• Eur. Respir. J. · Feb 2018

    Primary ciliary dyskinesia with normal ultrastructure: three-dimensional tomography detects absence of DNAH11.

    • Amelia Shoemark, Thomas Burgoyne, Robert Kwan, Mellisa Dixon, Mitali P Patel, Andrew V Rogers, Alexandros Onoufriadis, Juliet Scully, Farheen Daudvohra, Thomas Cullup, Michael R Loebinger, Robert Wilson, Chung Eddie M K EMK Genetics and Genomic Medicine, University College London, UCL Great Ormond Street Institute of Child Health, London, UK., Andrew Bush, Hannah M Mitchison, and Claire Hogg.
    • Royal Brompton and Harefield NHS Trust, London, UK a.shoemark@rbht.nhs.uk.
    • Eur. Respir. J. 2018 Feb 1; 51 (2).

    AbstractIn primary ciliary dyskinesia (PCD), motile ciliary dysfunction arises from ciliary defects usually confirmed by transmission electron microscopy (TEM). In 30% of patients, such as those with DNAH11 mutations, apparently normal ultrastructure makes diagnosis difficult. Genetic analysis supports diagnosis, but may not identify definitive causal variants. Electron tomography, an extension of TEM, produces three-dimensional ultrastructural ciliary models with superior resolution to TEM. Our hypothesis is that tomography using existing patient samples will enable visualisation of DNAH11-associated ultrastructural defects. Dual axis tomograms from araldite-embedded nasal cilia were collected in 13 PCD patients with normal ultrastructure (DNAH11 n=7, HYDIN n=2, CCDC65 n=3 and DRC1 n=1) and six healthy controls, then analysed using IMOD and Chimera software.DNAH11 protein is localised to the proximal ciliary region. Within this region, electron tomography indicated a deficiency of >25% of proximal outer dynein arm volume in all patients with DNAH11 mutations (n=7) compared to other patients with PCD and normal ultrastructure (n=6) and healthy controls (n=6). DNAH11 mutations cause a shared abnormality in ciliary ultrastructure previously undetectable by TEM. Advantageously, electron tomography can be used on existing diagnostic samples and establishes a structural abnormality where ultrastructural studies were previously normal.Copyright ©ERS 2018.

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