The Scientific World Journal

Volume 2014 (2014), Article ID 768038, 11 pages

http://dx.doi.org/10.1155/2014/768038

Review Article

Gene Technology for Papaya Ringspot Virus Disease Management

Md. Abul Kalam Azad,1,2 Latifah Amin,¹ and Nik Marzuki Sidik³

¹Centre for General Studies, Universiti Kebangsaan Malaysia (UKM), 43600 Bangi, Selangor, Malaysia

²Department of Agricultural Extension, Khamarbari, Farmgate, Dhaka 1215, Bangladesh

³Faculty of Science and Technology, Universiti Kebangsaan Malaysia (UKM), 43600 Bangi, Selangor, Malaysia

Received 19 December 2013; Accepted 1 February 2014; Published 17 March 2014

Academic Editors: R. Dinkins and S. Rodtong

Copyright © 2014 Md. Abul Kalam Azad et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Papaya (Carica papaya) is severely damaged by the papaya ringspot virus (PRSV). This review focuses on the development of PRSV resistant transgenic papaya through gene technology. The genetic diversity of PRSV depends upon geographical distribution and the influence of PRSV disease management on a sequence of PRSV isolates. The concept of pathogen-derived resistance has been employed for the development of transgenic papaya, using a coat protein-mediated, RNA-silencing mechanism and replicase gene-mediated transformation for effective PRSV disease management. The development of PRSV-resistant papaya via post-transcriptional gene silencing is a promising technology for PRSV disease management. PRSV-resistant transgenic papaya is environmentally safe and has no harmful effects on human health. Recent studies have revealed that the success of adoption of transgenic papaya depends upon the application, it being a commercially viable product, bio-safety regulatory issues, trade regulations, and the wider social acceptance of the technology. This review discusses the genome and the genetic diversity of PRSV, host range determinants, molecular diagnosis, disease management strategies, the development of transgenic papaya, environmental issues, issues in the adoption of transgenic papaya, and future directions for research.

1. Introduction

Papaya (Carica papaya L) belongs to the family Caricaceaeand is one of the most economically important fruit crops in many tropical and subtropical countries. Papaya is a dicotyledonous, polygamous, and diploid species. The geographical origin of papaya is Southern Mexico and Costa Rica [1]. Papaya has been cultivated in the USA, India, Brazil, Mexico, Nigeria, Jamaica, Indonesia, China, Taiwan, Peru, Thailand, and the Philippines [2]. Papaya fruit is known for its high nutritive and medicinal value [3]. Papaya is rich source of vitamin A, B, and C, as well as proteolytic enzymes like papain and chymopapain. It is an excellent source of beta carotene which may prevent cancer, diabetes, and heart disease [4]. Ripe fruits are usually eaten fresh and can be processed into jam, jelly, marmalade, and candy. The “green” or unripe fruits can be used as vegetables. Papaya is also utilized in the pharmaceutical and cosmetics industries [5].

Papaya crops are currently beset by disease problems especially those caused by the papaya ringspot virus (PRSV) [6, 7]. Symptoms of PRSV manifest as a prominent mosaic pattern on the leaf lamina, wet-oily streaks on the petioles and upper part of the trunk, and the distortion of young leaves. PRSV is the most serious threat to papaya production in the world [8]. PRSV has been recognized as a destructive disease in many tropical and subtropical areas including the USA, South America, Africa [9], India [10], Thailand, Taiwan, China and the Philippines [11], Mexico [12], Australia [13], Japan [14], French Polynesia, and the Cook islands [15] resulting in the decline in fruit production. This disease can cause up to 100% losses of crops in some regions [16]. PRSV is transmitted in a nonpersistent way by several species of aphids in a process involving coat protein (CP) and the helper component proteinase (HC-Pro) [17–19].

Papaya and the aphid transmitted virus are cosmopolitan in distribution [16]. PRSV is controlled by different methods such as rouging of infected plants, use of barrier crops, cross protection, and transgenic resistance [20]. PRSV disease management, via vector controlling, is very difficult to conduct whilst cross protection for controlling PRSV disease is not effective worldwide. Resistance against PRSV has not been found in Carica papaya [21]. On the other hand, several wild Carica species such as C. cauliflora, C. pubescens, and C. quercifolia are resistant to PRSV, but these are sexually incompatible with C. papaya [22]. The most effective method of controlling plant viruses is through enhancing population resistance [23]. Genetic transformation of plants has made it possible to introduce selected genes into plants for controlling plant diseases and pests. The concept of pathogen derived resistance has stimulated research into obtaining virus resistance in papaya through gene technology. Pathogen-derived resistance is mediated either by proteins encoded by transgenes (protein-mediated) or by the transcripts produced from the transgene (RNA-mediated). Recently, research has indicated that pathogen-derived resistance is mediated by an RNA-based posttranscriptional gene-silencing mechanism. Protein-mediated resistance provides moderate protection against a broad range of related viruses whilst RNA-mediated resistance offers high levels of protection to closely related strains of the virus [24]. The RNAi technology has enabled the induction of an immune reaction to PRSV. This technology has been at the forefront of the new era in the development of eco-friendly molecular tools, which can be suppressed by specific genes which are responsible for disease management.

Currently, transgenic Papaya is being grown in Hawaii and accounts for more than 70% of Hawaii’s Papaya acreage. SunUp and Rainbow have been widely grown in USA without any adverse effects on human health [25]. In countries such as Australia, Jamaica, Venezuela, Vietnam, Thailand, Taiwan, and Philippines, the CP gene from their geographic region has been used to develop region-specific transgenic Papaya for the control of PRSV [20]. There have been some studies upon the development of PRSV-resistant varieties of C. papaya through gene technology but no review article on PRSV disease management is available. Tecson Mendoza et al. [26] summarized the development of transgenic papaya technology and research activities by different countries but did not cover all areas of PRSV management. Therefore, this review paper aims to review recent development of PRSV, genomic, diversity of PRSV, molecular identification, host-range determinants and vector transmission, biosafety, major challenges, and future research directions.

2. The Genome of the Papaya Ringspot Virus (PRSV)

PRSV is of the genus Potyvirus and of the family Potyviridae. The genome of PRSV consists of 800–900 nm long nonenveloped flexuous filamentous particles with an ssRNA genome of about 10,324 nucleotides [27]. The virion contains 94.5% protein and 5.5% nucleic acid by weight. The PRSV genome encodes a single large protein (3,344 amino acids) which is subsequently cleaved into smaller proteins with various functions. The suggested map of the PRSV polyprotein is outlined in Figure 1.

Figure 1: The map of the PRSV polyprotein. Specific motifs are indicated, solid bars indicate cleavage sites in the polyprotein, and the dashed line indicates the potential internal cleavage site of the NIa protein.

The proposed locations of the cleavage sites predict eight to nine proteins consisting of P1 (63K), helper component (HC-Pro, 52K), P3 (46K), cylindrical inclusion protein (C1, 72K), nuclear inclusion protein a (NIa, 48K), nuclear inclusion protein b (NIb, 59K), and coat protein (CP, 35K) [27]. The P1 protein is encoded by the Potyvirus genome and autocatalytically cleaves. The P1 protein is the least conserved protein and can move systemically in infected plants [28]. The helper component (HC-Pro) is a multifunctional protein which mediates aphid transmission, symptom expression, long distance movement, genome amplification, and suppression of posttranscriptional gene silencing (PTGS). HC-Pro is a highly effective suppressor of RNA silencing [29]. It can affect the microRNA-mediated development pathway in plants and help in the establishment of the heterologous virus. The long distance movement and genome replication of HC-Pro depends on PTGS suppression [30]. HC-Pro is responsible for synergism between polyviruses and unrelated viruses that can cause severe symptoms and an accumulation of virus in infected leaves [31]. The C1 protein of PRSV has NTP binding, NTPase, RNA binding, and RNA helicase activity [32, 33]. The NIa has two domains defined as the N-terminal genome-linked protein (VPg) and C-terminal domain. The VPg is required for priming RNA synthesis. Nib is a codependent RNA polymerase that has been shown to have replicase activity. CP is involved in aphid transmission systemic movement and the encapsidation of the viral RNA [28]. The PRSV is divided into two major biotypes or strains based on their host range. The PRSV-W type affects cucurbits but not papaya while the PRSV-P type affects papaya and cucurbits.

3. The Genetic Diversity of PRSV

Knowledge of the genetic diversity of PRSV is important for effective evidence-based disease management. The genetic diversity of PRSV was observed in different regions of the world [34]. PRSV isolates and the sequence for PRSV CP genes have been presented in Table 1. Sequence diversity among isolates of the virus and their distribution are important for establishing virus origin, development, dispersion, and disease etiology, in the pursuit of effective virus disease management. There is little sequence variation among the CP genes of PRSV isolates from the USA and Australia [35, 36]. On the other hand, there is greater sequence variation amongst the CP genes of PRSV isolates from India [37] and Mexico [38]. The diversity at amino acid and nucleic acid levels was highest among the Asian population of PRSV isolates [37]. The PRSV isolates from India differed from the PRSV isolates from other countries. Bateson et al. [39] reported that the origin of PRSV was South Asia and found a greater diversity in PRSV isolates from India. The differences in PRSV were observed due to differences in the CP gene length [37]. The highest diversity of PRSV nucleotide sequences was found in the CP and HC-Pro genes collected from India [40]. PRSV might have been transported from India to America in the early 18th century and spread in 19th and 20th centuries [40]. Variation in the CP gene sequences of PRSV was observed in different parts of the world [35]. The genetic diversity of PRSV depends on geographical location. For example, the transgenic papaya incorporating CP gene (HA 5-1) isolated from USA showed resistance to PRSV infection by the severe USA isolate (HA) but did not show resistance against infection by the Australian and Thai isolates of PRSV [34].

Table 1: PRSV isolates and sequence for PRSV CP genes.

Name
Biotype
Origin
Gene Bank accession no.
Reference

USP-HW
P
USA
X67673
[39]

USW-FL
W
USA
D00594
[36]

USP-FL
P
USA
AF196839
[64]

AU-P
P
Australia
U14738
[35]

BD
P
Australia
U14736
[35]

BUN
P
Australia
U14737
[35]

WP
P
Australia
U14740
[96]

TWP-2
P
Taiwan
AB044341
[39]

TWP-YK
P
Taiwan
X78557
[44]

THP-11
P
Thailand
U14743
[39]

THW-03
W
Thailand
AF506895
[39]

THW-04
W
Thailand
AF506894
[39]

THP-14
P
Thailand
AF506898
[39]

THP-13
P
Thailand
AF506899
[39]

THP-12
P
Thailand
AF506900
[39]

INP-BR
P
India
AF305545
[38]

INW
P
India
AF063221
[39]

INP
P
India
AF063220
[39]

VNP-02-29
P
Vietnam
AF506862-89
[39]

VNW-30-32
W
Vietnam
AF506846-48
[39]

SRP
P
Sri Lanka
U14741
[35]

BZP-2
P
Brazil
AF344640
[39]

BZP-9
P
Brazil
AF344647
[39]

CHP
P
China
AF243496
[96]

JAP
P
Japan
AB044339
[39]

PHP-01
P
Philippines
AF506902
[39]

ChT-11
P
Mexico
AJ012650
[38]

VTB-6
P
Mexico
AJ012649
[38]

4. Host Range Determinants and Vector Transmission

Plant viruses spread from cell to cell with the interaction of virus and host factors. The plant viruses enter the host cell through wound sites, mechanically or via vector mechanisms. Viruses infect the plants by two further ways: short distance (cell to cell movement) and long distance. Virus movements within the plant are dependent on host specific reactions. PRSV has limited number of hosts belonging to the families Caricaceae, Chenopodiaceae, and Cucurbitaceae. The propagation hosts of PRSV are C. papaya, Cucurbita pepo, and Cucumis metuliferus. The lesion assay hosts of PRSV are Chenopodium quinoa and Chenopodium amaranticolor [8]. There are two strains of PRSV which can be differentiated on the basis of their host range [41]. The PRSV type P (PRSV-P) can infect the papaya, whereas PRSV type W (PRSV-W) can only infect cucurbits. Both strains are closely related. Chen et al. [42] reported that the CP gene is not a determinant for the infection of papaya. The NIa and a portion of the Nib gene of PRSV were responsible for papaya infection. Mutation of P1 and HC-Pro genes resulted in the attenuation of PRSV symptoms in papaya and local lesion formation in Chenopodium quinoa [43] while HC-Pro is the major determinant of lesion formation in Chenopodium quinoa. The interaction between host and PRSV is fundamental for biological interest and for developing disease management strategies. Although, cross protection is not clearly understood at the molecular level, posttranscriptional gene silencing (PTGS) is effective for PRSV management when cultivating Papaya. The virus is transmitted by several species of aphids in a nonpersistent manner. CP and HC-Pro are required for vector transmission of PRSV. Transmission occurs when aphids feed upon infected papaya plants and subsequently feed upon healthy papaya plants.

5. Molecular Diagnostic of PRSV

The most important step is identification of virus for effective PRSV control. PRSV diagnosis is very important as it exists in different strains [44]. The virus particle is very unstable and tends to aggregate with plant debris. PRSV is primarily diagnosed by assessment of symptoms; visual diagnosis is quick but it is also unreliable. The symptoms similar to PRSV can be due to the effects of micronutrient deficiency in soil and a variety of weather conditions. PRSV might be confirmed by molecular diagnosis such as ELISA, Immunocapture RT-PCR, RT-PCR, and DIBA. ELISA is widely used for rapid detection in the different parts of the world as a quick and reliable technique for PRSV detection in papaya [34, 45]. Immunocapture RT-PCR is a very reliable technique for quick determination of viruses and can detect the low concentrations of PRSV in papaya; it is a more sensitive technique than ELISA, RT-PCR, and DIBA [46]. Ruiz-Castro and Silva-Rosales [47] reported that reverse transcription and polymerase chain reaction (RT-PCR) showed reliable results for the detection of PRSV in papaya samples. Dot immune binding assay (DIBA) is useful for virus indexing, as it is a simple and cheap method for large scale virus detection [48].

6. Strategy for PRSV Disease Management

PRSV is the most destructive viral disease of papaya. Control of PRSV includes rouging infected plants and spraying them with aphicides. However, rouging cannot stop the spread of the disease once it is established. Similarly, spraying with aphicides is often ineffective since the virus is transmitted to the plants before the aphids are killed [49]. The PRSV disease management has been focused on developing tolerant or resistant varieties of papaya, but these varieties are rarely planted due to poor fruit quality and vigour [50]. PRSV-resistant gene is available in some wild varieties related to the Carica species. But the development of PRSV-resistant varieties through conventional breeding methods has been complicated due to the sexual incompatibility of wild species and cultivated papaya [51, 52]. Disease tolerance in back crosses with commercial papaya also limits this approach for PRSV disease management. Cross protection was used to control PRSV which involved the use of a mild virus strain against economic damage caused by severe strains of the same virus [6, 53]. The cross protection strategy of inoculating papaya with a mild strain of PRSV provides resistance against severe PRSV strain infection in Taiwan [54]. Cross protection depends on the availability of mild strains that can be used for effective protection against the target virus. Cross protection needs extra agricultural practice and care. However, strain specificity and the technical difficulties associated with propagating pure strains of mild forms of the virus and the unavailability of such mild strains limit the benefits of this approach [55]. Field evaluations revealed that cross protection was marginally effective for PRSV management evaluation in the field [8]. Researchers from Cornell University and the University of Hawaii initiated the development of PRSV-resistant papaya by gene technology. The concept of pathogen derived resistance was proposed by Sanford and Johnston [56] for developing resistance against pathogens. This research group has applied the concept of pathogen derived resistance which has stimulated research into obtaining virus resistance through gene technology. Pathogen derived resistance is governed either by protein-mediated or RNA-mediated methods. An alternative strategy using RNA-mediated gene silencing with transgenic plants expressing viral genes has been developed [57]. Resistance levels of PRSV differ with environmental factors and plant development stages despite of the success with this approach. Broad spectrum resistance against different PRSV isolates depends on the homology of transgenes with viral target genes and the genetic divergence of different PRSV strains which are correlated with their geographical distribution [58]. The transgenic papaya varieties resistant to PRSV against different viral strains must be developed individually for various papaya growing regions. The development of PRSV-resistant lines is generally considered the best strategy for efficient PRSV disease control in papaya for long-term protection [20].

7. Gene Technology for the Development of PRSV-Resistant Transgenic Papaya

Generally crops with resistance to viral disease may be developed through genes derived from viral sequences providing pathogen derived resistance (PDR), genes from various other sources that can interfere with target virus, and natural resistance genes. The concept of pathogen derived resistance (PDR) is a new approach for PRSV management. Pathogen derived genes interfere with the replication process of viruses in their host plants in different ways. So far, PRSV-resistant transgenic papaya has been developed through coat protein (CP), RNA silencing, and replicase gene technology.

7.1. Coat Protein (CP) Mediated Resistance

The development of transgenic papaya to prevent infection by PRSV has been employed after the successful development of transgenic tobacco, expressing the CP gene of the tobacco mosaic virus, which showed disease resistance. Fitch et al. [59] developed transgenic papaya containing CP genes resistant to PRSV using the gene transfer system of immature zygotic embryos with a plasmid construction containing the neomycin phosphotransferase II (nptII) gene. This was the first result that demonstrated that CP mediated resistance can be used to control PRSV. Cheng et al. [60] developed PRSV-resistant transgenic papaya using the CP gene of the Taiwanese strain of PRSV constructed with a Ti binary vector pBGCP through Agrobacterium mediated transformation. Many scientists have begun to develop PRSV-resistant transgenic papaya using different explants with plasmids containing the neomycin phosphotransferase II (nptII) gene [42, 61–63]. The CP mediated protection of PRSV has been adopted throughout the world [64]. Researchers have preferred CP genes as the agents utilized to develop PRSV-resistant papaya [65]. However, the effectiveness of CP mediated PRSV resistance depends upon the origin of PRSV isolates. The untranslatable and translatable constructs of PRSV-CP containing genes utilized in different countries have been shown in Table 2.

Table 2: Transgenic papaya developed by various research groups through gene technology.

Country
Cultivar
Construct
Type of coat protein
Transformation
Transgene expression
References

Australia
Local variety
uidA leader + CaMV35S promoter + PRSV Bridgeman Downs cp gene from Q/S start with stop codon in the middle of sequence
Translatable cp
Biolistics
cp not detected in ELISA and low levels of cp detection in northern analysis
[61]

Brazil
Sunrise solo, Sunset solo
CaMV35S + CMV leader + PRSV Bahia cp gene from Q/S start
Translatable cp
Biolistics
Low to high levels cp detected in ELISA
[97]

Brazil
Sunrise solo, Sunset solo
CaMV35S + CMV leader + PRSV Bahia cp gene from Q/S start
Untranslatable cp
Biolistics
Not tested
[97]

Florida
CV.F65
uidA leader + CaMV35S promoter + PRSV HIK cp gene from Q/S start
Translatable cp
Agrobacterium
cp is not detected in northern analysis
[98]

Florida
CV.F65
uidA leader + CaMV35S promoter + PRSV HIK cp gene from Q/S start in antisense
Untranslatable cp
Agrobacterium
cp is not detected in northern analysis
[98]

Florida
CV.F65
uidA leader + CaMV35S promoter + PRSV HIK cp gene from Q/S start with frame shift mutation
Untranslatable cp
Agrobacterium
cp is not detected in northern analysis
[98]

Florida
CV.F65
uidA leader + CaMV35S promoter + PRSV HIK cp gene from Q/S start with 3 in frame stop
Untranslatable cp
Agrobacterium
cp is not detection in northern analysis
[98]

Hawaii
Sunset solo
CMV leader + 16 aa CMV cp + PRSV HA 5-1 cp gene from Q/S start
Translatable cp
Biolistics
Low to high levels cp detected in ELISA and cp RNA detected by northern analysis
[99, 100]

Hawaii
Sunset solo
CaMV35S + CMV leader + PRSV Caymanas untranslatable cp
Untranslatable cp
Biolistics
cp RNA detected in northern analysis
[101]

Jamaica
Sunrise solo
CaMV35S + CMV leader + PRSV Caymanas untranslatable cp
Untranslatable cp
Biolistics
cp RNA detected in northern analysis
[62, 99]

Jamaica
Sunrise solo
CaMV35S + CMV leader + PRSV Caymanas cp from Q/S start
Translatable cp
Biolistics
cp RNA detected in northern analysis
[62, 99]

Taiwan
Tainung no. 2
uidA leader + CaMV35S promoter + PRSV YK cp gene from Q/S start
Translatable cp
Biolistics
cp transcript detected in northern analysis
[58, 78]

Thailand
KhakDum
CaMV35S + uidA leader + PRSV Ratchaburi province cp
Translatable cp
Biolistics
cp detected in western analysis
[73, 102]

Venezuela
Thailand red
CaMV35S + CMV leader + PRSV EV & VE from Q/S start
Translatable cp
Agrobacterium
cp RNA is not detected ELISA and low level cp detected in northern analysis
[87]

Gonsalves et al. [66] used gene gun technology when transferring an untranslatable CP gene for the development of a PRSV-resistant papaya variety. This showed resistance to homologous PRSV isolates from Hawaii, Australia, Taiwan, Mexico, Jamaica, the Bahamas, and Brazil. The PRSV-resistant (Hawaiian) transgenic papaya variety SunUp was developed through transformation of somatic embryos with the CP gene of the Hawaiian PRSV strain [59]. Tennant et al. [34] developed transgenic papaya expressing the CP gene of the mild PRSV strain from Hawaii (PRV HA 5-1). This transgenic papaya showed a high level of resistance against a severe strain of PRSV (PRV-HA). Bau et al. [67] developed transgenic papaya lines expressing a CP gene with broad-spectrum resistance PRSV of different strains in different geographical areas in Taiwan. Magdalita et al. [68] developed genetically engineered papaya using the CP gene of Philippine PRSV and regenerated putative transgenic R0 plantlets, which were moderately susceptible whilst R1 plantlets were completely resistant.

7.2. RNA-Interference-Mediated Resistance

RNA interference (RNAi) mediated virus resistance was first discovered by Waterhouse et al. [69] against the Potato virus Y in transgenic tobacco plants. RNA mediated gene control mechanism has provided a new platform for developing molecular tools for gene functions study and crop improvements [70]. RNA silencing pathways play a role in both biotic and abiotic stress responses in plants defence against pathogens and insects that will help humankind to face the challenges of productive agriculture in the increasingly unfavourable environmental conditions associated with climate change. This technology can be used for generating disease resistance by suppressing a specific gene or genes [71]. PRSV is an RNA virus containing a single open reading frame translated into a large polyprotein that produced the final protein products [72]. RNA-mediated protection would be effective only when the transgene is highly similar to the attacking virus. The differences between geographically distinct isolates have made the creation of PRSV-resistant transgenic plants difficult. The failure of PRSV resistance has frequently involved the silencing by suppressor proteins of viral origin [73]. This problem can be overcome by the silencing suppressor protein HcPro, through an RNA-silencing mechanism within transgenic papaya. The helper component proteinase (HcPro) has been shown to be a highly effective suppressor of RNA silencing. Mangrauthia et al. [74] suggested that HcPro is an important component which needs to be taken into consideration for the development of PRSV-resistant papaya on the Indian subcontinent. The mechanism of RNA-mediated virus resistance is also referred to as homology dependency resistance to reflect the specific mechanism of posttranscriptional gene silencing (PTGS) [75, 76]. PTGS is the accumulation of 21–25 nucleotide small-interfering RNAs, the sequence-specific degradation of target mRNAs, and the subsequent methylation of target gene sequences. Tennant et al. [77] reported that mechanisms of transgenic papaya resistance against PRSV are sequence homology dependent and mediated by RNA via PTGS. They found that an untranslatable CP gene was able to confer resistance to the homologous strain of the virus isolate of PRSV by PTGS. On the other hand, the silencing suppressor was the main factor for the suppression of PRSV transgenic resistance [78]. Ruanjan et al. [73] reported that transgenic papaya showed resistant to PRSV by suppressing posttranscriptional gene silencing (PTGS).

7.3. Replicase Gene-Mediated Resistance

The resistance mechanism is protein-based because the resistance phenotype is influenced by mutations affecting the primary structure of the protein encoded by the transgene. Replicase genes are different in structure within various genera. Resistance created by the introduction of replicase gene was first demonstrated for the tobacco mosaic virus (TMV) in Nicotiana tabacum [79]. Replicase genes with mutations have been shown to be able to confer virus resistance [80]. Chen et al. [42] reported that replicase gene (RP) conferred resistance to PRSV in transgenic papaya. Wei et al. [81] reported that transgenic papaya with mutated replicase genes (RP) showed high resistance to PRSV.

8. Factors to Be Considered for the Adoption of Transgenic Papaya

Despite the potential and benefits of transgenic papaya, the adoption rate of transgenic papaya is extremely low. Major challenges face the adoption of transgenic papaya which include the application of the biotechnological protocols for the development of transgenic papaya, its viability as a commercial product, biosafety regulatory issues, and trade regulations. Transgenic papayas were found to have no effect on the surrounding ecology such as adjacent nontransgenic papaya trees, microbial flora, beneficial insects, or soil [82]. Hsieh and Pan [83] reported that PRSV-resistant transgenic papaya had only limited effects on the microbial life within soil. Safety assessments by researchers have suggested that transgenic papaya may not have adverse effects as regards nutritional and toxicological parameters [84]. The successful adoption of transgenic papaya depends on regulatory issues concerning biosafety and the social acceptance of the technology. PRSV-resistant transgenic papayas have been released and adopted in the USA and China [85]. Gonsalves et al. [86] reported that the adoption rate of PRSV-resistant papaya was high among famers in Hawaii. Fermin et al. [87] found a variable adoption rate of transgenic papaya in Hawaii, Jamaica, and Venezuela which was influenced by the demand for papaya, biosafety regulations, and the social acceptance of the technology. The adoption rate of transgenic papaya is still slow due to lack of engagement from farmers, who are frequently persuaded against the technology by antigenetic engineering NGO networks. Some countries are also facing opposition to transgenic papaya by Greenpeace International (NGO). Some developing countries are lacking in biosafety laws, infrastructure, and the training sufficient to carry out the regulatory testing needed prior to commercialization. There are many countries with markets that are dependent on the political and consumer demands of importing countries. Moreover, cultural awareness, societal, political, and economic factors may influence the adoption of transgenic papaya.

9. Environment Issues and Food Safety

Transgenic crops are subject biosafety rules due to possibly negative impacts of the plants on the environment, human, and animal health. The environmental risks may come in the form of negative effects on beneficial insects, mammals, microbes, the possibility of crossing with nontransgenic species, and their persistence in the environment. CP expressed by the transgene within a transgenic plant may enter another invading virus infecting the plant via a process of heteroencapsidation. The CP gene can carry determinants for pathogenicity and the properties of the virus in transgenic plants might be changed. So, vector nontransmissible virus in transgenic plants would be transformed into a transmissible virus through heteroencapsidation resulting in new viral epidemics. But heteroencapsidation in transgenic papaya expressing virus CP gene has limited significance in practice and environmental effects would be negligible. Recombination refers to the exchange of genetic materials between two RNA molecules during virus replication. A recombinant virus has potentially negative effects on the environment such as increasing pathogenicity, expanding host range, and changing the vector. So far, no recombination has been found in PRSV transgenic papaya in the field [23]. Research into the effects of transgenic papaya on microbiology has been conducted. Phironrit et al. [88] reported that there were no distinct differences of microbial community in soil samples collected from transgenic and nontransgenic papaya fields. On the other hand, Hsieh and Pan [83] reported that PRSV-resistant transgenic plants had a limited effect on the microbial community of the soil. Transgenic flow is a major concern amongst growers, exporters, and consumers. Fuchs and Gonsalves [23] reported that gene flow is quite low among papaya as most of the papaya was hermaphrodite in Hawaii. Manshardt [89] showed that transgenic seeds were found in 7% of nontransgenic hermaphrodite. Food safety concerns toxins and allergens. Transgenic plants have potential allergenic properties due to the protein encoded by viral sequences [23]. Yeh and Gonsalves [90] reported that there were no ill effects after the consumption of PRSV-resistant transgenic papaya. Fermín et al. [91] observed that transgene derived PRSV CP did not pose any risk of food allergies. Transgenic papaya fruit can be recognised as an equivalent substitution for traditional papaya in food safety [92]. Benzyl isothiocyanate (BITC) is considered an antinutrient which has been identified in extracts of Cruciferae, Caricaceae, and Moringaceae [93]. BITC may endanger the foetus in pregnant women and enhance the risk of prostate cancer [94]. The BITC value of transgenic papaya and nontransgenic papaya is similar and consequently transgenic papaya does not pose any increased threat to human health. Therefore, PRSV-resistant papaya is environmentally safe and suitable for human consumption.

10. Current Challenges and Future Prospects

Transgenic papaya is the most advanced technology extant for plant disease management [95]. Transgenic papaya has had a great socioeconomic impact on the Hawaiian papaya industry [86]. However, the success of transgenic papaya depends on the continued stability of transgenic resistance and the desirable horticultural characteristics of papaya. The breakdown of PRSV resistance is the main problem associated with PRSV-resistant papaya. Tennant et al. [34] reported that R₁ transgenic papaya of line 55-1 showed narrow resistance after inoculation in greenhouse. R₁ transgenic papaya plants were resistant to PRSV isolates from Hawaii but remained susceptible to PRSV occurring in other countries. Moreover, transgenic resistance in papaya depends on growth stage, doses of transgene, and transgene homology [34]. Resistance to PRSV is positively correlated with a degree of homology between the CP of infecting virus and transgene [8]. For example, 97–100% of the sequence homology to transgene CP was found in PRSV isolates from Hawaii whilst 89–93% sequence homology of transgene CP was found in PRSV isolates from elsewhere [8]. Tripathi et al. [8] reported that the CP expression of transgenic papaya plants was lower in homozygous SunUp than hemizygous Rainbow. Transgenic resistance in Rainbow and SunUp has proven stable for nearly 10 years in Hawaii but resistance may breakdown in regions where new virus strains exist. There is great genetic diversity within PRSV isolates from different regions of the world. PRSV-resistant transgenic papaya faces major difficulties as no current strain has resistance against geographically distinct isolates. It is important that researchers monitor the PRSV population and its diversity to ensure the successful disease management of papaya. On the other hand, posttranscriptional gene silencing (PTGS) technology is possibly a more powerful and effective method for the development of PRSV-resistant transgenic papaya. Therefore, country-specific varieties of PRSV-resistant transgenic papaya should be developed through PTGS technology using geographically distinct PRSV isolates.

11. Conclusion

PRSV is the major threat for papaya production. Transgenic papaya via gene technology has been used for PRSV disease management. In this review, we find that PRSV-resistant papaya varieties have been developed using CP genes or RNA interference. The genetic diversity of PRSV has been identified throughout the world. The breakdown of PRSV resistance is the major challenge facing transgenic papaya cultivation. Although, the gene flow of PRSV-transgenic papaya is low, research towards minimizing this problem should be conducted. The adoption of PRSV-resistant transgenic papaya is still slow and it depends upon the demand for papaya, biosafety regulations, and social acceptance of the technology. Recent studies indicate that PRSV-resistant transgenic papaya is environmentally safe and has no adverse effects on human health. Posttranscriptional gene silencing (PTGS) technology may be suitable for the development of PRSV-resistant transgenic papaya in future. This review suggests that papaya producing countries should develop PRSV-resistant transgenic papaya using their own PRSV isolates through posttranscriptional gene silencing technology.

Conflict of Interests

The authors declare that there is no conflict of interests.

Acknowledgment

The authors would like to thank the Universiti Kebangsaan Malaysia for providing financial support for the publication of this paper under the UKM-AP-CMNB-2009/1 and DPP-2013-201 grant.

References

A. DeCandolle, Origin of Cultivated Plants, John Wiley & Sons, New York, NY, USA, 1984.

R. Jayavalli, T. N. Balamohan, N. Manivannan, and M. Govindaraj, “Breaking the intergeneric hybridization barrier in Carica papaya and Vasconcellea cauliflora,” Scientia Horticulturae, vol. 130, no. 4, pp. 787–794, 2011.

M. A. K. Azad, M. G. Rabbani, and L. Amin, “Plant regeneration and somatic embryogenesis from immature embryos derived through interspecific hybridization among different Carica species,” International Journal of Molecular Science, vol. 13, pp. 17065–17076, 2012.

G. Aravind, D. Bhowmik, S. Duraivel, and G. Harish, “Traditional and medicinal uses of Carica papaya,” Journal of Medicinal Plants Studies, vol. 1, no. 1, pp. 7–15, 2013.

A. M. O. Retuta, P. M. Magdalita, E. T. Aspuria, and R. R. C. Espino, “Evaluation of selected transgenic papaya (Carica papaya L) lines for inheritance of resistance to papaya ringspot virus and horticultural traits,” Plant Biotechnology, vol. 29, pp. 339–349, 2012.

S. D. Yeh and D. Gonsalves, “Evaluation of induced mutants of papaya ringspot virus for control by cross protection,” Phytopathology, vol. 74, pp. 1086–1091, 1984.

D. Gonsalves, “Control of papaya ringspot virus in papaya: a case study,” Annual Review of Phytopathology, vol. 36, pp. 415–437, 1998.

S. Tripathi, J. Y. Suzuki, S. A. Ferreira, and D. Gonsalves, “Papaya ringspot virus-P: characteristics, pathogenicity, sequence variability and control,” Molecular Plant Pathology, vol. 9, no. 3, pp. 269–280, 2008.

D. E. Purcifull, J. R. Edwardson, E. Hiebert, and D. Gonsalves, “Papaya ringspot virus,” in CMI/AAB Description of Plant Viruses, R. E. Coronel, Ed., vol. 292, no. 2, p. 8, Wageningen University, Wageningen, The Netherlands, 1984.

S. M. P. Khurana, “Studies on three virus diseases of papaya in Gorakhpur, India,” in Proceedings 19th International Horticulture Congress, vol. 7, p. 260, Warszawa, Poland, 1974.

D. Gonsalves, “Papaya ringspot virus,” in Compendium of Tropical Fruit Diseases, R. C. Ploetz, G. A. Zentmyer, W. T. Nishijima, K. G. Rohrbach, and H. D. Ohr, Eds., pp. 67–68, APS Press, St. Paul, Minn, USA, 1994.

H. F. Alvizo and C. Rojkind, “Resistencia al virus mancha anular del papayo en Carica cauliflora,” in Revista Mexicana De Fitopatología, vol. 5, pp. 61–62, 1987.

J. E. Thomas and R. L. Dodman, “The first record of papaya ringspot virus-p in Australia,” Australian Plant Pathology, vol. 22, pp. 2–7, 1993.

T. Maoka, S. Kawano, and T. Usugi, “Occurrence of the P strain of papaya ringspot virus in Japan,” Annals of the Phytopathological Society, vol. 61, pp. 34–37, 1995.

R. I. Davis, L. Mu, N. Maireroa et al., “First records of the papaya strain of Papaya ringspot virus (PRSV-P) in French Polynesia and the Cook Islands,” Australasian Plant Pathology, vol. 34, no. 1, pp. 125–126, 2005.

P. F. Tennant, G. A. Fermin, and R. E. Roye, “Viruses infecting papaya (Carica papaya L.): etiology, pathogenesis, and molecular biology,” Plant Viruses, vol. 1, pp. 178–188, 2007.

I. G. Maia, A.-L. Haenni, and F. Bernardi, “Potyviral HC-Pro: a multifunctional protein,” Journal of General Virology, vol. 77, no. 7, pp. 1335–1341, 1996.

Y.-H. Peng, D. Kadoury, A. Gal-On, H. Huet, Y. Wang, and B. Raccah, “Mutations in the HC-Pro gene of zucchini yellow mosaic potyvirus: effects on aphid transmission and binding to purified virions,” Journal of General Virology, vol. 79, no. 4, pp. 897–904, 1998.

T. P. Pirone and S. Blanc, “Helper-dependent vector transmission of plant viruses,” Annual Review of Phytopathology, vol. 34, pp. 227–247, 1996.

G. A. Fermin, L. T. Castro, and P. F. Tennant, “CP-transgenic and non-transgenic approaches for the control of papaya ringspot: current situation and challenges,” Transgenic Plant Journal, vol. 4, no. S1, pp. 1–15, 2010.

J. A. Teixeira da Silva, Z. Rashid, D. T. Nut, and et. al, “Papaya (Carica papaya L.) biology and biotechnology,” Tree and Forestry Science and Biotechnology, vol. 1, pp. 47–73, 2007.

S. Horovitz and H. Jimenez, “Cruzamientos interspecificos y intergenericos in Carica ceas y sus implicaciones fitotecnicas,” Agronomia Tropical (Maracay), vol. 17, pp. 323–343, 1967 (Spanish).

M. Fuchs and D. Gonsalves, “Safety of virus-resistant transgenic plants two decades after their introduction: lessons from realistic field risk assessment studies,” Annual Review of Phytopathology, vol. 45, pp. 173–202, 2008.

D. C. Baulcombe, “RNA as a target and an initiator of post-transcriptional gene silencing in trangenic plants,” Plant Molecular Biology, vol. 32, no. 1-2, pp. 79–88, 1996.

D. Gonsalves, S. Tripathi, J. B. Carr, and J. Y. Suzuki, “Papaya ringspot virus,” The Plant Health Instructor, 2010.

E. M. Tecson Mendoza, A. C. Laurena, and J. R. Botella, “Recent advances in the development of transgenic papaya technology,” Biotechnology Annual Review, vol. 14, pp. 423–462, 2008.

S.-D. Yeh and D. Gonsalves, “Translation of papaya ringspot virus RNA in vitro: detection of a possible polyprotein that is processed for capsid protein, cylindrical-inclusion protein, and amorphous-inclusion protein,” Virology, vol. 143, no. 1, pp. 260–271, 1985.

S. Urcuqui-Inchima, A.-L. Haenni, and F. Bernardi, “Potyvirus proteins: a wealth of functions,” Virus Research, vol. 74, no. 1-2, pp. 157–175, 2001.

R. Anandalakshmi, G. J. Pruss, X. Ge et al., “A viral suppressor of gene silencing in plants,” Proceedings of the National Academy of Sciences of the United States of America, vol. 95, no. 22, pp. 13079–13084, 1998.

K. D. Kasschau and J. C. Carrington, “Long-distance movement and replication maintenance functions correlate with silencing suppression activity of potyviral HC-Pro,” Virology, vol. 285, no. 1, pp. 71–81, 2001.

G. Pruss, X. Ge, X. M. Shi, J. C. Carrington, and V. B. Vance, “Plant viral synergism: the potyviral genome encodes a broad-range pathogenicity enhancer that transactivates replication of heterologous viruses,” Plant Cell, vol. 9, no. 6, pp. 859–868, 1997.

A. Fernandez, S. Lain, and J. A. Garcia, “RNA helicase activity of the plum pox potyvirus CI protein expressed in Escherichia coli. Mapping of an RNA binding domain,” Nucleic Acids Research, vol. 23, no. 8, pp. 1327–1332, 1995.

S. Lain, J. L. Riechmann, and J. A. Garcia, “RNA helicase: a novel activity associated with a protein encoded by a positive strand RNA virus,” Nucleic Acids Research, vol. 18, no. 23, pp. 7003–7006, 1990.

P. F. Tennant, C. Gonsalves, K. S. Ling et al., “Differential protection against papaya ringspot virus isolates in coat protein gene transgenic papaya and classically cross-protected Papaya,” Phytopathology, vol. 84, no. 11, pp. 1359–1366, 1994.

M. F. Bateson, J. Henderson, W. Chaleeprom, A. J. Gibbs, and J. L. Dale, “Papaya ringspot potyvirus: isolate variability and the origin of PRSV type P (Australia),” Journal of General Virology, vol. 75, no. 12, pp. 3547–3553, 1994.

H. Quemada, B. L'Hostis, D. Gonsalves et al., “The nucleotide sequences of the 3'-terminal regions of papaya ringspot virus strains W and P,” Journal of General Virology, vol. 71, no. 1, pp. 203–210, 1990.

R. K. Jain, J. Sharma, A. S. Sivakumar et al., “Variability in the coat protein gene of Papaya ringspot virus isolates from multiple locations in India,” Archives of Virology, vol. 149, no. 12, pp. 2435–2442, 2004.

L. Silva-Rosales, N. Becerra-Leor, S. Ruiz-Castro, D. Téliz-Ortiz, and J. C. Noa-Carrazana, “Coat protein sequence comparisons of three Mexican isolates of papaya ringspot virus with other geographical isolates reveal a close relationship to American and Australian isolates,” Archives of Virology, vol. 145, no. 4, pp. 835–843, 2000.

M. F. Bateson, R. E. Lines, P. Revill et al., “On the evolution and molecular epidemiology of the potyvirus Papaya ringspot virus,” Journal of General Virology, vol. 83, no. 10, pp. 2575–2585, 2002.

X. A. Olarte Castillo, G. Fermin, J. Tabima et al., “Phylogeography and molecular epidemiology of Papaya ringspot virus,” Virus Research, vol. 159, no. 2, pp. 132–140, 2011.

D. Gonsalves and M. Ishii, “Purification and serology of papaya ringspot virus,” Phytopathology, vol. 70, no. 11, pp. 1028–1032, 1980.

G. Chen, C. M. Ye, J. C. Huang, M. Yu, and B. J. Li, “Cloning of the papaya ringspot virus (PRSV) replicase gene and generation of PRSV-resistant papayas through the introduction of the PRSV replicase gene,” Plant Cell Reports, vol. 20, no. 3, pp. 272–277, 2001.

C.-H. Chiang, C.-Y. Lee, C.-H. Wang et al., “Genetic analysis of an attenuated Papaya ringspot virus strain applied for cross-protection,” European Journal of Plant Pathology, vol. 118, no. 4, pp. 333–348, 2007.

C. H. Wang, H. J. Bau, and S. D. Yeh, “Comparison of the nuclear inclusion b protein and coat protein genes of five papaya ringspot virus strains distinct in geographic origin and pathogenicity,” Phytopathology, vol. 84, no. 10, pp. 1205–1210, 1994.

S. D. Yeh, H. J. Bau, Y. H. Cheng, T. A. Yu, J. S. Yang, and R. A. Drew, “Greenhouse and field evaluations of coat-protein transgenic papaya resistant to papaya ringspot virus,” Acta Horticulturae, vol. 461, pp. 321–328, 1998.

M. Sreenivasulu and D. V. R. SaiGopal, “Development of recombinant coat protein antibody based IC-RT-PCR and comparison of its sensitivity with other immunoassays for the detection of papaya ringspot virus isolates from India,” Plant Pathology Journal, vol. 26, no. 1, pp. 25–31, 2010.

S. Ruiz-Castro and L. Silva-Rosales, “Use of RT-PCR for papaya ringspot virus detection in papaya (Carica papaya) plants from Veracruz, Tabasco and Chiapas,” Revista Mexicana de Fitopatologia, vol. 15, no. 1, pp. 83–87, 1997.

F. D. Smith and E. E. Bantari, “Dot ELISA on nitrocellulose membrane for detection of potato leaf roll virus,” Plant Disease, vol. 71, pp. 795–799, 1987.

K. Pernezny and R. E. Litz, “Some common diseases of papaya in Florida,” Florida Cooperative Extension Service Plant Pathology Fact Sheet, p. 35, 1999

S. Dillon, C. Ramage, S. Ashmore, and R. A. Drew, “Development of a codominant CAPS marker linked to PRSV-P resistance in highland papaya,” Theoretical and Applied Genetics, vol. 113, no. 6, pp. 1159–1169, 2006.

D. Gonsalves, A. Vegas, V. Prasartsee, R. A. Drew, J. Y. Suzuki, and S. Tripathi, “Developing papaya to control Papaya ringspot virus by transgenic resistance, intergeneric hybridization, and tolerance breeding,” in Plant Breeding Reviews, J. Janick, Ed., vol. 26, pp. 35–73, John Wiley & Sons, Hoboken, NJ, USA, 2006.

R. M. Manshardt, “Papaya,” in Biotechnology of Perennial Fruit Crops, F. A. Hammerschlag and R. E. Litz, Eds., pp. 489–511, Cambridge University Press, Oxford, UK, 1992.

D. Gonsalves and S. M. Garnsey, “Cross protection techniques for control of plant virus diseases in the tropics,” Plant Disease, vol. 73, no. 7, pp. 592–597, 1989.

S. D. Yeh, D. Gonsalves, H. L. Wang, et al., “Control of papaya ringspot virus by cross protection,” Plant Disease, vol. 22, pp. 375–380, 1988.

S. D. Yeh and Y. H. Cheng, “Use of resistant Cucumis metuliferus for selection of nitrous-acid induced attenuated strains of papaya ringspot virus,” Phytopathology, vol. 79, no. 11, pp. 1257–1261, 1989.

J. C. Sanford and S. A. Johnston, “The concept of parasite-derived resistance: deriving resistance genes from the parasite's own genome,” Journal of Theoretical Biology, vol. 113, no. 2, pp. 395–405, 1985.

C.-H. Chiang, J.-J. Wang, F.-J. Jan, S.-D. Yeh, and D. Gonsalves, “Comparative reactions of recombinant papaya ringspot viruses with chimeric coat protein (CP) genes and wild-type viruses on CP-transgenic papaya,” Journal of General Virology, vol. 82, no. 11, pp. 2827–2836, 2001.

H.-J. Bau, Y.-H. Cheng, T.-A. Yu, J.-S. Yang, and S.-D. Yeh, “Broad-spectrum resistance to different geographic strains of Papaya ringspot virus in coat protein gene transgenic papaya,” Phytopathology, vol. 93, no. 1, pp. 112–120, 2003.

M. M. M. Fitch, R. M. Manshardt, D. Gonsalves, J. L. Slightom, and J. C. Sanford, “Virus resistant papaya plants derived from tissues bombarded with the coat protein gene of papaya ringspot virus,” Nature Biotechnology, vol. 10, no. 11, pp. 1466–1472, 1992.

Y.-H. Cheng, J.-S. Yang, and S.-D. Yen, “Efficient transformation of papaya by coat protein gene of papaya ringspot virus mediated by Agrobacterium following liquid-phase wounding of embryogenic tissues with caborundum,” Plant Cell Reports, vol. 16, no. 3-4, pp. 127–132, 1996.

R. E. Lines, D. Persley, J. L. Dale, R. Drew, and M. F. Bateson, “Genetically engineered immunity to Papaya ringspot virus in Australian papaya cultivars,” Molecular Breeding, vol. 10, no. 3, pp. 119–129, 2002.

P. Tennant, M. H. Ahmad, and D. Gonsalves, “Transformation of Carica papaya L. with virus coat protein genes for studies on resistance to Papaya ringspot virus from Jamaica,” Tropical Agriculture, vol. 79, no. 2, pp. 105–113, 2002.

M. A. K. Azad, M. G. Rabbani, L. Amin, and N. M. Sidik, “Development of transgenic papaya through Agrobacterium mediated transformation,” International Journal of Genomics, vol. 2013, Article ID 235487, 5 pages, 2013.

M. J. Davis and Z. Ying, “Genetic diversity of the Papaya ringspot virus in Florida,” Proceedings of Florida State Horticulture Society, vol. 112, pp. 194–196, 1999.

M. M. M. Fitch, “Carica papaya Papaya,” in Biotechnology of Fruit and Nut Crops, R. E. Litz, Ed., Capter 6.1, pp. 174–207, CABI publishing, 2005.

C. Gonsalves, W. Cai, P. F. Tennant, and D. Gonsalves, “Effective development of papaya ringspot virus resistant papaya with untranslatable coat protein gene using a modified microprojectile transformation method,” Acta Horticulturae, vol. 461, pp. 311–319, 1998.

H. J. Bau, Y. H. Cheng, T. A. Yu et al., “Field evaluation of transgenic papaya lines carrying the coat protein gene of Papaya ringspot virus in Taiwan,” Plant Disease, vol. 88, no. 6, pp. 594–599, 2004.

P. M. Magdalita, L. D. Valencia, A. T. I. D. Ocampo, et al., “Towards development of PRSV resistant papaya by genetic engineering. In: New Directions for a Diverse Planet,” in Proceedings of the 4th International Crop Science Congress, Brisbane, Australia, October, 2004.

P. M. Waterhouse, M. W. Graham, and M.-B. Wang, “Virus resistance and gene silencing in plants can be induced by simultaneous expression of sense and antisense RNA,” Proceedings of the National Academy of Sciences of the United States of America, vol. 95, no. 23, pp. 13959–13964, 1998.

A. Eamens, M.-B. Wang, N. A. Smith, and P. M. Waterhouse, “RNA silencing in plants: yesterday, today, and tomorrow,” Plant Physiology, vol. 147, no. 2, pp. 456–468, 2008.

S. V. Ramesh, A. K. Mishra, and S. Praveen, “Hairpin RNA-mediated strategies for silencing of tomato leaf curl virus AC1 and AC4 genes for effective resistance in plants,” Oligonucleotides, vol. 17, no. 2, pp. 251–257, 2007.

S.-D. Yeh, F.-J. Jan, C.-H. Chiang et al., “Complete nucleotide sequence and genetic organization of papaya ringspot virus RNA,” Journal of General Virology, vol. 73, no. 10, pp. 2531–2541, 1992.

P. Ruanjan, S. Kertbundit, and M. Juříček, “Post-transcriptional gene silencing is involved in resistance of transgenic papayas to papaya ringspot virus,” Biologia Plantarum, vol. 51, no. 3, pp. 517–520, 2007.

S. K. Mangrauthia, R. K. Jain, and S. Praveen, “Sequence motifs comparisons establish a functional portrait of a multifunctional protein HC-Pro from papaya ringspot potyvirus,” Journal of Plant Biochemistry and Biotechnology, vol. 17, no. 2, pp. 201–204, 2008.

J. Meins F., “RNA degradation and models for post-transcriptional gene silencing,” Plant Molecular Biology, vol. 43, no. 2-3, pp. 261–273, 2000.

M. Wassenegger and T. Pélissier, “A model for RNA-mediated gene silencing in higher plants,” Plant Molecular Biology, vol. 37, no. 2, pp. 349–362, 1998.

P. Tennant, G. Fermin, M. M. Fitch, R. M. Manshardt, J. L. Slightom, and D. Gonsalves, “Papaya ringspot virus resistance of transgenic rainbow and SunUp is affected by gene dosage, plant development, and coat protein homology,” European Journal of Plant Pathology, vol. 107, no. 6, pp. 645–653, 2001.

S. Tripathi, H.-J. Bau, L.-F. Chen, and S.-D. Yeh, “The ability of Papaya ringspot virus strains overcoming the transgenic resistance of papaya conferred by the coat protein gene is not correlated with higher degrees of sequence divergence from the transgene,” European Journal of Plant Pathology, vol. 110, no. 9, pp. 871–882, 2004.

D. B. Golemboski, G. P. Lomonossoff, and M. Zaitlin, “Plants transformed with a tobacco mosaic virus nonstructural gene sequence are resistant to the virus,” Proceedings of the National Academy of Sciences of the United States of America, vol. 87, no. 16, pp. 6311–6315, 1990.

T. Nunome, F. Fukumoto, F. Terami, K. Hanada, and M. Hirai, “Development of breeding materials of transgenic tomato plants with a truncated replicase gene of cucumber mosaic virus for resistance to the virus,” Breeding Science, vol. 52, no. 3, pp. 219–223, 2002.

X. Wei, C. Lan, Z. Lu, and C. Ye, “Analysis on virus resistance and fruit quality for T4 generation of transgenic papaya,” Frontiers of Biology in China, vol. 2, no. 3, pp. 284–290, 2007.

S. Sakuanrungsirikul, N. Sarindu, V. Prasartsee et al., “Update on the development of virus-resistant papaya: virus-resistant transgenic papaya for people in rural communities of Thailand,” Food and Nutrition Bulletin, vol. 26, no. 4, pp. 422–426, 2005.

Y.-T. Hsieh and T.-M. Pan, “Influence of planting papaya ringspot virus resistant transgenic papaya on soil microbial biodiversity,” Journal of Agricultural and Food Chemistry, vol. 54, no. 1, pp. 130–137, 2006.

M. Roberts, D. A. Minott, P. F. Tennant, and J. C. Jackson, “Assessment of compositional changes during ripening of transgenic papaya modified for protection against papaya ringspot virus,” Journal of the Science of Food and Agriculture, vol. 88, no. 11, pp. 1911–1920, 2008.

R. Stone, “China plans $3.5 billion GM crops initiative,” Science, vol. 321, no. 5894, p. 1279, 2008.

C. Gonsalves, D. R. Lee, and D. Gonsalves, “The adoption of genetically modified papaya in Hawaii and its implications for developing countries,” Journal of Development Studies, vol. 43, no. 1, pp. 177–191, 2007.

G. Fermin, V. Inglessis, C. Garboza, S. Rangel, M. Dagert, and D. Gonsalves, “Engineered resistance against Papaya ringspot virus in Venezuelan transgenic papayas,” Plant Disease, vol. 88, no. 5, pp. 516–522, 2004.

N. Phironrit, B. Phuangrat, P. Burns, and W. Kositratana, “Determination of possible impact on the cultivation of PRSV resistant transgenic papaya to rhizosphere bacteria using the community-level physiological profiles (CLPP),” in Proceedings of the 6th Asian Crop Science Association Conference, p. 126, Bangkok, Thailand, November 2007.

R. Manshardt, “Is organic papaya production in Hawaii threatened by crosspollination with genetically engineered varieties,” University of Hawaii College Tropical Agriculture and Human Resource Biology, vol. 3, p. 2, 2002.

S. D. Yeh and D. Gonsalves, “Practices and perspective of control of papaya ringspot virus by cross protection,” in Advances in Disease Vector Research, K. F. Harris, Ed., vol. 10, pp. 237–257, Springer, New York, NY, USA, 1994.

G. Fermín, R. C. Keith, J. Y. Suzuki et al., “Allergenicity assessment of the papaya ringspot virus coat protein expressed in transgenic rainbow papaya,” Journal of Agricultural and Food Chemistry, vol. 59, no. 18, pp. 10006–10013, 2011.

H. T. Lin, G. C. Yen, T. T. Huang, L. F. Chan, and et. al, “Toxicity assessment of transgenic papaya ringspot virus of 823–2210 line papaya fruits,” Journal of Agricultural and Food Chemistry, vol. 61, no. 7, pp. 1585–1596, 2013.

M. G. Ettlinger and A. Kjaer, “Sulfur compounds in plants,” Recent Advances in Phytochemistry, vol. 1, pp. 49–144, 1968.

S. S. Hecht, P. M. J. Kenney, M. Wang, and P. Upadhyaya, “Benzyl isothiocyanate: an effective inhibitor of polycyclic aromatic hydrocarbon tumorigenesis in A/J mouse lung,” Cancer Letters, vol. 187, no. 1-2, pp. 87–94, 2002.

G. Fermin and P. Tennant, “Opportunities and constraints to biotechnological applications in the Caribbean: transgenic papayas in Jamaica and Venezuela,” Plant Cell Reports, vol. 30, no. 5, pp. 681–687, 2011.

A. C. Lima, R. Souza Jr., T. Monoel, R. Gilvan, and A. A. Lima, “Sequence of the coat protein gene from Brazilian isolates of papaya ringspot virus,” Fitopatologia Brasileira, vol. 27, pp. 263–267, 2002.

M. T. Souza, O. Nickel, and D. Gonsalves, “Development of virus resistant transgenic papayas expressing the coat protein gene from a Brazilian isolate of papaya ringspot virus,” Fitopatologia Brasileira, vol. 30, pp. 357–365, 2005.

M. J. Davis and Z. Ying, “Development of papaya breeding lines with transgenic resistance to Papaya ringspot virus,” Plant Disease, vol. 88, no. 4, pp. 352–358, 2004.

P. Tennant, M. H. Ahmad, and D. Gonsalves, “Field resistance of coat protein transgenic papaya to Papaya ringspot virus in Jamaica,” Plant Disease, vol. 89, no. 8, pp. 841–847, 2005.

S. A. Ferreira, K. Y. Pitz, R. Manshardt, M. Fitch, and D. Gonsalves, “Virus coat protein transgenic papaya provides practical control of Papaya ringspot virus in Hawaii,” Plant Disease, vol. 86, no. 2, pp. 101–105, 2002.

G. Fermin, Use, application and technology transfer of native and synthetic genes to engineering single and multiple transgenic viral resistance [Ph.D. thesis], Cornell University, Ithaca, NY, USA, 2002.

S. Kertbundit, N. Pongtanom, P. Ruanjan et al., “Resistance of transgenic papaya plants to Papaya ringspot virus,” Biologia Plantarum, vol. 51, no. 2, pp. 333–339, 2007.