Evidence for a non-replicative intracellular stage of nontypable Haemophilus influenzae in epithelial cells

Author:

Morey Pau12,Cano Victoria12,Martí-Lliteras Pau12,López-Gómez Antonio12,Regueiro Verónica12,Saus Carles3,Bengoechea José Antonio4512,Garmendia Junkal2641

Affiliation:

1. Centro de Investigación Biomédica en Red de Enfermedades Respiratorias (CIBERES), Bunyola, Spain

2. Programa de Infección e Inmunidad, Fundación Caubet-CIMERA, recinto Hospital Joan March, carretera Sóller, km 12, 07110, Bunyola, Spain

3. Servicio de Anatomía Patológica, Hospital Universitario Son Dureta, Palma Mallorca, Spain

4. Área Microbiología, Facultad de Biología, Universitat Illes Balears, carretera Valldemossa, km 7.5, 07122, Palma Mallorca, Spain

5. Consejo Superior de Investigaciones Científicas (CSIC), Madrid, Spain

6. Instituto Agrobiotecnología (UPNA-CSIC), Campus Arrosadía s/n, 31192 Mutilva Baja, Navarra, Spain

Abstract

Nontypable Haemophilus influenzae (NTHi) is a Gram-negative, non-capsulated human bacterial pathogen, a major cause of a repertoire of respiratory infections, and intimately associated with persistent lung bacterial colonization in patients suffering from chronic obstructive pulmonary disease (COPD). Despite its medical relevance, relatively little is known about its mechanisms of pathogenicity. In this study, we found that NTHi invades the airway epithelium by a distinct mechanism, requiring microtubule assembly, lipid rafts integrity, and activation of phosphatidylinositol 3-kinase (PI3K) signalling. We found that the majority of intracellular bacteria are located inside an acidic subcellular compartment, in a metabolically active and non-proliferative state. This NTHi-containing vacuole (NTHi-CV) is endowed with late endosome features, co-localizing with LysoTracker, lamp-1, lamp-2, CD63 and Rab7. The NTHi-CV does not acquire Golgi- or autophagy-related markers. These observations were extended to immortalized and primary human airway epithelial cells. By using NTHi clinical isolates expressing different amounts of phosphocholine (PCho), a major modification of NTHi lipooligosaccharide, on their surfaces, and an isogenic lic1BC mutant strain lacking PCho, we showed that PCho is not responsible for NTHi intracellular location. In sum, this study indicates that NTHi can survive inside airway epithelial cells.

Publisher

Microbiology Society

Subject

Microbiology

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