Chinese Journal of Tropical Crops ›› 2022, Vol. 43 ›› Issue (2): 361-368.DOI: 10.3969/j.issn.1000-2561.2022.02.017
• Plant Protection & Bio-safety • Previous Articles Next Articles
YU Haiying1, LAN Jianqiang2,*(), LIU Lin2
Received:
2021-06-03
Revised:
2021-10-12
Online:
2022-02-25
Published:
2022-02-22
Contact:
LAN Jianqiang
CLC Number:
YU Haiying, LAN Jianqiang, LIU Lin. Process of Mango Infected by Colletotrichum gloeosporioides and Host Histopathology[J]. Chinese Journal of Tropical Crops, 2022, 43(2): 361-368.
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Fig. 1 Formation of germ tube and appresorium and microcycle conidiation in slide (After 24 h) A: Single spore germination; B: The junction of the spore tube after germination of two spores; C: The spore may germinate to produce one or more appressoriums; D: Arrow indicates the secondary spores and tertiary spores produced by microcycle conidiation.
Fig. 2 Scanning electron micrographs of mango peel infected by C. gloeosporioides A: Valvular appressorium; B: Twisting and branching of hyphae on peel surface; C, E: Germ tube growing across stomata; D: The elongated germ tube has an ear like structure; F: Surface structure of healthy mango peel.
Fig. 3 Transmission electron and light micrographs of mango fruit infected by C. gloeosporioides A: Deformed cells of mango peel infected by hyphae (×10 000); B: Hyphae extending within and between pericarp cells under light microscope (×600); C: Secondary hyphae (SH) proliferates and expands in host cells; D: Cross section of primary mycelium (×5000); E: Longitudinal section of primary hyphae,arrow indicates septem (S) and vacuoles (V) (×5000); F: Secondary hyphae in host cells (×4000); G, H: Spore maturation and abscission (×150); I: Light micrographs of acervulus (×400); J: Cytological structure of the bottom of conidial disk under light microscope (×600). A, C-F: Transmission electron micrographs; B, G-J: Light micrographs.
Fig. 4 Transmission election and light micrograph of mango leaf infected by C. gloeosporioides A: The leaf cells were deformed and depressed under light microscope (×150); B: Hyphae invade mesophyll cells (×600); C: Funnel shaped bacterial tap (×5000); D: Constriction of primary hyphae through host cell wall (×4000); E: The arrow indicates the mycelial membrane (×5000); F: A longitudinal section of treated hyphae (×4000); G: The cross section of the hyphae in host cell (×4000). A, B: Light micrographs; C-G: Transmission electron micrographs.
Fig. 5 Pathology change of mango pericarp cells after mango fruit infected A: Cellular protoplasm of host cells became disorganized (×5000); B: The host cells borderline was lost (×8000); C: High electron- dense materials accumulated in host cell wall (×10 000); D: Second hyphae collected a bundle (×10 000); E: Healthy chloroplas of mango green epidermal cell (×20 000); F: Chloroplasts infected by mycelium formed vesicles (V) and grana thylakoids disintegrated (×12 000); G: Chloroplast envelope was distorted, and disorganized partly (×12 000).
Fig. 6 Pathology change of mango leaves infected by C. gloeosporioides A: Host cell wall deformation (×5000); B: The host organelles disintegrated and the protoplast membrane was completely lysed (×8000); C: Host cell wall became thinner (×8000); D: The host cell space became larger (×5000); E: Primary hyphae in host cells and second hyphae of intercellular space (×5000).
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