{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,5]],"date-time":"2026-05-05T12:24:49Z","timestamp":1777983889657,"version":"3.51.4"},"reference-count":34,"publisher":"Microbiology Society","issue":"3","license":[{"start":{"date-parts":[[2026,3,1]],"date-time":"2026-03-01T00:00:00Z","timestamp":1772323200000},"content-version":"unspecified","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2026,3,1]]},"abstract":"<jats:p>\n                    <jats:bold>Background.<\/jats:bold>\n                    The increasing prevalence of tigecycline and carbapenem-resistant\n                    <jats:italic>Klebsiella pneumoniae<\/jats:italic>\n                    (CRKP) poses a serious challenge, especially in resource-limited settings. Its ability to exchange resistance genes with other bacteria accelerates the spread of multidrug resistance. While carbapenems and tetracyclines have been used effectively against\n                    <jats:italic>K. pneumoniae<\/jats:italic>\n                    , resistance to these agents is now rising globally, narrowing available treatment options.\n                  <\/jats:p>\n                  <jats:p>\n                    <jats:bold>Objective.<\/jats:bold>\n                    The study aimed to determine the phenotypic and genotypic prevalence of carbapenem and tetracycline resistance in\n                    <jats:italic>K. pneumoniae<\/jats:italic>\n                    isolates along with the transferability pattern of carbapenem and tetracycline resistance genes in these isolates.\n                  <\/jats:p>\n                  <jats:p>\n                    <jats:bold>Methodology.<\/jats:bold>\n                    Clinical isolates from pus and respiratory samples were identified using biochemical tests and MALDI-TOF MS. Antimicrobial susceptibility test was performed by the Kirby\u2013Bauer disc diffusion method, and MICs were determined by the broth microdilution test method. PCR was performed to detect carbapenemase (\n                    <jats:italic>bla<\/jats:italic>\n                    <jats:sub>NDM<\/jats:sub>\n                    ,\n                    <jats:italic>bla<\/jats:italic>\n                    <jats:sub>OXA-48<\/jats:sub>\n                    and\n                    <jats:italic>bla<\/jats:italic>\n                    <jats:sub>KPC<\/jats:sub>\n                    ) and tetracycline resistance genes [\n                    <jats:italic>tet(A)<\/jats:italic>\n                    ,\n                    <jats:italic>tet(B)<\/jats:italic>\n                    ,\n                    <jats:italic>tet(K)<\/jats:italic>\n                    ,\n                    <jats:italic>tet(M)<\/jats:italic>\n                    and\n                    <jats:italic>tet(S)<\/jats:italic>\n                    ], followed by Sanger sequencing for validation. Conjugation assays assessed gene transferability.\n                  <\/jats:p>\n                  <jats:p>\n                    <jats:bold>Results.<\/jats:bold>\n                    Out of 152 CRKP isolates, 20.4% (31 out of 152) were found to be resistant to tigecycline. All tigecycline-resistant isolates exhibited complete resistance (31 out of 31; 100%) to ceftazidime, ciprofloxacin and omadacycline. Additionally, resistance to amikacin and cefoperazone-sulbactam was observed in 87.1% (27 out of 31) and 77.4% (24 out of 31) of the isolates. Resistance to minocycline and colistin was detected in 51.6% (16 out of 31) and 29.0% (9 out of 31) of the isolates, respectively.\n                  <\/jats:p>\n                  <jats:p>\n                    PCR analysis revealed that 51.6% (16 out of 31) of the isolates carried the\n                    <jats:italic>bla<\/jats:italic>\n                    <jats:sub>OXA-48<\/jats:sub>\n                    gene, and 29.0% (9 out of 31) carried the\n                    <jats:italic>bla<\/jats:italic>\n                    <jats:sub>NDM<\/jats:sub>\n                    gene. None of the isolates harboured the\n                    <jats:italic>bla<\/jats:italic>\n                    <jats:sub>KPC<\/jats:sub>\n                    gene. With respect to tetracycline resistance determinants, the\n                    <jats:italic>tet(A)<\/jats:italic>\n                    gene was detected in 12.9% (4 out of 31) of the isolates, and the\n                    <jats:italic>tet(B<\/jats:italic>\n                    ) gene in 3.2% (1 out of 31), while\n                    <jats:italic>tet(K)<\/jats:italic>\n                    ,\n                    <jats:italic>tet(M)<\/jats:italic>\n                    ,\n                    <jats:italic>tet(S)<\/jats:italic>\n                    and\n                    <jats:italic>bla<\/jats:italic>\n                    <jats:sub>KPC<\/jats:sub>\n                    were not detected in any isolate.\n                  <\/jats:p>\n                  <jats:p>\n                    Conjugation assays demonstrated that plasmids carrying\n                    <jats:italic>bla<\/jats:italic>\n                    <jats:sub>NDM<\/jats:sub>\n                    and\n                    <jats:italic>bla<\/jats:italic>\n                    <jats:sub>OXA-48<\/jats:sub>\n                    were transferable to a recipient strain, indicating their potential for horizontal gene transfer. In contrast, plasmids harbouring\n                    <jats:italic>tet(A)<\/jats:italic>\n                    and\n                    <jats:italic>tet(B)<\/jats:italic>\n                    genes were not transferable under the experimental conditions.\n                  <\/jats:p>\n                  <jats:p>\n                    <jats:bold>Conclusion.<\/jats:bold>\n                    Tigecycline-resistant\n                    <jats:italic>K. pneumoniae<\/jats:italic>\n                    isolates showed high multidrug resistance, with transferable\n                    <jats:italic>bla<\/jats:italic>\n                    <jats:sub>NDM<\/jats:sub>\n                    and\n                    <jats:italic>bla<\/jats:italic>\n                    <jats:sub>OXA-48<\/jats:sub>\n                    genes. In contrast, chromosome and plasmid-borne tetracycline resistance genes\n                    <jats:italic>tet(A)<\/jats:italic>\n                    and\n                    <jats:italic>tet(B)<\/jats:italic>\n                    were non-transferable, indicating limited horizontal spread.\n                  <\/jats:p>","DOI":"10.1099\/acmi.0.001017.v4","type":"journal-article","created":{"date-parts":[[2026,3,12]],"date-time":"2026-03-12T17:16:46Z","timestamp":1773335806000},"source":"Crossref","is-referenced-by-count":0,"title":["Molecular characterization and transmission pattern of tetracycline resistance determinants in tigecycline and carbapenem resistant Klebsiella pneumoniae isolates at a tertiary care hospital in India"],"prefix":"10.1099","volume":"8","author":[{"ORCID":"https:\/\/orcid.org\/0009-0001-1543-4499","authenticated-orcid":false,"given":"Jyoti","family":"Chaudhary","sequence":"first","affiliation":[{"name":"Department of Microbiology, Sanjay Gandhi Postgraduate 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