{"id":1260,"date":"2017-07-28T23:26:41","date_gmt":"2017-07-29T06:26:41","guid":{"rendered":"http:\/\/depts.washington.edu\/cfrtc\/?p=1260"},"modified":"2021-04-20T17:31:13","modified_gmt":"2021-04-21T00:31:13","slug":"rdp-pilot-hernandez","status":"publish","type":"post","link":"https:\/\/depts.washington.edu\/cfrtc\/rdp-pilot-hernandez\/","title":{"rendered":"RDP Pilot &#8211; Hernandez"},"content":{"rendered":"<p>[et_pb_section fullwidth=&#8221;on&#8221; specialty=&#8221;off&#8221;][et_pb_fullwidth_slider admin_label=&#8221;Fullwidth Slider&#8221; show_arrows=&#8221;on&#8221; show_pagination=&#8221;on&#8221; auto=&#8221;off&#8221; parallax=&#8221;off&#8221; parallax_method=&#8221;off&#8221; module_id=&#8221;interior&#8221;][et_pb_slide background_image=&#8221;https:\/\/depts.washington.edu\/cfrtc\/wp-content\/uploads\/2014\/12\/microscope11.jpg&#8221; background_color=&#8221;#ffffff&#8221; alignment=&#8221;center&#8221; background_layout=&#8221;dark&#8221; \/][\/et_pb_fullwidth_slider][\/et_pb_section][et_pb_section][et_pb_row][et_pb_column type=&#8221;1_4&#8243;][et_pb_sidebar admin_label=&#8221;Pilots Sidebar&#8221; orientation=&#8221;left&#8221; area=&#8221;et_pb_widget_area_7&#8243; background_layout=&#8221;light&#8221; \/][\/et_pb_column][et_pb_column type=&#8221;3_4&#8243;][et_pb_text admin_label=&#8221;Text&#8221; background_layout=&#8221;light&#8221; text_orientation=&#8221;left&#8221;]<\/p>\n<h1 style=\"text-align: center;\">RDP Pilot: Efflux Pumps in Nontuberculosis Mycobacteria<\/h1>\n<p><strong>P.I.:<\/strong> <a href=\"http:\/\/www.seattlechildrens.org\/medical-staff\/Rafael-E-Hernandez\/\" target=\"blank\">Rafael Hernandez, MD, PhD<\/a><br \/>\nAssistant Professor,<br \/>\nPediatrics<\/p>\n<p>Nontuberculosis mycobacteria (NTM) are environmental organisms that can cause pulmonary and other infections in susceptible hosts. Cystic fibrosis (CF) patients are at increased risk for NTM infections and recent epidemiologic studies suggest that the prevalence of NTM disease caused by both Mycobacterium avium complex (MAC) and M. abscessus (MABSC) in patients with CF may be increasing. The rapidly growing mycobacteria of the M. abscessus group are of particular concern as they can be associated with rapid decline in lung function and increased risk for poor outcomes following lung transplant. Like treatment for tuberculosis (TB), NTM infections require treatment with many months of potentially toxic antibiotics. There are a very limited number of antibiotics active against NTM, especially for M. abscessus, cure rates are low, and relapse is common. Therefore, new strategies are desperately needed for treatment of NTM infections; targeting bacterial efflux pumps (EPs) represents one such strategy. EPs are membrane transporters with promiscuous substrate specificity, which have been implicated in both intracellular survival and antibiotic tolerance in M. tuberculosis (Mtb). Furthermore, many of the EPs are conserved between Mtb and related NTM pathogens. Recent data from cell and animal models for TB suggest that the addition of efflux pump inhibitors to standard antibiotic regimens offers the potential for shorter and more efficacious treatment courses. The goal of this pilot project is test the hypotheses that EPs conserved between Mtb and NTM serve as virulence factors in NTM, and that EPs mediate both NTM antibiotic tolerance and NTM resistance to killing by macrophages.<\/p>\n<p><strong>Aim 1. Determine the expression dynamics of mycobacterial efflux pumps in NTM pathogens.<\/strong><br \/>\nHypothesis: Intracellular residence of NTM induces expression of mycobacterial efflux pumps.<br \/>\nApproach: We will infect a human macrophage cell line with either MAC or M. abscessus complex and isolate bacterial mRNA for RNAseq evaluation of expression of efflux pumps. We then will determine expression of efflux pumps in bacteria isolated directly from sputum to correlate gene expression in our cell culture model with expression of NTM efflux pumps within patients.<\/p>\n<p><strong>Aim 2. Determine whether efflux pump inhibitors will block intracellular growth or survival of NTM pathogens.<\/strong><br \/>\nHypothesis: NTM depend on efflux pumps for intracellular survival and\/or growth.<br \/>\nApproach: We will infect a human macrophage cell line with MAC or M. abscessus, using both reference and patient derived strains and then treat infected cells with efflux pump inhibitors. Bacterial growth\/survival will be assayed by enumerating colony-forming units.<\/p>\n<p><strong>Aim 3. Determine if efflux pumps contribute to either intrinsic antibiotic resistance or induced tolerance in NTM pathogens.<\/strong><br \/>\nHypothesis: Efflux pumps contribute to the broad intrinsic resistance of NTM pathogens and also underlie the poor correlation between in vitro susceptibility to antibiotics and in vivo activity.<\/p>\n<p>Approach: We will test the activity of antibiotics with and without the addition of efflux pump inhibitors both in vitro (broth culture) and in infected macrophages. We will also test whether growth of NTM within biofilms induces antibiotic tolerance and whether efflux pump inhibitors can overcome this tolerance.<\/p>\n<p>[\/et_pb_text][\/et_pb_column][\/et_pb_row][\/et_pb_section]<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Pilot 12: Identification of Biomarkers for Cystic Fibrosis Associated Nephrotoxicity<\/p>\n<p>P.I.:  \t<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_et_pb_use_builder":"on","_et_pb_old_content":"<p>P.I.: <a href=\"http:\/\/depts.washington.edu\/metab\/directory\/faculty\/steven-e-kahn-m-b-ch-b\/\" target=\"_blank\">Steven Kahn, MB, ChB<\/a><br \/> Professor of Medicine<br \/> Metabolism, Endocrinology and Nutrition<\/p><p><a href=\"http:\/\/depts.washington.edu\/metab\/directory\/faculty\/kristina-utzschneider-m-d\/\" target=\"_blank\">Kristina Utzschneider, MD<\/a><br \/> Associate Professor of Medicine<br \/> Metabolism, Endocrinology and Nutrition<\/p><p>With the increased life expectancy of patients with cystic fibrosis (CF), other co-morbidities have become apparent in these patients. One of these is abnormal glucose metabolism, where CF-related diabetes (CFRD) is common. More recently, another abnormality of glucose metabolism has been recognized; namely late hypoglycemia following oral glucose loading. In this study, we propose to test the hypothesis that the post-glucose load hypoglycemia observed in patients with CF results from a deficient counterregulatory hormone response and\/or an insulin response that is exaggerated and delayed. This increased insulin response could be the result of an exaggerated incretin hormone response or altered gastric emptying. To address this hypothesis, we will perform a 3-hour oral glucose tolerance test during which we will measure counterregulatory, islet and incretin hormone responses and determine the rate of gastric emptying using acetaminophen. To determine whether patients with CF and late hypoglycemia also have episodes of hypoglycemia during daily living that includes mixed meals, we will use a continuous glucose monitoring system (CGMS) to examine 24-hour glucose profiles for 3 days. All these measures will be compared between patients with CF who develop late hypoglycemia, CF patients who do not develop hypoglycemia, and age and body mass index-matched healthy controls. The findings from this study will provide important new information regarding the mechanism(s) responsible for the late hypoglycemia observed in patients with CF and the data could be used as the basis for future grant applications. The ultimate goal is to gain insight into the condition of late hypoglycemia in order to better manage patients with CF.<\/p>","_et_gb_content_width":"","_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"footnotes":"","_links_to":"","_links_to_target":""},"categories":[12],"tags":[],"_links":{"self":[{"href":"https:\/\/depts.washington.edu\/cfrtc\/wp-json\/wp\/v2\/posts\/1260"}],"collection":[{"href":"https:\/\/depts.washington.edu\/cfrtc\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/depts.washington.edu\/cfrtc\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/depts.washington.edu\/cfrtc\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/depts.washington.edu\/cfrtc\/wp-json\/wp\/v2\/comments?post=1260"}],"version-history":[{"count":2,"href":"https:\/\/depts.washington.edu\/cfrtc\/wp-json\/wp\/v2\/posts\/1260\/revisions"}],"predecessor-version":[{"id":1265,"href":"https:\/\/depts.washington.edu\/cfrtc\/wp-json\/wp\/v2\/posts\/1260\/revisions\/1265"}],"wp:attachment":[{"href":"https:\/\/depts.washington.edu\/cfrtc\/wp-json\/wp\/v2\/media?parent=1260"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/depts.washington.edu\/cfrtc\/wp-json\/wp\/v2\/categories?post=1260"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/depts.washington.edu\/cfrtc\/wp-json\/wp\/v2\/tags?post=1260"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}