<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>Journal of Medical Microbiology and Infectious Diseases</title>
<title_fa>Journal of Medical Microbiology and Infectious Diseases</title_fa>
<short_title>JoMMID</short_title>
<subject>Medical Sciences</subject>
<web_url>http://jommid.pasteur.ac.ir</web_url>
<journal_hbi_system_id>1</journal_hbi_system_id>
<journal_hbi_system_user>admin</journal_hbi_system_user>
<journal_id_issn>2345-5349</journal_id_issn>
<journal_id_issn_online>2345-5330</journal_id_issn_online>
<journal_id_pii>8</journal_id_pii>
<journal_id_doi>10.61882/JoMMID</journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid>14</journal_id_sid>
<journal_id_nlai>8888</journal_id_nlai>
<journal_id_science>13</journal_id_science>
<language>en</language>
<pubdate>
	<type>jalali</type>
	<year>1397</year>
	<month>10</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2019</year>
	<month>1</month>
	<day>1</day>
</pubdate>
<volume>7</volume>
<number>1</number>
<publish_type>online</publish_type>
<publish_edition>1</publish_edition>
<article_type>fulltext</article_type>
<articleset>
	<article>


	<language>en</language>
	<article_id_doi></article_id_doi>
	<title_fa></title_fa>
	<title>Isolation and Characterization of a Klebsiella pneumoniae Specific Lytic Bacteriophage from a Hospital Waste-water Treatment Plant</title>
	<subject_fa>Microbial pathogenesis </subject_fa>
	<subject>Microbial pathogenesis </subject>
	<content_type_fa>Original article</content_type_fa>
	<content_type>Original article</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;strong&gt;Introduction: &lt;/strong&gt;Phage therapy has gained interest as a potential alternative for treatment of infections caused by multidrug-resistant (MDR) pathogens. This study aimed to isolate a lytic bacteriophage with the potential to lyse clinical isolates of &lt;em&gt;Klebsiella pneumoniae.&lt;/em&gt; &lt;strong&gt;Methods: &lt;/strong&gt;Water samples were collected from a hospital waste-water treatment plant in Tehran. The samples were filtered and mixed with an overnight grown culture of &lt;em&gt;K. pneumoniae. &lt;/em&gt;(ATCC 10031) followed by incubation at 37&amp;deg;C overnight. Phage titration, latent period, and burst size measurements were carried out by the double-layer agar method using the &lt;em&gt;K. pneumoniae &lt;/em&gt;ATCC strain. The isolated phage w:as char:acterized by transmission electron microscopy (TEM), thermal, pH, and chloroform stability. Susceptibility of &lt;em&gt;Escherichia coli&lt;/em&gt;, &lt;em&gt;Acinetobacter baumannii&lt;/em&gt;, &lt;em&gt;Pseudomonas aeruginosa,&lt;/em&gt; ESBL producing &lt;em&gt;K. pneumoniae &lt;/em&gt;and 51 MDR &lt;em&gt;K. pneumoniae &lt;/em&gt;isolates was measured by placing 20 &amp;micro;l of the phage suspension (10&lt;sup&gt;8&lt;/sup&gt; PFU) onto bacterial lawns followed by incubation at 37&amp;deg;C overnight. Formation of clear zones indicated susceptibility. &lt;strong&gt;Results: &lt;/strong&gt;The isolated lytic bacteriophage formed small clear plaques with a latent period of 40 min and a burst time of 52 min, corresponding to 35-40 phage particles per infected cell. TEM results showed that the phage resembled the tailed &lt;em&gt;Siphoviridae&lt;/em&gt; family and was designated vB_KpnS-Teh.1. The phage vB_KpnS-Teh.1 was most stable at 37&amp;deg;C, pH 7 and was resistant to chloroform. &lt;strong&gt;Conclusion: &lt;/strong&gt;The isolated lytic phage showed specificity towards &lt;em&gt;K. pneumoniae. &lt;/em&gt;Further research will determine its potential in the treatment of &lt;em&gt;K. pneumoniae &lt;/em&gt;infections.</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Klebsiella pneumoniae, Bacteriophage, Waste-water, Siphoviridae</keyword>
	<start_page>6</start_page>
	<end_page>11</end_page>
	<web_url>http://jommid.pasteur.ac.ir/browse.php?a_code=A-10-176-2&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Mahboubeh</first_name>
	<middle_name></middle_name>
	<last_name>Soleimani Sasani</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>mahbobeh soleimani@yahoo.com</email>
	<code></code>
	<orcid>0000-0001-9310-894X</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Microbiology and Microbial Biotechnology, Faculty of Life Sciences and Biotechnology, Shahid Beheshti University</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Fereshteh</first_name>
	<middle_name></middle_name>
	<last_name>Eftekhar</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>f-eftekhar@sbu.ac.ir</email>
	<code></code>
	<orcid>0000-0002-2441-2582</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Department of Microbiology and Microbial Biotechnology, Faculty of Life Sciences and Biotechnology, Shahid Beheshti University</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Masoud</first_name>
	<middle_name></middle_name>
	<last_name>Hosseini</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>Ma_Hosseini@sbu.ac.ir</email>
	<code></code>
	<orcid>0000-0002-8906-5833</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Microbiology and Microbial Biotechnology, Faculty of Life Sciences and Biotechnology, Shahid Beheshti University</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


	</article>
</articleset>
</journal>
