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- Jaipal Singh Choudhary
- Aashish Kumar Anant
- C. Parameswaran
- G. Basana-Gowda
- Totan Adak
- P. Paneerselvam
- M. Annamalai
- Naveenkumar Patil
- Prakash Chandra Rath
- J. Berliner
- J. Alfred-Daniel
- Balaji Rajkumar
- H. C. Hombegowda
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- Rashid Parvez
- M. R. Khan
- Priyank Hanuman Mhatre
- Naiyar Naaz
- Enrico Ruzzier
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Govindharaj, Guru-Pirasanna-Pandi
- Population genetic structure and migration pattern of Nilaparvata lugens (Stål.) (Hemiptera: Delphacidae) populations in India based on mitochondrial COI gene sequences
Abstract Views :160 |
PDF Views:78
Authors
Guru-Pirasanna-Pandi Govindharaj
1,
Jaipal Singh Choudhary
2,
Aashish Kumar Anant
3,
C. Parameswaran
3,
G. Basana-Gowda
3,
Totan Adak
3,
P. Paneerselvam
3,
M. Annamalai
3,
Naveenkumar Patil
3,
Prakash Chandra Rath
3
Affiliations
1 Division of Crop Protection, ICAR-National Rice Research Institute, Cuttack 753 006, India
2 ICAR-Reseach Complex for Eastern Region, Farming Systems Research Centre for Hill and Plateau Region, Ranchi 834 010, India
3 Division of Crop Protection, ICAR-National Rice Research Institute, Cuttack 753 006, India
1 Division of Crop Protection, ICAR-National Rice Research Institute, Cuttack 753 006, India
2 ICAR-Reseach Complex for Eastern Region, Farming Systems Research Centre for Hill and Plateau Region, Ranchi 834 010, India
3 Division of Crop Protection, ICAR-National Rice Research Institute, Cuttack 753 006, India
Source
Current Science, Vol 123, No 3 (2022), Pagination: 461-470Abstract
Despite the economic and ecological impact of the brown planthopper, Nilaparvata lugens infestation associated with rice cultivation in India, studies on its genetic structure are lacking. Hence, the present study was conducted to assess the genetic variability of N. lugens in India. The study evaluated the diversity in N. lugens populations using mitochondrial cytochrome oxidase subunit I gene sequences from India, and compared them with the Bangladesh, China and Japan populations. In all, 47 unique haplotypes were identified and the haplotype number varied from 6 to 18 in the sampled populations. Genetic diversity indices like nucleotide diversity (0.004), average number of nucleotide differences (1.98), haplotype diversity (0.667) and haplotype number (47) of N. lugens populations from India revealed a low level of genetic diversity. A highly significant negative correlation of the demographic history of N. lugens populations along with no significant sum of square deviations indicated possible recent expansion of the brown planthopper in India. A non-significant correlation in isolation pattern by distance results indicated that geographic barriers present in the country are not sufficient for genetic differentiation among N. lugens from different migratory populations. In this study, the genetic diversity of N. lugens populations from India is compared with other Asian populationsReferences
- Pandi, G.G.P., Chander, S., Pal, M. and Pathak, H., Impact of elevated CO2 and temperature on brown planthopper population in rice ecosystem. Proc. Natl. Acad. Sci. India, Sect. B, 2016, 88(1), 57–64; doi:10.1007/s40011-016-0727-x.
- Jena, M. et al., Paradigm shift of insect pests in rice ecosystem and their management strategy. Oryza, 2018, 55, 82–89; doi:10.5958/2249-5266.2018.00010.3.
- Pandi, G. G. P., Chander, S., Pal, M. and Soumia, P. S., Impact of elevated CO2 on Oryza sativa phenology and brown planthopper, Nilaparvata lugens (Hemiptera: Delphacidae) population. Curr. Sci., 2018, 114(8), 1767–1777; doi:10.18520/cs/v114/i08/1767-1777.
- Li, S., Wang, H. and Zhoum, G. S., Synergism between Southern rice black-streaked dwarf virus and Rice ragged stunt virus enhances their insect vector acquisition. Phytopathology, 2014, 104(7), 794–799; doi:10.1094/PHYTO-11-13-0319-R. PMID: 24915431.
- Bottrell, D. G. and Schoenly, K. G., Resurrecting the ghost of green revolutions past: the brown planthopper as a recurring threat to high-yielding rice production in tropical. J. Asia-Pac. Entomol., 2012, 15(1), 122–140; https://doi.org/10.1016/j.aspen.2011.09.004.
- Otuka, A., Migration of rice planthoppers and their vectored reemerging and novel rice viruses in East Asia. Front. Microbiol., 2013, 4, 309; doi:10.3389/fmicb.2013.00309.
- Hu, G., Lu, M. H., Tuan, H. A. and Liu, W. C., Population dynamics of rice planthoppers, Nilaparvata lugens and Sogatella furcifera (Hemiptera, Delphacidae) in Central Vietnam and its effects on their spring migration to China. Bull. Entomol. Res., 2017, 107, 369–381; https://doi.org/10.1017/S0007485316001024.
- EPPO, European and Mediterranean Plant Protection Organization global database, 2021; https://gd.eppo.int/taxon/NILALU/distribution (accessed on 20 December 2021).
- Anant, A. K. et al., Genetic dissection and identification of candidate genes for brown planthopper, Nilaparvata lugens (Delphacidae: Hemiptera) resistance in farmers’ varieties of rice in Odisha. Crop Prot., 2021, 144, 105600; https://doi.org/10.1016/j.cropro.2021.105600.
- Matsumura, M., Takeuchi, H., Satoh, M., Sanada-Morimura, S., Otuka, A., Watanabe, T. and Van, T. D., Species specific insecticide resistance to imidacloprid and fipronil in the rice planthoppers Nilaparvata lugens and Sogatella furcifera in East and South-east Asia. Pest Manage. Sci., 2008, 64(11), 1115–1121; doi:10.1002/ps.1641. PMID: 18803329.
- Matsumoto, Y., Matsumura, M., Sanada-Morimura, S., Hirai, Y., Sato, Y. and Noda, H., Mitochondrial COX sequences of Nilaparvata lugens and Sogatella furcifera (Hemiptera, Delphacidae): low specificity among Asian planthopper populations. Bull. Entomol. Res., 2013, 103(4), 382–392; doi:10.1017/S000748531200082X. PMID: 23537548.
- Naeemullah, M., Sharma, P. N., Tufail, M., Mori, N., Matsumura, M., Takeda, M. and Nakamura, C., Characterization of brown planthopper strains based on their differential responses to introgressed resistance genes and on mitochondrial DNA polymorphism. Appl. Entomol. Zool., 2009, 44, 475–483; https://doi.org/10.1303/aez.2009.475.
- Rollins, L. A., Woolnough, A. P., Sinclair, R., Mooney, N. J. and Sherwin, W. B., Mitochondrial DNA offers unique insights into invasion history of the common starling. Mol. Ecol., 2011, 20(11), 2307–2317; doi:10.1111/j.1365-294X.2011.05101.x. PMID: 21507095.
- Wan, X., Liu, Y. and Zhang, B., Invasion history of the oriental fruit fly, Bactrocera dorsalis, in the Pacific-Asia region: two main invasion routes. PLOS ONE, 2012, 7(5), e36176; https://doi.org/10.1371/journal.pone.0036176.
- Choudhary, J. S., Naaz, N., Prabhakar, C. S. and Lemtur, M., Genetic analysis of oriental fruit fly, Bactrocera dorsalis (Diptera: Tephritidae) populations based on mitochondrial COX 1 and NAD 1 gene sequences from India and other Asian countries. Genetica, 2016, 144, 611–623; doi:10.1007/s10709-016-9929-7. PMID: 27699519.
- Choudhary, J. S., Naaz, N., Lemtur, M., Das, B., Singh, A.K., Bhatt, B. P. and Prabhakar, C. S., Genetic analysis of Bactrocera zonata (Diptera: Tephritidae) populations from India based on COX 1 and NAD 1 gene sequences. Mitochondrial DNA A, 2018, 29(5), 727–736; https://doi.org/10.1080/24701394.2017.1350952.
- Pandi, G. G. P. et al., Molecular diversity of Nilaparvata lugens (Stål.) (Hemiptera: Delphacidae) from India based on internal transcribed spacer 1 (ITSI) gene. Curr. Sci., 2022, 122(12), 1392–1400.
- Watanabe, S. and Melzer, M. J., A multiplex PCR assay for differentiating coconut rhinoceros beetle (Coleoptera: Scarabaeidae) from oriental flower beetle (Coleoptera: Scarabaeidae) in early life stages and excrement. J. Econ. Entomol., 2017, 110, 678–682; doi:10.1093/jee/tow299. PMID: 28115497.
- Noda, H., How can planthopper genomics be useful for planthopper management? In Planthoppers: New Threats to the Sustainability of Intensive Rice Production Systems in Asia (eds Heong, K. L. and Hardy, B.), International Rice Research Institute, Philippines, 2009, pp. 429–446.
- Roderick, G. K. and Navajas, M., Genes in new environments: genetics and evolution in biological control. Nature Rev. Genet., 2003, 4, 889–899; https://doi.org/10.1038/nrg1201.
- Wilson, M. R. and Claridge, M. F., Handbook for the Identification of Leafhoppers and Planthoppers of Rice, CAB International, London, UK, 1991, p. 143; ISBN 0-85198-692-7.
- Mun, J. H., Song, Y. H., Heong, K. L. and Roderick, G. K., Genetic variation among Asian populations of rice planthoppers, Nilaparvata lugens and Sogatella furcifera (Hemiptera: Delphacidae): mitochondrial DNA sequences. Bull. Entomol. Res., 1999, 89, 245–253; doi:10.1017/S000748539900036X.
- Huang, X. and Madan, A., CAP3: a DNA sequence assembly program. Genome Res., 1999, 9(9), 868–877; doi:10.1101/gr.9.9.868. PMID: 10508846.
- Tamura, K., Stecher, G., Peterson, D., Filipski, A. and Kumar, S., MEGA6: molecular evolutionary genetics analysis version 6.0. Mol. Biol. Evol., 2013, 30(12), 2725–2729; doi:10.1093/molbev/mst197. Epub 2013 Oct 16. PMID: 24132122.
- Librado, P. and Rozas, J., DnaSP V5: software for comprehensive analysis of DNA polymorphism data. Bioinformatics, 2009, 25(11), 1451–1452; https://doi.org/10.1093/bioinformatics/btp187.
- Excoffier, L. and Lischer, H. E. L., Arlequin suite ver. 3.5, a new series of programs to perform population genetics analyses under Linux and Windows. Mol. Ecol. Resour., 2010, 10(3), 564–567; doi:10.1111/j.1755-0998.2010.02847.x. PMID: 21565059.
- Bandelt, H., Forster, P. and Roehl, A., Median-joining networks for inferring intraspecific phylogenies. Mol. Biol. Evol., 1999, 16(1), 37–48; doi:10.1093/oxfordjournals.molbev.a026036. PMID: 10331250.
- Dupanloup, I., Schneider, S. and Excoffier, L., A simulated annealing approach to define the genetic structure of populations. Mol. Ecol., 2002, 11, 2571e2581; doi:10.1046/j.1365-294x.2002.01650.x. PMID: 12453240.
- Tajima, F., Statistical method for testing the neutral mutation hypothesis by DNA polymorphism. Genetics, 1989, 123(3), 585–595; doi:10.1093/genetics/123.3.585. PMID: 2513255.
- Fu, Y. X., Statistical tests of neutrality of mutations against population growth, hitchhiking and background selection. Genetics, 1997, 147, 915–925; doi:10.1093/genetics/147.2.915. PMID: 9335623.
- Rogers, A. R. and Harpending, H., Population growth makes waves in the distribution of pairwise differences. Mol. Biol. Evol., 1992, 9(3), 552–569; doi:10.1093/oxfordjournals.molbev.a040727.
- Mantel, N., The detection of disease and a generalized regression approach. Cancer Res., 1967, 27, 209–220. PMID: 6018555.
- Miller, M. P., Alleles in space (AIS): computer software for the joint analysis of interindividual spatial and genetic information. J. Hered., 2005, 96(6), 722–724; https://doi.org/10.1093/jhered/esi119.
- Beerli, P. and Felsenstein, J., Maximum-likelihood estimation of a migration matrix and effective population sizes in subpopulations by using a coalescent approach. Proc. Natl. Acad. Sci. USA, 2001, 98(8), 4563–4568; https://doi.org/10.1073/pnas.081068098.
- Rosetti, N. and Remis, M. I., Spatial genetic structure and mitochondrial DNA phylogeography of argentinean populations of the grasshopper Dichroplus elongatus. PLoS ONE, 2012, 7(7), e40807; https://doi.org/10.1371/journal.pone.0040807.
- Grant, W. S. and Bowen, B. W., Shallow population histories in deep evolutionary lineages of marine fishes: insights from sardines and anchovies and lessons for conservation. J. Hered., 1998, 89, 415–426; https://doi.org/10.1093/jhered/89.5.415.
- Suarez, A. V. and Tsutsui, N. D., The evolutionary consequences of biological invasions. Mol. Ecol., 2008, 17(1), 351–360; doi: 10.1111/j.1365-294X.2007.03456.x. PMID: 18173507.
- Grapputo, A., Bisazza, A. and Pilastro, A., Invasion success despite reduction of genetic diversity in the European populations of eastern mosquito fish (Gambusia holbrooki). Ital. J. Zool., 2006, 73, 67–73; https://doi.org/10.1080/11250000500502111.
- Slatkin, M. and Hudson, R. R., Pairwise comparison of mitochondrial DNA sequences in stable and exponentially growing populations. Genetics, 1991, 129(2), 555–562; doi:10.1093/genetics/129.2.555.
- Hereward, J. P., Cai, X., Matias, A. M. A., Walter, G. H., Xu, C. and Wang, Y., Migration dynamics of important rice pest: the brown planthopper (Nilaparvata lugens) across Asia-insights from population genomics. Evol. Appl., 2020, 13(9), 2449–2459; https://doi.org/10.1111/eva.13047.
- Harpending, H. C., Batzer, M. A., Gurven, M., Jorde, L. B., Rogers, A. R. and Sherry, S. T., Genetic traces of ancient demography. Proc. Natl. Acad. Sci. USA, 1998, 95, 1691–1697; https://doi.org/10.1073/pnas.95.4.1961.
- Slatkin, M., Gene flow in natural populations. Annu. Rev. Evol. Syst., 1985, 16, 393–430; https://doi.org/10.1146/annurev.es.16.110185.002141.
- Schneider, S. and Excoffier, L., Estimation of past demographic parameters from the distribution of pairwise differences when the mutation rates vary among sites: application to human mitochondrial DNA. Genetics, 1999, 152(3), 1079–1089.
- Wan, X., Nardi, F., Zhang, B. and Liu, Y., The oriental fruit fly, Bactrocera dorsalis, in China: origin and gradual inland range expansion associated with population growth. PLoS ONE, 2011, 6(10), e25238; https://doi.org/10.1371/journal.pone.0025238.
- Wei, S. J., Genetic structure and demographic history reveal migration of the diamondback moth Plutellaxylostella (Lepidoptera: Plutellidae) from the southern to northern regions of China. PLoS ONE, 2013, 8, e59654; https://doi.org/10.1371/journal.pone.0059654.
- Irwin, D. E., Phylogeographic breaks without geographic barriers to gene flow. Evolution, 2002, 56(12), 2383–2394; https://doi.org/10.1554/0014-3820(2002)056[2383:PBWGBT]2.0.CO;2.
- Fauna Associated with Wheat Cultivation in High Altitudes of the Nilgiris, India
Abstract Views :112 |
PDF Views:66
Authors
J. Berliner
1,
J. Alfred-Daniel
2,
Balaji Rajkumar
3,
H. C. Hombegowda
4,
B. Manimaran
5,
Rashid Parvez
5,
M. R. Khan
5,
Priyank Hanuman Mhatre
6,
Guru-Pirasanna-Pandi Govindharaj
7
Affiliations
1 ICAR-Indian Agricultural Research Institute, Regional Station, Wellington 643 231, IN
2 The Jacob Blaustein Institutes for Desert Research, Ben-Gurion University of the Negev 8499000, IL
3 ICAR-Indian Institute of Spices Research, Regional Station, Madikeri 571 201, IN
4 ICAR-Indian Institute of Soil and Water Conservation, Regional Station, Udagamandalam 643 004, IN
5 ICAR-Indian Agricultural Research Institute, New Delhi 110 012, IN
6 ICAR-Central Potato Research Institute, Regional Station, Udhagamandalam 643 004, IN
7 ICAR-National Rice Research Institute, Cuttack 753 006, IN
1 ICAR-Indian Agricultural Research Institute, Regional Station, Wellington 643 231, IN
2 The Jacob Blaustein Institutes for Desert Research, Ben-Gurion University of the Negev 8499000, IL
3 ICAR-Indian Institute of Spices Research, Regional Station, Madikeri 571 201, IN
4 ICAR-Indian Institute of Soil and Water Conservation, Regional Station, Udagamandalam 643 004, IN
5 ICAR-Indian Agricultural Research Institute, New Delhi 110 012, IN
6 ICAR-Central Potato Research Institute, Regional Station, Udhagamandalam 643 004, IN
7 ICAR-National Rice Research Institute, Cuttack 753 006, IN
Source
Current Science, Vol 124, No 4 (2023), Pagination: 426-433Abstract
Wheat cultivation in southern India is unique as it is grown in high altitudes (1500 m amsl), surrounded by the pristine environment of the Western Ghats. Also, it can be grown throughout the year, unlike only once a year in India’s central and northern plains. The faunal pressure on wheat cultivation in southern India is different from the other wheat-growing regions in the country. However, information on faunal diversity associated with wheat crops in this unique ecosystem is meagre. Hence, the present study aimed to acquire knowledge based on the fauna associated with and their influence on wheat cultivation in the Nilgiris, Tamil Nadu, South India. Our results indicated that the phylum Arthropoda dominated the ecosystem with 61 species, followed by the Chordata with 41 species, and the Nematoda with 22 species. The coleopterans were found to be dominant among arthropods followed by lepidopterans. In chordates, small birds such as spotted munia and common rosefinch were observed often, while among the Nematoda, the plant-parasitic order Tylenchida topped the list. During different phases of cultivation, the overall diversity was highest during the early stages of the crop and least during the vegetative phase. This study also highlights the human– animal interaction in the context of agriculture, as it was observed that the damage caused by Nilgiri gaur, spotted munia and common rosefinch was one of the major reasons for non-preference of wheat crops by the farmers besides the lack of cost-effective technologies to ward-off wild animals. This initiative may encourage researchers to perform more comprehensive studies on the faunal diversity of the entire crop-growing areas in the southern hill regions of India.Keywords
Agroecosystem, Animals, Biodiversity, Birds, Nematodes, Wheat.References
- Agricoop, Annual Report 2020–21. Department of Agriculture, Cooperation and Farmers’ Welfare Ministry of Agriculture and Farmers’ Welfare Government of India, Madras, 2021, pp. 1–13; https://agricoop.nic.in/sites/default/files/Web%20copy%20of%20-AR%20%28Eng%29_7.pdf
- Francis, W., The Nilgiris Madras District Gazateers, The Superintendent, Government Press, 1908.
- Myers, N., Mittermeier, R. A., Mittermeier, C. G., da Fonseca, G. A. B. and Kent, J., Biodiversity hotspots for conservation priorities. Nature, 2000, 403, 853–858.
- Cobb, N. A., Estimating the nema population of soil, with special reference to the sugar-beet and root-gall nemas, Heterodera schachtii Schmidt and Heterodera radicicola (Greef) Müller. Agricultural Technology Circular. Bureau of Plant Industry, US Department of Agriculture, Government Print Office, USA, 1918.
- Seinhorst, J. W., A rapid method for the transfer of nematodes from fixative to anhydrous glycerin. Nematologica, 1959, 4, 67–69.
- Goodey, T., Goodey, J. B. and Jenkins, W. R., Soil and freshwater nematodes. Soil Sci., 1964, 97, 291.
- Jairajpuri, M. S. and Ahmad, W., Dorylaimida – Free-Living, Predaceous and Plant-Parasitic Nematodes, Oxford and IBH Publishing Co, Delhi, 1992, pp. 1–458.
- Ahmad, W., Plant Parasitic Nematodes of India: An Identification Manual, Department of Zoology, Aligarh Press, Aligarh Muslim University, 1996, pp. 1–348.
- Siddiqi, M. R., Tylenchida: Parasites of Plants and Insects, CABI, London, UK, 2000, 2nd edn, pp. 86–121.
- Ahmad, W. and Jairajpuri, M. S., Mononchida, the Predatory Soil Nematodes, BRILL Publisher, Leiden, The Netherlands, 2010, pp. 51–238.
- Berliner, J., Mhatre, P. H., Kalai, P. V., Kalaiarasan, P., Parvez, R. and Manimaran, B., Nematode trophic diversity in the pristine and cultivated fields of Nilgiris using Sedgewick–Rafter slides. Indian J. Nematol., 2021, 51, 149–154.
- Shannon, C. E., A mathematical theory of communication. Bell Syst. Tech. J., 1948, 27, 379–423.
- Menhinick, E. F., Estimation of insect population density in herbaceous vegetation with emphasis on removal sweeping. Ecology, 1963, 44, 617–621.
- Evans, E. W., Rogers, R. A. and Opfermann, D. J., Sampling grasshoppers (Orthoptera: Acrididae) on burned and unburned tall-grass prairie: night trapping vs sweeping. Environ. Entomol., 1983, 12, 1449–1454.
- Gullan, P. J. and Cranston, P. S., Methods in entomology: collecting, preservation, curation, and identification. In The Insects: An Outline of Entomology, Wiley-Blackwell, Hoboken, NJ, USA, 2010, 2nd edn, pp. 443–459.
- Roulston, T. H., Smith, S. A. and Brewster, A. L., Short communication: a comparison of pan trap and intensive net sampling techniques for documenting a bee (Hymenoptera: Apiformes) fauna. J. Kansas Entomol. Soc., 2007, 80, 179–181.
- Daniel, J. A. H. S. and Hegde, D., Butterfly diversity in Tamil Nadu agricultural university campus, Coimbatore, Tamil Nadu, India. J. Entomol. Zool. Stud., 2018, 6, 1354–1361.
- Mitra, S. S. and Sheldon, F. H., Use of an exotic tree plantation by Bornean lowland forest birds. Auk, 1993, 110, 529–540.
- Ripley, S. D. and Ali, S., Handbook of the birds of India and Pakistan. Vol. 7, Oxford University Press, 1972, pp. 1–228.
- Berliner, J., Mhatre, P. H., Manimaran, B. and Parvez, R., The role of weeds in survival of root-knot nematode in Nilgiris. In Souvenir and Abstracts, Fifth National Symposium on Plant Protection in Horticulture (NSPPH-2021): Challenges and Roadmap Ahead, ICAR-Indian Institute of Horticultural Research, Bengaluru, 27–29 December 2021, p. 86.
- Rashid, P., Prevalence of plant parasitic and predatory nematodes associated with different crops of Badaun district (Uttar Pradesh). Curr. Nematol., 2004, 16, 43–46.
- Borad, C. K. and Parasharya, B. M., Community structure of birds in wheat crop fields of Central Gujarat. J. Entomol. Zool. Stud., 2018, 6, 19–24.
- Parasharya, B. M., Dodia, J. F., Mathew, K. L. and Yadav, D. N., The role of birds in the natural regulation of Helicoverpa armigera Hubner in wheat. Pavo, 1996, 1, 33–38.
- Baker, E. C., The Fauna of British India, Volume 5, Taylor and Francis, London, UK, 1930.
- https://ebird.org/view/checklist/S55009232 (accessed on 5 August 2022).
- https://ebird.org/checklist/S112360201 (accessed on 5 August 2022).
- Thapa, A., Singh, A., Pradhan, P. K., Joshi, B. D., Takur, M., Sharma, L. K. and Chandra, K., Is the Indian peafowl Pavo cristatus moving higher up in the mountains? Indian Birds, 2020, 15, 177–179.
- Kumar, A., Walker, S. and Molur, S., Prioritisation of endangered species. Report submitted to WWF-India, 1998.
- ICAR-IIWBR, Progress report of AICRP on wheat and barley 2017–18. In Crop Protection (eds Singh, D. P. et al.), ICAR-Indian Institute of Wheat and Barley Research, Karnal, 2018, p. 259.
- Ramesh, T., Milda, D., Kalle, R., Gayathri, V., Thanikodi, M., Ashish, K. and Giordano, A. J., Drivers of human–megaherbivore interactions in the Eastern and Western Ghats of southern India. J. Environ. Manage., 2022, 316, 115315; https://doi.org/10.1016/j.jenv-man.2022.115315.
- Genome Organization and Comparative Evolutionary Mitochondriomics of Rice Earhead Bug Leptocorisa oratoria (Fabricius)
Abstract Views :45 |
PDF Views:42
Authors
Guru-Pirasanna-Pandi Govindharaj
1,
M. Annamalai
1,
Jaipal Singh Choudhary
2,
G. Basana-Gowda
1,
Totan Adak
1,
Naiyar Naaz
2,
Naveenkumar Patil
1,
Enrico Ruzzier
3,
Prakash Chandra Rath
1
Affiliations
1 ICAR-National Rice Research Institute, Cuttack 753 006, IN
2 ICAR-Research Complex for the Eastern Region, Farming System Research Centre for Hill and Plateau Region, Ranchi 834 010, IN
3 World Biodiversity Association Onlus, C/o Museo Civico di Storia Naturale, Lungadige Porta Vittoria 9, 37129 Verona, IT
1 ICAR-National Rice Research Institute, Cuttack 753 006, IN
2 ICAR-Research Complex for the Eastern Region, Farming System Research Centre for Hill and Plateau Region, Ranchi 834 010, IN
3 World Biodiversity Association Onlus, C/o Museo Civico di Storia Naturale, Lungadige Porta Vittoria 9, 37129 Verona, IT
Source
Current Science, Vol 125, No 4 (2023), Pagination: 407-415Abstract
The rice earhead bug, Leptocorisa oratoria (Fabricius, 1794) is a critical rice pest in India. No mitochondrial genome of L. oratoria has been sequenced earlier, and the mitochondrial data are crucial for phylogenetic and population genetic studies of this significant rice pest. In the present study, the genome of L. oratoria is 17,584 bp long with 73.57% AT content. We observed tandem repeat in the control region. Analyses from genetic distance, sliding window and Ka/Ks ratio revealed a purifying selection of 13 protein-coding genes, with cox1 and nad2 reporting the lowest and highest rate of evolution respectively. Phylogenetic analysis was reconstructed using 65 pentatomid mitogenomes with Bayesian inference and maximum likelihood methods. The results help differentiate the Coreoidea superfamily from Lygaeoidea, Aradoidea and Pentatomoidea. There were two topologies at the family level, i.e. one clade formed with Coreidae + Rhopalidae + Alydidae, and the rest of the families of Pentatomomorpha formed in separate clades. Further, L. oratoria produced an independent subclade from the earlier reported Leptocorisa sp. genome. This study provides a source mitogenome for L. oratoria species to study population demography, individual differences and phylogeography of hemipterans.Keywords
Mitogenome, Next Generation Sequencing, Population Genetics, Phylogeny, Rice Earhead Bug.References
- Rao, J. and Prakash, A., Bio-deterioration of paddy seed quality due to insects and mites and its control using botanicals. Final report of ICAR Ad-hoch Scheme, Central Rice Research Institute, Cuttack, India, 1995.
- Aktera, U. S., Islam, K. S., Jahan, M., Rahman, M. S., Talukder, F. U. and Hasan, M. A., Extent of damage of rice bug (Leptocorisa acuta) and its control with insecticides. Acta Sci. Malays., 2020, 4(2), 82–87; doi:10.26480/asm.02.2020.82.87.
- Rai, A. B., Singh, J. and Rai, L., Evaluation of gundhi bug, Lepto corisavaricornis (F.) damage in rice. In International Symposium on Rice Research, Hyderabad, 1990.
- Gupta, K. and Kumar, A., Field efficacy of certain insecticides against rice gundhi bug (Leptocorisa acuta (Thonberg)) under agro-climatic condition of Allahabad, India. Int. J. Curr. Microbiol. Appl. Sci., 2017, 6(8), 343–345.
- Nugaliyadde, L., Dissanayake, N., Mitrasena, J. and Wijesundera, D. S., Advances of pest and disease management of rice in Sri Lanka: a review. In Annual Symposium of the Department of Agriculture, Sri Lanka, 2000, vol. 2, pp. 409–422.
- Jahn, G. C., Domingo, I., Liberty, M., Almazan, P. and Pacia, J., Effect of rice bug Leptocoris aoratorius (Hemiptera: Alydidae) on rice yield, grain quality and seed viability. J. Econ. Entomol., 2004, 97(6), 1923–1927; https://doi.org/10.1093/jee/97.6.1923.
- Lessinger, A. C. et al., The mitochondrial genome of the primary screwworm fly Cochliomyia hominivorax (Diptera: Calliphoridae). Insect Mol. Biol., 2000, 9(5), 521–529; https://doi.org/10.1046/j.1365-2583.2000.00215.x.
- Lewis, J. A., Huq, A., Liu, W. and Jacob, A., Induction of gene expression by intracellular interferon-: abrogation of the species specificity barrier. Virology, 1995, 212(2), 438–450; https://doi.org/10.1006/viro.1995.1501.
- Zhang, D. X., Szymura, J. M. and Hewitt, G. M., Evolution and structural conservation of the control region of insect mitochondrial DNA. J. Mol. Evol., 1995, 40(4), 382–391; https://doi.org/10.1007/BF00164024.
- Shao, R., Campbell, N. J. and Barker, S. C., Numerous gene rear-rangements in the mitochondrial genome of the wallaby louse, Heterodoxus macropus (Phthiraptera). Mol. Biol. Evol., 2001, 18(5), 858–865; https://doi.org/10.1093/oxfordjournals.molbev.a003867.
- Choudhary, J. S., Naaz, N., Prabhakar, C. S., Rao, M. S. and Das, B., The mitochondrial genome of the peach fruit fly, Bactrocera zonata (Saunders) (Diptera: Tephritidae): Complete DNA sequence, genome organization, and phylogenetic analysis with other tephritids using next generation DNA sequencing. Gene, 2015, 569(2), 191–202; https://doi.org/10.1016/j.gene.2015.05.066.
- Taanman, J. W., The mitochondrial genome: structure, transcription, translation and replication. Biochim. Biophys. Acta, 1999, 1410(2), 103–123; https://doi.org/10.1016/S0005-2728(98)00161-3.
- Boore, J. L., Animal mitochondrial genomes. Nucleic Acids Res., 1999, 27, 1767–1780; doi:10.1093/nar/27.8.1767.
- Cameron, S. L., Beckenbach, A. T., Dowton, M. P. and Whiting, M. F., Evidence from mitochondrial genomics on interordinal relationships in insects. Arthropod Syst. Phylogen., 2006, 64(1), 27–34.
- Ashlock, P. D. and Slater, A., Family Lygaeidae Schilling, 1829 (= Infericornes Amyot and Serville, 1843; Myodochidae Kirkaldy, 1899; Geocoridae Kirkaldy, 1902): the seed bugs and chinch bugs. In Catalog of the Heteroptera, or True Bugs of Canada and the Continental United States, CRC Press, Boca Raton, Florida, 2019, pp. 167–245.
- Schuh, R. T. and Slater, J. A., True Bugs of the Eorld (Hemiptera: Heteroptera): Classification and Natural History, Cornell University Press, Ithaca, New York, 1995, pp. 609–610.
- Chilana, P., Sharma, A. and Rai, A., Insect genomic resources: status, availability and future. Curr. Sci., 2012, 102(4), 571–580.
- Ribeiro, F. J. et al., Finished bacterial genomes from shotgun sequence data. Genome Res., 2012, 22(11), 2270–2277; http://www.genome.org/cgi/doi/10.1101/gr.141515.112.
- Kirkness, E. F. et al., Genome sequences of the human body louse and its primary endosymbiont provide insights into the permanent parasitic lifestyle. Proc. Natl. Acad. Sci. USA, 2010, 107(27), 12168–12173; https://doi.org/10.1073/pnas.1003379107.
- Knaus, B. J., Cronn, R., Liston, A., Pilgrim, K. and Schwartz, M. K., Mitochondrial genome sequences illuminate maternal lineages of conservation concern in a rare carnivore. BMC Ecol., 2011, 11(1), 1–4; https://doi.org/10.1186/1472-6785-11-10.
- Ma, P. F., Guo, Z. H. and Li, D. Z., Rapid sequencing of the bamboo mitochondrial genome using Illumina technology and parallel episodic evolution of organelle genomes in grasses. PLoS ONE, 2012, 7(1), e30297; https://doi.org/10.1371/journal.pone.0030297.
- Coates, B. S., Assembly and annotation of full mitochondrial genomes for the corn rootworm species, Diabrotica virgifera virgifera and Diabrotica barberi (Insecta : Coleoptera : Chrysomelidae), using next generation sequence data. Gene, 2014, 542(2), 190–197; https://doi.org/10.1016/j.gene.2014.03.035.
- Barrion, A. T. and Litsinger, J. A., Dichogaster nr. Curgensis Michaelsen (Annelida : Octochaetidae): an earthworm pest of terraced rice in the Philippine Cordilleras. Crop Prot., 1997, 16(1), 89–93; https://doi.org/10.1016/S0261-2194(96)00058-0.
- Govindharaj, G. P. et al., Genome organization and comparative evolutionary mitochondriomics of brown planthopper, Nilaparvata lugens biotype 4 using next generation sequencing (NGS). Life, 2022, 12(9), 1289; https://doi.org/10.3390/life12091289.
- Bernt, M. et al., MITOS: improved de novo metazoan mitochondrial genome annotation. Mol. Phylogenet. Evol., 2013, 69(2), 313–319; https://doi.org/10.1016/j.ympev.2012.08.023.
- Lowe, T. M. and Eddy, S. R., tRNAscan-SE: a program for improved detection of transfer RNA genes in genomic sequence. Nucleic Acids Res., 1997, 25(5), 955–964; https://doi.org/10.1093/nar/25.5.955.
- Grant, J. R. and Stothard, P., The CGView Server: a comparative genomics tool for circular genomes. Nucleic Acids Res., 2008, 36(2), W181–W184; https://doi.org/10.1093/nar/gkn179.
- Tamura, K., Stecher, G., Peterson, D., Filipski, A. and Kumar, S., MEGA6: molecular evolutionary genetics analysis version 6.0. Mol. Biol. Evol., 2013, 30(12), 2725–2729; https://doi.org/10.1093/molbev/mst197.
- Choudhary, J. S., Naaz, N., Lemtur, M., Das, B., Singh, A. K., Bhatt, B. P. and Prabhakar, C. S., Genetic analysis of Bactrocerazonata (Diptera : Tephritidae) populations from India based on cox1 and nad1 gene sequences. Mitochondrial DNA Part A, 2018, 29(5), 727–736; https://doi.org/10.1080/24701394.2017.1350952.
- Perna, N. T. and Kocher, T. D., Patterns of nucleotide composition at fourfold degenerate sites of animal mitochondrial genomes. J. Mol. Evol., 1995, 41(3), 353–358; https://doi.org/10.1007/BF0018-6547.
- Librado, P. and Rozas, J., DnaSP v5: a software for comprehensive analysis of DNA polymorphism data. Bioinformatics, 2009, 25(11), 1451–1452; https://doi.org/10.1093/bioinformatics/btp187.
- Katoh, K. and Standley, D. M., MAFFT multiple sequence alignment software version 7: improvements in performance and usability. Mol. Biol. Evol., 2013, 30(4), 772–780; https://doi.org/10.1093/molbev/mst010.
- Talavera, G. and Castresana, J., Improvement of phylogenies after removing divergent and ambiguously aligned blocks from protein sequence alignments. Syst. Biol., 2007, 56(4), 564–577; https://doi.org/10.1080/10635150701472164.
- Bu, R. et al., Tillage and straw-returning practices effect on soil dissolved organic matter, aggregate fraction and bacteria community under rice-rice-rapeseed rotation system. Agric. Ecosyst. Environ., 2020, 287, 106681; https://doi.org/10.1016/j.agee.2019.106681.
- Lanfear, R., Frandsen, P. B., Wright, A. M., Senfeld, T. and Calcott, B., PartitionFinder 2: new methods for selecting partitioned models of evolution for molecular and morphological phylogenetic analyses. Mol. Biol. Evol., 2017, 34(3), 772–773; https://doi.org/10.1093/molbev/msw260.
- Guindon, S. and Gascuel, O., A simple, fast, and accurate algorithm to estimate large phylogenies by maximum likelihood. Syst. Biol., 2003, 52(5), 696–704; https://doi.org/10.1080/10635150390235520.
- Huelsenbeck, J. P. and Ronquist, F., MRBAYES: bayesian inference of phylogenetic trees. Bioinformatics, 2001, 17(8), 754–755.
- Letunic, I. and Bork, P., Interactive tree of life (iTOL) v4: recent updates and new developments. Nucleic Acids Res., 2019, 47(W1), W256–W259; https://doi.org/10.1093/nar/gkz239.
- Crease, T. J., The complete sequence of the mitochondrial genome of Daphnia pulex (Cladocera: Crustacea). Gene, 1999, 233(1–2), 89–99; https://doi.org/10.1016/S0378-1119(99)00151-1.
- Yuan, M. L., Zhang, Q. L., Guo, Z. L., Wang, J. and Shen, Y. Y., The complete mitochondrial genome of Corizus tetraspilus (Hemiptera: Rhopalidae) and phylogenetic analysis of Pentatomomorpha. PLoS ONE, 2015, 10(6), e0129003; https://doi.org/10.1371/journal.pone.0129003.
- Zhang, K. J. et al., The complete mitochondrial genomes of two rice planthoppers, Nilaparvata lugens and Laodelphax striatellus: conserved genome rearrangement in Delphacidae and discovery of new characteristics of atp8 and tRNA genes. BMC Genomics, 2013, 14(1), 1–2; https://doi.org/10.1186/1471-2164-14-417.
- Anant, A. K. et al., Genetic dissection and identification of candidate genes for brown planthopper, Nilaparvata lugens (Delphacidae: Hemiptera) resistance in farmers’ varieties of rice in Odisha. Crop Prot., 2021, 144, 105600; https://doi.org/10.1016/j.cropro.2021.10-5600.
- Cha, S. Y. et al., The complete nucleotide sequence and gene organization of the mitochondrial genome of the bumblebee, Bombus ignitus (Hymenoptera: Apidae). Gene, 2007, 392(1–2), 206–220; https://doi.org/10.1016/j.gene.2006.12.031.
- Jiang, S. T., Hong, G. Y., Yu, M., Li, N., Yang, Y., Liu, Y. Q. and Wei, Z. J., Characterization of the complete mitochondrial genome of the giant silkworm moth, Eriogyna pyretorum (Lepidoptera: Saturniidae). Int. J. Biol. Sci., 2009, 5(4), 351; doi:10.7150/ijbs.5.351.
- Song, N. and Liang, A. P., Complete mitochondrial genome of the small brown planthopper, Laodelphax striatellus (Delphacidae: Hemiptera), with a novel gene order. Zool. Sci., 2009, 26(12), 851–860; https://doi.org/10.2108/zsj.26.851.
- Chen, M. M. et al., Complete mitochondrial genome of the Atlas moth, Attacus atlas (Lepidoptera: Saturniidae) and the phylogenetic relationship of Saturniidae species. Gene, 2014, 545(1), 95–101; https://doi.org/10.1016/j.gene.2014.05.002.
- Hua, J., Li, M., Dong, P., Cui, Y., Xie, Q. and Bu, W., Comparative and phylogenomic studies on the mitochondrial genomes of Pentatomomorpha (Insecta: Hemiptera: Heteroptera). BMC Genomics, 2008, 9(1), 1–5; https://doi.org/10.1186/1471-2164-9-610.
- Hou, W. R. et al., A complete mitochondrial genome sequence of Asian black bear Sichuan subspecies (Ursus thibetanus mupinensis). Int. J. Biol. Sci., 2007, 3(2), 85; doi:10.7150/ijbs.3.85.
- Hong, G., Jiang, S., Yu, M., Yang, Y., Li, F., Xue, F. and Wei, Z., The complete nucleotide sequence of the mitochondrial genome of the cabbage butterfly, Artogeia melete (Lepidoptera: Pieridae). Acta Biochim. Biophys. Sin., 2009, 41(6), 446–455; https://doi.org/10.1093/abbs/gmp030.
- Lv, L., Peng, X., Jing, S., Liu, B., Zhu, L. and He, G., Intraspecific and interspecific variations in the mitochondrial genomes of Nilaparvata (Hemiptera: Delphacidae). J. Econ. Entomol., 2015, 108(4), 2021–2029; https://doi.org/10.1093/jee/tov122.
- Thao, M. L., Baumann, L. and Baumann, P., Organization of the mitochondrial genomes of whiteflies, aphids, and psyllids (Hemiptera, Sternorrhyncha). BMC Evol. Biol., 2004, 4(1), 1–3; https://doi.org/10.1186/1471-2148-4-25.
- Zhu, Y. J., Zhou, G. L., Fang, R., Ye, J. and Yi, J. P., The complete sequence determination and analysis of Lymantria dispar (Lepidoptera: Lymantriidae) mitochondrial genome. Plant Quarantine, 2010, 24(4), 6–11.
- Valero, M. C., Ojo, J. A., Sun, W., Tamò, M., Coates, B. S. and Pittendrigh, B. R., The complete mitochondrial genome of Anoplocnemis curvipes F. (Coreinea, Coreidae, Heteroptera), a pest of fresh cowpea pods. Mitochondrial DNA, Part B, 2017, 2(2), 421–423; https://doi.org/10.1080/23802359.2017.1347829.
- Huang, Y. X. and Qin, D. Z., First mitogenome for the tribe Saccharosydnini (Hemiptera: Delphacidae: Delphacinae) and the phylogeny of three predominant rice planthoppers. Eur. J. Entomol., 2018, 30, 115.
- Ohtsuki, T., Kawai, G. and Watanabe, K., The minimal tRNA: unique structure of Ascaris suum mitochondrial tRNASerUCU having a short T arm and lacking the entire D arm. FEBS Lett., 2002, 514(1), 37–43; https://doi.org/10.1016/S0014-5793(02)02328-1.
- Sheffield, N. C., Song, H., Cameron, S. L. and Whiting, M. F., Nonstationary evolution and compositional heterogeneity in beetle mitochondrial phylogenomics. Syst. Biol., 2009, 58(4), 381–394; https://doi.org/10.1093/sysbio/syp037.
- Zhao, Q., Wang, J., Wang, M. Q., Cai, B., Zhang, H. F. and Wei, J. F., Complete mitochondrial genome of Dinorhynchus dybowskyi (Hemiptera: Pentatomidae: Asopinae) and phylogenetic analysis of Pentatomomorpha species. J. Insect Sci., 2018, 18(2), 44; https://doi.org/10.1093/jisesa/iey031.
- Lee, W., Kang, J., Jung, C., Hoelmer, K., Lee, S. H. and Lee, S., Complete mitochondrial genome of brown marmorated stink bug Halyomorpha halys (Hemiptera: Pentatomidae), and phylogenetic relationships of hemipteran suborders. Mol. Cells, 2009, 28(3), 155–165; https://doi.org/10.1007/s10059-009-0125-9.
- Li, H., Liu, H., Shi, A., Štys, P., Zhou, X. and Cai, W., The complete mitochondrial genome and novel gene arrangement of the unique-headed bug Stenopirates sp. (Hemiptera: Enicocephalidae). PLoS ONE, 2012, 7(1), e29419; https://doi.org/10.1371/journal.pone.0029419.
- Castellana, S., Vicario, S. and Saccone, C., Evolutionary patterns of the mitochondrial genome in Metazoa: exploring the role of mutation and selection in mitochondrial protein-coding genes. Genome Biol. Evol., 2011, 3, 1067–1079; https://doi.org/10.1093/gbe/evr040.
- Wang, Y., Chen, J., Jiang, L. Y. and Qiao, G. X., Hemipteran mitochondrial genomes: features, structures and implications for phylogeny. Int. J. Mol. Sci., 2015, 16(6), 12382–12404; https://doi.org/10.3390/ijms160612382.
- Zhao, L., Wei, J., Zhao, W., Chen, C., Gao, X. and Zhao, Q., The complete mitochondrial genome of Pentatoma rufipes (Hemiptera, Pentatomidae) and its phylogenetic implications. ZooKeys, 2021, 1042, 51; doi:10.3897/zookeys.1042.62302.
- Johnson, K. P. et al., Phylogenomics and the evolution of hemipteroid insects. Proc. Natl. Acad. Sci. USA, 2018, 115(50), 12775–12780; https://doi.org/10.1073/pnas.1815820115.