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<article article-type="research-article" dtd-version="1.0" xml:lang="en"
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    <front>
        <journal-meta>
            <journal-id journal-id-type="issn">0973-7510</journal-id>
            <journal-title-group>
                <journal-title>Journal of Pure and Applied Microbiology</journal-title>
            </journal-title-group>
            <issn pub-type="epub">2581-690X</issn>
            <publisher>
                <publisher-name>DR. M.N. Khan</publisher-name>
            </publisher>
        </journal-meta>
        <article-meta>
            <article-id pub-id-type="doi">10.22207/JPAM.16.2.13</article-id>
            <title-group>
                <article-title>Rapid Detection of Salmonella spp from Meat: Loop Mediated Isothermal Amplification (LAMP)</article-title>
            </title-group>
            <contrib-group>
				
				
				<contrib contrib-type="author">
                    <name>
                        <surname>Vittal</surname>
                        <given-names>Rajeshwari</given-names>
                    </name>
                    <xref ref-type="aff" rid="aff-1"/>
                </contrib>
				
						<contrib contrib-type="author">
                    <name>
                        <surname>Mohanraj</surname>
                        <given-names>Juliet Roshini</given-names>
                    </name>
                    <xref ref-type="aff" rid="aff-1"/>
                </contrib>
				
				
				
				
				<contrib contrib-type="author">
                    <name>
                        <surname>Chakraborty</surname>
                        <given-names>Gunimala</given-names>
                    </name>
                    <xref ref-type="aff" rid="aff-1"/>
					<xref ref-type="aff" rid="aff-2"/>
                </contrib>
				
				
								            		
            </contrib-group>
			
			
          <aff id="aff-1">NITTE University Center for Science Education and Research, NITTE (Deemed to be University), Mangalore – 575 018, Karnataka, India.</aff>
			 <aff id="aff-2">Division of Molecular Genetics and cancer, NITTE (Deemed to be University), Mangalore – 575 018, Karnataka, India.</aff>
			 			
			
            <pub-date publication-format="electronic" date-type="pub" iso-8601-date="2022-04-25">
                <day>25</day>
				<month>04</month>
                <year>2022</year>
            </pub-date>
            <volume>16</volume>
            <issue>2</issue>
            <fpage>929</fpage>
            <lpage>936</lpage>
            <permissions>
                <copyright-statement>Copyright &#x00A9; 2022 The Author(s)</copyright-statement>
                <copyright-year>2022</copyright-year>
                <license license-type="open-access"
                    xlink:href="https://creativecommons.org/licenses/by/4.0/">
                    <license-p>This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International License which permits unrestricted use, sharing, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.<uri 
					xlink:href="https://creativecommons.org/licenses/by/4.0/"
                            >https://creativecommons.org/licenses/by/4.0/</uri></license-p>
                </license>
            </permissions>
            <self-uri xlink:href="https://microbiologyjournal.org/rapid-detection-of-salmonella-spp-from-meat-loop-mediated-isothermal-amplification-lamp/"/>
            <abstract>
                <p> Loop-mediated isothermal amplification (LAMP) is a novel, high specific and sensitive method which amplifies nucleic acid under isothermal conditions. Salmonella is considered one of the threatening pathogens in food industries and these species are associated with distinct food poisoning called salmonellosis. Four primers (two outer and two inner primers) were designed to target six distinct regions on the target gene invA which is conserved in Salmonella species. The reaction was optimised for 60 mins at 65 ̊C. The sensitivity of the LAMP and PCR assay for Salmonella was 10 CFU/ml and 100 CFU/ml respectively. Artificial spiking of chicken meat shows detection of Salmonella even at dilution to extinction (&#60;1 CFU/ml) immediately after spiking as well after 48hr enrichment. All the LAMP experiments were compared to PCR method. This study reports the development of a highly sensitive, specific and a rapid diagnostic assay for the detection of Salmonella from food. The developed method could be very useful for routine pathogens point of care (POC) diagnostics. </p>
		</abstract>
		<kwd-group>
        <title>Keywords</title>
        <kwd>Food</kwd>
        <kwd>invA gene</kwd>
		<kwd>LAMP</kwd>
		<kwd>Pathogens</kwd>
        <kwd>PCR</kwd>
		<kwd>Salmonella</kwd>
			</kwd-group>
        </article-meta>
    </front>
    </article>
