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ARS Home » Southeast Area » Mayaguez, Puerto Rico » Tropical Crops and Germplasm Research » Research » Publications at this Location » Publication #390747

Research Project: Conservation and Utilization of Tropical and Subtropical Tree Fruit, Cacao and Bamboo Genetic Resources

Location: Tropical Crops and Germplasm Research

Title: First report of lasiodiplodia mahajangana causing canker of mango (mangifera indica) in Puerto Rico

Author
item QUIMBITA-REYES, ALEXIS - University Of Puerto Rico
item RIVERA-VARGAS, LYDIA - University Of Puerto Rico
item CABRERA-ASENCIO, IRMA - University Of Puerto Rico
item Serrato Diaz, Luz

Submitted to: Plant Disease
Publication Type: Peer Reviewed Journal
Publication Acceptance Date: 5/25/2022
Publication Date: 5/31/2022
Citation: Quimbita-Reyes, A., Rivera-Vargas, L., Cabrera-Asencio, I., Serrato Diaz, L.M. 2022. First report of lasiodiplodia mahajangana causing canker of mango (mangifera indica) in Puerto Rico. Plant Disease. https://doi.org/10.1094/PDIS-01-22-0149-PDN.
DOI: https://doi.org/10.1094/PDIS-01-22-0149-PDN

Interpretive Summary: Mango originated from the Indo-Burmese region, from where it rapidly expanded worldwide. Since 1948, Puerto Rico initiated a mango breeding and production program and currently produces considerable quantities of fruit, primarily for exportation to the US mainland and Europe. Dieback caused by fungi in the Botryosphaeriaceae family is an important disease affecting mango production. During 2019 and 2020, symptoms of dieback were observed on cv. Keitt trees planted in the mango germplasm collection of the Agricultural Experiment Station of the University of Puerto Rico located at Juana Díaz, PR. Sections of symptomatic tissue were disinfested by immersion in 70% ethanol, 10% sodium hypochlorite, rinsed with sterile-distilled-water for 1 minute at each step, and transferred to petri dishes containing PDA acidified with 85% lactic acid. One representative isolate was selected and identified Lasiodiplodia mahajangana (syn. L. caatinguensis) (Lm) isolate 17 using morphology and DNA sequencing of four nuclear genes. Pathogenicity tests were performed on 6-month-old mango trees of cv. Keitt. Four healthy trees were inoculated with 5 mm mycelial disks of Lc, on branches, with and without wounds. Controls were inoculated with PDA disks only. The inoculated trees were covered with plastic bags for 3 days. Bags were then removed and trees kept in shaded conditions for an additional 9 days. Twelve days after inoculation, Lm isolates caused stem necrosis and canker, with lesions sizes ranging from 2 to 17 mm2 with wounds, and 0 to 6 mm2 without wounds. Untreated controls showed no symptoms. Lasiodiplodia mahajangana was re-isolated from diseased branches fulfilling Koch's postulates. Lasiodiplodia mahajangana has been reported to cause stem-end rot of mango in Malaysia. Knowing L. mahajangana as a new pathogen that causes canker of mango is important to establish an adequate and effective control management of this disease in mango producing countries worldwide.

Technical Abstract: Mango originated in the Indo-Burmese region (Alphonse de Candolle, 1885). In the Caribbean, Puerto Rico currently produces and exports mangoes to the United States and Europe. Globally, an important disease affecting mango production is dieback, caused by fungi belonging to Botryosphaeriaceae family. During a one-year survey from 2019 to 2020, conducted at the mango germplasm collection of the Agricultural Experiment Station of the University of Puerto Rico, located at Juana Díaz, PR, symptoms of dieback were observed in shoots, descending towards the woody part, and vascular necrosis. We sampled bimonthly, 35 Keitt trees for one year. At the end of the evaluation, we detected that a 74% disease incidence was caused by Botryosphaeriaceae. Lasiodiplodia mahajangana (syn. L. caatinguensis) was associated with 4% disease incidence. In addition, we identified other Botryosphaeriaceae species causing 70% of disease incidence. To identify the causal agent, sections of symptomatic tissue (4mm2) were surface disinfected by immersion in 70% ethanol, 10% sodium hypochlorite and rinsed with sterile-distilled water for 1 minute at each solution. Sections were transferred to petri dishes containing potato dextrose agar acidified with 85% lactic acid (aPDA). Ten fungal isolates were obtained with similar morphological characteristics such as colony color and texture, after 12 days. Of these, one representative (isolate 17) was selected and identified as L. mahajangana (Lm) using morphological parameters and sequences of four nuclear genes (Zhang, W. et al., 2021). In aPDA, Lm colonies showed sparse and slow-growing aerial mycelium with dark gray-greenish color at the center and light gray edges. Black pycnidia were observed after 15 days of incubation at 28°C and dark conditions. Hyaline, ovoid to ellipsoid immature conidia (n=40) with average size of 22 µm long and 12 µm wide were observed. Mature bicellular pigmented conidia (n=40) had longitudinal striate and its average size was 23 µm long and 12 µm wide. Internal transcribed spacer (ITS), ß-tubulin (ßtub), elongation factor 1-alpha (EF1-a) and large ribosomal subunit (LSU) genetic regions were amplified by PCR from the original and pathogenicity test recovered isolates. Sequences of PCR products were compared with NCBI database BLAST tool with other Lm sequences. Sequence accession numbers of the four genetic regions of Lm are as follows: OL375401 and OL375402 for the ITS region; OL405579 and OL405580 for ß-tubulin; OL455922 and OL455923 for EF1-a; and OL375648 and OL375649 for LSU. All the sequences were grouped with the ex-type CMM1325 of Lm (BS=84). Pathogenicity tests were performed on 6-month-old mango trees of cv. Keitt. Three healthy trees were inoculated with 5 mm mycelial disks of Lm, on stems, with and without wounds. Controls were inoculated with aPDA disks only. Inoculated trees were covered for 3 days with plastic bags, keeping them in conditions of high relative humidity with constant irrigation, temperature of 28°C, and 12 hours of light and 12 hours of darkness for 12 days. Twelve days after inoculation, Lm isolates caused stem necrosis and canker, with differences in lesion severity from 2 to 17 mm2 with wound, and 0 to 6 mm2 without wound. Untreated controls showed no symptoms of canker. Lasiodiplodia mahajangana was re-isolated from diseased stems fulfilling Koch's postulates, and a sequence of the recovered isolate from the pathogenicity test was compared and included in the phylogenetic analysis. Lasiodiplodia mahajangana has been reported to cause stem-end rot of mango in Malaysia (Li, L. et. al., 2021). To our knowledge, this is the first report of Lm causing canker of mango in Puerto Rico. Knowing L. mahajangana as a new pathogen that causes canker of mango is important to establish an adequate and effective control management of this disease in mango producing co