Sialic acids consist of nine-carbon keto sugars that are commonly found at the terminal end of mucins. This positional
feature of sialic acids contributes to host cell interactions but is also exploited by some pathogenic bacteria in evasion of
host immune system. Moreover, many commensals and pathogens use sialic acids as an alternative energy source to survive
within the mucus-covered host environments, such as the intestine, vagina, and oral cavity. Among the various biological
events mediated by sialic acids, this review will focus on the processes necessary for the catabolic utilization of sialic acid in
bacteria. First of all, transportation of sialic acid should be preceded before its catabolism. There are four types of transporters
that are used for sialic acid uptake; the major facilitator superfamily (MFS), the tripartite ATP-independent periplasmic
C4-dicarboxilate (TRAP) multicomponent transport system, the ATP binding cassette (ABC) transporter, and the sodium
solute symporter (SSS). After being moved by these transporters, sialic acid is degraded into an intermediate of glycolysis
through the well-conserved catabolic pathway. The genes encoding the catabolic enzymes and transporters are clustered into
an operon(s), and their expression is tightly controlled by specific transcriptional regulators. In addition to these mechanisms,
we will cover some researches about sialic acid utilization by oral pathogens.
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Livestock pigs and porcine norovirus could be candidate tools
for future studies on the geographic isolation of norovirus.
In this study, we provide the first evidence for geographic
isolation of the host as a determinant of the distribution of
subgenotypes of the porcine norovirus genogroup II (GII)
genotype 11. Environmental water samples were collected
from peri-urban streams and estuaries in South Korea between
2014 and 2020. In total, 488 GII region C sequences of
norovirus open reading frame 2 were isolated. A total of 14
genotypes were detected, two of which (GII.11 and GII.18)
corresponded to porcine norovirus. Five human norovirus
genotypes (GII.2, GII.3, GII.4, GII.6, and GII.17) and one
porcine norovirus genotype (GII.11) comprised the subgenotypes.
Integrated analysis of seasonal and geographical factors
revealed that the possibility of the co-emergence of different
GII.11 subgenotypes in the same province was lower
than that of human norovirus subgenotypes in the same province.
Additional algorithms designed to eliminate potential
biases further supported the estimated restricted geographical
spread of the GII.11 subgenotypes. Fecal contamination
source tracking revealed low detection rates of porcine norovirus
in the absence of upstream pig farms. These results suggest
that a one-sided viral transmission route, mainly dependent
on indirect contact owing to the limited chance of direct
contact between geographically separated livestock pig populations,
may be responsible for the restricted geographical
spread of the GII.11 subgenotypes.
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