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Groundnut Host Plant and Vector Aphid (Aphis craccivora) Interaction in the Transmission of Groundnut Rosette Disease as a Basis for Physiological Studies

Received: 19 January 2025     Accepted: 5 February 2025     Published: 20 February 2025
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Abstract

Groundnut (Arachis hypogaea L.) is an important food crop in sub-Saharan Africa. Among the major causes for low yields is the susceptibility of cultivated varieties to the Groundnut Rosette Disease (GRD). The Groundnut Rosette is a viral disease, the most destructive where groundnut is grown, that can lead to 100% yield loss. The objectives of the study were to; 1) investigate the effect of leaf colour and plant architecture on aphid colonization; 2) determine the relationship between aphid colonization and disease development. An experiment was carried out in the glasshouse during winter of the 2018/19 and 2019/2020 growing seasons. Sixteen (16) test genotypes with known field reaction to the groundnut rosette disease were used. The results for disease severity concur with field ratings as all genotypes rated resistant had severity score of <1.39 and all genotypes rated moderate resistant, had scores <1 while susceptible genotypes recorded scores > 2.8. All susceptible genotypes had high aphid population (40 aphids on average per plant) whereby CG 7 had the highest. The results clearly show that, genotypes with dark green colour attracted more aphids (52.6) than the light green. Plant architecture may play a role in the migration of aphids within plants but does not influence plant preference by aphids. Genotypes ICGV-SM 01514, ICGV-SM 06637 and ICGV-SM 07544 attracted minimal number of aphids and were resistant to the rosette disease, a similar behaviour to ICG 12991, that is known to be aphid resistant. It can be concluded that these 3 genotypes are resistant to aphids. Genotypes ICGV-SM 01709, ICGV-SM 03710, ICGV-SM 08503 and ICGV-SM 01731 had considerable infestation by aphids (>40) but did not show any signs of the rosette disease, a trait that is common with ICGV-SM 90704, a variety resistant to grounndut rosette virus (GRV strain), an implication that they are resistant to the virus. The valuable results about these genotypes forms a basis for further characterization of these genotypes using molecular markers to understand the physiological basis of the varied reaction to vector and disease incidence. Sequencing the genome of the aphid species on groundnut is crucial to inform the diversity of the vector and give insights on how microbial effector proteins, host targets and plant immune receptors co-evolve.

Published in Journal of Plant Sciences (Volume 13, Issue 1)
DOI 10.11648/j.jps.20251301.11
Page(s) 1-8
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2025. Published by Science Publishing Group

Keywords

Aphids, GRV, Genotypes, Characterization, Physiological

1. Introduction
Groundnut (Arachis hypogaea L.) is an important oil, food forage crop grown in many countries of sub-Saharan Africa. The average yields of 800 kg/ha is below potential and one of the reasons for low yields is the susceptibility of currently grown cultivars to the groundnut rosette disease (GRD) . The Rosette disease is known to be endemic to sub-Saharan Africa and its off-shore islands, including Madagascar. There are two main forms of the disease; chlorotic rosette and green rosette described based on symptoms. The disease is caused by a complex of three agents: Groundnut Rosette Virus (GRV), and its satellite RNA (sat RNA), and Groundnut Rosette Assistor Virus (GRAV). The three agents of the disease must be present in the host plant for successful transmission by the vector . Disease symptoms are largely due to sat RNA and variants of sat RNA are responsible for the different forms of rosette. The symptoms occur in two predominant forms, chlorotic and green rosette although other symptomatic forms have been reported. The groundnut aphid, Aphis craccivora, is the principal vector of the disease. Rosette disease has been and continues to be responsible for devastating losses to groundnut production in Africa .
According to reviews by , there is evidence for behavioural response of aphids to colours. This was proved from an experiment where aphids were exposed to a number of illuminated papers. It was found out that there was a considerable number of probing made by aphids on differently coloured and illuminated paper with the highest in orange, yellow and green, and low on red, grey and blue. This was classified as evidence for colour vision in aphids. With an extensive series of experiments, it was further demonstrated the effect of coloured stimuli on aphid landing in the field. Pure yellow without UV showed the strongest attraction for winged aphids, with orange, yellow-green and green following, whereas the aphids responded with low landing rates to red, blue, purple, white, grey and black. Current knowledge on epidemiology with respect to the predominant colours for groundnut; green, dark green and light green as well the general plant architecture is very scanty and yet these may be important factor for attracting or promoting migration of aphids. Such information may help shape groundnut breeding programs or to form the basis designing comprehensive disease management strategies.
The study was premised on the fact that field observations showed that most resistant genotypes are Virginia which are generally green to dark green in colour with bunched stem structures. The varieties that are light green in colour with an open stem architecture are Spanish or Valencia and often susceptible to groundnut rosette disease. However, whether these traits contribute to aphid attraction and eventually the observed disease reactions is not known. Further investigation is important to elucidate the doubts existing on host plant aphid relationship. Therefore, an experiment was carried out to; 1) investigate the effect of leaf colour and plant architecture on aphid colonization and 2) investigate whether aphid colonization translate into high disease incidence.
2. Materials and Methods
2.1. Test Lines
The experiment was established at ICRISAT Malawi glasshouses during winter of the 2018/2019 and 2019/2020 growing season. Sixteen (16) test genotypes with known field reaction to rosette of the three botanical groups of groundnuts; Virginia, Spanish and Valencia were obtained from the groundnut breeding program. These test lines included; CG 7, Chalimbana, JL 24, ICG 12991, ICGV-SM 01514, ICGV-SM 01709, ICGV-SM 01731, ICGV-SM 01739, ICGV-SM 03710, ICGV-SM 06637, ICGV-SM 06711, ICGV-SM 07544, ICGV-SM 07599, ICGV-SM 08503, ICGV-SM 90704 and ICGV-SM 99568. These varieties had also been evaluated under the Regional Groundnut Variety Trials (RGVT) with high rosette pressure using an infector row technique. Among them, six (6) of these materials had already been released in Malawi and often used as resistant (ICG 12991 (aphid resistant), ICGV-SM 90704 (GRV resistant) and ICGV-SM 99568 (moderate resistant)) and susceptible (JL 24, CG 7 and Chalimbana) checks. Each botanical group had genotypes classified as resistant, moderate resistant and susceptible using a 0-5 scoring scale where; 0-1.5 was resistant, 1.6-3.9 moderate resistant and 4-5 susceptible. These groups were further divided into two categories; 1) three groups based on the prevalent leaf colour for the groundnut varieties; light green, green and dark green and 2) the structural arrangement of the stems grouping them into bunch and open types (Table 1).
Table 1. Genotype characterization based on colour and architecture.

Colour

Stem structure

Light green

Green

Dark green

Bunch

Open

ICGV-SM 01514

ICGV-SM 01739

ICGV-SM 07599

ICGV-SM 01739

ICGV-SM 01514

ICG 12991

ICGV-SM 90704

ICGV-SM 08503

ICGV-SM 90704

ICG 12991

ICGV-SM 99568

ICGV-SM 01731

CG 7

ICGV-SM 01731

ICGV-SM 99568

JL 24

ICGV-SM 06637

ICGV-SM 03710

ICGV-SM 03710

JL 24

ICGV-SM 07544

ICGV-SM 6711

ICGV-SM 06637

Chalimbana

ICGV-SM 01709

ICGV-SM 01709

ICGV-SM 6711

Chalimbana

CG 7

ICGV-SM 07544

ICGV-SM 08503

ICGV-SM 07599

2.2. Experimental Layout and Aphid Inoculation
The experiments planted in a glasshouse were arranged in a Complete Randomized Design (CRD). There were three replications for each experiment. Each genotype had three pots per replication, three plants were planted in each pot, and eventually thinned to two (Figure 1). All test plants were flanked on one side with a row of JL 24, a rosette susceptible variety from the front of the bench to serve as the infector row technique used to transfer viruliferous aphids under field conditions. The infector row technique involves planting a test row of uninfected plants flanked on either side by a row of plants infested with aphids reared in glass house . This infector row technique is the only known method for rapid screening of large number of segregating populations and breeding lines for resistance to the groundnut rosette disease. Ninety-nine (99%) percent success rate in spreading the disease to susceptible plants has been recorded. Test plants were placed 30cm away from the infector row. Two weeks after emergence, the infector row (JL 24) was inoculated by placing three viruliferous aphids on each plant. There was no direct inoculation of aphids onto the test plants. Watering was done by pouring water straight onto the soil to avoid draining aphids off the plants.
Figure 1. Experiment site at ICRISAT Malawi.
Figure 2. Aphid colonization on test plants.
2.3. Management of the Experiment
Soils used in this experiment were collected from low lying virgin lands near Chitedze Research station and were sterilized via heat. Phosphorus fertilizer was applied as P2O5 at the rate of 200kg/ha. Before inoculation, all test and infector row plants were sprayed against fungal infection using BRAVO® 720 (contains chlorothalonil 720 g/l (Reg. no. L7005, Act no. 36 of 1947) of Syngenta Group Company. Once inoculation had been done, there was no more chemical spraying to avoid killing aphids. Plants were watered twice per day, in the morning and late afternoon through the base or directly onto the pot to avoid washing aphids from the leaves. Frequent monitoring was undertaken to ensure the experiments were weed free.
2.4. Data Collection
Data collected included; date of first colonisation by aphids, no of aphids per plant (collected twice a week for five weeks, date to first symptoms and rosette severity. Severity rating was done on a 0-5 scoring scale where; 0 - 1.5 was resistant, 1.6-3.9 moderate resistant 4-5 susceptible.
2.5. Statistical Analysis
Quantitative data was subjected to analysis of variance (ANOVA) using GenStat, 22nd edition (https://vsni.co.uk/software/genstat), to assess genotype and vector colonization differences and interaction effects on groundnut rosette disease development. The number of aphids was log transformed (log10) to normalize their distribution before subjecting them to ANOVA. Figures were generated using Microsoft excel. Where significant differences among variables were found, means were compared using Fishers Protected Least Significant Difference (LSD) at 5% level of probability or using the standard error of the difference of means (SED).
3. Results and Discussion
3.1. Aphid Colonization and Rosette Severity
Significant differences (P<0.05) were observed for aphid infestation as well as rosette severity on the test genotypes (Table 2). Results for severity concur with field ratings as all genotypes rated resistant had severity score of <1.39 and all genotypes rated moderate resistant, had scores <1 while susceptible genotypes recorded scores > 2.8. All susceptible genotypes; CG 7, JL 24, ICGV-SM 06711 and ICGV-SM 07599 had an average aphid population of 40 per 12 plants under observation. Among these varieties, CG 7 had the highest number of 124 followed by ICGV-SM 07599 with 117 aphids. The resistant and moderate resistant genotypes constituting 68% of the test plants had the lowest number (< 15). Genotype ICG 12991 attracted the least number of aphids confirming its status as an aphid resistant variety. Only one genotype, ICGV-SM 01709 that was moderate resistant in the field, had high aphid population similar to that of the susceptible genotypes.
The implication of the results was that, the ability of host plants to allow minimal aphid colonization is an important factor for plants to check disease progression. It may also infer that, attracting high aphid population may result into inability for a plant to resist infection, and this concur with findings by , who reported that resistance to groundnut rosette virus is controlled by two recessive genes responsible for the production of antiviral substances by plants, but when these plants are subjected to massive inoculum pressure from viruliferous aphids, the resistant plants could be infected with GRV. Genotype ICGV-SM 01709 may be an example of those genotypes that produce sufficient amounts of antiviral substance hence being resistant despite the heavy aphid load.
Table 2. Aphid population infestation by genotypes.

Genotype

Description

Aphid accumulation

Disease severity

CG 7

Susceptible

123.5

2.9

Chalimbana

Susceptible

40.4

2.8

ICG 12991

Resistant

1.9

1

ICGV-SM 01514

Resistant

3.8

1

ICGV-SM 01709

Moderate resistant

42.8

1

ICGV-SM 01731

Resistant

11.3

1

ICGV-SM 01739

Moderate resistant

6.0

1

ICGV-SM 03710

Resistant

14.8

1

ICGV-SM 06637

Moderate resistant

3.2

3.8

ICGV-SM 06711

Susceptible

67.3

3

ICGV-SM 07544

Moderate resistant

4.3

1

ICGV-SM 07599

Susceptible

116.7

4.1

ICGV-SM 08503

Resistant

11.6

1

ICGV-SM 90704

Resistant

6.7

1.4

ICGV-SM 99568

Moderate resistant

5.15

1

JL 24

Susceptible

105.7

3.7

Mean

35.3

1.8

Fpr

<0.001

<0.001

SED

13.86

0.3751

3.2. Trend of Aphid Infestation on Six Selected Genotypes
Aphids appeared on both groups (three (3) resistant and three (3) susceptible genotypes) in the second week after inoculating the infector rows. At the onset, more aphids were recorded on ICGV-SM 08503, ICGV-SM 01514 and ICG 12991, the three resistant genotypes than the susceptible ones (Figure 3). This trend was followed by a sharp decline in the level of aphids for the genotypes stabilizing for two weeks at low levels before a second wave of high population especially among the susceptible genotypes. Susceptible genotypes had a high population of aphids throughout the experimental period. Only ICGV-SM 01514 from the resistant group attracted more aphids by the fith week of experimentation, but reduced quickly after two weeks.
Highly contrasting trends were observed bewteen JL 24, a susceptible check and ICG 1299, an aphid resistant check. The aphid population declined sharply 14 Days After Inoculation (DAI) for ICG 12991 leveling off to zero confirming its status as an aphid resistant genotype. The study revealed two cycles of aphid population in JL 24, with the first cycle ending 21 DAI and high population building up at 28 DAI. This shows that JL 24 is an aphid susceptible genotypes. These observations tally with findings by , who carried out experiments exposing groundnut genotypes including ICGV-SM 90704, JL 24 and ICG 12991 to viruliferous aphids, whereby 10 DAI, increased numbers of aphids were observed on ICGVSM 90704 and JL 24 with an average of 93 and 96 aphids per plant respectively. In contrast, aphid number on ICG 12991 fell from 5 to 3 per plant. The increased number of aphids on both ICGV SM 90704 and JL 24 were an indication of susceptibility to aphids while the reduction on ICG 12991 was an indication of resistance to aphids.
Figure 3. Aphid trend performance in susceptible and resistant genotypes.
3.3. Aphid and Severity Levels on Susceptible and Resistant Genotypes
The six (6) genotypes; three susceptible and three resistant, were compared to determine the general trend on aphid population and rosette disease incidence. Significant differences, P<0.05 in reaction to rosette disease for the three groups were observed (Table 3). Resistant genotypes had fewer aphid population on average (8.4) than the susceptible (90.7), implying there is underlying mechanisms in resistant genotypes that limit aphid colonization. Further observations show geonotypes being classified into three groups in relation to aphid and disease incidence namely; 1) resistant with low aphid population, 2) resistant with higher levels of aphid populaton and 3) susceptible without regard to levels of aphids (Figure 4). Genotypes CG7, Chalimbana and JL 24 had high levels of aphids that translated into high levels of rosette severity. The increase in the number of aphids hovever did not translate into high disease severity in some genotypes, for example, ICGV-SM 90704, a GRV resistant variety as reported by , that had considerable levels of aphids with low rosette disease severity. Four (4) other pipeline genotypes; ICGV-SM 01709, ICGV-SM 03710, ICGV-SM 08503 and ICGV-SM 01731 shared this trait, an implication that these genotypes may be confering resistance by dealing with the virus itself (GRV) or its trasmission mechanism by producing antiviral biochemical components that enable it to survive high pressure. The lowest number of aphids were on ICGV-SM 01514, ICGV-SM 06637 and ICGV-SM 07544, similar to ICG 12991 a known aphid resistant genotype as confirmed by , thus it may be concluded these are aphid resistant genotypes.
Table 3. Effect of genotype on aphid colonization by diseases reaction category.

Reaction to rosette

Aphid accumulation

Resistant genotypes

8.4

Moderate resistant genotypes

12.3

Susceptible genotypes

90.7

Mean

35.3

Fpr

<0.001

SED

7.22

It is imperative that resistance associated with low aphid population may be through impediment of colonisation and multiplication of aphids, while resistance despite high aphid population is likely due to internal mechanisms dealing with the three agents of the groundnut rosette disease. The results from the current study concur with observations by that suggested resistance mechanisms in groundnut deter colonization by immigrant alatae and also reduce their fecundity.
Figure 4. Relationship between aphid colonization and rosette severity.
3.4. Relationship Between Host Physical Characteristis and Aphid Infestation
Significant differences P < 0.05, were observed for aphid population with respect to colour and plant architecture among the tested genotypes (Table 4). The results indicated that aphids were more attracted to dark green followed by green and then light green colors. This corroborates with findings by , who reported strongest attraction for winged aphids by orange, yellow-green and green background, as opposed to red, blue, purple, white, grey and black colours.
Table 4. Relationship between colour and plant architecture on aphid population.

Colour of genotypes

Aphid population

Plant architecture

Aphid population

Dark green

52.6

Bunch

58.54

Green

29.8

Open

18

Light green

29.2

Mean

35.3

Mean

38.3

Fpr

0.002

Fpr

<0.001

SED

9.45

SED

11.15

The results revealed that plant architecture does not play any role on attraction of aphids and/or selection of plants by aphids. The results show that the bunch types were either dark green or green, thus had more aphids, though colour did not necessarily influence groundnut rosette disease incidence and severity (Figure 4). Overall, the results show that there was no significant correlation (-0.005) between levels of aphid population and groundnut rosette severity among the genotypes, though within the light green coloured genotypes, increase in aphid population resulted into an increase in rosette severity, and this was so for the susceptible genotypes only. High severity in this group however, was attained even with relatively low level of aphids with the exception of ICG 12991, an aphid resistant check and ICGV-SM 01514, a new variety that has given responses similar to the aphid resistant check. These insights are the first step towards efforts to exploit more approaches to understand molecular mechanisms for sustainable aphid control strategies in tandem with proposal by .
4. Conclusions
Based on the reuslts from the study, aphids get attracted to genotypes with greener than lighter leaf colour. However it was evident that colour had no influence on the reaction to the grounndut rosette diease. These findings disagree with general blanket observation in the fields that most light green genotypes were susceptible due to their ability to attract aphids. It is therefore important that greener genotypes that are susceptible to the rosette disease require good field management to avoid or minimise aphid populations. In addition, it was evident that plant architecture does not have any role on attraction of aphids or selection of plants by aphids. We conclude that genotypes; ICGV-SM 01514, ICGV-SM 06637 and ICGV-SM 07544 are aphid resistant similar to ICG 12991, while ICGV-SM 01709, ICGV-SM 03710, ICGV-SM 08503 and ICGV-SM 01731 are GRV resistant since their reaction was simmilar to that of ICGV-SM 90704, a key genetic resource in breeding for resistance. The genotype ICGV-SM 01709 proved to be resistant to the rosette diseases, despite being highly infested by aphids, the vector for the disease. This may be a helpful trait for breeders as it is an example of genotypes that produce sufficient amounts of antiviral substance as their resistance mechanism. The genotype however may be a good source of inoculum and not advisable to have it planted close to susceptible varieties. The results opens a field of enquiry as a basis for further research, whereby there is need for further characterization of these sets of genotypes using molecular and biochemical markers to understand the physiological basis of the varied reaction to vector and disease incidence among the genotypes. This will help in understanding the biochemical basis of resistance and or susceptibility to the groundnut rosette disease. Further, sequencing the genome of the aphid species on groundnut is crucial to inform the diversity of the vector and give insights on how microbial effector proteins, host targets and plant immune receptors co-evolve.
Abbreviations

GRD

Groundnut Rosette Disease

GRV

Groundnut Rosette Virus

DAI

Days after Inoculation

Acknowledgments
The authors thank research technicians for their support and engagement in the work contributing to the Eastern and Southern Africa Groundnut Breeding Program of the International Crops Research Institute for the Semi-Arid Tropics (ICRISAT).
Author Contributions
Mwololo James: Conceptualization, Data curation, Methodology, Supervision, Validation, Writing – original draft, Writing – review & editing
Njoroge Samuel: Validation, Writing – review & editing
Munthali Wills: Data curation, Writing – original draft, Writing – review & editing
Okori Patrick: Funding acquisition, Project administration
Funding
The study was made possible through the generous support of the Tropical Legumes III project funded by Bill and Melinda Gates Foundation.
Data Availability Statement
The data is available from the corresponding author upon reasonable request.
Conflicts of Interest
There is no conflict of interest reported by authors.
References
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[2] Murant, A. F. and Kumar, I. K. 1990. Different variants of the satellite RNA of groundnut rosette virus are responsible for the chlorotic and green forms of groundnut rosette diseases. Annals of applied Biology 117: 85–92.
[3] Barbara, W, Aleksandra O. 2024. Small non‐coding satellite RNAs – the ‘game changers’ at the virus–host plant interaction? Biological Reviews, 100: 19-34.
[4] Subrahmanyam, P. and Van Der Merwe, P. J. A. 2003. Management of rosette, the past, present and the future. Chitedze Agriculture Research Station, Lilongwe Malawi.
[5] Thomas, F. Döring, 2014. How aphids find their host plants, and how they don't.
[6] Bock, K. R. and Nigam, S. N. 1988. Methodology of groundnut rosette resistance screening and vector-ecology studies in Malawi. In: Coordinated research on Groundnut Rosette Virus Disease: Summary Proceedings of the Consultative Group Meeting, 8-10 mar 1987, Lilongwe, Malawi.
[7] Reshmi, K. R., B. Baisakh, B., Tripathy, S. K., Devraj, l., Pradhan, B., Mishra, M. K., Salini, K. and Mohanty, M. R. 2019. Screening for Mungbean Yellow Mosaic Virus Resistance in Green Gram (Vigna radiata (L.) Wilczek). International Journal of Current Microbiology and Applied Sciences 8: 666-670.
[8] Berchoux, C. de. 1960. La rosette de l'arachide en Haute-Volta. Comportement des lignes resistantes. Oleagineux 15: 229-233.
[9] Nigam, S. N. and Bock, K. R. 1990. Inheritance of Resistance to Rosette Virus Disease in Groundnut. Annals of Applied Biology 117: 553-560.
[10] Van der Merwe, P. J. A., Subrahmanyam, P., Kimmins, F. M. and Willekens, J. 2001. Mechanisms of Resistance to Groundnut Rosette. International Crops Research Institute for the Semi-Arid Tropics.
[11] Minja, E. M., van der M e r w e, P. J. A. and Subrahmanyam, P. 1999. Screening groundnut breeding lines for resistance to aphids. Aphis craccivora Koch. International Arachis Newsletter 19: 21-23.
[12] Subrahmanyam, P., van der M e r w e, P. J. A., Reddy, L. J., Chiyembekeza, A. J., Kimmins, F. M. and Naidu, R. A. 2000. Identification of elite short-duration rosette resistant lines in world germplasm collections. International Arachis Newsletter 20: 46-50.
[13] Amin, P. W. 1985. Resistance of wild species of groundnut to insect and mite pests. In Cytogenetics of Arachis. Proceedings of the International Workshop, 31 Oct -2 Nov 1983, ICRISAT Center, India. Patancheru, Andhra Pradesh 502 324, India: International Crops.
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    James, M., Samuel, N., Wills, M., Patrick, O. (2025). Groundnut Host Plant and Vector Aphid (Aphis craccivora) Interaction in the Transmission of Groundnut Rosette Disease as a Basis for Physiological Studies. Journal of Plant Sciences, 13(1), 1-8. https://doi.org/10.11648/j.jps.20251301.11

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    James, M.; Samuel, N.; Wills, M.; Patrick, O. Groundnut Host Plant and Vector Aphid (Aphis craccivora) Interaction in the Transmission of Groundnut Rosette Disease as a Basis for Physiological Studies. J. Plant Sci. 2025, 13(1), 1-8. doi: 10.11648/j.jps.20251301.11

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    AMA Style

    James M, Samuel N, Wills M, Patrick O. Groundnut Host Plant and Vector Aphid (Aphis craccivora) Interaction in the Transmission of Groundnut Rosette Disease as a Basis for Physiological Studies. J Plant Sci. 2025;13(1):1-8. doi: 10.11648/j.jps.20251301.11

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  • @article{10.11648/j.jps.20251301.11,
      author = {Mwololo James and Njoroge Samuel and Munthali Wills and Okori Patrick},
      title = {Groundnut Host Plant and Vector Aphid (Aphis craccivora) Interaction in the Transmission of Groundnut Rosette Disease as a Basis for Physiological Studies
    },
      journal = {Journal of Plant Sciences},
      volume = {13},
      number = {1},
      pages = {1-8},
      doi = {10.11648/j.jps.20251301.11},
      url = {https://doi.org/10.11648/j.jps.20251301.11},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.jps.20251301.11},
      abstract = {Groundnut (Arachis hypogaea L.) is an important food crop in sub-Saharan Africa. Among the major causes for low yields is the susceptibility of cultivated varieties to the Groundnut Rosette Disease (GRD). The Groundnut Rosette is a viral disease, the most destructive where groundnut is grown, that can lead to 100% yield loss. The objectives of the study were to; 1) investigate the effect of leaf colour and plant architecture on aphid colonization; 2) determine the relationship between aphid colonization and disease development. An experiment was carried out in the glasshouse during winter of the 2018/19 and 2019/2020 growing seasons. Sixteen (16) test genotypes with known field reaction to the groundnut rosette disease were used. The results for disease severity concur with field ratings as all genotypes rated resistant had severity score of  2.8. All susceptible genotypes had high aphid population (40 aphids on average per plant) whereby CG 7 had the highest. The results clearly show that, genotypes with dark green colour attracted more aphids (52.6) than the light green. Plant architecture may play a role in the migration of aphids within plants but does not influence plant preference by aphids. Genotypes ICGV-SM 01514, ICGV-SM 06637 and ICGV-SM 07544 attracted minimal number of aphids and were resistant to the rosette disease, a similar behaviour to ICG 12991, that is known to be aphid resistant. It can be concluded that these 3 genotypes are resistant to aphids. Genotypes ICGV-SM 01709, ICGV-SM 03710, ICGV-SM 08503 and ICGV-SM 01731 had considerable infestation by aphids (>40) but did not show any signs of the rosette disease, a trait that is common with ICGV-SM 90704, a variety resistant to grounndut rosette virus (GRV strain), an implication that they are resistant to the virus. The valuable results about these genotypes forms a basis for further characterization of these genotypes using molecular markers to understand the physiological basis of the varied reaction to vector and disease incidence. Sequencing the genome of the aphid species on groundnut is crucial to inform the diversity of the vector and give insights on how microbial effector proteins, host targets and plant immune receptors co-evolve.
    },
     year = {2025}
    }
    

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  • TY  - JOUR
    T1  - Groundnut Host Plant and Vector Aphid (Aphis craccivora) Interaction in the Transmission of Groundnut Rosette Disease as a Basis for Physiological Studies
    
    AU  - Mwololo James
    AU  - Njoroge Samuel
    AU  - Munthali Wills
    AU  - Okori Patrick
    Y1  - 2025/02/20
    PY  - 2025
    N1  - https://doi.org/10.11648/j.jps.20251301.11
    DO  - 10.11648/j.jps.20251301.11
    T2  - Journal of Plant Sciences
    JF  - Journal of Plant Sciences
    JO  - Journal of Plant Sciences
    SP  - 1
    EP  - 8
    PB  - Science Publishing Group
    SN  - 2331-0731
    UR  - https://doi.org/10.11648/j.jps.20251301.11
    AB  - Groundnut (Arachis hypogaea L.) is an important food crop in sub-Saharan Africa. Among the major causes for low yields is the susceptibility of cultivated varieties to the Groundnut Rosette Disease (GRD). The Groundnut Rosette is a viral disease, the most destructive where groundnut is grown, that can lead to 100% yield loss. The objectives of the study were to; 1) investigate the effect of leaf colour and plant architecture on aphid colonization; 2) determine the relationship between aphid colonization and disease development. An experiment was carried out in the glasshouse during winter of the 2018/19 and 2019/2020 growing seasons. Sixteen (16) test genotypes with known field reaction to the groundnut rosette disease were used. The results for disease severity concur with field ratings as all genotypes rated resistant had severity score of  2.8. All susceptible genotypes had high aphid population (40 aphids on average per plant) whereby CG 7 had the highest. The results clearly show that, genotypes with dark green colour attracted more aphids (52.6) than the light green. Plant architecture may play a role in the migration of aphids within plants but does not influence plant preference by aphids. Genotypes ICGV-SM 01514, ICGV-SM 06637 and ICGV-SM 07544 attracted minimal number of aphids and were resistant to the rosette disease, a similar behaviour to ICG 12991, that is known to be aphid resistant. It can be concluded that these 3 genotypes are resistant to aphids. Genotypes ICGV-SM 01709, ICGV-SM 03710, ICGV-SM 08503 and ICGV-SM 01731 had considerable infestation by aphids (>40) but did not show any signs of the rosette disease, a trait that is common with ICGV-SM 90704, a variety resistant to grounndut rosette virus (GRV strain), an implication that they are resistant to the virus. The valuable results about these genotypes forms a basis for further characterization of these genotypes using molecular markers to understand the physiological basis of the varied reaction to vector and disease incidence. Sequencing the genome of the aphid species on groundnut is crucial to inform the diversity of the vector and give insights on how microbial effector proteins, host targets and plant immune receptors co-evolve.
    
    VL  - 13
    IS  - 1
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    1. 1. Introduction
    2. 2. Materials and Methods
    3. 3. Results and Discussion
    4. 4. Conclusions
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