The presence of ESAT-6 and CFP 10 and other gene orthologs of the RD 1 region in non-tuberculous mycobacteria, mycolicibacteria, mycobacteroides and mycolicibacter as possible impediments for the diagnosis of (animal) tuberculosis

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Authors

Gcebe, Nomakorinte
Hlokwe, Tiny Motlatso
Bouw, Agnes
Michel, Anita Luise
Rutten, Victor P.M.G.

Journal Title

Journal ISSN

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Publisher

MDPI

Abstract

The Esx-1 family proteins of the Type VII secretion systems of Mycobacterium bovis and Mycobacterium tuberculosis have been assessed and are frequently used as candidates for tuberculosis (TB) diagnosis in both humans and animals. The presence of ESAT-6 and CFP 10 proteins, which are the most immunogenic proteins of the Esx-1 system and have been widely investigated for the immunodiagnosis of tuberculosis, in some Mycobacteriaceae and in Mycobacterium leprae, poses limitations for their use in specific diagnoses of TB. As such, to improve the specificity of the ESAT-6/CFP 10-based cell-mediated immunity (CMI) assays, other proteins encoded by genes within and outside the RD 1 region of the esx-1 locus have been evaluated as candidate antigens for CMI, as well as to investigate humoral responses in combination with ESAT-6 and or CFP 10, with varying specificity and sensitivity results. Hence, in this study, we evaluated various non-tuberculous mycobacteria (NTM), Mycolicibacterium, Mycolicibacter and Mycobacteroides species genomes available on the NCBI database for the presence and composition of the RD1 region of the esx-1 locus. In addition, we also assayed by polymerase chain reaction (PCR) and sequencing of Mycobacteriaceae available in our culture collection for the presence and sequence diversity of esxA and esxB genes encoding ESAT-6 and CFP 10, respectively. Whole genome sequence (WGS) data analysis revealed the presence of RD 1 gene orthologs in 70 of the over 100 published genomes of pathogenic and non- pathogenic Mycobcteriaceae other than tuberculosis. Among species evaluated from our culture collection, in addition to earlier reports of the presence of esxA and esxB in certain Mycolicibacterium, Mycolicibacterium septicum/peregrinum, Mycolicibacterium porcinum and Mycobacterium sp. N845T were also found to harbour orthologs of both genes. Orthologs of esxA only were detected in Mycobacterium brasiliensis, Mycolicibacterium elephantis and Mycolicibacterium flouroantheinivorans, whereas in Mycolicibacter engbackii, Mycolicibacterium mageritense and Mycobacterium paraffinicum, only esxB orthologs were detected. A phylogenetic analysis based on esxA and esxB sequences separated slow-growing from rapidly growing bacteria. These findings strengthen previous suggestions that esxA and esxB may be encoded in the majority of Mycobacteriaceae. The role of the Esx-1 system in both pathogenic and non-pathogenic Mycobacteriaceae needs further investigation, as these species may pose limitations to immunological assays for TB.

Description

DATA AVAILABILITY STATEMENT : In this study, we used publicly available data which were accessed from NCBI (https://www.ncbi.nlm.nih.gov/), Smegmlist (https://mycobrowser.epfl.ch/genes/) and Bovilist (http://genolist.pasteur.fr/BoviList/genome.cgi?; accessed on 20 January 2022) databases. All other data generated or analysed in the current study are available upon request.
SUPPLEMENTARY INFORMATION : FIGURE S1: Gel electrophoresis image illustrating amplification of esxA gene fragment using M. smegmatis derived primers. Lane ‘M’ is 100 bp Molecular weight markers (O’ gene ruler from Thermofisher Scientific), Lanes 6, 7 and 8 are positive samples, Lanes 2, 3, 4, 9, 10,11,12,13,14, and 15 are negative samples, and lane PC is M. smegmatis positive control and lane NC1 and NC2 are negative controls. FIGURE S2: Gel electrophoresis image illustrating amplification of esxB gene fragment using M. smegmatis derived primers. Lane 1 is a positive sample, lane NC is a negative control, while lane PC is M. smegmatis positive control, and lane M is a 100 bp Molecular weight marker (100 bp O’gene Ruler from Thermo Fisher Scientific); FIGURE S3: Gel electrophoresis image illustrating amplification of esxA gene fragment using M. bovis derived primers. Lanes 1 and 4 are negative samples, Lane 2, is a positive sample and lane 3 is M. bovis control while lane 5 is a negative control, and lane M, a 100 bp Molecular weight marker (100 bp O’gene Ruler from Thermo Fisher Scientific); FIGURE S4: Gel electrophoresis image illustrating amplification of esxB gene fragment using M. bovis derived primers. Lanes 1 is M. bovis control, Lane 2, is a negative sample and lane 3 is a positive sample while lane 4 is a negative control, and lane M, a 100 bp Molecular weight marker (100 bp O’gene Ruler from Thermo Fisher Scientific).

Keywords

Esx-1, RD1, Mycobacteriaceae, Tuberculosis (TB), Mycobacterium bovis (M. bovis), Mycobacterium tuberculosis (MTB), ESAT-6 protein, CFP 10 protein, SDG-03: Good health and well-being

Sustainable Development Goals

SDG-03:Good heatlh and well-being

Citation

Gcebe, N.; Hlokwe, T.M.; Bouw, A.; Michel, A.; Rutten, V.P.M.G. The Presence of esat-6 and cfp10 and Other Gene Orthologs of the RD 1 Region in Non-Tuberculous Mycobacteria, Mycolicibacteria, Mycobacteroides and Mycolicibacter as Possible Impediments for the Diagnosis of (Animal) Tuberculosis. Microorganisms 2024, 12, 1151. https://DOI.org/10.3390/microorganisms12061151.