Rapid diagnosis and genotyping of Leishmania isolates from cutaneous and visceral leishmaniasis by microcapillary cultivation and polymerase chain reaction–restriction fragment length polymorphism of miniexon region
We have performed a combination of microcapillary cultivation method and restriction fragment length polymorphism (RFLP) analysis of amplified products by 1 single PCR of miniexon region of Leishmania for molecular diagnosis and genotyping of different Leishmania species isolated from cutaneous leis...
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Published in | Diagnostic microbiology and infectious disease Vol. 53; no. 3; pp. 209 - 214 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Elsevier Inc
01.11.2005
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Abstract | We have performed a combination of microcapillary cultivation method and restriction fragment length polymorphism (RFLP) analysis of amplified products by 1 single PCR of miniexon region of
Leishmania for molecular diagnosis and genotyping of different
Leishmania species isolated from cutaneous leishmaniasis (CL) and visceral leishmaniasis. We have analyzed 10 microcapillary cultivated isolates from cutaneous cases and 5 microcapillary cultivated isolates from visceral cases (totally 15) by polymerase chain reaction–RFLP (PCR-RFLP). Of 10 isolates, 3 (30%) were genotyped as
Leishmania infantum and 7 (70%) of 10 isolates were genotyped as
Leishmania tropica from the microcapillary cultivated isolates of cutaneous cases. On the other hand, all 5 isolates (100%) were genotyped as
L. infantum from microcapillary cultivated visceral cases. Our most interesting finding is the presence of 3
L. infantum isolates in CL cases without kala-azar history. Therefore, we suggest that further investigations must be done about this subject. On the other hand, we suggest the combination of microcapillary culture method and PCR-RFLP of miniexon region of leishmaniae can be used in routine laboratory experimentation because of their simple, cheap, and rapid benefits (within a week), whereas other different approaches offer a multitude of valid taxonomic characters for species identification. |
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AbstractList | We have performed a combination of microcapillary cultivation method and restriction fragment length polymorphism (RFLP) analysis of amplified products by 1 single PCR of miniexon region of
Leishmania for molecular diagnosis and genotyping of different
Leishmania species isolated from cutaneous leishmaniasis (CL) and visceral leishmaniasis. We have analyzed 10 microcapillary cultivated isolates from cutaneous cases and 5 microcapillary cultivated isolates from visceral cases (totally 15) by polymerase chain reaction–RFLP (PCR-RFLP). Of 10 isolates, 3 (30%) were genotyped as
Leishmania infantum and 7 (70%) of 10 isolates were genotyped as
Leishmania tropica from the microcapillary cultivated isolates of cutaneous cases. On the other hand, all 5 isolates (100%) were genotyped as
L. infantum from microcapillary cultivated visceral cases. Our most interesting finding is the presence of 3
L. infantum isolates in CL cases without kala-azar history. Therefore, we suggest that further investigations must be done about this subject. On the other hand, we suggest the combination of microcapillary culture method and PCR-RFLP of miniexon region of leishmaniae can be used in routine laboratory experimentation because of their simple, cheap, and rapid benefits (within a week), whereas other different approaches offer a multitude of valid taxonomic characters for species identification. We have performed a combination of microcapillary cultivation method and restriction fragment length polymorphism (RFLP) analysis of amplified products by 1 single PCR of miniexon region of Leishmania for molecular diagnosis and genotyping of different Leishmania species isolated from cutaneous leishmaniasis (CL) and visceral leishmaniasis. We have analyzed 10 microcapillary cultivated isolates from cutaneous cases and 5 microcapillary cultivated isolates from visceral cases (totally 15) by polymerase chain reaction-RFLP (PCR-RFLP). Of 10 isolates, 3 (30%) were genotyped as Leishmania infantum and 7 (70%) of 10 isolates were genotyped as Leishmania tropica from the microcapillary cultivated isolates of cutaneous cases. On the other hand, all 5 isolates (100%) were genotyped as L. infantum from microcapillary cultivated visceral cases. Our most interesting finding is the presence of 3 L. infantum isolates in CL cases without kala-azar history. Therefore, we suggest that further investigations must be done about this subject. On the other hand, we suggest the combination of microcapillary culture method and PCR-RFLP of miniexon region of leishmaniae can be used in routine laboratory experimentation because of their simple, cheap, and rapid benefits (within a week), whereas other different approaches offer a multitude of valid taxonomic characters for species identification. We have performed a combination of microcapillary cultivation method and restriction fragment length polymorphism (RFLP) analysis of amplified products by 1 single PCR of miniexon region of Leishmania for molecular diagnosis and genotyping of different Leishmania species isolated from cutaneous leishmaniasis (CL) and visceral leishmaniasis. We have analyzed 10 microcapillary cultivated isolates from cutaneous cases and 5 microcapillary cultivated isolates from visceral cases (totally 15) by polymerase chain reaction-RFLP (PCR-RFLP). Of 10 isolates, 3 (30%) were genotyped as Leishmania infantum and 7 (70%) of 10 isolates were genotyped as Leishmania tropica from the microcapillary cultivated isolates of cutaneous cases. On the other hand, all 5 isolates (100%) were genotyped as L. infantum from microcapillary cultivated visceral cases. Our most interesting finding is the presence of 3 L. infantum isolates in CL cases without kala-azar history. Therefore, we suggest that further investigations must be done about this subject. On the other hand, we suggest the combination of microcapillary culture method and PCR-RFLP of miniexon region of leishmaniae can be used in routine laboratory experimentation because of their simple, cheap, and rapid benefits (within a week), whereas other different approaches offer a multitude of valid taxonomic characters for species identification.We have performed a combination of microcapillary cultivation method and restriction fragment length polymorphism (RFLP) analysis of amplified products by 1 single PCR of miniexon region of Leishmania for molecular diagnosis and genotyping of different Leishmania species isolated from cutaneous leishmaniasis (CL) and visceral leishmaniasis. We have analyzed 10 microcapillary cultivated isolates from cutaneous cases and 5 microcapillary cultivated isolates from visceral cases (totally 15) by polymerase chain reaction-RFLP (PCR-RFLP). Of 10 isolates, 3 (30%) were genotyped as Leishmania infantum and 7 (70%) of 10 isolates were genotyped as Leishmania tropica from the microcapillary cultivated isolates of cutaneous cases. On the other hand, all 5 isolates (100%) were genotyped as L. infantum from microcapillary cultivated visceral cases. Our most interesting finding is the presence of 3 L. infantum isolates in CL cases without kala-azar history. Therefore, we suggest that further investigations must be done about this subject. On the other hand, we suggest the combination of microcapillary culture method and PCR-RFLP of miniexon region of leishmaniae can be used in routine laboratory experimentation because of their simple, cheap, and rapid benefits (within a week), whereas other different approaches offer a multitude of valid taxonomic characters for species identification. |
Author | Tezcan, Seda Emekdas, Gurol Allahverdiyev, Adil Uzun, Soner Daglioglu, Kenan Kayar, Begum Vural, Zeynep Yetkin, Mesut Koksal, Fatih Serin, Mehmet S. Bagirova, Melahat Aslan, Gonul |
Author_xml | – sequence: 1 givenname: Mehmet S. surname: Serin fullname: Serin, Mehmet S. email: serinmss@cu.edu.tr, serinmss@yahoo.com organization: Department of Microbiology, Faculty of Pharmacy, Mersin University, Mersin 33343, Turkey – sequence: 2 givenname: Kenan surname: Daglioglu fullname: Daglioglu, Kenan organization: Experimental Surgery Research Center, Cukurova University, Adana 01330, Turkey – sequence: 3 givenname: Melahat surname: Bagirova fullname: Bagirova, Melahat organization: Tropical Diseases Research Center, Cukurova University, Adana 01330, Turkey – sequence: 4 givenname: Adil surname: Allahverdiyev fullname: Allahverdiyev, Adil organization: Tropical Diseases Research Center, Cukurova University, Adana 01330, Turkey – sequence: 5 givenname: Soner surname: Uzun fullname: Uzun, Soner organization: Department of Dermatology, Faculty of Medicine, Cukurova University, Adana 01330, Turkey – sequence: 6 givenname: Zeynep surname: Vural fullname: Vural, Zeynep organization: Tropical Diseases Research Center, Cukurova University, Adana 01330, Turkey – sequence: 7 givenname: Begum surname: Kayar fullname: Kayar, Begum organization: Tropical Diseases Research Center, Cukurova University, Adana 01330, Turkey – sequence: 8 givenname: Seda surname: Tezcan fullname: Tezcan, Seda organization: Department of Microbiology, Faculty of Medicine, Mersin University, Mersin 33343, Turkey – sequence: 9 givenname: Mesut surname: Yetkin fullname: Yetkin, Mesut organization: Tropical Diseases Research Center, Cukurova University, Adana 01330, Turkey – sequence: 10 givenname: Gonul surname: Aslan fullname: Aslan, Gonul organization: Department of Microbiology, Faculty of Medicine, Mersin University, Mersin 33343, Turkey – sequence: 11 givenname: Gurol surname: Emekdas fullname: Emekdas, Gurol organization: Department of Microbiology, Faculty of Medicine, Mersin University, Mersin 33343, Turkey – sequence: 12 givenname: Fatih surname: Koksal fullname: Koksal, Fatih organization: Tropical Diseases Research Center, Cukurova University, Adana 01330, Turkey |
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Keywords | Microcapillary culture L. tropica L. infantum Miniexon PCR RFLP Kinetoplastida Protozoa Skin disease Protozoal disease Typing Microbiology Genotype Kala azar Leishmaniasis Parasitosis Infection Cutaneous leishmaniasis Polymerase chain reaction Restriction fragment length polymorphism Leishmania Isolate Diagnosis L. infautum |
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SubjectTerms | Animals Biological and medical sciences Culture Media Deoxyribonucleases, Type II Site-Specific - metabolism Exons - genetics Fundamental and applied biological sciences. Psychology Human protozoal diseases Humans Infectious diseases L. infantum L. tropica Leishmania - classification Leishmania - genetics Leishmania - isolation & purification Leishmania infantum Leishmania tropica Leishmaniasis, Cutaneous - diagnosis Leishmaniasis, Cutaneous - parasitology Leishmaniasis, Visceral - diagnosis Leishmaniasis, Visceral - parasitology Leshmaniasis Medical sciences Microbiology Microcapillary culture Miniexon Parasitic diseases Parasitology - instrumentation Parasitology - methods PCR Polymerase Chain Reaction - methods Polymorphism, Restriction Fragment Length Protozoal diseases RFLP Time Factors |
Title | Rapid diagnosis and genotyping of Leishmania isolates from cutaneous and visceral leishmaniasis by microcapillary cultivation and polymerase chain reaction–restriction fragment length polymorphism of miniexon region |
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