|Year : 2013 | Volume
| Issue : 2 | Page : 134-137
Isolation and identification of bacterial endophytes from pharmaceutical agarwood-producing Aquilaria species
Subhash J Bhore1, Jagadesan Preveena1, Kodi I Kandasamy2
1 Department of Biotechnology, Faculty of Applied Sciences, AIMST University, Bedong Semeling Road, Semeling 08100, Kedah, Malaysia
2 Tissue Culture Laboratory, Forest Research Institute Malaysia, 52109 Kepong, Selangor; Malaysian Biotechnology Corporation, Level 23, Menara Atlan, 161B, Jalan Ampany, 50450 Kuala Lumpur, Malaysia
|Date of Submission||25-Aug-2012|
|Date of Decision||08-Oct-2012|
|Date of Web Publication||15-Apr-2013|
Subhash J Bhore
Department of Biotechnology, Faculty of Applied Sciences, AIMST University, Bedong-Semeling Road, Semeling 08100, Kedah
Source of Support: Ministry of Agriculture and Agro-Based Industry (MoA), Malaysia,, Conflict of Interest: None
| Abstract|| |
Background: Resins and gums are used in traditional medicine and do have potential applications in pharmacy and medicine. Agarwood is the fragrant resinous wood, which is an important commodity from Aquilaria species and has been used as a sedative, analgesic, and digestive in traditional medicine. Endophytic bacteria are potentially important in producing pharmaceutical compounds found in the plants. Hence, it was important to understand which types of endophytic bacteria are associated with pharmaceutical agarwood-producing Aquilaria species. Objective: This study was undertaken to isolate and identify endophytic bacteria associated with agarwood-producing seven (7) Aquilaria species from Malaysia. Materials and Methods: Botanical samples of seven Aquilaria species were collected, and endophytic bacteria were isolated from surface-sterilized-tissue samples. The 16S rRNA gene fragments were amplified using PCR method, and endophytic bacterial isolates (EBIs) were identified based on 16S rRNA gene sequence similarity based method. Results: Culturable, 77 EBIs were analyzed, and results of 16S rRNA gene sequences analysis suggest that 18 different types of endophytic bacteria are associated with (seven) Aquilaria species. From 77 EBIs, majority (36.4%) of the isolates were of Bacillus pumilus. Conclusion: These findings indicate that agarwood-producing Aquilaria species are harboring 18 different types of culturable endophytic bacteria.
Keywords: 16S rRNA, biodiversity, endophytes, Malaysia, medicine, natural products, ribosomal DNA, traditional medicine
|How to cite this article:|
Bhore SJ, Preveena J, Kandasamy KI. Isolation and identification of bacterial endophytes from pharmaceutical agarwood-producing Aquilaria species. Phcog Res 2013;5:134-7
|How to cite this URL:|
Bhore SJ, Preveena J, Kandasamy KI. Isolation and identification of bacterial endophytes from pharmaceutical agarwood-producing Aquilaria species. Phcog Res [serial online] 2013 [cited 2021 Feb 28];5:134-7. Available from: http://www.phcogres.com/text.asp?2013/5/2/134/110545
| Introduction|| |
Naturally produced resins by plants has been used in traditional medicine around the world from the earliest times and have several potential applications in pharmacy and medicine.  Aquilaria species (family: Thymelaeaceae) are known to produce dark resinous heartwood, known as agarwood.  This agarwood is also known as Oud, Oodh, and Agar etc. Agarwood-producing Aquilaria species includes Aquilaria beccariana van Tiegh., A. crassna Pierre, , A. hirta Ridl., A. malaccensis Lamk.,  A. microcarpa Baill., , A. sinensis (Lour) Gilg,  and A. subintegra Ding Hou. Currently, there is a huge demand for agarwood, and Indonesia, Malaysia, Thailand, and Vietnam are the major producers of agarwood.
As stated by Lardos et al. (2011), agarwood is known to have many pharmacological functions that include analgesic, anti-inflammatory, anti-microbial, immunomodulatory, and wound healing properties.  Agarwood is also used as a digestive in traditional medicine, and its medico-pharmacological analysis using model mice indicated the laxative effect. , Furthermore, the essential oil obtained from agarwood is also known to have anti-microbial properties. 
Endophytes are microorganisms that live inside plants (inter or intra cellular in nature) without causing any plant disease. Although its true functions in the plants are poorly understood, reports suggest that bacterial endophytes can produce bioactive compounds found in their host  and have potential in providing new drugs,  plant hormones,  and novel natural products.  As a part of a broad study to explore bacterial endophytes for its various potential applications, research work on isolation, identification, and characterization of bacterial endophytes was initiated at AIMST University. The isolated and identified bacterial endophytes of the economically and pharmaceutically important agarwood-producing (seven) Aquilaria species have been reported in this paper.
| Materials and Methods|| |
Nutrient medium, bacto-agar powder, and agarose-gel powder were purchased from Sisco Research Laboratories Pvt. Ltd. MEGAquick-spin TM PCR, and agarose-gel DNA Extraction System was procured from NHK Bioscience Solutions Sdn. Bhd. PCR components were purchased from Fermentas and SBS Genetech, and DNA markers were supplied by Dongsheng Biotechnology Pte. Ltd., China. Forward [Bak11W-F; 5'- AGT TTG ATC MTG GCT CAG-3'] and reverse [Bak-R; 5'- GGA CTA CHA GGG TAT CTA AT-3'] primers used in the study were supplied by First Base and SBS Genetech, and all other chemicals were procured from the Sigma-Aldrich Corporation (St. Louis, MO), USA.
Stem and leaf (along with their petiole) samples of A. beccariana, A. crassna, A. hirta, A. malaccensis, A. microcarpa, A. sinensis, and A. subintegra were collected. All seven Aquilaria species in sampling were from the plants collection of Forest Research Institute of Malaysia (FRIM), Malaysia.
Surface-sterilization of plant material samples
The surface-sterilization of the collected botanical samples was carried out as described elsewhere.  The surface sterilized stem, leaf, and petiole tissues were used in isolation of EBIs.
Isolation and identification of bacterial endophytes
The isolation of EBIs, amplification of 16S rRNA gene fragments, and identification of the EBIs was carried out as described by Bhore et al. 
| Results|| |
As a result of botanical samples' incubation, culturable bacterial endophytes were able to grow on nutrient agar. Seventy-seven (77) EBIs were isolated from the seven Aquilaria species, and their pure cultures were examined. From the 77 EBIs, PCR-amplified 16S rRNA gene fragments were sequenced, and all isolates were identified as a result of nucleotide blast (megablast) hits analysis.
Seventy-seven EBI's annotated 16S rRNA gene fragments nucleotide sequences have been submitted to the GenBank/DDBJ/EMBL under accession numbers: JF819666-JF819685, and JF938917-JF938973.
Analysis of identified 77 EBIs revealed that agarwood-producing 7 Aquilaria species are harboring 18 different types of bacterial endophytes. [Figure 1] show the total number of isolates of identified 18 types of bacterial endophytes, and the identified bacterial endophytes and their respective host (Aquilaria) species are depicted in [Table 1].
|Figure 1: Eighteen (18) types of bacterial endophytes found in agarwood-producing Aquilaria species and total number of bacterial endophytes isolates representing each type.|
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|Table 1: Seven (7) agarwood-producing Aquilaria species and their bacterial endophytes as revealed by 16S rRNA gene sequence similarity based method of bacterial identification|
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| Discussion|| |
Almost every plant on the earth hosts endophytic bacteria that could serve as potential source of novel natural products, which are of a great potential not only in medicine but also in various other sectors of the biotechnology industry. , However, endophytes from medicinally important plants are of a great interest, especially in understanding their potential medicinal properties and to explore their potential applications. , In this study, we isolated and identified 77 strains of bacterial endophytes from seven agarwood-producing Aquilaria species. Likewise, bacterial endophytes have been reported from various medicinal plants; for examples, Gynura procumbens, Piper nigrum, Strobilanthes crispa, and Vernonia amygdalina. ,, However, this is the first study to elucidate diverse types of bacterial endophytes in (seven) agarwood-producing Aquilaria species.
The 16S rRNA gene sequence of each bacterium is species-specific, and hence can be used for accurate bacterial identification.  Thus, we amplified the 16S rRNA gene for rapid and precise identification of the isolated EBIs. The 16S rRNA gene fragment sequences comparison from the 77 isolated strains with the sequences from nucleotide sequence database of GenBank/DDBJ/EMBL using blast revealed the identity of these isolates. The 16S rRNA gene sequence similarity % was >95%, except for one isolate, where the similarity % was only 82%. This isolate (from A. subintegra) was putatively identified as Pantoea agglomerans (Accession no: JF819683) and need further verification.
Though 9 species of the bacterial endophytes are represented by only one isolate, it cannot be inferred that they are respective Aquilaria species-specific, because sample numbers used in the study were limited (in number) and samples were from only one plant of each Aquilaria species. The seasonal fluctuation of the endophytes has been reported in other plant species; , hence, it is possible that various other types of bacterial endophytes might be also associated with agarwood-producing Aquilaria species. In addition, it should be noted that soil type in which plants are growing can influence the diversity of bacterial endophytes in plants.  Therefore, if Aquilaria species are collected from other locations, then some other types of bacterial endophytes could also be detected.
Bacterial endophytes can produce novel natural products found in their host plant;  and therefore, bacterial endophytes are potential sources of the novel natural products including novel antibiotics. The anti-microbial (anti-bacterial, anti-fungal, and anti-viral) activities of some bacterial endophytes has also been reported by other researchers. ,,,,,, Similarly, it has been reported that the endophytic fungi associated with agarwood have potential anti-microbial and anti-tumor activity.  Therefore, further research is needed in order to explore the potential applications of the isolated bacterial endophytes. Furthermore, the in-depth understanding of symbiotic association between Aquilaria species and their bacterial (and fungal) endophytes could be helpful in the protection of threatened Aquilaria' species. 
On the basis of the results obtained, it could be concluded that agarwood-producing Aquilaria species are harboring diverse 18 types of culturable bacterial endophytes. However, the benefits of these 18 bacterial endophytes to Aquilaria species are not clearly understood. We hypothesize that isolated bacterial endophytes might be useful to its respective host Aquilaria species and might be producing economically and pharmaceutically important bioactive compounds. Nonetheless, our research findings could be useful, as a foundation for further research on both the agarwood-producing Aquilaria species, as well as its endophytic bacteria.
| References|| |
|1.||Lardos A, Prieto-Garcia J, Heinrich M. Resins and gums in historical iatrosophia texts from Cyprus-A botanical and medico-pharmacological approach. Front Pharmacol 2011;2:32. |
|2.||Kumeta Y, Ito M. Genomic organization of δ-guaiene synthase genes in Aquilaria crassna and its possible use for the identification of Aquilaria species. J Nat Med 2011;65:508-13. |
|3.||Eurlings MC, van Beek HH, Gravendeel B. Polymorphic microsatellites for forensic identification of agarwood (Aquilaria crassna). Forensic Sci Int 2010;197:30-4. |
|4.||Gunasekera SP, Kinghorn AD, Cordell GA, Farnsworth NR. Plant anticancer agents. XIX constituents of Aquilaria malaccensis. J Nat Prod 1981;44:569-72. |
|5.||Kenmotsu Y, Yamamura Y, Ogita S, Katoh Y, Kurosaki F. Transcriptional activation of putative calmodulin genes am-cam-1 and am-cam-2 from Aquilaria microcarpa, in response to external stimuli. Biol Pharm Bull 2010;33:1911-4. |
|6.||Kenmotsu Y, Ogita S, Katoh Y, Yamamura Y, Takao Y, Tatsuo Y, et al. Methyl jasmonate-induced enhancement of expression activity of Am-FaPS-1, a putative farnesyl diphosphate synthase gene from Aquilaria microcarpa. J Nat Med 2011;65:194-7. |
|7.||Chen H, Yang Y, Xue J, Wei J, Zhang Z. Comparison of compositions and antimicrobial activities of essential oils from chemically stimulated agarwood, wild agarwood and healthy Aquilaria sinensis (Lour.) gilg trees. Molecules 2011;16:4884-96. |
|8.||Kakino M, Izuta H, Ito T, Tsuruma K, Araki Y, Shimazawa M, et al. Agarwood induced laxative effects via acetylcholine receptors on loperamide-induced constipation in mice. Biosci Biotechnol Biochem 2010;74:1550-5. |
|9.||Kakino M, Tazawa S, Maruyama H, Tsuruma K, Araki Y, Shimazawa M, et al. Laxative effects of agarwood on low-fiber diet-induced constipation in rats. BMC Complement Altern Med 2010;10:68. |
|10.||Mehanni MM, Safwat MSA. Endophytes of medicinal plants. Acta Hort (ISHS) 2010;854:31-9. |
|11.||Strobel G, Daisy B. Bioprospecting for microbial endophytes and their natural products. Microbiol Mol Biol Rev 2003;67:491-502. |
|12.||Bhore SJ, Ravichantar N, Loh CY. Screening of endophytic bacteria isolated from leaves of Sambung Nyawa [Gynura procumbens (Lour.) Merr.] for cytokinin-like compounds. Bioinformation 2010;5:191-7. |
|13.||Guo B, Wang Y, Sun X, Tang K. Bioactive natural products from endophytes: A review. Prikl Biokhim Mikrobiol 2008;44:153-8. |
|14.||Strobel GA. Rainforest endophytes and bioactive products. Crit Rev Biotechnol 2002;22:315-33. |
|15.||Qin S, Xing K, Jiang JH, Xu LH, Li WJ. Biodiversity, bioactive natural products and biotechnological potential of plant-associated endophytic actinobacteria. Appl Microbiol Biotechnol 2011;89:457-73. |
|16.||Aravind R, Kumar A, Eapen SJ, Ramana KV. Endophytic bacterial flora in root and stem tissues of black pepper (Piper nigrum L.) genotype: Isolation, identification and evaluation against Phytophthora capsici. Lett Appl Microbiol 2009;48:58-64. |
|17.||Bhore SJ, Tiong OK. Bacterial endophytes of therapeutically important Strobilanthes crispa (L.) Bremek and Vernonia amygdalina Del. J Pharm Biomed Sci 2012;14:1-3. |
|18.||Clarridge JE. Impact of 16S rRNA gene sequence analysis for identification of bacteria on clinical microbiology and infectious diseases. Clin Microbiol Rev 2004;17:840-62. |
|19.||Gao XX, Zhou H, Xu DY, Yu CH, Chen YQ, Qu LH. High diversity of endophytic fungi from the pharmaceutical plant, Heterosmilax japonica Kunth revealed by cultivation-independent approach. FEMS Microbiol Lett 2005;249:255-66. |
|20.||Forchetti G, Masciarelli O, Izaguirre MJ, Alemano S, Alvarez D, Abdala G. Endophytic bacteria improve seedling growth of sunflower under water stress, produce salicylic acid, and inhibit growth of pathogenic fungi. Curr Microbiol 2010;61:485-93. |
|21.||Hardoim PR, Hardoim CC, van Overbeek LS, van Elsas JD. Dynamics of seed-borne rice endophytes on early plant growth stages. PLoS One 2012;7:e30438. |
|22.||Ding L, Maier A, Fiebig HH, Lin WH, Hertweck C. A family of multicyclic indolosesquiterpenes from a bacterial endophyte. Org Biomol Chem 2011;9:4029-31. |
|23.||Ding L, Münch J, Goerls H, Maier A, Fiebig HH, Lin WH, et al. Xiamycin, a pentacyclic indolosesquiterpene with selective anti-HIV activity from a bacterial mangrove endophyte. Bioorg Med Chem Lett 2010;20:6685-7. |
|24.||Castillo UF, Strobel GA, Ford EJ, Hess WM, Porter H, Jensen JB, et al. Munumbicins, wide-spectrum antibiotics produced by Streptomyces NRRL 30562, endophytic on Kennedia nigriscans. Microbiology 2002;148:2675-85. |
|25.||Castillo U, Harper JK, Strobel GA, Sears J, Alesi K, Ford E, et al. Kakadumycins, novel antibiotics from Streptomyces sp NRRL 30566, an endophyte of Grevillea pteridifolia. FEMS Microbiol Lett 2003;224:183-90. |
|26.||Castillo UF, Strobel GA, Mullenberg K, Condron MM, Teplow DB, Folgiano V, et al. Munumbicins E-4 and E-5: Novel broad-spectrum antibiotics from Streptomyces NRRL 3052. FEMS Microbiol Lett 2006;255:296-300. |
|27.||Harrison L, Teplow DB, Rinaldi M, Strobel G. Pseudomycins, a family of novel peptides from Pseudomonas syringae possessing broad-spectrum antifungal activity. J Gen Microbiol 1991;137:2857-65. |
|28.||Miller CM, Miller RV, Garton-Kenny D, Redgrave B, Sears J, Condron MM, et al. Ecomycins, unique antimycotics from Pseudomonas viridiflava. J Appl Microbiol 1998;84:937-44. |
|29.||Cui JL, Guo SX, Xiao PG. Antitumor and antimicrobial activities of endophytic fungi from medicinal parts of Aquilaria sinensis. J Zhejiang Univ Sci B 2011;12:385-92. |
|30.||CITES. Convention on international trade in endangered species of wild fauna and flora-amendments to appendices I and II of CITES, thirteenth meeting of the conference of the parties. Bangkok, Thailand 3-14 Oct 2004. |
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