Monitoring the impact of anthropogenic and naturogenic threats on orchid community through diversity, taxonomy and conservation studies is necessary. Reintroduction of these species to their natural habitat associates with their resilience, selection of suitable trees and sites for regeneration and restoration efforts, drives the conservation initiative. Upon obtaining an accurate estimate of the diversity for genetic resource conservation, integrative methods of classical morphological taxonomy, anatomy (micromorphology), and molecular genetics are crucial to solve the taxonomic uncertainty. Changes in microclimatic conditions and habitat structures are the key determinants of both epiphytic and terrestrial orchids assemblages following disturbance. Any assessments of biodiversity and ecosystem service must include variable forest types and management regimes to provide impartial views on the effect of forest and ecological disturbance on the orchid community. Accordingly, a plant-microbial ecology study should be included to study the extent of human-induced climatic variability towards the orchid diversification.

As an attempt to examine the causes of forest disturbance and degradation of the orchid community, a comparative study on diversity and ecology in eight undisturbed and ten disturbed forests in Peninsular Malaysia was conducted that varied in areas, elevations, vegetation types, and disturbance regimes. Density and individual-based rarefaction curves were used to describe the abundance. Univariate and multivariate analyses were also performed to explore the associations of species abundance with biotic and abiotic factors. The study reported 239 orchid species belonging to 65 genera. Species richness, abundance, density, and diversity of orchids varied by locality. Higher density of orchids (2.433 plants/km²) occurred in the undisturbed forests than in the disturbed forests (0.228 plants/km²). As with the character of undisturbed forests, the temperature was between 27.8 ± 0.3 °C and 31.2 ± 0.2 °C, humid (77.1 ± 1.2%–89.6 ± 0.9%), and with low light intensity (23.8 ± 3.3 μmol m⁻²s⁻¹–171.7 ± 18.8 μmol m⁻²s⁻¹), thus supporting the high density of the plants. Disturbed forests had higher diversity (H = 4.934 and 1-D = 0.990) and abundance (183 species of 57 genera) but were determined to be highly influenced by the higher abundance of epiphytic orchids on the fallen trees and ease of accessibility in the logged forests. Terrestrial and mycoheterotroph orchids were much lower in density and abundance in the disturbed habitat indicating a gradual reduction in their niche availability following the disturbance. Additionally, the ecology data show that the microclimate conditions of the canopy-covered forest was influenced by proximity to the logged area which had eventually reduced the orchids’ habitat quality. Furthermore, the results show that the abundance of epiphytic orchid communities was associated with the host plant characteristics. Host types and bark texture preference were apparent for the epiphytic orchid species, with certain types and textures hosting more orchid species than others. Overall results show that extreme temperature, humidity, and light intensity caused by the canopy opening inflicted damages to the habitat conditions and bark textures of the host plants and limits recolonisation of the orchids in the disturbed forests. The species diversity and density patterns of orchids in undisturbed and disturbed forests revealed in this study provide a baseline for conservationists, policy makers, and forest authorities in expanding the understanding of the forest ecology and vegetation along the disturbance gradient, forest regeneration, and criteria for plant selection for forest restoration in Peninsular Malaysia.

Stevia rebaudiana, a perennial herb native to northeastern Paraguay, has gained immense attention globally over the recent decades due to the natural sweetness of its leaves. Like in most plants, this particular species contains high amount of secondary metabolites, thus rendering the isolation of high quality and quantity RNA extract for molecular applications rather challenging. An effective, high-yield and high-quality RNA isolation protocol for this economically important plant species was devised here based on the cetyltrimethylammonium bromide (CTAB) extraction method, with an additional genomic DNA (gDNA) removal step. DNA and other contaminants that may affect downstream applications were effectively removed. Our results exhibited that RNA samples isolated from the leaves and stems of Stevia rebaudiana using this improvised method are high in integrity and quality with RNA integrity number (RIN) of more than 8 and low in contaminants. Kajian ini melaporkan biodiversiti strain bakteria selulosa termofilik yang terdapaStevia rebaudiana, satu tumbuhan herba saka yang berasal dari timur laut Paraguay, telah mendapat perhatian yang banyak untuk beberapa dekad kebelakangan ini kerana kemanisan semula jadi daun-daunnya. Seperti kebanyakan tumbuhan, spesies ini mengandungi kandungan metabolit sekunder yang tinggi, dengan itu menyebabkan pengasingan RNA yang berkualiti dan berkuantiti tinggi untuk aplikasi-aplikasi hiliran menjadi agak mencabar. Sebuah protokol pengasingan RNA yang efektif, dapat memberikan hasil yang banyak dan berkualiti tinggi telah dirumuskan berdasarkan kaedah pengekstrakan setiltrimetilamonium bromida (CTAB), dengan penambahan langkah pembuangan DNA genom (gDNA). DNA dan bahan kontaminasi lain yang berkemungkinan mempengaruhi aplikasi hiliran juga disingkirkan secara efektif. Hasil kajian ini menunjukkan bahawa sampelsampel RNA yang diasingkan daripada daun-daun dan batang-batang Stevia rebaudiana menggunakan kaedah yang direka ubah ini adalah dalam kualiti dan integriti yang tinggi dengan nombor integriti RNA (RIN) yang melebihi 8 dan tahap pencemaran yang rendah.

The cynomolgus macaque (Macaca fascicularis) is an extensively utilised nonhuman primate model for biomedical research due to its biological, behavioural, and genetic similarities to humans. Genomic information of cynomolgus macaque is vital for research in various fields; however, there is presently a shortage of genomic information on the Malaysian cynomolgus macaque. This study aimed to sequence, assemble, annotate, and profile the Peninsular Malaysian cynomolgus macaque transcriptome derived from three tissues (lymph node, spleen, and thymus) using RNA sequencing (RNA-Seq) technology. A total of 174,208,078 paired end 70 base pair sequencing reads were obtained from the Illumina Hi-Seq 2500 sequencer. The overall mapping percentage of the sequencing reads to the M. fascicularis reference genome ranged from 53–63%. Categorisation of expressed genes to Gene Ontology (GO) and KEGG pathway categories revealed that GO terms with the highest number of associated expressed genes include Cellular process, Catalytic activity, and Cell part, while for pathway categorisation, the majority of expressed genes in lymph node, spleen, and thymus fall under the Global overview and maps pathway category, while 266, 221, and 138 genes from lymph node, spleen, and thymus were respectively enriched in the Immune system category. Enriched Immune system pathways include Platelet activation pathway, Antigen processing and presentation, B cell receptor signalling pathway, and Intestinal immune network for IgA production. Differential gene expression analysis among the three tissues revealed 574 differentially expressed genes (DEG) between lymph and spleen, 5402 DEGs between lymph and thymus, and 7008 DEGs between spleen and thymus. Venn diagram analysis of expressed genes revealed a total of 2,630, 253, and 279 tissue-specific genes respectively for lymph node, spleen, and thymus tissues. This is the first time the lymph node, spleen, and thymus transcriptome of the Peninsular Malaysian cynomolgus macaque have been sequenced via RNA-Seq. Novel transcriptomic data will further enrich the present M. fascicularis genomic database and provide future research potentials, including novel transcript discovery, comparative studies, and molecular markers development.