Neisseria meningitidis filamentous phage MDA promotes colonisation by selecting hyperadhesive pili variants

C Clémence Mouville A Antoine Brizard M Morgane Wuckelt M Mélanie Montabord H Hervé Lécuyer J Julie Meyer (INSERM U1151, CNRS UMR8253, Institut Necker-Enfants Malades, Université Paris Cité) A Anne Jamet B Béatrice Durel C Charlotte Izabelle X Xavier Nassif (INSERM U1151, CNRS UMR8253, Institut Necker-Enfants Malades, Université Paris Cité) M Mathieu Coureuil (INSERM U1151, CNRS UMR8253, Institut Necker-Enfants Malades, Université Paris Cité) E Emmanuelle Bille (INSERM U1151, CNRS UMR8253, Institut Necker-Enfants Malades, Université Paris Cité)

Abstract

Abstract Filamentous phages are non-lytic phages mutually beneficial to their bacterial hosts. In Neisseria meningitidis , the filamentous phage MDA is associated with invasive diseases thanks to its key role in the formation of biofilm during epithelium colonisation. The infection model for filamentous phages has been defined for phages Ff and CTX. These phages bind to the tips of bacterial pili before being translocated into the periplasm of their hosts. The aim of this study is to investigate the relationship between filamentous phage infection and type IV pili, using the bacterium Neisseria meningitidis and the bacteriophage MDA as model organisms. We show that MDAΦ rather binds to type IV pili along their entire length with preferential binding to positively charged variants of the major fibre-forming pilin, demonstrating a role for antigenic variation in phage infection. Strikingly, bacteria expressing the more positively charged pilin are also the most adhesive, suggesting that MDAΦ primarily target the most adhesive bacteria. Finally, we show that adhesion to human cells is sufficient to amplify the phage-positive meningococcal population. Overall, this study reveals how a filamentous phage can target hyperadhesive bacterial variants and promote their selection, thereby establishing a link between phage infection and bacterial colonisation.

Article Details

Volume / Issue Vol. 17, Issue 1
Published December 20, 2025
ISSN 2041-1723
Publisher Nature Portfolio

Journal Info

Nature Communications

Nature Portfolio

ISSN: 2041-1723 Open Access Life Sciences

Authors (12)

C

Clémence Mouville

A

Antoine Brizard

M

Morgane Wuckelt

M

Mélanie Montabord

H

Hervé Lécuyer

J

Julie Meyer

INSERM U1151, CNRS UMR8253, Institut Necker-Enfants Malades, Université Paris Cité

A

Anne Jamet

B

Béatrice Durel

C

Charlotte Izabelle

X

Xavier Nassif

INSERM U1151, CNRS UMR8253, Institut Necker-Enfants Malades, Université Paris Cité

M

Mathieu Coureuil

INSERM U1151, CNRS UMR8253, Institut Necker-Enfants Malades, Université Paris Cité

E

Emmanuelle Bille

INSERM U1151, CNRS UMR8253, Institut Necker-Enfants Malades, Université Paris Cité