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Comparison of Nested Polymerase Chain Reaction and Real-Time Polymerase Chain Reaction With Parasitological Methods for Detection of Strongyloides Stercoralis in Human Fecal Samples Publisher Pubmed



Sharifdini M1 ; Mirhendi H1 ; Ashrafi K1 ; Hosseini M1 ; Mohebali M1 ; Khodadadi H1 ; Kia EB1
Authors
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Authors Affiliations
  1. 1. Center for Resr. of Endemic Parasites of Iran (CREPI), Tehran Univ. of Med. Sciences, Tehran, Iran
  2. 2. Dept. of Med. Parasitology and Mycology, School of Public Health, Tehran Univ. of Med. Sciences, Tehran, Iran
  3. 3. Dept. of Med. Parasitology and Mycology, School of Med., Isfahan Univ. of Med. Sci., Isfahan, Iran
  4. 4. Dept. of Med. Microbiology, School of Med., Guilan Univ. of Med. Sci., Rasht, IRN
  5. 5. Dept. of Biostatistics and Epidemiology, School of Public Health, Tehran Univ. of Med. Sci., Tehran, IRN
  6. 6. Dept. of Med. Parasitology and Mycology, School of Med., Shiraz Univ. of Med. Sci., Shiraz, IRN
  7. 7. Center for Research of Endemic Parasites of Iran (CREPI), Tehran University of Medical Sciences, Tehran, Iran
  8. 8. Department of Medical Parasitology and Mycology, School of Public Health, Tehran University of Medical Sciences, P.O. Box 14155-6446, Tehran, Iran
  9. 9. Department of Medical Parasitology and Mycology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran
  10. 10. Department of Medical Microbiology, School of Medicine, Guilan University of Medical Sciences, Rasht, Iran
  11. 11. Department of Biostatistics and Epidemiology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
  12. 12. Department of Medical Parasitology and Mycology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran

Source: American Journal of Tropical Medicine and Hygiene Published:2015


Abstract

This study was performed to evaluate nested polymerase chain reaction (PCR) and real-time PCR methods for detection of Strongyloides stercoralis in fecal samples compared with parasitological methods. A total of 466 stool samples were examined by conventional parasitological methods (formalin ether concentration [FEC] and agar plate culture [APC]). DNA was extracted using an in-house method, and mitochondrial cytochrome c oxidase subunit 1 and 18S ribosomal genes were amplified by nested PCR and real-time PCR, respectively. Among 466 samples, 12.7% and 18.2% were found infected with S. stercoralis by FEC and APC, respectively. DNA of S. stercoralis was detected in 18.9% and 25.1% of samples by real-time PCR and nested PCR, respectively. Considering parasitological methods as the diagnostic gold standard, the sensitivity and specificity of nested PCR were 100% and 91.6%, respectively, and that of real-time PCR were 84.7% and 95.8%, respectively. However, considering sequence analyzes of the selected nested PCR products, the specificity of nested PCR is increased. In general, molecular methods were superior to parasitological methods. They were more sensitive and more reliable in detection of S. stercoralis in comparison with parasitological methods. Between the two molecular methods, the sensitivity of nested PCR was higher than real-time PCR. © 2015 by The American Society of Tropical Medicine and Hygiene.