Growth Analysis of Trichomonas vaginalis in Different Culture Media: Leveraging Large Language Models (LLMs) to Predict and Optimize In Vitro Growth Conditions
{"title":"Growth Analysis of Trichomonas vaginalis in Different Culture Media: Leveraging Large Language Models (LLMs) to Predict and Optimize In Vitro Growth Conditions","authors":"Shernica L Ferguson, Loria Brown Gordon","doi":"10.1101/2024.09.12.612589","DOIUrl":null,"url":null,"abstract":"Trichomonas vagnalis is a tiny protozoan universally known to have one of the highest prevalance rates of any common sexually transmitted disease. Its popularity in HIV transmission and preterm labor highlights its importance in clinical, biological, and epidemiological investigations worldwide. Propagation of T vaginalis in vitro uses modified Diamonds media in commercial and clinical culture environments. Several modifications of this medium exist, but a more recent modification proved the most efficient. Our study aimed to investigate media modifications that could optimize the growth of T. vaginalis in routine laboratory cultivation. RSMT media enriched with quantitated media components was compared to modified Diamond's, Oxoid, and In Pouch culture mediums. Several growth studies were employed to select eight isolates (n=8) of T. vaginalis, including an ATCC reference isolate. These isolates were examined for several days at 37 degrees C in an anaerobic environment. Tests revealed that isolates in RSMT media had over 85% higher concentrations of T vaginalis growth than our testing mediums, with a maximum growth increase of 250%. The composite counts of T. vaginalis in RSMT showed a significant difference (p <0.05) from those of T. vaginalis in the standard Diamonds media Oxoid or In Pouch mediums. This data suggests that more efficient culturing and growth of T. vaginalis requires more vitamins and other growth factors beyond what would conventionally be expended in standard Trichomonas culture mediums.","PeriodicalId":501471,"journal":{"name":"bioRxiv - Pathology","volume":"29 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"bioRxiv - Pathology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2024.09.12.612589","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Trichomonas vagnalis is a tiny protozoan universally known to have one of the highest prevalance rates of any common sexually transmitted disease. Its popularity in HIV transmission and preterm labor highlights its importance in clinical, biological, and epidemiological investigations worldwide. Propagation of T vaginalis in vitro uses modified Diamonds media in commercial and clinical culture environments. Several modifications of this medium exist, but a more recent modification proved the most efficient. Our study aimed to investigate media modifications that could optimize the growth of T. vaginalis in routine laboratory cultivation. RSMT media enriched with quantitated media components was compared to modified Diamond's, Oxoid, and In Pouch culture mediums. Several growth studies were employed to select eight isolates (n=8) of T. vaginalis, including an ATCC reference isolate. These isolates were examined for several days at 37 degrees C in an anaerobic environment. Tests revealed that isolates in RSMT media had over 85% higher concentrations of T vaginalis growth than our testing mediums, with a maximum growth increase of 250%. The composite counts of T. vaginalis in RSMT showed a significant difference (p <0.05) from those of T. vaginalis in the standard Diamonds media Oxoid or In Pouch mediums. This data suggests that more efficient culturing and growth of T. vaginalis requires more vitamins and other growth factors beyond what would conventionally be expended in standard Trichomonas culture mediums.