Rajkumar Venkatesan , Taju Gani , Abdul Majeed Seepoo , Philip Samuel Paulraj , Govindarajan Renu , Gowri Sankar Subbiah , Vijesh Sreedhar Kuttiatt , Nafeez Ahmed Abdul , Suryakodi Selvam , Abdul Wazith Mohamed Jaffer , Kanimozhi Kumarasamy , Vimal Sugumar , Sahul Hameed Azeez Sait
{"title":"人恙虫病东方体(恙虫病)感染分子和免疫学诊断工具的建立","authors":"Rajkumar Venkatesan , Taju Gani , Abdul Majeed Seepoo , Philip Samuel Paulraj , Govindarajan Renu , Gowri Sankar Subbiah , Vijesh Sreedhar Kuttiatt , Nafeez Ahmed Abdul , Suryakodi Selvam , Abdul Wazith Mohamed Jaffer , Kanimozhi Kumarasamy , Vimal Sugumar , Sahul Hameed Azeez Sait","doi":"10.1016/j.mimet.2025.107124","DOIUrl":null,"url":null,"abstract":"<div><div>Scrub typhus is a disease caused by a bacterial pathogen, <em>Orientia tsutsugamushi</em> which spreads through bites of infected chigger mite. Fever, headache, body aches and rash are common symptoms of scrub typhus. The absence of specific signs and symptoms of the disease makes diagnosis extremely difficult. In the present study, the blood samples from individuals with infections were obtained and analyzed for IgM and IgG antibodies using a commercial ELISA test kit. The present work was carried out to develop a molecular and immunological based technique which are more sensitive and accurate for the early detection of infected persons. The molecular diagnostics like PCR and nested PCR used for amplification of the 56 kDa type specific antigen (TSA) are more specific, sensitive and accurate. The PCR amplified partial 56 kDa TSA gene was cloned into the vector pET27b (+), and expressed in the BL21 host. The recombinant protein was purified by Ni-NTA column, and then the purified protein was used for production of polyclonal antibody in mice and rabbits. The antibody was used to develop immunological based diagnostic tools like ELISA, Western blot and dot blot for the early detection of scrub typhus infection. Totally, 141 infected samples were screened by PCR, nPCR, ELISA and western blot developed in the present study and the results were compared to commercial ELISA kit. Out of 141 samples analyzed, 58.8 % (83 samples) tested positive by PCR, 73 % (103 samples) by nPCR, and 86.5 % (122 samples) by ELISA. Western blot analysis of the 14 selected positive samples showed positive results (100 %). The newly developed immunological diagnostic tools and PCR techniques demonstrated high sensitivity and enhanced specificity, allowing for early detection of scrub typhus infection.</div></div>","PeriodicalId":16409,"journal":{"name":"Journal of microbiological methods","volume":"232 ","pages":"Article 107124"},"PeriodicalIF":1.9000,"publicationDate":"2025-04-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Development of molecular and immunological based diagnostic tools to detect Orientia tsutsugamushi (scrub typhus) infection in human\",\"authors\":\"Rajkumar Venkatesan , Taju Gani , Abdul Majeed Seepoo , Philip Samuel Paulraj , Govindarajan Renu , Gowri Sankar Subbiah , Vijesh Sreedhar Kuttiatt , Nafeez Ahmed Abdul , Suryakodi Selvam , Abdul Wazith Mohamed Jaffer , Kanimozhi Kumarasamy , Vimal Sugumar , Sahul Hameed Azeez Sait\",\"doi\":\"10.1016/j.mimet.2025.107124\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Scrub typhus is a disease caused by a bacterial pathogen, <em>Orientia tsutsugamushi</em> which spreads through bites of infected chigger mite. Fever, headache, body aches and rash are common symptoms of scrub typhus. The absence of specific signs and symptoms of the disease makes diagnosis extremely difficult. In the present study, the blood samples from individuals with infections were obtained and analyzed for IgM and IgG antibodies using a commercial ELISA test kit. The present work was carried out to develop a molecular and immunological based technique which are more sensitive and accurate for the early detection of infected persons. The molecular diagnostics like PCR and nested PCR used for amplification of the 56 kDa type specific antigen (TSA) are more specific, sensitive and accurate. The PCR amplified partial 56 kDa TSA gene was cloned into the vector pET27b (+), and expressed in the BL21 host. The recombinant protein was purified by Ni-NTA column, and then the purified protein was used for production of polyclonal antibody in mice and rabbits. The antibody was used to develop immunological based diagnostic tools like ELISA, Western blot and dot blot for the early detection of scrub typhus infection. Totally, 141 infected samples were screened by PCR, nPCR, ELISA and western blot developed in the present study and the results were compared to commercial ELISA kit. Out of 141 samples analyzed, 58.8 % (83 samples) tested positive by PCR, 73 % (103 samples) by nPCR, and 86.5 % (122 samples) by ELISA. Western blot analysis of the 14 selected positive samples showed positive results (100 %). The newly developed immunological diagnostic tools and PCR techniques demonstrated high sensitivity and enhanced specificity, allowing for early detection of scrub typhus infection.</div></div>\",\"PeriodicalId\":16409,\"journal\":{\"name\":\"Journal of microbiological methods\",\"volume\":\"232 \",\"pages\":\"Article 107124\"},\"PeriodicalIF\":1.9000,\"publicationDate\":\"2025-04-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of microbiological methods\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0167701225000405\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"BIOCHEMICAL RESEARCH METHODS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of microbiological methods","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0167701225000405","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
Development of molecular and immunological based diagnostic tools to detect Orientia tsutsugamushi (scrub typhus) infection in human
Scrub typhus is a disease caused by a bacterial pathogen, Orientia tsutsugamushi which spreads through bites of infected chigger mite. Fever, headache, body aches and rash are common symptoms of scrub typhus. The absence of specific signs and symptoms of the disease makes diagnosis extremely difficult. In the present study, the blood samples from individuals with infections were obtained and analyzed for IgM and IgG antibodies using a commercial ELISA test kit. The present work was carried out to develop a molecular and immunological based technique which are more sensitive and accurate for the early detection of infected persons. The molecular diagnostics like PCR and nested PCR used for amplification of the 56 kDa type specific antigen (TSA) are more specific, sensitive and accurate. The PCR amplified partial 56 kDa TSA gene was cloned into the vector pET27b (+), and expressed in the BL21 host. The recombinant protein was purified by Ni-NTA column, and then the purified protein was used for production of polyclonal antibody in mice and rabbits. The antibody was used to develop immunological based diagnostic tools like ELISA, Western blot and dot blot for the early detection of scrub typhus infection. Totally, 141 infected samples were screened by PCR, nPCR, ELISA and western blot developed in the present study and the results were compared to commercial ELISA kit. Out of 141 samples analyzed, 58.8 % (83 samples) tested positive by PCR, 73 % (103 samples) by nPCR, and 86.5 % (122 samples) by ELISA. Western blot analysis of the 14 selected positive samples showed positive results (100 %). The newly developed immunological diagnostic tools and PCR techniques demonstrated high sensitivity and enhanced specificity, allowing for early detection of scrub typhus infection.
期刊介绍:
The Journal of Microbiological Methods publishes scholarly and original articles, notes and review articles. These articles must include novel and/or state-of-the-art methods, or significant improvements to existing methods. Novel and innovative applications of current methods that are validated and useful will also be published. JMM strives for scholarship, innovation and excellence. This demands scientific rigour, the best available methods and technologies, correctly replicated experiments/tests, the inclusion of proper controls, calibrations, and the correct statistical analysis. The presentation of the data must support the interpretation of the method/approach.
All aspects of microbiology are covered, except virology. These include agricultural microbiology, applied and environmental microbiology, bioassays, bioinformatics, biotechnology, biochemical microbiology, clinical microbiology, diagnostics, food monitoring and quality control microbiology, microbial genetics and genomics, geomicrobiology, microbiome methods regardless of habitat, high through-put sequencing methods and analysis, microbial pathogenesis and host responses, metabolomics, metagenomics, metaproteomics, microbial ecology and diversity, microbial physiology, microbial ultra-structure, microscopic and imaging methods, molecular microbiology, mycology, novel mathematical microbiology and modelling, parasitology, plant-microbe interactions, protein markers/profiles, proteomics, pyrosequencing, public health microbiology, radioisotopes applied to microbiology, robotics applied to microbiological methods,rumen microbiology, microbiological methods for space missions and extreme environments, sampling methods and samplers, soil and sediment microbiology, transcriptomics, veterinary microbiology, sero-diagnostics and typing/identification.