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PHRP : Osong Public Health and Research Perspectives

OPEN ACCESS. pISSN: 2210-9099. eISSN: 2233-6052

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"ELISA"

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"ELISA"

Original Articles
Study on the Prevalence of Leptospirosis among Fever Cases Reported from Private Clinics in the Urban areas of Villupuram District, Tamil Nadu, India
Parasuraman Basker, Pichai Kannan, Karumana Gounder Kolandaswamy
Osong Public Health Res Perspect 2014;5(1):54-67.
Published online February 28, 2014
DOI: https://doi.org/10.1016/j.phrp.2014.01.003
Objectives
To know the prevalence of leptospirosis cases reported in private clinics among fever cases in Villupuram District, Tamil Nadu, India to know its real magnitude of the problem and to diagnose Leptospirosis among fever cases from differential diagnosis.
Methods
1502 Blood serum samples collected from three urban towns namely Kallakurichi (Latitude: 11° 73′ N; Longitude: 78° 97′ E), Villupuram (Latitude: 11° 75′ N; Longitude: 79° 92′ E) and Thindivanam (Latitude: 12° 25′ N; Longitude: 79° 65′ E) in fifteen clinics based on case definition of leptospirosis delineated by the National Vector Borne Disease Control Programme (NVBDCP), Government of India. Samples were tested in the laboratory of the Zonal Entomological Team (ZET), Cuddalore with Macroscopic Slide Agglutination Test (MSAT) and Ig-M ELISA.
Result
There were 65 positive cases detected from 1502 blood serum samples in both MSAT and Ig-M ELISA. It could be known that there was 4% cases contributed from private clinics among fever cases. From this study, further it was known that all age groups of people affected irrespective of sexes based on their living condition associated with the environment prevailed of the disease.
Conclusion
From this study, it was quantified that 4% of cases reported in private clinics among fever cases and its findings ascertained both the importance of differential diagnosis as well as reports that should be included to the Government for knowing its real magnitude for planning.

Citations

Citations to this article as recorded by  Crossref logo
  • Molecular surveillance of Leptospira infection in domestic dogs in Soledad, Northern Colombia
    Carlos Alberto Beltrán-Sánchez, Alfonso Carlos Bettin, Karina Castellanos-Romero, Adriana Santodomingo, Elber Osorio-Rodríguez, Richard Thomas, Alveiro Pérez-Doria, Marlon Mauricio Ardila
    Veterinary Research Communications.2026;[Epub]     CrossRef
  • Molecular and genomic characterization of Leptospira isolates in humans and its relation to disease severity
    Anitha Thattamparambil Ravindranathan, Aiswarya Mukundan, Sithara Nasar Thottathil Puthanpurayil, Bijesh Kavuthodi, Sunitha Karunakaran, Reena John
    Indian Journal of Medical Microbiology.2025; 56: 100910.     CrossRef
  • Leptospirosis in the Delta Region of Tamil Nadu: A Retrospective Analysis in South India
    P B Praveen Kumar, Eunice Swarna Jacob, A Shanthi
    Cureus.2025;[Epub]     CrossRef
  • Seroprevalence of acute leptospirosis in a tertiary care hospital of western India
    Bhumika Baveja, Meghna S. Palewar, Suverna Joshi, Rajesh Karyakarte
    MGM Journal of Medical Sciences.2022; 9(4): 517.     CrossRef
  • Leptospirosis in Wardha District, Central India—Analysis of hospital based surveillance data
    Pradeep Deshmukh, Rahul Narang, Jyoti Jain, Manish Jain, Kiran Pote, Pratibha Narang, R.Vimal Raj, Praveen Kumar, Paluru Vijayachari
    Clinical Epidemiology and Global Health.2019; 7(1): 102.     CrossRef
  • Effects of gamma radiation exposure on PANI-Fe(X) -Ni(1−X) (X = 0.2,0.4,0.6,0.8) nanocomposite thin film for Leptospira detection
    Huda Abdullah, Jamal Jurait, Ravinder Singh Sidhu Amrik Singh, Iskandar Yahya, Siti Khairani Bejo
    Materials Research Express.2018; 6(2): 026507.     CrossRef
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Application of the Microagglutination Test for Serologic Diagnosis of Human Brucellosis
Sang-Hee Park, Yoo-Hoon Lee, Hyuk Chu, Seon-Do Hwang, Kyu-Jam Hwang, Hee-Yeol Choi, Mi-Yeoun Park
Osong Public Health Res Perspect 2012;3(1):19-23.
Published online December 31, 2011
DOI: https://doi.org/10.1016/j.phrp.2012.01.003
Objectives
Brucellosis is one of the most common zoonoses in the world, and occurs mainly in farmers, slaughterhouse workers, and veterinarians via direct or indirect contact with infected animals or their products. The clinical symptoms of human brucellosis are nonspecific, such as fever, headache, chills, and sweating. Diagnosis and treatment of brucellosis requires laboratory tests. Although the serum tube agglutination test (SAT) is the standardized gold method, it is laborious, time consuming, and requires a number of reagents. A microagglutination test (MAT) variant of the SAT or enzyme-linked immunosorbent assay (ELISA) is recommended for serological diagnoses. For the simple and rapid diagnosis of brucellosis, the MAT was standardized using samples for the SAT to define positive and negative categories, and we then compared the sensitivity and specificity of the MAT and ELISA.
Methods
Thirty SAT-positive sera and 60 SAT-negative sera were used in this study. Antibody titers of ≥1:160 were considered positive readings in both the SAT and MAT. <i>Brucella abortus</i> antigens and <i>Brucella</i>-positive control antiserum were used in the SAT and MAT. ELISAs of IgM and IgG were performed according to the manufacturers’ instructions.
Results
The titers of the MAT differed according to antigen concentration. The optimal concentration of <i>B abortus</i> antigen was determined to compare the sensitivity and specificity between the MAT and SAT. The sensitivity and specificity of the MAT were 93.3% and 96.7%, respectively, for IgG with reference to ELISA, and 96.7% and 98.3%, respectively, for IgM.
Conclusions
The optimal concentration of antigen for the MAT was 1:10. The MAT is less time consuming and requires less antigen and serum than the SAT. The results of the MAT showed good agreement with those of ELISA. The results of this study suggest that the MAT could be useful for diagnosis of brucellosis.

Citations

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  • Serological and molecular diagnostics of combined infection "brucellosis + toxoplasmosis" among the population of Azerbaijan
    A. E. Salekhov, Sh. G. Gasanova
    Yakut Medical Journal.2025; (1): 72.     CrossRef
  • Brucellosis in the omics era: integrative perspectives on Brucella genomic architecture, host-pathogen interactions, and disease dynamics
    Shashi Bhushan Kumar, Giridhar Goudar, Manne Munikumar, Shanvanth R. Arnipalli, Puneeta Singh Yaduvanshi, Virendra V. Panpatil
    World Journal of Microbiology and Biotechnology.2025;[Epub]     CrossRef
  • Using Fluorescence Polarization Immunoassay for the Determination of Flunixin in Milk
    D. A. Arutyunyan, L. I. Mukhametova, I. A. Shanin, S. E. Kondakov, S. A. Eremin
    Journal of Analytical Chemistry.2025; 80(6): 1030.     CrossRef
  • Determination of IgG and IgA Antibodies by Fluorescence Polarization Using Fluorescently Labeled Recombinant Nanobodies
    L. I. Mukhametova, S. A. Eremin, I. V. Mikhura, O. S. Goryainova, T. I. Ivanova, S. V. Tillib
    Russian Journal of Bioorganic Chemistry.2025; 51(6): 2602.     CrossRef
  • Seroprevalence, Risk Factors, and Diagnostic Accuracy of Brucellosis in Upper Dir District, Khyber Pakhtunkhwa, Pakistan
    Sidra Sanam, Kamran Khan
    Journal of Bioresource Management.2025; 12(3): 40.     CrossRef
  • Two cases of MPO-ANCA-positive hypertrophic pachymeningitis mimicking as intracranial infection
    Jirui Wang, Shan Wang, Meiqing Lin, Xiuli Shang
    BMC Neurology.2024;[Epub]     CrossRef
  • Spatial prediction of human brucellosis susceptibility using an explainable optimized adaptive neuro fuzzy inference system
    Ali Jafari, Ali Asghar Alesheikh, Iman Zandi, Aynaz Lotfata
    Acta Tropica.2024; 260: 107483.     CrossRef
  • The Development of Diagnostic and Vaccine Strategies for Early Detection and Control of Human Brucellosis, Particularly in Endemic Areas
    Ayman Elbehiry, Musaad Aldubaib, Eman Marzouk, Adil Abalkhail, Abdulaziz M. Almuzaini, Mohammed Rawway, Ali Alghamdi, Abdullah Alqarni, Mohammed Aldawsari, Abdelmaged Draz
    Vaccines.2023; 11(3): 654.     CrossRef
  • New insights into the genetic predisposition of brucellosis and its effect on the gut and vaginal microbiota in goats
    Ahmed M. Sallam, Ibrahim Abou-souliman, Henry Reyer, Klaus Wimmers, Alaa Emara Rabee
    Scientific Reports.2023;[Epub]     CrossRef
  • Bovine brucellosis – a comprehensive review
    Sandip Kumar Khurana, Anju Sehrawat, Ruchi Tiwari, Minakshi Prasad, Baldev Gulati, Muhammad Zubair Shabbir, Rajesh Chhabra, Kumaragurubaran Karthik, Shailesh Kumar Patel, Mamta Pathak, Mohd. Iqbal Yatoo, Vivek Kumar Gupta, Kuldeep Dhama, Ranjit Sah, Wanpe
    Veterinary Quarterly.2021; 41(1): 61.     CrossRef
  • Microbiological Laboratory Diagnosis of Human Brucellosis: An Overview
    Giovanni Di Bonaventura, Silvia Angeletti, Andrea Ianni, Tommasangelo Petitti, Giovanni Gherardi
    Pathogens.2021; 10(12): 1623.     CrossRef
  • The spatiotemporal distribution of human brucellosis in mainland China from 2007-2016
    Peifeng Liang, Yuan Zhao, Jianhua Zhao, Dongfeng Pan, Zhongqin Guo
    BMC Infectious Diseases.2020;[Epub]     CrossRef
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    Soumaya Rammeh, Emna Romdhane, Hend Riahi, Meriem Ksentini, Mouna Chelli Bouaziz, Rahma Ayadi, Aida Berriche, Yosra Chebbi, Mohamed Fethi Ladeb
    Journal of Clinical Neuroscience.2020; 78: 360.     CrossRef
  • A case report of neurobrucellosis mimicking Guillain–Barré syndrome
    Parastoo Paydarnia, Soroush Moradi, Arman Habibi, Ladan Abbasian, Mojdeh Ghabaee
    Neurology, Psychiatry and Brain Research.2019; 31: 27.     CrossRef
  • A compact laser diode based photoacoustic spectral response technique to differentiate Brucellosis infected goat tissue from normal tissues
    A. Gorey, S. Shukla, J.G. Prasad, S. Verma, A. Sharma, S. Vasudevan
    Journal of Instrumentation.2019; 14(05): P05017.     CrossRef
  • Laboratory Diagnosis of Human Brucellosis
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    Clinical Microbiology Reviews.2019;[Epub]     CrossRef
  • Real-time PCR assays for diagnosing brucellar spondylitis using formalin-fixed paraffin-embedded tissues
    Man Li, Xingang Zhou, Jingjing Li, Lei Sun, Xiangmei Chen, Peng Wang
    Medicine.2018; 97(9): e0062.     CrossRef
  • Incidence of human brucellosis in the Kilimanjaro Region of Tanzania in the periods 2007–2008 and 2012–2014
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    Transactions of The Royal Society of Tropical Medi.2018; 112(3): 136.     CrossRef
  • Seroreactivity and Risk Factors Associated with Human Brucellosis among Cattle Slaughterhouse Workers in South Korea
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    International Journal of Environmental Research an.2018; 15(11): 2396.     CrossRef
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