Literature DB >> 31541428

Development and evaluation of LAMP-coupled lateral flow device for the detection of MAP in livestock at point of care resource-limited areas.

Rudrama Devi Punati1,2,3, Prudhvi Chand Mallepaddi1,2,3, Revathi Poonati1,2,3, Soumendra Nath Maity2,3, Jagdip Singh Sohal4, Kavi Kishor B Polavarapu5,6, Rathnagiri Polavarapu1,2,3,7.   

Abstract

The Mycobacterium avium subspecies paratuberculosis (MAP) causes paratuberculosis (Johne's disease), a systemic and chronic inflammation of intestine that affects bovine, small ruminants like goat and sheep. The disease has a greater economic importance in cattle and in small ruminants. But its effective control is impeded due to lack of rapid and accurate diagnostics. The present study is aimed at developing a LAMP-coupled lateral flow device (LFD) for rapid detection of paratuberculosis in livestock animal species such as cattle and in small ruminants at resource-limited areas. LAMP primers with biotin and FITC end tags were designed for IS900 gene specific for MAP. To determine sensitivity of LAMP assay, 10-fold serial dilutions were made from 10 ng/μl MAP stock DNA and were compared with PCR. The detection limits of LAMP-coupled LFD were defined and reactions were repeated for reproducibility. The specificity was evaluated using other infectious bacteria such as M. bovis, M. tuberculosis, Brucella abortus, Leptospira interrogan, Yersinia enterocolitica, Salmonella typhimurium, Listeria monocytogens, and Staphylococcus aureus. A total of 95 samples turned positive for LAMP-coupled LFD out of 389 fecal samples. All the cultural-positive and PCR-positive samples showed positive in LAMP-coupled LFD. Nine samples with negative cultures turned positive in LAMP assay. The overall sensitivity and specificity of the LAMP-coupled LFD assays were 100% and 97.02% respectively in comparison with the culture as the gold standard method. The sensitivity detection limit of developed assay was 10 fg/μl and specificity was 100%. This assay successfully detected MAP not only by using bacterial DNA but also in clinical fecal samples. The clear band formation at control and test positions was observed on LAMP-coupled LFD. The developed assay is a simple, rapid, easy to perform, and is very useful in early diagnosis of Mycobacterium avium subsp. paratuberculosis at point of care resource-limited areas.

Entities:  

Keywords:  Fluorescein isothiocyanate (FITC); Insertion sequence 900 (IS900) gene; Lateral flow device (LFD); Loop-mediated isothermal amplification (LAMP); Mycobacterium avium subsp. paratuberculosis (MAP); Point of care (POC); Polymerase chain reaction (PCR)

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Year:  2019        PMID: 31541428      PMCID: PMC6863330          DOI: 10.1007/s42770-019-00116-z

Source DB:  PubMed          Journal:  Braz J Microbiol        ISSN: 1517-8382            Impact factor:   2.476


  36 in total

1.  Loop-mediated isothermal amplification of DNA.

Authors:  T Notomi; H Okayama; H Masubuchi; T Yonekawa; K Watanabe; N Amino; T Hase
Journal:  Nucleic Acids Res       Date:  2000-06-15       Impact factor: 16.971

2.  Comparison of real-time, quantitative PCR with molecular beacons to nested PCR and culture methods for detection of Mycobacterium avium subsp. paratuberculosis in bovine fecal samples.

Authors:  Ying Fang; Wai-Hong Wu; Jessica L Pepper; Jill L Larsen; Salvatore A E Marras; Eric A Nelson; William B Epperson; Jane Christopher-Hennings
Journal:  J Clin Microbiol       Date:  2002-01       Impact factor: 5.948

3.  Evaluation of four serological tests for bovine paratuberculosis.

Authors:  D C Sockett; T A Conrad; C B Thomas; M T Collins
Journal:  J Clin Microbiol       Date:  1992-05       Impact factor: 5.948

4.  Development of Loop-Mediated Isothermal Amplification-Based Lateral Flow Device Method for the Detection of Malaria.

Authors:  Prudhvi Chand Mallepaddi; Meng-Yee Lai; Sudhakar Podha; Choo-Huck Ooi; Jonathan Wee-Kent Liew; Rathnagiri Polavarapu; Yee-Ling Lau
Journal:  Am J Trop Med Hyg       Date:  2018-06-21       Impact factor: 2.345

5.  Isolation and diagnostic potential of ISMav2, a novel insertion sequence-like element from Mycobacterium avium subspecies paratuberculosis.

Authors:  B Strommenger; K Stevenson; G F Gerlach
Journal:  FEMS Microbiol Lett       Date:  2001-03-01       Impact factor: 2.742

6.  ELISA and fecal culture for paratuberculosis (Johne's disease): sensitivity and specificity of each method.

Authors:  R H Whitlock; S J Wells; R W Sweeney; J Van Tiem
Journal:  Vet Microbiol       Date:  2000-12-20       Impact factor: 3.293

7.  Detection of Mycobacterium avium subsp. paratuberculosis in bovine fecal samples: comparison of three polymerase chain reaction-based diagnostic tests with a conventional culture method.

Authors:  Simone Taddei; Chiara Robbi; Camilla Cesena; Ilenia Rossi; Emiliana Schiano; Norma Arrigoni; Gaddo Vicenzoni; Sandro Cavirani
Journal:  J Vet Diagn Invest       Date:  2004-11       Impact factor: 1.279

8.  Culture of Mycobacterium avium subspecies paratuberculosis from the blood of patients with Crohn's disease.

Authors:  Saleh A Naser; George Ghobrial; Claudia Romero; John F Valentine
Journal:  Lancet       Date:  2004 Sep 18-24       Impact factor: 79.321

Review 9.  Mycobacterium avium subspecies paratuberculosis diagnosis and strain typing--present status and future developments.

Authors:  J S Sohal; S V Singh; Swati Subhodh; A V Singh; P K Singh; Neelam Sheoran; Komal Sandhu; K Narayansamy; A Maitra
Journal:  Indian J Exp Biol       Date:  2007-10       Impact factor: 0.818

10.  Comparison of polymerase chain reaction tests and faecal culture for detecting Mycobacterium paratuberculosis in bovine faeces.

Authors:  D M Collins; D M Stephens; G W de Lisle
Journal:  Vet Microbiol       Date:  1993-09       Impact factor: 3.293

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  1 in total

1.  The development and use of Actiphage® to detect viable mycobacteria from bovine tuberculosis and Johne's disease-infected animals.

Authors:  Benjamin M C Swift; Nathan Meade; Elsa Sandoval Barron; Malcolm Bennett; Tania Perehenic; Valerie Hughes; Karen Stevenson; Catherine E D Rees
Journal:  Microb Biotechnol       Date:  2019-12-03       Impact factor: 5.813

  1 in total

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