Ultrastructural study of anther parasitism of Ficus laevigata by Ficophagus laevigatus (Aphelenchoididae)

Author:

Giblin-Davis Robin M.1,Kanzaki Natsumi12,Williams Donna S.3

Affiliation:

1. 1 Fort Lauderdale Research and Education Center, Department of Entomology and Nematology, University of Florida/IFAS , 3205 College Avenue , Davie , FL , United States of America

2. 2 Kansai Research Center, Forestry and Forest Products Research Institute , 68 Nagaikyutaroh, Fushimi , Kyoto , Japan

3. 3 Department of Microbiology and Cell Science, University of Florida-IFAS , P.O. Box 10700 , Gainesville , FL , United States of America

Abstract

Abstract Transmission electron microscopy (TEM) was used to compare the ultrastructural differences between healthy male florets (anthers) and one floret parasitized by Ficophagus laevigatus in late phase C syconia of Ficus laevigata from southern Florida. Previous light-microscopic examination of paraffin-sectioned material showed that F. laevigatus-infested anthers of F. laevigata manifested as malformed, often with aberrant pollen and hypertrophied epidermal cells closest to regions containing propagating nematodes. Female florets or fig wasp-parasitized female florets were not observed to be parasitized by nematodes. Considering that plant-feeding in the Aphelenchoididae is purportedly much less specialized than in certain groups of the Tylenchomorpha, where specialized hypertrophied feeder cells are produced in response to nematode feeding, we examined the putative induced response in this unusual aphelenchoidid system with the higher resolution afforded by TEM. TEM confirmed the expression of significant epidermal cell hypertrophy of the anther and anther filament in the presence of propagating nematodes, which was expressed as cell enlargement (2-5X), fractionation of large electron-dense stores into smaller aggregates, irregularly shaped nuclei enclosed by an elongated nuclear envelope, nucleolus enlargement, increased organelle production, and apparent metabolism with increased numbers of mitochondria, pro-plastids, and endoplasmic reticulum, as well as increased thickening of the cell walls. Pathological effects were observed in adjacent cells/tissue (e.g., anther and anther filament parenchymal cells, pollen tubes, pollen, and endothecium) with apparent diminishment as the distance from propagating nematodes increased (which was also probably affected by number of nematodes). Some TEM sections captured previously undocumented ultrastructural highlights of propagating individuals of F. laevigatus.

Publisher

Walter de Gruyter GmbH

Reference14 articles.

1. Center, B. J., Giblin-Davis, R. M., Herre, E. A., and Chung-Schickler, G. 1999. Histological comparisons of parasitism by Schistonchus spp. (Nemata: Aphelenchoididae) in Neotropical Ficus spp. Journal of Nematology 31:393-406.

2. Davis, E. L., Hussey, R. S., and Baum, T. J. 2004. Getting to the roots of parasitism by nematodes. Trends in Parasitology 20:134-141. DOI: 10.1016/j.pt.2004.01.005.

3. Davies, K. A., Bartholomaeus, F., Kanzaki, N., Ye, W., and Giblin-Davis, R. M. 2015. A review of the taxonomy, phylogeny, distribution and co-evolution of Schistonchus (Nematoda: Aphelenchoididae) and proposal of Ficophagus n. gen. and Martininema n. gen. Nematology 17:761-829. DOI: 10.1163/15685411-00002907

4. DeCrappeo, N., and Giblin-Davis, R. M. 2001. Schistonchus aureus n. sp. and Schistonchus laevigatus n. sp. (Aphelenchoididae): associates of native Floridian Ficus spp. and their Pegoscapus pollinators (Agaonidae). Journal of Nematology 33:91-103.

5. Dropkin, V. H. 1969. Cellular responses of plants to nematode infections. Annual Review of Phytopathology 7:101-122. DOI: 10.1146/annurev.py.07.090169.000533

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