסמו את המחקר הראשון שהוכיח תפקיד קריטי עבור IL-9 בתגובה החיסונית נגד N. brasiliensis. באמצעות עכברי דיווח, מחקר זה תיאר תאי T (בעיקר T עוזר 9) ותאי לימפה מולדים מסוג 2 (ILC2s) כתת-קבוצות התאיות העיקריות המבטאות IL-9 בעת זיהום4.
בידוד ואפיון של תאי מערכת החיסון מריאות נגועות בהלמינת'ס הוא אפשרי, ודווח בהרחבה 3,4. עם זאת, בגלל שיפוץ הרקמה האינהרנטית וייצור הריר, לעשות זאת במעיים הנגועים התגלה כאתגר טכני, עד לפרסום האחרון של Ferrer-Font et al.5. הקבוצה התוותה פרוטוקול לבידוד וניתוח תרחיפים חד-תאיים של תת-קבוצות חיסוניות ממעי מורין נגועים בפוליגירוס Heligmosomoides. בהתבסס על זה, יש לנו עכשיו סטנדרטיזציה פרוטוקול לבידוד וניתוח ציטוטומטרי של תאי לימפה המבטאים IL-9 מן המעי נגוע N. brasiliensis. בנוסף, ביססנו קינטיקה IL-9 ממקורות תאיים שונים וממיקומים אנטומיים שונים במהלך הזיהום.
אפיון אוכלוסיות התאים השונות המעורבות בזיהום זה חיוני להבנה רחבה יותר של התגובה החיסונית לטפיל והאינטראקציה שלו עם הפונדקאי. פרוטוקול מקיף זה מספק מסלול ברור לבידוד וניתוח תאים מייצרי IL-9 מאיברים רצויים בשלבי מחלה, ומאפשר שיפור חד של הידע על תפקידם של תאים אלה בזיהום N. brasiliensis ובזיהומים טפילים בכלל.

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a strategy for the study of il-9-producing lymphoid cells in the nippostrongylus brasiliensis infection model

IL-9 הוא ציטוקין פליוטרופי הקשור לתהליכים שונים, כולל חסינות אנטי-סרטנית, השראת פתולוגיות אלרגיות והתגובה החיסונית נגד זיהומי הלמינת'ס, שם הוא ממלא תפקיד חשוב בגירוש הטפיל. במודל מוריני של זיהום Nippostrongylus brasiliensis, IL-9 מיוצר בעיקר על ידי לימפוציטים מסוג CD4+ T ותאי לימפה מולדים הנמצאים בריאה, במעי הדק ובבלוטות הלימפה המנקזות. בהתחשב בקשיים הטכניים הכרוכים בצביעה תוך-תאית של IL-9, כמו גם המורכבות של בידוד תאים המטופויטיים מהמעי הדק בעת זיהום, יש צורך דחוף בפרוטוקול מקיף אך פשוט לניתוח הביטוי של IL-9 ברקמות לימפואידיות ולא לימפואידיות שונות במודל זה. הפרוטוקול המתואר כאן מתאר את הקינטיקה של IL-9 המיוצרת על ידי תאי T CD4+ ותאי לימפה מולדים בריאה ובמעי הדק, האיברים העיקריים הממוקדים על ידי N. brasiliensis, כמו גם בבלוטות הלימפה mediastinal ו mesenteric, לאורך כל הזיהום. בנוסף, הוא מפרט את מספר הזחלים הדרושים לזיהום, בהתאם לסוג התא והאיבר המעניין. פרוטוקול זה נועד לסייע בסטנדרטיזציה של בדיקות כדי לחסוך זמן ומשאבים על ידי מתן הזדמנות להתמקד בתאים, איברים ושלבי מחלה ספציפיים של עניין במודל זיהום N. brasiliensis.

Watch this Scientific Journal Video about A Strategy for the Study of IL-9-Producing Lymphoid Cells in the Nippostrongylus brasiliensis Infection Model at JoVE.com

A Strategy for the Study of IL-9-Producing Lymphoid Cells in the Nippostrongylus brasiliensis Infection Model

תאי T ו-ILC2 המבטאים IL-9 מושרים במהלך זיהום ב-N. brasiliensis , אך האפיון שלהם התעלם במידה רבה במעי הנגוע בשל התדירות הנמוכה והקינטיקה הדיפרנציאלית שלהם. פרוטוקול זה מתאר בידוד של תאים אלה מאיברי מטרה שונים ואישור זהותם באמצעות ציטומטריית זרימה בשלבי זיהום שונים.

אסטרטגיה לחקר תאי לימפה מייצרי IL-9 במודל זיהום Nippostrongylus brasiliensis

IL-9 is a pleiotropic cytokine associated with various processes, including antitumor immunity, induction of allergic pathologies, and the immune response ...

This protocol allows for the isolation and characterization of lymphoid cells expressing IL-9 in N.brasiliensis non-lymphoid infected tissues including the infected cut which recently was technically invisible.This protocol also provides an alternative to analyze populations of cells from peripheral tissues previously unappreciated in infection due to the intrinsic difficulties of isolating cells from these anatomical sites.This method allows the study of difficult-to-isolate populations from N.brasiliensis infected cut and could be applied to other helminthic infections, broadening our understanding of hookworm infections in humans.Demonstrating the procedure will be Ofelia Mu

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A Strategy for the Study of IL-9-Producing Lymphoid Cells in the Nippostrongylus brasiliensis Infection Model

1.2K Views.  Universidad Nacional Autónoma de México. This protocol allows for the isolation and characterization of lymphoid cells expressing IL-9 in N.brasiliensis non-lymphoid infected tissues including the infected cut which recently was technically invisible.This protocol also provides an alternative to analyze populations of cells from peripheral tissues previously unappreciated in infection due to the intrinsic difficulties of isolating cells from these anatomical sites.This method allows the study of difficult-to-isolate populations from...

Video: A Strategy for the Study of IL-9-Producing Lymphoid Cells in the Nippostrongylus brasiliensis Infection Model

Introducing Shear Stress in the Study of Bacterial Adhesion

During bacterial infections a sequence of interactions occur between the pathogen and its host. Bacterial adhesion to the host cell surface is often the initial and determining step of the pathogenesis. Although experimentally adhesion is mostly studied in static conditions adhesion actually takes place in the presence of flowing liquid. First encounters between bacteria and their host often occur at the mucosal level, mouth, lung, gut, eye, etc. where mucus flows along the surface of epithelial cells. Later in infection, pathogens occasionally access the blood circulation causing life-threatening illnesses such as septicemia, sepsis and meningitis. A defining feature of these infections is the ability of these pathogens to interact with endothelial cells in presence of circulating blood. The presence of flowing liquid, mucus or blood for instance, determines adhesion because it generates a mechanical force on the pathogen. To characterize the effect of flowing liquid one usually refers to the notion of shear stress, which is the tangential force exerted per unit area by a fluid moving near a stationary wall, expressed in dynes/cm2. Intensities of shear stress vary widely according to the different vessels type, size, organ, location etc. (0-100 dynes/cm2). Circulation in capillaries can reach very low shear stress values and even temporarily stop during periods ranging between a few seconds to several minutes 1. On the other end of the spectrum shear stress in arterioles can reach 100 dynes/cm2 2. The impact of shear stress on different biological processes has been clearly demonstrated as for instance during the interaction of leukocytes with the endothelium 3. To take into account this mechanical parameter in the process of bacterial adhesion we took advantage of an experimental procedure based on the use of a disposable flow chamber 4. Host cells are grown in the flow chamber and fluorescent bacteria are introduced in the flow controlled by a syringe pump. We initially focused our investigations on the bacterial pathogen Neisseria meningitidis, a Gram-negative bacterium responsible for septicemia and meningitis. The procedure described here allowed us to study the impact of shear stress on the ability of the bacteria to: adhere to cells 1, to proliferate on the cell surface 5and to detach to colonize new sites 6 (Figure 1). Complementary technical information can be found in reference 7. Shear stress values presented here were chosen based on our previous experience1 and to represent values found in the literature. The protocol should be applicable to a wide range of pathogens with specific adjustments depending on the objectives of the study.

During the infection process, a key step is the adhesion of pathogens with host cells. In most instances this adhesion step occurs in the presence of mechanical stress generated by flowing liquid. We describe a technique that introduces shear stress as an important parameter in the study of bacterial adhesion.

היכרות עם מתח שאר בחקר הדבקה חיידקית

During bacterial infections a sequence of interactions occur between the pathogen and its host. Bacterial adhesion to the host cell surface is often the ...

Following Cell-fate in E. coli After Infection by Phage Lambda

The system comprising bacteriophage (phage) lambda and the bacterium E. coli has long served as a paradigm for cell-fate determination1,2. Following the simultaneous infection of the cell by a number of phages, one of two pathways is chosen: lytic (virulent) or lysogenic (dormant)3,4. We recently developed a method for fluorescently labeling individual phages, and were able to examine the post-infection decision in real-time under the microscope, at the level of individual phages and cells5. Here, we describe the full procedure for performing the infection experiments described in our earlier work5. This includes the creation of fluorescent phages, infection of the cells, imaging under the microscope and data analysis. The fluorescent phage is a "hybrid", co-expressing wild- type and YFP-fusion versions of the capsid gpD protein. A crude phage lysate is first obtained by inducing a lysogen of the gpD-EYFP (Enhanced Yellow Fluorescent Protein) phage, harboring a plasmid expressing wild type gpD. A series of purification steps are then performed, followed by DAPI-labeling and imaging under the microscope. This is done in order to verify the uniformity, DNA packaging efficiency, fluorescence signal and structural stability of the phage stock. The initial adsorption of phages to bacteria is performed on ice, then followed by a short incubation at 35&deg;C to trigger viral DNA injection6. The phage/bacteria mixture is then moved to the surface of a thin nutrient agar slab, covered with a coverslip and imaged under an epifluorescence microscope. The post-infection process is followed for 4 hr, at 10 min interval. Multiple stage positions are tracked such that ~100 cell infections can be traced in a single experiment. At each position and time point, images are acquired in the phase-contrast and red and green fluorescent channels. The phase-contrast image is used later for automated cell recognition while the fluorescent channels are used to characterize the infection outcome: production of new fluorescent phages (green) followed by cell lysis, or expression of lysogeny factors (red) followed by resumed cell growth and division. The acquired time-lapse movies are processed using a combination of manual and automated methods. Data analysis results in the identification of infection parameters for each infection event (e.g. number and positions of infecting phages) as well as infection outcome (lysis/lysogeny). Additional parameters can be extracted if desired.

Following Cell-fate in E. coli After Infection by Phage Lambda

This article describes the procedure for preparing a fluorescently-labeled version of bacteriophage lambda, infection of E. coli bacteria, following the infection outcome under the microscope, and analysis of infection results.

בעקבות Cell-גורל ב<em&gt; א coli</em&gt; לאחר זיהום על ידי phage מבדה

The system comprising bacteriophage (phage) lambda and the bacterium E. coli has long served as a paradigm for cell-fate determination1,2. Following the ...

Cutaneous Leishmaniasis in the Dorsal Skin of Hamsters: a Useful Model for the Screening of Antileishmanial Drugs

Traditionally, hamsters are experimentally inoculated in the snout or the footpad. However in these sites an ulcer not always occurs, measurement of lesion size is a hard procedure and animals show difficulty to eat, breathe and move because of the lesion. In order to optimize the hamster model for cutaneous leishmaniasis, young adult male and female golden hamsters (Mesocricetus auratus) were injected intradermally at the dorsal skin with 1 to 1.5 x l07 promastigotes of Leishmania species and progression of subsequent lesions were evaluated for up to 16 weeks post infection. The golden hamster was selected because it is considered the adequate bio-model to evaluate drugs against Leishmania as they are susceptible to infection by different species. Cutaneous infection of hamsters results in chronic but controlled lesions, and a clinical evolution with signs similar to those observed in humans. Therefore, the establishment of the extent of infection by measuring the size of the lesion according to the area of indurations and ulcers is feasible. This approach has proven its versatility and easy management during inoculation, follow up and characterization of typical lesions (ulcers), application of treatments through different ways and obtaining of clinical samples after different treatments. By using this method the quality of animal life regarding locomotion, search for food and water, play and social activities is also preserved.

Optimization of the experimental hamster model for cutaneous leishmaniasis by intradermal injection of Leishmania promastigotes at the dorsal skin. This approach is useful during inoculation, follow-up, characterization of lesions, application of treatments and obtaining of clinical samples. Locomotion, search for food and water, play and social activities are preserved.

Leishmaniasis עורית בעור הגב של אוגרים: מודל שימושי להקרנה של תרופות Antileishmanial

Traditionally, hamsters are experimentally inoculated in the snout or the footpad. However in these sites an ulcer not always occurs, measurement of ...

Use of Galleria mellonella as a Model Organism to Study Legionella pneumophila Infection

Legionella pneumophila, the causative agent of a severe pneumonia named Legionnaires&#39; disease, is an important human pathogen that infects and replicates within alveolar macrophages. Its virulence depends on the Dot/Icm type IV secretion system (T4SS), which is essential to establish a replication permissive vacuole known as the Legionella containing vacuole (LCV). L. pneumophila infection can be modeled in mice however most mouse strains are not permissive, leading to the search for novel infection models. We have recently shown that the larvae of the wax moth Galleria mellonella are suitable for investigation of L. pneumophila infection. G. mellonella is increasingly used as an infection model for human pathogens and a good correlation exists between virulence of several bacterial species in the insect and in mammalian models. A key component of the larvae&#39;s immune defenses are hemocytes, professional phagocytes, which take up and destroy invaders. L. pneumophila is able to infect, form a LCV and replicate within these cells. Here we demonstrate protocols for analyzing L. pneumophila virulence in the G. mellonella model, including how to grow infectious L. pneumophila, pretreat the larvae with inhibitors, infect the larvae and how to extract infected cells for quantification and immunofluorescence microscopy. We also describe how to quantify bacterial replication and fitness in competition assays. These approaches allow for the rapid screening of mutants to determine factors important in L. pneumophila virulence, describing a new tool to aid our understanding of this complex pathogen.

Use of Galleria mellonella as a Model Organism to Study Legionella pneumophila Infection

The larva of the wax moth Galleria mellonella was recently established as an in vivo model to study Legionella pneumophila infection. Here, we demonstrate fundamental techniques to characterize the pathogenesis of Legionella in the larvae, including inoculation, measurement of bacterial virulence and replication as well as extraction and analysis of infected hemocytes.

שימוש<em&gt; Mellonella Galleria</em&gt; כאורגניזם מודל לחקר<em&gt; הלגיונלה pneumophila</em&gt; זיהום

Legionella pneumophila, the causative agent of a severe pneumonia named Legionnaires&#39; disease, is an important human pathogen that infects and ...

A Rapid Strategy for the Isolation of New Faustoviruses from Environmental Samples Using Vermamoeba vermiformis

The isolation of giant viruses is of great interest in this new era of virology, especially since these giant viruses are related to protists. Giant viruses may be potentially pathogenic for many species of protists. They belong to the recently described order of Megavirales. The new lineage Faustovirus that has been isolated from sewage samples is distantly related to the mammalian pathogen African swine fever virus. This virus is also specific to its amoebal host, Vermamoeba vermiformis, a protist common in health care water systems. It is crucial to continue isolating new Faustovirus genotypes in order to enlarge its genotype collection and study its pan-genome. We developed new strategies for the isolation of additional strains by improving the use of antibiotic and antifungal combinations in order to avoid bacterial and fungal contaminations of the amoeba co-culture and favoring the virus multiplication. We also implemented a new starvation medium to maintain V. vermiformis in optimal conditions for viruses co-culture. Finally, we used flow cytometry rather than microscopic observation, which is time-consuming, to detect the cytopathogenic effect. We obtained two isolates from sewage samples, proving the efficiency of this method and thus widening the collection of Faustoviruses, to better understand their environment, host specificity and genetic content.

A Rapid Strategy for the Isolation of New Faustoviruses from Environmental Samples Using Vermamoeba vermiformis

We describe here the latest advances in viral isolation for the characterization of new genotypes of Faustovirus, a new asfarvirus-related lineage of giant viruses. This protocol can be applied to the high throughput isolation of viruses, especially giant viruses infecting amoeba.

אסטרטגית ראפיד עבור הבידוד של ניו Faustoviruses ממדגמים סביבת שימוש<em&gt; Vermiformis Vermamoeba</em

The isolation of giant viruses is of great interest in this new era of virology, especially since these giant viruses are related to protists. Giant ...

Assessment of the Synaptic Interface of Primary Human T Cells from Peripheral Blood and Lymphoid Tissue

The current understanding of the dynamics and structural features of T-cell synaptic interfaces has been largely determined through the use of glass-supported planar bilayers and in vitro-derived T-cell clones or lines1,2,3,4. How these findings apply to the primary human T cells isolated from blood or lymphoid tissues is not known, partly due to significant difficulties in obtaining a sufficient number of cells for analysis5. Here we address this through the development of a technique exploiting multichannel flow slides to build planar lipid bilayers containing activating and adhesion molecules. The low height of the flow slides promotes rapid cell sedimentation in order to synchronize cell:bilayer attachment, thereby allowing researchers to study the dynamic of the synaptic interface formation and the kinetics of the granules release. We apply this approach to analyze the synaptic interface of as few as 104 to 105 primary cryopreserved T cells isolated from lymph nodes (LN) and peripheral blood (PB). The results reveal that the novel planar lipid bilayer technique enables the study of the biophysical properties of primary human T cells derived from blood and tissues in the context of health and disease.

The protocol describes a technique to study the ability of primary polyclonal human T cells to form synaptic interfaces using planar lipid bilayers. We use this technique to show the differential synapse formation capability of human primary T cells derived from lymph nodes and peripheral blood.

הערכה של הממשק סינפטית של תאי T האנושי העיקרי של דם היקפיים ורקמות הלימפה

The current understanding of the dynamics and structural features of T-cell synaptic interfaces has been largely determined through the use of ...

The Galleria mellonella Waxworm Infection Model for Disseminated Candidiasis

Candida species are common fungal commensals of humans colonizing the skin, mucosal surfaces, and gastrointestinal tract. Under certain conditions, Candida can overgrow their natural niches resulting in debilitating mucosal infections as well as life-threatening systemic infections, which are a major focus of investigation due to their associated high mortality rates. Animal models of disseminated infection exist for studying disease progression and dissecting the characteristics of Candida pathogenicity. Of these, the Galleria mellonella waxworm infection model provides a cost-effective experimental tool for high-throughput investigations of systemic virulence. Many other bacterial and eukaryotic infectious agents have been effectively studied in G. mellonella to understand pathogenicity, making it a widely accepted model system. Yet, variation in the method used to infect G. mellonella can alter phenotypic outcomes and complicate interpretation of the results. Here, we outline the benefits and drawbacks of the waxworm model to study systemic Candida pathogenesis and detail an approach to improve reproducibility. Our results highlight the range of mortality kinetics in G. mellonella and describe the variables which can modulate these kinetics. Ultimately, this method stands as an ethical, rapid, and cost-effective approach to study virulence in a model of disseminated candidiasis.

The Galleria mellonella Waxworm Infection Model for Disseminated Candidiasis

Galleria mellonella serves as an invertebrate model for disseminated candidiasis. Here, we detail the infection protocol and provide supporting data for the model&#39;s effectiveness.

לדוגמא Galleria mellonella Waxworm זיהום קנדידה המופץ

Candida species are common fungal commensals of humans colonizing the skin, mucosal surfaces, and gastrointestinal tract. Under certain conditions, ...

A Galleria mellonella Oral Administration Model to Study Commensal-Induced Innate Immune Responses

The investigation of the immunogenic potential of commensal bacteria on the host immune system is one essential component when studying intestinal host-microbe interactions. It is well established that different commensals exhibit a different potential to stimulate the host intestinal immune system. Such investigations involve vertebrate animals, especially rodents. Since increasing ethical concerns are linked with experiments involving vertebrates, there is a high demand for invertebrate replacements models. 
Here, we provide a Galleria mellonella oral administration model using commensal non-pathogenic bacteria and the possible assessment of the immunogenic potential of commensals on the G. mellonella immune system. We demonstrate that G. mellonella is a useful alternative invertebrate replacement model that allows the analysis of commensals with different immunogenic potential such as Bacteroides vulgatus and Escherichia coli. Interestingly, the bacteria exhibited no killing effect on the larvae, which is similar to mammals. The immune responses of G. mellonella were comparable with vertebrate innate immune responses and involve recognition of the bacteria and production of antimicrobial molecules. We propose that G. mellonella was able to restore previous microbiota balance, which is well known from healthy mammalian individuals. Although providing comparable innate immune responses in both G. mellonella and vertebrates, G. mellonella does not harbor an adaptive immune system. Since the investigated components of the innate immune system are evolutionary conserved, the model allows a prescreening and first analysis of bacterial immunogenic properties.

A Galleria mellonella Oral Administration Model to Study Commensal-Induced Innate Immune Responses

Here, we provide a detailed protocol for an oral administration model using Galleria mellonella larvae and how to characterize induced innate immune responses. Using this protocol, researchers without practical experience will be able to use the G. mellonella force-feeding method.

גלרייה mellonella מודל הניהול אוראלי את תגובות מערכת החיסון מולדים Study Commensal-Induced

The investigation of the immunogenic potential of commensal bacteria on the host immune system is one essential component when studying intestinal ...

Use of the Invertebrate Galleria mellonella as an Infection Model to Study the Mycobacterium tuberculosis Complex

Tuberculosis is the leading global cause of infectious disease mortality and roughly a quarter of the world&#8217;s population is believed to be infected with Mycobacterium tuberculosis. Despite decades of research, many of the mechanisms behind the success of M. tuberculosis as a pathogenic organism remain to be investigated, and the development of safer, more effective antimycobacterial drugs are urgently needed to tackle the rise and spread of drug resistant tuberculosis. However, the progression of tuberculosis research is bottlenecked by traditional mammalian infection models that are expensive, time consuming, and ethically challenging. Previously we established the larvae of the insect Galleria mellonella (greater wax moth) as a novel, reproducible, low cost, high-throughput and ethically acceptable infection model for members of the M. tuberculosis complex. Here we describe the maintenance, preparation, and infection of G. mellonella with bioluminescent Mycobacterium bovis BCG lux. Using this infection model, mycobacterial dose dependent virulence can be observed, and a rapid readout of in vivo mycobacterial burden using bioluminescence measurements is easily achievable and reproducible. Although limitations exist, such as the lack of a fully annotated genome for transcriptomic analysis, ontological analysis against genetically similar insects can be carried out. As a low cost, rapid, and ethically acceptable model for tuberculosis, G. mellonella can be used as a pre-screen to determine drug efficacy and toxicity, and to determine comparative mycobacterial virulence prior to the use of conventional mammalian models. The use of the G. mellonella-mycobacteria model will lead to a reduction in the substantial number of animals currently used in tuberculosis research.

Use of the Invertebrate Galleria mellonella as an Infection Model to Study the Mycobacterium tuberculosis Complex

Galleria mellonella was recently established as a reproducible, cheap, and ethically acceptable infection model for the Mycobacterium tuberculosis complex. Here we describe and demonstrate the steps taken to establish successful infection of G. mellonella with bioluminescent Mycobacterium bovis BCG lux.

השימוש חסרי חוליות גלריה מלאבלה כמודל זיהום לחקור את מתחם שחפת של פטרת

Tuberculosis is the leading global cause of infectious disease mortality and roughly a quarter of the world&#8217;s population is believed to be infected ...

Lentiviral CRISPR/Cas9-Mediated Genome Editing for the Study of Hematopoietic Cells in Disease Models

Manipulating genes in hematopoietic stem cells using conventional transgenesis approaches can be time-consuming, expensive, and challenging. Benefiting from advances in genome editing technology and lentivirus-mediated transgene delivery systems, an efficient and economical method is described here that establishes mice in which genes are manipulated specifically in hematopoietic stem cells. Lentiviruses are used to transduce Cas9-expressing lineage-negative bone marrow cells with a guide RNA (gRNA) targeting specific genes and a red fluorescence reporter gene (RFP), then these cells are transplanted into lethally-irradiated C57BL/6 mice. Mice transplanted with lentivirus expressing non-targeting gRNA are used as controls. Engraftment of transduced hematopoietic stem cells are evaluated by flow cytometric analysis of RFP-positive leukocytes of peripheral blood. Using this method, ~90% transduction of myeloid cells and ~70% of lymphoid cells at 4 weeks after transplantation can be achieved. Genomic DNA is isolated from RFP-positive blood cells, and portions of the targeted site DNA are amplified by PCR to validate the genome editing. This protocol provides a high-throughput evaluation of hematopoiesis-regulatory genes and can be extended to a variety of mouse disease models with hematopoietic cell involvement.

Described are protocols for the highly efficient genome editing of murine hematopoietic stem and progenitor cells (HSPC) by the CRISPR/Cas9 system to rapidly develop mouse model systems with hematopoietic system-specific gene modifications.

לנטינגיו CRISPR/Cas9 בתיווך הגנום עריכה לחקר התאים המטפאות במודלים למחלות

Manipulating genes in hematopoietic stem cells using conventional transgenesis approaches can be time-consuming, expensive, and challenging. Benefiting ...