Characterization of the Genetic Diversity of Acid Lime (Citrus aurantifolia (Christm.) Swingle) Cultivars of Eastern Nepal Using Inter-Simple Sequence Repeat Markers

Acid lime (Citrus aurantifolia (Christm.) Swingle) is an important fruit crop, which has high commercial value and is cultivated in 60 out of the 77 districts representing all geographical landscapes of Nepal. A lack of improved high-yielding varieties, infestation with various diseases, and pests,...

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Main Authors: Nabin Narayan Munankarmi, Neesha Rana, Tribikram Bhattarai, Ram Lal Shrestha, Bal Krishna Joshi, Bikash Baral, Sangita Shrestha
Format: Article
Language:English
Published: MDPI AG 2018-06-01
Series:Plants
Subjects:
PCR
Online Access:http://www.mdpi.com/2223-7747/7/2/46
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spelling doaj-5cbaf3aca47e4e2caf468d9e786f3ccf2020-11-24T21:12:34ZengMDPI AGPlants2223-77472018-06-01724610.3390/plants7020046plants7020046Characterization of the Genetic Diversity of Acid Lime (Citrus aurantifolia (Christm.) Swingle) Cultivars of Eastern Nepal Using Inter-Simple Sequence Repeat MarkersNabin Narayan Munankarmi0Neesha Rana1Tribikram Bhattarai2Ram Lal Shrestha3Bal Krishna Joshi4Bikash Baral5Sangita Shrestha6Central Department of Biotechnology, Tribhuvan University (CDBt-TU), GPO Box 44613, Kirtipur, Kathmandu, NepalMolecular Biotechnology Unit, Faculty of Science, Nepal Academy of Science and Technology (NAST), GPO Box 3323, Khumaltar, Lalitpur, NepalCentral Department of Biotechnology, Tribhuvan University (CDBt-TU), GPO Box 44613, Kirtipur, Kathmandu, NepalNepal Agriculture Research Council (NARC), GPO Box 5459, Khumaltar, Lalitpur, NepalNepal Agriculture Research Council (NARC), GPO Box 5459, Khumaltar, Lalitpur, NepalDepartment of Biochemistry, University of Turku, FIN-20014 Turku, FinlandMolecular Biotechnology Unit, Faculty of Science, Nepal Academy of Science and Technology (NAST), GPO Box 3323, Khumaltar, Lalitpur, NepalAcid lime (Citrus aurantifolia (Christm.) Swingle) is an important fruit crop, which has high commercial value and is cultivated in 60 out of the 77 districts representing all geographical landscapes of Nepal. A lack of improved high-yielding varieties, infestation with various diseases, and pests, as well as poor management practices might have contributed to its extremely reduced productivity, which necessitates a reliable understanding of genetic diversity in existing cultivars. Hereby, we aim to characterize the genetic diversity of acid lime cultivars cultivated at three different agro-ecological gradients of eastern Nepal, employing PCR-based inter-simple sequence repeat (ISSR) markers. Altogether, 21 polymorphic ISSR markers were used to assess the genetic diversity in 60 acid lime cultivars sampled from different geographical locations. Analysis of binary data matrix was performed on the basis of bands obtained, and principal coordinate analysis and phenogram construction were performed using different computer algorithms. ISSR profiling yielded 234 amplicons, of which 87.18% were polymorphic. The number of amplified fragments ranged from 7–18, with amplicon size ranging from ca. 250–3200 bp. The Numerical Taxonomy and Multivariate System (NTSYS)-based cluster analysis using the unweighted pair group method of arithmetic averages (UPGMA) algorithm and Dice similarity coefficient separated 60 cultivars into two major and three minor clusters. Genetic diversity analysis using Popgene ver. 1.32 revealed the highest percentage of polymorphic bands (PPB), Nei’s genetic diversity (H), and Shannon’s information index (I) for the Terai zone (PPB = 69.66%; H = 0.215; I = 0.325), and the lowest of all three for the high hill zone (PPB = 55.13%; H = 0.173; I = 0.262). Thus, our data indicate that the ISSR marker has been successfully employed for evaluating the genetic diversity of Nepalese acid lime cultivars and has furnished valuable information on intrinsic genetic diversity and the relationship between cultivars that might be useful in acid lime breeding and conservation programs in Nepal.http://www.mdpi.com/2223-7747/7/2/46citrus breedingdiversitygenetic similaritylimemolecular markersPCR
collection DOAJ
language English
format Article
sources DOAJ
author Nabin Narayan Munankarmi
Neesha Rana
Tribikram Bhattarai
Ram Lal Shrestha
Bal Krishna Joshi
Bikash Baral
Sangita Shrestha
spellingShingle Nabin Narayan Munankarmi
Neesha Rana
Tribikram Bhattarai
Ram Lal Shrestha
Bal Krishna Joshi
Bikash Baral
Sangita Shrestha
Characterization of the Genetic Diversity of Acid Lime (Citrus aurantifolia (Christm.) Swingle) Cultivars of Eastern Nepal Using Inter-Simple Sequence Repeat Markers
Plants
citrus breeding
diversity
genetic similarity
lime
molecular markers
PCR
author_facet Nabin Narayan Munankarmi
Neesha Rana
Tribikram Bhattarai
Ram Lal Shrestha
Bal Krishna Joshi
Bikash Baral
Sangita Shrestha
author_sort Nabin Narayan Munankarmi
title Characterization of the Genetic Diversity of Acid Lime (Citrus aurantifolia (Christm.) Swingle) Cultivars of Eastern Nepal Using Inter-Simple Sequence Repeat Markers
title_short Characterization of the Genetic Diversity of Acid Lime (Citrus aurantifolia (Christm.) Swingle) Cultivars of Eastern Nepal Using Inter-Simple Sequence Repeat Markers
title_full Characterization of the Genetic Diversity of Acid Lime (Citrus aurantifolia (Christm.) Swingle) Cultivars of Eastern Nepal Using Inter-Simple Sequence Repeat Markers
title_fullStr Characterization of the Genetic Diversity of Acid Lime (Citrus aurantifolia (Christm.) Swingle) Cultivars of Eastern Nepal Using Inter-Simple Sequence Repeat Markers
title_full_unstemmed Characterization of the Genetic Diversity of Acid Lime (Citrus aurantifolia (Christm.) Swingle) Cultivars of Eastern Nepal Using Inter-Simple Sequence Repeat Markers
title_sort characterization of the genetic diversity of acid lime (citrus aurantifolia (christm.) swingle) cultivars of eastern nepal using inter-simple sequence repeat markers
publisher MDPI AG
series Plants
issn 2223-7747
publishDate 2018-06-01
description Acid lime (Citrus aurantifolia (Christm.) Swingle) is an important fruit crop, which has high commercial value and is cultivated in 60 out of the 77 districts representing all geographical landscapes of Nepal. A lack of improved high-yielding varieties, infestation with various diseases, and pests, as well as poor management practices might have contributed to its extremely reduced productivity, which necessitates a reliable understanding of genetic diversity in existing cultivars. Hereby, we aim to characterize the genetic diversity of acid lime cultivars cultivated at three different agro-ecological gradients of eastern Nepal, employing PCR-based inter-simple sequence repeat (ISSR) markers. Altogether, 21 polymorphic ISSR markers were used to assess the genetic diversity in 60 acid lime cultivars sampled from different geographical locations. Analysis of binary data matrix was performed on the basis of bands obtained, and principal coordinate analysis and phenogram construction were performed using different computer algorithms. ISSR profiling yielded 234 amplicons, of which 87.18% were polymorphic. The number of amplified fragments ranged from 7–18, with amplicon size ranging from ca. 250–3200 bp. The Numerical Taxonomy and Multivariate System (NTSYS)-based cluster analysis using the unweighted pair group method of arithmetic averages (UPGMA) algorithm and Dice similarity coefficient separated 60 cultivars into two major and three minor clusters. Genetic diversity analysis using Popgene ver. 1.32 revealed the highest percentage of polymorphic bands (PPB), Nei’s genetic diversity (H), and Shannon’s information index (I) for the Terai zone (PPB = 69.66%; H = 0.215; I = 0.325), and the lowest of all three for the high hill zone (PPB = 55.13%; H = 0.173; I = 0.262). Thus, our data indicate that the ISSR marker has been successfully employed for evaluating the genetic diversity of Nepalese acid lime cultivars and has furnished valuable information on intrinsic genetic diversity and the relationship between cultivars that might be useful in acid lime breeding and conservation programs in Nepal.
topic citrus breeding
diversity
genetic similarity
lime
molecular markers
PCR
url http://www.mdpi.com/2223-7747/7/2/46
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