Investigating bark, ambrosia and nitidulid beetle (Coleoptera : Scolytinae and Nitidulidae) communities and their potential role in the movement of Ceratocystis manginecans in commercial forestry plantations in Riau, Indonesia
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Wiley
Abstract
Ceratocystis Canker and Wilt Disease (CCWD), caused by the fungal pathogen Ceratocystis manginecans, poses a significant threat to Acacia and Eucalyptus plantations in Indonesia. Infections typically occur through wounds on the main stems of trees, and infected trees, particularly Acacia, are often co-infested by various wood-associated beetles. The aim of this study was to identify the beetle species associated with Ceratocystis-infected trees and to assess their potential role in dispersing C. manginecans.
Beetle and frass samples were collected from Ceratocystis-infected compartments of Acacia and Eucalyptus propagated as monocultures in Riau, Indonesia, either by using traps or by direct collection from infected trees. The samples were screened for the presence and viability of Ceratocystis propagules using a quantitative polymerase chain reaction-high-resolution melting analysis (qPCR-HRMA) diagnostic tool and a carrot baiting technique, respectively.
Fourteen beetle species, predominantly collected from traps, representing nine genera of the Scolytinae and Nitidulidae, were identified from the two plantation types.
The qPCR tool detected the presence of Ceratocystis DNA on 13 of the 14 beetle species at concentrations as low as 0.015–0.0019 ng. However, viable Ceratocystis propagules could not be recovered from these beetles using culture-based methods.
Of the 105 frass samples screened, qPCR detected Ceratocystis DNA in 67 samples; however, only one Ceratocystis isolate was obtained using the carrot baiting method.
The results of this study suggest that the beetles and beetle frass can harbour Ceratocystis propagules, as indicated by the detection of fungal DNA. However, the viability of the propagules and the ability of the beetles and/or beetle frass to spread C. manginecans requires further investigation.
Description
DATA AVAILABILITY STATEMENT : All data are openly available in the supporting information. All consensus DNA sequences generated in this study have been deposited in the NCBI GenBank database (https://www.ncbi.nlm.nih.gov/). Accession numbers for every sequence are provided in Table S1.
SUPPORTING INFORMATION
TABLE S1. Beetle collections from clonal Eucalyptus pellita and Acacia crassicarpa compartments and the detection of Ceratocystis using carrot baiting and qPCR detection.
TABLE S2. Frass samples collected and detection of Ceratocystis using carrot baiting and qPCR detection.
FIGURE S1. Figures of several of the morpho-species collected in infected Acacia crassicarpa and clonal Eucalyptus pellita compartments (a) Mature Beaverium sp. collected from modified Bambara beetle trap in infected A. crassicarpa compartments. Bar = 500 μm. (b) Mature Hypothenemus sp. collected from modified Bambara beetle trap in infected A. crassicarpa and clonal E. pellita compartments. Bar = 200 μm. (c) Mature Epuraea sp. collected from modified Bambara beetle trap in infected A. crassicarpa and clonal E. pellita compartments. Bar = 500 μm. (d) Mature Stictodex dimidiatus (syn. Xyleborus decumans) collected from modified Bambara beetle trap in infected clonal E. pellita compartments. Bar = 200 μm. (e) Mature Xyleborus affinis collected from modified Bambara beetle trap in infected A. crassicarpa and clonal E. pellita compartments. Bar = 200 μm. (f) Mature Xylosandrus crassiusculus collected from modified Bambara beetle trap in infected A. crassicarpa and clonal E. pellita compartments. Bar = 200 and 500 μm. (g) Mature Xyleborinus exiguus collected from modified Bambara beetle trap in infected A. crassicarpa and clonal E. pellita compartments. Bar = 200 μm. (h) Mature Xyleborus perforans collected from modified Bambara beetle trap in infected A. crassicarpa and clonal E. pellita compartments. Bar = 200 μm. (i) Mature Xyleborinus sharpae collected from modified Bambara beetle trap in infected A. crassicarpa and clonal E. pellita compartments. Bar = 200 μm.
FIGURE S2. Macerated beetle mix susceptions when placed onto carrot baits yielded sporulation characteristic of C. manginecans.
FIGURE S3. Association of beetle wounding and Ceratocystis infection on Acacia crassicarpa. (a) Typical staining of vascular tissue due to Ceratocystis infection on Acacia crassicarpa surrounding a borer hole. (b) Ceratocystis perithecia colonizing wood from and below borer wound.
FIGURE S4. Artificially wounded Acacia crassicarpa stem colonized by Ceratocystis. Ceratocystis colonized tissue being fed upon by (a) a fly and (b) a nitidulid beetle.
Keywords
Ceratocystidaceae, Tropical plantation forestry, Quantitative polymerase chain reaction (qPCR), Insect-fungus interactions, Fungal pathogen detection, Quantitative polymerase chain reaction-high-resolution melting analysis (qPCR-HRMA)
Sustainable Development Goals
SDG-15: Life on land
Citation
Lynn, K.M.T., Wingfield, M.J., Tarigan, M., Durán, A., Santos, S.A., Nel, W.J. & Barnes, I. Investigating bark, ambrosia and nitidulid beetle (Coleoptera: Scolytinae and Nitidulidae) communities and their potential role in the movement of Ceratocystis manginecans in commercial forestry plantations in Riau, Indonesia', Agricultural and Forest Entomology, vol. 27, no. 4, pp. 707-722, doi : 10.1111/afe.12698.
