Selection of Potential Bacteria in Termite Nest and Gut for Sustainable Agriculture

Authors

  • Phanukit Kunhachan National Institute of Health, Department of Medical Sciences, Ministry of Public Health, Nonthaburi 11000, Thailand
  • Wandee Sirithana Faculty of Science and Technology, Suan Dusit University, Bangkok 10700, Thailand
  • Orapin Komutiban Faculty of Science and Technology, Suan Dusit University, Bangkok 10700, Thailand
  • Vassanasak Limkhuansuwan Faculty of Science and Technology, Suan Dusit University, Bangkok 10700, Thailand
  • Phanchai Menchai Faculty of Science and Technology, Suan Dusit University, Bangkok 10700, Thailand
  • Chanaporn Trakunjae Kasetsart Agricultural and Agro-Industrial Product Improvement Institute (KAPI), Kasetsart University, Bangkok 10900, Thailand
  • Thanasak Lomthong Division of Biology, Faculty of Science and Technology, Rajamangala University of Technology Thanyaburi, Pathum Thani 12110, Thailand
  • Kriangsak Ruchusatsawat National Institute of Health, Department of Medical Sciences, Ministry of Public Health, Nonthaburi 11000, Thailand
  • Srisuda Samaimai Faculty of Science and Technology, Suan Dusit University, Bangkok 10700, Thailand

DOI:

https://doi.org/10.48048/tis.2024.7794

Keywords:

Bacillus, Termite nest, Termite gut, Phythium parasitica

Abstract

In this study, bacteria with the best abilities in cellulose degradation, siderophore production, phosphate solubility, and Pythium parasitica inhibition were selected from termite nests and guts. The isolate BTNASP 5-2, BTPK 5-3 and BTNA 5-1 from termite guts exhibited highest in siderophore production index (SPI) (4.16 ± 0.21), phosphate solubilizing index (PSI) (2.10 ± 0.14) and percentage inhibition of radial growth (PIRG) (67.07 ± 4.02 %), respectively. The BGNACMC 4-3 isolated from termite nest gave the highest cellulolytic index (CI) of 5.17 ± 0.24. Bacterial classification was performed using 16s rRNA gene sequencing. The isolates BTPK 5-3, BGNACMC 4-3 and BTNA 5-1 were found closely related to Bacillus cereus, whereas the bacterial isolate BTNASP 5-2 was closely related to Bacillus subtilis. It is also suggested that the Bacillus cereus exhibited a variety of biological activities, denoting the highest cellulase, phosphate-solubilizing and antifungal activities, while Bacillus subtilis produced only a siderophore. The results obtained suggest that the bacteria selected will be used to develop bio-compost to promote plant growth, leading to sustainable farming. 

HIGHLIGHTS

  • Bacillus cereus exhibited a variety of biological activities, denoting the highest cellulase, phosphate-solubilizing, and antifungal activities
  • Bacillus subtilis produced a siderophore
  • The highest cellulose-degrading bacteria ( cereus BGNACMC4-3) found in termite mound nest

GRAPHICAL ABSTRACT

Downloads

Download data is not yet available.

Metrics

Metrics Loading ...

References

FAO, IFAD, UNICEF, WFP & WHO. The state of food security and nutrition in the world 2023: Urbanization, agrifood systems transformation and healthy diets across the rural-urban continuum. FAO; IFAD; UNICEF; WFP; WHO, Rome, Italy, 2023, p. 316.

T Mahanty, S Bhattacharjee, M Goswami, P Bhattacharyya, B Das, A Ghosh and P Tribedi Biofertilizers: A potential approach for sustainable agriculture development. Environ. Sci. Pollut. Res. 2016; 24, 3315-35.

AM Pirttilä, HMP Tabas, N Baruah, and JJ Koskimäki. Biofertilizers and biocontrol agents for agriculture: How to identify and develop new potent microbial strains and traits. Microorganisms 2021; 9, 817.

M Tariq, F Jameel, U Ijaz, M Abdullah and K Rashid. Biofertilizer microorganisms accompanying pathogenic attributes: A potential threat. Physiol. Mol. Biol. Plants 2022; 28, 77-90.

M Verma, J Mishra and NK Arora. Plant growth-promoting rhizobacteria: Diversity and applications. In: RC Sobti, NK Arora and R Kothari (Eds.). Environmental Biotechnology: For sustainable future. Springer, Singapore, 2018, p. 129-73.

D Nandika, L Karlinasari, A Arinana, I Batubara, PS Sitanggang, D Santoso, LD Witasari, Y Rachmayanti, D Firmansyah, IK Sudiana and DM Hertanto. Chemical components of fungus comb from indo-malayan termite Macrotermes gilvus Hagen mound and its bioactivity against wood-staining fungi. Forests 2021, 12, 159.

R Duponnois, M Kisa, K Assigbetse, Y Prin, J Thioulouse, M Issartel, P Moulin and M Lepage. Fluorescent pseudomonads occuring in Macrotermes subhyalinus mound structures decrease Cd toxicity and improve its accumulation in sorghum plants. Sci. Total Environ. 2006; 370, 391-400.

AK Chauhan, DK Maheshwari, S Dheeman and VK Bajpai. Termitarium-inhabiting Bacillus spp. enhanced plant growth and bioactive component in turmeric (Curcuma longa L.). Curr. Microbiol. 2017; 74, 184-92.

S Fall, J Hamelin, F Ndiaye, K Assigbetse, M Aragno, JL Chotte and A Brauman. Differences between bacterial communities in the gut of a soil-feeding termite (Cubitermes niokoloensis) and its mounds. Appl. Environ. Microbiol. 2007; 73, 5199-208.

PS Costa, PL Oliveira, E Chartone-Souza and AMA Nascimento. Phylogenetic diversity of prokaryotes associated with the mandibulate nasute termite Cornitermes cumulans and its mound. Biol. Fertil. Soils. 2013; 49, 567-74.

A Manjula, S Suresh, M Pushpanathan, P Gunasekaran and J Rajendhran. Microbial diversity in termite nest. Curr. Sci. 2014; 106, 1430-4.

KH Kim, TR Ramadhar, C Beemelmanns, S Cao, M Poulsen, CR Currie and J Clardy. Natalamycin A, an ansamycin from a termite-associated Streptomyces sp. Chem. Sci. 2014; 5, 4333-8.

R Devi, R Thakur and M Gupta. Isolation and molecular characterization of bacterial strains with antifungal activity from termite mound soil. Int. J. Curr. Microbiol. Appl. Sci. 2018; 7, 1-7.

R Devi and R Thakur. Screening and identification of bacteria for plant growth promoting traits from termite mound soil. J. Pharmacogn. Phytochem. 2018; 7, 1681-6.

D Sharma, B Joshi, MR Bhatt, J Joshi, R Malla, T Bhattarai and L Sreerama. Isolation of cellulolytic organisms from the gut contents of termites native to Nepal and their utility in saccharifcation and fermentation of lignocellulosic biomass. J. Biomass Biofuel. 2015; 2, 11-20.

CP Sreena, NK Resna and D Sebastian. Isolation and characterization of cellulase producing bacteria from the gut of termites (Odontotermes and Heterotermes species). Br. Biotechnol. J. 2015; 9, 1-10.

GM Mathew, YM Ju, CY Lai, DC Mathew and CC Huang. Microbial community analysis in the termite gut and fungus comb of Odontotermes formosanus: the implication of Bacillus as mutualists. FEMS Microbiol Ecol. 2012; 79, 504-17.

D Oktiarni, H Hermansyah, Hasanudin, Miksusanti, E Nofyan and G Kasmiarti. Isolation and identification cellulolytic bacteria from termite gut obtained from Indralaya Peatland area. IOP Conf. Series: Earth Environ. Sci. 2021; 926, 012024.

HRK Ali, NF Hemeda and YF Abdelaliem. Symbiotic cellulolytic bacteria from the gut of the subterranean termite Psammotermes hypostoma Desneux and their role in cellulose digestion. AMB Express 2019; 9, 111.

N Sujada, R Sungthong and S Lumyong. Termite nests as an abundant source of cultivable actinobacteria for biotechnological purposes. Microbes Environ. 2014; 29, 211-9.

BJ Enagbonm and OO Babalola. Potentials of termite mound soil bacteria in ecosystem engineering for sustainable agriculture. Ann. Microbiol. 2019; 69, 211-9.

P Gupta, K Samant and A Sahu. Isolation of cellulose-degrading bacteria and determination of their cellulolytic potential. Int. J. Microbiol. 2012; 2012, 578925.

A Ferbiyanto, I Rusmana and R Raffiudin. Characterization and identification of cellulolytic bacteria from gut of worker Macrotermes gilvus. HAYATI J. Biosci. 2016; 22, 1-4.

D Sharma, B Joshi, MR Bhatt, J Joshi, R Malla, T Bhattarai and L Sreerama. Isolation of cellulolytic organisms from the gut contents of termites native to Nepal and their utility in saccharification and fermentation of lignocellulosic biomass. J. Biomass Biofuel 2015; 2, 11-20.

SF Fu, PF Sun, HY Lu, JY Wei, HS Xiao, WT Fang, BY Cheng and JY Chou. Plant growth-promoting traits of yeasts isolated from the phyllosphere and rhizosphere of Drosera spatulata Lab. Fungal Biol. 120, 433-48.

EP Kyaw, MM Soe, SS Yu, ZK Latt and TM Lynn. Study on plant growth promoting activities of Azotobacter isolates for sustainable agriculture in Myanmar. J. Biotech. Biores. 2019; 1, 1-6.

S Nacoon, S Jogloy, N Riddech, W Mongkolthanaruk, TW Kuyper and SS Boonlue. Interaction between phosphate solubilizing bacteria and arbuscular mycorrhizal fungi on growth promotion and tuber inulin content of Helianthus tuberosus L. Sci. Rep. 2020; 10, 4916.

S Sudewi, A Ala, B Patandjengi and MBDR Farid. Isolation of phosphate solubilizing bacteria from the rhizosphere of local aromatic rice in Bada Valley Central Sulawesi, Indonesia. IOP Conf. Ser.: Earth Environ. Sci. 2020; 575, 012017.

F Ahmad, I Ahmad and MS Khan. Screening of free-living rhizospheric bacteria for their multiple plant growth promoting activities. Microbiol. Res. 2008; 168, 173-81.

BC Louden, D Haarmann and AM Lynne. Use of blue agar CAS assay for siderophore detection. J. Microbiol. Biol. Educ. 2011; 12, 51-3.

GA Abo-Zaid, NAM Soliman, AS Abdullah, EE El-Sharouny, SM Matar and SAF Sabry. Maximization of siderophores production from biocontrol agents, Pseudomonas aeruginosa F2 and Pseudomonas fluorescens JY3 using batch and exponential fed-batch fermentation. Processes 2020; 8, 455.

W Intana, P Yenjit, T Suwanno, S Sattasakulchai, M Suwanno and C Chamswarng. Efficacy of antifungal metabolites of Bacillus spp. for controlling tomato damping-off caused by Pythium aphanidermatum. Walailak J. Sci. Tech. 2008; 5, 29-38.

K Sookchaoy, S Panthachode and J Thipchu. Screening of Trichoderma spp. for phytophthora root and foot rot on Citrus sinensis biocontrol. In: International Conference on the Role of Universities in Hands-On Education, Rajamangala University of Technology Lanna, Chiang-Mai, Thailand. 2009, p. 356-62.

K Tamura, G Stecher and S Kumar. MEGA 11: Molecular evolutionary genetics analysis version 11. Mol. Biol. Evol. 2021; 38, 3022-7.

N Saitou and M Nei. The neighbor-joining method: A new method for reconstructing phylogenetic trees. Mol. Biol. Evol. 1987; 4, 406-25.

M Kimura. A simple method for estimating evolutionary rate of base substitutions through comparative studies of nucleotide sequences. J. Mol. Evol. 1980; 16, 111-20.

P Jouquet, N Guilleux, RR Shanbhag and S Subramanian. Influence of soil type on the properties of termite mound nests in southern India. Appl. Soil. Ecol. 2015; 96, 282-7.

JA Breznak and A Brune. Role of microorganisms in the digestion of lignocellulose by termites. Annu. Rev. Entomol. 1994; 39, 453-87.

BJ Enagbonma and OO Babalola. Metagenomics reveals the microbiome multifunctionalities of environmental importance from termite mound soils. Bioinform. Biol. Insights 2023; 17, 1-10.

W Lertlumnaphakul, R Ngoen-Klan, C Vongkaluang and T Chareonviriyaphap. A review of termite species and their distribution in Thailand. Insects 2022; 13, 186.

S Fall, J Hamelin, F Ndiaye, K Assigbetse, M Aragno, JL Chotte and A Brauman. Differences between bacterial communities in the gut of a soil-feeding termite (Cubitermes niokoloensis) and its mounds. Appl. Environ. Microbiol. 2007; 73, 5199-208.

DB Alexander and DA Zuberer. Use of chrome azurol S reagents to evaluate siderophore production by rhizosphere bacteria. Biol. Fertil. Soils 1991; 12, 39-45.

GA Abo-Zaid, NA-M Soliman, AS Abdullah, EE El-Sharouny, SM Matar and SA-F Sabry. Maximization of siderophores production from biocontrol agents, Pseudomonas aeruginosa F2 and Pseudomonas fluorescens JY3 using batch and exponential fed-batch fermentation. Processes 2020; 8, 455.

GAA Aguado-Santacruz, BA Moreno-Gómez, B Jiménez-Francisco, EG Moya and RE Preciado-Ortiz. Impact of the microbial siderophores and phytosiderophores on the iron assimilation by plants: A synthesis. Rev. Fitotec. Mex. 2012, 35, 9-21.

J Köhl, R Kolnaar and WJ Ravensberg. Mode of action of microbial biological control agents against plant diseases: Relevance beyond efficacy. Front. Plant Sci. 2019; 10, 845.

VS Kumar, S Menon, H Agarwal and D Gopalakrishnan. Characterization and optimization of bacterium isolated from soil samples for the production of siderophores. Resource-Efficient Tech. 2017; 3, 434-9.

PS Bama and AD Ravindran. Dynamics of P sorption and solubilising activity in termite nest material. Asian J. Res. Soc. Sci. Hum. 2012; 2, 231-7.

H Chakdar, SG Dastager, JM Khire, D Rane and MS Dharne. Characterization of mineral phosphate solubilizing and plant growth promoting bacteria from termite soil of arid region. 3 Biotech 2018; 8, 463.

S Um, A Fraimout, P Sapountzis, DC Oh and M Poulsen. The fungus-growing termite Macrotermes natalensis harbors bacillaene-producing Bacillus sp. that inhibit potentially antagonistic fungi. Sci. Rep. 2013; 3, 3250.

W Raab. Natamycin (Pimaricin): Its properties and possibilities in medicine. Mycoses 1972; 17, 21.

KH Kim, TR Ramadhar, C Beemelmanns, S Cao, M Poulsen, CR Currie and J Clardy. Natalamycin A, an ansamycin from a termite-associated Streptomyces sp. Chem. Sci. 2014; 5, 4333-8.

AK Chauhan, DK Maheshwari, K Kim and VK Bajpai. Termitarium-inhabiting Bacillus endophyticus TSH42 and Bacillus cereus TSH77 colonizing Curcuma longa L.: Isolation, characterization, and evaluation of their biocontrol and plant-growth-promoting activities. Can. J. Microbiol. 2016; 62, 10.

M Wenzel, M Schonig, M Berchtold, P Kämpfer, H KÖnig. Aerobic and facultatively anaerobic cellulolytic bacteria from the gut of termite Zootermopsis angusticollis. J. App. Microbiol. 2002; 92, 32-40.

P Paejaroen, C Phaenark, S Chunchob and W Sawangproh. Morphological and physicochemical properties of termite mounds in the mixed deciduous forests of Thailand. Floresta e Ambient. 2021; 28, e20210040.

P Shelke, M Waghmode, R Mene, A Gunjal, N Patil, N Bhujbal, U Dhangar, S Jagtap and S Shinde. Morphological and elemental analysis of termite mound and ant nest in agriculturally prominent area. Nep. J. Environ. Sci. 2023; 11, 1-10.

J Paul and A Varma. Characterization of cellulose and hemicellulose degrading Bacillus sp. from termite infested soil. Curr. Sci. 1993; 64, 262-6.

S Sexana, J Bahadur and A Varma. Cellulose and hemi-cellulose degrading bacteria from termite gut and mound soils of India. Int. J. Micro. 1993; 33, 55-60.

HM Makonde, R Mwirichia, Z Osiemo, HI Boga and HP Klenk. 454 pyrosequencing-based assessment of bacterial diversity and community structure in termite guts, mounds and surrounding soils. SpringerPlus. 2015; 4, 471.

S Wasi, S Tabrez and M Ahmad. Use of Pseudomonas spp. for the bioremediation of environmental pollutants: A review. Environ. Monit. Assess. 2013; 185, 8147-55.

R Duponnois, M Kisa, K Assigbetse, Y Prin, J Thioulouse, M Issartel, P Moulin and M Lepage. Fluorescent pseudomonads occuring in Macrotermes subhyalinus mound structures decrease Cd toxicity and improve its accumulation in sorghum plants. Sci. Total Environ. 2006; 370, 391-400.

T Chouvenc, CA Efstathion, ML Elliott and NY Su. Extended disease resistance emerging from the faecal nest of a subterranean termite. Proc Biol Sci. 2013; 280, 20131885.

AK Chauhan, DK Maheshwari, K Kim and VK Bajpai. Termitarium-inhabiting Bacillus endophyticus TSH42 and Bacillus cereus TSH77 colonizing Curcuma longa L.: isolation, characterization, and evaluation of their biocontrol and plant-growth-promoting activities. Can J. Microbiol. 2016; 62, 880-92.

TH Do, TK Dao, HD Nguyen and NH Truong. Understanding the role of free-living bacteria in the gut of the lower termite Coptotermes gestroi based on metagenomic DNA analysis. Insects 2023; 14, 832.

IN Istina, H Widiastuti, B Joy and M Antralina. Phosphate-solubilizing microbe from saprists peat soil and their potency to enhance oil palm growth and P uptake. Proc. Food. Sci. 2015; 3, 426-35.

Downloads

Published

2024-05-30

How to Cite

Kunhachan, P. ., Sirithana, W. ., Komutiban, O. ., Limkhuansuwan, V. ., Menchai, P. ., Trakunjae, C. ., Lomthong, T. ., Ruchusatsawat, K. ., & Samaimai, S. . (2024). Selection of Potential Bacteria in Termite Nest and Gut for Sustainable Agriculture . Trends in Sciences, 21(8), 7794. https://doi.org/10.48048/tis.2024.7794