Publications by authors named "Qibing Gu"

Streptococcus suis (S. suis) is an important gram-positive pathogen and an emerging zoonotic pathogen that causes meningitis in swine and humans. Although several virulence factors have been characterized in S.

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Integrative and conjugative elements (ICEs) play a vital role in bacterial evolution by carrying essential genes that confer adaptive functions to the host. Despite their importance, the mechanism underlying the stable inheritance of ICEs, which is necessary for the acquisition of new traits in bacteria, remains poorly understood. Here, we identified SezAT, a type II toxin-antitoxin (TA) system, and AbiE, a type IV TA system encoded within the ICESsuHN105, coordinately promote ICE stabilization and mediate multidrug resistance in Streptococcus suis.

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Bovine coronavirus (BCoV) is a major cause of infectious disease in cattle, causing huge economic losses to the beef and dairy industries worldwide. BCoV can infect humans and multiple other species of animals. A rapid, reliable, and simple test is needed to detect BCoV infection in suspected farms.

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Article Synopsis
  • Serotype 2 (SS2) is a zoonotic pathogen linked to diseases in pigs and cases of severe human illness, specifically streptococcal toxic shock syndrome.
  • The study identified an RNA-binding protein (RbpA) with an S1 domain that enhances SS2's ability to adhere to host cells and increases its pathogenicity.
  • A proteomic analysis revealed 145 differentially expressed proteins, including key virulence factors, and demonstrated that RbpA influences gene expression through various post-transcriptional mechanisms, shedding light on bacterial pathogenicity.
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Streptococcus suis (S. suis) is one of the important pathogens that cause bacterial meningitis in pigs and humans. Evading host immune defences and penetrating the blood-brain barrier (BBB) are the preconditions for S.

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Toxin-antitoxin (TA) systems are ubiquitous genetic elements that play an essential role in multidrug tolerance and virulence . So far, little is known about the TA systems in . In this study, the Xress-MNTss TA system, composed of the MNTss toxin in the periplasmic space and its interacting Xress antitoxin, was identified in .

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