solated bacteria from the sputum of a patient that seemed somewhat resistant to their antibiotic ce multiple weeks of treatment had yielded no satisfactory improvement of their active disease. er had then resuspended the patient's sputum in saline and used a mouse model to measure the a phage selected for its capacity to target M. mycobacterium, as a single therapy, and as a herapy with antibiotics. Here is a schematic representation of the experiment: Group 1 Control (saline) oculate mice th patient utum Group 2 wait for active disease to show Treated with phage Collect lung sample every 2 weeks Group 3 Treated with Abx Split mice showing active disease in 4 Group 4 Treated with Abx and Count bacteria in sample groups phage itum from patients were isolated and resuspended in saline. Mice were given equal amounts of sputum intra-nasally and were left to develop active disease. Once the mice developed active were split into 4 group: a control group treated with saline (group 1), a group treated with the e only (group 2), a group treated with antibiotics (Abx) only (group 3) and a group treated with both eriophage (group 4). Group 1 was injected with saline (i.v.) every week, to mimic the treatment oup 2 was given a single dose of bacteriophage on day one of active disease, Group3 was treated every week, and Group 4 was treated with one dose of bacteriophage on day 1 of active disease oses of Abx. Once the 4 treatments started, several mice from each group were culled every 2 weeks , and their lung lavage were collected to count the number of bacteria growing on agar plates with esults from this experiment that Ahmed presented at the lab meeting: Control Figure 5. Bacterial growth in mice model of tuberculosis. Mice were inoculated with the same number of M.tuberculosis and treatment with control (saline), Abx, phage, or Abx with phage started at onset of active disease. Mice lung lavage (sputum samples) were collected Abx and phage
solated bacteria from the sputum of a patient that seemed somewhat resistant to their antibiotic ce multiple weeks of treatment had yielded no satisfactory improvement of their active disease. er had then resuspended the patient's sputum in saline and used a mouse model to measure the a phage selected for its capacity to target M. mycobacterium, as a single therapy, and as a herapy with antibiotics. Here is a schematic representation of the experiment: Group 1 Control (saline) oculate mice th patient utum Group 2 wait for active disease to show Treated with phage Collect lung sample every 2 weeks Group 3 Treated with Abx Split mice showing active disease in 4 Group 4 Treated with Abx and Count bacteria in sample groups phage itum from patients were isolated and resuspended in saline. Mice were given equal amounts of sputum intra-nasally and were left to develop active disease. Once the mice developed active were split into 4 group: a control group treated with saline (group 1), a group treated with the e only (group 2), a group treated with antibiotics (Abx) only (group 3) and a group treated with both eriophage (group 4). Group 1 was injected with saline (i.v.) every week, to mimic the treatment oup 2 was given a single dose of bacteriophage on day one of active disease, Group3 was treated every week, and Group 4 was treated with one dose of bacteriophage on day 1 of active disease oses of Abx. Once the 4 treatments started, several mice from each group were culled every 2 weeks , and their lung lavage were collected to count the number of bacteria growing on agar plates with esults from this experiment that Ahmed presented at the lab meeting: Control Figure 5. Bacterial growth in mice model of tuberculosis. Mice were inoculated with the same number of M.tuberculosis and treatment with control (saline), Abx, phage, or Abx with phage started at onset of active disease. Mice lung lavage (sputum samples) were collected Abx and phage
Biology: The Dynamic Science (MindTap Course List)
4th Edition
ISBN:9781305389892
Author:Peter J. Russell, Paul E. Hertz, Beverly McMillan
Publisher:Peter J. Russell, Paul E. Hertz, Beverly McMillan
Chapter17: Bacterial And Viral Genetics
Section: Chapter Questions
Problem 1ITD
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