P: ISSN No. 0976-8602 RNI No.  UPENG/2012/42622 VOL.- XII , ISSUE- II April  - 2023
E: ISSN No. 2349-9443 Asian Resonance
Aphid Transmission on Chilli (Capsicum frutescens) in Doon Valley, Uttarakhand
Paper Id :  17478   Submission Date :  2023-04-01   Acceptance Date :  2023-04-19   Publication Date :  2023-04-25
This is an open-access research paper/article distributed under the terms of the Creative Commons Attribution 4.0 International, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
For verification of this paper, please visit on http://www.socialresearchfoundation.com/resonance.php#8
Vijaylaxmi
Research Scholar
Department Of Botany
D.B.S. (P.G.) College
Dehradun,Uttarakhand, India
Nirmala Koranga
Associate Professor
Department Of Botany
D.B.S. (P.G.) College
Dehradun, Uttarakhand, India
Abstract
Plant viruses are affected by insects, which cause severe crop loss and economic loss. The majority of plant viruses observed thus far have been demonstrated to be transmissible by insects, the majority of which are aphids, white flies, mites, grasshoppers, plant bugs, leaf hoppers and other insects that have been identified as plant virus vectors. The number of plant viral agents causing plant diseases like Chilli leaf curl virus (CLCV), Chilli veinal mottle virus (ChiVMV) Begomovirus, Tymovirus, Potyvirus, Zucchini yellow mosaic virus and Cucumber mosaic virus (CMV) viz. cause disease in Capsicum frutescens. India is the largest producer of chilli and due to the presence of alluvial soil, Uttarakhand is more fertile for chilli crops. The three aphid species, Aphis craccivora koch, Aphis gossypii golvz, Myzus persica, and Bemisia tabaci (white flies), are common on chilli plants in Doon valley, Uttarakhand.
Keywords Aphid Transmission, Virus Isolation, Pre-Acquisition Fasting.
Introduction
Capsicum frutescens belong to the family of Solanaceae. The Begomovirus, Tymovirus, Potyvirus, Chilli veinal mottle virus, Zucchini yellow mosaic virus and Cucumber mosaic virus cause infection in chilli species. The large numbers of plant viruses reported thus far have been shown to be transmissible by insects such as aphids, grasshoppers, mites, mealy bugs, plant bugs, and white flies. Aphid gossypii, A. craccivora, and Myzus persicae and Bemisia tabaci transmitted the yellow mosaic virus.
Objective of study
Most plant viruses are transmitted by Aphids which work as a vector. During the study identify the aphid spices and protect the chilli crop.
Review of Literature

 

Fig1. (A). Myzus persica feeding time on Capsicum frutescens (B). Aphis craccivora

Aphids and whiteflies transmitted the virus isolates that cause mosaic and leaf curl diseases in chilli cultivars (Khan et al., 2006). Although Aphis gossypii (Glov.) transmitted ChiVMV to its natural host chilli pepper. The plants caused systemic vein mottling symptoms, which were confirmed by DAS-ELISA (Shah et al., 2008). Cucumber mosaic virus (CMV) and Chilli veinal mottle virus (ChiVMV) are major destructive viruses spread by aphids that affect chilli crops (Naresh et.,al 2016 and Myti et.,al 2014). Papaya ring spot virus affected the behaviour and biology of its vector, the melon aphid (Aphis gossypii Glover), as well as the non-vector, silver leaf whitefly (Bemisia tabaci Gennadius) (Gadhave et.,al 2019). The genetic diversity of mosaic and chlorosis-inducing Cucumber mosaic virus (CMV) strains infecting chilli. It was discovered to contain a cryptic mutation of Threonine amino acid, which is conserved for aphid transmission (Vinodhini et.,al 2022).

Main Text

Materials and Methods

During the month of June to November a field study was undertaken in the village of Badripur area of Dehradun district, Uttarakhand. The infection was found in Adhoyiwala, Badripur, and Prem nagar area, Dehradun. Back inoculation on healthy chilli seedlings was used to determine whether the plant species was a latent host of the viruses in plants where no symptoms emerged. The majority of plant viruses transmitted by the three aphid species, Aphis craccivora koch, Aphis gossypii golvz, Myzus persica, and Bemisia tabaci (white flies), which are common on chilli plants in Doon velly, Uttarakhand, were tested for their ability to spread chilli mosaic virus isolates within that study.

Fig2.(A) Aphids collection on Capsicum frutescens

(B). Aphid transmission on four-leaf seedlings

Vector virus association of mild and severe isolates with Aphis craccivora

Aphis craccivora is a common species found in Dehradun's solanaceae crops. During preliminary transmission testing, this aphid was determined to be the most efficient vector of chilli mosaic virus isolates, both mild and severe. A.craccivora association with these two isolates was determined by changing pre-acquisition fasting periods, acquisition feeding time, number of aphids, minimum infection feeding required time, post-acquisition fasting periods, and virus persistence in the vector.

Methodology
Materials and methodology are briefly described after the Discussion and Result.
Result and Discussion

Discussion and Result

The presence of A. gossypii within five minutes of feeding on a diseased plant massively increased the extent of transmission (Swenson et al.,1952). However M. persicae and A. gossypii transmitted pepper vein banding virus at 90 and 100%, respectively. M. persicae, A. gossypii, and A. craccivora transmitted pepper veinal mottle potyvirus, resulting in 90, 100, and 30% infection, respectively (Gowda et al., 1989). Overall, the appropriate integrated pest management strategies for A. gossypii and CVMV in small farm agro-ecosystems in the tropics (Hussein et.,al 1993).Whereas After a minute of acquisition, the virus from the chilli pepper leaf was transferred by the peach potato aphid, Myzus persicae, to immature chilli pepper plants (Chiemsombat et al., 1998).

Barrier cropping will be interconnected with other disease management strategies, and its use as a strategy for managing aphid-transmitted virus diseases will be improved (Hooks & Fereres, 2006). In different circumstances the DAG motif, which is common in aphid-transmitted potyviruses, was found in all isolates like pepper vein banding virus (PVBV), chilli vein-banding mottle virus (CVbMV) and Chiengmai isolate (Tsai et al., 2008).

The aphids were fasted for three hours pre-acquisition. Fasted aphids were given a two-minute acquisition feeding time on infected chilli plants. As test plants, young vigorously growing chilli seedlings were used (Table -1).

Chilli mosaic virus mild and severe isolates were transmitted by aphids.

Table 1

 Aphids

Number of aphids in per chilli plants  

Mild

Severe

Ist trial

2ed trial

Transmission percentage (%)

Ist trial

2ed trial

Transmission percentage (%)

Bemisia tabaci

10

5

6

55

4

6

50

Aphis craccivora

10

7

7

70

7

8

75

Aphis gossypii

10

5

4

45

6

6

60

Myzus persica

10

7

6

65

5

7

60

← Number of Aphids →

Table 1 indicates that all aphid species can efficiently transfer both isolates from infected to healthy plants. Within 8-12 days, symptoms occurred on the infected seedlings. Aphis craccivora was found to be the most effective vector, causing 75% ChiMV severe and 70% ChiMV mild infection. 60% A.gossypii and 60% Myzus persicas.

Effect of pre-acquisition fasting and acquisition eating timings on mild and severe isolate transmission:

According to experiment during the virus's assimilation, it comes into contact with some chemical that partially or completely damages its infectivity. It is assumed that this chemical is either not generated at all or is produced at a significantly reduced rate in fasting insects. During the present study, when an aphid is given a short feeding 1-2 minutes after hunger, the amount of inactivater is insufficient to inactivate the virus taken in, resulting in greater infection. However, with a 5 minute increase in acquisition feeding time, the benefit of fasting begins to fade and the quantity of inactivater increases, resulting in reduced infection. When aphids are not starving, the quantity of inactivater already present in the insect reaches a peak, inactivating a high proportion of the virus ingested during the acquisition feeding phase, resulting in decreased infections. Table-2 shows the results.

Table 2

Isolates

Pre–acquisition fasting time (hrs)

Acquisition Feeding time min

Total

0.5

1.0

2.0

3.0

4.0

5.0

Mild isolates

0.0

-

1

2

3

2

3

11

Severe isolates

0.0

1

1

2

3

3

2

12

Mild isolates

1.0

1

2

3

4

2

2

14

Severe isolates

1.0

2

3

4

5

4

3

22

Mild isolates

2.0

2

4

3

6

5

4

24

Severe isolates

2.0

3

5

5

7

5

4

29

Mild isolates

3.0

3

5

6

5

4

3

26

Severe isolates

3.0

4

6

7

7

4

4

32

Mild isolates

4.0

4

5

2

3

5

3

22

Severe isolates

4.0

3

7

5

4

3

2

24

Mild isolates

5.0

0

0

1

3

2

1

07

Severe isolates

5.0

0

1

2

3

2

1

09

Mild isolates

Total

10

17

17

24

20

16

 

Severe isolates

12

22

23

26

18

16

Transmission of CMV mild and CMV severe isolates by A.craccivora with varying pre-acquisition fasting and acquisition eating times:

The effect of the number of aphids on the transmission of mild and severe isolates: Some viruses were only transmitted when a high number of vectors were used. This has frequently resulted in the conclusion that insects can inject virus with sub-minimal infective concentrations into plants. These have a cumulative impact, and none of them could have caused infection on its own. After getting enough of these dosages, a plant will become infected. Table 11 shows the results of an experiment conducted in two trials to determine the impact of the number of aphids on the transmission of the present virus isolate. According to the data in table 11 and figure -1, even a single aphid can spread the virus, however the percentage of transmission is relatively low. However, for optimal transmission of both strains, a group of 5 or 10 aphids per plant is recommended. When 15 and 20 aphids per plant were sampled, the percentage transmission declined steadily.

Table 3

Isolates 

Number of Aphids per plant        

No of trials

Out of 20 treated total number plant infected

Transmission percentage      (%)

Trial I

Trial II

Mild isolates

01

2

2

4

20

Severe isolates

01

2

3

5

25

Mild isolates

05

3

2

5

25

Severe isolates

05

4

3

7

35

Mild isolates

10

5

6

11

55

Severe isolates

10

7

7

14

70

Mild isolates

15

6

6

12

60

Severe isolates

15

7

6

13

65

Mild isolates

20

4

4

8

40

Severe isolates

20

3

5

8

40

Minimum infection feeding time necessary for mild and severe isolate transmission:

An experiment was conducted to determine the minimum infection feeding time needed for transmission of isolates of chilli mosaic virus, and the findings are provided in table-3.

Based on the findings in Table 3 it is concluded that viruliferous aphids may spread mild and severe isolates to healthy plants in as little as two minutes of infection feeding time. In both cases, however, optimum infection is reached in 30 to 60 minutes after infection feeding.

Table 4

Isolates

Aphids infection feeding time

No of trials

Out of 20 treated total number plant infected

Transmission percentage     (%)

Trial I

Trial II

Mild isolates

02

1

1

2

10

Severe isolates

02

1

2

3

15

Mild isolates

05

2

2

4

20

Severe isolates

05

3

3

6

30

Mild isolates

15

5

4

9

45

Severe isolates

15

4

5

9

45

Mild isolates

20

6

7

13

65

Severe isolates

20

6

6

12

60

Mild isolates

30

7

8

15

75

Severe isolates

30

8

6

14

70

Mild isolates

60

7

7

14

70

Severe isolates

60

6

8

15

75

Mild isolates

120

6

8

14

70

Severe isolates

120

6

9

15

75

ChiMV mild and ChiMV severe isolate minimum feeding time for aphids transmission:

Mild and severe isolates transmission of post-acquisition fasting effect:

Fig.3 Post-acquisition fasting periods

 An experiment was conducted to determine the effect of aphid starvation after acquisition feeding, and the findings are presented in table 4.

Table 4 demonstrate that percentage transmission lowered transmission, but only when the aphids fasted following acquisition feeding. Fasting for 30 minutes reduced transmission slightly, but the reduction became more significant as post-acquisition fasting duration increased to 4 hours in mild isolates and 6 hours in severe isolates, after which no infection occurred.





Table 5

Isolates

Post–acquisition fasting time

Number of plants infected out of 10 treated 

Total plants infected out of 20 treated

Transmission percentage     (%)

Trial  I

Trial II

Mild isolates

0.0

7

8

15

75

Severe isolates

0.0

8

8

16

80

Mild isolates

0.5

7

6

13

65

Severe isolates

0.5

6

7

13

65

Mild isolates

1.0

5

6

11

55

Severe isolates

1.0

6

6

12

60

Mild isolates

2.0

4

4

8

40

Severe isolates

2.0

3

3

6

30

Mild isolates

3.0

3

3

6

30

Severe isolates

3.0

2

3

5

25

Mild isolates

4.0

1

1

2

10

Severe isolates

4.0

2

2

4

20

Mild isolates

5.0

1

-

1

5

Severe isolates

5.0

1

1

2

10

Mild isolates

6.0

-

-

-

-

Severe isolates

6.0

1

-

1

5

Mild isolates

7.0

-

-

-

-

Severe isolates

7.0

-

-

-

-

Mild isolates

8.0

-

-

-

-

Severe isolates

8.0

-

-

-

-

Mild and severe isolates persist in the vector:
An experiment was carried out to find out how many plants a single viruliferous aphid may infect when fed on a series of plants. Table 5 displays the acquired data.
According to the results, seven of the ten aphids infected mild isolates only on the first plant and three on the second plant. None of the aphids were capable of producing more than one infection. In the event of severs, segregate all 10 aphids to feed initially. The remaining plants were unaffected. This demonstrates that a single viruliferous aphid is incapable of causing more than one infection and loses its infectivity after that.
Table 6

ChiMV Isolates

Number of aphids   

Plants in series

1

2

3

4

   Mild

1

+

_

_

_

  Severe

1

+

_

_

_

   Mild

2

-

+

_

_

  Severe

2

+

_

_

_

   Mild

3

+

_

_

_

  Severe

3

+

_

_

_

   Mild

4

-

_

_

_

  Severe

4

+

_

_

_

   Mild

5

+

_

_

_

  Severe

5

+

_

_

_

   Mild

6

-

+

_

_

  Severe

6

+

_

_

_

   Mild

7

+

_

_

_

  Severe

7

+

+

_

_

   Mild

8

+

_

_

_

  Severe

8

+

_

_

_

   Mild

9

+

_

_

_

  Severe

9

+

_

_

_

   Mild

10

+

_

_

_

  Severe

10

+

_

_

_

 (+) Mild and severe infection (-) No infection on mild and severe isolates 

Conclusion
On the bases of studies showing that barrier on chilli crop is a promising tactic for mitigating yield losses caused by chilli mosaic disease transfer by aphids. Virus cause economic losses in agriculture due to non-persistently aphid transmitted viruses impact on chilli. In the Doon valley region Aphis craccivora was found to be the most effective vector, causing 75% ChiMV severe and 70% ChiMV mild infection. 60% A.gossypii and 60% Myzus persicas.
Acknowledgement The authors would like to thank the Department of Botany DBS (PG) College Dehradun for providing technical assistance during community visits and collecting.
References
1. Chiemsombat, P., Sae-Ung, N., Attathom, S., Patarapuwadol, S., & Siriwong, P. (1998). Molecular taxonomy of a new potyvirus isolated from chilli pepper in Thailand. Archives of virology, 143(10), 1855-1863. 2. Gadhave, K. R., Dutta, B., Coolong, T., & Srinivasan, R. (2019). A non-persistent aphid-transmitted Potyvirus differentially alters the vector and non-vector biology through host plant quality manipulation. Scientific Reports, 9(1), 1-12. 3. Gowda, K. T. P., & Reddy, H. R. (1989). Aphid transmitted viruses infecting chilli. Current Research-University of Agricultural Sciences (Bangalore), 18(5), 71-72. 4. Gowda, K. T. P., & Reddy, H. R. (1989). Aphid transmitted viruses infecting chilli. Current Research-University of Agricultural Sciences (Bangalore), 18(5), 71-72. 5. Hooks, C. R., & Fereres, A. (2006). Protecting crops from non-persistently aphid-transmitted viruses: a review on the use of barrier plants as a management tool. Virus research, 120(1-2), 1-16. 6. Hussein, M. Y., & Samad, N. A. (1993). Intercropping chilli with maize or brinjal to suppress populations of Aphis gossypii Glov., and transmission of chilli viruses. International journal of pest management, 39(2), 216-222. 7. Khan, S. M., Raj, S. K., Bano, T., & Garg, V. K. (2006). Incidence and management of mosaic and leaf curl diseases in cultivars of chilli (Capsicum annuum). Journal of Food Agriculture and Environment, 4(1), 171. 8. Myti, S., Shabbir, A. K., Akhter, S., Uddin, A., Kamruzzaman, M., Faruq, M. O., & Biswas, G. C. (2014). Identification of the most prevalent and spatially disperse virus on chilli at Northern and Eastern part of Bangladesh. Int J Biosci, 5(7), 40-49. 9. Naresh, P., Reddy, M. K., Reddy, P., & Reddy, K. M. (2016). Screening chilli (Capsicum spp.) germplasm against Cucumber mosaic virus and Chilli veinal mottle virus and inheritance of resistance. European journal of plant pathology, 146(3), 451-464. 10. Shah, H., Yasmin, T., Fahim, M., Hameed, S. H. A. H. I. D., & Haque, M. I. (2008). Transmission and host range studies of Pakistani isolate of chilli veinal mottle virus. Pakistan Journal of Botany, 40, 2669-2681. 11. Swenson, K. G. (1952). Aphid transmission of a strain of Alfalfa mosaic virus. Phytopathology, 42(5). 12. Tsai, W. S., Huang, Y. C., Zhang, D. Y., Reddy, K., Hidayat, S. H., Srithongchai, W., ... & Jan, F. J. (2008). 13. Molecular characterization of the CP gene and 3′ UTR of Chilli veinal mottle virus from South and Southeast Asia. Plant Pathology, 57(3), 408-416. 14. Vinodhini, J., Rajendran, L., & Karthikeyan, G. (2022). Comparative coat protein annotation of two biologically distinct strains of Cucumber mosaic virus in chilli.