PCPimrawee Chaemlek

Pimrawee Chaemlek

*This is an algorithmically generated author record based on publicly available information.

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Pimrawee Chaemlek has a total of 24 co-authors. Here are the top co-authors by number of shared publications:


Latest Publications

  • Open Access

    Low-Molecular-Weight Chitosan Produced by Gamma Irradiation and Hydrogen Peroxide Promotes Immune Readiness, Antioxidant Responses, and Survival in Photobacterium damselae-Challenged Asian Seabass (Lates calcarifer)

    by Thitirat Rattanawongwiboon, Natthapong Paankhao, Ratchanon Chumchuen, Nattaset Chinnabutra, Wasin Saisin, Benchawan Kumwan, Pakapon Meachasompop, Yosapon Adisornprasert, Pimrawee Chaemlek, Prapansak Srisapoome, et al.

    Low-molecular-weight chitosan may exhibit improved dispersion and biological accessibility compared with high-molecular-weight chitosan, but direct comparisons in Asian seabass remain limited. This study evaluated dietary low-molecular-weight chitosan produced by combined gamma irradiation and hydrogen peroxide depolymerization. The untreated and degraded preparations had apparent GPC-derived molecular weights of approximately 85 and 10 kDa, respectively. Juvenile Asian seabass (Lates calcarifer) were fed a Control diet of 1.0% high-molecular-weight chitosan or low-molecular-weight chitosan at 0.25%, 0.5%, or 1.0% for four weeks. Growth, serum antioxidant and humoral immune parameters, tissue-specific gene expression, and resistance to Photobacterium damselae were evaluated. No treatment significantly affected growth or feed utilization. Both high- and low-molecular-weight chitosan reduced serum MDA relative to the Control, whereas selected antioxidant and immune responses differed among inclusion levels. The 0.5% low-molecular-weight treatment increased GSH and GPx activity, the 1.0% low-molecular-weight treatment produced the highest CAT activity, and the 0.25% low-molecular-weight treatment produced the highest total serum IgM. Low-molecular-weight chitosan generally produced broader tissue-specific transcriptional responses than 1.0% high-molecular-weight chitosan. Following bacterial challenge, all chitosan treatments improved survival relative to the Control, with the highest numerical RPS observed in the 0.5% low-molecular-weight group. These results indicate that molecular-weight reduction influenced the biological response to dietary chitosan. Among the tested levels, 0.5% produced the most consistent combined response, although the optimal level was endpoint-specific and requires longer-term validation.

  • Open Access

    Whole-Genome Sequencing Reveals Virulence and Antimicrobial Resistance Determinants of Lactococcus garvieae Causing Lactococcosis in Cage-Cultured Nile Tilapia (Oreochromis niloticus) in Thailand

    by Putita Chokmangmeepisarn, Yosapon Adisornprasert, Pakapon Meachasompop, Benchawan Kumwan, Pimrawee Chaemlek, Prapansak Srisapoome, Kednapat Sriphairoj, Sittichai Hatachote, Niyada Umputhorn, Chonthicha Choppradit, et al.

    Lactococcosis is an important bacterial disease affecting farmed fish worldwide and is primarily associated with Lactococcus garvieae, Lactococcus petauri, and Lactococcus formosensis. In Thailand, information on L. garvieae infection in tilapia remains limited, particularly regarding genome-based identification, virulence determinants, and antimicrobial resistance profiles. This study characterized two L. garvieae isolates, AAHM-LG2501 and AAHM-LG2509, recovered from a lactococcosis outbreak in cage-cultured Nile tilapia (Oreochromis niloticus) in Ubon Ratchathani province, Thailand. Both isolates exhibited typical phenotypic characteristics of L. garvieae, including Gram-positive cocci, alpha hemolysis, positive capsule staining, and positive carbohydrate fermentation. Whole-genome sequencing confirmed both isolates as L. garvieae, with genome sizes of approximately 1.95 Mb and a G + C content of 38.9%. Genome-based taxonomic analysis supported species identification based on dDDH and ANI values, and both isolates were assigned to sequence type ST95 and serotype I. Virulence factor analysis identified 288 virulence-associated genes representing 97 virulence factors across 14 functional categories. Capsule-associated genes were prominent, together with genes involved in heme uptake, adhesion, hemolysis, stress survival, biofilm formation, and host adaptation. Ten capsule biosynthesis genes, including cpsABCFGKO, cps4A, and cps4I, as well as LPxTG cell wall anchor protein genes, were detected. Antimicrobial susceptibility testing showed resistance to nalidixic acid, oxolinic acid, and oxacillin, while reduced inhibition zones were observed for enrofloxacin and sulfamethoxazole-trimethoprim. Genome analysis identified predicted antimicrobial resistance determinants, including lsaD, vanT, vanY, and mdtA. Resistance-associated protein variants were detected in gyrA and gyrB, suggesting that target alteration may contribute to fluoroquinolone resistance. Overall, this study provides genome-level evidence of virulence and antimicrobial resistance determinants in L. garvieae from Thai tilapia and highlights the importance of whole-genome sequencing for accurate diagnosis, epidemiological surveillance, and disease management in aquaculture.

  • Sequential nanoimmersion and hydrogel-based multivalent vaccination induce durable multilayered immunity against four bacterial pathogens in Nile tilapia (Oreochromis niloticus)

    by Benchawan Kumwan, Pakapon Meachasompop, Yosapon Adisornprasert, Chonlatat Rajitdumrong, Pimrawee Chaemlek, Prapansak Srisapoome, Jitraporn Phaksopa, Wararut Buncharoen, Patcharapong Thangsunan, Pattanapong Thangsunan, et al.


  • Open Access

    Isolation, Identification, Virulence and Pathogenic Features of Lactococcus garvieae from Cage-Cultured Tilapia (Oreochromis niloticus) in Thailand

    by Yosapon Adisornprasert, Benchawan Kumwan, Pakapon Meachasompop, Chonlatat Rajitdumrong, Pimrawee Chaemlek, Prapansak Srisapoome, Wararut Buncharoen, Natthapong Paankhao, Niyada Umputhorn, Chonthicha Choppradit, et al.

    Lactococcosis caused by Lactococcus garvieae is an emerging threat to warmwater aquaculture, yet evidence integrating field outbreaks with robust molecular confirmation and controlled virulence testing remains limited for Thailand’s cage-cultured tilapia. From May to October 2025, acute mortality events were investigated in cage-cultured Nile tilapia (Oreochromis niloticus) in a reservoir in Ubon Ratchathani Province, Thailand. Suspected outbreaks were defined by abrupt daily mortality exceeding 5% accompanied by septicemia-like clinical signs. Water quality during sampling covered the following ranges: temperature 28.6–31.9 °C, pH 6.5–7.0, salinity 0.02–0.03 ppt, electrical conductivity 0.036–0.046 mS/cm, TDS 22.20–26.50 mg/L, total alkalinity 17.0–34.0 mg/L as CaCO3, total hardness 12.0–60.0 mg/L as CaCO3, dissolved oxygen 6.5–7.0 mg/L, and NH3 were below the limit of detection. Full-length 16S rRNA tissue profiling revealed strong tissue partitioning: blood microbiomes were consistently dominated by Lactococcus and L. garvieae at the species level, whereas gills showed higher richness and mixed communities with multiple opportunistic taxa. Culture isolation was more reliable from blood than gills, yielding 16 Gram-positive, catalase-negative isolates (AAHM-LG2501–AAHM-LG2516) that clustered within the L. garvieae clade in near full-length 16S rRNA phylogenetic analysis and were separated from closely related Lactococcus lineages. A representative blood isolate (AAHM-LG2501) showed dose-dependent virulence in controlled challenges, with an LD50 of ~1.05 × 105 CFU/fish by intraperitoneal injection and an LC50 of ~1.20 × 106 CFU/mL by immersion. Histopathology supported systemic dissemination, with injection producing more consistent multi-organ lesions than immersion, particularly in head kidney, liver, and spleen, while gills exhibited route-associated epithelial and vascular alterations. Together, these findings confirm L. garvieae as a major etiological agent of septicemic outbreaks in cage-cultured tilapia in Thailand and support a practical surveillance framework prioritizing blood sampling, molecular confirmation, and risk-based monitoring to guide biosecurity and vaccine-oriented prevention.