The polymorphic bacterial oncoprotein, CagA shows geography-
dependent variation in the C-terminal Glu-Pro-Ile-
Tyr-Ala (EPIYA) motifs; East-Asian H. pylori isolates carry
the ABD type while Western isolates carry the ABC type. In
Western isolates, the EPIYA-C motif is sometimes found in
multi-copy and this genotype is associated with disease severity.
Interestingly, a small number of East-Asian H. pylori
isolates have been found to carry Western ABC-type CagA.
To gain a better understanding of these unusual isolates, the
genomes of four Korean H. pylori clinical isolates carrying
ABC-type CagA were sequenced via third generation (Pac-
Bio SMRT) sequencing technology. The obtained data were
utilized for phylogenetic analysis as well as comparison of
additional virulence factors that are known to show geographic-
dependent polymorphisms. Three of four isolates indeed
belonged to the hpEastAsia group and showed typical East-
Asian polymorphism in virulence factors such as homA/B/C,
babA/B/C, and oipA. One isolate grouped to HpAfrica and
showed typical Western polymorphism of virulence factors
such as cagA, homA/B/C, and oipA. To understand the occurrence
of the multi-copy EPIYA-C motif genotype in an East-
Asian H. pylori background, the Korean clinical isolate, K154
was analyzed; this strain belonged to hpEastAsia but encoded
CagA EPIYA-ABCCCC. Based on DNA sequence homology
within the CagA multimerization (CM) sequence that flanked
the EPIYA-C motifs, we predicted that the number of C motifs
might change via homologous recombination. To test this
hypothesis, K154 was cultured for one generation and 287
single colonies were analyzed for the number of EPIYA-C
motifs using PCR-based screening and DNA sequencing verification.
Three out of 284 (1%) single colony isolates showed
changes in the number of EPIYA-C motifs in vitro; one isolate
increased to five EPIYA-C motifs, one decreased to three
EPIYA-C motifs, and one completely deleted the EPIYA-C
motifs. The capacity for dynamic changes in the number of
EPIYA-C repeats of CagA may play a role in generating important
intraspecies diversity in East-Asian H. pylori.
Citations
Citations to this article as recorded by
Virulence gene polymorphisms in Shandong Helicobacter pylori strains and their relevance to gastric cancer Zhijing Xue, Weijia Li, Hailing Ding, Fengyan Pei, Jianzhong Zhang, Yanan Gong, Ruyue Fan, Fang Wang, Youjun Wang, Qing Chen, Yanran Li, Xinyu Yang, Yan Zheng, Guohai Su, Saeid Ghavami PLOS ONE.2024; 19(9): e0309844. CrossRef
Amino acid deletions at positions 893 and 894 of cytotoxin-associated gene A protein affect Helicobacter pylori gastric epithelial cell interactions Zhi-Jing Xue, Ya-Nan Gong, Li-Hua He, Lu Sun, Yuan-Hai You, Dong-Jie Fan, Mao-Jun Zhang, Xiao-Mei Yan, Jian-Zhong Zhang World Journal of Gastroenterology.2024; 30(41): 4449. CrossRef
Characteristics of different types of Helicobacter pylori: New evidence from non-amplified white light endoscopy Weidong Liu, Wenjie Kong, Wenjia Hui, Chun Wang, Qi Jiang, Hong Shi, Feng Gao Frontiers in Microbiology.2023;[Epub] CrossRef
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.
Citations
Citations to this article as recorded by
Swine Norovirus: Past, Present, and Future Lara Cavicchio, Andrea Laconi, Alessandra Piccirillo, Maria Serena Beato Viruses.2022; 14(3): 537. CrossRef