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Pharmacol."],"abstract":"<jats:sec>\n                    <jats:title>Introduction<\/jats:title>\n                    <jats:p>\n                      Various systemic and enteric diseases have been attributed to\n                      <jats:italic>C. perfringens<\/jats:italic>\n                      , including healthcare-associated infections and intoxications. Humans and animals are thus exposed to serious health risks from these bacteria. Infections caused by these antibiotic-resistant bacteria are becoming an increasing concern. Bacteriophages (phages), which possess specific lytic activity, offer a viable alternative for the treatment of\n                      <jats:italic>Clostridium perfringens<\/jats:italic>\n                      .\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      In this study, a novel lytic\n                      <jats:italic>C. perfringens<\/jats:italic>\n                      phage designed as CpP_VarHS was isolated from wastewater and targeted the host\n                      <jats:italic>C. perfringens<\/jats:italic>\n                      type A ATCC 13124. The phage was then characterized using Transmission Electron Microscope (TEM), molecular sequencing, and bioinformatics tools.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Transmission electron microscopy (TEM) analysis revealed that CpP_VarHS possesses a short, non-contractile tail (31.55 \u00b1 2.5\u00a0nm in length) and a regular icosahedral head (44.23 \u00b1 2.1\u00a0nm in diameter), characteristic of the podovirus morphotype. Whole-genome analysis showed that the CpP_VarHS genome is 17,814 bp long, linear double-stranded DNA with a GC content of 28.30%. Among the 21 identified open reading frames, 12 were functional genes (GenBank accession number PP973485). Whole-genome sequence comparison showed 94.37% and 94.31% nucleotide identity with\n                      <jats:italic>Clostridium<\/jats:italic>\n                      phage vB_CpeP_HN02 and\n                      <jats:italic>Clostridium<\/jats:italic>\n                      phage CPS1. No tRNA, bacterial virulence gene, lysogenic gene, or antibiotic resistance gene was identified in the genome of CpP_VarHS. Phylogenetic analysis indicated that phage CpP_VarHS represents a novel species within the genus\n                      <jats:italic>Gregsiragusavirus<\/jats:italic>\n                      of the family\n                      <jats:italic>Guelinviridae<\/jats:italic>\n                      .\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>\n                      To the best of our knowledge, this is the first report of the isolation of a\n                      <jats:italic>C. perfringens<\/jats:italic>\n                      phage in T\u00fcrkiye. In conclusion, these findings suggested that phage CpP_VarHS has promising potential for preventing and controlling\n                      <jats:italic>C. perfringens<\/jats:italic>\n                      .\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.3389\/fphar.2026.1807000","type":"journal-article","created":{"date-parts":[[2026,5,22]],"date-time":"2026-05-22T04:51:35Z","timestamp":1779425495000},"update-policy":"https:\/\/doi.org\/10.3389\/crossmark-policy","source":"Crossref","is-referenced-by-count":0,"title":["Morphological and complete genome analysis of a novel Clostridium perfringens phage CpP_VarHS, isolated from wastewater"],"prefix":"10.3389","volume":"17","author":[{"given":"Hamza","family":"Saghrouchni","sequence":"first","affiliation":[{"name":"Department of Biotechnology, Institute of Natural and Applied Sciences, \u00c7ukurova University","place":["Adana, T\u00fcrkiye"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Semra","family":"Tasdurmazli","sequence":"additional","affiliation":[{"name":"Department of Molecular Biology and Genetics, Yildiz Technical University","place":["Istanbul, T\u00fcrkiye"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ibrahim Halil","family":"Kilic","sequence":"additional","affiliation":[{"name":"Department of Biology, Faculty of Arts and Sciences, Gaziantep University","place":["Gaziantep, T\u00fcrkiye"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Isil","family":"Var","sequence":"additional","affiliation":[{"name":"Department of Food Engineering, Engineering Faculty, \u00c7ukurova University","place":["Adana, T\u00fcrkiye"]}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"1965","published-online":{"date-parts":[[2026,5,22]]},"reference":[{"key":"B1","doi-asserted-by":"publisher","first-page":"1","DOI":"10.1007\/978-1-4939-9173-0_1","article-title":"tRNAscan-SE: searching for tRNA genes in genomic sequences","volume":"1962","author":"Chan","year":"2019","journal-title":"Methods Mol. 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