Mycobacterium tuberculosis does not show evidence of molecular DNA in human cadaveric ocular tissues in an endemic setting.


Journal

Clinical & experimental ophthalmology
ISSN: 1442-9071
Titre abrégé: Clin Exp Ophthalmol
Pays: Australia
ID NLM: 100896531

Informations de publication

Date de publication:
01 2020
Historique:
received: 21 04 2019
revised: 23 09 2019
accepted: 29 09 2019
pubmed: 7 10 2019
medline: 5 6 2021
entrez: 7 10 2019
Statut: ppublish

Résumé

Mycobacterium tuberculosis (MTB) in latent infection has been demonstrated in pulmonary/extra-pulmonary locations (lung, spleen, liver, kidney, adipose tissue) in autopsy studies, but its presence in ocular tissues in the latent state is not known. We conducted molecular and histopathological study of 100 cadaver eyes (50 humans) who died from causes other than tuberculosis (TB) (and were potential candidates for corneal transplantation) to detect MTB in ocular tissues in an endemic setting. After removal of the corneal button, an 8 to 10 mm block of tissue (choroid, retina and part of the vitreous) was excised from the remaining globe for DNA isolation. Gel-based IS6110 and devR3 polymerase chain reaction (PCR) assays were done, followed by real-time PCR using beta actin gene as an internal control. Sixteen randomly selected DNA samples were double checked using a commercial kit for MTB and non-tuberculous mycobacteria (NTM) DNA. The remaining larger part of the globe was subjected to histopathology. The mean age was 65.14 ± 18 years. All 100 samples were negative for both IS6110 and devR, and all 16 samples were negative with NTM MTB commercial kit. All samples were negative with Ziehl-Neelsen stain for acid fast bacilli and none showed any inflammation or granulomatous pathology. MTB could not be detected in human ocular tissues in latent state in India, a TB-endemic country. This may suggest the inability of MTB to seed ocular tissues in the latent state, unlike other organs which serve as reservoirs for the bacilli in the absence of manifest disease.

Sections du résumé

BACKGROUND
Mycobacterium tuberculosis (MTB) in latent infection has been demonstrated in pulmonary/extra-pulmonary locations (lung, spleen, liver, kidney, adipose tissue) in autopsy studies, but its presence in ocular tissues in the latent state is not known.
METHODS
We conducted molecular and histopathological study of 100 cadaver eyes (50 humans) who died from causes other than tuberculosis (TB) (and were potential candidates for corneal transplantation) to detect MTB in ocular tissues in an endemic setting. After removal of the corneal button, an 8 to 10 mm block of tissue (choroid, retina and part of the vitreous) was excised from the remaining globe for DNA isolation. Gel-based IS6110 and devR3 polymerase chain reaction (PCR) assays were done, followed by real-time PCR using beta actin gene as an internal control. Sixteen randomly selected DNA samples were double checked using a commercial kit for MTB and non-tuberculous mycobacteria (NTM) DNA. The remaining larger part of the globe was subjected to histopathology.
RESULTS
The mean age was 65.14 ± 18 years. All 100 samples were negative for both IS6110 and devR, and all 16 samples were negative with NTM MTB commercial kit. All samples were negative with Ziehl-Neelsen stain for acid fast bacilli and none showed any inflammation or granulomatous pathology.
CONCLUSIONS
MTB could not be detected in human ocular tissues in latent state in India, a TB-endemic country. This may suggest the inability of MTB to seed ocular tissues in the latent state, unlike other organs which serve as reservoirs for the bacilli in the absence of manifest disease.

Identifiants

pubmed: 31587479
doi: 10.1111/ceo.13654
doi:

Substances chimiques

DNA, Bacterial 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

69-77

Informations de copyright

© 2019 Royal Australian and New Zealand College of Ophthalmologists.

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Auteurs

Harish Chauhan (H)

Advanced Eye Centre, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Reema Bansal (R)

Advanced Eye Centre, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Aman Kumar (A)

Advanced Eye Centre, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Surya P Sharma (SP)

Advanced Eye Centre, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Geethanjali Gude (G)

Department of Histopathology, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Uma Nahar (U)

Department of Histopathology, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Ramandeep Singh (R)

Advanced Eye Centre, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Arun K Jain (AK)

Advanced Eye Centre, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Vishali Gupta (V)

Advanced Eye Centre, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

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