Staphylococcus pseudintermedius is a zoonotic pathogen that can cause life-threatening infections in animals and humans. The study of methicillin-resistant S. pseudintermedius (MRSP) and its ability to produce biofilms is important to select the most suitable treatment. The prevalence and characteristics of S. pseudintermedius isolated from dogs admitted at the Veterinary Teaching Hospital, Prince of Songkla University, Thailand were assessed. Results showed that 28.30% (15/53) of the isolates were MRSP. Amplification of the mecA gene was observed in 93.33% (14/15) MRSP. Methicillin-resistant strains revealed co-resistant patterns against other antibiotics, including chloramphenicol, clindamycin, tetracycline, clarithromycin, ciprofloxacin, and trimethoprim. In this study, all bacterial isolates produced biofilms, while 90.55% of S. pseudintermedius isolates were strong or moderate biofilm producers. Most (45–60%) of the resistant strains were strong biofilm producers, while the correlation between biofilm production and antibiotic resistance was not statistically significant. This is the first study in southern Thailand to investigate the drug-resistant profile of S. pseudintermedius and its ability to form biofilm. The results will contribute to a better understanding of the emergence and prevalence of antimicrobial resistance in S. pseudintermedius.

Background and Aim: Bullfighting is booming in South Thailand, attracting tourists, and stimulating local economies. The bulls are well raised and practiced, but in many cases, the owners lack knowledge and understanding of the prevention of animal diseases, including parasitic infections. This study aimed to determine the occurrence of gastrointestinal (GI) parasite infection in fighting bulls. Materials and Methods: A total of 1501 fecal samples were collected from bulls aged 2-5 years visiting the animal hospital of Prince of Songkla University during 2016-2019. The formalin ethylether concentration method was used to detect GI parasites in feces. Results: The overall rate of GI parasite infection was 94.27%. Rumen fluke eggs were detected in 97.17% of all infected animals, followed in prevalence by strongyles (26.29%), Eurytrema spp. (2.83%), Fasciola spp. (2.47%), Trichuris spp. (0.35%), and Moniezia spp. (0.14%). Two protozoan genera were identified, Balantidium coli (6.64%) and Eimeria spp. (3.53%). Coinfection was observed in 33.99%. The five most common coinfections were rumen fluke with strongyles (20.85%), B. coli (4.66%), Eimeria spp. (1.55%), Eurytrema spp. (1.34%), and Fasciola spp. (1.06%). Conclusion: In addition to high GI parasite infection rates, zoonotic parasites were observed. Therefore, it is recommended that farmers should follow good sanitation and prevention practices to control parasitic infections in bulls, and proper hygienic precautions should be taken by the owners. Implementation of deworming programs using appropriate anthelmintic drugs as well as rotation of anthelmintic drug that have different chemical agent to prevent further drug resistance should be considered. The promotion of bull health management is highly recommended to protect humans from zoonotic diseases.

Background and Aim: Fighting bulls have a high risk of eye injuries, and opportunistic conjunctival bacterial flora may cause subsequent eye diseases. There is little information about the ocular health care of fighting bulls in Thailand. Thus, this study aimed to estimate the prevalence of Staphylococcus spp. from the eyes of fighting bulls and investigate their antimicrobial susceptibility. Materials and Methods: The samples were collected from the right conjunctival sacs of 105 fighting bulls. Biochemical tests and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry were used to identify bacteria to genus and species levels. Antimicrobial susceptibility was tested by agar disk diffusion. Results: Staphylococcus spp. (36.84%, 56/152) were the most detected bacteria. The most prevalent Staphylococcus spp. was Staphylococcus chromogenes (37.50%, 21/56). The susceptibility test revealed that all isolates were susceptible to sulfamethoxazole/trimethoprim (56/56, 100%) and most were susceptible to chloramphenicol and gentamicin (54/56, 96.43%). The highest resistance rates were seen for tetracycline and doxycycline (23.21%, 13/56) followed by erythromycin (19.64%, 11/56). In addition, S. chromogenes isolates were evaluated for their ability to produce biofilms by a quantitative biofilm production assay. A total of 21 isolates exhibited biofilm production, independent of their antimicrobial susceptibility. Three multidrug-resistant isolates were found, including two Staphylococcus epidermidis isolates and a single S. chromogenes isolate. Conclusion: As antimicrobial resistant bacteria were detected on the eye surface, veterinarians should always conduct antimicrobial susceptibility testing before using antimicrobial agents. The results from this study will help to improve the standard of eye treatment for fighting bulls in Thailand.

Conventional glass ionomer cement (GIC) is widely used as a restorative base and liner owing to its chemical adhesion to dentine, fluoride release, and favourable biocompatibility. Nevertheless, its intrinsic antibacterial activity and regenerative capacity remain limited. To enhance these properties, a series of modified GIC formulations, referred to as BIOGIC, incorporating tricalcium phosphate (TCP), TCTP-derived peptides, and 10% chlorhexidine (CHX), were developed. This study evaluated their antibacterial efficacy, cytocompatibility, and pulpal responses in a rabbit-tooth model. Six formulations were examined: GIC, BIOGIC, BIOGIC+TCP, BIOGIC+TCP+3 µg TCTP, BIOGIC+TCP+10 µg TCTP, and BIOGIC+10% CHX. Antibacterial activity against Streptococcus mutans and Enterococcus faecalis was assessed using liquid culture assays and spread-plate analysis. Dental pulp cell viability was evaluated using a metabolic assay. In vivo pulpal responses were examined in rabbit incisors restored with each material and assessed histologically after 21 days, focusing on inflammation, collagen formation, and pulp-dentine integrity. BIOGIC+10% CHX demonstrated the strongest antibacterial activity, significantly reducing S. mutans and E. faecalis. Dental pulp cell viability decreased significantly in the GIC, BIOGIC+TCP+10 µg TCTP, and BIOGIC+10% CHX groups, with BIOGIC+10% CHX showing the greatest cytotoxicity. In contrast, BIOGIC, BIOGIC+TCP, and BIOGIC+TCP+3 µg TCTP significantly enhanced pulp cell proliferation. Histological analysis revealed no pulpal inflammation in any group. Mild collagen deposition was noted only in the BIOGIC group, whereas the remaining formulations exhibited normal pulp morphology without adverse reactions. Incorporation of 10% CHX markedly enhanced the antibacterial properties of BIOGIC but increased cytotoxicity. BIOGIC formulations containing TCP and low-dose TCTP improved pulp cell viability and maintained favourable pulpal responses. These modified BIOGIC materials show promise as bioactive, pulp-compatible alternatives to conventional GIC, although CHX-containing formulations should be used with caution owing to their cytotoxic effects.

Oral infections are common health problems in companion animals, often associated with bacterial colonization, biofilm formation, and inflammation. This study investigates the efficacy of hypertonic salt tablets as an antibacterial approach and their effect on bacteria-associated inflammatory stimulation against important oral pathogens, Staphylococcus aureus and Pasteurella canis. Agar well diffusion showed that 0.3 g salt tablets exhibited antibacterial activity, with inhibition zones of 13.33 ± 0.89 mm for S. aureus and 28.75 ± 1.18 mm for P. canis, compared with 23.10 ± 0.87 mm and 31.43 ± 0.81 mm for 0.12% chlorhexidine, respectively. In vitro cytotoxicity assessment demonstrated that 1% v/v and 10% v/v released salt solutions maintained high cell viability (>80%), while morphology assays confirmed non-cytotoxicity of 1% v/v 24 h released salt solution. The 1% v/v and 10% v/v 10 min-released salt solution reduced relative biofilm formation in S. aureus to approximately 61% and 45%, respectively, and in P. canis to approximately 89% and 52%, respectively. Salt-treated bacterial suspensions induced lower NO production in RAW264.7 macrophages, decreasing NO levels from 33.17 ± 2.01 to 4.34 ± 0.65 µM for S. aureus and from 60.73 ± 0.99 to 36.33 ± 0.69 µM for P. canis, suggesting attenuation of bacteria-associated inflammatory stimulation. In a preliminary mouse oral mucosal wound model, local application of NaCl crystals for 30 min reduced total bacterial counts from 8.9 × 10² to 2.0 × 10² CFU/mL, corresponding to a 77.5% reduction. These findings suggest that hypertonic sodium chloride tablets may provide a simple localized approach for short-term reduction in oral bacterial burden and bacteria-associated inflammatory stimulation; however, further validation is required in clinically relevant oral disease models and companion animals.

The research aimed to study the genome of Cryptococcus neoformans isolated from bird excreta. Thirteen isolates were cultured, colony stained, and underwent biochemical testing confirmation by nested polymerase chain reaction using ITS1-ITS4 and CN4-CN5 primers, respectively. Antifungal susceptibility testing and whole-genomic sequencing were analyzed. The results determined that all isolates were susceptible to amphotericin B (100%), fluconazole, and itraconazole (92.3%). One isolate (DOP3) showed resistance to fluconazole and itraconazole (MIC >64 and >8 µg/mL, respectively). A phylogenetic tree showed the identity of C. neoformans (serotype A). The genome of resistant (DOP3) and non-resistant isolates (DOP3.1) had 14 chromosomes. DOP3 consisted of 38 candidate antifungal resistance genes, which were the most active against azoles (14). The annotated genes in the azole group mostly were in the ATP-binding cassette transporter transmembrane superfamily. Resistance genes against FCZ were in the transcription factors (HAP2, HAP5), zinc finger (NRG1), cytochrome P450 (ERG11), and Myb-like DNA-binding domain (REB1). The most frequent resistance genes against ITZ were cytochrome P450 (ERG5 and ERG11) and a transcription factor (HAP5). DOP3.1 also consisted of 26 candidate resistance genes against azoles. Resistance genes against the azole group belong to the ABC transporter transmembrane superfamily. Resistance genes against FCZ belong to cytochrome P450 (ERG11), the zinc finger (NRG1), and the CCAAT binding transcription factor (HAP2). Resistance genes belonging to cytochrome P450 (ERG5) were found against ITZ. This research provides the first report of C. neoformans (serotype A) in zebra dove excreta, drug susceptibility to a resistant strain, and identification of resistance genes. Farm sanitation should be strictly applied, and immunocompetent people should avoid contact with zebra dove excreta.