1. End, M.J.; Daymond, A.J.; Hadley, P. (Eds.) Technical Guidelines for the Safe Movement of Cacao Germplasm; Revised from the FAO/IPGRI Technical Guidelines No. 20 (Third Update, October 2017); Global Cacao Genetic Resources Network (CacaoNet), Bioversity International: Rome, Italy, 2017.
2. Muller, E.; Ullah, I.; Dunwell, J.M.; Daymond, A.J.; Richardson, M.; Allainguillaume, J.; Wetten, A. Identification and distribution of novel badnaviral sequences integrated in the genome of cacao (Theobroma cacao). Sci. Rep. 2021, 11, 8270. [CrossRef]
3. Chingandu, N.; Zia-Ur-Rehman, M.; Sreenivasan, T.N.; Surujdeo-Maharaj, S.; Umaharan, P.; Gutierrez, O.A.; Brown, J.K. Molecular characterization of previously elusive badnaviruses associated with symptomatic cacao in the New World. Arch. Virol. 2017, 162, 1363–1371. [CrossRef] [PubMed]
4. Kirkpatrick, T.W. Insect transmission of cacao virus disease in Trinidad. Bull. Entomol. Res. 1950, 41, 99–117. [CrossRef]
5. Swarbrick, J.T. Cacao virus in Trinidad. Trop. Agric. Trin. 1961, 38, 245–249.
Ramos-Sobrinho, R.; Ferro, M.M.M.; Nagata, T.; Puig, A.S.; Von Keith, C.; Britto, D.S.; Gutierrez, O.A.; Marelli, J.-P.; Brown, J.K. Complete genome sequences of three newly discovered cacao mild mosaic virus isolates from Theobroma cacao L. in Brazil and Puerto Rico and evidence for recombination. Arch. Virol. 2021, 166, 2027–2031. [CrossRef] [PubMed]
7. Ciferri, R. Una virosis del cacao en Colombia y en la República Dominicana. Rev. Fac. Nac. Agron. Medellín 1948, 8, 79–84.
8. Posnette, A.F.; Palma, M. Observations on cacao in the Paria Peninsula, Venezuela. Trop. Agric. Trinidad. 1944, 21, 104.
9. Simangu, H. Gedjala-Gedjala Mosiak Pada Daun Tjoklat; Universitas Gadjah Mada: Jogjakarta, Indonesia, 1961; Volume 2, 13p.
10. Kenten, R.H.; Woods, R.D. A virus of the Cocoa Swollen Shoot group infecting cocoa in North Sumatra. PANS 1976, 22, 488–490. [CrossRef]
11. Legg, J.T. Cocoa swollen-shoot disease—Know your enemy. In Proceedings of the 5th International Cocoa Research Conference, Ibadan, Nigeria, 1–9 September 1979; pp. 397–402.
12. Turner, P.D.; Shepherd, R. Cocoa diseases in Malaysia and Indonesia: Their present and potential importance. In Proceedings of the International Conference Cocoa Coconuts, Kuala Lumpur, Malaysia, 21–24 June 1978; pp. 308–321.
13. Lockwood, R. MEMORANDUM: Subject: Suspected Cocoa Virus in Malaysia. 1992, pp. 1–4. Available online: http://www.icgd. reading.ac.uk/icqcdata/Lockwood_1992_Report_on_Malaysian_virus_2_Mar1992.pdf (accessed on 17 October 2021).
14. Daymond, A.J. Detection of Symptoms Characteristic of Viral Infection on the Clone BR 25; Report from ICQC-Reading. 2018, pp. 1–2. Available online: http://www.icgd.reading.ac.uk/icqc/data/Detection_of_Viral_Symptom_on_the_clone_BR_25.pdf (accessed
on 17 October 2021).
15. Osorio-Guarín, J.A.; Quackenbush, C.R.; Cornejo, O.E. Ancestry informative alleles captured with reduced representation library sequencing in Theobroma cacao. PLoS ONE 2018, 13, 10. [CrossRef]
16. Kane, N.; Sveinsson, S.; Dempewolf, H.; Yang, J.Y.; Zhang, D.; Engels, J.M.; Cronk, Q. Ultra-barcoding in cacao (Theobroma spp.; Malvaceae) using whole chloroplast genomes and nuclear ribosomal DNA. Am. J. Bot. 2012, 99, 2. [CrossRef]
17. Cornejo, O.E.; Yee, M.C.; Dominguez, V.; Andrews, M.; Sockell, A.; Strandberg, E.; Livingstone, D., 3rd; Stack, C.; Romero, A.; Umaharan, P.; et al. Population genomic analyses of the chocolate tree, Theobroma cacao L., provide insights into its domestication process. Commun. Biol. 2018, 1, 167. [CrossRef]
18. Langmead, B.; Salzberg, S.L. Fast gapped-read alignment with Bowtie 2. Nat. Methods 2012, 9, 357–359. [CrossRef] [PubMed]
19. Li, H.; Handsaker, B.; Wysoker, A.; Fennell, T.; Ruan, J.; Homer, N.; Marth, G.; Abecasis, G.; Durbin, R. The sequence align�ment/map format and SAMtools. Bioinformatics 2009, 25, 2078–2079. [CrossRef] [PubMed]
20. Robinson, J.T.; Thorvaldsdottir, H.; Wenger, A.M.; Zehir, A.; Mesirov, J.P. Variant review with the integrative genomics viewer. Cancer Res. 2017, 77, e31–e34. [CrossRef] [PubMed]
21. Muhire, B.M.; Varsani, A.; Martin, D.P. SDT: A virus classification tool based on pairwise sequence alignment and identity calculation. PLoS ONE 2014, 9, e108277. [CrossRef] [PubMed]
22. Kumar, S.; Stecher, G.; Tamura, K. MEGA7: Molecular evolutionary genetics analysis version 7.0 for bigger datasets.
Mol. Biol. Evol. 2016, 33, 1870–1874. [CrossRef] [PubMed]
23. Kimura, M. A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences. J. Mol. Evol. 1980, 16, 111–120. [CrossRef] [PubMed]
24. Puig, A.; Ramos-Sobrinho, R.; Keith, C.; Kitchen, N.; Gutierrez, O.; Goenaga, R.; Brown, J.K. First report of Cacao mild mosaic virus (CaMMV) associated with symptomatic commercial cacao (Theobroma cacao L.) trees in Puerto Rico. Plant Dis. 2020, 104, 3089. [CrossRef]
25. Pecman, A.; Kutnjak, D.; Gutiérrez-Aguirre, I.; Adams, I.; Fox, A.; Boonham, N.; Ravnikar, M. Next generation sequencing for detection and discovery of plant viruses and Viroids: Comparison of two approaches. Front. Microbiol. 2017, 8, 1998. [CrossRef]
26. Glasa, M.; Hanˇcinský, R.; Šoltys, K.; Predaj ˇna, L.; Tomašechová, J.; Hauptvogel, P.; Mrkvová, M.; Mihálik, D.; Candresse, T. Molecular characterization of Potato Virus Y (PVY) using high-throughput sequencing: Constraints on full genome reconstructions imposed by mixed infection involving recombinant PVY strains. Plants 2021, 10, 753. [CrossRef]
27. Sukal, A.C.; Kidanemariam, D.B.; Dale, J.J.; Harding, R.M.; James, A.P. Assessment and optimization of rolling circle amplification protocols for the detection and characterization of badnaviruses. Virology 2019, 529, 73–80. [CrossRef] [PubMed]
28. Baker, R.E.; Dale, W.T. Notes on a virus disease of cacao. Ann. Appl. Biol. 1947, 34, 60–65. [CrossRef] [PubMed]
29. Staginnus, C.; Richert-Pöggeler, K.R. Endogenous pararetroviruses: Two-faced travelers in the plant genome. Trends Plant Sci. 2006, 11, 485–491. [CrossRef] [PubMed]
30. Chen, S.; Saito, N.; Encabo, J.R.; Yamada, K.; Choi, I.-R.; Kishima, Y. Ancient endogenous pararetroviruses in oryza genomes provide insights into the heterogeneity of viral gene macroevolution. Genome Biol. Evol. 2018, 10, 2686–2696. [CrossRef]
31. Chabannes, M.; Gabriel, M.; Aksa, A.; Galzi, S.; Dufayard, J.-F.; Iskra-Caruana, M.-L.; Muller, E. Badnaviruses and banana genomes: A long association sheds light on Musa phylogeny and origin. Mol. Plant Pathol. 2021, 22, 216–230. [CrossRef] [PubMed]
32. Serfraz, S.; Sharma, V.; Maumus, F.; Aubriot, X.; Geering, A.D.W.; Teycheney, F.-Y. Insertion of badnaviral DNA in the late blight resistance gene (R1a) of brinjal eggplant (Solanum melongena). Front. Plant Sci. 2021. [CrossRef]
33. Catoni, M.; Noris, E.; Vaira, A.M.; Jonesman, T.; Mati´c, S.; Soleimani, R.; Behjatnia, S.A.A.; Vinals, N.; Paszkowski, J.; Accotto, G.P. Virus-mediated export of chromosomal DNA in plants. Nat. Commun. 2018, 9, 5308. [CrossRef]
34. Kreuze, J.F.; Perez, A.; Gargurevich, M.G.; Cuellar, W.J. Badnaviruses of sweet potato: Symptomless coinhabitants on a global scale. Front. Plant Sci. 2020, 11, 313. [CrossRef]
35. Marais, A.; Umber, M.; Filloux, D.; Gomez, R.M.; Faure, C.; Pavis, C.; Julian, C.; Roumagnac, P.; Acina-Mambole, I.;
Bonheur, L.; et al. Yam asymptomatic virus 1, a novel virus infecting yams (Dioscorea spp.) with significant prevalence in a germplasm collection. Arch. Virol. 2020, 165, 2653–2657. [CrossRef] [PubMed]
36. Marshall, P.L.; King, J.L.; Budowle, B. Utility of amplification enhancers in low copy number DNA analysis. Int. J. Legal Med. 2015, 129, 43–52. [CrossRef] [PubMed]
37. Armani, A.; Giusti, A.; Guardone, L.; Castigliego, L.; Gianfaldoni, D.; Guidi, A. Universal primers used for species identification of foodstuff of animal origin: Effects of oligonucleotide tails on PCR amplification and sequencing performance. Food Anal. Methods 2016, 9, 1199–1209. [CrossRef]
38. Bartley, B.G.D. The Genetic Diversity of Cacao and Its Utilization; CABI Publishing: Wallingford, UK, 2005; p. 341. ISBN 0851996191.
39. Mahas, A.; Hassan, N.; Aman, R.; Marsic, T.; Wang, Q.; Ali, Z.; Mahfouz, M.M. LAMP-Coupled CRISPR–Cas12a module for rapid and sensitive detection of plant DNA viruses. Viruses 2021, 13, 466. [CrossRef] [PubMed]
40. Sherrill-Mix, S.; Hwang, Y.; Roche, A.M.; Glascock, A.; Weiss, S.R.; Li, Y.; Haddad, L.; Deraska, P.; Monahan, C.; Kromer, A.; et al. Detection of SARS-CoV-2 RNA using RT-LAMP and molecular beacons. Genome Biol. 2021, 22, 169. [CrossRef] [PubMed