Abstract
Background: Cutaneous leishmainasis (CL) is highly prevalent in several provinces of Iran,
having increased during the recent decades. The diagnosis of CL in most of clinical laboratories is
usually performed using routine microscopy. However, this method is not sensitive enough, and the
assessment and utilization of other methods, including a variety of PCR techniques, have been taken
to consideration. In the present study, a direct PCR, based on kDNA primers, in comparison with
the microscopic examination and in vitro NNN culture was evaluated for the detection of CL.
Materials & Methods: The scrapings were taken from 73 patients from Mirjaveh, Sistan &
Baluchestan province, and subjected to the comparative diagnoses.
Results: The results showed that 38.4%, 55.5% and 63.2% of the specimens were positive by
microscopy, PCR and NNN culture, respectively. The parasite species were also characterized by
the current PCR. Separate comparisons of both microscopy and PCR methods with NNN culture,
showed that the sensitivity of the PCR (76%) is higher than that of microscopy (61%). The
calculated specificity, however, was 100% for microscopy and 73% for PCR.
Conclusion: In addition to the higher sensitivity, this particular PCR, which uses species-specific
primers, has a major advantage of identification of Leishmania species at the same time. It is,
therefore, concluded that this PCR technique can be a suitable complement to the routine
microscopic examination for diagnosis and identification of the parasite species from suspected
leishmaniasis.
having increased during the recent decades. The diagnosis of CL in most of clinical laboratories is
usually performed using routine microscopy. However, this method is not sensitive enough, and the
assessment and utilization of other methods, including a variety of PCR techniques, have been taken
to consideration. In the present study, a direct PCR, based on kDNA primers, in comparison with
the microscopic examination and in vitro NNN culture was evaluated for the detection of CL.
Materials & Methods: The scrapings were taken from 73 patients from Mirjaveh, Sistan &
Baluchestan province, and subjected to the comparative diagnoses.
Results: The results showed that 38.4%, 55.5% and 63.2% of the specimens were positive by
microscopy, PCR and NNN culture, respectively. The parasite species were also characterized by
the current PCR. Separate comparisons of both microscopy and PCR methods with NNN culture,
showed that the sensitivity of the PCR (76%) is higher than that of microscopy (61%). The
calculated specificity, however, was 100% for microscopy and 73% for PCR.
Conclusion: In addition to the higher sensitivity, this particular PCR, which uses species-specific
primers, has a major advantage of identification of Leishmania species at the same time. It is,
therefore, concluded that this PCR technique can be a suitable complement to the routine
microscopic examination for diagnosis and identification of the parasite species from suspected
leishmaniasis.
Keywords
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Copyright
© 2007, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.