Literature DB >> 35923212

Cassava mosaic disease (CMD) in Benin: Incidence, severity and its whitefly abundance from field surveys in 2020.

Jerome Anani Houngue1, Serge Sètondji Houédjissin1, Corneille Ahanhanzo1, Justin S Pita2, Mélaine S Ella Houndénoukon3, Martine Zandjanakou-Tachin3.   

Abstract

Cassava mosaic disease (CMD) is the main threat to cassava (Manihot esculenta Crantz) production in Benin. This study was conducted to assess CMD incidence, disease severity, and adult whitefly (Bemisia tabaci) populations in 11 regions of Benin. A total of 180 cassava fields across the country were assessed during June-December 2020 following the harmonized protocol of the Central and West African Virus Epidemiology program. Based on symptoms observation, CMD was present in all surveyed fields in Ouémé and Alibori regions. The highest disease incidence levels were observed in Malanville (100%), Kpomassè (86.67%), Kandi and Zagnanado (both 81.67%), Ségbanan (80%), and Avrankou (76.67%) districts. The highest mean severity scores were in Couffo (3.68), Mono (3.63), and Atlantique (3.33) regions, while the lowest was in Alibori (2.37). Adult whitefly populations (mean number/plant) were highest in Couffo (15.88) and Mono (13.00) regions and lowest in Donga (0.06). Significant relationships were found between CMD severity and whitefly abundance (P = 0.0010) but there was no significant relationship between whitefly numbers and CMD incidence (P = 0.0577). These findings indicate that CMD has expanded its range across Benin. They also provide a basis for designing a response strategy for the control of cassava virus diseases such as CMD.
© 2022 The Authors.

Entities:  

Keywords:  ACMV, African cassava mosaic virus; Bemisia tabaci; CMD symptoms; CMD, cassava mosaic disease; Cassava mosaic virus; EACMV, East African cassava mosaic virus; Manihot esculenta; Virus vector

Year:  2022        PMID: 35923212      PMCID: PMC9168543          DOI: 10.1016/j.cropro.2022.106007

Source DB:  PubMed          Journal:  Crop Prot        ISSN: 0261-2194            Impact factor:   3.036


Introduction

Cassava (Manihot esculenta Crantz) is one of the most important root crops in Africa as well as for millions of people in the tropics worldwide (Legg, 1999). This importance can be attributed to the ability of cassava to thrive in adverse climatic conditions and poor soils (Ntawuruhunga et al., 2007), thus making it an ideal food security crop in the tropics. It is the second most commonly crop grown after maize in Benin but it is the most important plant in multi-crop systems. It is found in a wide range of markets and provides a stable source of income and food for many households (Houngue et al., 2018). The average cassava yield in Benin is 14 t/ha (FAOSTAT, 2021), which is lower than the estimated potential of 80 t/ha (FAO, 2013). This lower yield may be due to abiotic and biotic factors that affect cassava cultivation including cassava diseases. Cassava diseases are an important factor as they prevail even with Benin's acceptable agricultural biotic conditions. Several diseases hamper cassava production, but the most important ones are virus-related; in Benin, cassava mosaic disease (CMD) is the most serious (Sseruwagi et al., 2004). This disease of cassava is caused by cassava mosaic begomoviruses (genus Begomovirus, family Geminiviridae). It is transmitted by whitefly (Bemisia tabaci) and perpetuated through infected cuttings, which is the usual crop propagation method (Fauquet et al., 2005). To date, 11 species of cassava mosaic viruses have been described and cause disease in Africa and the Indian sub-continent (Patil and Fauquet, 2009; Legg et al., 2015; Fondong, 2017). Cassava viruses may cause 20–95% yield losses; their effects are more severe when plants are infected in early growth stages than in later stages (Torkpo et al., 2018). The disease is manifested by leaf mosaic patterns, leaf reduction, and leaf chlorosis, followed by plant dieback, thereby causing important economic losses for farmers (Thresh et al., 1997). Cassava viruses exhibit diverse infection dynamics such as symptom expression, progression, recovery, severity, and host range (Bull et al., 2007; Patil and Fauquet, 2009); symptoms can vary among leaves, shoots, and plants within the same cassava variety. This variation in symptoms may depend on virus strain, virus species, host plant susceptibility, plant age, and environmental factors, such as soil fertility and soil moisture availability (Hillocks and Thresh, 2000). Furthermore, high disease incidence is closely related to the use of infected cuttings and density of whitefly populations in fields (Houngue et al., 2019b), whereas high severity may be due to a high concentration of virus in plants (Tsai et al., 2022). Previous studies on CMD have been limited by the fact that they were conducted within the borders of a single country raising issues related to small sample sizes, incomplete/missing data, inadequate methods to collect/store/process data, inadequate statistical methods selected to analyze the data among others. Central and West African Virus Epidemiology (WAVE) program have attempted to address these limitations by harmonizing a data collection protocol across 10 Central and West African countries. Thus, the data was collected and stored-edge database that contains the most comprehensive set of data on CMD, allowing for more thorough investigations and development of risk mitigation strategies. High disease incidence, disease severity, and abundant whitefly populations in farmers' fields throughout Benin were found in 2015 and 2017 together with indications of the viruses possibly present (unpublished data). With the potential risk of contamination and propagation of the redoubtable EACMV-UG (East African cassava mosaic virus-Uganda) to new areas of cassava production, there was a need for an extensive survey to assess the current status of CMD in Benin. The aim of this survey was first to provide an updated status of CMD in Benin including incidence, symptom severity, and infection type; and second to assess adult whitefly populations in cassava fields in Benin.

Materials and methods

Survey locations

The study was carried out in 72 districts across 11 cassava-producing regions in Benin (Fig. 1). These regions have a rainfall range of 700–1500 mm per year and their soils are suitable for cassava cultivation. These regions are within three climatic zones, the Sudanian (I), Sudano-Guinean (II), and Guinean (III) zones (Fig. 1):
Fig. 1

Climatic zones of Benin.

Zone I is characterized by 950–1300 mm of annual rainfall with one rainy season and average temperature of 17–33 °C and relative humidity of 20–47%; Zone II is characterized by 1200 mm of annual rainfall with two rainy and dry seasons. The temperature average is 22.5–35.2 °C and relative humidity is 30–83%; Zone III is characterized by 950–1500 mm annual rainfall with two rainy and dry seasons. Annual average temperature is 24–31 °C and relative humidity is 58–95% (Afloukou et al., 2020). Climatic zones of Benin. Seven of the regions surveyed are major cassava-producing regions: Mono, Couffo, Atlantique, Ouémé, Plateau, Zou, and Collines.

Survey method

Using the harmonized WAVE sampling protocol, 72 districts in 11 regions, and a total of 180 fields were surveyed in Benin between June and December 2020 (Table 1). The surveyed fields were approximately 10 km apart, depending on the availability of fields on the accessible roads. Thirty cassava plants aged 3–6 months were randomly examined along two diagonals in an “X” pattern in each field and 15 plants were selected along each diagonal.
Table 1

Characteristics of regions and districts surveyed.

RegionsSurveyed districtsGeographical locationClimate zonesMajor crops
AliboriMalanville, Kandi, Ségbanan, Banikouara, GogounouNorth-EstISorghum, maize, rice, cotton
AtacoraKérou, Pehounco, Kouandé, Natitingou, Toukountouna, Tanguiéta, Matéri, Boukoumbé, CoblyNorth-westISorghum, maize, yam, cotton, cassava
AtlantiqueKpomassè, Ouidah, Toffo, Allada, Zè, Abomey-Calavi, Torri-Bossito,South-centralIIIPineapple, maize, tomato, cassava
BorgouTchaourou, Parakou, N'dali, Bemberèkè, Pèrèrè, Nikki, KalaléNorth-EstI and IICereal, yam, cassava, cotton
CollinesDassa, Glazoué, Savè, Ouèssè, SavalouBantèCentralIICereal, cassava, yam, cotton
CouffoDogbo, Aplahoué, Klouékanmè, Toviclin, DjakotomeySouth-EstII and IIIMaize, cassava, cowpea, cotton
DongaCopargo, Djougou, Ouaké, BassilaNorth-WestI and IIMaize, cassava, cowpea, cotton
MonoCome, Bopa, Houéyogbé, Grang-Popo, Athiémé, LokossaSouth-EstIIIMaize, cassava, cowpea, tomato, pepper
OuéméSèmè-Kpodji, Porto-Novo, Adjarra, Avrankou, Bonou, Adjohoun, Dangbo, Akpro-MissérétéSouth-WestIIIMaize, cassava, groundnut, tomato, pepper
PlateauSakété, Ifangni, Adjaouèrè, Pobè, KétouSouth-WestII and IIICassava, yam, maize, groundnut, tomato, pepper
ZouOuinhi, Zagnanado, Covè, Zakpota, Djidja, Abomey, Agbangnizoun, Bohicon, ZogbodomeyCentralII and IIIMaize, cassava, groundnut, bean, tomato, pepper
Characteristics of regions and districts surveyed.

Data collection and recording

Field data were recorded in accordance with the WAVE survey protocol. Four leaf samples per field were collected and stored in a herbarium press. The samples were labeled with an identifier composed of field and plant number and collection date. Cuttings were taken from each sampled plant and grown under greenhouse conditions in 1-L black polythene bags for observation of disease symptom expression. In each field, whiteflies were counted on the five apical leaves of the plants examined. They were collected using an aspirator and stored in Eppendorf tubes containing 70% ethanol (Sseruwagi et al., 2004). Data were recorded using a tablet and a data collection application (built in iForm 9.12.7) which was developed for the WAVE program by the University of Cambridge, UK's Epidemiological Modelling Group. The data were then uploaded from the tablet to iForm's cloud-based database and then integrated into the WAVE Cube multi-dimensional database – according to the WAVE survey protocols (Soro et al., 2021). Information recorded included cassava plant details as well as the location coordinates (latitude and longitude), and altitude of fields recorded using a global positioning system (Garmin eTrex, Summit HC). When recording disease information, CMD severity was assessed based on a severity scale with range 1–5 as defined by the International Institute of Tropical Agriculture (IITA): 1, absence of infection; 2, mild infection; 3, moderate infection; 4, severe infection; and 5, very severe infection (IITA, 1990). In each field, we recorded the adult whitefly population (on the top five leaves), the number of visible cassava fields nearby, and the size of the field. The CMD incidence was determined by the proportion of diseased plants expressed as a percentage of the total number of plants assessed per field. When determining severity, asymptomatic plants (score 1) were excluded from calculations to avoid the underestimation of the disease severity; thus field severity analysis used data on infected plants only (scores 2–5) (Sseruwagi et al., 2004). Whiteflies were counted on the five top apical leaves of the 30 plants evaluated in each field, and the mean whitefly number was expressed as the total number of whiteflies in the field divided by 30.

Data processing

Data stored in the WAVE Cube could be visualized at plant, field, district and region levels as tables, graphs, or histograms to assist our analysis. Geographic coordinates (longitude and latitude) were used to map the geographic distribution of CMD, incidence, and severity in Benin. Disease incidence and severity maps were produced by means of Microsoft's Power BI tool and associated map-generating software, using the coordinates stored in the Cube. Means of CMD incidence and adult whitefly population were presented in tables and histograms. The means of incidence, severity, and adult whitefly numbers were compared using XLSTAT™ one-way analysis of variance. Regression analyses were run to examine the relationships between whitefly number and CMD incidence and severity.

Results

CMD symptoms assessment

CMD was observed in 145 of the 180 fields surveyed (80.55%). The disease prevalence was highest in Ouémé and Alibori regions (100%), moderate in Donga (66.67%), and lowest in Couffo (33.33%) regions (Table 2). Both mild and severe CMD symptoms were observed in the cassava fields surveyed. Symptoms comprising chlorotic blotches, leaf distortion, and mosaic were observed in eight regions: Alibori, Atacora, Atlantique, Borgou, Collines, Donga, Ouémé, and Plateau (Fig. 2).
Table 2

Fields showing CMD-infected fields by region.

Regions surveyedNumber of surveyed fieldsNumber of infected fieldsInfected fields (%)
Alibori88100.00
Atacora171270.59
Atlantique151173.33
Borgou252288.00
Collines262180.77
Donga9666.67
Couffo12433.33
Mono151280.00
Ouémé1010100.00
Plateau222195.45
Zou211885.71
Total18014580.56
Fig. 2

CMD symptoms in the surveyed fields: A, asymptomatic; B, mild infection; C, moderate infection; D, severe infection; and E, very severe infection.

Fields showing CMD-infected fields by region. CMD symptoms in the surveyed fields: A, asymptomatic; B, mild infection; C, moderate infection; D, severe infection; and E, very severe infection.

CMD incidence

Disease incidence differed significantly (P < 0.0001) among the 11 regions (Table 3). Disease incidence range was 9.44–74.58% among regions (Table 3). The highest disease incidence (74.58%) was found in Alibori region whereas the lowest (9.44%) was in Couffo. Moderate disease incidence levels of range 25–50% were found in seven regions (Atlantique, Borgou, Collines, Donga, Ouémé, Plateau, and Zou), while mean disease incidence of 0–25% was found in three regions (Atacora, Mono, and Couffo). Kandi and Malanville districts in Alibori region presented severe disease incidence of 81.67% and 100%, respectively (Table 3).
Table 3

CMD incidence in the regions and districts surveyed.

RegionsDistrictsNumber of fieldsNumber of plants evaluatedNumber of CMD-infected plantsCMD incidence (%)
AliboriMalanville13030100.00
Kandi2604981.67
Ségbanan2604880.00
Banikouara2604575.00
Gogounou130723.33
Mean incidence74.58
AtacoraKérou1302170.00
Pehounco3903033.33
Kouandé41201113.33
Natitingou26085.00
Toukountouna26011.67
Tanguiéta13000.00
Matéri26058.33
Boukoumbé13013.33
Cobly1301963.33
Mean incidence18.82
AtlantiqueKpomassè1305286.67
Ouidah3901921.11
Toffo260815.00
Allada2602135.00
2603050.00
Abomey-Calavi2602745.00
Torri-Bossito39005.56
Mean incidence30.44
BorgouTchaourou927013359.63
Parakou2605748.33
N'dali41204840.00
Bembèrèkè130710.00
Nikki61806536.11
Pèrèrè13000.00
Kalalé2601016.67
Mean incidence42.80
CollinesDassa41205124.29
Glazoué3902831.11
Savè41203121.67
Ouèssè41206351.67
Savalou72106530.48
Bantè41206454.17

Mean incidence



34.36
Regions
Districts
Number of fields
Number of plants evaluated
Number of CMD-infected plants
CMD incidence (%)
CouffoDogbo26046.67
Aplahoué41201815.00
Klouékanmè26011.67
Toviclin2601118.33
Djakotomey26000.00
Mean incidence9.44
DongaCopargo26000.00
Djougou2601118.33
Ouaké2602033.33
Bassila3904044.44
Mean incidence26.30
MonoCome2602440.00
Bopa2601423.33
Houéyogbé2602846.67
Grand-Popo39022.22
Athiémé3901820.00
Lokossa13000.00
Mean incidence24.22
OuéméSèmè-Kpodji2603253.33
Porto-Novo130310.00
Adjarra1302273.33
Avrankou1302376.67
Bonou2602745.00
Adjohoun130620.00
Dangbo1301446.67
Akpro-missérété130723.33
Mean incidence45.33
PlateauSakété41206856.67
Ifangni3905864.44
Adja-ouèrè2601015.00
Pobè3901626.67
Kétou92709836.67
Mean incidence39.24
ZouOuinhi3905965.56
Zagnanado2605081.67
Covè3904651.11
Zakpota3905055.56
Djidja41201210.00
Abomey1301550.00
Agbangnizoun26000.00
Bohicon130930.00
Zogbodomey3901112.22
Mean incidence35.87
P-valueDistricts0.211
Regions<0.0001
CMD incidence in the regions and districts surveyed. We found low CMD incidence (0–25%) in 51 cassava fields, medium incidence (25–50%) in 38 fields, high incidence (50–75%) in 33 fields, and very high incidence (75–100%) in 23 fields (Fig. 3). Symptoms of CMD were found in all regions where cassava is produced in Benin. In some cassava fields, disease incidence reached 100%, e.g. Alibori region in northern Benin (see Fig. 4).
Fig. 3

Number of fields by disease incidence level.

Fig. 4

CMD incidence levels (%) by region.

Number of fields by disease incidence level. CMD incidence levels (%) by region.

CMD severity

Severity of CMD did not significantly differ among the regions (P = 0.1000) and among districts (P = 0.0610) (Table 4). Throughout the regions, CMD severity range was 2.37–3.68, with the severity of 3.68 in Couffo and 2.37 in Alibori region (Fig. 5). Across all plants surveyed, the overall mean CMD severity score for infected plants was 2.85.
Table 4

Analysis of variance of disease severity throughout the regions and districts.

SourceDegrees of freedomSum of squaresAverage of squaresFPr > F
Regions1011.68021.16801.63630.1000
Districts6961.62140.89311.38970.0610
Fig. 5

Mean of CMD severity scores (for infected plants) in regions surveyed.

Analysis of variance of disease severity throughout the regions and districts. Mean of CMD severity scores (for infected plants) in regions surveyed. Of the 1836 plants that exhibited CMD symptoms in other all fields, 1154 plants were assigned a severity score of 3 whereas 495 plants were assigned a severity score of 2 (Fig. 6). The severe symptoms were seen on 187 plants, with 162 plants assigned a severity score 4 and 25 plants a severity score 5) (Fig. 6).
Fig. 6

Distribution of CMD severity scores across symptomatic plants.

Distribution of CMD severity scores across symptomatic plants.

Whitefly populations, CMD severity, and CMD incidence by region

The mean numbers of whitefly on the plants that have been infested by whitefly varied significantly (P < 0.0001) 226 among regions, ranging from 0.06 (Donga region) to 15.88 (Couffo region; Table 5). With regard to the maximum number of whitefly per plant, the lowest value was found in Donga (2.00) while the largest number was observed in Ouémé (125; Table 5). In total, only 16 whiteflies were counted across 9 surveyed fields in Donga whereas 5849 whiteflies were counted across 15 surveyed fields in Mono (Table 5). By field, the lowest mean number of whitefly was observed in Donga (1.78) and the highest mean number of whitefly was found in Couffo region (476.50; Table 5).
Table 5

Whitefly numbers observed in surveyed fields, per region.

RegionMaximum no. of whitefly per plantMean no. of whitefly per plantMinimum no. of whitefly per plantTotal no. of whiteflyNo. of surveyed plantsNo. of surveyed fieldsMean no. of whitefly per field (based on 30 plants/field)
Alibori2.000.10 ± 0.000.0023.00240.0082.88 ± 0.01
Atacora8.000.09 ± 0.000.0048.00510.00172.82 ± 0.01
Atlantique28.002.01 ± 0.020.00905.00450.001560.33 ± 3.72
Borgou12.000.39 ± 0.000.00290.00750.002511.60 ± 1.02
Collines17.001.22 ± 0.010.00954.00780.002636.69 ± 2.16
Couffo76.0015.88 ± 0.910.005718.00360.0012476.50 ± 37.10
Donga8.000.06 ± 0.000.0016.00270.0091.78 ± 0.01
Mono100.0013.00 ± 1.210.005849.00450.0015389.93 ± 34.01
Ouémé125.002.74 ± 0.020.00821.00300.001082.10 ± 4.23
Plateau28.001.87 ± 0.010.001233.00660.002256.05 ± 3.15
Zou24.001.84 ± 0.010.001160.00630.002155.24 ± 3.57
Mean/sum125.003.150.0017,017.005400.0018077.87
Whitefly numbers observed in surveyed fields, per region. There was no proportional relationship between disease incidence and mean number of whitefly per plant. For example, a low value for mean number whitefly/plant (0.10) was associated with a high mean CMD incidence (74.58%) in Alibori region, whereas a higher mean number whitefly/plant (15.88) was associated with a lower mean CMD incidence (9.44%) in Couffo region (Table 6).
Table 6

Variation of CMD incidence and severity according to the mean number of whitefly per plant.

RegionMean CMD incidenceMean no. of whitefly per plantMean CMD severity
Alibori74.58 ± 4.100.10 ± 0.002.37 ± 0.11
Atacora18.82 ± 1.170.09 ± 0.002.50 ± 0.12
Atlantique30.44 ± 2.212.01 ± 0.023.33 ± 0.13
Borgou42.80 ± 3.110.39 ± 0.002.86 ± 0.09
Collines34.36 ± 2.021.22 ± 0.012.85 ± 0.14
Couffo9.44 ± 0.9715.88 ± 0.913.68 ± 0.33
Donga26.30 ± 1.420.06 ± 0.002.92 ± 0.12
Mono24.22 ± 1.2413.00 ± 1.213.63 ± 0.35
Ouémé45.33 ± 3.262.74 ± 0.022.62 ± 0.14
Plateau39.24 ± 2.961.87 ± 0.012.66 ± 0.12
Zou35.87 ± 2.261.84 ± 0.012.88 ± 0.15
Overall mean34.00%3.152.84
Variation of CMD incidence and severity according to the mean number of whitefly per plant. The mean number of whitefly in different fields was significantly related (R2 = 0.7171; P = 0.0010) to CMD disease severity (Table 7), whereas there was no significant relationship (R2 = 0.3444; P = 0.0577) between whitefly mean per field per regions and CMD disease incidence mean per regions (Table 7). However, CMD incidence mean was significantly related (R2 = 0.4685; P = 0.0202) to CMD severity mean among the regions (Table 7).
Table 7

Relationship between whitefly mean density per field per region, CMD severity mean, and CMD incidence mean per region.

VariablesCMD incidence – meanWhitefly – meanCMD severity – mean
Coefficient of determination (R2):CMD incidence – mean1
Whitefly – mean0.34441
CMD severity – mean0.4685*0.7171*1
Correlation matrix (PearsonCMD incidence – mean1
Whitefly – mean−0.58691
CMD severity – mean−0.68440.84681
p-values):CMD incidence – mean0
Whitefly – mean0.05770
CMD severity – mean0.0202*0.0010*0

Values with star (*) are different from 0 with a significance level alpha = 0.05.

Relationship between whitefly mean density per field per region, CMD severity mean, and CMD incidence mean per region. Values with star (*) are different from 0 with a significance level alpha = 0.05.

Discussion

Effective management of cassava viral diseases such as CMD and cassava brown streak requires sound knowledge about these diseases and the factors that can affect their emergence. In this work, the incidence and severity of CMD were assessed in various districts of Benin, following which the relationship between this disease and whitefly abundance was established. The work consisted of surveying cassava fields throughout the territory to assess CMD prevalence and the abundance of its associated biological vector (B. tabaci). The survey results indicated that 145 out of 180 of these fields (i.e. 80.55%) showed CMD symptoms. This high rate of infected fields can be explained by the extensive spread of the disease in cassava production areas (Chikoti et al., 2019). In Alibori region, all of the fields surveyed were infected. Alibori constitutes a high-risk area in which the renewal of planting material is necessary even though it is not a high cassava production area. The ease of trading cuttings within and outside the country poses a strong epidemic risk because all fields in a region could become hotspots for the virus to spread. The extensive spread of CMD can be linked to the cultural practice of farmers exchanging cuttings with one another, as well as to ignorance of the disease and the considerable damage it can cause to cassava cultivation (Chikoti et al., 2015; Houngue et al., 2018). The moderate-to-severe severity symptoms observed in the fields may be related to the use of specific CMD-susceptible cultivars, but could also be linked to the recycle of infected cuttings (Chikoti et al., 2015), which have accumulated a high viral load. The existence of several co-infected variants can also cause severe CMD symptoms (Fondong et al., 2000). The incidence of CMD is very high in most production areas and has reached 75–100% in the districts of Malanville, Kandi, Ségbanan, Banikouara, Zagnanado, Kpomassè, and Avrankou. Torkpo et al. (2018) also showed that the use of infected cuttings increases the CMD incidence and can lead to a considerable reduction in yield. Thus, the practice of exchanging plant material among farmers poses a serious problem for CMD management in Benin due to the potentially unlimited source of virus inoculum in the fields. This problem is exacerbated by the non-existence or inaccessibility of healthy planting material for farmers (Houngue et al., 2018). The mean disease severity recorded in the regions could be linked to the susceptibility to CMD of cassava varieties cultivated by farmers (Houngue et al., 2019b), the existence of several virus variants in co-infections (Pita et al., 2001), viral load accumulation over several cycles, or the appearance of new severe variants (Njock and Sama, 2015; Igwe et al., 2020). The degree of susceptibility is related to the level of expression of mosaic symptoms in specific cassava varieties, as shown by Ntawuruhunga et al. (2007) in their work on Ugandan varieties TME204 and I/92/0067. The average number (3.15) of whitefly obtained in this latest survey was not higher than that reported for 2015 and 2017 (unpublished data), but also did not exceed that reported in previous studies (4.2 in transition forest and 3.4 in dry savannah) in Benin (Legg and James, 2005). This study showed that the whitefly population was relatively low in the high-altitude regions of Borgou, Alibori, Donga, and Atacora. This observation accords with previous studies that indicated that high altitude can hamper whitefly multiplication (Cudjoe et al., 2005; Legg and James, 2005). Although previous studies (Legg and Raya, 1998) have shown a clear relationship between whitefly abundance and infection transmitted by whiteflies, such a relationship is difficult to justify due to the temporal variation of the whitefly population (Fishpool et al., 1995), and the latency time varying from 3 to 5 weeks between transmission and first symptom (Fargette et al., 1993). In our survey, we took into account the whitefly population and disease incidence variation, and found that the whitefly population in Alibori and Borgou was low whereas CMD incidence was high or medium; by contrast, we observed the opposite in southern Benin. Whitefly is not only the vector of CMD viruses, this insect also spreads other viruses (Chikoti et al., 2013). The CMD incidence is due not only to whiteflies but also to humans spreading infected cuttings. In this study, we found a significant and positive relationship between disease severity and whitefly population. This could be explained by the fact that whiteflies may transmit different variants of virus causing a co-infection which then leads to severe disease symptoms. Cultivar response to CMD was also noted during the survey (pers. obs.). This could be linked to the substantial genetic variability that exists within cassava germplasm grown in the regions surveyed (Houngue et al., 2019a). Although virtually all of the landraces we encountered were infected by CMD, the degree of infection was variable. However, since in most cases the disease is transmitted through infected cuttings, the data collected are insufficient to draw any conclusion on the state of resistance or susceptibility of the local varieties. Therefore, these cultivars should be evaluated under a known inoculum pressure to determine the relative levels of resistance or susceptibility as shown by Houngue et al. (2019b). In most fields, cassava is grown in combination with other crops such as sweet potato, maize, okra, yam, chili, and tomato as well as weeds (the latter have been observed to harbor whitefly). This intercropping cultivation could also affect disease severity because these other species could serve as alternative host plants for vectors of the virus (Bellotti and Arias, 2001). We suggest that a monoculture of cassava would be advantageous as this might make it possible to keep the fields clear of weeds and other crops that might harbor the viruses that cause CMD.

Conclusion

This study established that CMD is widespread in all regions of Benin and that it continues to spread to new cassava-growing areas of the country. The prevalence of the disease reached 100% in some districts. Plants showing very severe mosaic symptoms were observed in most of the growers’ fields, leading to the risk of high yield losses. The incidence and high severity of CMD recorded during the survey are also of concern. It is therefore necessary that awareness-raising and training campaigns are also carried out by agricultural extension agents, non-governmental organizations, and research institutions on the use of healthy planting material and the adoption of varieties or resistant cultivars. We propose that future research efforts should be aimed at the characterization of begomoviruses associated with CMD in Benin in order to gain knowledge on the existing virus strains prevalent in the country.

Data availability statement

The data that support the findings of this study are available from the corresponding author upon request.

Authors’ contributions

JSP and CA designed the study; JAH, SSH, and MSEH conducted the work; CA and MZ supervised the research; SSH analyzed the data; JAH wrote the manuscript; JAH and MZ reviewed the article; all authors read, corrected and approved the manuscript.

Ethical approval

This article does not contain any studies with human participants or animals performed by any of the authors.

Declaration of competing interest

The authors declare that they have no conflict of interest in this publication.
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Review 1.  Methods of surveying the incidence and severity of cassava mosaic disease and whitefly vector populations on cassava in Africa: a review.

Authors:  P Sseruwagi; W S Sserubombwe; J P Legg; J Ndunguru; J M Thresh
Journal:  Virus Res       Date:  2004-03       Impact factor: 3.303

2.  Cassava virus diseases: biology, epidemiology, and management.

Authors:  James P Legg; P Lava Kumar; T Makeshkumar; Leena Tripathi; Morag Ferguson; Edward Kanju; Pheneas Ntawuruhunga; Wilmer Cuellar
Journal:  Adv Virus Res       Date:  2014-12-10       Impact factor: 9.937

3.  Infectivity, pseudorecombination and mutagenesis of Kenyan cassava mosaic begomoviruses.

Authors:  Simon E Bull; Rob W Briddon; William S Sserubombwe; Kahiu Ngugi; Peter G Markham; John Stanley
Journal:  J Gen Virol       Date:  2007-05       Impact factor: 3.891

Review 4.  The Search for Resistance to Cassava Mosaic Geminiviruses: How Much We Have Accomplished, and What Lies Ahead.

Authors:  Vincent N Fondong
Journal:  Front Plant Sci       Date:  2017-03-24       Impact factor: 5.753

5.  Evaluation of resistance to cassava mosaic disease in selected African cassava cultivars using combined molecular and greenhouse grafting tools.

Authors:  Jerome Anani Houngue; Martine Zandjanakou-Tachin; Hermine Bille Ngalle; Justin S Pita; Gilles Habib Todjro Cacaï; Sergine E Ngatat; Joseph Martin Bell; Corneille Ahanhanzo
Journal:  Physiol Mol Plant Pathol       Date:  2019-01       Impact factor: 2.747

Review 6.  Cassava mosaic disease: a review of a threat to cassava production in Zambia.

Authors:  Patrick Chiza Chikoti; Rabson Mpundu Mulenga; Mathias Tembo; Peter Sseruwagi
Journal:        Date:  2019-02-12

7.  Phenotypic and molecular screenings for determination of cassava mosaic disease (CMD) status in farmers' fields in Ebonyi State, Nigeria.

Authors:  David Okeh Igwe; Chidinma Blessing Anyanwu; Celestine Azubuike Afiukwa; Catherine Veronica Nnamani; Friday Nwalo Nweke; George Nkem Ude; Benjamin Ewa Ubi
Journal:  Mol Biol Rep       Date:  2020-12-10       Impact factor: 2.316

8.  Effects of Elevated Temperature on the Susceptibility of Capsicum Plants to Capsicum Chlorosis Virus Infection.

Authors:  Wei-An Tsai; Jonathan R Shafiei-Peters; Neena Mitter; Ralf G Dietzgen
Journal:  Pathogens       Date:  2022-02-02

9.  Survey of farmers' knowledge of cassava mosaic disease and their preferences for cassava cultivars in three agro-ecological zones in Benin.

Authors:  Jerome Anani Houngue; Justin S Pita; Gilles Habib Todjro Cacaï; Martine Zandjanakou-Tachin; Emmanuel A E Abidjo; Corneille Ahanhanzo
Journal:  J Ethnobiol Ethnomed       Date:  2018-04-25       Impact factor: 2.733

10.  Response of cassava cultivars to African cassava mosaic virus infection across a range of inoculum doses and plant ages.

Authors:  Jerome Anani Houngue; Justin S Pita; Hermine Bille Ngalle; Martine Zandjanakou-Tachin; Apollin Fotso Kuate; Gilles Habib Todjro Cacaï; Joseph Martin Bell; Corneille Ahanhanzo
Journal:  PLoS One       Date:  2019-12-23       Impact factor: 3.240

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