The Scientific World JournalVolume 2012 (2012), Article ID 359413, 8 pagesdoi:10.1100/2012/359413

Research Article

Plant Regeneration and Cellular Behaviour Studies inCelosia cristata Grown In Vivo and In Vitro

Rosna Mat Taha and Sharifah Nurashikin Wafa

Institute of Biological Sciences, Faculty of Science, University of Malaya, 50603 Kuala Lumpur, Malaysia

Received 19 October 2011; Accepted 21 November 2011

Academic Editors: S. Jogloy and I. V. Sharakhov

Copyright © 2012 Rosna Mat Taha and Sharifah Nurashikin Wafa. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Tissue culture studies of Celosia cristata were established from various explants and the effects of various hormones on morphogenesis of this species were examined. It was found that complete plant regeneration occurred at highest percentage on MS medium supplemented with 2.0 mg/L NAA and 1.5 mg/L BAP, with the best response showed by shoot explants. In vitro flowering was observed on MS basal medium after six weeks. The occurrence of somaclonal variation and changes in cellular behavior from in vivo and in vitro grown plants were investigated through cytological studies and image analysis. It was observed that Mitotic Index (MI), mean chromosome numbers, and mean nuclear to cell area ratio of in vitro root meristem cells were slightly higher compared to in vivo values. However, in vitro plants produced lower mean cell areas but higher nuclear areas when compared to in vivo plants. Thus, no occurrence of somaclonal variation was detected, and this was supported by morphological features of the in vitro plants.

1. Introduction

Celosia cristata is native to South America and now is widespread in Asia, especially, Malaysia. It is now becoming more important as ornamental plant and often used for landscaping and roadside plants due to the various attractive colours of the flowers. Due to its high demands, in vitro cloning has been introduced for this species. In vitro cloning has many advantages. Specifically, propagation in vitro is more rapid than in vivo, with the possibility of producing disease-free plants using little starting materials. In addition, through the use of in vitro methods, the effect of the seasons can be eliminated and year-round production can be achieved, or a new cultivar can be made commercially available more quickly [1]. Celosia cristata was found to be able to produce purplish or reddish pigment in tissue culture system and when analysed was found to contain cyanidin, a kind of anthocyanin. This species was also capable of producing in vitro flowers after only 6 weeks in culture [2]. Because of these abilities, and the popularity of this plant, Celosia cristata was cultured to study the morphogenesis in vitro and the effect of various hormones on plant regeneration in attempt to achieve efficient mass propagation of this species. Cellular behavior studies, such as mean cell and nuclear areas, Mitotic index (MI) and ploidy level are also very important in plants, for example, for differentiating between embryogenic and nonembryogenic calli [3]. In addition, the rate of cell division correlates with growth rates [4]. Some cellular investigations have revealed the occurrence of somaclonal variation, even at an early stage. Hence, in the current work, cellular behaviours, such as Mitotic index (MI), chromosome counts, mean cell, and nuclear areas and their ratios were also investigated, in regenerants and intact plants, to determine if somaclonal variations occurred during the culture protocols. Although in vitro flowering of this species has been previously reported [2], changes in cellular behaviour during in vitro flowering have never been reported before. Therefore, the objectives of the present work are to establish efficient regeneration system for this species, to compare cellular behaviours in root meristem cells of in vivo and in vitro grown plants, to detect whether any somaclonal variation had occurred during tissue culture protocols and finally, to observe the changes in cellular behavior during in vitro flowering.

2. Materials and Methods

2.1. The Effects of Various Hormones on Tissue Culture of Celosia cristata

Celosia cristata seeds were obtained from nurseries around Kuala Lumpur and were sterilised in standard tissue culture protocols [5, 6]. Seeds were treated with 100%, 70%, 50%, 20%, and 10% (v/v) commercial bleach (chlorox) for 3-4 min at each concentration. At 100% (v/v) concentrations of chlorox, 3 drops of Tween-20 were added, in order to facilitate sterilisation. Surface sterilisation of the seeds was accomplished by submersion in 70% (v/v) ethanol, followed by rinsing 3 times with sterile distilled water under aseptic conditions using a laminar flow chamber. Subsequently, seeds were cultured on MS basal medium. One-month-old aseptic seedlings were used as explant sources. Leaves (0.5 × 0.5 cm), stems (0.5 cm), root segments (0.5 cm), and shoot tips (1.0 cm) were excised from aseptic seedlings to initiate cultures. MS medium supplemented with various hormones, such as benzyl aminopurine (BAP), naphthalene acetic acid (NAA), indole acetic acid (IAA), kinetin and zeatin were used at different concentrations with different combinations. Throughout the experiment, the culture media used was Murashige and Skoog (MS) media supplemented with 3% sucrose and 0.8% agar. The pH of the media was adjusted to 5.8 ± 0.1 before autoclaving at 121°C for 15 min. Twenty replicates were used for each experiment. Cultures were maintained at 25 ± 1°C with 16 h light and 8 h dark, except for in vitro flowering experiments, where cultures were subjected to 12 h light and 12 h dark. Regenerants were acclimatised in garden soil as previously described [7]. Full-grown plantlets were transferred to flower pots containing a mixture of black soil and sand at a ratio of 3 : 1 and covered with transparent polyethylene bags to prevent plant dehydration. Plantlets were kept in the culture room at 25 ± 1°C under 16-hour light and 8-hour dark. After 2 weeks, well-grown and healthy plantlets were transferred to a greenhouse.

2.2. Cytological Investigations on Roots Grown In Vivo versus In Vitro

One hundred (100) seeds of Celosia cristata were germinated on moist cotton wool in Petri dishes for 2 weeks, and also on MS basal medium (for comparison), to obtain standard growth curves for the primary roots. The primary root length of the population was measured once per day at a fixed time and the mean root length of each sample was recorded and was plotted against time. Roots were then cut and soaked in alcohol and acetic acid (3 : 1) overnight for preservation. Based on the standard curve, the mean root length of the sample displaying the highest growth rate before the emergence of secondary roots was determined. For subsequent experiments, the mean root length of the sample was chosen, fixed, and made into permanent slides. Permanent slides were prepared by soaking primary roots in 5 M Hydrochloric acid (HCl) and stained with Feulgen. Subsequently, roots were transferred onto slides, mounted with 45% (v/v) acetic acid, sprayed with freeze spray, and rinsed. Cover slides were then mounted on the slides by DPX (Di-N-Butyle Phthalate in Xylene). Primary roots produced in vitro were also made into permanent slides and analysed for cellular behaviours, such as Mitotic index, chromosome count, mean nuclear and cell areas, and their ratios. For measurement of mean cell and nuclear areas, standard protocols using an image analyser were followed. The experiments were conducted using a light microscope (Zeiss Axioscope, Germany) connected to a Sony video camera, images from 500 interphase cells were captured and transferred to a host computer for image analyzing. The system was supported by two macros programs, that are, DNA for calculation of DNA C value and VIDAS for cell and nuclear area measurement (Kontron Electronic, Germany). The DNA C value was determined by calibrating the integrated optical density with reference nuclei [3].

3. Results and Discussion

In general, callus growth in Celosia cristata was observed after as early as 7–10 days in culture. Stem, leaf, shoot, and even root explants were able to produce reddish purple calli on MS medium containing 0.5–2.0 mg/L BAP and 0.5 mg/L NAA. When shoot explants were cultured on MS basal medium (Figure 1(a)) and MS medium supplemented with 2.0 mg/L NAA, 1.0 mg/L NAA + 0.5 mg/L BAP, or 1.5 mg/L NAA + 2.0 mg/L BAP, or 1.0 mg/L IAA, 1.0 mg/L Kinetin + 1.0 mg/L Zeatin; 100% direct regeneration of C. cristata was obtained in 35 days. In addition, direct regeneration of C. cristata was achieved in 20 days when shoot explants were cultured on MS medium supplemented with 2.0 mg/L NAA + 0.5 mg/L BAP, or 2.0 mg/L NAA + 1.5 mg/L BAP. Roots were obtained on most of the media tested; for example, MS supplemented with 0.5–2.0 mg/L NAA and 0.5–2.0 mg/L BAP, or MS basal medium. In vitro flowering (Figure 1(b)) was observed when shoot explants were cultured on MS basal media after being exposed to 12 h light and 12 h dark (Data not shown). Some plantlets with abnormal stems (swollen) were observed when shoot tips were cultured on MS supplemented with 0.5–2.0 mg/L BAP, applied singly. The responses of various explants to different concentrations of hormones are shown in Table 1.

Table 1: Effects of different hormones on the tissue culture of Celosia cristata initiated from various explants maintained at 25 ± 1°C with 16 h light and 8 h dark.

Hormone concentration (mg/l)
Explants
Callus (%)
Direct regeneration (%)
Observations

NAA
BAP
IAA
KIN
ZEA

—
—
—
—
—
Leaves
—
—
—

Stem
—
—
—

Root
—
—
—

Shoot
—
100
Multiple shoots and roots after 35 days

—
0.5
—
—
—
Leaves
25
—
White callus and root

Stem
50
—
Orange callus

Root
—
—
—

Shoot
—
90
Multiple shoots, abnormal stem

—
1.0
—
—
—
Leaves
65
—
White callus and later dormant

Stem
100
—
Red, black, and white callus

Root
—
—
—

Shoot
—
80
multiple shoots, abnormal stem

—
1.5
—
—
—
Leaves
65
—
White callus and later dormant

Stem
100
—
White, green, and black callus

Root
50
—
Callus

Shoot
—
100
Multiple shoots, abnormal stem

—
2.0
—
—
—
Leaves
40
—
White callus and later dormant

Stem
100
10
Orange callus and shoot, necrosis

Root
65
—
Callus

Shoot
—
100
Multiple shoots, abnormal stem

0.5
—
—
—
—
Leaves
95
—
Yellow callus and root

Stem
100
—
White callus, necrosis

Root
55
—
Callus

Shoot
—
100
Multiple shoots

1.0
—
—
—
—
Leaves
20
—
White callus and roots

Stem
30
—
Callus and roots

Root
—
—
Roots

Shoot
—
85
Direct regeneration after 35 days

1.5
—
—
—
—
Leaves
10
—
Callus and roots

Stem
80
—
Callus and roots

Root
30
—
Roots

Shoot
—
50
Multiple shoots and roots

2.0
—
—
—
—
Leaves
5
—
Callus and roots

Stem
15
—
Callus and roots

Root
5
—
Roots

Shoot
—
100
Direct regeneration after 35 days

0.5
0.5
—
—
—
Leaves
40
—
White callus and roots

Stem
100
—
Red, yellow, and green callus, roots

Root
30
—
Callus

Shoot
—
90
Direct regeneration after 30 days

0.5
1.0
—
—
—
Leaves
70
—
Yellow and red callus

Stem
80
—
Yellow and red callus

Root
55
—
Callus

Shoot
—
100
Multiple shoots and roots

0.5
1.5
—
—
—
Leaves
85
—
White callus

Stem
95
—
Orange and red callus

Root
65
—
Callus and roots

Shoot
—
100
Multiple shoots and roots

0.5
2.0
—
—
—
Leaves
100
—
White, red, green, and black callus

Stem
100
—
Yellow and red callus, roots

Root
75
—
Roots

Shoot
—
90
Direct regeneration after 30 days

1.0
0.5
—
—
—
Leaves
35
—
White callus and roots

Stem
55
—
Roots

Root
5
—
Roots

Shoot
—
100
Direct regeneration after 35 days

1.0
1.0
—
—
—
Leaves
—
—
—

Stem
—
—
—

Root
—
—
—

Shoot
—
—
—

1.0
1.5
—
—
—
Leaves
65
—
White and black callus, roots

Stem
80
—
Callus and roots

Root
30
—
Roots

Shoot
—
50
Multiple shoots and roots

1.0
2.0
—
—
—
Leaves
20
—
Callus

Stem
45
—
Yellow and black callus

Root
35
—
Roots

Shoot
—
95
Multiple shoots and roots

1.5
0.5
—
—
—
Leaves
15
—
White callus and roots

Stem
45
—
Roots

Root
10
—
Roots

Shoot
—
90
Multiple shoots and roots

1.5
1.0
—
—
—
Leaves
25
—
Roots

Stem
60
—
Roots

Root
10
—
Roots

Shoot
—
100
Multiple shoots and roots

1.5
1.5
—
—
—
Leaves
45
—
Callus and roots

Stem
85
—
Callus and roots

Root
70
—
Roots

Shoot
—
95
Direct regeneration after 35 days

1.5
2.0
—
—
—
Leaves
80
—
Callus and roots

Stem
100
—
Callus and roots

Root
70
—
Roots

Shoot
—
100
Direct regeneration after 35 days

2.0
0.5
—
—
—
Leaves
5
—
Roots

Stem
20
—
Roots

Root
20
—
Roots

Shoot
—
90
Direct regeneration after 20 days

2.0
1.0
—
—
—
Leaves
10
—
Roots

Stem
20
—
Roots

Root
25
—
Roots

Shoot
—
100
Multiple shoots

2.0
1.5
—
—
—
Leaves
65
—
Callus and roots

Stem
95
—
Orange callus and roots

Root
75
—
Roots

Shoot
—
100
Direct regeneration after 20 days

2.0
2.0
—
—
—
Leaves
65
—
Callus

Stem
70
—
Yellow callus and roots

Root
—
—
—

Shoot
—
100
Multiple shoots

—
—
1.0
—
—
Leaves
20
—
Necrosis

Stem
45
—
White callus and roots

Root
15
—
Roots

Shoot
—
100
Direct regeneration after 35 days

—
—
—
1.0
—
Leaves
5
—
Necrosis

Stem
10
—
Roots

Root
10
—
Roots

Shoot
—
100
Direct regeneration after 35 days

—
—
—
—
1.0
Leaves
10
—
Necrosis

Stem
15
—
Roots

Root
10
—
Roots

Shoot
—
100
Direct regeneration after 35 days

(a)

(b)

Figure 1: (a) Complete in vitro plant regeneration of Celosia cristata derived from a shoot explant cultured in MS basal medium after 35 days of culture. (b) In vitro flowering of Celosia cristata in MS basal medium after 2 months of culture at 25 ± 1°C under 12 h light and 12 h dark.

The mean primary root length of the sample after 7 days of germination was determined. In subsequent experiments, only primary roots which achieved this mean root length were chosen. Permanent slides of the primary roots were prepared as previously described [8]. In meristematic cells of intact roots which achieved the mean root length of the sample, the mean MI value was determined to be 39.03 ± 4.67. The chromosome count was 33.23 (Table 2) and the mean cell and nuclear areas were 252.48 ± 25.88 μm² and 49.06 ± 2.16 μm², respectively (Table 3; Figures 2(a) and 3(a)). Primary roots obtained in vitro after 4 weeks were made into squashed preparations as previously described [9]. The MI value for normal in vitro grown plantlets was 45.64 ± 3.16 and the chromosome count was 36.05 (Table 2), in agreement with the chromosome number of intact C. cristata plants reported by Grant (1954) [10]. The mean cell and nuclear areas for root meristem cells from in vitro grown plants were 228.13 ± 19.44 μm² and 84.26 ± 3.07 μm², respectively, while the ratio of mean nuclear to cell area was 0.37 ± 0.01 (Figures 2(b) and 3(b); Table 3). In abnormal plantlets (swollen stems), the MI was found to be 43.65 ± 2.75, with a chromosome count of 36.98 (Table 2). Plantlets that exhibited in vitro flowering had a mean MI value of 46.35 ± 0.99, with a chromosome count of 42.07, higher than the value of 33.23 found for in vivo grown plants. In contrast, nonflowering regenerants had a slightly lower mean MI value (42.27 ± 2.86) and a lower mean chromosome number (38.24) compared to in vitro flowering plants (Table 2). Because the in vivo mean chromosome count was 36, some changes may have taken place during tissue culture with respect to cellular and nuclear behaviour: perhaps due to media, hormones, environmental cultural factors, and/or explants, and so forth. Consistent with this notion, in a study by Tabur and Oney [11], high concentrations of artificial fertilisers had negative effects on the Mitotic index and chromosome behaviour in Vicia hybrida L.

Table 2: The Mitotic Index and mean chromosome numbers in meristem cells of intact Celosia cristata plants and regenerants.

Celosia cristata
Mitotic Index (%)
Chromosome number (mean)

In vivo
Plant
39.03 ± 4.67
33.23

In vitro
PLANTLET

    Normal
45.64 ± 3.16
36.05

    Abnormal
43.65 ± 2.75
36.98

FLOWERING
46.35 ± 0.99
42.07

NON-FLOWERING
42.27 ± 2.86
38.24

Table 3: The mean nuclear and cell areas and their ratios in root meristem cells of in vivo and in vitro grown Celosia cristata plants.

Celosia cristata
Mean (μm²)

Nucleus (N)
Cell (C)
Ratio (N/C)

In vivo
49.06 ± 2.16
252.48 ± 25.88
0.19 ± 0.01

In vitro (normal)
84.26 ± 3.07
228.13 ± 19.25
0.37 ± 0.01

In vitro (abnormal)
71.24 ± 3.56
228.37 ± 13.69
0.33 ± 0.02

(a)

(b)

(c)

Figure 2: (a) Mean nuclear areas for in vivo primary root cells. (b) Mean nuclear areas for in vitro primary root cells (normal). (c) Mean nuclear areas for in vitro primary root cells (abnormal).

(a)

(b)

(c)

Figure 3: (a) Mean cell areas for in vivo primary root cells. (b) Mean cell areas for in vitro primary root cells (normal). (c) Mean cell areas for in vitro primary root cells (abnormal).

Figures 2(c) and 3(c) show the mean nuclear and cell areas for root cells from abnormal plants. While the mean nuclear area was observed to be increased (71.24 ± 3.56) versus intact plants, the mean cell area decreased and was almost equal to that observed for in vitro cells. Although the ratio of mean nuclear to cell area was larger than that found for intact plants, this ratio was slightly smaller than that measured for in vitro plants (Table 3). These results suggest that cell and nuclear areas may have changed independently of each other: since mean cell areas decreased while mean nuclear areas increased. This is in agreement with the work of Taha and Francis [12] on Vicia faba. Furthermore the results obtained in the present study is supported by the findings of Thomas and Davidson [13], whereby they found that the relationship between nuclear and cell size of Vicia faba can change abruptly without affecting mitotic activity, and the nuclei can remain constant in size, despite a decrease in cell sizes. In addition, Taha and Francis also reported that chromosome numbers and MI values increased with culture age, consistent with results observed in the present study. This could be due to cellular instability upon transfer from one environment to another, in this case from in vivo to in vitro conditions. Besides, the cells could experience shock effect during transfer. Possibly the mechanisms regulating cell and nuclear size and other cellular parameters are disturbed when cells are brought into culture, coupled with a loss of the organising influences imposed on cells by intact plants.

MI values observed in the present study for C. cristata were very high compared to many other species: for example in V. faba, the MI value was only 25% [14]. This is consistent with the readiness of C. cristata to respond actively in culture, as shown in Table 1, whereas in V. Faba, regeneration was not easily achieved. All C. cristata explant sources could regenerate or were able to produce shoots in vitro, whereas, in V. faba, it is comparatively more difficult to induce callus and regeneration in vitro [15]. Unfortunately, very few reports have been published in the literature discussing changes to cellular behaviour when cells are grown in tissue culture systems. The cellular behaviour parameters investigated in the present study do not appear to follow any particular pattern. Even in abnormal stems, the MI, mean chromosome number, mean cell and nuclear areas, and their ratio were nearly similar to the normal and in vitro flowering plantlets. Interestingly, nearly all cellular parameters examined increased in vitro, with the exception of mean cell area. However, this decrease in cell area did not hinder callus formation, plant regeneration, or in vitro flowering in C. cristata. Usually, cultures that form shoots or roots exhibit reduced cell sizes for example in shoot forming tobacco callus cultures [16]. It is hoped that more research on the cellular behaviour of plant species will be carried out, to pinpoint exactly the pattern of changes that occur when cells are transferred from in vivo to in vitro environments. Cellular behaviour is also important for the regeneration potential of a particular species.

4. Conclusion

Direct regeneration and in vitro flowering of C. cristata have been obtained from shoot explants cultured on MS basal medium. The highest percentage of plant regeneration was achieved on MS medium supplemented with 2.0 mg/L NAA and 1.5 mg/L BAP. Use of BAP alone on MS medium was associated with abnormalities during plant regeneration. No differences were observed with respect to mitotic index (MI), chromosome number, mean nuclear, and cell areas between normal and abnormal plants. Further investigations must be conducted to enable a better understanding of cellular behaviour in relation to plant regeneration and in vitro flowering.

Acknowledgment

The authors would like to thank University of Malaya for the financial support and facilities provided to successfully carry out this research.

References

R. L. M. Pierik, In Vitro Culture of Higher Plants, Martinus Nijhoff, Dordrecht, The Netherlands, 1987.

R. M. Taha, “In vitro flowering of Celosia cristata,” Jurnal Sains, vol. 8, no. 1, pp. 1027–1031, 2000.

B. E. Moghaddam and R. M. Taha, “Cellular behavior in embryogenic and non-embryogenic sugar beet calluses,” In Vitro Cellular and Developmental Biology, vol. 41, no. 4, pp. 465–469, 2005.

A. M. Ekanem and J. O. Osuji, “Mitotic index studies on edible cocoyams (Xanthosoma and Colocasia spp.),” African Journal of Biotechnology, vol. 5, no. 10, pp. 846–849, 2006.

R. M. Taha, “Tissue culture studies of Citrus hystrix D.C. and Severinia buxifolia (poir) tenore,” Asia-Pacific Journal of Molecular Biology and Biotechnology, vol. 1, no. 1, pp. 36–42, 1993.

R. M. Taha, “In vitro flowering of Murraya paniculata (Jack) Linn,” Asia-Pacific Journal of Molecular Biology and Biotechnology, vol. 5, no. 2, pp. 68–71, 1997.

R. M. Taha and M. Tijan, “An in vitro production and field transfer protocol for Solanum melongena L. plants,” South African Journal of Botany, vol. 68, no. 4, pp. 447–450, 2002.

A. D. Conger and L. M. Fairchild, “A quick-freeze method for making smear slides permanent,” Stain Technology, vol. 28, no. 6, pp. 281–283, 1953.

D. Francis, “Effects of red and far-red light on cell division in the shoot apex of Silene coeli-rosa L,” Protoplasma, vol. 107, no. 3-4, pp. 285–299, 1981.

W. F. Grant, “A cytological study of Celosia argentea, C. argentea Var. cristata and their hybrids,” Botanical Gazette, vol. 115, no. 4, pp. 323–336, 1954.

S. Tabur and S. Oney, “Effect of artificial fertilizers on mitotic index and chromosome behaviour in Vicia hybrida, L,” Journal of Agricultural Research, vol. 47, no. 1, pp. 1–9, 2009.

R. M. Taha and D. Francis, “Cell and Nuclear areas in mitotic cells of primary roots of Vicia faba L. in vivo and in vitro,” Malaysian Journal of Science, vol. 13, pp. 23–28, 1991.

J. E. Thomas and D. Davidson, “Cell and nuclear size in Vicia faba roots: changes during germination and in response to levels of ambient water,” Annals of Botany, vol. 51, no. 3, pp. 353–361, 1983.

R. M. Taha and D. Francis, “The relationship between polyploidy and organogenetic potential in embryo- and root-derived tissue cultures of Vicia faba L,” Plant Cell, Tissue and Organ Culture, vol. 22, no. 3, pp. 229–236, 1990.

R. M. Taha, Studies on the cellular behaviour of roots of Vicia faba L., in vivo and in vitro, Ph.D. thesis, Wales University, Cardiff, UK, 1989.

M. K. Ross, T. A. Thorpe, and J. W. Costerton, “Ultrastructural aspects of shoot initiation in tobacco callus cultures,” American Journal of Botany, vol. 60, no. 8, pp. 788–795, 1973.