An Antimicrobial Role for Zinc in Innate Immune Defense Against Group A Streptococcus
The Journal of infectious diseases, 2014•academic.oup.com
Background. Zinc plays an important role in human immunity, and it is known that zinc
deficiency in the host is linked to increased susceptibility to bacterial infection. In this study,
we investigate the role of zinc efflux in the pathogenesis of Streptococcus pyogenes (group
A Streptococcus [GAS]), a human pathogen responsible for superficial infections, such as
pharyngitis and impetigo, and severe invasive infections. Methods. The clinically important
M1T1 wild-type strain was used in this study, and isogenic mutants were constructed with …
deficiency in the host is linked to increased susceptibility to bacterial infection. In this study,
we investigate the role of zinc efflux in the pathogenesis of Streptococcus pyogenes (group
A Streptococcus [GAS]), a human pathogen responsible for superficial infections, such as
pharyngitis and impetigo, and severe invasive infections. Methods. The clinically important
M1T1 wild-type strain was used in this study, and isogenic mutants were constructed with …
Abstract
Background. Zinc plays an important role in human immunity, and it is known that zinc deficiency in the host is linked to increased susceptibility to bacterial infection. In this study, we investigate the role of zinc efflux in the pathogenesis of Streptococcus pyogenes (group A Streptococcus [GAS]), a human pathogen responsible for superficial infections, such as pharyngitis and impetigo, and severe invasive infections.
Methods. The clinically important M1T1 wild-type strain was used in this study, and isogenic mutants were constructed with deletions in the czcD gene (Spy0653; which encodes a putative zinc efflux pump) and adjacent gczA gene (Spy0654; which encodes a putative zinc-dependent activator of czcD). Wild-type, isogenic mutants and complemented strains were tested for resistance against zinc stress, intracellular zinc accumulation, and virulence.
Results. Both czcD and gczA mutants exhibited increased sensitivity to zinc. Transcriptional analyses indicate that GczA upregulates czcD in response to zinc. Both mutants displayed increased susceptibility to human neutrophil killing and reduced virulence in a murine infection model. Furthermore, we showed that neutrophils mobilize zinc in response to GAS.
Conclusions. These data indicate that the innate immune system may use zinc as an antimicrobial agent and that zinc efflux is an important contributor to GAS pathogenesis.
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