Rapid Urine Test Detects Active Visceral Leishmaniasis
By LabMedica International staff writers Posted on 14 Jun 2013 |

Image: Bone marrow section showing Leishmania within macrophages (Photo courtesy of University of Thessaly).
A specific urine test has been developed to identify patients with active visceral leishmaniasis (VL), also known as kala-azar.
A capture enzyme linked immunosorbent assays (ELISA) has been designed to detect individually each of three Leishmania infantum antigens in the urine of VL patients.
Scientists from The Forsyth Institute (Cambridge, MA, USA) in conjunction with those at DetectoGen Inc. (Grafton, MA, USA; www.detectogen.com), have developed a single assay assembled with the combination of the reagents used to individually detect three Leishmania antigens in the urine of VL patients. They combed reverse-phase high-performance liquid chromatography (RP-HPLC) with mass spectroscopy, to identify the three distinct L. infantum proteins. These were L. infantum iron superoxide dismutase 1, L. infantum tryparedoxin 1, and L. infantum nuclear transport factor 2.
In a sample of 20 confirmed and diagnosed VL patients, each L. infantum protein was identified in approximately 10 to 12 overlapping and nonoverlapping urine samples. Moreover, in one sample no leishmanial antigen could be identified by any of the three assays. None of the antigens was detected in the urine of patients with cutaneous leishmaniasis, Chagas disease, schistosomiasis, or tuberculosis (TB). The urinary antigen detection ELISA had a sensitivity of 89%, specificity of 100%, and limit of detection of 4 pg to 10 pg of antigen per mL of urine. This new urine-based assay identified 20/20 VL patients and did not react with 62 urine samples obtained from control subjects.
The authors concluded that the urine based capture ELISA is a noninvasive VL diagnostic test that can differentiate active disease from parasitic exposure and from cured VL patients. The assay will be useful for the diagnosis of VL in patients coinfected with the human immunodeficiency virus (HIV) as the conventional serological diagnosis of VL in these patients is problematic and not sensitive. It is likely that the combined capture ELISA test will be equally useful for the diagnosis of VL patients from the Old World. This prediction is based on the fact that the three antigens discovered in the urine of patients with VL from the New World are 98% homologous to the same group of proteins produced by L. donovani.
Kala-azar or VL is a serious and debilitating disease that affects economic productivity and quality of life, and is nearly 100% fatal if not treated promptly, and there are 500,000 new cases of disease per year around the world. The disease occurs on four continents and is endemic in 47 countries, with approximately 200 million people at risk of infection. Due to the deterioration of social and economic conditions and coinfection with HIV, the number of cases is increasing. Most of the approximately 50,000 deaths that occur each year due to VL occur in children. The study was published on May 30, 2013, in the Public Library of Science Neglected Tropical Diseases.
Related Links:
The Forsyth Institute
DetectoGen Inc.
A capture enzyme linked immunosorbent assays (ELISA) has been designed to detect individually each of three Leishmania infantum antigens in the urine of VL patients.
Scientists from The Forsyth Institute (Cambridge, MA, USA) in conjunction with those at DetectoGen Inc. (Grafton, MA, USA; www.detectogen.com), have developed a single assay assembled with the combination of the reagents used to individually detect three Leishmania antigens in the urine of VL patients. They combed reverse-phase high-performance liquid chromatography (RP-HPLC) with mass spectroscopy, to identify the three distinct L. infantum proteins. These were L. infantum iron superoxide dismutase 1, L. infantum tryparedoxin 1, and L. infantum nuclear transport factor 2.
In a sample of 20 confirmed and diagnosed VL patients, each L. infantum protein was identified in approximately 10 to 12 overlapping and nonoverlapping urine samples. Moreover, in one sample no leishmanial antigen could be identified by any of the three assays. None of the antigens was detected in the urine of patients with cutaneous leishmaniasis, Chagas disease, schistosomiasis, or tuberculosis (TB). The urinary antigen detection ELISA had a sensitivity of 89%, specificity of 100%, and limit of detection of 4 pg to 10 pg of antigen per mL of urine. This new urine-based assay identified 20/20 VL patients and did not react with 62 urine samples obtained from control subjects.
The authors concluded that the urine based capture ELISA is a noninvasive VL diagnostic test that can differentiate active disease from parasitic exposure and from cured VL patients. The assay will be useful for the diagnosis of VL in patients coinfected with the human immunodeficiency virus (HIV) as the conventional serological diagnosis of VL in these patients is problematic and not sensitive. It is likely that the combined capture ELISA test will be equally useful for the diagnosis of VL patients from the Old World. This prediction is based on the fact that the three antigens discovered in the urine of patients with VL from the New World are 98% homologous to the same group of proteins produced by L. donovani.
Kala-azar or VL is a serious and debilitating disease that affects economic productivity and quality of life, and is nearly 100% fatal if not treated promptly, and there are 500,000 new cases of disease per year around the world. The disease occurs on four continents and is endemic in 47 countries, with approximately 200 million people at risk of infection. Due to the deterioration of social and economic conditions and coinfection with HIV, the number of cases is increasing. Most of the approximately 50,000 deaths that occur each year due to VL occur in children. The study was published on May 30, 2013, in the Public Library of Science Neglected Tropical Diseases.
Related Links:
The Forsyth Institute
DetectoGen Inc.
Latest Microbiology News
- Viral Load Tests Can Help Predict Mpox Severity
- Gut Microbiota Analysis Enables Early and Non-Invasive Detection of Gestational Diabetes
- Credit Card-Sized Test Boosts TB Detection in HIV Hotspots
- Fecal Metabolite Profiling Predicts Mortality in Critically Ill Patients
- Portable Molecular POC System Rules Out UTIs in Just 35 Minutes
- POC Lateral Flow Test Detects Deadly Fungal Infection Faster Than Existing Techniques
- Rapid Diagnostic Test Slashes Sepsis Mortality by 39%
- Blood Culture Assay Enhances Diagnostic Stewardship Through Targeted Panel Selection
- Real-Time Genome Sequencing Detects Dangerous Superbug Causing Hospital Infections
- Diagnostic Test Accurately Detects Colorectal Cancer by Identifying Microbial Signature in Gut Bacteria
- Rapid Bedside Test Predicts Sepsis with Over 90% Accuracy
- New Blood Test Detects Up to Five Infectious Diseases at POC
- Molecular Stool Test Shows Potential for Diagnosing TB in Adults with HIV
- New Test Diagnoses Bacterial Meningitis Quickly and Accurately
- Handheld Device Delivers Low-Cost TB Results in Less Than One Hour
- New AI-Based Method Improves Diagnosis of Drug-Resistant Infections
Channels
Clinical Chemistry
view channel
New Clinical Chemistry Analyzer Designed to Meet Growing Demands of Modern Labs
A new clinical chemistry analyzer is designed to provide outstanding performance and maximum efficiency, without compromising affordability, to meet the growing demands of modern laboratories.... Read more
New Reference Measurement Procedure Standardizes Nucleic Acid Amplification Test Results
Nucleic acid amplification tests (NAATs) play a key role in diagnosing a wide range of infectious diseases. These tests are generally known for their high sensitivity and specificity, and they can be developed... Read moreMolecular Diagnostics
view channel
RNA-Seq Based Diagnostic Test Enhances Diagnostic Accuracy of Pediatric Leukemia
A new unique test is set to reshape the way Acute Lymphoblastic Leukemia (BCP-ALL) samples can be analyzed. Qlucore (Lund, Sweden) has launched the first CE-marked RNA-seq based diagnostic test for pediatric... Read more
New Technique for Measuring Acidic Glycan in Blood Simplifies Schizophrenia Diagnosis
Polysialic acid is a unique acidic glycan predominantly found in brain regions associated with memory and emotion, but it is also present in the bloodstream. Research has shown that blood levels of polysialic... Read moreHematology
view channel
Disposable Cartridge-Based Test Delivers Rapid and Accurate CBC Results
Complete Blood Count (CBC) is one of the most commonly ordered lab tests, crucial for diagnosing diseases, monitoring therapies, and conducting routine health screenings. However, more than 90% of physician... Read more
First Point-of-Care Heparin Monitoring Test Provides Results in Under 15 Minutes
Heparin dosing requires careful management to avoid both bleeding and clotting complications. In high-risk situations like extracorporeal membrane oxygenation (ECMO), mortality rates can reach about 50%,... Read moreImmunology
view channel
Blood Test Detects Organ Rejection in Heart Transplant Patients
Following a heart transplant, patients are required to undergo surgical biopsies so that physicians can assess the possibility of organ rejection. Rejection happens when the recipient’s immune system identifies... Read more
Liquid Biopsy Approach to Transform Diagnosis, Monitoring and Treatment of Lung Cancer
Lung cancer continues to be a major contributor to cancer-related deaths globally, with its biological complexity and diverse regulatory processes making diagnosis and treatment particularly difficult.... Read more
Computational Tool Exposes Hidden Cancer DNA Changes Influencing Treatment Resistance
Structural changes in tumor DNA are among the most damaging genetic alterations in cancer, yet they often go undetected, particularly when tissue samples are degraded or of low quality. These hidden genomic... Read morePathology
view channel
AI Performs Virtual Tissue Staining at Super-Resolution
Conventional histopathology, essential for diagnosing various diseases, typically involves chemically staining tissue samples to reveal cellular structures under a microscope. This process, known as “histochemical... Read more
AI-Driven Preliminary Testing for Pancreatic Cancer Enhances Prognosis
Pancreatic cancer poses a major global health threat due to its high mortality rate, with 467,409 deaths and 510,992 new cases reported worldwide in 2022. Often referred to as the "king" of all cancers,... Read more
Cancer Chip Accurately Predicts Patient-Specific Chemotherapy Response
Esophageal adenocarcinoma (EAC), one of the two primary types of esophageal cancer, ranks as the sixth leading cause of cancer-related deaths worldwide and currently lacks effective targeted therapies.... Read more
Clinical AI Solution for Automatic Breast Cancer Grading Improves Diagnostic Accuracy
Labs that use traditional image analysis methods often suffer from bottlenecks and delays. By digitizing their pathology practices, labs can streamline their work, allowing them to take on larger caseloads... Read moreTechnology
view channel
Inexpensive DNA Coated Electrode Paves Way for Disposable Diagnostics
Many people around the world still lack access to affordable, easy-to-use diagnostics for diseases like cancer, HIV, and influenza. Conventional sensors, while accurate, often rely on expensive equipment... Read more
New Miniature Device to Transform Testing of Blood Cancer Treatments
Chimeric antigen receptor (CAR) T cell therapy has emerged as a groundbreaking treatment for blood cancers like leukemia, offering hope to patients when other treatments fail. However, despite its promise,... Read moreIndustry
view channel
Lunit and Microsoft Collaborate to Advance AI-Driven Cancer Diagnosis
Lunit (Seoul, South Korea) and Microsoft (Redmond, WA, USA) have entered into a collaboration to accelerate the delivery of artificial intelligence (AI)-powered healthcare solutions. In conjunction with... Read more