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Relevant bibliographies by topics / Banana bunchy top disease

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Academic literature on the topic 'Banana bunchy top disease'

Author: Grafiati

Published: 4 June 2021

Last updated: 27 January 2023

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Journal articles on the topic "Banana bunchy top disease"

1

Qazi, Javaria. "Banana bunchy top virus and the bunchy top disease." Journal of General Plant Pathology 82, no. 1 (December 8, 2015): 2–11. http://dx.doi.org/10.1007/s10327-015-0642-7.

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2

KHALID, S., and M. H. SOOMRO. "Banana bunchy top disease in Pakistan." Plant Pathology 42, no. 6 (December 1993): 923–26. http://dx.doi.org/10.1111/j.1365-3059.1993.tb02678.x.

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3

Arubi, D., Giyanto, D. Dinarty, A. Sutanto, and S. H. Hidayat. "Response of banana germplasms to banana bunchy top virus." IOP Conference Series: Earth and Environmental Science 948, no. 1 (December 1, 2021): 012022. http://dx.doi.org/10.1088/1755-1315/948/1/012022.

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Abstract Banana bunchy top virus (BBTV) is one of the important viruses causing disease in bananas and its infection has the potential to cause yield loss. This study was conducted to evaluate the response of several commercial cultivars (Cavendish, Bebek, Goroho, Tanduk, and Barangan Merah) and wild accessions (Klutuk NTT, Halabanensis, SPn 001, LNT 001, and Microcarpa) of banana to BBTV infection. Transmission of BBTV was carried out through banana aphid Pentalonia nigronervosa, using 20 adult aphids per plant with an acquisition feeding period of 24 hours on BBTV-infected plants and an inoculation feeding period on healthy test plants for 48 hours. Observation on plant growth and disease intensity was conducted for 8 weeks after inoculation. At the end of the observation period, only 5 cultivars, i.e. Cavendish, Bebek, Goroho, Barangan Merah, and Halabanensis showed typical symptoms of BBTV with disease incidence reached 80%, 60%, 20%, 20%, and 20% respectively. Significant inhibition of plant height and leaves width occurred in Cavendish, Bebek, and Goroho i.e. 44.60%, 36.31%; 12.62%, 41.08%; and 25%, 10.13%, respectively. This paper discusses the need for banana germplasm exploration to find sources of resistance to BBTV.

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Prasetyo, Joko, and Sudiono Sudiono. "PEMETAAN PERSEBARAN PENYAKIT BUNCHY TOP PADA TANAMAN PISANG DI PROVINSI LAMPUNG." Jurnal Hama dan Penyakit Tumbuhan Tropika 4, no. 2 (September 16, 2004): 94–101. http://dx.doi.org/10.23960/j.hptt.2494-101.

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Distribution mapping of bunchy top of banana in Lampung Province. Studies on the occurrence of banana bunchy top were conducted in Lampung province from March to May 2003. This study were aimed to make distribution map of banana bunchy top in Lampung. The stratified random sampling were used. The sample comprised 6 districts out of 10 districts in Lampung. Three subdistrics were randomly selected in each district and then 3 villages were also selected in each subdistrict. In each village 3 famer”s gardens were selected as observation area. The distribution map shows that banana bunchy top has spread throughout the 6 districts visually observed, but only 4 districts, that bunchy top incidence could be examined. Banana bunchy top incidence in Bandar Lampung, South Lampung, Central Lampung, and North Lampung were 2.31, 2.23, 1.06, and 0.84 % respectively. Bunchy top virus attacked various types, among them are janten (55.23%), muli (38.88%), kepok (30.47%), ambon (21.52%), raja sere (19.76%), nangka 4.64%), and lilin (3.84%). There were no disease incidence on cultivar tanduk, rejang and susu, thus this fact might be indicated resistance phenomena of these cultivars.

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5

Kakati, Nilakshi, and P. D. Nath. "Genetic Diversity of Banana Bunchy Top Virus (BBTV) Prevalent in Assam Causing Banana Bunchy Top Disease." International Journal of Current Microbiology and Applied Sciences 7, no. 11 (November 10, 2018): 1547–60. http://dx.doi.org/10.20546/ijcmas.2018.711.178.

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6

S. R. Adat, S. S. Waghmare, V. K. Mohite A. A. Waghule, and S. S. Patale. "Study of Bunchy Top of Banana Virus (BBTV) and its Control by Integrated Disease Management (IDM)." International Journal of Current Microbiology and Applied Sciences 10, no. 11 (November 10, 2021): 416–29. http://dx.doi.org/10.20546/ijcmas.2021.1011.047.

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India is the top country by Banana production in the world as of 2019, bananas production in India was 30.5 million tonnes that accounts for 26.02% of the world's bananas production. The top 5 countries (others are China, Indonesia, Brazil, and Ecuador) account for 53.94% of it. The world's total bananas production was estimated at 117 million tonnes in 2019.In India, states like Andhra Pradesh, Gujarat, Tamil Nadu, Maharashtra, Kerala, Uttar Pradesh, Bihar and Madhya Pradesh contribute more than 70 per cent of the country's banana production. Banana and plantain (Musa spp.), produced in 10.3 million ha in the tropics, are among the world's top 10 food crops. They are vegetative propagated using suckers or tissue culture plants and grown almost as perennial plantations. They are vulnerable to pests and pathogens, especially viruses which causes reduction in yield and are also hinders to the international exchange of germplasm. The most economically important viruses of banana and plantain are Banana bunchy top virus (BBTV), a complex of banana streak viruses (BSVs) and Banana bract mosaic virus (BBrMV). BBTV is known to cause the most serious economic losses contributing to yield reduction of up to 100% and responsible for a dramatic reduction in cropping area. The BSVs exist as episomal and endogenous forms are known to be worldwide in distribution. In India and the Philippines, BBrMV is known to be economically important.

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7

Sutrawati, Mimi, and Sempurna Ginting. "First Report of Banana Bunchy Top Disease on Banana in Bengkulu." AGRITROPICA : Journal of Agricultural Sciences 3, no. 2 (December 1, 2020): 82–87. http://dx.doi.org/10.31186/j.agritropica.3.2.82-87.

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Banana is a horticulture crop that has economic value and is widely cultivated in tropical countries. Banana production in Bengkulu province reached 259,748 quintals, then durian (110,387 quintals), tangerines (94,396 quintals) (BPS 2015). Banana bunchy top disease caused by Banana bunchy top virus (BBTV) infection is considered the most crucial virus disease affecting yield losses of a banana plantation in Asia, Africa, and the South Pacific. However, the incidence and molecular characters of BBTV has never been reported in Bengkulu. This research aims to characterize symptom variations, disease incidence, and disease severity of BBTV infection in Bengkulu and virus detection using molecular methods by polymerase chain reaction (PCR). Disease incidence of BBTV was measured based on field symptoms. The disease survey was conducted in Bengkulu city, Bengkulu Utara district, and Rejang Lebong district. The study showed that the incidence of BBTV in Bengkulu City, Bengkulu Utara, and Rejang Lebong ranged from 0% to 100%. The most common symptoms observed in the field involved vein clearing, upturned leaf, chlorotic, and ragged margins, reducing petiole length, distance, lamina width, and stunting. Banana crops that are infected with BBTV in the vegetative phase will not produce fruit. In contrast, viral infection in the generative phase causes the formation of stunted fruit that is not suitable for harvesting. Thus, the potential loss of yield due to stunted disease can reach 100%. This study's results are the first reports of BBTV infection in banana crops in Bengkulu. Disease diagnosis will form the basis of disease control strategies in banana crops.

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8

Oben, T. T., R. Hanna, J. Ngeve, O. J. Alabi, R. A. Naidu, and P. Lava Kumar. "Occurrence of Banana Bunchy Top Disease Caused by the Banana bunchy top virus on Banana and Plantain (Musa sp.) in Cameroon." Plant Disease 93, no. 10 (October 2009): 1076. http://dx.doi.org/10.1094/pdis-93-10-1076c.

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Banana bunchy top virus (BBTV; genus Babuvirus, family Nanoviridae) is a serious pathogen of banana (AAA genome) and plantain (AAB genome) (Musa sp.). It is transmitted by the banana aphid (Pentalonia nigronervosa) in a persistent manner (1). In recent years, BBTV has emerged as a major constraint to banana and plantain production in several countries of Africa and had been previously confirmed in viz., Burundi, Central African Republic, Republic of Congo, Democratic Republic of Congo, Egypt, Equatorial Guinea, Gabon, Malawi, and Rwanda (1) and more recently in Mozambique and Zambia (2) and Angola (3). To assess the potential threat of BBTV in West-Central Africa, we conducted surveys in August and September 2008 in 36 major banana- and plantain-producing regions of Littoral, South, Southwest, and Western Provinces of Cameroon. DNA was extracted from 520 plants and tested by PCR with primers specific for a conserved domain of BBTV DNA-R segment (4). A 240-bp DNA fragment specific to the virus was amplified in 31 samples from 18 plantain and 13 banana plants from Southwest, Western, and Southern Cameroon. Among virus-positive samples, symptoms (upright leaf growth, small leaves with pale chlorotic margins that choked the throat of the plant creating the bunchy appearance at the top) typical of bunchy top disease were observed only in banana (cv. Cavendish Williams) from Muea in the Southwest Province. PCR products obtained from the symptomatic and asymptomatic banana (Cavendish Williams) from Muea and Abang, respectively, were cloned into pCR2.1 (Invitrogen, Carlsbad, CA) and two independent clones from each isolate were sequenced in both directions. Pairwise comparison of these sequences showed 100% sequence homology. A comparison of these sequences (Accession No. F580970) with corresponding sequences in GenBank showed 99% nt sequence identity with a BBTV isolate from Angola (Accession No. EU851977) and 96 to 98% identity with BBTV isolates belonging to the South Pacific group (Australia, Africa, South Asia, and South Pacific). However, the BBTV isolate from Cameroon showed 85 to 90% sequence identity with isolates belonging to the Asian group (China, Indonesia, Japan, Taiwan, Philippines, and Vietnam). To further confirm the virus identity, complete nucleotide sequence of the DNA-SCP segment that encodes for the virus coat protein was determined using PCR amplification of viral DNA (1), cloning of products into pCR2.1 vector, and sequencing. The derived sequence (1,075 nt; Accession No. GQ249344) in BLAST search at NCBI database revealed 98% nt sequence identity with coat protein gene of BBTV isolate from Burundi (Accession No. AF148943). These results, together with phylogenetic analysis, indicate that BBTV isolates from Cameroon have greater affinity to the South Pacific group. To our knowledge, this is the first report of BBTV in West-Central Africa. The occurrence of BBTV in the Western and Southern provinces of Cameroon, neighboring north of Gabon, suggests a possible spread of the virus from Gabon. This report also underscores the need to monitor other countries of West Africa for BBTV and enforce quarantine measures to prevent further spread through infected suckers from endemic areas of West and Central Africa. References: (1) I. Amin et al. Virus Genes 36:191, 2008. (2) W. T. Gondwe et al. InfoMusa 16:38, 2007. (3) P. L. Kumar et al. Plant Pathol. 58:402, 2009. (4) S. Mansoor et al. Mol. Biotechnol. 30:167, 2005.

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9

Wirya, Gusti Ngurah Alit Susanta, I. Putu Sudiarta, and Dewa Gede Wiryangga Selangga. "Disease Severity and Molecular Identification of Banana bunchy top virus, Infecting Local Banana in Bali Island." Jurnal Perlindungan Tanaman Indonesia 24, no. 1 (July 7, 2020): 11. http://dx.doi.org/10.22146/jpti.54882.

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Bunchy top symptoms on banana has been reported in Bali Island since early 2011. Symptoms variation were observed in the field similar to infection of Banana bunchy top virus (BBTV). The identity of the BBTV in Bali on the basis of DNA-S nucleotide sequence has not been studied, therefore research was conducted to identify the species of BBTV infecting local banana in Bali based on sequence analysis. Research activities were initiated by collecting field samples from several local banana growing areas in Bali Island. Incidence of bunchy top disease in all locations reached 8% to 44% with disease severity ranged from 2.6% to 30%. Identification of BBTV from field samples were done by polymerase chain reaction using specific primers for BBTV (CPF/CPR) followed by sequence analysis of amplified DNA target. Specific BBTV DNA fragment was successfully amplified from 10 field samples; sequence analysis of DNA fragments showed their highest homology with BBTV. In addition the phylogenetic analysis confirmed the close relationship of BBTV isolates from Bali with various BBTV isolates from Indonesia and other isolates from the Asian group in GeneBank.

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10

Allen, RN. "Further studies on epidemiological factors influencing control of banana bunchy top disease and evaluation of control measures by computer simulation." Australian Journal of Agricultural Research 38, no. 2 (1987): 373. http://dx.doi.org/10.1071/ar9870373.

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The basic infection rate of bunchy top disease in established bananas averaged 0.0342 new infections per infectious plant per day, but varied seasonally with a maximum in summer. The mean distance of spread for the aphid vector was 15.2 m. The latent period was 59.8 days and correlated with the time required for the growth of 3.7 new banana leaves. A microcomputer program was written to simulate spread of banana bunchy top disease in space and time. In the absence of disease control, disease spread from an initial primary infection in July or January to 124 or 153 infected plants, respectively, in one year. When disease control was maintained by removing diseased plants whenever the number of infected plants exceeded a given threshold, the numbers of diseased plants detected each inspection were positively correlated with the infection threshold, but the numbers of inspections required to maintain control increased markedly as the infection threshold was decreased. A practice of removing apparently healthy plants within 5 m of plants detected with bunchy top disease symptoms in five or more leaves was found to locate about 30% of the remaining undetected infected plants when disease was first detected in a plantation. However, its use as a routine control measure was ineffective in reducing the number of inspections required to maintain control or in reducing the risk of disease spreading to adjoining plantations. Removal of apparently healthy plants within 5 m had some bearing on disease control when applied around plants with disease symptoms in two leaves or less, but also caused a significant loss of healthy plants.

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Dissertations / Theses on the topic "Banana bunchy top disease"

1

Wanitchakorn, Raktham. "Gene functions in banana bunchy top virus." Thesis, Queensland University of Technology, 1999.

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2

Burns, Thomas Michael. "Genome organisation of banana bunchy top virus." Thesis, Queensland University of Technology, 1994.

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3

Dugdale, Benjamin. "Promoter activity associated with the intergenic regions of banana bunchy top virus." Thesis, Queensland University of Technology, 1999. https://eprints.qut.edu.au/37001/6/37001_Digitised_Thesis.pdf.

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4

Hafner, Gregory. "Replication of banana bunchy top virus : mechanisms and interference." Thesis, Queensland University of Technology, 1998.

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5

Beetham, Peter Ronald. "Transcription of mRNAs from the banana bunchy top virus genome." Thesis, Queensland University of Technology, 1998.

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6

Soko, Misheck Mica Mafeni. "Evaluation of transgenic RNAi banana and plantain lines for resistance to banana bunchy top disease." Thesis, Queensland University of Technology, 2022. https://eprints.qut.edu.au/228515/1/Misheck%20Mica%20Mafeni_Soko_Thesis.pdf.

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This project evaluated genetically modified Cavendish bananas and plantains for field and glasshouse resistance to banana bunchy top virus in Malawi in Africa, over a three-and-a-half-year period. The study identified several GM lines with significant resistance to the virus and provided a rare insight into virus-vector relations and the climate. The research showed that rigorous field assessment of GM plants for disease resistance is critical and that immunity to this virus will likely only be achieved using a multi-faceted resistance strategy.

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7

Karan, Mirko. "Sequence diversity of DNA components associated with banana bunchy top virus." Thesis, Queensland University of Technology, 1995.

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Horser, Cathryn Louise. "Characterisation of the putative satellite DNAs associated with banana bunchy top virus." Thesis, Queensland University of Technology, 2000.

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Becker, Douglas Kenneth. "The transformation of banana with potential virus resistance genes." Thesis, Queensland University of Technology, 1999. https://eprints.qut.edu.au/37023/6/37023_Digitised_Thesis.pdf.

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One approach to reducing the yield losses caused by banana viral diseases is the use of genetic engineering and pathogen-derived resistance strategies to generate resistant cultivars. The development of transgenic virus resistance requires an efficient banana transformation method, particularly for commercially important 'Cavendish' type cultivars such as 'Grand Nain'. Prior to this study, only two examples of the stable transformation of banana had been reported, both of which demonstrated the principle of transformation but did not characterise transgenic plants in terms of the efficiency at which individual transgenic lines were generated, relative activities of promoters in stably transformed plants, and the stability of transgene expression. The aim of this study was to develop more efficient transformation methods for banana, assess the activity of some commonly used and also novel promoters in stably transformed plants, and transform banana with genes that could potentially confer resistance to banana bunchy top nanovirus (BBTV) and banana bract mosaic potyvirus (BBrMV). A regeneration system using immature male flowers as the explant was established. The frequency of somatic embryogenesis in male flower explants was influenced by the season in which the inflorescences were harvested. Further, the media requirements of various banana cultivars in respect to the 2,4-D concentration in the initiation media also differed. Following the optimisation of these and other parameters, embryogenic cell suspensions of several banana (Musa spp.) cultivars including 'Grand Nain' (AAA), 'Williams' (AAA), 'SH-3362' (AA), 'Goldfinger' (AAAB) and 'Bluggoe' (ABB) were successfully generated. Highly efficient transformation methods were developed for both 'Bluggoe' and 'Grand Nain'; this is the first report of microprojectile bombardment transformation of the commercially important 'Grand Nain' cultivar. Following bombardment of embryogenic suspension cells, regeneration was monitored from single transfom1ed cells to whole plants using a reporter gene encoding the green fluorescent protein (gfp). Selection with kanamycin enabled the regeneration of a greater number of plants than with geneticin, while still preventing the regeneration of non-transformed plants. Southern hybridisation confirmed the neomycin phosphotransferase gene (npt II) was stably integrated into the banana genome and that multiple transgenic lines were derived from single bombardments. The activity, stability and tissue specificity of the cauliflower mosaic virus 358 (CaMV 35S) and maize polyubiquitin-1 (Ubi-1) promoters were examined. In stably transformed banana, the Ubi-1 promoter provided approximately six-fold higher p-glucuronidase (GUS) activity than the CaMV 35S promoter, and both promoters remained active in glasshouse grown plants for the six months they were observed. The intergenic regions ofBBTV DNA-I to -6 were isolated and fused to either the uidA (GUS) or gfjJ reporter genes to assess their promoter activities. BBTV promoter activity was detected in banana embryogenic cells using the gfp reporter gene. Promoters derived from BBTV DNA-4 and -5 generated the highest levels of transient activity, which were greater than that generated by the maize Ubi-1 promoter. In transgenic banana plants, the activity of the BBTV DNA-6 promoter (BT6.1) was restricted to the phloem of leaves and roots, stomata and root meristems. The activity of the BT6.1 promoter was enhanced by the inclusion of intron-containing fragments derived from the maize Ubi-1, rice Act-1, and sugarcane rbcS 5' untranslated regions in GUS reporter gene constructs. In transient assays in banana, the rice Act-1 and maize Ubi-1 introns provided the most significant enhancement, increasing expression levels 300-fold and 100-fold, respectively. The sugarcane rbcS intron increased expression about 10-fold. In stably transformed banana plants, the maize Ubi-1 intron enhanced BT6.1 promoter activity to levels similar to that of the CaMV 35S promoter, but did not appear to alter the tissue specificity of the promoter. Both 'Grand Nain' and 'Bluggoe' were transformed with constructs that could potentially confer resistance to BBTV and BBrMV, including constructs containing BBTV DNA-1 major and internal genes, BBTV DNA-5 gene, and the BBrMV coat protein-coding region all under the control of the Ubi-1 promoter, while the BT6 promoter was used to drive the npt II selectable marker gene. At least 30 transgenic lines containing each construct were identified and replicates of each line are currently being generated by micropropagation in preparation for virus challenge.

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10

Hastie, Marcus Lachlan. "In vitro activities of BBTV-REP." Thesis, Queensland University of Technology, 2001. https://eprints.qut.edu.au/37077/1/37077_Digitised%20Thesis.pdf.

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Books on the topic "Banana bunchy top disease"

1

Suresh, S. Banana bunchy top disease & its ahpid [sic] vector: An annotated bibliography. Coimbatore: Keerthi Pub. House, 1987.

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Book chapters on the topic "Banana bunchy top disease"

1

Lantican, Gaudencia A. "Field Screening of Gamma-Irradiated Cavendish Bananas." In Efficient Screening Techniques to Identify Mutants with TR4 Resistance in Banana, 97–109. Berlin, Heidelberg: Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-662-64915-2_7.

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AbstractIn our search for Cavendish bananas to withstand Fusarium oxysporum f. sp. cubense (Foc TR4) and other diseases, field screening of tissue-cultured Grand Nain banana seedlings derived from gamma-irradiated shoot tips was explored. Six months after irradiation and multiplication in the laboratory, the plantlets (M1V6) were individually grown in seedling bags under screen house conditions for 8 weeks, side-by-side with non-irradiated plantlets of the same clone. Once acclimatized, the banana plants were grown in an area confirmed positive of Foc TR4 (based on previous farm records stating that more than 50% of the plant population succumbed to the disease). Seedlings from each treatment (dose of radiation) were divided into four replicates, regardless of the number of plants. Each plant was given a unique identification code for traceability during disease monitoring, bunch and fruit quality evaluation.Incidences of Foc TR4, Moko disease (Ralstonia solanacearum) and virus diseases were monitored weekly. Plants found positive of any disease were eradicated immediately. The plant population for the succeeding generation was managed by removing the unwanted suckers, 12 weeks from planting using a spade gouge and keeping only one sucker per plant for the next generation. Agronomic characters of each plant were taken at the flowering stage. These included age to flower, height, pseudostem circumference, number of leaves and height of the sucker. The bunch was harvested 12 weeks from flowering. The number of hands in a bunch, the number of fingers and weight of a hand were recorded. The same agronomic characters of the plant were taken for the succeeding generations.Plants left standing in the field without any disease symptoms 3 years after planting were considered as putative mutants and were selected as candidate lines for multiplication and second-generation field screening. Only healthy suckers (free from viruses) were further multiplied via tissue culture technique to reach M1V6. Clean suckers from each line free of soil debris or dirt were sent to the laboratory for multiplication. At least 1000 plantlets were produced from each line for the second-generation field screening. These were grown in two locations – with and without records of Foc TR4. Field monitoring activities including plant population management, disease incidence assessment and fruit quality evaluation were carried out following the same protocols used in the establishment of the first-generation plants. Lines with population showing ≤10% Foc TR4 after the first harvest, with good vigor, fruit quality and productivity were considered as candidates for further multiplication, farmers distribution and field planting under semi-commercial scale.

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2

Dale, James L. "Banana Bunchy Top: An Economically Important Tropical Plant Virus Disease." In Advances in Virus Research, 301–25. Elsevier, 1987. http://dx.doi.org/10.1016/s0065-3527(08)60321-8.

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3

Thomas, J. E. "Banana Bunchy Top Virus." In Encyclopedia of Virology, 272–79. Elsevier, 2008. http://dx.doi.org/10.1016/b978-012374410-4.00636-1.

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Thomas, John E. "Banana Bunchy Top Virus (Nanoviridae)." In Reference Module in Life Sciences. Elsevier, 2020. http://dx.doi.org/10.1016/b978-0-12-809633-8.21235-1.

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Selvarajan, R., V. Balasubramanian, and C. Anuradha. "Population Structure and Diversity of Banana Bunchy Top Virus and Banana Bract Mosaic Virus." In Plant Viruses, 149–70. CRC Press, 2018. http://dx.doi.org/10.1201/b22221-9.

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Conference papers on the topic "Banana bunchy top disease"

1

Hanna, Rachid. "Prospects of biological control and other management options of the banana aphidPentalonia nigronervose, the vector of banana bunchy top virus in Africa." In 2016 International Congress of Entomology. Entomological Society of America, 2016. http://dx.doi.org/10.1603/ice.2016.115540.

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