“…The fungus does not appear to enter through the stigma, but rather enters from nectaries or other natural openings below the ovary and then moves upward into the developing boll (Klich and Chmielewski, 1 985; Klich et al ., 1984, 1986). Ultrastructural evidence indicates that the fungus may be entering the seeds via the vascular tissue (Huizar et al ., 1990). Early season bolls and those under water stress (water potentials between –1.6 and –1.9 MPa) at anthesis are more susceptible to infection than later season bolls or those under more or less stress at anthesis (Klich, 1987, 1990).…”
Section: Factors Influencing Aflatoxin Formation In the Fieldmentioning
“…The fungus does not appear to enter through the stigma, but rather enters from nectaries or other natural openings below the ovary and then moves upward into the developing boll (Klich and Chmielewski, 1 985; Klich et al ., 1984, 1986). Ultrastructural evidence indicates that the fungus may be entering the seeds via the vascular tissue (Huizar et al ., 1990). Early season bolls and those under water stress (water potentials between –1.6 and –1.9 MPa) at anthesis are more susceptible to infection than later season bolls or those under more or less stress at anthesis (Klich, 1987, 1990).…”
Section: Factors Influencing Aflatoxin Formation In the Fieldmentioning
“…After analyzing cotton plants inoculated at cotyledonary leaf scars, unopened flower buds, and involucral nectaries or the peduncle of newly opened flowers for aflatoxin contamination in cotton bolls, Klich and her colleagues [6][7][8] concluded that the fungus might gain entry through the vascular bundles, primarily through xylem vessels. Hamsa and Ayres [9] observed that hyphal invasion in stored cottonseeds proceeded via chalaza, micropyle, and cracks that developed in the seed coat during ginning.…”
Section: Introductionmentioning
confidence: 99%
“…Hamsa and Ayres [9] observed that hyphal invasion in stored cottonseeds proceeded via chalaza, micropyle, and cracks that developed in the seed coat during ginning. Likewise, after microscopic analyses of contaminated cottonseeds, Lee et al [10] and Huizar et al [8] hypothesized that the fungus may enter through nonlignified layers of the seed coat. However, clear evidence regarding entry of the fungus and the infection process during pre-or post-harvest phases of contamination has not been available from these studies.…”
Cotton bolls were inoculated with a green fluorescent protein (GFP)-expressing Aspergillus flavus (strain 70) to monitor fungal growth, mode of entry, colonization of cottonseeds, and production of aflatoxins. The GFP strain and the wild-type did not differ significantly in pathogen aggressiveness as indicated by similar reductions in inoculated locule weight. GFP fluorescence was at least 10 times higher than the blue green yellow fluorescence (BGYF) produced in response to infection by A. flavus. The GFP produced by the strain made it possible to identify and monitor specific plant tissues colonized by the fungus. For example, the inner seed coat and cotyledon were colonized by the fungus within 72 h of inoculation and the mode of entry was invariably through the porous chalazal cap in intact seeds. The amount of GFP fluorescence was shown to be an indicator of fungal growth, colonization and, to some extent, aflatoxin production. The A. flavus strain expressing GFP should be very useful for rapidly identifying cotton lines with enhanced resistance to A. flavus colonization developed through genetic engineering or traditional plant breeding. In addition, development of GFP expressing A. flavus strain provides an easy and rapid assay procedure for studying the ecology, etiology, and epidemiology of cotton boll rot caused by A. flavus resulting in aflatoxin contamination.
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