<?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>1401</year>
	<month>12</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2023</year>
	<month>3</month>
	<day>1</day>
</pubdate>
<volume>11</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>Prevalence of Extended Spectrum β-Lactamases-Producing Escherichia coli Isolated from Clinical Samples and Their Antibiotic Resistance Pattern</title>
	<subject_fa>Anti-microbial agents, resistance and treatment protocols </subject_fa>
	<subject>Anti-microbial agents, resistance and treatment protocols </subject>
	<content_type_fa>Original article</content_type_fa>
	<content_type>Original article</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;b&gt;&lt;span style=&quot;font-size:9.0pt&quot;&gt;&lt;span style=&quot;line-height:107%&quot;&gt;&lt;span new=&quot;&quot; roman=&quot;&quot; style=&quot;font-family:&quot; times=&quot;&quot;&gt;&lt;span style=&quot;color:black&quot;&gt;Introduction:&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/b&gt;&lt;span style=&quot;font-size:9.0pt&quot;&gt;&lt;span style=&quot;line-height:107%&quot;&gt;&lt;span new=&quot;&quot; roman=&quot;&quot; style=&quot;font-family:&quot; times=&quot;&quot;&gt;&lt;span style=&quot;color:black&quot;&gt; Infections caused by&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;b&gt; &lt;/b&gt;&lt;span style=&quot;font-size:9.0pt&quot;&gt;&lt;span style=&quot;line-height:107%&quot;&gt;&lt;span new=&quot;&quot; roman=&quot;&quot; style=&quot;font-family:&quot; times=&quot;&quot;&gt;&lt;span style=&quot;color:black&quot;&gt;ESBL-producing bacteria are a growing concern worldwide, especially in developing countries like Nigeria. Hence, this study aimed to isolate, screen, and identify ESBL-producing &lt;i&gt;Escherichia&lt;/i&gt; &lt;i&gt;coli&lt;/i&gt; from clinical samples and analyze their antibiotic resistance patterns. &lt;b&gt;Methods: &lt;/b&gt;200&lt;b&gt; &lt;/b&gt;clinical samples were collected, consisting of 60 stool, 88 urine, and 52 wound pussamples. We used the pour-plate method on MaCconkey agar (MAC) for isolation. After suspected &lt;i&gt;E. coli&lt;/i&gt; was isolated, we sub-cultured it on eosin methylene blue (EMB) agar. To confirm &lt;i&gt;E. coli&lt;/i&gt; identification, we used cultural and biochemical assays. Disc and double disc diffusion methods were employed to screen and confirm ESBL-producing &lt;i&gt;E&lt;/i&gt;. &lt;i&gt;coli&lt;/i&gt;. Antimicrobial susceptibility testing was conducted by disc diffusion technique, and the results were interpreted using CLSI standards. &lt;b&gt;Results: &lt;/b&gt;A total of 47 &lt;i&gt;E. coli&lt;/i&gt; isolates were obtained, with 48.5% of the isolates originating from urine samples. These isolates were among six different genera of bacteria. Among the &lt;i&gt;E. coli&lt;/i&gt; isolates, 16 were confirmed to be ESBL producers. The ESBL-producing &lt;i&gt;E. coli&lt;/i&gt; demonstrated high resistance to amoxicillin-clavulanic acid (87.5%), ampicillin (75.0%), and cefotaxime (50.0%). Before plasmid curing, the bacteria demonstrated a high susceptibility to chloramphenicol (81.3%) and amikacin (56.3%). However, varying antibiotic resistance and susceptibility degrees were observed after plasmid curing. &lt;b&gt;Conclusion:&lt;/b&gt; &lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-size:9.0pt&quot;&gt;&lt;span style=&quot;line-height:107%&quot;&gt;&lt;span new=&quot;&quot; roman=&quot;&quot; style=&quot;font-family:&quot; times=&quot;&quot;&gt;&lt;span style=&quot;color:#c00000&quot;&gt;ESBL-producing &lt;i&gt;E. coli&lt;/i&gt; showed a high resistance level (34.0%) against most discs used. &lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;span style=&quot;font-size:9.0pt&quot;&gt;&lt;span style=&quot;line-height:107%&quot;&gt;&lt;span new=&quot;&quot; roman=&quot;&quot; style=&quot;font-family:&quot; times=&quot;&quot;&gt;&lt;span style=&quot;color:black&quot;&gt;However, chloramphenicol and amikacin showed promise as potential treatments for ESBL-producing&lt;i&gt; E. coli&lt;/i&gt; infections&lt;i&gt;.&lt;/i&gt; In addition, it is recommended that clinical laboratories should include routine ESBL detection methods for ongoing surveillance of antibiotic-resistant isolates. This will serve as a helpful guide for empirically treating bacterial infections.&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;&lt;/span&gt;</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Escherichia coli, Antibiotics resistance, ESBL, Nosocomial infections</keyword>
	<start_page>34</start_page>
	<end_page>40</end_page>
	<web_url>http://jommid.pasteur.ac.ir/browse.php?a_code=A-10-445-1&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Mohammed</first_name>
	<middle_name></middle_name>
	<last_name>Ja'afaru</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>mijaafaru@mautech.edu.ng</email>
	<code></code>
	<orcid>0000-0002-9800-4450</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Microbiology, Modibbo Adama University, Yola, PMB 2076, Adamawa State, Nigeria</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Abubakar</first_name>
	<middle_name></middle_name>
	<last_name>Gaure</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>sk.siniya@gmail.com</email>
	<code></code>
	<orcid></orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Microbiology, Modibbo Adama University, Yola, PMB 2076, Adamawa State, Nigeria</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Joel</first_name>
	<middle_name></middle_name>
	<last_name>Ewansiha</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>ewansihajoel@mau.edu.ng</email>
	<code></code>
	<orcid>0000-0003-0331-8885</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Microbiology, Faculty of Life Sciences, Modibbo Adama University, Yola</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Olumuyiwa</first_name>
	<middle_name></middle_name>
	<last_name>Adeyemo</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>omadeyemo@mau.edu.ng</email>
	<code></code>
	<orcid>0000000318041153</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Department of Biotechnology, Modibbo Adama University, Yola, PMB 2076, Adamawa State, Nigeria</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


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