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| Materyal Türü: | Recurso digital |
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Zenodo
2023
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| Konular: | |
| Online Erişim: | https://doi.org/10.5281/zenodo.10249875 |
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- <p><b><i>Neodeightonia chamaeropicola</i> D.S. Pereira & A.J.L. Phillips <i>sp. nov.</i>, MycoBank MB847703</b></p><p>(Figure 10)</p><p><i>Etymology</i>: Named after the host genus from which it was isolated, <i>Chamaerops humilis</i>.</p><p><i>Type</i>: <b>PORTUGAL</b>, Lisbon, Parque das Nações, on foliar lesions of <i>Chamaerops humilis</i> (<i>Arecaceae</i>), 8 May 2021, Diana S. Pereira (<b>specimen</b> HDP 089, <b>holotype</b> AVE-F-16, culture ex-type CDP 1446 = CBS KNAW culture collection, ITS sequence OQ 996231, <i>tef1</i> sequence OR 233669).</p><p>Associated with foliar lesions. <b>Sexual morph</b>: Undetermined. <b>Asexual morph</b>: <i>Conidiomata</i> on palm leaf pieces in culture pycnidial, globose to subglobose, slightly papillate, non-stromatic, uniloculate, dark brown to black, solitary, occasionally aggregated, scattered, semi-immersed to superficial or immersed in the host becoming erumpent when mature, glabrous, exuding a creamy, whitish mucoid mass or cirrus of conidia. <i>Conidiophores</i> reduced to conidiogenous cells. <i>Conidiogenous cells</i> lining the pycnidial cavity, hyaline, smooth- and thin-walled, simple, indeterminate, cylindrical, often swollen at the base, ampulliform, straight or curved, aseptate, occasionally 1-septate, enteroblastic, proliferating at the same level giving rise to periclinal thickenings, or proliferating percurrently to form 1–3 annellations, occasionally enteroblastic proliferating percurrently after the formation of a new conidiogenous cell by apical wallbuilding, variable in size, 8.28–24.23 × 3.38–8.55 μm, 95 % confidence limits = 13.80–15.81 × 4.65–5.19 μm (mean ± SD = 14.80 ± 3.63 × 4.92 ± 0.98 μm, n = 50). <i>Conidia</i> broadly ellipsoid to obovoid, apex and base broadly rounded, widest in the middle, thick-walled, initially hyaline and aseptate, becoming pale to dark brown and 1-septate, with melanin deposits on the inner surface of the wall arranged longitudinally giving a striate appearance to the conidia, mostly eguttulate, 6.80–12.42 × 2.71–4.60 μm, 95 % confidence limits = 7.82–8.32 × 3.60–3.81 μm (mean ± SD = 8.07 ± 0.91 × 3.70 ± 0.38 μm), mean ± SD conidium length/width ratio = 2.20 ± 0.29 (n = 50).</p><p><i>Culture characteristics</i>: Colonies on 1/2 PDA, reaching 80 mm diam. after 7 at 20 ℃ in darkness. Surface raised, cottony, with abundant aerial mycelium, with entire, filamentous margin, circular shape, whitish, becoming pale to light brown towards the centre, opaque. Reverse pale, becoming brownish towards the centre. No diffusible pigment.</p><p><i>Additional material examined</i>: PORTUGAL, Lisbon, Parque das Nações, on foliar lesions of <i>Chamaerops humilis</i> (<i>Arecaceae</i>), 8 May 2021, Diana S. Pereira (specimen HDP 089), living culture CDP 1447 (ITS sequence OQ996232, <i>tef1</i> sequence OR233670); Parque das Nações, on foliar lesions of <i>C. humilis</i> (<i>Arecaceae</i>), 8 May 2021, Diana S. Pereira (specimen HDP 090), living culture CDP 1512 (ITS sequence OQ996233, <i>tef1</i> sequence OR233671); Parque das Nações, on foliar lesions of <i>C. humilis</i> (<i>Arecaceae</i>), 8 May 2021, Diana S. Pereira (specimen HDP 091), living culture CDP 1566 (ITS sequence OQ996236, <i>tef1</i> sequence OR233673).</p><p><i>Hosts</i>: <i>Chamaerops humilis</i> (present study), <i>Phoenix dactylifera</i> (Al-Sadi <i>et al</i>. 2012), <i>Syagrus romanzoffiana</i> (da Silva Fonseca <i>et al</i>. 2020) (<i>Arecaceae</i>).</p><p><i>Distribution</i>: Brazil (Pato Branco, Paraná) (da Silva Fonseca <i>et al</i>. 2020), Oman (Al-Sadi <i>et al</i>. 2012), Portugal (Lisbon) (present study).</p><p><i>Notes</i>: Based on ITS and <i>tef1</i> sequence data, <i>Neodeightonia chamaeropicola</i> (CDP 1446) is most closely related to <i>N. phoenicum</i> (CBS 122528) (Figure 4) and can be distinguished from it based on 10 fixed unique single nucleotide polymorphisms (SNP) and seven fixed deletion/insertion polymorphisms (DIP) in the partial sequences of those two gene regions (three in ITS and seven in <i>tef1</i>). Thus, <i>N. chamaeropicola</i> and <i>N. phoenicum</i> differ in seven and 10 nucleotide positions in ITS and <i>tef1</i> partial loci, respectively. Moreover, two additional SNP are observed in the <i>tef1</i> sequence data between the ex-type strain of <i>N. chamaeropicola</i> and <i>N. phoenicum</i>, although they were not considered fixed, since they are not observed in the remaining <i>N. chamaeropicola</i> strains studied. In short, the ex-type strains of <i>N. chamaeropicola</i> (CDP 1446) and <i>N. phoenicum</i> (CBS 122528) display 98.62 % (501/508, including 4 gaps) and 95.77 % (272/284, including 3 gaps) sequence similarity in ITS and <i>tef1</i>, respectively. Morphologically, <i>N. chamaeropicola</i> (CDP 1446) and <i>N. phoenicum</i> (CBS 122528) are similar, both producing dark brown to black pycnidial conidiomata and ellipsoid, hyaline and aseptate conidia that become pigmented, 1-septate and striate after discharge from the conidiomata (Phillips <i>et al</i>. 2008) (Figure 10, Table 4). Nonetheless, they can be distinguished from one another based on conidial morphology (Phillips <i>et al</i>. 2008) (Figure 10, Table 4). Conidia of <i>N. chamaeropicola</i> (CDP 1446) (mean = 8.07 × 3.70 μm; L/W = 2.20) are substantially smaller, with a higher L/W ratio than those of <i>N. phoenicum</i> (CBS 122528) (mean = 19.1 × 11.5 μm; L/W = 1.7) (Phillips <i>et al</i>. 2008). Four strains of <i>N. chamaeropicola</i> were isolated, namely CDP 1446 (ex-type), CDP 1447, CDP 1512 and CDP 1566. They exhibited a minute degree of variation in colony morphology when cultured on 1/2 PDA, which is expressed by the amount of aerial mycelium produced. No relevant variation in micromorphology was observed between these strains. The nucleotide sequence similarity between them was 99.41–100 % for ITS, which result from a single nucleotide position difference in CDP 1566 (i.e. an additional G in ITS1) and three nucleotide positions differences in CDP 1512 (i.e. the insertions of an A and G and a deletion of a G in ITS1), and 99.29 % for <i>tef1</i>, resulting from two nucleotide position differences that were only present in the partial <i>tef1</i> sequence of the ex-type strain CDP 1446. The isolates of <i>N. chamaeropicola</i> studied were recorded from foliar lesions of <i>Chamaerops humilis</i>, but pathogenicity has not been tested. <i>Neodeightonia chamaeropicola</i> (as “ <i>N. phoenicum</i> ”) has been previously isolated and characterized as a weak pathogen causing root necrosis of <i>Phoenix dactylifera</i> (Al-Sadi <i>et al</i>. 2012).</p>