- Research article
- Open Access
Induction of hairy roots by various strains of Agrobacterium rhizogenes in different types of Capsicum species explants
© Md Setamam et al.; licensee BioMed Central Ltd. 2014
Received: 25 July 2013
Accepted: 19 June 2014
Published: 30 June 2014
Capsicum annuum and Capsicum frutescens, also known as “chilies”, belong to the Solanaceae family and have tremendous beneficial properties. The application of hairy root culture may become an alternative method for future development of these species by adding value, such as by increasing secondary metabolites and improving genetic and biochemical stability compared with normal Capsicum plants. Therefore, in this research, different types of explants of both species were infected with various Agrobacterium rhizogenes strains to provide more information about the morphology and induction efficiency of hairy roots. After 2 weeks of in vitro seed germination, young seedling explants were cut into three segments; the cotyledon, hypocotyl, and radical. Then, the explants were co-cultured with four isolated A. rhizogenes strains in Murashige & Skoog culture media (MS) containing decreasing carbenicillin disodium concentrations for one month.
In this experiment, thick and short hairy roots were induced at all induction sites of C. annuum while thin, elongated hairy roots appeared mostly at wound sites of C. frutescens. Overall, the hairy root induction percentages of C. frutescens were higher compared with C. annuum. Hairy root initiation was observed earliest using radicles (1st week), followed by cotyledons (2nd week), and hypocotyls (3rd week). Cotyledon explants of both species had the highest induction frequency with all strains compared with the other explants types. Strains ATCC 13333 and ATCC 15834 were the most favourable for C. frutescens while ATCC 43056 and ATCC 43057 were the most favourable for C. annuum. The interactions between the different explants and strains showed significant differences with p-values < 0.0001 in both Capsicum species.
Both Capsicum species were amenable to A. rhizogenes infection and hairy root induction is recommended for use as an alternative explants in future plant-based studies.
Capsicum annuum and Capsicum frutescens also known as “chilies” belong to the Solanaceae family . These species have tremendous economic value as vegetables crops and medicinal plants in numerous countries. Capsicum species have multiple usages as medicinal drugs for various diseases because of their analgesic, anti-inflammatory, antioxidant and anticancer properties [2, 3]. These beneficial properties of Capsicum species usually come from their major secondary metabolites such as capsaicinoids, capsinoids, quercetin and luteolin [4–7]. Currently, one of the developing trends is hairy root culture techniques that enable high production of these secondary metabolites for extensive industrial applications [8–10].
In recent years, hairy root culture has been chosen as an alternative method for the development of crops and medicinal plants such as Capsicum species because of its many advantages [11, 12]. Hairy root cultures have been proven to increase secondary metabolite levels in various plants including Capsicum species for industrial purposes [8, 13, 14]. Another advantage is the improvement of the plant system with better genetic and biochemical stability compared with normal plants [15–17].
One of the main factors that contribute to achieving hairy root induction is the type of explant used. Several studies on hairy roots in Capsicum species have used various explants such as hypocotyls , cotyledons , leaves  and mesophyll protoplasts . In this research, different types of explants of both C. annuum and C. frutescens were infected with various A. rhizogenes strains. The objective of this research was to provide information on the establishment of hairy roots for both C. annuum and C. frutescens in term of morphology and induction efficiency.
Results and discussion
Effect on morphology of hairy root induction
In this experiment, young seedlings of C. annuum and C. frutescens germinated in vitro were used as study plants. Three types of explants—cotyledon, hypocotyl, and radical—from each Capsicum species were co-cultured with four isolated A. rhizogenes wild type strains (ATCC 15834, ATCC 43056, ATCC 13333, and ATCC 43057). After 1 month, hairy roots were induced by all A. rhizogenes strains for all explants types in both Capsicum species.
Wound sites are a common location for hairy root induction since they serve as a genetic transfer point for A. rhizogenes[24, 25]. In hypocotyl explants of both species, hairy roots were induced at the wound site except for hypocotyls of C. annuum with ATCC 43056 and ATCC 43057 (Figure 2). However, in radicle explants of both species, hairy roots were only induced far from the wound sites with the exception of C. annum with ATCC 13333 and ATCC 43057 (Figure 2). Additionally, hairy roots were induced at the wound sites of C. frutescens cotyledon explants by all strains (Figure 3).
The formation of callus in plant cultures is usually caused by additional plant hormones present in the medium. However, in hairy root cultures, the active expression of rol genes due to the presence vir genes on the A. rhizogenes Ri-plasmid may cause extreme synthesis of endogenous auxin and cytokinin in the host cells . This may lead to the production of both hairy roots and callus simultaneously . In our experiment, C. annuum was able to produce both callus and hairy roots at the same time, in contrast to C. frutescens. Both hypocotyl and radicle explants of C. annuum with strains ATCC 43056 and ATCC 43057 (Figure 2) were able to establish whitish, soft-textured callus at the wound sites. C. annuum treated with ATCC 15834 and ATCC 13333 (Figure 3) also produced callus at the wound sites of cotyledon explants.
Direct co-culturing with A. rhizogenes strains can result in bacteria residing in the plant cells [28, 29]. However, active infection can cause cells to rupture and cell death known as necrosis. In in vitro cultures, the remaining necrotic cells may secrete phenolic compounds and fungal avirulence proteins that are highly toxic . The presence of necrosis and antibiotics also may affect hairy root induction and contamination in samples [31, 32].
Effect on hairy root induction
In this experiment, three parameters were used to estimate the hairy root induction efficiencies of both C. annuum and C. frutescens. These parameters were hairy root induction percentage per total explants, hairy root initiation days per total explants and hairy root induction frequency per single explant.
Overall, the results showed that the hairy root induction percentages of C. frutescens were higher compared with C. annuum. Hypocotyl explants for both Capsicum species showed induction percentages of 55–75% with all strains. The mean percentages for C. frutescens radicle and cotyledon explants with all strain types were the highest at 100% hairy root induction.
Hairy roots were induced faster from radicle explants than cotyledon explants in both species. This is because of the ability of the radicle to initiate pericycle cells around the root for greater hairy root establishment. The cotyledon explants in both species had slower initiation times because the meristematic cells specifically accentuate the formation of new leaves and axillary buds .
The hypocotyl explants of C. annuum and C. frutescens in all strain treatments had the highest hairy roots initiation times (Figures 6 and 7), which may have been due to lower cell division activities. These inactive cells may require more time to regulate the cell toward decisive factors such plant hormones, turgor pressures and cyclic-dependent kinases (CDKs) for cell expansion and differentiation [36, 37]. Therefore, hairy root initiation was deferred up to the third week.
Hairy root induction frequency per single explant (mean ± standard deviation) in both Capsicum spp. after 1 month
List of species
2.15 ± 0.90
2.45 ± 0.63
1.40 ± 0.47
2.75 ± 0.61
10.32 ± 0.96
13.20 ± 0.78
12.05 ± 0.61
13.35 ± 0.58
13.50 ± 0.49
14.05 ± 0.46
12.80 ± 0.79
13.8 ± 0.96
1.55 ± 0.68
1.15 ± 0.96
1.70 ± 0.53
1.45 ± 0.76
7.50 ± 0.69
6.75 ± 0.47
7.75 ± 0.85
7.00 ± 0.50
10.30 ± 0.82
7.70 ± 0.93
15.75 ± 0.67
9.45 ± 0.51
Two-way ANOVA (α = 0.05) for hairy root induction frequency per single explant of Capsicum annum after 1 month
Source of variation
Sum of squares (SS)
Degree of freedom (DF)
Mean square (MS)
Significant level (p-value)
A: Types of explants
B: Types of strains
A × B
Two-way ANOVA (α = 0.05) for hairy root induction frequency per single explant of Capsicum frutescens after 1 month
Source of variation
Sum of squares (SS)
Degree of freedom (DF)
Mean square (MS)
Significant level (p-value)
A: Types of explants
B: Types of strains
A × B
In this study, both C. annuum and C. frutescens were amenable to A. rhizogenes infection. Both species showed positive responses, yielding hairy roots without the presence of exogenous plant hormones. These hairy roots exhibited whitish, fungus needle-like structures and plagiotropic growth similar to those in other plant studies. However, morphological variations were still seen between the two species in terms of length, thickness and the site of hairy root induction. Variations in species, strain and explant type led to different hairy root induction efficiencies. C. annuum was more amenable to ATCC 43056 and ATCC 43057 compared with ATCC 15834 and ATCC 13333, while C. frutescens was more amenable to ATCC 15834 and ATCC 13333 compared with ATCC 43056 and ATCC 43057. Despite the antagonistic response demonstrated by these two species, the various explant types showed similar results. In ascending order, the most suitable explant types for maximum hairy root induction were cotyledons, radicles and hypocotyls. Overall, our results suggest that hairy root induction could be used for alternative explants in future plant-based studies such as plant regeneration, somatic embryogenesis, molecular analysis or phytochemical studies.
Seed sterilization and in vitro seed germination
Seeds of C. annuum var. cayenne pepper and C. frutescens var. bird’s eye chili were obtained from a local supplier. The seed edges were cut approximately 1 mm before soaking them in sterilised water for a day. Then, the seeds were washed under tap water for 5 minutes before the seed surfaces were sterilised in 15% sodium hypochlorite (NaClO) with two drops of Tween 80 for 10 minutes. The seeds were then rinsed twice with sterile water before being sterilised with 70% ethanol for 3 minutes. Finally, the seeds were rinsed again several times with sterile water. Ten sterilised seeds were cultured in individual Petri dishes that contained half-strength MS solid media. The seeds were left to germinate under a 16/8 h (light/dark) photoperiod for two weeks.
Culture medium preparation
Full-strength MS medium was prepared by adding 4.4 g of MS powder, 1 g myo-inositol, and 30 g sucrose to 1 L of sterile distilled water. The solution pH was adjusted to approximately 5.7 to 6.0 using hydrochloric acid (HCl) or sodium hydroxide (NaOH). About 4 g gelrite was added to the medium before autoclaving at 121°C and 15 psi for 20 minutes. Half-strength MS solid medium was prepared similarly but the MS powder, myo-inositol and sucrose amounts were reduced by half.
Preparation of sterile explants and pre-culturing
After 2 weeks of in vitro seed germination, 20 young seedling explants were cut into three segments (cotyledon, hypocotyl, and radicle) about 7–10 mm long. The cut segments were pre-cultured in Petri dishes containing half-strength MS solid medium for 1 day.
Bacterial strains and cultures
Four wild A. rhizogenes strains (ATCC 15834, ATCC 43056, ATCC 13333 and ATCC 43057) were used for hairy root induction. The isolated strains were cultured in 0.01 L nutrient broth (NB) medium. The NB culture medium was prepared by weighing out 8 g/L NB powder and transferring it into 1 L of sterile water. Then, the solution was autoclaved and 0.01Lwas transferred into individual universal bottles. After three days, 10 μL of each isolated strain was inoculated into the NB cultures for three more days at a temperature of 26°C. The bacterial cultures with an optical density (OD) of 500–600 nm were used for co-culture after being shaken at 300 rpm for an hour. For culture preservation, 1mLeach of the main cultures were kept in 0.009 L nutrient broth at 10−1 dilution at a temperature of 26°C for not more than 1 week. The unused working cultures were stored in 20% glycerol and kept frozen in −20°C freezer.
Co-culture and hairy root culture establishment
Each explant was immersed in 10 μL of the isolated strains in Petri dishes containing half-strength MS solid medium for a day. Then, the co-cultured explants were decontaminated using washing medium containing MS liquid medium with carbenicillin disodium (1 g/L) for 2 hours. The co-cultured explants were dried with sterile filter paper to remove excess bacteria before culture on full-strength MS solid medium containing 0.5 g/L carbenicillin disodium. The explants were sub-cultured each week on MS solid medium containing decreasing carbenicillin disodium concentrations (0.2, 0.1, 0.05 mg/L) for 1 month. Explants without A. rhizogenes strain treatment were used as controls. The experiments were performed with 20 replications per each treatment (n = 20).
The data were collected after one month and analysed using a two-way analysis of variance (ANOVA) with SAS 9.0 and standard deviation mean values expressed as mean ± SD.
The authors are deeply indebted to the Faculty of Applied Science of University Technology Mara, for their research facilities and the Faculty of Science and Technology, Academic Centre of Bioscience and Biotechnology of Universiti Kebangsaan Malaysia for providing Agrobacterium rhizogenes strains. This research study was funded by the Research Management Institute (UiTM) under FRGS/2/2010/SG/UiTM/03/22.
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