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1.
Summary The two most serious diseases of cassava (Manihot esculenta Crantz) are cassava mosaic disease (CMD) and cassava bacterial blight (CBB) (Xanthomonas manihotis Starr). Clone 58308, derived from the third backcross of the interspecific cross of cassava (M. esculenta) x ceara rubber (M. glaziovii), showed a high level of resistance to both diseases. Crosses of 58308 with several other clones which varied from susceptible to moderately susceptible to both diseases gave progenies with a significant genotypic correlation between resistance to both diseases (r=0.90), apparently due to linkage. The heritabilities of resistance to the diseases were estimated at 50–70% for CMD and 25–65% for CBB. Resistance to both diseases is assumed to be polygenic. The correlated response to selection for CMD and for CBB was estimated.  相似文献   

2.
Summary Cassava (Manihot esculenta) is a tropical crop that is grown in Africa, Latin America and Southeast Asia. Cassava was introduced from Latin America into West and East Africa at two independent events. In Uganda a serious threat to cassava's survival is the cassava mosaic disease (CMD). Uganda has had two notable CMD epidemics since the introduction of cassava in the 1850s causing severe losses. SSR markers were used to study the effect of CMD on the genetic diversity in five agroecologies in Uganda with high and low incidence of CMD. Surprisingly, high gene diversity was detected. Most of the diversity was found within populations, while the diversity was very small among agroecological zones and the high and low CMD incidence areas. The high genetic diversity suggests a mechanism by which diversity is maintained by the active involvement of the Ugandan farmer in continuously testing and adopting new genotypes that will serve their diverse needs. However, in spite of the high genetic diversity we found a loss of rare alleles in areas with high CMD incidence. To study the effect of the introgression history on the gene pool the genetic differentiation between East and West Africa was also studied. Genetic similarities were found between the varieties in Uganda and Tanzania in East Africa and Ghana in West Africa. Thus, there is no evidence for a differentiation of the cassava gene pool into a western and an eastern genetic lineage. However, a possible difference in the genetic constitution of the introduced cassava into East and West Africa may have been diminished by germplasm movement.  相似文献   

3.
The aim of this study was to obtain information on the response of cassava(Manihot esculenta Crantz) to root-knot nematode infestation. To achieve this aim, a novel in vitro dual root/nematode culture method was used, where root cultures of several cassava cultivars were inoculated with axenic Meloidogyne javanica eggs. Following an incubation period,cassava roots were stained, weighed and dissected to determine the number of galls produced on the roots, as well as the number of mature females embedded in the galls. The number of eggs and larvae produced during this time were also determined. Results indicated that the modified in vitro nematode culture medium used was suitable for most root cultures of cassava cultivars. It was found that some cassava cultivars were highly susceptible to root-knot nematode infestation, with some cultivars showing very high numbers of galls and up to 50 mature females inside each gall. Some cassava cultivars screened, however, showed low numbers of galls and mature females, even though the presence of larvae was high. Some of these cultivars formed callus-like structures instead of galls, and this may be a resistance mechanism. This method may be useful as a screening tool, to determine the response and resistance or susceptibility of cassava cultivars to root-knot nematode infestation. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

4.
Deployment of resistant varieties is one major approach to controlling cassava bacterial blight (CBB), caused by Xanthomonas axonopodis pv. manihotis (Xam). To understand the genetic determinism of resistance to CBB, the use of reliable parameters measuring resistance is necessary. In order to test a relevant method for evaluation of quantitative resistance for mapping QTL (quantitative trait loci), the response of 150 F1 individuals, inoculated with four different Xam strains (CIO-84, CIO-1, CIO-136 and CIO-295), was assessed under controlled conditions. We used two types of evaluations at different intervals after inoculation, one based on a scale of 0 to 5 and the second based on the determination of the bacterial population in the vascular system. Both evaluation types revealed interaction between strains and F1 genotypes. Population values at 3 and 6 cm from the point of inoculation showed a high level of correlation. By performing an association analysis, at 7 and 15 days after inoculation, a significant positive correlation between both evaluation types was obtained. However, the disease rating at 30 days did not correlate with bacterial populations at either 7 or 15 days after inoculation, except for one strain, CIO-84. Evaluation of the bacterial population in stem tissues is time and labour consuming, consequently, for a rapid and reliable assessment of CBB resistance for QTL analysis, we strongly recommend evaluation based on the use of a symptom scale.  相似文献   

5.
The virological situation of cassava in Africa is increasing in complexity due to the number and types of viruses isolated from different locations within the continent. Here, we report the complete nucleotide sequences of both A and B components of two geminivirus species infecting cassava in the Ivory Coast and review the current knowledge of the molecular and biological diversity of the African cassava geminiviruses. As a whole, newly obtained sequences are compared with those of the African cassava mosaic geminiviruses identified to date. Results indicate that all isolates of African cassava mosaic virus (ACMV), irrespective of their geographical origin are clustered together with little or no variation in their genomic sequence. On the contrary, the genomes of the East African cassava mosaic virus (EACMV) are more genetically diverse due to the frequent occurrence of recombinations within their two components. Indeed, the EACMV-like viruses vary so much that their classification is becoming problematic. In addition, there is also a large range of phenotypic symptom variation for each of these virus species, irrespective of the location of isolation. Furthermore, it has been shown that ACMV and EACMV can be synergistic in cassava, resulting in a greater DNA accumulation and consequently inducing severe symptoms. For all these reasons, this paper initiates a discussion concerning the species demarcation for cassava geminivirus. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

6.
Summary Methodology, based on starch and polyacrylamide gel electrophoresis, was developed for determining isozyme electrophoregrams (patterns) of 16 enzymes of cassava (Manihot esculenta Grantz) varieties as potential genotype markers. Extracts of five different tissues (root, stem, leaf, petiole and bud) were examined. In general, the nodal portions of the shoots gave isozyme patterns with the largest number of bands. Petiole extracts gave similar results but bud extracts gave poor patterns. The limited number of varieties that were examined could be distinguished by sequential classification on the basis of the isozyme patterns of acid phosphatase, esterase, glutamate oxaloacetase transaminase and phosphoglucoisomerase.Joint publication of the Centro Internacional de Agricultura Tropical and the Department of Plant Science (No. 716), University of Manitoba. Presented in part at the 2nd International Symposium on Biochemical Approaches to Identification of Cultivars and Evaluation of Their Properties, 5–9 May, 1985, Braunschweig, West Germany.  相似文献   

7.
Cassava mosaic disease (CMD) caused by a group of begomoviruses and transmitted by whitefly vector is a serious disease in all the cassava-growing areas of Africa. Field evaluation with replication was conducted in 2003 and 2004 in three agroecologies in Nigeria to study the response of 40 cassava genotypes to CMD and to investigate genotype × environment (GE) interactions on their reactions to CMD, using the rank-sum classification and site regression analysis model. The 40 genotypes were separated into resistant (n = 17), moderately resistant (n = 6), moderately susceptible (n = 2) and susceptible (n = 15) groups. Environments, genotypes and GE interactions were all highly significant (P < 0.0001) for the virus disease contributing 9.5%, 71.36% and 19.14%, respectively to total variation. More than 40% of the genotypes were identified as resistant to the disease. Genotypes TMS 98/0581, TMS 99/3073, TMS 97/4763, TMS M98/0040, TMS 98/0505, TMS 97/0211, TMS 97/4769, TMS 99/2123, TMS M98/0068 and TMS 97/0162 were shown to have high resistance to CMD. The study also identified Umudike, in south-east Nigeria, as having high disease severity and the most appropriate site for CMD resistance screening of genotypes. Most of the genotypes exhibited stable resistance to CMD. The implication that the availability of these resistant genotypes as identified in this study could be a source of CMD resistance for further breeding is discussed.  相似文献   

8.
Summary Cassava (Manihot esculenta Crantz) germplasm collections are conventionally maintained by continuous vegetative propagation in the field. Tissue culture techniques provide a more convenient way to conserve germplasm. The cassava in vitro gene bank held in trust at CIAT comprises nearly 6000 accessions. A study was carried out to determine whether any DNA rearrangements resulting from in vitro storage under slow growth could be detected by molecular analysis in retrieved plants. RFLPs with homologous probes, RAPDs with twenty primers and DNA fingerprinting with M13 probe were tested to detect variation at DNA level in cassava plants after ten-years in vitro storage. The molecular marker data obtained in this study supports the stability of the cassava germplasm under the in vitro storage conditions described in this work.  相似文献   

9.
Summary The diploid (2C) amount of DNA in cassava (Manihot esculenta Crantz) is 1.67 picograms (pg) per cell nucleus. This value corresponds to 772 mega-base pairs in the haploid genome. The size of the nuclear genome in cassava is very small in comparison with other Angiosperms. Flow cytometry techniques were used to screen ploidy levels in a large population of in vitro plantlets treated with colchicine and oryzalin (3,5-dinitro-N4,N-dipropylsulphate). Culture of axillary node cuttings for 48 hours in liquid medium supplemented with 2.5 to 5.0 mM colchicine in combination with 2% dimethyl sulfoxide (DMSO) resulted in a high frequency (23 to 42%) of non-chimeric tetraploids in the V3 generation. Although mixoploidy may persist in as many as four cycles of vegetative propagation of node cuttings, solid (non-chimeric) tetraploids can be identified by flow cytometry among in vitro plantlets and then rapidly propagated for field testing. A somatic polyploidization system is proposed for implementation in cassava breeding programmes.Dedicated to the memory of the late Dr. Novak. Correspondence to M. van Duren  相似文献   

10.
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11.
The storage roots of cassava (Manihot esculenta Crantz) suffer from a rapid post-harvest deterioration that is a major constraint to their increased exploitation. In many ways this deterioration resembles wound responses in other better studied plant systems, though it appears to lack an adequate wound repair response. A cDNA clone (cMeHRGP1) for a hydroxyproline-rich glycoprotein expressed during the deterioration response was isolated and characterised. This clone proved to be an antisense pairing, coding for part of phosphoserine aminotransferase on its complementary strand. Messenger RNA corresponding to cMeHRGP1 accumulated in deteriorating cassava roots from day three after harvest, by which time the deterioration response was well advanced. There by confirming that aspects of the wound repair response were inadequate in harvested cassava roots. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

12.
The most widespread disease of economic importance of cassava is caused by whitefly vector, both as a single strain or combination of strains. A B1P2 family was generated from the crosses of an inter-specific F1 hybrid (CW 198-11) as a female parent with a commercial cassava cultivar (MTAI-8) as male parent at CIAT headquarters and evaluated in a high-pressure zone for whiteflies in Colombia. 227 genotypes were scored using a scale ranging from 1 (no leaf damage) to 6 (considerable leaf necrosis and defoliation, sooty mould on mid and lower leaves and young stems). The rest were considered promising. The most promising resistance was for damage ratings below 2 for 17.8% of the genotypes. The availability of the pest resistance genotypes, will serve as a means to combat the problem of CMD in Africa provided that resistance to A. socialis is also effective against B. tabaci with different virus strains that is capable of been introduced.  相似文献   

13.
Cassava bacterial blight (CBB), caused by Xanthomonas axonopodis pv. manihotis (Xam), is a particularly destructive disease in South America and Africa. The movement of infected asymptomatic stems is a major means of pathogen dispersal as well as infected seeds. The success of a cassava-seed certification program depends on the availability of reliable tests to detect the pathogen in vegetative planting materials and true seeds. We report here the different methods that permitted to detect the pathogen in cassava tissues. A polymerase chain reaction (PCR) test was developed for this pathogen. The PCR assay worked well for pathogen detection in extracts from leaf and stem lesions and the minimum number of cells that could be detected ranged from 3 × 102 to 104 CFU per ml. Nested-PCR worked well for Xam detection from naturally infected seeds. This technique was specific, sensitive, and rapid for detecting Xam in cassava true seeds. The highest detection level found was 1–2 viable cells per reaction. A dot-blot assay was developed by evaluating a 898 bp DNA fragment unique to Xam strains as a diagnostic DNA probe. The probe detected Xam strains in crude extracts of leaf and stem lesions, cassava fruits and sexual seeds that were naturally infected. Overall sensitivity of the dot-blot method was about103CFU per reaction. The dot-blot hybridization technique can be easily used for culture indexing. A monoclonal antibody (MAb) was also used for an enzyme-linked immunosorbent assay (ELISA) and tested with various infected tissues. Overall sensitivity of the method was about103CFU per reaction. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

14.
The propagation of cassava through true seeds (sexual seeds) rather than by clones is a promising option due to its manifold advantages such as enhancing the multiplication rate, keeping the dreaded cassava mosaic disease (CMD) under check, longer seed viability, ease of storage and transport. The high genetic heterogeneity and consequent variation among seedlings is the major stumbling block in sexual propagation. In the present study, a CMD resistant exotic accession MNga-1 and a promising cultivar Ambakadan with profuse fruit setting, seed output and male sterility were identified to be promising parents for the TCS programme. The rate of sexual propagation could be more than 20-fold over the traditional clonal propagation. Seed treatment with 1% KNO3 or 300 ppm GA promoted uniform seed germination and seedling vigour and reduced the transplanting period from 45 days after planting (DAS) to 30 DAS. Removal of taproots of seedlings while transplanting enhanced tuber development. Tuber yield of first clones (C1) was significantly superior to that of the seedlings. The dry matter content and starch output of seedlings and first clones were comparable to that of the commercial varieties. Similarly, the HCN and cooking quality of seedlings and first clones were at acceptable levels. In the open pollinated (OP) progenies of the Ambakadan the CMD infection increased drastically due to secondary spread of the pathogen. The hybrid progenies of Ambakadan and the CMD resistant line MNga-1 revealed higher percentage of CMD free seedlings and first clonal progenies in the evaluation trials conducted at CTCRI Thiruvananthapuram and ARS, Peddapuram during 2001–2002 and 2002–2003. Nearly homogeneous hybrid population resistant to CMD could be obtained by systematic roguing at seedling and first clonal stage.  相似文献   

15.
Crossing patterns were investigated in an experimental garden of ethnovarieties ofManihot esculenta (Euphorbiaceae) inPiracicaba, São Paulo, Brazil. A model of evolutionary dynamics for cassava presupposes genetic recombination by means of crossing within cassava gardens as a source that amplifies genetic diversity. Quantitative analysis of mating system parameters was performed using progeny arrays assayed for eight allozyme markers. The multilocus outcrossing rate (t m)estimate (0.915±0.04)revealed that outcrossing was prevalent, but that a low level of self-pollination also occurred. The multilocus outcrossing rate ranged from 0.69 to 1.00 among eight varieties. The high value found for the outcrossing rate indicates that the ethnovarieties studied are preferentially allogamous. Genetic recombination occurred through crossing within the cassava garden, in agreement with an assumption of the model of evolutionary dynamics for this species.  相似文献   

16.
An SSR-based molecular genetic map of cassava   总被引：7，自引：2，他引：7  
E. Okogbenin  J. Marin  M. Fregene 《Euphytica》2006,147(3):433-440
Summary Microsatellites or simple sequence repeats (SSR) are the markers of choice for molecular genetic mapping and marker-assisted selection in many crop species. A microsatellite-based linkage map of cassava was drawn using SSR markers and a F2 population consisting of 268 individuals. The F2 population was derived from selfing the genotype K150, an early yielding genotype from an F1 progeny from a cross between two non-inbred elite cassava varieties, TMS 30572 and CM 2177-2 from IITA and CIAT respectively. A set of 472 SSR markers, previously developed from cassava genomic and cDNA libraries, were screened for polymorphism in K150 and its parents TMS 30572 and CM 2177-2. One hundred and twenty two polymorphic SSR markers were identified and utilized for linkage analysis. The map has 100 markers spanning 1236.7 cM, distributed on 22 linkage groups with an average marker distance of 17.92 cM. Marker density across the genome was uniform. This is the first SSR based linkage map of cassava and represents an important step towards quantitative trait loci mapping and genetic analysis of complex traits in M. esculenta species in national research program and other institutes with minimal laboratory facilities. SSR markers reduce the time and cost of mapping quantitative trait loci (QTL) controlling traits of agronomic interest, and are of potential use for marker-assisted selection (MAS).  相似文献   

17.
Cassava root rot disease is an increasing problem in Africa where yield losses of about 80% have been recorded. We evaluated 290 African landraces and 306 improved genotypes from the germplasm collections of the International Institute of Tropical Agriculture (IITA), for sources of resistance using root slice laboratory assay. Disease severity was assessed quantitatively by direct percentage estimation (PS) and by use of a rating scale (RS). Both methods of assessment were compared for identification of variability in the germplasm, and genotypes were classified into response groups using an enlarged rank-sum method that combined the PS and RS assessments. The two scoring methods revealed continuous variation (P < 0.001) for resistance in the sets of germplasm. Disease assessments based on PS and RS were highly correlated in both the improved germplasm (r = 0.75) and the landraces (r = 0.72). Based on PS assessment, 50 improved genotypes (16.3%) and 53 landraces (18.3%) showed significantly lower disease scores than the resistant control. The rank-sum method separated each set of collections into highly resistant, resistant, moderately resistant, moderately susceptible, susceptible and highly susceptible groups. Fifty-nine improved genotypes (16.4%) and 61 African landraces (16.9%) were identified as either highly resistant or resistant. Generally, these genotypes exhibited resistance by limiting the growth of the pathogen (reduced amount of invaded surface area). This type of rate-reducing resistance is highly heritable and a quantitative trait which can be harnessed in breeding. Genotypes subsets were identified for further studies into the genetic basis of resistance to root rot disease.  相似文献   

18.
F. Lefèvre  A. Charrier 《Euphytica》1992,66(3):171-178
Summary Starch gel electrophoresis was used to assess isozyme polymorphism in two Manihot species. Crude extracts were obtained from leaves and pollen. Ten enzymes were examined for their polymorphism in a germplasm collection of 365 cultivated plus 109 wild accessions, mainly from Africa. The inheritance of these enzymes was examined using 13 intra and interspecific progenies. Seventeen polymorphic loci were found for the ten enzyme systems, with 59 alleles. All the markers showed disomic heredity and three linkage groups were identified.  相似文献   

19.
Twenty-two improved and local cassava genotypes were evaluated for their bacterial blight symptom types in reaction to infection by Xanthomonas axonopodis pv. manihotis under field conditions in the forest, forest savanna transition and wet savanna zones of Togo. High genotype × environment interactions in development of each symptom type were observed. Combining data on environments and genotypes, spot, blight and wilt symptoms were positively correlated. Analysing genotype reactions across environments, indications for independent mechanisms of resistance on leaf and stem level, varying by genotype, were found. Genotypes Main27 with resistance to spot and blight symptoms and TMS4(2)1425 with resistance to wilt symptoms are recommended to breeders to introgress their resistance characteristics. Significant negative correlations were generally observed between blight and wilt symptom development and root yield across ecozones, with blight being more important under lower, and wilt under higher inoculum pressure. Genotypes TMS30572, CVTM4, TMS92/0429 and TMS91/02316 showed low spot, blight and wilt symptoms combined with high root yield across ecozones.  相似文献   

20.
Summary To elucidate the role of leaf surface structures as first barriers to confer resistance to bacterial blight, leaf stomata and their occlusion with leaf waxes were studied in cassava genotypes. For the first time, cassava leaf waxes were quantitatively and qualitatively analysed. Comparing the susceptible and resistant standard genotypes BEN86052 and TMS30572, respectively, the total quantity of triterpenes was significantly higher in the resistant genotype, grown in three ecozones of Benin. In cuticular leaf waxes of seven cassava genotypes the triterpenes beta amyrins, epi-taraxerol, taraxerone and taraxerol were dominant constituents across genotypes, and alkanes (C25-C33) and acids (C30 and C32) occurred in minor concentrations. Comparing seven genotypes, no clear relation between resistance or ecozones and total quantities of the major wax constituents was observed. Only the highly resistant genotype TMS30572 showed high triterpene levels irrespective of ecozone. Scanning electron-microscopy revealed a regular distribution of waxes at the abaxial leaf surface, covering and occluding stomatal pores of susceptible and resistant genotypes, while on the adaxial leaf surface waxes were in form of crystalloids and did not occlude the stomata. The number of stomata on the abaxial surfaces was about 7–11 fold higher than on the adaxial surfaces, where stomata were located along the midrib and major veins. No significant differences in stomata number were observed between genotypes varying in resistance to bacterial blight. It is suggested, that stomata on the adaxial surface might be portals of entry for the bacteria.  相似文献   

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