“…In addition, NCBA shows numerous advantages compared to SSM: (a) the ability of NCBA to form GMNP-AFB complexes and concentrate AFB [ 20 ], through the glycan-glycoprotein interaction between the GMNP surface and the mycobacterial cell wall [ 21 ]; (b) after cell enrichment with GMNP, disaggregation of complexes with Tween 80 improves the microscopic quantification of AFB; (c) a larger volume of sample analyzed (by concentrating it with GMNP) in the same proportion of examined area may facilitate the ability to obtain higher AFB counts [ 22 ]; (d) the AFB detected and captured by GMNP, followed by ZN staining of concentrated aliquots, allows easy identification by colorimetry, which may increase the possibility to identify bacilli from paucibacillary cases [ 21 ]; (e) it is a fast method, since the complete processing can be obtained in 30–40 min from sample acquisition to final diagnostic result; (f) it is a direct and quantitative detection technique where bacilli can be viewed and counted through a microscope; (g) it is a low-cost method: one test, including materials, labor and infrastructure overhead, costs approximately USD 3.20 for NCBA and USD 4.20 with Tween 80, compared to other methods, such as culture (USD 16.50) [ 67 ], and molecular tests, such as GeneXpert (USD 12.90) [ 68 ]; (h) it does not require complex infrastructure, allowing its applicability in settings where TB is a burden, but resources are limited; and (i) offers bio-safety, since the NCBA-GMNP assay does not require centrifugation to concentrate AFB, thus reducing the generation of infectious aerosols, and the addition of Tween 80 may also reduce infectivity, due to the loss of virulence factors from the mycobacterial cell wall [ 60 , 61 , 64 ].…”