The Gut-Brain Axis 2016
DOI: 10.1016/b978-0-12-802304-4.00011-6
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Long-Term Implications of Antibiotic Use on Gut Health and Microbiota in Populations Including Patients With Cystic Fibrosis

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Cited by 4 publications
(5 citation statements)
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References 224 publications
(277 reference statements)
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“…What is meaningful, we observed down-regulation of genes involved in β-oxidation of the fatty acids, which may result in changes of the membranes structure, fluidity and consequently cell shape. This statement can be supported by an observed higher minimum inhibitory concentration for colistin 56,57 that acts as a surface active agent (see Fig. 3C).…”
Section: Discussionmentioning
confidence: 58%
“…What is meaningful, we observed down-regulation of genes involved in β-oxidation of the fatty acids, which may result in changes of the membranes structure, fluidity and consequently cell shape. This statement can be supported by an observed higher minimum inhibitory concentration for colistin 56,57 that acts as a surface active agent (see Fig. 3C).…”
Section: Discussionmentioning
confidence: 58%
“…Therefore, ESBL producing bacteria respond poorly to β-lactams, leading to higher medical costs, prolonged hospital stays, loss of prophylactic protection, and increased mortality [3,4]. ESBLs are not effective in hydrolyzing cephamycins (e.g., cefoxitin and cefotetan) and carbapenems (e.g., imipenem and meropenem), therefore, these antibiotic agents-notably carbapenems, are recommended for the treatment of infections due to ESBL producers [5,6]. ESBL enzymes are mediated by genes, commonly bla CTX-M , bla TEM, and bla SHV , which are harbored by self-transmissible conjugative plasmids that are horizontally shared within the same and different species of bacteria [7,8].…”
Section: Introductionmentioning
confidence: 99%
“…Therefore, ESBL producing bacteria respond poorly to β-lactams, leading to higher medical costs, prolonged hospital stays, loss of prophylactic protection, and increased mortality [ 3 , 4 ]. ESBLs are not effective in hydrolyzing cephamycins (e.g., cefoxitin and cefotetan) and carbapenems (e.g., imipenem and meropenem), therefore, these antibiotic agents—notably carbapenems, are recommended for the treatment of infections due to ESBL producers [ 5 , 6 ].…”
Section: Introductionmentioning
confidence: 99%
“…Lincosamides are mainly used to treat anaerobic infections caused by gram-positive organisms, including infections developed by methicillin resistant Staphylococcus aureus [90]. Originally this class of antibiotics comes from natural product lincomycin, but derivatives also include clindamycin and pirlimycin, from which clindamycin is the most clinically relevant lincosamide [90,91]. Drugs such as lincomycin and clindamycin are bacteriostatic and inhibit protein synthesis.…”
Section: Lincosamidesmentioning
confidence: 99%