The study comprised the main citrus-producing areas of Central-Northern Veracruz in commercial orchards of C. sinensis, C. latifolia, C. reticulata, and C. paradisi of different ages, located in the municipalities of Alamo, Castillo de Teayo, Cazones, Cuitlahuac, Martinez de la Torre, Papantla, Tihuatlan, and Tuxpan. Sampling focused on trees with yellowing symptoms, decline, death of annual branches, and small fruits. From up to two trees, samples included four vegetative shoots in active growth from each orchard (one shoot per cardinal direction).

The number of samples per municipality varied: six in Cuitlahuac, nine in Martinez, 10 in Papantla, 15 in Alamo, 18 in Tihuatlan, 18 in Castillo de Teayo, 22 in Cazones, and 22 in Tuxpan. Samples per species divided as seven of C. paradisi, 22 of C. latifolia, 24 of C. reticulata and 67 of C. sinensis, as in some sampling areas only one citrus species is grown.

RNA extraction followed this protocol: 0.2 g of the midrib of leaves was macerated in a mortar with liquid nitrogen until obtaining a fine powder; the powder was transferred into a 2 mL microcentrifuge tube with 750 µL of EB1 and 75 µL of 20% SDS and mixed on a vortex (BenchMixerTM). The tubes were incubated at 65˚C for 20 min in a Dry Block Heater (Select BioProducts), mixing them with inversion every 5 min; 250 µL of 5M KOAC were added and incubated at 4˚C for 20 min. Subsequently, they were centrifuged at 13,500 rpm at 10˚C for 20 min; 600 µL of the supernatant was transferred to a 1.5 mL microcentrifuge tube with 540 µL of isopropanol, incubated at −20˚C for 30 min, then centrifuged at 13,500 rpm at 10˚C for 15 min. The supernatant was discarded, and the pellet was allowed to dry. The pellet was then dissolved with 700 µL of EB2 at 4˚C for 12 h. The tubes were centrifuged at 13,500 rpm at 4˚C for 15 min. 600 µL of the supernatant were transferred into a 1.5 mL microcentrifuge tube containing 500 µL of isopropanol and 75 µL of 3M NaOAC. The tube was mixed by inversion five to 10 times and centrifuged at 13,500 rpm at 4˚C for 10 min. The supernatant was discarded, 1 ml of 75% ethanol was added to the formed pellet, and the mixture was centrifuged at 13,500 rpm at 4˚C for 10 min. The supernatant was removed, and the pellet was allowed to dry; once dried, the pellet was resuspended in DNase-free water. Nucleic acid concentration and purity were verified with a NanoDropTM 2000 spectrophotometer.

Two-step RT-PCR was performed. Synthesis of cDNA was performed using M-MLV reverse transcriptase (PROMEGA) with modification in the reverse transcription reaction (RT), 0.5 µL of each forward and reverse primer (Table 1) [12] [16] were added into a 0.2 mL microcentrifuge tube with 4 µL water and 2 µL

of RNA (200 µg·µL⁻¹) from each sample. The tubes were incubated at 72˚C for 5 min and then placed on ice for 10 min. Into each microcentrifuge tube, 4 µL of the mix containing 2 µL Buffer 5X of M-MLV (PROMEGA), 1 µL of DTT 0.1 M (PROMEGA), 0.5 µL of dNTP’s Mix (PROMEGA), and 0.15 µL of M-MLV reverse transcriptase (PROMEGA). Reverse transcription was performed at 42˚C for 60 min, followed by inactivation at 72˚C for 10 min.

PCR was performed in a total reaction volume of 9 µL of the reaction mix. This mix contained 2 µL of Green buffer GoTaq DNA polymerase (PROMEGA), 0.4 µL of MgCl₂, 0.2 µL of dNTP’s mix, 0.6 µL of each primer F and R [12] [16], 0.1 µL of GoTaq DNA polymerase (PROMEGA), 5.1 µL of DNase-free water, and 2 µL of cDNA. The PCR conditions proposed by [16] were followed, and the five strains (T36, VT, T3, B165, and T30) were those proposed by Roy [12]. The products were visualized on a 2% agarose gel with ethidium bromide.

The samples that tested positive were sent to Macrogen Corp. for Sanger sequencing. The sequences were assembled with the DNA BASER software and compared with those deposited in the National Center for Biotechnology Information (NCBI). Five sequences obtained in this study were deposited in the GenBank database (MN545966, MN545967, MN545968, MN545969, and MN545970). The phylogenetic analysis was performed with the Neighbor-Joining (NJ) method and the nucleotide substitution model obtained was K2 (Kimura 2 parameters); a bootstrap of 500 repetitions was performed with the MEGA software.

In six out of the eight municipalities, the percentage of samples positive for CTV was higher than 50% (Figure 1). The reason might be that C. sinensis dominates

in Alamo, Castillo de Teayo, Cazones, Papantla, and Tihuatlan, and most of the cultivars from this species produce three vegetative sprouting per year. In contrast, C. reticulata (in Tuxpan) produces a single vegetative sprouting per year, while in Cuitlahuac, C. latifolia, the prevalent species, has three to four vegetative sprouting affected by the weather. These species then become the preferred hosts for the main vectors (aphids). Our results agree with [17], who mentioned that CTV is semi-persistently transmitted by A. gossypii, T. citricida, and T. auranti, among other aphids. The results for Martinez de la Torre are enigmatic as C. latifolia dominates, similarly to Cuitlahuac, yet their outcomes differ; a more intensive technology usage that increases the number of pest control applications might be the reason for this discrepancy.

It is essential to indicate that since 1986, [18] mentions CTV detection in Ixtacuaco, Veracruz, a community located on the limits of Martinez de la Torre. The time between studies (32 years) presumes a higher incidence percentage. This situation occurred in Brazil and Argentina with the brown citrus aphid (T. citricida) as a vector, and the rapid spread of the Citrus tristeza virus caused the death of millions of trees grafted onto C. aurantium in the 1930s and 1940s [19]. In Mexico, CTV was first detected in 1983 and then the primary vector in 2000; it is probably for this reason that it took longer for the disease to spread.

The results obtained in Veracruz coincide with findings in Spain, where the disease took 54 years to become an epidemic as there was no vector; while in Brazil, where a vector existed, the process took five to 10 years [20]. The detection of T. citricida in Quintana Roo [21] resulted in predictions of an increase in strains and severe CTV symptoms as in other countries [22]; however, the reasons for the lack of correlation between vector dispersion in Mexico and disease spread are unknown.

The virus may have already infected most producing orchards in the state of Veracruz, but it is necessary to verify this. Extensive surveys are necessary for all citrus-producing areas in Mexico as the virus might be present in other citrus-producing states.

This study found CTV in 100% of the C. paradisi samples, followed by C. latifolia in 82% of the samples, C. sinensis in 60%, and C. reticulata in 46% (Figure 2). Differences in cultivar incidences may depend on various factors that influence the CTV transmission rate, such as cultivars that produce more shoots per year,

aphid species and their reproduction rates changing with the local environmental conditions [23], use of non-certified vegetative material, and orchard management (e.g., pruning) with infected tools [24].

The presence of CTV in all the municipalities and cultivars sampled may result from using infected material as most producers acquired their plants in non-certified nurseries and with sour orange (C. aurantium) rootstock. Thus, certification programs are essential to prevent the introduction of severe CTV strains or other pathogens associated with citruses. Besides the main insect vectors, four species of aphids have shown the ability to transmit CTV: A gossypii, A. spiraecola, T. aurantia, and T. citricida. The last species mentioned is a highly efficient transmission vector for CTV, up to 25 times. Where T. citricida is absent, A. gossypii becomes the primary vector of CTV [25] [26] [27].

Nevertheless, in Mexico, the distribution and transmissibility of CTV, or the main citrus-associated aphids in Central and Northern Veracruz, is not known. A pest currently widely in most citrus-producing areas, Diaphorina citri, acts as a CTV vector [28]. In some states of Mexico, given the conditions of humidity, temperature, and alternate hosts, D. citri can be found throughout the year [29].

This study employed RT-PCR for five different strains with specific primers: T30, T3, B165, VT, and T36. Out of the 120 samples analyzed, 76 were positive for CTV. All eight municipalities studied contained the T30 strain (Figure 3): the incidence ranged from 17 in Tihuatlan to 83% in Cuitlahuac. Thus, all municipalities studied have the disease and, indeed, most other municipalities of Veracruz. Notoriously, visible symptoms do not appear under the T30 strain, even in key lime (C. aurantifolia) indicator plants [30]. The lack of symptoms may explain why no tree deaths have occurred in Mexico.

The VT strain, considered severe [31], was found in seven municipalities, with incidence from 7% in Alamo to 50% in Tihuatlan (Figure 3). This prevalence might explain the observed tree deaths in the north of Veracruz and put the country’s citrus industry at risk since C. aurantium is the principal rootstock. Epidemics related to CTV have occurred at different times in Ghana (1938), California (1939), Florida (1951), Spain (1957), Israel (1970), and Venezuela (1980); those countries had C. aurantium as a rootstock [32]. We highlight the above as the observed symptoms in the field coincide with those reported in the literature

by [12] [33]: small fruits attached to the plant, defoliation, and quick tree death. The T3 strain was detected in six municipalities, from 20% in Castillo de Teayo to 50% in Papantla.

In Tihuatlan, CTV-positive samples for T30 and VT strains (Figure 4), also tested positive for T36 (33%), which is considered the most aggressive type worldwide [14] [31]. All strains are associated with severe leaf symptoms (vein clearing or leaf cupping), mild to moderate stem pitting on all replicates of key lime, as well as little or no stunting (depending on replicate) on this host [34]. Our results conclude that this strain should be present in other municipalities; thus, more exhaustive studies are required.

The results indicate rapid progression affecting Veracruz and other producing states; NOM-031-FITO-2000 and NOM-079-FITO-2002 standards, CTV continues spreading. Moreover, in the Mexican citrus orchards, sour orange (C. aurantium) is the prevailing rootstock, making it even more vulnerable to CTV.

In most municipalities, sampled trees showed yellowing of shoots, leaves, and small fruits, dieback of twigs, and debarking of the trunk and branches. In Cazones and Tihuatlan, the cultivars sampled corresponded to C. sinensis and C. reticulata, in most cases grafted onto C. aurantium; current knowledge indicates that CTV symptoms vary depending on the virus strain and the cultivar/rootstock combination [35]. The most often described symptoms are deterioration and death in cultivars of C. sinensis, C. reticulata, and C. paradisi. In C. aurantium, “stem pitting” is commonly observed resulting from aberrant phloem development. “Yellowing” is characterized by growth retardation and leaf chlorosis in C. sinensis and C. paradisi [36]. Aggressive strains and the cultivar/rootstock combination cause tree death and substantially decrease plant yield and vigor, resulting in cumulative economic losses. The CTV positive trees in Cazones, Cuitlahuac, and Tihuatlan showed yellowing of shoots, leaves, and small fruits, dieback of twigs, and rapid deterioration.

The sequences of each isolate were read in Bioedit, aligned, and compared with GenBank and showed a similarity of up to 100% with CTV strains. For phylogenetic analysis, three sequences (AF260651.1, EU857538.1, and MN545966) were selected. Therefore, based on this analysis, strains of the virus can be detected with specific primers as proposed by Roy et al. [11] for an endpoint RT-PCR. The dendrogram (Figure 5) shows three groupings: CTV type T30, T3, and VT. The Citrus tristeza virus has caused epidemics in citrus cultivation worldwide for two centuries. Stain T36 and VT mainly caused quick tree decline. Stem pitting, often caused by T3 or T68, substantially reduces the growth and fruit quality of C. paradisi, C. sinensis, and C. aurantifolia trees, regardless of the rootstock used, which limits the type of rootstock and varieties that can be grown commercially where these strains are present [12] [25] [26].

The high incidence of CTV in the prominent citrus-producing municipalities in the state of Veracruz allows us to conclude that: 1) Producers generally do not use certified material; 2) The required prophylactic measures are not applied in the handling of pruning tools; 3) The nursery certification program to produce citrus plants used in Mexico is only partially applied. It is vital to acknowledge the current situation in Veracruz, where citrus farming is the basis for the livelihood of more than 50,000 families; furthermore, C. latifolia is the primary fruit exported to other countries.

Our results can explain the causes of the accelerated decline of citrus farming in Central-Northern Veracruz: most sampled plants had damaged trunks, as well as damaged main branches from second to fifth or sixth order, showed psosoris (CPsV), exocortis (CEVd), cachexia (CVd-II), and HLB (CLas). Additional factors like associated diseases caused by Phytophthora, Lasiodiplodia, and Colletotrichum species and the lack of pruning and fertilization further promote the decline. The effects show particularly on Persian lime, mandarin, orange orchards, and to a lesser extent, grapefruit.

The potential for future citrus losses from CTV is more significant than previously recorded. Therefore, pre-immunization using attenuated strains is the only means to deal with severe Citrus tristeza virus strains. According to [37], it has been the best way to control CTV in Brazil, South Africa, Australia, and Japan. Pre-immunization as a management strategy for CTV could resolve one of the phytosanitary problems in Mexican citrus farming. Additionally, the production must be done in certified nurseries and on a scientific and professional basis. In addition, the understanding of the relationship between CTV isolates, plants, and vectors, which in Mexico is scarce, should be strengthened. The combination of the use of certified and pre-immunized buds is undoubtedly the best way to control the losses induced by CTV. Before you begin to format your paper, first write and save the content as a separate text.