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Natural infection and phylogenetic classification of Leishmania spp. infecting Rhombomys opimus, a primary reservoir host of zoonotic cutaneous leishmaniasis in northeast Iran

Background In the northeast and central parts of Iran, Rhombomys opimus (great gerbil) is the primary reservoir host of zoonotic cutaneous leishmaniasis (ZCL). This study used both parasitological and molecular methods to identify Leishmania spp. and their different haplotypes that were circulating...

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Published in:Transactions of the Royal Society of Tropical Medicine and Hygiene 2013-09, Vol.107 (9), p.550-557
Main Authors: Hajjaran, Homa, Mohebali, Mehdi, Abaei, Mohammad Reza, Oshaghi, Mohammad Ali, Zarei, Zabih, Charehdar, Sorour, Mirjalali, Hamed, Sharifdini, Meysam, Teimouri, Aref
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cited_by cdi_FETCH-LOGICAL-c356t-48a3b5f8ca53dbf43a1e82e79398c9d28caebc14d44a61d6fff853d2dc3d78793
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container_title Transactions of the Royal Society of Tropical Medicine and Hygiene
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creator Hajjaran, Homa
Mohebali, Mehdi
Abaei, Mohammad Reza
Oshaghi, Mohammad Ali
Zarei, Zabih
Charehdar, Sorour
Mirjalali, Hamed
Sharifdini, Meysam
Teimouri, Aref
description Background In the northeast and central parts of Iran, Rhombomys opimus (great gerbil) is the primary reservoir host of zoonotic cutaneous leishmaniasis (ZCL). This study used both parasitological and molecular methods to identify Leishmania spp. and their different haplotypes that were circulating in the great gerbil populations in ZCL foci from northeastern Iran. Methods A cross-sectional study using microscopy, culturing and molecular methods was conducted to detect Leishmania parasites in 194 live R. opimus in ZCL foci from northeastern Iran during 2010-2011. Results Leishmania spp. were found in 38.1% (74/194) of the samples by microscopy and in 41.2% (80/194) by culturing. Small papules and skin thickening on the upper edge of the ears were observed in 25 (12. 9%) of the R. opimus. PCR-RFLP and PCR direct sequencing of internal transcribed spacer 1 (ITS1) rRNA showed similar infection rates for L. major and L. turanica in 60 eligible R. opimus, only one mixed infection containing both L. major and L. turanica was found. Phylogenetic analysis was conducted using the ITS1 sequences of 32 isolates that were successfully aligned by comparison of their base sequences with the ITS1 DNA sequence database using ClustalW and MEGA5. The samples were classified into monophyletic clusters (>97% bootstrap). Six haplotypes were observed for L. major and seven for L. turanica. Conclusion In northeast Iran, L. major, and L. turanica naturally circulate in R. opimus, and L. major/L. turanica co-infections also exist. Phylogenetic analysis suggested that Leishmania spp. isolated from R. opimus are not a monophyletic group.
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This study used both parasitological and molecular methods to identify Leishmania spp. and their different haplotypes that were circulating in the great gerbil populations in ZCL foci from northeastern Iran. Methods A cross-sectional study using microscopy, culturing and molecular methods was conducted to detect Leishmania parasites in 194 live R. opimus in ZCL foci from northeastern Iran during 2010-2011. Results Leishmania spp. were found in 38.1% (74/194) of the samples by microscopy and in 41.2% (80/194) by culturing. Small papules and skin thickening on the upper edge of the ears were observed in 25 (12. 9%) of the R. opimus. PCR-RFLP and PCR direct sequencing of internal transcribed spacer 1 (ITS1) rRNA showed similar infection rates for L. major and L. turanica in 60 eligible R. opimus, only one mixed infection containing both L. major and L. turanica was found. Phylogenetic analysis was conducted using the ITS1 sequences of 32 isolates that were successfully aligned by comparison of their base sequences with the ITS1 DNA sequence database using ClustalW and MEGA5. The samples were classified into monophyletic clusters (&gt;97% bootstrap). Six haplotypes were observed for L. major and seven for L. turanica. Conclusion In northeast Iran, L. major, and L. turanica naturally circulate in R. opimus, and L. major/L. turanica co-infections also exist. Phylogenetic analysis suggested that Leishmania spp. isolated from R. opimus are not a monophyletic group.</description><identifier>ISSN: 0035-9203</identifier><identifier>EISSN: 1878-3503</identifier><identifier>DOI: 10.1093/trstmh/trt060</identifier><identifier>PMID: 23868742</identifier><identifier>CODEN: TRSTAZ</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Animals ; Biological and medical sciences ; Cross-Sectional Studies ; Disease Reservoirs - parasitology ; Disease Reservoirs - veterinary ; General aspects ; Gerbillinae - parasitology ; Haplotypes ; Human protozoal diseases ; Infectious diseases ; Iran - epidemiology ; Leishmania - classification ; Leishmaniasis, Cutaneous - parasitology ; Leishmaniasis, Cutaneous - transmission ; Leishmaniasis, Cutaneous - veterinary ; Leshmaniasis ; Medical sciences ; Parasitic diseases ; Phylogeny ; Polymerase Chain Reaction - methods ; Polymorphism, Restriction Fragment Length ; Protozoal diseases ; Rodent Diseases - parasitology ; Rodent Diseases - transmission ; Zoonoses</subject><ispartof>Transactions of the Royal Society of Tropical Medicine and Hygiene, 2013-09, Vol.107 (9), p.550-557</ispartof><rights>The Author 2013. Published by Oxford University Press on behalf of Royal Society of Tropical Medicine and Hygiene. All rights reserved. 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This study used both parasitological and molecular methods to identify Leishmania spp. and their different haplotypes that were circulating in the great gerbil populations in ZCL foci from northeastern Iran. Methods A cross-sectional study using microscopy, culturing and molecular methods was conducted to detect Leishmania parasites in 194 live R. opimus in ZCL foci from northeastern Iran during 2010-2011. Results Leishmania spp. were found in 38.1% (74/194) of the samples by microscopy and in 41.2% (80/194) by culturing. Small papules and skin thickening on the upper edge of the ears were observed in 25 (12. 9%) of the R. opimus. PCR-RFLP and PCR direct sequencing of internal transcribed spacer 1 (ITS1) rRNA showed similar infection rates for L. major and L. turanica in 60 eligible R. opimus, only one mixed infection containing both L. major and L. turanica was found. Phylogenetic analysis was conducted using the ITS1 sequences of 32 isolates that were successfully aligned by comparison of their base sequences with the ITS1 DNA sequence database using ClustalW and MEGA5. The samples were classified into monophyletic clusters (&gt;97% bootstrap). Six haplotypes were observed for L. major and seven for L. turanica. Conclusion In northeast Iran, L. major, and L. turanica naturally circulate in R. opimus, and L. major/L. turanica co-infections also exist. 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This study used both parasitological and molecular methods to identify Leishmania spp. and their different haplotypes that were circulating in the great gerbil populations in ZCL foci from northeastern Iran. Methods A cross-sectional study using microscopy, culturing and molecular methods was conducted to detect Leishmania parasites in 194 live R. opimus in ZCL foci from northeastern Iran during 2010-2011. Results Leishmania spp. were found in 38.1% (74/194) of the samples by microscopy and in 41.2% (80/194) by culturing. Small papules and skin thickening on the upper edge of the ears were observed in 25 (12. 9%) of the R. opimus. PCR-RFLP and PCR direct sequencing of internal transcribed spacer 1 (ITS1) rRNA showed similar infection rates for L. major and L. turanica in 60 eligible R. opimus, only one mixed infection containing both L. major and L. turanica was found. Phylogenetic analysis was conducted using the ITS1 sequences of 32 isolates that were successfully aligned by comparison of their base sequences with the ITS1 DNA sequence database using ClustalW and MEGA5. The samples were classified into monophyletic clusters (&gt;97% bootstrap). Six haplotypes were observed for L. major and seven for L. turanica. Conclusion In northeast Iran, L. major, and L. turanica naturally circulate in R. opimus, and L. major/L. turanica co-infections also exist. Phylogenetic analysis suggested that Leishmania spp. isolated from R. opimus are not a monophyletic group.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>23868742</pmid><doi>10.1093/trstmh/trt060</doi><tpages>8</tpages></addata></record>
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source Oxford University Press:Jisc Collections:OUP Read and Publish 2024-2025 (2024 collection) (Reading list)
subjects Animals
Biological and medical sciences
Cross-Sectional Studies
Disease Reservoirs - parasitology
Disease Reservoirs - veterinary
General aspects
Gerbillinae - parasitology
Haplotypes
Human protozoal diseases
Infectious diseases
Iran - epidemiology
Leishmania - classification
Leishmaniasis, Cutaneous - parasitology
Leishmaniasis, Cutaneous - transmission
Leishmaniasis, Cutaneous - veterinary
Leshmaniasis
Medical sciences
Parasitic diseases
Phylogeny
Polymerase Chain Reaction - methods
Polymorphism, Restriction Fragment Length
Protozoal diseases
Rodent Diseases - parasitology
Rodent Diseases - transmission
Zoonoses
title Natural infection and phylogenetic classification of Leishmania spp. infecting Rhombomys opimus, a primary reservoir host of zoonotic cutaneous leishmaniasis in northeast Iran
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