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Understanding the prey preference of Malayan tiger (Panthera tigris jacksoni) in Malaysia is important to guide conservation planning initiatives. The utilisation of DNA metabarcoding provides valuable insights, particularly in the field of carnivora diet research. This technique has been proven to be effective for identifying various species within complex mixtures such as scat materials, where visual identification is challenging. The Cytochrome c oxidase subunit I (COI) locus has been selected as it is a widely used as an effective non-invasive approach for diet studies. Hence, given this advance approach, Malayan tiger scats were collected on the basis of existing records of their presence in two types of habitats, namely, protected areas (PA) and human–tiger conflict (HTC) areas. This study aimed to identify prey species in Peninsular Malaysia, based on Malayan tiger scat samples using DNA metabarcoding. Based on the partial mitochondrial COI region, DNA metabarcoding led to the taxonomic resolution of prey DNA remnants in scats and the identification of prey species consumed by Malayan tiger, which were predominately small-to-medium-sized prey, including livestock. The dominant DNA prey detected belongs to the family Canidae, followed by Bovidae, Vespertilionidae, Homonidae, Felidae, Phasianidae and Muridae. A significant difference (p < 0.05) was observed in alpha and beta diversity using the Shannon index and PERMANOVA with regard to prey richness and evenness in two different habitat groups, namely, PA and HTC. Our finding provides insights into Malayan tiger dietary requirements, which can be used to develop conservation plans and strategies for Malayan tiger, particularly for habitat priorities.

BackgroundWhile oral mirobial dysbiosis due to tobacco smoking has been studied thoroughly, there is limited data on the effect of waterpipe smoking on the oral microbiome. This study aims to compare the salivary microbiome between waterpipe smokers and non-smokers.Materials and methodsUnstimulated saliva samples were collected from 60 participants, 30 smokers and 30 non-smokers in Kuala Lumpur and Klang Valley, Malaysia. DNA extraction was performed using the Qiagen DNA mini kit, and the 16S rRNA bacterial gene was amplified and sequenced using the Illumina MiSeq platform. Sequencing reads were processed using DADA2, and the alpha and beta diversity of the bacterial community was assessed. Significantly differentiated taxa were identified using LEfSe analysis, while differentially expressed pathways were identified using MaAsLin2.ResultsA significant compositional change (beta diversity) was detected between the two groups (PERMANOVA P

Complete mitochondrial genome sequences have significant relevance in the study of phylogenetic relationships, evolution, and population genetics. In this paper, we present the complete mitochondrial genome of the red junglefowl (Gallus gallus spadiceus) from Peninsular Malaysia, inferred using next-generation sequencing (NGS). The mitogenome is 16,785 bp in length with the structural organization of an avian mitochondrial arrangement compromising 13 proteincoding regions, 22 tRNAs, 2 rRNAs, and 1 control region. No internal stop codon was found in the protein-coding genes. Overall base composition is A: 30.3%, C: 32.5%, G: 13.5%, and T: 23.7%, indicating a high A + T content of 54.0%. Phylogenetic tree analysis revealed that red junglefowl from Peninsular Malaysia is grouped together with other members of Gallus gallus specifically from Southeast Asia, with 89% bootstrap value support. These research findings might be beneficial for red junglefowl genetic identification, molecular systematic studies, and conservation management interest in the future. [ABSTRACT FROM AUTHOR]