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Communication

Protocols for Adventitious Regeneration of Amelanchier alnifolia var. cusickii and Lonicera kamtschatica ‘Jugana’

by
Júlia Hunková
,
Monika Szabóová
and
Alena Gajdošová
*
Plant Science and Biodiversity Center, Institute of Plant Genetics and Biotechnology, Slovak Academy of Sciences, 950 07 Nitra, Slovakia
*
Author to whom correspondence should be addressed.
Plants 2021, 10(6), 1155; https://doi.org/10.3390/plants10061155
Submission received: 18 March 2021 / Revised: 3 June 2021 / Accepted: 5 June 2021 / Published: 6 June 2021
(This article belongs to the Special Issue Plant Tissue Culture II)
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Abstract

:
The aim of this work was to assess the regeneration capacity of Amelanchier alnifolia var. cusickii and Lonicera kamtschatica cv. ‘Jugana’ from different types of explants under various hormonal treatments. The whole leaves, petioles, and internodal segments of in vitro plants were examined as explants. Several plant growth regulators (cytokinins and auxins) were evaluated for their ability to induce adventitious regeneration. Direct and indirect organogenesis was achieved under certain culture conditions in both species. The frequency of shoot regeneration was strongly dependent on concentrations of plant growth regulators in the induction media (L. kamtschatica ‘Jugana’) or concentrations of plant growth regulators in the induction media and type of explant (A. alnifolia var. cusickii). Results showed that leaves were not suitable explants for A. alnifolia var. cusickii. Both species were able to regenerate shoots from internodal segments and petioles. The highest induction of shoots was obtained on Murashige and Skoog (MS) medium enriched with 2 mg/L thidiazuron (TDZ) and 0.5 mg/L indole-3-butyric acid (IBA) for Amelanchier alnifolia and with 1 mg/L TDZ and 0.2 mg/L indole-3-acetic acid (IAA) for L. kamtschatica ‘Jugana’. Obtained adventitious shoots were further proliferated in order to investigate their multiplication capacity. The multiplication of shoots was successful in all cultivars, with the best results reported in A. alnifolia var. cusickii (7.07 shoots/explant on average).

1. Introduction

Berries belong to the group of economically important crops mostly due to their benefits on human health [1]. It is known that many non-traditional small fruit species are being recognized for their content of biologically active compounds and serve as a valuable and natural source of vitamins, antioxidants, anthocyanins, and polyphenols with strong health-promotion effect [2,3,4,5]. Amelanchier alnifolia Nutt. (saskatoon berry) is a fruit bearing shrub native to the Canadian prairies and southern and northern territories of the United States. This berry is potentially attractive because of its frost-resistance, disease-resistance, and decorative purposes [6], moreover also of its high yields and fruit quality, which is very similar to blueberry. Saskatoon fruit could be a suitable supplement for modern human nutrition, as the berries are rich source of polyphenols, flavonoids (gallic acid, rutin, quercetin), and anthocyanines [7]. Lonicera kamschatica (honeysuckle) is a deciduous shrub native to Russia and Japan. Similarly to saskatoon, it is frost- and disease-resistant and can be grown in lowlands as well as mountain regions [8]. This species has dark-blue, elongated-shape fruits, which contain a high amount of vitamin C, anthocyanins, and flavonoids (quercetin, rutin) [9,10].
The demand for small fruit is continuously growing, especially in the food industry for a variety of products [11]. Both saskatoon and honeysuckle berries can be eaten fresh or dried, or be processed to other products like jam, syrup, desserts, or vines [12,13]. In order to fulfill the increasing demand for healthy planting material, tissue culture techniques are being used as an alternative to traditional propagation methods. They are less time-demanding and in case of adventitious regeneration they can also serve as a prerequisite for the transformation approaches used in genetic improvement of selected cultivars [14,15]. However, plant regeneration in vitro depends on such factors as species, genotype, and explant. Environmental conditions (culture medium, plant growth regulators) also significantly influence the rate of regeneration [16]. Thus, there is still a need for development of new or optimization of existing procedures, especially for less commercialized cultivars and species.
Reports about adventitious regeneration in Lonicera spp. are rather limited. Shoot induction was achieved from leaf explants in Lonicera nitida, Lonicera japonica and Lonicera macranthoides [17,18,19], stem segments in Lonicera tatarica [20], or calli cultures in Lonicera japonica [21]. The combinations of cytokinins 6-benzylaminopurine (BAP), thidiazuron (TDZ), and kinetin (KIN) with different auxins were used in a wide range of concentrations. However, due to some inconsistencies, no general recommendations can be made for Lonicera spp. as each protocol needs to be modified to the individual species. No study has been published yet dealing with adventitious regeneration of L. kamtschatica ‘Jugana’ and the same is also valid for A. alnifolia var. cusickii.
The research presented in this study was undertaken because of a total absence of relevant data for these two species. The primary goal was to examine adventitious plant regeneration in saskatoon and honeysuckle using three different types of tissues. The effect of different combinations of plant growth regulators (PGR) for callogenesis and organogenesis, shoot induction and multiplication were evaluated. The reported results clarify factors controlling adventitious shoot regeneration of A. alnifolia var. cusickii and L. kamtschatica ‘Jugana’ and provide rapid protocols allowing further plant multiplication and improvements by in vitro techniques and genetic engineering.

2. Results

2.1. Amelanchier alnifolia var. cusickii Shoot Induction and Multiplication

Testing of explant type showed that A. alnifolia var. cusickii leaves of in vitro plants were not suitable for adventitious shoot induction. The same outcome was observed with petioles as the majority of them had necrotized shortly after being placed on an induction medium. The significantly highest induction of shoots was recorded after using internodal segments (IS) as explants (Table 1, Figure 1).
The type of explant and type of cytokinin (BAP vs. TDZ) was a statistically significant factor for callogenesis and shoot induction, while the type of cytokinin was not significant for the number of induced adventitious shoots. Under the influence of BAP, no calli emerged and only direct regeneration was observed. With the use of TDZ, shoots originated both directly and indirectly. The highest rate of induction was observed after cultivation on MS medium with 2 mg/L TDZ and 0.5 mg/L IBA. It is worth mentioning that TDZ in concentrations higher than 2 mg/L led more frequently to shortened stems with longer, occasionally deformed leaves, while no such traits were observed under the influence of BAP.
ANOVA suggests a significant effect (p ≤ 0.05) of explant type on the callus formation, shoot induction, and number of induced adventitious shoots. Plant growth regulator was a significant factor for callus formation and also shoot induction but did not affect the number of shoots. The interaction of both factors was significant for shoot induction as well as their number (Table 2). The mean number of shoots induced on media with BAP or TDZ reached 3.58 and 3.22, respectively. The average number of shoots per explant type was 0.17 (leaf), 1.33 (petiole), and 4.05 (IS) (Supplementary Table S1).
Both cytokinins were examined during multiplication phase to evaluate whether prolonged influence of TDZ will result in worsened shoot growth. Multiplication index of shoots reached 7.07 shoots/explant for BAP and 6.57 shoots/explant for TDZ. The mean number of shoots evaluated after each subculture did not rise significantly under the influence of TDZ (6.93, 6.13, and 6.67, respectively). In the presence of BAP, the highest mean number of shoots was recorded after 1st subculture, followed by a significant decrease in the next two subcultures (10.57, 4.57, and 6.10, respectively) (Figure 2).

2.2. Lonicera Kamtschatica ‘Jugana’ Shoot Induction and Multiplication

The organogenesis efficiency in L. kamtschatica ´Jugana´ was rather low compared to A. alnifolia var. cusickii (Supplementary Table S2). The highest rate of induction was observed when petioles were used, internodal segments were also suitable explants. The use of leaves resulted in their necrosis. Significant differences were observed in callogenesis and shoot organogenesis depending on the hormone type (Table 3). Shoots induced from explants cultivated on media with BAP were chlorotic, very fragile, and thin, without active growth. They perished shortly after transferring on multiplication medium. The same result was observed also on medium containing both BAP and kinetin (data not evaluated). On the contrary, shoots induced under the influence of TDZ had thicker stems with larger leaves and occasional chlorosis (Figure 3).
They originated only indirectly from green, proliferating calli and were actively growing and elongating during the whole induction phase. The significantly highest number of regenerated shoots was recorded after cultivation on MS medium with 1 mg/L TDZ and 0.2 mg/L IAA.
ANOVA suggests a highly significant (p ≤ 0.01) effect only of PGR treatment on callus formation, shoot induction and the number of induced adventitious shoots (Table 4). The mean number of shoots cultivated on media with BAP or TDZ reached 0.36 and 3.07, respectively. The average number of shoots per explant type was 0.29 (leaf), 1.64 (petiole), and 2.82 (IS) (Supplementary Table S2). Multiplication of shoots was successful under the influence of 1 mg/L TDZ and 0.2 mg/L IAA on MS medium supplemented with 36.7 mg/L FeNaEDTA to avoid shoot chlorosis. Most of the shoots multiplied formed big clumps with a massive callus on the base part but their elongation was reduced (Figure 4). The average multiplication index after three months of cultivation reached 7.03 shoots/explant.

3. Discussion

According to our knowledge, no study was reported concerning adventitious regeneration of Amelanchier spp. so far, therefore comparison of our results is possible only with related members of Rosaceae family. Mahmood and Hassanein [22] achieved 36.7% regeneration of adventitious shoots from leaf discs of Rosa hybrida ‘Eiffel Tower’ cultivated on modified MS medium with 0.5 mg/L BAP, 1 mg/L GA3, and 0.5 mg/L NAA. Thidiazuron in the concentration of 1 mg/L did not result in shoot induction but increasing its concentration led to a higher rate of callogenesis which was observed also in our study. Reports were published concerning regeneration from other types of explants, such as internode sections [23], cotyledons [24], and petioles [25]. Shoot induction was not observed from Prunus avium leaves on MS medium with 2 mg/L TDZ and 0.5 mg/L IBA. The regeneration was confirmed only on QL (Quoirin and Lepoivre) medium [26] with the same growth regulators [23]. As in our study, the internode sections as explants resulted in more effective shoot formation in almost all cultivars. Feyissa et al. [25] observed that TDZ was superior to BAP in callus induction and shoot regeneration from leaves of Hagenia abyssinica. Previous studies on H. abyssinica showed that low concentration of TDZ (<0.2 mg/L) enhanced direct shoot regeneration while high concentrations promoted callus induction and shoot regeneration. However, high concentration of TDZ led to shoot elongation inhibition [25], what confirms findings in our research. The regeneration rate was improved significantly only after the increase of BAP above 5 mg/L which might indicate that concentration in our study was too low for successful induction. According to Vujović et al. [27], a sudden decrease in the multiplication index can be caused by repeated subcultivation as it was observed for two Prunus spp. cultivars. This might be a possible explanation because the mother plants in this experiment were already cultivated for at least one year. The multiplication index (7.1 shoots/explant) in this study was comparable with the results already published for shoots of A. alnifolia var. cusickii which originated from axillary buds [28].
As far we know, no protocol has been published for adventitious regeneration of L. kamtschatica ´Jugana´ yet. Leaves and stem internodes were used as explants in existing studies with other honeysuckle species [18,19,20]. Leaves of L. japonica ‘Hall’s Profilic’ cultivated on ½ LS (Linsmaier and Skoog) medium [29] with 1 or 3 mg/L BAP were the most responsive explants in the work of Georges et al. [18] (48–53%, respectively), while TDZ resulted in no induction. This does not coincide with our results where TDZ was significantly better cytokinin compared to BAP. However, the species-dependent response might alter the outcome of the experiment. Differentiation of shoots from callus cultures of L. japonica Thunb. was evaluated by Hui et al. [21]. The best results (5.50 shoots/explant) were obtained after cultivation on WPM medium with 0.5 mg/L BAP and 1.5 mg/L NAA. Moreover, NAA resulted in significantly higher differentiation than IAA. This supports the findings in our study about PGR treatment directly influencing the induction of shoots. The multiplication index (7.0 shoots/explant) achieved in our study was comparable with the results already published for L. kamtschatica (Sevast.) Pojark shoots propagated from axillary buds [8]. According to our previous experiences with Amaranthus spp. adventitious regeneration and shoot multiplication [30], we suppose that reduced elongation growth of shoot clumps formed on medium with 1 mg/L TDZ and 0.2 mg/L IAA could be stimulated by their transfer on medium with 1 mg/L BAP, as was also reported by Van Le et al. [31]. Fira et al. [32] reported that L. kamtschatica represent a challenge for micropropagation due to a relatively low proliferation rates in some cases, shorts shoots, physiological problems like necrosis of the apices and hyperdricity on media with high BAP concentration, which confirms our findings.
In conclusion, this study presents protocols for adventitious regeneration of two economically important small fruit species. As far as is known, this study is the first describing adventitious shoot induction and proliferation of saskatoon (A. alnifolia var. cusickii) and honeysuckle (L. kamtschatica ´Jugana´). Recommendations presented herein could be applied to related species or used for further genetic improvement of selected cultivars via transformation or other biotechnology techniques.

4. Materials and Methods

4.1. Plant Material

In vitro cultures of Amelanchier alnifolia var. cusickii, Lonicera kamschatica ´Jugana´ were established according to the procedure by Hunková et al. [27,33,34]. Sprouts bearing several axillary or apical buds were taken from mature plants, cut into smaller pieces (1–1.5 cm), and sterilized with 70% (v/v) ethanol for 2 min followed by immersion in 0.1% (w/v) HgCl2 with Tween for 5 min along with three rinses in sterile distilled water.

4.2. Shoot Initiation and Multiplication

Single-node explants were placed vertically in sterile Petri dishes (6 cm in diameter) filled with the culture medium. In vitro cultures of Amelanchier alnifolia var. cusickii and Lonicera kamschatica ´Jugana´ were established at MS (Murashige and Skoog) medium supplemented with 30 g/L sucrose (Slavus, Bratislava, SK) and 8 g/L plant agar (Duchefa Biochemie, Haarlem, NL). Medium pH was adjusted to 5.6 before autoclaving 20 min at 1 kg cm3 and 121 °C. Growth regulators for shoot initiation were used as follows: 1 mg/L BAP and 0.5 mg/L IBA for A. alnifolia var. cusickii; 2 mg/L BAP and 0.2 mg/L IAA for L. kamtschatica ´Jugana´. After six weeks, 10–15 shoots from each cultivar were transferred to Combiness vessels (Microbox Combiness, Nevele, BE) containing multiplication medium. All plant growth regulators were filter-sterilized before being added to the culture medium. The concentration of plant growth regulators followed the earlier published protocols [27,35,36]. Proliferating shoots were subcultured every 4 weeks. All cultures were maintained in a growth chamber at 22 ± 2 °C with 16 h light period using cool white fluorescent light at a photosynthetic photon flux density 50 μM/m2s.

4.3. Adventitious Shoot Regeneration

Explants were taken from the upper third part of the shoots two weeks after the last subculture from cultures that had been cultivated for one year. Three types of explants were chosen to compare their ability to induce organogenesis, e.g., whole leaves, petioles, and internodal segments (IS). Initial explants were fully developed parts of the plantlet (no buds etc.). The leaf had been cut together with the petiole, then the petiole was separated and both parts (leaf, petiole) were used whole as individual initial explants. All leaves were cut transversally three-times. Explants were placed horizontally and abaxially on the induction medium and subjected to treatments with various plant growth regulators (Table 5). From each explant type, 25 pieces were used per treatment in one repetition. After eight weeks of induction phase, all explants were examined, and the number of shoots was calculated for each explant individually. The number of shoots was used for statistical evaluation. Following the induction phase, isolated adventitious shoots were transferred to the multiplication medium (Table 5). Due to problems with chlorosis, 36.7 mg/L of FeNaEDTA was added to MS medium for L. kamtschatica ´Jugana´. The number of multiplied shoots from 30 randomly chosen explants was recorded after each subculture, once every four weeks. The duration of the experiment was 12 weeks (with three subcultures of the shoots on the fresh culture medium in 4-week interval). Multiplication index was calculated as the amount of shoots/number of explants ratio and indicated the total average number of adventitious shoots per explant.

4.4. Statistical Analysis

Statistical analysis of the obtained data were performed by using Statistica 10 software (StatSoft Inc., Tulsa, OK, USA). Analysis of variance (ANOVA) and Fisher LSD test were employed to identify significant differences among the different processes at p ≤ 0.05.

Supplementary Materials

The following are available online at https://www.mdpi.com/article/10.3390/plants10061155/s1, Table S1: Adventitious shoot induction rate (%) and number of induced shoots from leaves, petioles and internodal segments of Amelanchier alnifolia var. cusickii grouped according to different explants and planth growth regulators (PGR) treatments, Table S2: Adventitious shoot induction rate (%) and number of induced shoots from leaves, petioles and internodal segments of Lonicera kamtschatica ´Jugana´ grouped according to different explants and planth growth regulators (PGR) treatments.

Author Contributions

Conceptualization, J.H. and A.G.; formal analysis, M.S.; funding acquisition, A.G.; supervision, A.G.; writing—original draft, J.H. and A.G.; writing—review and editing, J.H. and M.S. All authors have read and agreed to the published version of the manuscript.

Funding

This research was co-funded by Research Centre AgroBioTech built in framework of European Community Project Building Research Centre “AgroBioTech” ITMS 26220220180 and by the Scientific Grant Agency of the Ministry of Education of the Slovak Republic and the Slovak Academy of Sciences (VEGA 2/0052/17).

Conflicts of Interest

The authors declare no conflict of interest.

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Plants 10 01155 g001 550
Figure 1. A. alnifolia adventitious shoot induction from leaves (A), petioles (B), and internodal segments (C) on induction media. Explants after eight weeks of cultivation on MS medium with 1 mg/L BAP and 0.5 mg/L IBA. The length of the scale bar is 1 cm.
Figure 1. A. alnifolia adventitious shoot induction from leaves (A), petioles (B), and internodal segments (C) on induction media. Explants after eight weeks of cultivation on MS medium with 1 mg/L BAP and 0.5 mg/L IBA. The length of the scale bar is 1 cm.
Plants 10 01155 g001
Plants 10 01155 g002 550
Figure 2. Effect of 0.5 mg/L TDZ and 1 mg/L BAP in combination with 0.5 mg/L IBA on A. alnifolia var. cusickii multiplication. Adventitious shoots after four weeks of cultivation on MS medium. The length of the scale bar is 1 cm.
Figure 2. Effect of 0.5 mg/L TDZ and 1 mg/L BAP in combination with 0.5 mg/L IBA on A. alnifolia var. cusickii multiplication. Adventitious shoots after four weeks of cultivation on MS medium. The length of the scale bar is 1 cm.
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Figure 3. Adventitious shoots of L. kamtschatica ´Jugana´ after eight weeks of cultivation on MS medium with 0.2 mg/L IAA, 1 mg/L BAP, and 1 mg/L TDZ. The length of the scale bar is 1 cm.
Figure 3. Adventitious shoots of L. kamtschatica ´Jugana´ after eight weeks of cultivation on MS medium with 0.2 mg/L IAA, 1 mg/L BAP, and 1 mg/L TDZ. The length of the scale bar is 1 cm.
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Figure 4. Adventitious shoots of L. kamtschatica ´Jugana´ after four weeks of cultivation on MS medium supplemented with 36.7 mg/L FeNaEDTA, 1 mg/L TDZ and 0.2 mg/L IAA. The length of the scale bar is 1 cm.
Figure 4. Adventitious shoots of L. kamtschatica ´Jugana´ after four weeks of cultivation on MS medium supplemented with 36.7 mg/L FeNaEDTA, 1 mg/L TDZ and 0.2 mg/L IAA. The length of the scale bar is 1 cm.
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Table
Table 1. Effect of plant growth regulators (PGR) treatments and explant type on adventitious shoot regeneration of A. alnifolia var. cusickii.
Table 1. Effect of plant growth regulators (PGR) treatments and explant type on adventitious shoot regeneration of A. alnifolia var. cusickii.
PGR Combinations (mg/L)Shoot InductionRegenerated Shoots
LPISLPIS
1 BAP + 0.5 IBA0.000 e0.040 de0.160 cd0.000 c0.280 c0.240 c
2 BAP + 0.5 IBA0.000 e0.040 de0.040 de0.000 c0.040 c0.640 bc
3 BAP + 0.5 IBA0.000 e0.000 e0.320 b0.000 c0.000 c1.520 ab
1 TDZ + 0.5 IBA0.040 de0.000 e0.240 bc0.040 c0.000 c0.360 c
2 TDZ + 0.5 IBA0.000 e0.000 e0.680 a0.000 c0.000 c2.120 a
3 TDZ + 0.5 IBA0.000 e0.000 e0.320 b0.000 c0.000 c2.240 a
L—leaves, P—petioles, IS—internodal segments. Means with different letters (a–e) for each group within three columns indicate significant differences by LSD test (p ≤ 0.05).
Table
Table 2. Summary of two-way ANOVA results for examining the effect of explant and hormone and their interaction of A. alnifolia var. cusickii.
Table 2. Summary of two-way ANOVA results for examining the effect of explant and hormone and their interaction of A. alnifolia var. cusickii.
Effect Callus FormationShoot InductionNumber of Shoots
dfFpFpFP
explant24.4820.012 *61.7780.000 *23.2490.000 *
hormone56.3040.000 *5.2030.000 *1.9610.083
explant * hormone101.8290.0546.5980.000 *2.5210.005 *
Error432
Note: df—degrees of freedom; F—F-value; p—probability value; statistical significance at * p ≤ 0.05 in the same colum.
Table
Table 3. Effect of plant growth regulators (PGR) treatments on callus formation and adventitious shoot regeneration of L. kamtschatica ´Jugana´.
Table 3. Effect of plant growth regulators (PGR) treatments on callus formation and adventitious shoot regeneration of L. kamtschatica ´Jugana´.
PGR Combinations (mg/L)Callus FormationShoot InductionRegenerated Shoots
1 BAP + 0.2 IAA0.000 b0.040 ab0.040 bc
2 BAP + 0.2 IAA0.000 b0.000 b0.000 c
3 BAP + 0.2 IAA0.000 b0.000 b0.000 c
0.5 BAP + 1.5 KIN + 0.2 IAA0.000 b0.027 ab0.027 bc
1 TDZ + 0.2 IAA0.133 a0.080 a0.360 a
2 TDZ + 0.2 IAA0.200 a0.053 ab0.227 ab
3 TDZ + 0.2 IAA0.173 a0.013 b0.027 bc
Means with different letters (a–c) indicate significant differences by LSD test (p ≤ 0.05) in the same column.
Table
Table 4. Summary of two-way ANOVA results for examining the effect of explant and hormone and their interaction in Lonicera kamtschatica ´Jugana´.
Table 4. Summary of two-way ANOVA results for examining the effect of explant and hormone and their interaction in Lonicera kamtschatica ´Jugana´.
Effect Callus FormationShoot InductionNumber of Shoots
dfFpFpFp
explant21.0020.3682.8670.0582.8630.058
hormone65.5180.000 *2.2890.034 *3.5010.002 *
explant * hormone120.5620.8731.6220.0821.6920.0653
Error504
Note: df—degrees of freedom; F—F-value; p—probability value; statistical significance at * p ≤ 0.05 in the same column.
Table
Table 5. Different plant growth regulators (PGR) treatments for adventitious regeneration of A. alnifolia var. cusickii and L. kamtschatica ´Jugana´.
Table 5. Different plant growth regulators (PGR) treatments for adventitious regeneration of A. alnifolia var. cusickii and L. kamtschatica ´Jugana´.
SpeciesPGR (in mg/L)
Shoot InductionShoot Multiplication
A. alnifolia var. cusickii1–3 BAP + 0.5 IBA1 BAP + 0.5 IBA
1–3 TDZ + 0.5 IBA0.5 TDZ + 0.5 IBA
L. kamtschatica ‘Jugana’1–3 BAP + 0.2 IAA1 TDZ + 0.2 IAA
1–3 TDZ + 0.2 IAA
0.5 BAP + 1.5 KIN + 0.2 IAA
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Hunková, J.; Szabóová, M.; Gajdošová, A. Protocols for Adventitious Regeneration of Amelanchier alnifolia var. cusickii and Lonicera kamtschatica ‘Jugana’. Plants 2021, 10, 1155. https://doi.org/10.3390/plants10061155

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Hunková J, Szabóová M, Gajdošová A. Protocols for Adventitious Regeneration of Amelanchier alnifolia var. cusickii and Lonicera kamtschatica ‘Jugana’. Plants. 2021; 10(6):1155. https://doi.org/10.3390/plants10061155

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Hunková, Júlia, Monika Szabóová, and Alena Gajdošová. 2021. "Protocols for Adventitious Regeneration of Amelanchier alnifolia var. cusickii and Lonicera kamtschatica ‘Jugana’" Plants 10, no. 6: 1155. https://doi.org/10.3390/plants10061155

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