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Pinlaor, P.

Publications and source records attributed to Pinlaor, P..

3 recordsLinked to original sources

Alterations of metagenomics and metaproteomics associate kidney disease in a combination of opisthorchiasis and nonalcoholic fatty liver disease

BackgroundNon-alcoholic fatty liver disease (NAFLD) is prevalent worldwide and is associated with chronic kidney disease (CKD). Opisthorchis viverrini (Ov) infection and consumption of high- fat and high-fructose (HFF) diets exacerbate NAFLD leading to nonalcoholic steatohepatitis. Here, we aimed to investigate the effects of a combination of HFF diets and O.viverrini infection on kidney pathology via changes in the gut microbiome and host proteome in hamsters. Methodology/Principal findingsTwenty animals were divided into four groups; Normal diet feeding and non-infected Ov (Normal); HFF diets feeding (HFF); Ov infection (Ov); and feeding with a combination of HFF diets and infection with Ov (HFFOv). Fecal samples were extracted and used for Illumina Miseq sequencing platform based on the V3-V4 region of the 16S rRNA gene, along with LC/MS-MS analysis. Histopathological studies and biochemical assays were also conducted. The results indicated that the HFFOv group exhibited the most severe kidney injury, as elevated KIM-1 expression and accumulation of fibrosis in kidney tissue. In comparison with the HFF group, the combined group showed higher diversity and composition. An increased number of Ruminococaceae, Lachospiraceae, Desulfovibrionaceae and Akkermansiaceae, and a lower number of Eggerthellaceae were observed. A total of 243 significant host proteome were identified in all groups. Analysis using STITCH predicted that host proteome associated leaky gut such as soluble CD14 and p-cresol may play a role in the development of kidney disease. Among host proteome, TGF-beta, involving in fibrogenesis, was significantly expressed in HFFOv. Conclusions/SignificanceThe combination of HFF diets and O.viverrini infection may promote kidney injury through the alterations in the gut microbiome and host proteome. This knowledge may be an effective strategy to prevent the progression of CKD beyond the early stages. Author summaryA diets high in fat and fructose causes nonalcoholic fatty liver disease (NAFD), which is increasing worldwide. Liver fluke (Opisthorchis viverrini, Ov) infection is endemic in the Mekong subregion including in the northeastern Thailand. The prevalence of opisthorchiasis caused by the infection with O. viverrini is associated with fatty liver and bile duct cancer. We have previously demonstrated that infection with O. viverrini exacerbates NAFD progression to non-alcoholic steatohepatitis (NASH) in animal models. NASH exists kidney disease severity higher than ingestion of high-fat and high-fructose (HFF) diets or infection with O. viverrini. Here, we further investigate whether metagenomics is more likely to change in NASH than in NAFD or opisthorchiasis conditions. The combined group had higher diversity and composition. Elevated levels of Ruminococaceae, Lachospiraceae, Desulfovibrionaceae and Akkermansiaceae and decreased levels of Eggerthellaceae were observed, suggesting that HFF+Ov may cause gut dysbiosis in NASH. Differentially expressed proteins were also associated with these gut microbiomes in NASH condition. In addition, we found that the association of metagenomics and metaproteomics in NASH was related to kidney disease. Analysis using STITCH predicted that host proteome may be involved in leaky gut such as soluble CD14 and p-cresol to promote kidney disease. A significantly expressed TGF-beta involving fibrogenesis was found to be associated with kidney fibrosis. Therefore, alterations of metagenomics and metaproteomics is associated with kidney disease in a combination of opisthorchiasis and nonalcoholic fatty liver disease.

bioinformatics↗

Fecal microbiota dysbiosis in macaques and humans within a shared environment

Traditional zoonotic disease research focuses on detection of recognized pathogens and may miss opportunities to understand broader microbial transmission dynamics between humans, animals, and the environment. We studied human-macaque microbiome overlap in Kosum Phisai District, Maha Sarakham Province, Thailand, where a growing population of long-tailed macaques (Macaca fascicularis) in Kosumpee Forest Park interact with humans from an adjacent village. We surveyed workers in or near the park with elevated exposure to macaques to characterize tasks resulting in exposure to macaque feces in addition to dietary and lifestyle factors that influence gut microbiome composition. Fecal samples were collected from 12 exposed workers and 6 controls without macaque exposure, as well as 8 macaques from Kosumpee Forest Park and 4 from an isolated forest patch with minimal human contact. The V4 region of the 16S rRNA gene from fecal sample extracted DNA was amplified and sequenced using Illumina HiSeq to characterize the microbial community. A permuted betadisper test on the weighted UniFrac distances revealed significant differences in the dispersion patterns of gut microbiota from exposed and control macaques (p=0.03). The high variance in gut microbiota composition of macaques in contact with humans has potential implications for gut microbiome stability and susceptibility to disease, described by the Anna Karenina principle (AKP). Human samples had homogenous variance in beta diversity but different spatial medians between groups (p=0.02), indicating a shift in microbial composition that may be explained by fundamental lifestyle differences between the groups unrelated to exposure status. SourceTracker was used to estimate the percent of gut taxa in exposed humans that was contributed by macaques. While one worker showed evidence of elevated contribution, the overall trend was not significant. Task observations among workers revealed opportunities to employ protective measures or training to reduce exposure to occupational hazards. These results suggest the potential for hygiene measures to mitigate negative aspects of contact between humans and macaques in order to optimize the health of both populations.

microbiology↗

Differential protein expression marks the transition from infection with Opisthorchis viverrini to cholangiocarcinoma

Parts of Southeast Asia have the highest incidence of intrahepatic cholangiocarcinoma (CCA) in the world due to infection by the liver fluke Opisthorchis viverrini (Ov). Ov-associated CCA is the culmination of chronic Ov-infection, with the persistent production of the growth factors and cytokines associated with persistent inflammation, which can endure for years in Ov-infected individuals prior to transitioning to CCA. Isobaric labelling and tandem mass spectrometry of liver tissue from a hamster model of CCA was used to compare protein expression profiles from inflammed tissue (Ov-infected but not cancerous) versus cancerous tissue (Ov-induced CCA). Immunohistochemistry and immunoblotting were used to verify dysregulated proteins in the animal model and in human tissue. We identified 154 dysregulated proteins that marked the transition from Ov-infection to Ov-induced CCA, i.e. proteins dysregulated during carcinogenesis but not Ov-infection. The verification of dysregulated proteins in resected liver tissue from humans with Ov-associated CCA showed the numerous parallels in protein dysregulation between human and animal models of Ov-induced CCA. To identify potential circulating markers for CCA, dysregulated proteins were compared to proteins isolated from exosomes secreted by a human CCA cell line (KKU055) and 27 proteins were identified as dysregulated in CCA and present in exosomes. These data form the basis of potential diagnostic biomarkers for human Ov-associated CCA. The profile of protein dysregulation observed during chronic Ov-infection and then in Ov-induced CCA provides insight into the etiology of an infection-induced inflammation-related cancer.\n\nAbbreviations

cancer biology↗