In situ Detection and Investigation of the Ultrastructural Modiflcations of Phytoplasma Infection on Daffodil (Narcissus tazetta) Using a Combined Microscopy Approaches


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Derecik K., Boztaş K., Çağlayan K., Tulum I.

Agrica, cilt.13, ss.12-20, 2024 (Hakemli Dergi)

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 13
  • Basım Tarihi: 2024
  • Doi Numarası: 10.5958/2394-448x.2024.00002.1
  • Dergi Adı: Agrica
  • Derginin Tarandığı İndeksler: Index Copernicus
  • Sayfa Sayıları: ss.12-20
  • Hatay Mustafa Kemal Üniversitesi Adresli: Evet

Özet

Phytoplasmas are one of the most aggressive

phloem-limited pathogens that are obligate parasites of

plants transmitted by sap-feeding insects which also

serve as their hosts. Phytoplasma infection leads to

massive changes on plant morphology associated with a

severely impaired ultrastructure of the host cells.

However, the detailed aspects of the intricate

modiÞcations that phytoplasmas cause on their host

plants remain unclear. In this study, we conducted a

morphological comparison between healthy and

phytoplasma-infected daffodil (Narcissus tazetta) leaves

and utilized light microscopy, epißuorescence

microscopy and transmission electron microscopy

(TEM) to comprehensively examine how phytoplasma

infection modiÞes the ultrastructure of phloem cell

walls, sieve tubes and plasmodesmata. We also describe

a method based on the use of Syto 9/PI dual staining,

adaptable for preliminary detection studies of

phytoplasmas. TEM examinations visually conÞrmed

the presence of phytoplasmas within the sieve tubes and

identiÞed changes in plant cells due to infection. In the

phytoplasma infected daffodil leaves, pleomorphic

bodies (PBs) were observed within the sieve elements.

Additionally, an elevation in callose collars at the ends of

the pore-plasmodesma units of the sieve elements,

conformational changes in phloem proteins, and cell

wall thickening were noted in the phytoplasma infected

leaves compared to healthy ones. This study offers fresh

perspectives on as a structural point of view for

enhancing our comprehension of intracellular obligate

cell wall-less prokaryotes and host phloem structures,

and will aid in understanding of their interactions