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In this work, we investigated how exposure to positive electric pulses affects the growth characteristics of <jats:italic>Klebsiella pneumonia<\/jats:italic> (<jats:italic>K. pneumonia<\/jats:italic>), a common cause of pneumonia. We explored the impact of varying exposure frequencies (0.2\u20132\u00a0Hz) and time (15\u201390\u00a0min, at resonance frequency) on bioelectric signals produced during cell division, biofilm formation, and bacterial antibiotic susceptibility. Our research found that an extremely low-frequency pulsed electric field (ELF-PEF) significantly inhibited <jats:italic>K. pneumonia<\/jats:italic> growth. Specifically, exposure to 0.8\u00a0Hz for one hour increased the antibiotic susceptibility of <jats:italic>K. pneumonia<\/jats:italic> to inhibitors of cell wall formation, proteins, \u03b2-lactamase, DNA, and other substances. We also noticed a notable decrease in <jats:italic>K. pneumonia<\/jats:italic> biofilm development exposed to ELF-PEF. Our results suggest that the interaction of <jats:italic>K. pneumonia<\/jats:italic> cells with ELF-PEF at the specified frequency and time alters cellular activity and bacterial structure. This technique may be used in the future to treat <jats:italic>K. pneumonia<\/jats:italic> infections both in vitro and <jats:italic>in vivo.<\/jats:italic>\n          <\/jats:p>","DOI":"10.1007\/s00253-024-13330-z","type":"journal-article","created":{"date-parts":[[2024,11,5]],"date-time":"2024-11-05T19:01:42Z","timestamp":1730833302000},"update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":5,"title":["Pulsed electric field at resonance frequency combat Klebsiella pneumonia\u00a0biofilms"],"prefix":"10.1007","volume":"108","author":[{"given":"Dorria H.","family":"Mohamed","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-6055-9514","authenticated-orcid":false,"given":"Haitham","family":"Mohammed","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Reem H.","family":"El-Gebaly","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mohamed","family":"Adam","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Fadel M.","family":"Ali","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2024,11,5]]},"reference":[{"issue":"8","key":"13330_CR1","doi-asserted-by":"publisher","first-page":"203","DOI":"10.20546\/ijcmas.2016.501.028","volume":"6","author":"AGM Al-Agha","year":"2017","unstructured":"Al-Agha AGM, Al-Khafaji NJM, Al-Azawi AKS (2017) Isolation and identification of Klebsiella pneumoniae using API-20E analytical system and conventional PCR assay. 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