Acid-fast bacilli (AFB) were detected in the autopsy lung tissue homogenate samples of four cows (variety Frisian cross) in a dairy farm in Bangladesh. Histopathological examination of the lung tissue demonstrated prominent granulomas, caseating necrosis and calcification indicative of tuberculosis (TB) infection. Mycobacteria could not be cultured from the tissue homogenate samples by Lowenstein-Jensen based conventional culture method though AFB were evident by Ziehl-Neelsen (ZN) staining of the smears of tissue homogenate and in paraffin embedded tissue slices. Spoligotyping performed on DNA extracts of paraffin embedded lung tissue samples confirmed the AFB as a member of the M. tuberculosis complex (MTBC) with a pattern assigned to M. africanum subtype I. This characterization by spoligotyping was confirmed by subjecting M. africanum subtype I isolates from other parts of the world to an alternative identification method based on DNA polymorphism in the gyrB gene (Hain Life Science, GmbH, Nehren, Germany). Since M. africanum is believed to be a human pathogen, general infection in cattle may be a public health threat. The presence of these bacteria in the animal reservoir most likely originated from a caretaker.

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Article Synopsis
  • - The study focused on characterizing the different lineages of Mycobacterium tuberculosis (M. tuberculosis) that cause childhood pulmonary tuberculosis in developing countries, specifically Ethiopia, where limited data exists.
  • - Using 54 stored cultures, researchers employed methods like polymerase chain reaction (PCR) and spoligotyping to determine the lineage and drug sensitivity patterns of the bacteria.
  • - Results revealed that a majority of the isolates belonged to the Euro-American lineage, with high drug susceptibility rates (91.9% phenotypic and 97.4% molecular), while the overall prevalence of drug resistance was low at 7.8%.
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Tuberculosis (TB), caused by the human pathogens () and , has plagued humanity for millennia and remains the deadliest infectious disease in the modern world. and can be subdivided phylogenetically into seven lineages exhibiting a low but significant degree of genomic diversity and preferential geographic distributions. Human genetic variability impacts all stages of TB pathogenesis ranging from susceptibility to infection with , progression of infection to disease, and the development of distinct clinical subtypes.

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Three-reaction high-resolution melting assay for rapid differentiation of Mycobacterium tuberculosis complex members.

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Section of Veterinary Bacteriology, Institute for Food Safety and Hygiene, Vetsuisse Faculty, University of Zurich, Zurich, Switzerland.

The possibility of introducing a reliable assay for a quick identification and differentiation of the main species of Mycobacterium tuberculosis complex (MTBC) supports the improvement of efficient tuberculosis combating strategies worldwide. Commercially available assays are often based on cultured samples; however, due to the long cultivation time of mycobacteria, results are delayed. Developed PCR approaches have been published previously, though, when testing intricate veterinary samples, the complex composition of multiplex qPCRs frequently leads to assay failure.

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