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Citrus leprosis disease

Citrus leprosis (CL) is an economically important viral disease affecting citrus crops. This emerging disease is widely distributed in South and Central America, from Argentina to Mexico. The disease is associated with up to three different non-systemic viruses, which cause similar symptoms in the citrus hosts and are transmitted by the same vector, mites of the genus Brevipalpus; although they have vastly different genomes. Citrus leprosis virus nuclear type (CiLV-N) is found in the nuclei and cytoplasm of infected cells, while Citrus leprosis virus cytoplasmic type (CiLV-C) is found in the endoplasmic reticulum. In 2012, a new virus causing similar symptoms was found in Colombia and it was named Citrus leprosis virus cytoplasmic type 2 (CiLV-C2) due to its close similarity to CiLV-C. The cytoplasmic type viruses are the most prevalent and widely distributed of the three species.

Structure and genome Edit

CiLV-N has short, rod-shaped particles, 120 to 130 nanometers (nm) long and 35 to 40 nm wide, occurring in the nucleus or cytoplasm of the infected cells, and associated with the presence of viroplasm in the nucleus.[1] The CiLV-N genome is a bipartite, negative-sense, single stranded RNA ((-)ssRNA). Both RNAs have 3'-terminal poly(A) tails. CiLV-N RNA1 (6,268 nucleotides (nt)) contains five Open Reading Frames (ORF) encoding the nucleocapsid protein (N), putative phosphoprotein (P), cell-to-cell movement protein (MP), matrix protein (M), and glycoprotein (G). CiLV-N RNA2 (5,847 nt) contains one ORF encoding the RNA-dependent RNA polymerase (RdRp) replication module. The size and structure of the CiLV-N genome closely resembles the genome organization of Orchid fleck virus (OFV)[2] and is likely to be a member of the newly proposed genus Dichorhavirus.

CiLV-C has short, membrane-bound bacilliform particles, 120 to 130 nm long and 50 to 55 wide; it is found in the endoplasmic reticulum in the cytoplasm of infected cells, and large electron dense viroplasm is observed in the cytoplasm.[3] CiLV-C has a bipartite, positive-sense, single stranded, RNA ((+)ssRNA) genome. Both RNAs had 3'-terminal poly(A) tails. CiLV-C RNA1 (8,729 to 8,730 nt) contains two ORFs, encoding a 286 kiloDaltons (kDa) polyprotein, putatively involved in virus replication, with four conserved domains: methyltransferase, protease, helicase, and RNA-dependent RNA polymerase (RdRp); and a 29 kDa protein, of unknown function. CiLV-C RNA2 (4,969 to 4,975 nt) contains four ORFs, encoding 15, 61, 32, and 24 kDa proteins. The 32-kDa protein is apparently involved in cell-to-cell movement of the virus (MP), but none of the other proteins showed any conserved protein domain.[4][5]

CiLV-C2 is associated with short bacilliform virions, 100 to 110 nm long and 40 to 50 nm wide[6] The genome of CiLV-C2 is composed of RNA1 (8,717) and RNA2 (4,989 nt). Both RNAs also had 3'-terminal poly(A) tails. The structure of the CiLV-C2 genome closely resembles the genome organization of CiLV-C. CiLV-C2 RNA1 have two ORFs encoding a large polyprotein (285 kDa), putative involve in virus replication, with five conserved domains (two methyltransferase, protease, helicase and RdRp); and a putative coat protein (CP) of 29 kDa. CiLV-C2 RNA2 contains five ORFs that potentially encoded five proteins: 15, 7, 61, 32, and 24 kDa, similar to those predicted protein masses for CiLV-C. The 32 kDa protein has a conserved cell-to-cell movement protein domain, and the small hypothetical protein (7 kDa), that is not present in CiLV-C, has a putative trans-membrane domain.[6]

Taxonomic position Edit

CiLV-N probably belongs to the proposed genus Dichorhavirus, related to the family Rhabdoviridae, which has Orchid fleck virus (OFV) as the type member.[7] CiLV-C is the type member of the new accepted genus Cilevirus.[8] CiLV-C2 has been proposed as a new member of the genus Cilevirus.[6]

Transmission Edit

 
The Brevipalpus phoenicis carries the Leprosis Citrus leprosis disease, a disease currently in South America but moving North

CiLV-N, CiLV-C, and CiLV-C2 are transmitted by false spider mites or flat mites, belonging to the genus Brevipalpus (Acari: Tenuipalpidae). Three mites species within this genus have been reported as CiLV vectors: B. californicus Banks, B. obovatus Donnadieu, and B. phoenicis Geijskes, the latter is considered the main vector.[9] The three mites species have a broad host range and are widely distributed.[10] All active stages of the mite (larvae, nymph, and adult) can acquire and transmit the virus,[11] although it has been reported that larvae transmit the virus more efficiently.[12] It is known that there is no transovarial transmission from female to its descendants,[13] and that after acquisition (an acquisition access period of 2 days), the mite remains viruliferous during entire life-span (persistent transmission), but it is not clear if the virus replicates inside the vector.[9]

Agricultural importance Edit

CiLV produces localized symptoms in leaves, stems, and fruits. In leaves, characteristic lesions are often circular (from 5 to 12 millimetres (316 to 1532 in) in diameter), chlorotic or necrotic, colored light yellow to dark brown. In older lesions, a darker central point can also be observed.[14] In young stems, lesions are small, chlorotic and shallow; with time they become darker brown or reddish and prominent. In old stems lesions can join together and appearing larger.[14] In fruits, dark and depressed lesions are found in large numbers and affecting only the external part.[15] Commercial losses result from undesirable appearance and fruits falling. Some differences in symptoms produced by CiLV-C and CiLV-N have been reported; in leaves and fruits, lesions caused by the nuclear type are smaller and more numerous than those caused by the cytoplasmic type. Lesions caused by CiLV-C shows additional halos, making them look larger.[16][17] This disease is considered an important problem in citriculture in countries where it has been established, and is considered the major viral disease in citrus in Brazil.[9] Damage by leprosis in plants and in orange production has caused an annual cost of approximately US$90 million for miticides to control the disease, this represents about 40% of fertilizer and pesticide expenses and about 16% of the total costs of a grove.[18] Because of its widespread occurrence and potential for high damage, the disease can cause 100% yield losses, depending on the susceptibility of the citrus variety, isolate and control of the vector.[19] Because CL is considered a quarantine disease, international marketing is restricted to those regions where the disease is not reported.[20]

CiLV-C was long considered restricted to the genus Citrus, where species exhibit different grades of susceptibility, with sweet oranges (Citrus sinensis (L.) Osbeck) being highly susceptible, mandarins (C. reticulata Blanco) and grapefruits (C. paradisi Macfad.) moderately susceptible, and lemons (C. limon (L.) Osbeck) practically immune.[9] Nevertheless, CiLV-C was also found naturally infecting non-Citrus species as Swinglea glutinosa Merr., used as hedgerows around citrus orchards in Villavicencio, Colombia,[21] and Commelina benghalensis L., a weed present in citrus orchards in Brazil.[22] Mechanical transmission experiments have showed that CiLV-C could be transmitted to other species, causing localized lesions,[23] and it also can be mite transmitted to a quite wide range of experimental plant species.[24] B. phoenicis transmission to the common bean was also demonstrated[25] and this species has been proposed as an experimental indicator.[26]

Diagnosis Edit

Citrus leprosis is principally detected by the observation of local lesions with characteristic symptoms. Presence of CiLV-N and CiLV-C particles in affected tissue can be confirmed by transmission electron microscopy (TEM).[1][3] Other laboratory detection methods are also available, as double antibody sandwich-enzyme-linked-immunosorbent-assay (DAS-ELISA), indirect ELISA, dot-blot immunoassay, and immunocapture-reverse transcription-polymerase chain reaction using monoclonal and polyclonal;[27][28][29] and reverse transcription-polymerase chain reaction (RT-PCR).[6][30][31][32]

Epidemiology Edit

CL was initially described in what is now Philippe Park, Florida in 1907 by Fawett who called it "scaly bark" and "nail-head rust".[33][34] However, the disease appears to have disappeared from Florida since the 1960s,[35][33] perhaps due to reduction of vector population caused by freezing weather and intensive sulfur application.[36] There is evidence that CL was caused by the nuclear type.[37] The first report of CL in South America was in 1920 in Paraguay,[38] later it was reported in Brazil,[39] Argentina and Uruguay.[40] CiLV-C has been detected in Bolivia, Venezuela, and Colombia, and it is spreading northward through Panama, Costa Rica, Nicaragua, Guatemala, Honduras, El Salvador, and Mexico.[9][41] CiLV-N has also been reported from the states of São Paulo, Rio Grande do Sul, and Minas Gerais in Brazil, Boquete in Panama, and in the state of Querétaro, Mexico.[2][9] Recently, a mixed infection of the same plant with the two viruses CiLV-N and CiLV-C2, was reported in Casanare, Colombia.[32] The recent establishment of citrus leprosis in Central America represents a potential threat to citriculture in North America, where the vector is also present.

Management Edit

CL is mainly controlled through the management of mites. Most of the currently available miticides are effective,[42] although mite resistance has already been detected.[43][44] Biological alternatives as mite predators and entomopathogenic fungi have been reported with promising results.[41][45] Virus inoculum can be reduced implementing some cultural practices as remove affected branches, use of windbreaks to decrease vector wind spread, control of weeds (alternative mite hosts), use of healthy plants sources, and controlling the movement of people and material in orchard.[41] Although resistance has been observed between different Citrus species, few studies have been conducted in this area in order to identify commercial resistant varieties. One study developed using a hybrid population suggests that inheritance of resistance to leprosis may be controlled by only a few genes.[46]

Resources Edit

References Edit

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citrus, leprosis, disease, citrus, leprosis, economically, important, viral, disease, affecting, citrus, crops, this, emerging, disease, widely, distributed, south, central, america, from, argentina, mexico, disease, associated, with, three, different, systemi. Citrus leprosis CL is an economically important viral disease affecting citrus crops This emerging disease is widely distributed in South and Central America from Argentina to Mexico The disease is associated with up to three different non systemic viruses which cause similar symptoms in the citrus hosts and are transmitted by the same vector mites of the genus Brevipalpus although they have vastly different genomes Citrus leprosis virus nuclear type CiLV N is found in the nuclei and cytoplasm of infected cells while Citrus leprosis virus cytoplasmic type CiLV C is found in the endoplasmic reticulum In 2012 a new virus causing similar symptoms was found in Colombia and it was named Citrus leprosis virus cytoplasmic type 2 CiLV C2 due to its close similarity to CiLV C The cytoplasmic type viruses are the most prevalent and widely distributed of the three species Contents 1 Structure and genome 2 Taxonomic position 3 Transmission 4 Agricultural importance 5 Diagnosis 6 Epidemiology 7 Management 8 Resources 9 ReferencesStructure and genome EditCiLV N has short rod shaped particles 120 to 130 nanometers nm long and 35 to 40 nm wide occurring in the nucleus or cytoplasm of the infected cells and associated with the presence of viroplasm in the nucleus 1 The CiLV N genome is a bipartite negative sense single stranded RNA ssRNA Both RNAs have 3 terminal poly A tails CiLV N RNA1 6 268 nucleotides nt contains five Open Reading Frames ORF encoding the nucleocapsid protein N putative phosphoprotein P cell to cell movement protein MP matrix protein M and glycoprotein G CiLV N RNA2 5 847 nt contains one ORF encoding the RNA dependent RNA polymerase RdRp replication module The size and structure of the CiLV N genome closely resembles the genome organization of Orchid fleck virus OFV 2 and is likely to be a member of the newly proposed genus Dichorhavirus CiLV C has short membrane bound bacilliform particles 120 to 130 nm long and 50 to 55 wide it is found in the endoplasmic reticulum in the cytoplasm of infected cells and large electron dense viroplasm is observed in the cytoplasm 3 CiLV C has a bipartite positive sense single stranded RNA ssRNA genome Both RNAs had 3 terminal poly A tails CiLV C RNA1 8 729 to 8 730 nt contains two ORFs encoding a 286 kiloDaltons kDa polyprotein putatively involved in virus replication with four conserved domains methyltransferase protease helicase and RNA dependent RNA polymerase RdRp and a 29 kDa protein of unknown function CiLV C RNA2 4 969 to 4 975 nt contains four ORFs encoding 15 61 32 and 24 kDa proteins The 32 kDa protein is apparently involved in cell to cell movement of the virus MP but none of the other proteins showed any conserved protein domain 4 5 CiLV C2 is associated with short bacilliform virions 100 to 110 nm long and 40 to 50 nm wide 6 The genome of CiLV C2 is composed of RNA1 8 717 and RNA2 4 989 nt Both RNAs also had 3 terminal poly A tails The structure of the CiLV C2 genome closely resembles the genome organization of CiLV C CiLV C2 RNA1 have two ORFs encoding a large polyprotein 285 kDa putative involve in virus replication with five conserved domains two methyltransferase protease helicase and RdRp and a putative coat protein CP of 29 kDa CiLV C2 RNA2 contains five ORFs that potentially encoded five proteins 15 7 61 32 and 24 kDa similar to those predicted protein masses for CiLV C The 32 kDa protein has a conserved cell to cell movement protein domain and the small hypothetical protein 7 kDa that is not present in CiLV C has a putative trans membrane domain 6 Taxonomic position EditCiLV N probably belongs to the proposed genus Dichorhavirus related to the family Rhabdoviridae which has Orchid fleck virus OFV as the type member 7 CiLV C is the type member of the new accepted genus Cilevirus 8 CiLV C2 has been proposed as a new member of the genus Cilevirus 6 Transmission Edit The Brevipalpus phoenicis carries the Leprosis Citrus leprosis disease a disease currently in South America but moving NorthCiLV N CiLV C and CiLV C2 are transmitted by false spider mites or flat mites belonging to the genus Brevipalpus Acari Tenuipalpidae Three mites species within this genus have been reported as CiLV vectors B californicus Banks B obovatus Donnadieu and B phoenicis Geijskes the latter is considered the main vector 9 The three mites species have a broad host range and are widely distributed 10 All active stages of the mite larvae nymph and adult can acquire and transmit the virus 11 although it has been reported that larvae transmit the virus more efficiently 12 It is known that there is no transovarial transmission from female to its descendants 13 and that after acquisition an acquisition access period of 2 days the mite remains viruliferous during entire life span persistent transmission but it is not clear if the virus replicates inside the vector 9 Agricultural importance EditCiLV produces localized symptoms in leaves stems and fruits In leaves characteristic lesions are often circular from 5 to 12 millimetres 3 16 to 15 32 in in diameter chlorotic or necrotic colored light yellow to dark brown In older lesions a darker central point can also be observed 14 In young stems lesions are small chlorotic and shallow with time they become darker brown or reddish and prominent In old stems lesions can join together and appearing larger 14 In fruits dark and depressed lesions are found in large numbers and affecting only the external part 15 Commercial losses result from undesirable appearance and fruits falling Some differences in symptoms produced by CiLV C and CiLV N have been reported in leaves and fruits lesions caused by the nuclear type are smaller and more numerous than those caused by the cytoplasmic type Lesions caused by CiLV C shows additional halos making them look larger 16 17 This disease is considered an important problem in citriculture in countries where it has been established and is considered the major viral disease in citrus in Brazil 9 Damage by leprosis in plants and in orange production has caused an annual cost of approximately US 90 million for miticides to control the disease this represents about 40 of fertilizer and pesticide expenses and about 16 of the total costs of a grove 18 Because of its widespread occurrence and potential for high damage the disease can cause 100 yield losses depending on the susceptibility of the citrus variety isolate and control of the vector 19 Because CL is considered a quarantine disease international marketing is restricted to those regions where the disease is not reported 20 CiLV C was long considered restricted to the genus Citrus where species exhibit different grades of susceptibility with sweet oranges Citrus sinensis L Osbeck being highly susceptible mandarins C reticulata Blanco and grapefruits C paradisi Macfad moderately susceptible and lemons C limon L Osbeck practically immune 9 Nevertheless CiLV C was also found naturally infecting non Citrus species as Swinglea glutinosa Merr used as hedgerows around citrus orchards in Villavicencio Colombia 21 and Commelina benghalensis L a weed present in citrus orchards in Brazil 22 Mechanical transmission experiments have showed that CiLV C could be transmitted to other species causing localized lesions 23 and it also can be mite transmitted to a quite wide range of experimental plant species 24 B phoenicis transmission to the common bean was also demonstrated 25 and this species has been proposed as an experimental indicator 26 Diagnosis EditCitrus leprosis is principally detected by the observation of local lesions with characteristic symptoms Presence of CiLV N and CiLV C particles in affected tissue can be confirmed by transmission electron microscopy TEM 1 3 Other laboratory detection methods are also available as double antibody sandwich enzyme linked immunosorbent assay DAS ELISA indirect ELISA dot blot immunoassay and immunocapture reverse transcription polymerase chain reaction using monoclonal and polyclonal 27 28 29 and reverse transcription polymerase chain reaction RT PCR 6 30 31 32 Epidemiology EditCL was initially described in what is now Philippe Park Florida in 1907 by Fawett who called it scaly bark and nail head rust 33 34 However the disease appears to have disappeared from Florida since the 1960s 35 33 perhaps due to reduction of vector population caused by freezing weather and intensive sulfur application 36 There is evidence that CL was caused by the nuclear type 37 The first report of CL in South America was in 1920 in Paraguay 38 later it was reported in Brazil 39 Argentina and Uruguay 40 CiLV C has been detected in Bolivia Venezuela and Colombia and it is spreading northward through Panama Costa Rica Nicaragua Guatemala Honduras El Salvador and Mexico 9 41 CiLV N has also been reported from the states of Sao Paulo Rio Grande do Sul and Minas Gerais in Brazil Boquete in Panama and in the state of Queretaro Mexico 2 9 Recently a mixed infection of the same plant with the two viruses CiLV N and CiLV C2 was reported in Casanare Colombia 32 The recent establishment of citrus leprosis in Central America represents a potential threat to citriculture in North America where the vector is also present Management EditCL is mainly controlled through the management of mites Most of the currently available miticides are effective 42 although mite resistance has already been detected 43 44 Biological alternatives as mite predators and entomopathogenic fungi have been reported with promising results 41 45 Virus inoculum can be reduced implementing some cultural practices as remove affected branches use of windbreaks to decrease vector wind spread control of weeds alternative mite hosts use of healthy plants sources and controlling the movement of people and material in orchard 41 Although resistance has been observed between different Citrus species few studies have been conducted in this area in order to identify commercial resistant varieties One study developed using a hybrid population suggests that inheritance of resistance to leprosis may be controlled by only a few genes 46 Resources EditCitrus Diseases Leprosis USDA University of Florida Citrus leprosis rhabdovirus European and Mediterranean Plant Protection Organization References Edit a b Kitajima E W Muller G W Costa A S Yuki W 1972 Short rodlike particles associated with citrus leprosis Virology 50 1 254 258 doi 10 1016 0042 6822 72 90366 2 PMID 4117125 a b Roy A Stone A Otero Colina G Wei G Choudhary N Achor D Shao J Levy L Nakhla M K Hollingsworth C R Hartung J S Schneider W L Brlansky R H 2013 Genome assembly of Citrus leprosis virus nuclear type reveals a close association with orchid fleck virus Genome Announcements 1 4 e00519 e613 doi 10 1128 genomea 00519 13 PMC 3735072 PMID 23887919 a b Kitajima E W Chagas C M Rodrigues J C V 2003 Brevipalpus transmitted plant virus and virus like diseases cytopathology and some recent cases Exp Appl Acarol 30 1 3 135 160 doi 10 1023 b appa 0000006546 55305 e3 PMID 14756414 S2CID 45072508 Locali Fabris E C Freitas Astu J Souza A A Takita M A Astua Monge G Antonioli Luizon R Rodrigues V Targon M L P N Machado M A 2006 Complete nucleotide sequence genomic organization and phylogenetic analysis of Citrus leprosis virus cytoplasmatic type J Gen Virol 87 9 2721 2729 doi 10 1099 vir 0 82038 0 PMID 16894213 Pascon R C Kitajima J P Breton M C Assumpcao L Greggio C Zanca A S Okura V K Alegria M C Camargo M E Silva G G Cardozo J C Vallim M A Franco S F Silva V H Junior H J Oliveira F Giachetto P F Ferrari F Aguilar Vildoso C I Franchiscini F J B Silva J M F Arruda P Ferro J A Reinach F Silva A C R 2006 The complete nucleotide sequence and genomic arganization of Citrus leprosis associated virus cytoplasmatic type CiLVC Virus Genes 32 3 289 298 doi 10 1007 s11262 005 6913 1 PMID 16732481 S2CID 22217705 a b c d Roy A Choudhary N Guillermo L M Shao J Govindarajulo A Anchor D Wei G Picton D D Levy L Nakhla M K Hartung J S Brlansky R H 2006 A novel virus of the genus Cilevirus causing symptoms similar of citrus leprosis Phytopathology 103 5 488 500 doi 10 1094 PHYTO 07 12 0177 R PMID 23268581 Kondo H Maeda T Shirako Y Tamada T 2006 Orchid fleck virus is a rhabdovirus with an unusual bipartite genome Journal of General Virology 87 Pt 8 2413 2421 doi 10 1099 vir 0 81811 0 PMID 16847138 Locali Fabris E C Freitas Astua J Machado M A 2012 Genus Cilevirus Virus Taxonomy Classification and Nomenclature of Viruses Ninth Rep Int Committee on Taxonomy of Viruses Elsevier San Diego CA 1139 1142 a b c d e f Bastianel M Noveli V M Kubo K S Kitajima E M Bassanezi R Machado M A Freitas Astua J 2010 Citrus leprosis centennial of an unusual mite virus pathosystem Plant Disease 94 3 284 292 doi 10 1094 pdis 94 3 0284 PMID 30754248 Childers C C Rodrigues J C V Welbourn W C 2003 Host plants of Brevipalpus californicus B obovatus and B phoenisis Acari Tenuipalpidae and their potential involvement in the spread of one or more viral disease vectored by these mites Experimental and Applied Acarology 30 1 3 29 105 doi 10 1023 b appa 0000006544 10072 01 PMID 14756412 S2CID 29730760 Chiavegato L 1996 Aspectos biologicos e transmissao de leprose pelo acaro Brevipalpus phoenicis Geijskes em citros Laranja 17 1 229 235 Chagas M Rosseti V Chiavegato L 1983 Influence of the biological cycle of Brevipalpus phoenicis on leprosis transmission Annals IX Conference of the International Organization of Citrus Virologists Riverside CA 69 Boaretto M A C Chiavegato L G Silva C A D 1993 Transmissao da leprose atraves de femeas de Brevipalpus phoenicis Geijskes 1939 Acari Tenuipalpidae e de seus descendentes em condicoes de laboratorio Cientifica Sao Paulo 21 2 245 253 a b Bastianel M Freitas Astua J Kitajima E W Machado M A 2006 The citrus leprosis pathosystem Summa Phytopathologica 32 3 211 220 doi 10 1590 s0100 54052006000300001 Rodrigues J C V Kitajima E W Childers C C Chagas C M 2003 Citrus leprosis virus vectored by Brevipalpus Phoenisis Acari Tenuipalpirae on citrus in Brazil Experimental and Applied Acarology 30 1 3 161 179 doi 10 1023 b appa 0000006547 76802 6e PMID 14756415 S2CID 13542435 Kitajima E W Ferrereira P T O Freitas Astua J Machado M A 2004 Ocorrencia da leprose dos citros tipo nuclear CiLV N nos municipios paulistas de Montealegre do Sul e Amparo Summa Phythopathologica 30 68 Marques J P R Kitajima E W Freitas Atua J Appezzato Da Gloria B 2010 Comparative morpho anatomical studies of the lesion caused by citrus leprosis virus on sweet orange Anais da Academia Brasileira de Ciencias 82 2 501 511 doi 10 1590 s0001 37652010000200025 PMID 20563430 Ayres A Citrus disease control in Brazil www fao org Retrieved 29 November 2014 Rodrigues J C V 2000 The relationships among the pathogen vector and plant in the citrus leprosis system PhD dissertation Piracicaba SP Brazil Sao Paulo University Leon G 2012 Current status of the Citrus leprosis virus CiLV C and its vector Brevipalpus phoenicis Geijskes Agronomia Colombiana 30 2 242 250 Leon G A Becerra C H Freitas Astua J Salaroli R B Kitajima E W 2008 Natural infection of Swinglea glutinosa by the Citrus leprosis virus citoplsmatic type CiLV C in Colombia Plant Disease 92 9 1364 doi 10 1094 pdis 92 9 1364c PMID 30769432 Nunes M A Bergamini M P Coerini L F Bastianel M Novelli V M Kitajima E W Freitas Astua J 2012 Citrus leprosis virus C naturally infecting Commelina benghalensis a prevalent monocot weed of citrus orchards in Brazil Plant Disease 96 5 770 doi 10 1094 pdis 11 11 0925 pdn PMID 30727543 Colariccio A Lovisolo O Chagas C M Galleti S R Rossetti V Kitajima E W 1995 Mechanical transmission and ultrastructural aspects of citrus leprosis disease Fitopatol Bras 20 208 213 Nunes M A Oliveira C A Oliveira M L Kitajima E W Hilf M E Gottwald R T Freitas Astua J 2012 Transmission of Citrus leprosis virus cytoplamatic type by Brevipalpus phoenicis Geijskes to alternate host plants found in citrus orchards Plant Disease 96 7 968 972 doi 10 1094 pdis 06 11 0538 PMID 30727203 Groot T V Freitas Astua J Kitajima E W 2006 Brevipalpus phoenicis transmits citrus leprosis virus cytoplasmatic type CiLV C to common bean Phaseolus vulgaris under experimental conditions Virus Rev Res 11 67 68 Garita L C Tassi A D Calegario R F Kitajima E W Carbonell S A M Freitas Astua J 2013 Common bean Experimental indicator plant for Citrus leprosis virus C and some other cytoplasmatic type Brevipalpus trinsmitted viruses Plant Disease 97 10 1346 1351 doi 10 1094 pdis 12 12 1143 re PMID 30722150 Calegario R F Locali E C Stach Machado D R Peroni L A Caserta R Salaroli R B Freitas Astua J Machado M A Kitajima E W 2013 Polyclonal antibodies to the putative coat protein of Citrus leprosis virus C expressed in Escherichia coli Production and use in immunodiagnosis Trop Plant Pathol 38 3 188 197 doi 10 1590 s1982 56762013005000005 Choudhary N Roy A Leon M G Picton D D Wei G Nakhla M K Levy L Brlan Sky R H 2013 Immunodiagnosis of Citrus leprosis virus C using a polyclonal antibody to an expressed putative coat protein J Virol Methods 193 2 548 553 doi 10 1016 j jviromet 2013 07 035 PMID 23911294 Choudhary N Roy A Govindarajulu A Nakhla M K Levy L Brlansky R H 2014 Production of monoclonal antibodies for detection of Citrus leprosis virus C in ezyme linked immuno assays and immunocapture reverse transcription polymerase chain reaction Journal of Virological Methods 206 144 149 doi 10 1016 j jviromet 2014 06 010 PMID 24956418 Kubo K S Novelli V M Bastianel M Locali Fabris E C Antonioli Luizon R Machado M A Freitas Astua J 2011 Detection of Brevipalpus transmitted viruses in their mite vectors by RT PCR Exp Appl Acarol 54 1 33 39 doi 10 1007 s10493 011 9425 9 PMID 21279538 S2CID 31600294 Locali E C Freitas Astua J Souza de A A Takita M A Astua Monge G Antonioli R Kitajima E W Machado M A 2003 Development of a molecular tool for the diagnosis of leprosis a major threat to citrus production in the Americas Plant Disease 87 11 1317 1321 doi 10 1094 pdis 2003 87 11 1317 PMID 30812546 a b Roy A Leon M G Stone A L Schneider W L Hartung J S Brlansky R H 2014 First report of Citrus leprosis virus nuclear type in sweet orange in Colombia Plant Disease 98 8 1162 doi 10 1094 pdis 02 14 0117 pdn PMID 30708809 a b Childers Carl C Rodrigues Jose C V 2011 12 20 An overview of Brevipalpus mites Acari Tenuipalpidae and the plant viruses they transmit Zoosymposia Magnolia Press 6 180 192 doi 10 11646 zoosymposia 6 1 28 ISSN 1178 9913 Fawcett Howard Samuel 1911 Scaly Bark or Nail Head Rust of Citrus Bulletin of the Florida Agricultural Experiment Station Gainesville FL USA Florida Agricultural Experiment Station University of Florida 106 41 ASIN B00089SF00 ISSN 0096 607X OCLC 18160315 OCLC 903637507 Google Books AGRIS id US201300451845 AGRIS id US201300067868 Childers C C Rodrigues J C V Derrick K S Achor D S French J V Welbourn W C Ochoa R Kitajima E W 2003 Citrus leprosis and its status in Florida and Texas Past and present Experimental and Applied Acarology 30 1 3 181 202 doi 10 1023 b appa 0000006548 01625 72 PMID 14756416 S2CID 19178892 Childers C C Rodriguez J C V Kitajima E W Derrick K S Rivera C Welbourn W 2001 A control strategy for breaking the virus vector cycle of Brevipalpus spp and Rhabdovirus disease citrus leprosis Manejo Integrado de Plagas Costa Rica 60 76 79 Kitajima E W Chagas C M Harakava R Calegario R F Freitas Astua J Rodrigues J C V Childers C C 2011 Citrus leprosis in Florida USA apperars to have been caused by the Nuclear Type of Citrus Leprosis Virus CiLV N Virus Rev Res 16 1 2 1 5 doi 10 17525 vrr v16i1 2 51 Spegazzini C 1920 Sobre algunas enfermedades y hongos que afectan las plantas de agrios en el Paraguay Ann Soc Cient 90 155 188 Bitancourt A A 1934 Relacao das doencas e fungus parasitas observados na seccao de Fitopatologia durante os anos de 1931 e 1932 Arq Inst Biol 5 39 45 Bitancourt A A 1940 A leprose dos citrus O Biologico 6 39 45 a b c CABI Citrus leprosis virus C In Invasive Species Compendium www cabi org Retrieved 28 November 2014 Prates H S Rodrigues J C V 1996 Citris leprosis Cati SAA Technical Bull Campinas SP Omoto C Albes E B Ribeiro P C 2000 Detection and monitoring of resistance in Brevipalpus phoenicis Geijkes Acari Tenuipalpidae to dicofol Anais da Sociedade Entomologica do Brasil 29 4 757 764 doi 10 1590 s0301 80592000000400016 Omoto C Alves E 2004 A resistencia dos acaros a acaricidas em citros Visao Agricola 2 82 86 Magalhaes B P Rodrigues J C Boucias D G Childers D G 2005 Pathogenicity of Metarhizium anisoplae var Acridum to the false spider mite Brevipalpus phoenicis Acari Tenuipalpidae Florida Entomologist 88 2 195 198 doi 10 1653 0015 4040 2005 088 0195 pomava 2 0 co 2 Bastianel M de Oliveira A C Cristofani M Filho O G Freitas Astua J Rodrigues V Astua Monge G Machado M A 2006 Inheritance and heridability of resistance to citrus leprosis Phytopathology 96 10 1092 1096 doi 10 1094 phyto 96 1092 PMID 18943497 Retrieved from https en wikipedia org w index php title Citrus leprosis disease amp oldid 1170568547, wikipedia, wiki, book, books, library,

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