Sialylation of Lipooligosaccharides Promotes Biofilm Formation by Nontypeable Haemophilus influenzae

WE Swords, ML Moore, L Godzicki… - Infection and …, 2004 - Am Soc Microbiol
WE Swords, ML Moore, L Godzicki, G Bukofzer, MJ Mitten, J VonCannon
Infection and immunity, 2004Am Soc Microbiol
ABSTRACT Nontypeable Haemophilus influenzae (NTHi) is a major cause of opportunistic
respiratory tract infections, including otitis media and bronchitis. The persistence of NTHi in
vivo is thought to involve bacterial persistence in a biofilm community. Therefore, there is a
need for further definition of bacterial factors contributing to biofilm formation by NTHi. Like
other bacteria inhabiting host mucosal surfaces, NTHi has on its surface a diverse array of
lipooligosaccharides (LOS) that influence host-bacterial interactions. In this study, we show …
Abstract
Nontypeable Haemophilus influenzae (NTHi) is a major cause of opportunistic respiratory tract infections, including otitis media and bronchitis. The persistence of NTHi in vivo is thought to involve bacterial persistence in a biofilm community. Therefore, there is a need for further definition of bacterial factors contributing to biofilm formation by NTHi. Like other bacteria inhabiting host mucosal surfaces, NTHi has on its surface a diverse array of lipooligosaccharides (LOS) that influence host-bacterial interactions. In this study, we show that LOS containing sialic (N-acetyl-neuraminic) acid promotes biofilm formation by NTHi in vitro and bacterial persistence within the middle ear or lung in vivo. LOS from NTHi in biofilms was sialylated, as determined by comparison of electrophoretic mobilities and immunochemical reactivities before and after neuraminidase treatment. Biofilm formation was significantly reduced in media lacking sialic acid, and a siaB (CMP-sialic acid synthetase) mutant was deficient in biofilm formation in three different in vitro model systems. The persistence of an asialylated siaB mutant was attenuated in a gerbil middle ear infection model system, as well as in a rat pulmonary challenge model system. These data show that sialylated LOS glycoforms promote biofilm formation by NTHi and persistence in vivo.
American Society for Microbiology