OPTIMIZING MOLECULAR TECHNIQUES FOR ACCURATE EXAMINATION OF LEPTOSPIRA SPECIES: A COMPREHENSIVE PRIMER FOR RESEARCHERS

Background: Leptospirosis is a potentially life-threatening disease caused by bacteria of the genus Leptospira. The accurate identification and characterization of Leptospira species are critical for disease surveillance, outbreak investigation, and treatment strategies. Molecular techniques, such a...

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Main Authors: Aldiana Astuti, Farida Dwi Handayani
Format: Article
Language:Indonesian
Published: Universitas Airlangga 2024-11-01
Series:Journal of Vocational Health Studies
Subjects:
Online Access:https://e-journal.unair.ac.id/JVHS/article/view/46298
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author Aldiana Astuti
Farida Dwi Handayani
author_facet Aldiana Astuti
Farida Dwi Handayani
author_sort Aldiana Astuti
collection DOAJ
description Background: Leptospirosis is a potentially life-threatening disease caused by bacteria of the genus Leptospira. The accurate identification and characterization of Leptospira species are critical for disease surveillance, outbreak investigation, and treatment strategies. Molecular techniques, such as Polymerase Chain Reaction (PCR) and Deoxyribonucleic acid (DNA) sequencing, have revolutionized the field of microbiology, providing rapid and accurate identification of Leptospira strains. However, optimizing these molecular techniques for accurate examination of Leptospira species can be challenging due to the genetic diversity and complexity of these bacteria. Purpose: This research aims to identify the most suitable primers for the precise identification of pathogenic Leptospira strains. Method: This research used the PCR method, using LipL32, rrs2, seqY, LipL41, IcdA, and Adk primers. A total of 17 isolates of pathogenic Leptospira bacteria were cultured from Institute of Vector Control and Reservoir Disease (IVRCD) in Salatiga, Indonesia. Result: The results of the research showed that the LipL41 and IcdA primers were found to be effective in distinguishing pathogenic strains, while the seqY, LipL32, Adk, and rrs2 primers required further refinement. The suitable Melting Temperature (TM) or annealing temperature is 58°C with 35 cycles of amplification. DNA concentration and purity had an A260/A280 ratio ranging between 1.8 and 2.8. Conclusion: LipL41 (500 bp) and IcdA (700 bp) are suitable primers for identifying pathogenic Leptospira.
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institution Kabale University
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2580-717X
language Indonesian
publishDate 2024-11-01
publisher Universitas Airlangga
record_format Article
series Journal of Vocational Health Studies
spelling doaj-art-275d054d2c5e47a4a57e2b4caa4551422024-11-28T00:45:52ZindUniversitas AirlanggaJournal of Vocational Health Studies2580-71612580-717X2024-11-018210811510.20473/jvhs.V8.I2.2024.108-11544384OPTIMIZING MOLECULAR TECHNIQUES FOR ACCURATE EXAMINATION OF LEPTOSPIRA SPECIES: A COMPREHENSIVE PRIMER FOR RESEARCHERSAldiana Astuti0https://orcid.org/0000-0001-9400-304XFarida Dwi Handayani1Medical Laboratory Technology Study Program, Kupang Ministry of Health Polytechnic, KupangNational Research and Innovation Agency of Indonesia (BRIN), SalatigaBackground: Leptospirosis is a potentially life-threatening disease caused by bacteria of the genus Leptospira. The accurate identification and characterization of Leptospira species are critical for disease surveillance, outbreak investigation, and treatment strategies. Molecular techniques, such as Polymerase Chain Reaction (PCR) and Deoxyribonucleic acid (DNA) sequencing, have revolutionized the field of microbiology, providing rapid and accurate identification of Leptospira strains. However, optimizing these molecular techniques for accurate examination of Leptospira species can be challenging due to the genetic diversity and complexity of these bacteria. Purpose: This research aims to identify the most suitable primers for the precise identification of pathogenic Leptospira strains. Method: This research used the PCR method, using LipL32, rrs2, seqY, LipL41, IcdA, and Adk primers. A total of 17 isolates of pathogenic Leptospira bacteria were cultured from Institute of Vector Control and Reservoir Disease (IVRCD) in Salatiga, Indonesia. Result: The results of the research showed that the LipL41 and IcdA primers were found to be effective in distinguishing pathogenic strains, while the seqY, LipL32, Adk, and rrs2 primers required further refinement. The suitable Melting Temperature (TM) or annealing temperature is 58°C with 35 cycles of amplification. DNA concentration and purity had an A260/A280 ratio ranging between 1.8 and 2.8. Conclusion: LipL41 (500 bp) and IcdA (700 bp) are suitable primers for identifying pathogenic Leptospira.https://e-journal.unair.ac.id/JVHS/article/view/46298leptospirapcrprimersdna purityoptimizing
spellingShingle Aldiana Astuti
Farida Dwi Handayani
OPTIMIZING MOLECULAR TECHNIQUES FOR ACCURATE EXAMINATION OF LEPTOSPIRA SPECIES: A COMPREHENSIVE PRIMER FOR RESEARCHERS
Journal of Vocational Health Studies
leptospira
pcr
primers
dna purity
optimizing
title OPTIMIZING MOLECULAR TECHNIQUES FOR ACCURATE EXAMINATION OF LEPTOSPIRA SPECIES: A COMPREHENSIVE PRIMER FOR RESEARCHERS
title_full OPTIMIZING MOLECULAR TECHNIQUES FOR ACCURATE EXAMINATION OF LEPTOSPIRA SPECIES: A COMPREHENSIVE PRIMER FOR RESEARCHERS
title_fullStr OPTIMIZING MOLECULAR TECHNIQUES FOR ACCURATE EXAMINATION OF LEPTOSPIRA SPECIES: A COMPREHENSIVE PRIMER FOR RESEARCHERS
title_full_unstemmed OPTIMIZING MOLECULAR TECHNIQUES FOR ACCURATE EXAMINATION OF LEPTOSPIRA SPECIES: A COMPREHENSIVE PRIMER FOR RESEARCHERS
title_short OPTIMIZING MOLECULAR TECHNIQUES FOR ACCURATE EXAMINATION OF LEPTOSPIRA SPECIES: A COMPREHENSIVE PRIMER FOR RESEARCHERS
title_sort optimizing molecular techniques for accurate examination of leptospira species a comprehensive primer for researchers
topic leptospira
pcr
primers
dna purity
optimizing
url https://e-journal.unair.ac.id/JVHS/article/view/46298
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