Insights into Non-Enzymatic Carbapenem Resistance: Role of Porin Alterations among <i>Klebsiella pneumoniae</i>

<p id="p1">Carbapenem resistance in <em><italic xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">Klebsiella pneumoniae</italic></em> is a growing public health concern, with loss or deficiency of outer mem...

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Autores principales: Hamzaoui, Zaineb, Ferjani, Sana, Boubaker, Ilhem Boutiba-Ben
Formato: Capítulo de libro
Lenguaje:inglés
Publicado: IntechOpen 2025
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Acceso en línea:https://www.intechopen.com/chapters/89397
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Sumario:<p id="p1">Carbapenem resistance in <em><italic xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">Klebsiella pneumoniae</italic></em> is a growing public health concern, with loss or deficiency of outer membrane porins (OMPs) and &beta;-lactamases production, including extended-spectrum-&beta;-lactamase (ESBL) and cephalosporinases, playing a significant role. <em><italic xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">K. pneumoniae</italic></em> is often found in urinary tract infections, pneumonia, and severe bacteremia, playing a significant role in hospital-acquired infections worldwide. The emergence of ESBL-producing <em><italic xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">K. pneumoniae</italic></em> is closely related to the overuse of expanded-spectrum cephalosporins, a critical factor in its rise. Carbapenems were once the last resort against multidrug-resistant strains producing ESBLs. However, their overuse and misuse have led to resistance mechanisms emerging. This has resulted in carbapenem-resistant Enterobacteriaceae becoming a major public health concern, with limited treatment options, fast transmission, and high mortality rates. Resistance to carbapenems may result from the production of carbapenemases or ESBL and/or AmpC &beta;-lactamases in association with alteration in the outer membrane porins. <em><italic xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">K. pneumoniae</italic></em>, which normally lacks a chromosomally encoded class C &beta;-lactamase, can easily acquire a plasmid encoding AmpC or another broad-spectrum-&beta;-lactamase. These enzymes can confer high-level carbapenem resistance in porin-deficient strains. In addition, ESBL-producing <em><italic xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">K. pneumoniae</italic></em> with deficiency in OmpK35 and OmpK36 may contribute to the antibiotic resistance. These enzymes can confer high-level carbapenem resistance in porin-deficient strains.</p>
ISBN:978-1-83634-842-9
DOI:10.5772/intechopen.114946