Jatuporn - Rattanasrisomporn

Prof. Dr. Jatuporn - Rattanasrisomporn

Kasetsart University, Bangkok, Krung Thep Maha Nakhon, Thailand
orcid

Research Focus & Metrics

Academic Career Length

8Years (2019-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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5 July 2022 in Veterinary World
Verified
Journal Article
Open access
OROumaporn - Rungsuriyawiboon
Oumaporn - Rungsuriyawiboon
TJThitichai Jarudecha
Thitichai Jarudecha
SHSupa Hannongbua
Supa Hannongbua
KCKiattawee Choowongkomon
Kiattawee Choowongkomon
CBChaiwat Boonkaewwan
Chaiwat Boonkaewwan
Jatuporn - RattanasrisompornJatuporn - Rattanasrisomporn
Jatuporn - Rattanasrisomporn
Background and Aim: Feline leukemia virus (FeLV) and feline immunodeficiency virus (FIV) are retroviruses associated with chronic and neoplastic diseases in domestic and non-domestic cats. There has been increasing interest in the clinical importance of feline retroviruses in Thailand and the identification of associated risk factors in domestic cats. To prevent the spread of retroviral diseases and improve the management of retrovirus-infected cats, risk factors and associated clinical laboratory data must be clearly understood. This study aimed to identify the influence of household, lifestyle, health status, sterilization, clinical presentations, and laboratory findings on FIV- and FeLV-infected cats in Bangkok, Thailand. Materials and Methods: A total of 480 cats were evaluated for FeLV p27 antigen and FIV antibodies using Witness FeLV-FIV Rapid Test and SNAP FIV/FeLV Combo Test at a veterinary hospital service. Results: Of the 480 cats tested, 113 were positivefor virus infection, including 60 for FeLV (12.5%), 40 for FIV (8.3%), and 13 for both FeLV and FIV (2.7%). The findings revealed that the risk factors for cats infected with FeLV, FIV, or both FeLV and FIV were significantly different compared with those for non-infected cats (p < 0.05). Multivariate analysis showed that multi-cat ownership is a risk factor for the high prevalence of feline retrovirus infection, as multi-cat households exhibited a higher prevalence of infection than single-cat households. Anemic and sick cats were also at a greater risk of testing positive for specific retrovirus infections. FeLV-infected cats had a higher risk of anemia and low erythrocyte and thrombocyte counts (p ≤ 0.0001), whereas FIV-infected cats were more likely to have anemia and leukocytopenia than controls. Conclusion: Knowledge of the risk factors for retroviral diseases and associated clinical and laboratory findings can be used to develop strategies to reduce FIV and FeLV infections in cats.

1 January 2024 in Journal of Advanced Veterinary and Animal Research
Verified
Journal Article
Open access
WMWassamon Moyadee
Wassamon Moyadee
SSSupita Sunpongsri
Supita Sunpongsri
KCKiattawee Choowongkomon
Kiattawee Choowongkomon
SRSittiruk Roytrakul
Sittiruk Roytrakul
ARAmonpun Rattanasrisomporn
Amonpun Rattanasrisomporn
Jatuporn - RattanasrisompornJatuporn - Rattanasrisomporn
Jatuporn - Rattanasrisomporn
Objective: This study aimed to investigate the clinical and laboratory characteristics of naturally occurring feline infectious peritonitis (FIP) and estimate the median survival time of FIP cats treated with prednisolone to guide further therapeutic planning. Materials and Methods: In this retrospective study, data from a total of 116 cats with effusion were fully recorded. Forty-five FIP-diagnosed cats were enrolled for analysis. Results: The study findings indicate that FIP was a disease affecting cats aged 1–2 years and was highly prevalent among male cats. Clinical manifestations of FIP affected the digestive (60%), hematological (53.3%), respiratory (33.3%), neurological (6.7%), and ocular (4.4%) systems. Blood profiles revealed mild anemia, lymphopenia, thrombocytopenia, hypoalbuminemia, hyperglobulinemia, and an albumin to globulin ratio of 0.4. Fluid analysis and cytology of FIP cats demonstrated a transparent yellow fluid with a protein content of 6 gm/dl and a total nucleated cell count of approximately 5,000–10,000 cells. During the observation period, FIP cats treated with prednisolone exhibited a median survival time of 31 days. Conclusion: Confirming FIP cases can be challenging; therefore, a tentative diagnosis of FIP must be made with care. This study provided practical diagnostic tools to diagnose FIP based on clinical signs and multiple abnormalities, which allowed for more efficient and rapid detection.

14 August 2022 in Animals
Verified
Journal Article
Open access
PDF file
WRWitsanu Rapichai
Witsanu Rapichai
WSWichayet Saejung
Wichayet Saejung
KKKotchaporn Khumtong
Kotchaporn Khumtong
CBChaiwat Boonkaewwan
Chaiwat Boonkaewwan
STSupansa Tuanthap
Supansa Tuanthap
Jatuporn - RattanasrisompornJatuporn - Rattanasrisomporn
Jatuporn - Rattanasrisomporn
Feline infectious peritonitis (FIP) is a worldwide fatal disease caused by a mutant feline coronavirus (FCoV). Simple and efficient molecular detection methods are needed. Here, sensitive, specific, rapid, and reliable colorimetric reverse transcription loop-mediated isothermal amplification (RT-LAMP) was developed to detect the ORF1a/1b gene of FCoV from cats with suspected FIP using neutral red as an indicator. Novel LAMP primers were specifically designed based on the gene of interest. The isothermal assay could visually detect FCoV at 58 °C for 50 min. The RT-LAMP assay was highly specific and had no cross-reactivity with other related feline viruses. The detection limit of FCoV detection by RT-LAMP was 20 fg/µL. A blind clinical test (n = 81) of the developed RT-LAMP procedure was in good agreement with the conventional PCR method. In the light of its performance specificity, sensitivity, and easy visualization, this neutral-red-based RT-LAMP approach would be a fruitful alternative molecular diagnostic tool for veterinary inspection of FCoV when combined with nucleotide sequencing or specific PCR to affirm the highly virulent FIP-associated FCoV.

31 March 2022 in Animals
Verified
Journal Article
Open access
PDF file
SSSupita Sunpongsri
Supita Sunpongsri
Attawit KovitvadhiAttawit Kovitvadhi
Attawit Kovitvadhi
Jatuporn - RattanasrisompornJatuporn - Rattanasrisomporn
Jatuporn - Rattanasrisomporn
VTViphavee Trisaksri
Viphavee Trisaksri
NJNichakorn Jensirisak
Nichakorn Jensirisak
Tassanee JaroensongTassanee Jaroensong
Tassanee Jaroensong
Feline leukemia virus (FeLV) infection is considered a poor prognostic factor for feline lymphoma. This study investigated the prevalence of cats suffering from feline lymphoma with natural infection of the feline leukemia virus, as well as clinical signs, adverse events, and survival time after cyclophosphamide, vincristine and prednisolone (COP) chemotherapy. This retrospective study involved 92 cats diagnosed with mediastinal or mediastinal plus other anatomical sites of lymphoma and treated with COP chemotherapy. FeLV-antigen-positive was observed in all cats. Clinical signs and adverse events were observed after the 1st, 2nd, and 3rd inductions. Clinical signs improved after the 3rd induction of COP chemotherapy. The response rate was 96.74% (81.52% complete response, 15.22% partial response, and 3.26% no response). The overall median survival time was 338 days (range 62–1057 days). The overall response rate and median survival time of cats with feline lymphoma that were FeLV-antigen-positive and treated with COP chemotherapy were higher than from other studies. This study found that cats aged <4 years survived longer than those aged at least 4 years. Anemia (before COP), azotemia (after 2nd induction), and elevated alanine aminotransferase (after 1st induction) were associated with an increased chance of mortality.

11 September 2021 in Heliyon
Verified
Journal Article
Open access
PTPaiboon Tunsagool
Paiboon Tunsagool
SPSekkarin Ploypetch
Sekkarin Ploypetch
JJJanthima Jaresitthikunchai
Janthima Jaresitthikunchai
SRSittiruk Roytrakul
Sittiruk Roytrakul
KCKiattawee Choowongkomon
Kiattawee Choowongkomon
Jatuporn - RattanasrisompornJatuporn - Rattanasrisomporn
Jatuporn - Rattanasrisomporn
Microsporum canis (M. canis) is a dermatophyte fungal pathogen that causes ringworms. Cats are considered to be a dominant reservoir host enabling M. canis transmission to humans. The concerns of dermatophyte resistance were raised among the usage of antifungal drugs to treat the ringworm. This study aimed to evaluate the fungal activity of cyclic lipopeptides (CLPs) obtained from Bacillus subtilis (B. subtilis) as an alternative method for the inhibition of M. canis growth. The culture plate of M. canis from confirmed cats with ringworm infection was provided. The purification of CLP extract, fengycin, iturin A, and surfactin was carried out from B. subtilis by preparative thin-layer chromatography (PTLC) coupled with solid-phase extraction (SPE) methods. Half-maximal effective concentration (EC50) and agar well diffusion assays were performed to determine the efficacy of Bacillus CLP extract, fengycin, iturin A, and surfactin to inhibit the growth of M. canis isolated from cats. All purified Bacillus substances displayed antifungal activity to control the growth of M. canis when compared with 80% ethanol (control). EC50 values for CLP extract, fengycin, iturin A, and surfactin were 0.23, 0.05, 0.17, and 0.08 mg/mL, respectively. In agar well diffusion assay, the ability of CLP extract, fengycin, iturin A, and surfactin on fungal inhibition had no statistically significant difference at 24 and 48 h after treatment (p < 0.05). However, CLP extract showed a statistically significant difference on M. canis inhibition at 62.21% followed by surfactin with 59.04% at 72 h after treatment. In vitro, Bacillus CLPs revealed an inhibitory effect on M. canis growth which is a zoonotic pathogen that causes ringworms. This study suggests an alternative approach to control the growth of M. canis using substances obtained from B. subtilis as a biomedicine agent with antifungal activity.

7 August 2021 in Archives of Virology
Verified
Journal Article
Closed access
PDF file
STSupansa Tuanthap
Supansa Tuanthap
NCNatdaroon Chiteafea
Natdaroon Chiteafea
Jatuporn - RattanasrisompornJatuporn - Rattanasrisomporn
Jatuporn - Rattanasrisomporn
KCKiattawee Choowongkomon
Kiattawee Choowongkomon