African Journal of
Plant Science

  • Abbreviation: Afr. J. Plant Sci.
  • Language: English
  • ISSN: 1996-0824
  • DOI: 10.5897/AJPS
  • Start Year: 2007
  • Published Articles: 692

Full Length Research Paper

Effects of different hormones on organogenesis in vitro of some varieties of cassava (Manihot esculenta CRANTZ) grown in Senegal

Abdoulaye FAYE
  • Abdoulaye FAYE
  • Laboratory Campus of Plant Biotechnology, Faculty of Sciences and Technology, University Cheikh Anta Diop of Dakar, BP: 5005 Dakar-Fann, Senegal.
  • Google Scholar
Maurice SAGNA
  • Maurice SAGNA
  • Laboratory Campus of Plant Biotechnology, Faculty of Sciences and Technology, University Cheikh Anta Diop of Dakar, BP: 5005 Dakar-Fann, Senegal.
  • Google Scholar
Papa Demba KANE
  • Papa Demba KANE
  • Senegalese Institute of Agricultural Research (ISRA), BP: 3120 Dakar, Senegal.
  • Google Scholar
Djibril SANE
  • Djibril SANE
  • Laboratory Campus of Plant Biotechnology, Faculty of Sciences and Technology, University Cheikh Anta Diop of Dakar, BP: 5005 Dakar-Fann, Senegal.
  • Google Scholar

  •  Received: 12 November 2014
  •  Accepted: 13 July 2015
  •  Published: 30 August 2015


Cassava (Manihot esculenta) is a perennial euphorbiaceous shrub grown mainly for its starchy tubers and its leaves rich in protein. The most known method of propagation of this crop is the classical cuttings’ planting. However, in vitro propagation appears most useful and permits to obtain high quantity of healthy vegetable material in a short period. In this work, it was to study the impact of different hormones on the organogenetic capacities in vitro of five cassava varieties cultivated in Senegal. Axillary uninodal sections were disinfected and cultured in Murashige and Skoog (MS) basal medium added or not of different concentrations (0.1, 0.5 and 1 mg/L) of auxin (α-naphthalene acetic acid (NAA)) or cytokines (benzyl aminopurine (BAP) and kinetin). Best shoot growth and rooting was observed in MS medium containing 0.1 mg/L kinetin with normal development of the leaves. Highest proliferation of shoots and leaves was obtained with medium MS + BAP 1 mg/L. Callus formation was observed in all media containing hormone but most in MS + NAA 1 mg/L. This work proposes a rapid and economic technique for cassava multiplication.
Key words: Organogenesis in vitro, cassava, varieties, hormones, Senegal.


Manihot esculenta known as cassava is a plant-tubers grown mainly in tropical regions where it presents a high economic importance. According to FAO (1995) it is the most important locally-produced food in a third of the world's low-income and food-deficit countries, especially in Africa. Its starchy roots and high-protein leaves are consumed at home or sold, in fresh or in processed form. Because of its simple technology of culture and large flexibility, cassava is often grown in rural areas where other crops fail (Thro et al., 1998). However, cassava propagation using cuttings classical method is not adequate for rapid and healthy multiplication. The annual production of vegetable material of this plant is very low (average 10 cuttings per plant per year) and yields are reduced by pests and diseases attack, essentially by the cassava african mosaic, the cassava bacterial blight due to Xanthomonas campestris and the floury cochineal (Phenacoccus manihotis). An alternative method that proves to remediate the low coefficient of multiplication and infections of cassava is micropropagation in vitro. It consists of regenerating whole plants by cultivating explants in artificial medium, sterile conditions and controlled environment (light and temperature). Several plants conserving genetic identity are obtained from successive generations and can be multiplied to infinity. According to Guo and Liu (1995), hundreds of millions of plants derived from culture in vitro are produced annually in the world. Micropropagation is therefore a rapid and powerful technique of multiplication that permits to obtain plants in sufficient quantity to satisfy continuous production independent of the seasons. Indeed, contrarily to the classical method that gives a single individual by seed or cutting, in vitro propagation may produce as many copies as liked from a single explant (Rancillac, 1981) and help to overcome constraints related to the availability of high quality of planting material (Wheatley et al., 2005; Vaillant et al., 2005). The work of Fereol (1978) highlighted perfectly the interest of culture in vitro in cassava. The ability of vegetative propagation in vitro has been estimated in African clones, to a potential of production of a million plants a year from a single cutting (Lourd, 1981). Thus, with this method of propagation, research can make a significant contribution to food security and economic development in the areas of culture of cassava (Thro et al., 1998). This contribution is more interesting when it comes to propagate resistant or tolerant varieties to major constraints to the culture. In this present study, it was made to study the effect of some hormones on organogenetic capacities in vitro of 5 varieties of cassava grown in Senegal and selected for their tolerance to termites ravaging cuttings Odontotermes sp. aff. erraticus (Faye et al., 2014). The general objective of the study was to determine the best medium for an optimal response of cassava to multiplication in vitro. Specific objectives were to assess the effects of different hormone concentrations on the growth and development (caulogenesis, rooting, shoot and root growth, phyllogenesis and callus formation) in vitro of the different varieties of cassava.


Plant material

The plant material was composed of five cassava varieties cultivated in the Department of Tivaouane (Senegal) including 3 local: Soya, Cololi and Niargi and 2 Brazilian: Cacau and Cacau roja. Cuttings were collected from farms and transplanted into pots placed in a greenhouse. They were watered every two days at 1/2 L per cutting. Fungicide and insecticide treatments using respectively 50 mg/L mancozeb and 2 ml/L chlorpyrifos-ethyl were conducted in this culture. Plants obtained have provided explants which were used for material of introduction in vitro.



After a brief wash with soap followed by 3 successive rinses, explants have been soaked for 20 min in a solution of 80 g/L calcium hypochlorite with 2-3 drops of tween 20, then in bleach for 10 min. Each soaking was immediately followed by 3 successive rinses with sterile water.


Culture media and control

The basal nutrient used was the complete MS (Murashige and Skoog) (1962) medium. It was solidified with 8 g.L-1 agar at pH adjusted 5.7 and contained 25 g.L-1 of sucrose. This medium was or not supplemented with NAA (α-naphthalene acetic acid), BAP (benzyl aminopurine) or kinetin at different concentrations (0.1, 0.5 and 1 mg/L). The media were distributed in glass test tubes at 20 ml/tube and then sterilized by autoclaving at 110°C for 20 min. The surface disinfected explants were placed vertically on the media, in sterile conditions. Cultures were incubated in the dark for 24 h and then transferred to the culture chamber lighted with 4000 lux where they were maintained at 27 ± 1°C, under a photoperiod of 13 h day.

A sample of 12 tubes per medium per variety was considered for the parameters assessment. Weekly measures have been conducted on the 3rd generation plantlets during 30 days of culture. The parameters evaluated were the shoot and root numbers and growth, the number of leaves and the rate of callus formation.


Statistical analyses

Data collected on this study were entered on Excel and analyzed with software Costat. They have been subjected to analysis of variance of the Student, Newman and Keuls test at the 0.05 level of significance.


Effect of hormones on caulogenesis in vitro of the different varieties of cassava

Figure 1 shows that the addition of hormones in the basal medium MS favored multiple shoots formation in all the varieties of cassava. Indeed, average 5.3 shoots by plantlet were count in the variety Soya in the MS + BAP 0.1 mg/L medium after four weeks of culture. Highest numbers of shoots were observed in medium containing BAP or kinetin. Medium with NAA were however less favorable to caulogenesis. The variation of shoots number were significant (F = 0.383; P = 0.05) among the different hormonal concentrations experimented, according to statistics.



Effect of hormones on rooting in vitro of the different varieties of cassava

The extent of root formation in vitro in cassava depends on the culture medium. We noted that the addition of BAP, especially at high doses in the MS medium reduced strongly the formation of roots. Indeed, no rooting was observed among the varieties Niargi, Cacau and Cacau roja in the MS + BAP 1 mg/L medium during 1 month of culture. In contrast, highest numbers of roots (average 10.4 per plantlet in variety Niargi) were found in MS + NAA 0.1 mg/L after 4 weeks of culture (Figure 2). According to ANOVA, the number of roots in the 5 varieties of cassava varied significantly (F = 3.453; P = 0.05) among the hormonal concentrations tested.



Effect of hormones on shoots’ growth in vitro of the different varieties of cassava

Explants cultured in media containing kinetin showed best growth of shoots. Respectively 3.56, 3.44 and 3.33 cm averages of shoots’ lengths were observed among varieties Cacau, Niargi and Soya in MS + KIN 1 mg/L after four weeks of culture (Figure 3). However BAP and NAA were less favorable to shoots’ growth. Therefore shortest shoots with averages 0.45 and 0.32 cm long, respectively have been observed among varieties Cololi and Cacau roja in the media MS + NAA 0.5 mg/L and MS + BAP 0.5 mg/L after 1 month of culture.



According to the analysis of variance, the variation of the shoots’ length among the different culture media tested was significant (F = 0.639; P = 0.05).


Effect of hormones on roots’ growth in vitro of the different varieties of cassava


The elongation of plantlets’ roots varied depending on the culture medium. Thus, we have seen that the addition of hormone, especially in high concentrations, in the medium MS enhanced the roots growth. Kinetin proved however best elongation of roots in some varieties. Thus, we could record respectively 4.62 and 3.58 cm averages of roots’ lengths among varieties Cacau and Soya in the MS + KIN 1 mg/L medium after 1 month of culture. In contrast, the lowest root growth occurred in media containing the NAA where very short roots not exceeding 0.06 cm average have been observed in the variety Cacau roja in the medium MS + NAA 1 mg/L after 4 weeks of culture (Figure 5). The variation of the roots’ length was significant (F = 1.554; P = 0.05) among the culture media experienced, according to the ANOVA.


Effect of hormones on the phyllogenesis in vitro of the different cassava varieties

Figures 4 and 7 show that explants cultured in medium with BAP produced more leaves than those cultured in medium containing kinetin. Indeed, after four weeks of culture we could count up to 16.4 leaves average in plantlets of the variety Niargi in the MS + BAP 0.5 mg/L medium. Leaves produced in media addition of kinetin presented however the best development. In contrast, NAA appeared to be a hormone unfavorable to the phyllogenesis in all varieties. Thus the number of leaves per plantlet could fall up to 1.5 average after 4 weeks of culture in the medium MS + NAA 0.5 mg/L in the variety Cololi (Figure 6).






The number of leaves formed in vitro was significantly variable (F = 10.310; P = 0.05) among the different culture media tested, according to the analysis of variance.


Effect of hormones on the callus formation in vitro of the different varieties of cassava

Callus formation in plantlets appeared to be induced by the addition of growth regulators in the basal medium MS. Figure 8 shows that NAA, especially at high concentration, were more favorable to the callus formation, compared to the BAP and the kinetin which had the least. Indeed, after 4 weeks of culture, we recorded 100% of callus formation in all varieties in media MS + NAA 0.5 mg/L and MS + NAA 1 mg/L against 25 and 58.3%, respectively in varieties Soya and Cololi in the MS + KIN 0.1 mg/L medium. No callus formation was observed however in the basal medium MS (Figure 4). The analysis of variance showed that the callus formation’s rate varied significantly (F = 32.538; P = 0.05) among the different media tested.



Our results showed that the response of cassava to micropropagation in vitro depends on the culture medium. Thus, the addition of growth regulators at different concentrations in the basal culture medium MS oriented the organogenesis in vitro of this plant. In our experimental conditions, we could note that the application of a low concentration (0.1 mg/L) of NAA, BAP or kinetin favored more than high concentration (1 mg/L), best growth of organs except callus. Such observations are confirmed by the results obtained by Cacai et al. (2012) according to which the effect of kinetin on the shoots’ growth varies depending on the applied concentration. Das et al. (2013) also found that the nature and the concentration of cytokinin determined significant growth’ variations in some genotypes of Dioscorea sp. ; reflecting the results of Ondo et al. (2007) who, using high concentration (2 mg/l) of kinetin, have noticed a reduction of the length of roots in the Dioscorea cayenensis – Dioscorea rotundata complex.

In our experiment, explants cultured in media containing BAP produced highest numbers of shoots and leaves in all the cassava varieties. Kinetin resulted better growth of shoots, roots and leaves, while NAA induced more importantly the formation of callus, compared to the 2 cytokinins (BAP and kinetin). These results are confirmed by the works of Malaurie et al. (1995), Miller and Skoog (1957), James and Newton (1977), Navatel (1979), Ammirato (1984), Bennett et al. (1986), Lalmohanlal et al. (1990), Romano et al. (1992), Boniface (1992), Yepez et al. (2001), Kbiach (2002), Namwenje et al. (2003) and Ahanhanzo et al. (2008) reported by Cacai et al. (2012), which have shown that kinetin induces more roots than BAP. Indeed, these cytokinins, unlike auxin (NAA), would encourage more development and growth of the aerial organs (shoots and leaves) than of roots. Therefore, according to Phil et al. (1995) the variations of the ratio auxin/cytokinin have specific effects on the development of the explants and then determine the organogenesis tendency. These authors have shown that a high ratio (more auxin than cytokinin) resulted in differentiation of roots, while a low ratio (more cytokinin than auxin) resulted in differentiation of shoots. However, Ahanhanzo et al. (2008), using NAA (0.5 mg/l) + BAP (0.5 mg/l) on one hand and NAA (0.5 mg/l) + KIN (0.5 mg/l) on the other hand, have not observed callus formation in three varieties of cassava (RB 89509, BEN 86052 and TMS 30572). This would be explained by the fact that there was some interaction between growth regulators so that shoot or root differentiation would depend on the type of hormonal combination made.

Our results also show that the organogenesis in vitro of the different varieties of cassava were ideal in the culture medium MS, without any addition of hormone. Plantlets were well rooted and showed good vegetative develop-ment in this basal medium in all varieties. Such findings agree with results obtained by Boher (1988) and Lourd (1981) which could successfully multiply 65 cassava cultivars without using growth regulator. It appeared according to this researcher that the plantlets’ growth in vitro could however be extremely variable depending on the cultivars or the type of explants of the same cultivar.

Therefore, according to our results, the variety would also have an influence on organogenesis in vitro of cassava. Thus, varieties Soya, Cacau and Niargi have presented best growth and development of organs, compared to varieties Cololi and Cacau roja in the culture medium MS. Such observations are confirmed by the work of Cacai et al. (2012) according to which the reaction of explants in different culture media is not the same from one variety to another. According to these authors, MS + KIN and MS + NAA media gave the highest shoots’ length average in beninese cultivars Agric Sazoue (3.54 ± 0.4 cm) and Gbeze (6.36 ± 0, 3 cm) on one hand and Ahouandjan (8.62 ± 0.8 cm) on the other hand respectively.

In varieties 92/0057 (1.63±0, 1 cm), BEN 86052 (4.20 ± 0.6 cm), Sekandji (6.6 ± 0.4 cm) and Okoyao (1.85 ± 0.3 cm) however, it was the NAA + KIN combination that gave the highest averages of shoot length. Similarly, work conducted by Ahanhanzo et al. (2010) on different genotypes of yam have confirmed that the response of the microcuttings to cytokinins’ action depended on the genotype of the plant.


Organogenesis in vitro of cassava explants depends on the culture medium and the variety. The addition of different growth regulators (NAA, BAP and kinetin) at different concentrations (0.1, 0.5 and 1 mg/L) each in the basal Murashige & Skoog (MS) medium allowed to observe different tendencies in organs’ development among 5 varieties Soya, Niargi, Cololi, Cacau and Cacau roja put in experience. The cytokinin BAP enabled to obtain more shoots, more leaves and fewer roots, while NAA has the most promoted callus formation in all varieties. Kinetin was found to be more favorable to best elongation of shoots and roots and the normal development of the leaves. In all media, rooting and growth of shoots and roots, conversely to number of shoots as well as the phyllogenesis and the callus formation, were more favored with low (0.1 mg/L) than with high (1 mg/L) hormonal concentration. However, the ideal response was observed with the basal culture medium MS in all the cassava varieties, so that the use of hormones appears not necessary for propagation in vitro of this plant.


The authors have not declared any conflict of interest.


The authors thank the Regional Studies Centre for Adaptation to Drought (CERAAS) for its financial support through the WAAPP (Agricultural Productivity Program in West Africa). Our thanks also go to Mr. Assane NDIAYE, national supervisor of cassava program and member of the National Federation of the cassava producers in Senegal for his collaboration which was very helpful.


Ahanhanzo C, Agbangla C, Agassounon DTM, Cacaï GHT, Dramane K (2008). Comparative study of the influence of growth' regulators on morphogenesis in vitro of some cassava varieties (Manihot esculenta) in Benin. Rev. CAMES – Ser. A, 07:47-52.
Ahanhanzo C, Gandonou C, Agbidinoukoun A, Dansi A, Agbangla C (2010). Effect of two cytokinins in combination with acetic acide α- naphthalene on yams (Discorea spp.) genotypes response to in vitro morphogenesis. Afr. J. Biotech. 9(51):8837- 8843.
Ammirato PV (1984). Yams. In Handbook of Plant Cell Culture (vol. 3). Crop Species Macmillan; New York: 336-354.
Bennett LK, Davies FTJ (1986). In vitro propagation of Quercus shumardii seedlings. Hort. Sci. 21(4):1045-1047.
Boher B (1988). Cassava healthy material production by in vitro culture. Plant Cell Tissue and Orqan Cidture. Agron. 6(3):221-228.
Cacai GHT, Ahanhanzo C, Dangou JS (2012). Effect of different hormonal combinations on organogenesis in vitro of some local improved varieties of cassava (Manihot esculenta-Euphorbiaceae) cultivated in Benin. Int. J. Biol. Chem. Sci. 6(4):1593-1607.
Das S, Dutta MC, Mazumdar PB (2013). Micropropagation of Dioscorea alata L. through nodal segments. Afr. J. Biotech. 12(47):6611-6617.
FAO/GIEWS (Global Information and Early Warning System on Food and Agriculture) (1995). Food supply situation and crop prospects in sub-Saharan Africa. Special Africa Report, April 1995.
Faye A, Kane PD, Sall-Sy D, Sane D, Mbaye DF (2014). Study of the cassava varietal sensitivity to termites ravaging cuttings planted in farms in the department of Tivaouane (Senegal) Int. J. Sc. Adv. Tech. 4(6):6-16.
Fereol C (1978). Vegetative multiplication and elimination of the cassava mosaic disease by thermothérapy inplants cultivated in vitro. Diseases of Tropical Food Crops. Int. J. Corpus Linguist. 65(7):285-295.
Guo JY, Liu YQ (1995). Rapid propagation of cassava by tissue culture and its application in rural districts in China. In Proceedings of the Second International Scientific Meeting, Cassava Biotechnology Network, Bogor, Indonesia, 25-28 Aug. 1994, CIAT Working Doc. No. 150:183-189.
James DJ, Newton B (1977). Auxin-cytokinin interactions in the in vitro micropropagation of strawberry. Acta Hort. 78:321-331.
Kbiach ML, Lamart A, Abdali A, Badoc A (2002). In vitro buds' culture of the oak-cork (Quercus suber). Bull. Soc. Pharm. Bordeau 141:73-78.
Lourd M (1981). Cultivation in vitro of a collection of cassava variéties. Balance after 4 months of experimentation. ORSAY, 1981.
Miller CO, Skoog F (1957). Chemical regulation of growth and organ formation in plant tissues cultured in vitro. Symp. Soc. Exp. Biol. 11:118-130.
Murashige T, Skoog F (1962). A revised medium for rapid growth and bio assays with tissue culture. Physiol. Plant. 15:473-497.
Nweke F (1996). Processing Potential for Cassava Production Growth in Sub- Saharan Africa. COSCA Working. Collaborative Study of Cassava in Africa, IITA Ibadan, Nigeria; Paper No 11.
Ondo OP, Kevers C, Dommes J (2007). Bud an tuber proliferation in vitro of Dioscorea cayenensis-D. rotundata complex. Plant Cell. Tiss. Organ Cult. 91:107-114.
Rancillac M (1981). Making a vegetative multiplication in vitro method of the maritime pine (Pinus pinaster Sol.) for clones constitution by seeds, AFOCEL, pp. 41-48.
Romano A, Noronha C, Martins-Loução MA (1992). Influence of growth regulators on shoot proliferation in vitro of Quercus suber L. Ann. Bot. 70(6):531-536.
Saleil V, Degras L, Jonard R (1990). Obtention of plants without virus of the yam mosaic (YMV) by in vitro culture of apex in american yam Dioscorea trifida L. Agronomy Elsevier/ INRA 10:605-615.
Sane D, Borgel A, Chevallier MA, Gassama-Dia YK (2001). In vitro induction of Acacia tortilis subsp. raddiana micro-cuttings' rooting by transitory auxin treatment. Ann. For. Sci. 58:431-437.
Thro AM, Taylor N, Raemakers K, Visser R, Puonti-Kaerlas J, Schopke C, Iglesias C, Roca W, Sampaio MJ (1998b). Biotechnology and the cassava farmer: an agenda to make a difference. Nat. Biotech. 16:428-430.
Vaillant V, Bade P, Constant C (2005). Photoperiod affects the growth and development of yam plantlets obtained by in vitro propagation. Biol. Plant. 49:355-359.
Wheatley AO, Ahmed MH, Asemota HN (2005). Development in vitro and salt adaptation of greater yam (Dioscorea alata) plantlets. In vitro Cell. Dev. Biol. Plant. 39:346-353.