Evaluation of some molecular biological methods’ detection capacity for staphylococcus aureus

Authors

  • З.Урангоо АШУҮИС, Био-АС, Молекул биологи-Удамзүйн тэнхим , ХСҮТ, Эмнэлзүйн лабораторийн тасаг Author
  • Д.Амгаланзаяа Этүгэн их сургууль, Био-Анагаахын тэнхим Author
  • Н.Нямтуяа Экспресс лаборатори Author
  • Ц.Гэрэлсүх ХСҮТ, Эмнэлзүйн лабораторийн тасаг Author
  • Ц.Хишигбуян ХСҮТ, Эмнэлзүйн лабораторийн тасаг Author
  • Э.Отгонцэцэг АШУҮИС, Био-АС, Молекул биологи-Удамзүйн тэнхим Author
  • Б.Баярлах АШУҮИС, Био-АС, Молекул биологи-Удамзүйн тэнхим Author
  • Ж.Сарантуяа АШУҮИС, Био-АС, Молекул биологи-Удамзүйн тэнхим Author
  • Я.Мөнхдэлгэр АШУҮИС, Био-АС, Молекул биологи-Удамзүйн тэнхим Author

Keywords:

Polymerase chain reaction (PCR), Loop-Mediated Isothermal amplification (LAMP), nuc A, S.aureus

Abstract

Background: Staphylococcus aureus (S.aureus) is a highly virulence pathogen that responsible for various tissues infection and a wide range of diseases, including food borne infection, skin infections, pneumonia, mastitis and bacteremia in humans and animals. Aim: To compare PCR and LAMP methods in detecting S.aureus. Materials and Methods: In our study, we analyzed a comparison of PCR and LAMP results on S.aureus (ATCC 6538) standard strain used quality control strain solution which diluted, 0.1fg/µL, 1fg/µL, 10fg/µL, 100fg/µL, 1pg/µL, 10pg/ µL, 100pg/µL, 1ng/μL, 10ng/μL, and 100ng/μL DNA concentration from BP agar cultures. A comparison was made using PCR and LAMP methods to detect diluted DNA concentrations. Results: The nuc A gene sensitivity in PCR results is positive in 10fg/µL DNA solution and negative in 0.1fg/µL and 1fg/L DNA. In LAMP test results, it showed a positive response to all concentrations. Conclusion: The LAMP method’s sensitivity is 100 times more than PCR for detecting S.aureus. Therefore this method might be more practical in near future.

In the MNUMS Digital Library

View this article in the digital library →

Author research profiles: Б.Баярлах

Published

2023-05-18

Issue

Section

Original Articles