Chayanard Phukhamsakda

Ms. Chayanard Phukhamsakda

Engineering Research Center of Chinese Ministry of Education for Edible and Medicinal Fungi, Jilin Agricultural University, Changchun, China
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Research Focus & Metrics

Academic Career Length

9Years (2018-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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27 March 2022 in Fungal Diversity
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Chitrabhanu Sharma BhunjunChitrabhanu Sharma Bhunjun
Chitrabhanu Sharma Bhunjun
TNTuula Niskanen
Tuula Niskanen
Nakarin SuwannarachNakarin Suwannarach
Nakarin Suwannarach
NWNopparat Wannathes
Nopparat Wannathes
YCYi-Jyun Chen
Yi-Jyun Chen
SLSAISAMORN LUMYONG
SAISAMORN LUMYONG
Fungi play vital roles in ecosystems as endophytes, pathogens and saprobes. The current estimate of fungal diversity is highly uncertain, ranging from 1.5 to 12 million, but only around 150,000 species have been named and classified to date. Since the introduction of DNA based methods for species identification, the number of newly described taxa has increased from approximately 1000 to around 2000 yearly. This demonstrates the importance of DNA based methods to identify and distinguish species, especially cryptic species. Many novel species from recent studies have been found in historically understudied regions and habitats, but these still represent only a small percentage of the estimated species. In this paper, we examine 16 genera from the top 40 most speciose genera as listed in Species Fungorum as case studies to examine the diversity of taxa in each genus. The genera treated herein are Cercospora, Diaporthe, Meliola, Passalora, Phyllachora, Phyllosticta, Pseudocercospora, Ramularia (ascomycetes) and Cortinarius, Entoloma, Inocybe, Marasmius, Psathyrella, Puccinia, Russula, Uromyces (basidiomycetes). We critically evaluate the number of species in these genera and correlate these numbers with the number of entries in GenBank. We introduce 18 new species Apiospora multiloculata, Candolleomyces thailandensis, Cortinarius acutoproximus, Cortinarius melleoalbus, Cortinarius pacificus, Cortinarius parvoacetosus, Diaporthe guizhouensis, Entoloma pseudosubcorvinum, Inocybe meirensongia, Marasmius albulus, Marasmius obscuroaurantiacus, Meliola camporesii, Phyllachora siamensis, Phyllosticta doitungensis, Picipes yuxiensis, Pseudocercospora vignae, Puccinia maureanui and Russula inornata. We also introduce a new record of Candolleomyces cladii-marisci and Inocybe iringolkavensis. We discuss the genera Colletotrichum and Pleurotus that are speciose, but do not occur in the top 40. We hypothesize whether there might be more species in these genera and discuss why these genera have some of the largest number of species.

28 April 2022 in Fungal Diversity
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Chayanard PhukhamsakdaChayanard Phukhamsakda
Chayanard Phukhamsakda
HNHenrik Nilsson
Henrik Nilsson
Chitrabhanu Sharma BhunjunChitrabhanu Sharma Bhunjun
Chitrabhanu Sharma Bhunjun
AFAntonio Roberto Gomes de Farias
Antonio Roberto Gomes de Farias
YSYa-Ru Sun
Ya-Ru Sun
KHKevin D. Hyde
Kevin D. Hyde
The global diversity of fungi has been estimated using several different approaches. There is somewhere between 2–11 million estimated species, but the number of formally described taxa is around 150,000, a tiny fraction of the total. In this paper, we examine 12 ascomycete genera as case studies to establish trends in fungal species descriptions, and introduce new species in each genus. To highlight the importance of traditional morpho-molecular methods in publishing new species, we introduce novel taxa in 12 genera that are considered to have low species discovery. We discuss whether the species are likely to be rare or due to a lack of extensive sampling and classification. The genera are Apiospora , Bambusicola , Beltrania , Capronia , Distoseptispora , Endocalyx , Neocatenulostroma , Neodeightonia , Paraconiothyrium , Peroneutypa , Phaeoacremonium and Vanakripa . We discuss host-specificity in selected genera and compare the number of species epithets in each genus with the number of ITS (barcode) sequences deposited in GenBank and UNITE. We furthermore discuss the relationship between the divergence times of these genera with those of their hosts. We hypothesize whether there might be more species in these genera and discuss hosts and habitats that should be investigated for novel species discovery.

16 March 2023 in Fungal Diversity
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Chitrabhanu Sharma BhunjunChitrabhanu Sharma Bhunjun
Chitrabhanu Sharma Bhunjun
Chayanard PhukhamsakdaChayanard Phukhamsakda
Chayanard Phukhamsakda
KHKevin D. Hyde
Kevin D. Hyde
EMEric Hugh Charles McKenzie
Eric Hugh Charles McKenzie
RSRamesh K. Saxena
Ramesh K. Saxena
QLQirui Li
Qirui Li
Fungi are an essential component of any ecosystem and have diverse ecological roles, ranging from endophytes to epiphytes and pathogens to saprobes. The current estimate of fungal endophytes is around 1 million species, however, we estimate that there is likely over 3 million species and only about 150,000 fungal species have been named and classified to date. Endophytes inhabit internal plant tissues without causing apparent harm to the hosts. Endophytes occur in almost every plant from the coldest climates to the tropics. They are thought to provide several benefits to host plants and improve the hosts’ ability to tolerate several abiotic and biotic stresses. Endophytes produce secondary metabolites with biotechnological, industrial and pharmaceutical application. Some endophytes appear to be host-specific, while some are associated with a wide range of hosts. We discuss the importance of endophytes. The ability to switch lifestyles from endophytes to pathogens or saprobes is discussed. Interactions between endophytes and hosts based on fossil data is also highlighted. Factors that influence the specificity in endophytes are discussed. We argue that the endophytic lifestyle is a common strategy in most fungi and that all fungi have endophytic ancestors. We critically evaluate the influence of co-evolution based on fossil data. We hypothesise the influence of specificity on the estimated number of endophytes and overall species numbers, and present examples of metabolites that they produce. We argue that studying endophytes for novel compounds has limitations as the genera recovered are limited. However, if saprobes were chosen instead, this would result in a much higher species diversity and undoubtedly chemical diversity.

19 April 2021 in Life
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Saowaluck TibprommaSaowaluck Tibpromma
Saowaluck Tibpromma
LZLu Zhang
Lu Zhang
Samantha C. KarunarathnaSamantha C. Karunarathna
Samantha C. Karunarathna
Tian-Ye DuTian-Ye Du
Tian-Ye Du
Chayanard PhukhamsakdaChayanard Phukhamsakda
Chayanard Phukhamsakda
YWYue-Hu Wang
Yue-Hu Wang
Algae, bacteria, and fungi, as well as higher plants, produce a wide variety of secondary metabolites known as natural products. Natural products are well known as remarkable sources of many therapeutic agents. The genus Nemania is a wood-decaying fungus that belongs to family Xylariaceae. Nemania is often found as an endophyte in diverse hosts and some species are known to produce useful secondary metabolites. In this study, two Nemania species were isolated as an endophytic fungus from Aquilaria sinensis. Multi-gene phylogenetic studies showed that the newly described strains of Nemania are new to science, and this is the first report of Nemania from the host Aquilaria. One of the fermented species, Nemania aquilariae (KUMCC 20-0268), resulted in five sesquiterpenoids, which were previously reported from agarwood, and their structures were identified by gas chromatography-mass spectrometry (GC-MS). In addition, five different media were investigated in vitro to optimize conditions for growing the fungal biomass of Nemania aquilariae and N. yunnanensis.

22 March 2024 in MycoKeys
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RXRui-Fang Xu
Rui-Fang Xu
Samantha C. KarunarathnaSamantha C. Karunarathna
Samantha C. Karunarathna
Chayanard PhukhamsakdaChayanard Phukhamsakda
Chayanard Phukhamsakda
DDDong-Qin Dai
Dong-Qin Dai
AEAbdallah Elgorban
Abdallah Elgorban
Saowaluck TibprommaSaowaluck Tibpromma
Saowaluck Tibpromma
The tropical areas in southern and south-western Yunnan are rich in fungal diversity. Additionally, the diversity of seed flora in Yunnan Province is higher than in other regions in China and the abundant endemic species of woody plants provide favourable substrates for fungi. Rubber plantations in Yunnan Province are distributed over a large area, especially in Xishuangbanna. During a survey of rubber-associated fungi in Yunnan Province, China, dead rubber branches with fungal fruiting bodies were collected. Morphological characteristics and multigene phylogenetic analyses (ITS, LSU, SSU, rpb2 and tef1-α) revealed four distinct new species, described herein as Melomastia puerensis, Nigrograna lincangensis, Pseudochaetosphaeronema lincangensis and Pseudochaetosphaeronema xishuangbannaensis. Detailed descriptions, illustrations and phylogenetic trees are provided to show the taxonomic placements of these new species.

23 August 2021 in Fungal Diversity
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TWThilini Chethana Kandawatte Wedaralalage
Thilini Chethana Kandawatte Wedaralalage
RJRuvishika Shehali Jayawardena
Ruvishika Shehali Jayawardena
YCYi-Jyun Chen
Yi-Jyun Chen
SKSirinapa Konta
Sirinapa Konta
STSaowaluck Tibpromma
Saowaluck Tibpromma
KHKevin D. Hyde
Kevin D. Hyde
Fungi have evolved diverse strategies to acquire nutrients as endophytes, saprobes, symbionts, or pathogens. Appressoria have been intensively studied due to their importance in attaching and breaching the host surface. These specialized infection structures have evolved into various morpho-types: proto-appressoria, hyaline appressoria, melanized (dark) appressoria, and compound appressoria. In this review, we discuss the differences in the formation, differentiation, and function of appressoria among fungi with diverse life strategies. Using DNA sequence information, LSU, 5.8S, SSU and rpb2 gene fragments, we reconstructed the ancestral states for appressorial types in the main phyla of fungi and fungus-like organisms and found that the hyaline appressoria was the most ancestral form. Our analysis estimated proto-appressoria diversification during the Mesozoic period (92–239 million years ago), however, its origin remains inconclusive. Our data suggest that these hyaline appressoria diversified into melanized or compound appressoria, with evidence of adaptive radiation.