Molecular characterization of necromenic nematode Pristionchus pacificus and associated bacteria: A new record


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Authors

  • ASHISH KUMAR SINGH ICAR-Vivekanada Parvatiya Krishi Anusandhan Sansthan, Almora, Uttarakhand 263 601, India
  • AMIT U PASCHAPUR ICAR-Vivekanada Parvatiya Krishi Anusandhan Sansthan, Almora, Uttarakhand 263 601, India
  • TILAK MONDAL ICAR-Vivekanada Parvatiya Krishi Anusandhan Sansthan, Almora, Uttarakhand 263 601, India
  • MANOJ PARIHAR ICAR-Vivekanada Parvatiya Krishi Anusandhan Sansthan, Almora, Uttarakhand 263 601, India
  • K K MISHRA ICAR-Vivekanada Parvatiya Krishi Anusandhan Sansthan, Almora, Uttarakhand 263 601, India
  • LAKSHMI KANT ICAR-Vivekanada Parvatiya Krishi Anusandhan Sansthan, Almora, Uttarakhand 263 601, India

https://doi.org/10.56093/ijas.v92i10.120837

Keywords:

Myroides marinus, Necromenic nematode, North-western Himalaya, Phylogenetic analysis, Pristionchus pacificus

Abstract

The vast diversity of nematodes has adapted to endure in different trophic groups as free living and parasites of plants and animals. In search of potential entomopathogenic nematodes (EPNs), soil samples were collected from, the rhizosphere of Apple orchard in Darima, Nainital, Uttarakhand, India north-western Himalaya in August 2019. The whole experimental activity carried out at ICAR-Vivekanada Parvatiya Krishi Anusandhan Sansthan, Almora during 2019–2021. In present study, Pristionchus pacificus was isolated using Corcyra bait trap, identified based on morphological and molecular approaches, studied its host range, evaluated the phylogenetic tree of P. pacificus and isolated and characterized the nematode associated bacteria. The reproduction potential and frequency of emergence of P. pacificus differs significantly among the tested hosts on Corcyra, Spodoptera and Holotrichia larvae. The molecular diagnostics of associated bacteria based on 16S gene displayed the highest homology with Myroides marinus strain. The discovery of P. pacificus VLPP01 represents the first record from India and Himalayan region.

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References

Bower C A and Wilcox L V. 1965. Soluble salts. Methods of Soil Analysis, pp 433–45. Black CA (Eds). ASA, Inc Madison, Wisconsin, USA.

Cho S H, Chae S H, Im W T and Kim S B. 2011. Myroides marinus sp. nov., a member of the family Flavobacteriaceae, isolated from seawater. International Journal of Systematic and Evolutionary Microbiology 61(4): 938–41. DOI: https://doi.org/10.1099/ijs.0.024067-0

De Ley P, De Ley I T, Morris K, Abebe E, Mundo-Ocampo M, Yoder M, Heras J, Waumann D, Rocha-Olivares A, Jay Burr A H and Baldwin J G. 2005. An integrated approach to fast and informative morphological vouchering of nematodes for applications in molecular barcoding. Philosophical Transactions of the Royal Society B: Biological Sciences 360(1462): 1945–58. DOI: https://doi.org/10.1098/rstb.2005.1726

Gomez K A and Gomez A A. 1984. Statistical Procedures for Agricultural Research, 2nd edn, pp 680. John Wiley and Sons, New York.

Hassani-Kakhki M, Karimi J and Shokoohi E. 2013. Molecular and morphological characterization of Pristionchus pacificus (Nematoda: Rhabditida: Neodiplogastridae), a new record of an entomophilic nematode from Iran. Biologia 68: 910–17. DOI: https://doi.org/10.2478/s11756-013-0232-0

Herrmann M, Kienle S, Rochat J, Mayer W E and Sommer R J. 2010. Haplotype diversity of the nematode Pristionchus pacificus on reunion in the Indian Ocean suggests multiple in-dependent invasions. Biological Journal of the Linnean Society 100: 170–79 DOI: https://doi.org/10.1111/j.1095-8312.2010.01410.x

Herrmann M, Mayer W E and Sommer R J. 2006. Sex, bugs and Haldane’s rule: The nematode genus Pristionchus in the United States. Frontiers in Zoology 3: 14 DOI: https://doi.org/10.1186/1742-9994-3-14

Holmes B, Snell J J S and Lapage S P. 1977. Revised description from clinical isolates of Flavobacterium odoratum Stutzer and Kwaschnina 1929, and designation of the neotype strain. International Journal of Systematic and Evolutionary Microbiology 27: 330–36. DOI: https://doi.org/10.1099/00207713-27-4-330

Holterman M, Van der Wurff A, Van den Elsen S, Van Megen H, Bongers T, Holovachov O, Bakker J and Helder J. 2006. Phylum-wide analysis of SSU rDNA reveals deep phylogenetic relationships among nematodes and accelerated evolution toward crown Clades. Molecular Biology and Evolution 23(9): 1792–800. DOI: https://doi.org/10.1093/molbev/msl044

Hong R L and Sommer R J. 2006. Pristionchus pacificus: a well-rounded nematode. Bioessays 28: 651–59. DOI: https://doi.org/10.1002/bies.20404

Jackson M L. 1967. Soil Chemical Analysis. Prentice Hall of India Private Ltd, New Delhi, pp. 263–93

Johnson T E and Lithgow G J. 1992. The search for the genetic basis of aging: the identification of gerontogenes in the nematode Caenorhabditis elegans. Journal of the American Geriatrics Society 40(9): 936–45. DOI: https://doi.org/10.1111/j.1532-5415.1992.tb01993.x

Jones J T. 2013. Top 10 plant-parasitic nematodes in molecular plant pathology. Molecular Plant Pathology 14: 946–61. DOI: https://doi.org/10.1111/mpp.12057

Kanzaki N, Taki H, Masuya H, Okabe K, Tanaka R and Abe F. 2011. Diversity of stag beetle-associated nematodes in Japan. Environmental Entomology 40(2) 281–88. DOI: https://doi.org/10.1603/EN10182

Kanzaki N, Ragsdale E J, Herrmann M, Mayer W E and Sommer R J. 2012. Description of three Pristionchus species (Nematoda: Diplogastridae) from Japan that form a cryptic species complex with the model organism P. pacificus. Zoological Science 29: 403–17 DOI: https://doi.org/10.2108/zsj.29.403

Li P, Dai C, Bao H, Chen L, Gao D, Wang G, Wang J, Wang H, Yedid G and Zhang K. 2015. A new species of Pristionchus (Rhabditida: Diplogastridae) and its bacterial symbiont from Yixing, China. Journal of Nematology 47(3): 190–97.

Lindsay W L and Norvell W A. 1978. Development of soil test for zinc, iron, manganese and copper. Soil Science Society of America Journal 42: 421–28 DOI: https://doi.org/10.2136/sssaj1978.03615995004200030009x

Muhling M, Woolven-Allen J, Murrell J C and Joint I. 2008. Improved group-specific PCR primers for denaturing gradient gel electrophoresis analysis of the genetic diversity of complex microbial communities. ISME: 379–92. DOI: https://doi.org/10.1038/ismej.2007.97

Olsen S R, Cole C V, Watanabe F S and Dean L A. 1954. Estimation of available phosphorus in soils by extraction with sodium bicarbonate. Circular No. 939. USDA, Washington, DC, USA.

Pereira T J and Baldwin J G. 2016. Contrasting evolutionary patterns of 28S and ITS rRNA genes reveal high intragenomic variation in Cephalenchus (Nematoda): implications for species delimitation. Molecular Phylogenetics and Evolution 98: 244–42 DOI: https://doi.org/10.1016/j.ympev.2016.02.016

Pires-daSilva A. 2013. Pristionchus pacificus protocols. The C. elegans Research Community, WormBook. DOI: https://doi.org/10.1895/wormbook.1.114.2

Powers T. 2004. Nematode molecular diagnostics: from bands to barcodes. Annual Review of Phytopathology 42: 367–83. DOI: https://doi.org/10.1146/annurev.phyto.42.040803.140348

Rae R, Riebesell M, Dinkelacker I, Wang Q, Herrmann M, Weller A M, Dieterich C and Sommer R J. 2008. Isolation of naturally associated bacteria of necromenic Pristionchus nematodes and fitness consequences. Journal of Experimental Biology 211(12): 1927–36. DOI: https://doi.org/10.1242/jeb.014944

Schollenberger C J and Simon R H. 1945. Determination of exchange capacity and exchangeable bases in soil – ammonium acetate method. Soil science 59: 13–24 DOI: https://doi.org/10.1097/00010694-194501000-00004

Seinhorst J W. 1959. A rapid method for the transfer of nematodes from fixative to anhydrous glycerin. Nematologica 4: 67–69. DOI: https://doi.org/10.1163/187529259X00381

Singh A K. 2021. Entomopathogenic nematodes: a sustainable option for insect pest management. Biopesticides: Advances in Bio-inoculant Science, pp. 73–92. Rakshit A, Meena V S, Abhilash P C, Sarma B K , Singh H B, Leonardo Fraceto, Parihar M, Singh A K (Eds). Woodhead Publishing. DOI: https://doi.org/10.1016/B978-0-12-823355-9.00007-9

Sommer R J and McGaughran A. 2013. The nematode Pristionchus pacificus as a model system for integrative studies in evolutionary biology. Molecular Ecology 22: 2380–93. DOI: https://doi.org/10.1111/mec.12286

Subbiah B V and Asija G L. 1956. A rapid test procedure for assessment of available nitrogen in soils. Current Science 25: 259–60

White G F. 1927. A method for obtaining infective nematode larvae from cultures. Science 66: 302–03. DOI: https://doi.org/10.1126/science.66.1709.302-b

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2022-01-31

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2022-10-04

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How to Cite

SINGH, A. K., PASCHAPUR, A. U., MONDAL, T., PARIHAR, M., MISHRA, K. K., & KANT, L. (2022). Molecular characterization of necromenic nematode Pristionchus pacificus and associated bacteria: A new record. The Indian Journal of Agricultural Sciences, 92(10), 1253–1257. https://doi.org/10.56093/ijas.v92i10.120837
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