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<Article>
<Journal>
				<PublisherName>Baqiyatallah University of Medical Sciences</PublisherName>
				<JournalTitle>Journal of Applied Biotechnology Reports</JournalTitle>
				<Issn>2322-1186</Issn>
				<Volume>13</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2026</Year>
					<Month>03</Month>
					<Day>30</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Comparative Analysis of Pseudomonas aeruginosa Isolated from Different Clinical Sources Using Whole Genome Sequencing and Bioinformatics</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>1953</FirstPage>
			<LastPage>1962</LastPage>
			<ELocationID EIdType="pii">242582</ELocationID>
			
<ELocationID EIdType="doi">10.30491/jabr.2025.555514.1934</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Ansejam</FirstName>
					<LastName>Yaaqop Khadem</LastName>
<Affiliation>College of Education for Pure Science, Diyala University, Diyala, Iraq</Affiliation>
<Identifier Source="ORCID">0009-0004-2267-8530</Identifier>

</Author>
<Author>
					<FirstName>Munim</FirstName>
					<LastName>Radwan Ali</LastName>
<Affiliation>College of Science, Mustansiriyah University, Baghdad, Iraq</Affiliation>
<Identifier Source="ORCID">0000-0003-0989-0620</Identifier>

</Author>
<Author>
					<FirstName>Ali</FirstName>
					<LastName>Jaffar Saleem</LastName>
<Affiliation>College of Education for Pure Science, Diyala University, Diyala, Iraq</Affiliation>
<Identifier Source="ORCID">0000-0001-5758-1895</Identifier>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2025</Year>
					<Month>10</Month>
					<Day>26</Day>
				</PubDate>
			</History>
		<Abstract>&lt;span class=&quot;fontstyle0&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;This study aimed to evaluate the antibiotic resistance patterns, virulence characteristics, and genetic and epidemiological relationships of clinical isolates of &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;&lt;em&gt;Pseudomonas aeruginosa&lt;/em&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;obtained from various sources in hospitals and clinics in the city of Baqubah, Iraq.&lt;/span&gt;&lt;br&gt;&lt;span class=&quot;fontstyle0&quot;&gt;&lt;strong&gt;Materials and Methods:&lt;/strong&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;&lt;em&gt;P. aeruginosa&lt;/em&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;isolates (n = 80) were tested for antimicrobial susceptibility. Eight isolates, selected for diversity, underwent Whole Genome Sequencing (WGS). Analyses included the identification of Antibiotic Resistance Genes (ARGs), antimicrobial Resistance (AMR) Mechanism, Multi-Locus Sequence Typing (MLST), and Virulence Factors (VFs). A biofilm production assay was performed, and results were correlated with resistance patterns.&lt;/span&gt;&lt;br&gt;&lt;span class=&quot;fontstyle0&quot;&gt;&lt;strong&gt;Results:&lt;/strong&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;High resistance rates were observed for the isolates, with the majority being multi-drug resistant: MDR 42.5%, XDR 27.5%, and PDR 10%. The highest resistance rates were recorded against Piperacillin (97.5%) and Polymyxin B (97.5%). Statistically significant resistance was also documented against Cefepime (70%, &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;&lt;em&gt;p&lt;/em&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;= 0.0003) and Meropenem (36.3%, &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;&lt;em&gt;p&lt;/em&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;= 0.013). 100% of the isolates were biofilm producers (68.75% strong, 31.25% moderate). Statistical analysis revealed a significant correlation between resistance patterns (MDR/XDR/PDR) and the capacity for strong biofilm formation (X squared = 18, &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;&lt;em&gt;p&lt;/em&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;= 0.0004). Using MLST and WGS, the spread of high-risk clones was confirmed: ST-235 (in PA4 and PA18) and ST-244 (in PA7 and PA40). A substantial accumulation of ARGs was identified. Isolate PA 56 (ST-654) carried the most dangerous combination: bla_NDM-1, bla_KPC-2 (carbapenemases), and rmtF (high-level aminoglycoside resistance). The core set of essential VFs (such as the Type III Secretion System (TTSS), Exotoxin A, and Quorum Sensing) was conserved across all eight isolates.&lt;/span&gt;&lt;br&gt;&lt;span class=&quot;fontstyle0&quot;&gt;&lt;strong&gt;Conclusions:&lt;/strong&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;Findings confirm widespread Multidrug-Resistant &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;P. aeruginosa &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;in Iraqi hospitals, driven by high-risk international clones and acquired &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;&lt;em&gt;carbapenemase&lt;/em&gt; &lt;/span&gt;&lt;span class=&quot;fontstyle2&quot;&gt;genes. The combination of Mobile Genetic Elements (MGEs) in resistance transfer and strong biofilm formation presents a major therapeutic and epidemiological challenge, necessitating strict genomic surveillance and infection control. However, these findings are based on a local, small-scale comparison.&lt;/span&gt; </Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Pseudomonas aeruginosa</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Whole Genome Sequencing</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Comparative Genomics</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Antimicrobial Resistance</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Virulence factors</Param>
			</Object>
		</ObjectList>
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