edexcel a level biology cystic fibrosiswendy williams sister lawyer
However, while humans have long benefited from antimicrobials, mechanisms of resistance to classical antimicrobials have emerged and spread among bacteria [, Hence, antivirulence therapy (AVT) consists of the use of drugs targeting pathways important for pathogenesis but not essential for microbial growth [, Selective pressure is not a consequence of the AVT approach, as it aims to prevent attacks on the host rather than eliminate pathogens. Cystic fibrosis (CF) is the number-one life-shortening inherited disease of young people. * The process of transcription and translation In this context, drugs already used against, To date, there is not a consolidated standard drug regimen to treat MABSC infections, although the US Cystic Fibrosis Foundation and the European Cystic Fibrosis Society published consensus recommendations for the management of NTM in patients with CF [. In fact, alongside symptom therapy, personalized therapies are now starting to treat the basic defect in some CFTR mutations [, Thanks to scientific research, new therapeutic approaches have indeed emerged that can correct the defects underlying CF. ; Smith, B.E. ; Catanzaro, A.; Daley, C.; Gordin, F.; Holland, S.M. Mycobacterium abscessus Infections in Cystic Fibrosis Individuals: A Review on Therapeutic Options. Bacteria Percentage of people with cystic fibrosis who have a lung infection (%) 5 years old 15 years old 25 years old 35 years old 45 years old P. aeruginosa 34 70 82 82 75 S. aureus 42 45 35 31 25 (i) Using the information in the table, describe the relationship between the age US Cystic Fibrosis Foundation and European Cystic Fibrosis Society. 2.14 (i): Understand how errors in DNA replication can give rise to mutations (substitution, insertion and deletion of bases) Available online: OSullivan, B.P. Normally, mucus in the lungs traps germs, which are then cleared out of the lungs. 2.13 (ii): Understand patterns of inheritance, including the interpretation of genetic pedigree diagrams, in the context of monohybrid inheritance They have been successfully used to treat a plethora of diseases, from cancer to infections and as putative wound dressing [, Recently, those tools have been also investigated as putative weapons against, One example is gallium-based nanoparticles, which showed significant results in blocking, The efficacy of liposome encapsulated rifampicin compared to free rifampicin, in an ex vivo, Nanoniosomes are vesicles with a composition similar to that of the cell membrane (named niosomes) that have been loaded with antibiotics or lignin-silver nanoparticles. A Test for Concentration of Electrolytes in Sweat in Cystic Fibrosis of the Pancreas Utilizing Pilocarpine by Iontophoresis. Recently, Dedrick et al. ; Bach, H. Targeting intracellular mycobacteria using nanosized niosomes loaded with antibacterial agents. Exercise to dislodge the mucus P1b 1c Very big and very small numbers H PBworks. Shanthikumar, S.; Neeland, M.N. [, Therefore, being as this preliminary evidence very promising, it is advisable to continue to study the use of NO as an alternative strategy to treat, Phage therapy (PT) represents an old idea which has acquired renewed importance thanks to the successful recent case reports, where antibiotic-resistant lung infections in CF people were treated [, PT refers to the use of phages to fight bacterial infections. In a healthy person, the pancreas produces chemicals (enzymes) which pass into the gut as food leaves the stomach. Currently, there have been few reported cases of phage therapy in humans, e.g., a clinical trial done in London reached phase II for the treatment of chronic otitis from, Of particular interest is a study carried out in Tbilisi (Georgia), in which CF people with pulmonary infections were treated by nebulization with phage preparations, combined with conventional antibiotics, anti-mucus drugs, and vitamins. Chan, B.K. ; Pasca, M.R. I am constantly thinking of new ways to engage a student with a topic and try to implement that in the design of the lessons. Smaller fleas ad infinitum: Therapeutic bacteriophage redux. What happens if there is too little water in the airways of an individual with cystic fibrosis? * The meaning of key genetic terms These people are called "carriers" of the CF gene. * The structure of proteins If you have cystic fibrosis, this mucus is excessively thick and sticky and cannot perform this role properly. The aim is to provide a snapshot of some of the movement of particles from an area of high concentration to an area of lower concentration Fick's law the rate of diffusion is inversely proportional to the thickness of the gas exchange surface surfactant a complex mixture of phospholipids and proteins that reduces surface tension at the air-liquid interface of the alveolus dipeptide Dorfman, R.; For the CFMD/CFTR1 Team. Active transport, endocytosis & exocytosis (Edexcel A-level Biology A) Some of the key biological topics are covered in topic 2 of the Pearson Edexcel A-level Biology A (Salters Nuffield) course and include the transport of materials across cell membranes, DNA structure and replication, protein synthesis and monohybrid inheritance. Treatment of nontuberculous mycobacterial pulmonary disease: An official ATS/ERS/ESCMID/IDSA clinical practice guideline. In conclusion cystic fibrosis is genetic and if you have this disease you dont have long to live with an average life expectancy of 32. It follows that the level of knowledge required to understand the mechanism of action of VFs in the pathogenesis process must be high, whereas in many cases this knowledge is lacking. Recent advances on antimicrobial wound dressing: A review. ; Cheung, G.Y.C. The site of infection may also play a role in the expression of VFs, varying it accordingly [, Despite these limitations, currently, AVT compounds against, To understand bacteria from a pathophysiological perspective, it may be important to obtain information on both the complete sets of causative genetic variants and the complex genegene (or epistatic) interactions [, Among the most recent discoveries, antimicrobial peptides (AMPs) are becoming an increasingly promising weapon against bacterial infections. 8. ; Degiacomi, G.; Chiarelli, L.R. ; Lima, L.D. [6]. This video explains about Cystic Fibrosis as a whole and how it affects the human body. These enzymes break down the fat. 1) The CFTR protein is missing or non-functional so chloride ions are not secreted into the mucus. Gibson, L.E. * The roles of the template strand, mRNA and tRNA Heifets, L. Mycobacterial infections caused by nontuberculous mycobacteria. Forstermann, U.; Sessa, W.C. Nitric oxide synthases: Regulation and function. basement membrane ; Bourne, S. Phage as an antimicrobial agent: dHerelles heretical theories and their role in the decline of phage prophylaxis in the West. Cystic fibrosis is a genetic disorder of cell membranes It results in the body producing large amounts of thick, sticky mucus in the air passages Over time, this may damage the lungs and stop them from working properly Cystic fibrosis is caused by a recessive allele ( f) This means: Nontuberculous mycobacterial infections in cystic fibrosis. - DNA fragments in the mothers blood plasma and detects cell-free fetal DNA (cffDNA) and analysed ; Nelson, D.; Moore, R.E. * The structure of DNA and RNA COVID-19 vaccine development and a potential nanomaterial path forward. ; Wallace, R.J., Jr. A novel gene, erm(41), confers inducible macrolide resistance to clinical isolates of. The Cystic Fibrosis Foundation is a leading healthcare nonprofit organization like no other. 1) Chloride ions are pumped into the epithelial cell causing a concentration gradient and the CFTR channel protein opens. Chitambar, C.R. Cystic fibrosis affects over 7,500 people in the UK [2]. If you want to see what we offer before purchasing, we have a free membership with sample revision materials. All of the questions included in the lesson have mark schemes which are embedded into the PowerPoint and this allows the students to assess their progress. Although the severity of the disease differs greatly from person to person, the persistence of infection and lung inflammation, which causes the progressive deterioration of lung tissue, is the major cause of morbidity in people with CF. The nearest thing for a cure for cystic fibrosis is gene therapy. ; Kuo, H.P. Some of the key biological topics are covered in topic 2 of the Pearson Edexcel A-level Biology A (Salters Nuffield) course and include the transport of materials across cell membranes, DNA structure and replication, protein synthesis and monohybrid inheritance. * The formation of polypeptides and proteins * Simple and facilitated diffusion as methods of passive transport Deppisch, C.; Herrmann, G.; Graepler-Mainka, U.; Wirtz, H.; Heyder, S.; Engel, C.; Marschal, M.; Miller, C.C. Cystic fibrosis is a genetic disorder caused by a recessive allele. Another mutation reduces the quantity of CFTR protein in membranes. As well as explaining that this channel allows chloride ions to flow across the apical membrane of the epithelial cells, time is taken to emphasise the importance of its inhibition on the ENaC, which prevents the flow of sodium ions back into the cells. ; writingreview and editing, D.R., G.S., D.L.G., A.S., L.R.C., G.D. and M.R.P. Although the majority of the lesson is described with reference to the gaseous exchange system, the impaired functioning of the digestive system in terms of the blockage of the pancreas and liver secretions is considered and discussed and the students are challenged on their understanding through a range of exam-style questions. * The structures of DNA and RNA ; Magombedze, G.; Srivastava, S.; Deshpande, D.; Gumbo, T. Systematic review and meta-analyses of the effect of chemotherapy on pulmonary, Chen, J.; Zhao, L.; Mao, Y.; Ye, M.; Guo, Q.; Zhang, Y.; Xu, L.; Zhang, Z.; Li, B.; Chu, H. Clinical Efficacy and Adverse Effects of Antibiotics Used to Treat, Nash, K.A. Kortright, K.E. ; et al. ; Philley, J.V. The table below shows two of these classes and their effects on the CFTR protein. 3.20 (i): Phenotype is an interaction between genotype and the environment ; Koff, J.L. What happens if there is too little water in an unaffected person's airways? Miller, C.; McMullin, B.; Ghaffari, A.; Stenzler, A.; Pick, N.; Roscoe, D.; Ghahary, A.; Road, J.; Av-Gay, Y. Gaseous nitric oxide bactericidal activity retained during intermittent high-dose short duration exposure. ; van Hoesel, Q.; le Cesne, A.; van Oosterom, A.T.; Clemons, M.J.; Kamby, C.; Hermans, C.; et al. What happens if there is excess water in an unaffected person's airways? Less than half the price of our monthly plan. most exciting work published in the various research areas of the journal. ; De Santis, F.; Henrici De Angelis, L.; Ciciriello, F.; DAndrea, M.M. ; Sennato, S.; De Santis, F.; Forte, J.; Fraziano, M.; Casciardi, S.; Marianecci, C.; Bordi, F.; Carafa, M. Rifampicin-liposomes for, Poerio, N.; Riva, C.; Olimpieri, T.; Rossi, M.; Lor, N.I. Coordination, Response & Gene Technology, 8.2 How a Response is Generated by Effectors, 8.7 The Effects of Drugs on Nervous Transmission, 8.12 Core Practical 18: Amylase in Germinating Cereal Grains, 8.17 Drug Production from Genetically Modified Organisms, 8.19 Transfer of Recombinant DNA into Other Cells, The polypeptide can affect the phenotype, e.g. 3.8 (ii): The linkage of genes on a chromosome and sex linkage Not ready to purchase the revision kit yet? ; Ortega-Rivera, O.A. This lesson bundle contains 16 lessons which have been designed to cover the Pearson Edexcel A-level Biology A (Salters Nuffield) specification points which focus on the structure of DNA and RNA, their roles in replication and protein synthesis, and genetics and inheritance. ; Teschler, H.; Konietzko, N.; Ratjen, F. Effect of L-arginine infusion on airway NO in cystic fibrosis and primary ciliary dyskinesia syndrome. A Science teacher by trade, I've also been known to be found teaching Maths and PE! 3.12: Understand how cells become specialised through differential gene expression, producing active mRNA leading to synthesis of proteins, which in turn control cell processes or determine cell structure in animals and plants, including the lac operon Cystic Fibrosis is caused by a single faulty gene that controls the movement of salt in the body [4]. Food leaves the stomach the mucus P1b 1c Very big and Very small H... Is missing or non-functional so chloride ions are pumped into the gut as food leaves stomach! ( ii ): the linkage of genes on a chromosome and sex linkage not ready to the! Concentration of Electrolytes in Sweat in cystic fibrosis as a whole and how affects... Pancreas Utilizing Pilocarpine by Iontophoresis offer before purchasing, we have a membership... 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