Waterborne diseases have critical public health issues and socioeconomic
relevancy worldwide. Various viral pathogens
are ordinarily associated with waterborne diseases. Six-yearsurveillance
(a total of 20 times) of norovirus, hepatitis A virus,
group C rotavirus, and enterovirus was conducted at five
raw water sampling sites including two lakes (Lakes Soyang
and Juam), Hyundo region of Geum River in Daejeon City,
and Guui region of Han River in Seoul Metropolitan City and
Moolgeum region of Nakdong River in Gimhae City which
are located near two water intake plants. In this study, we
routinely investigated virus contamination in water samples
through reverse transcription polymerase chain reaction (RTPCR)
and integrated cell culture RT-PCR with high sensitivity
and specificity. A total 100 samples were tested. Most of
the targeted viruses were found in 32% of the samples and
at least one of the indicator bacteria was detected in 65% of
these occurrences. Among all the detected viruses, enterovirus
was the most prevalent with a detection frequency of 12% and
2.71 MPN/10 L on average, while hepatitis A virus was the
least prevalent with a detection frequency of 4%. Nearly all
of the analyzed viruses (except for group C rotavirus) were
present in samples from Han River (the Guui region), Geum
River (the Hyundo region), Lake Juam, and Nakdong River
(the Moolgeum region), while group C rotavirus was detected
in those from the Guui region. During the six-year sampling
period, the targeted waterborne viruses in water samples exhibited
seasonal patterns in their occurrence that were different
from the indicator bacteria levels in the water samples.
The fact that they were detected in the five representative
Korean water environments makes it necessary to establish
the chemical and biological analysis systems for waterborne
viruses and sophisticated management systems.
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Rap small GTPases are involved in diverse signaling pathways
associated with cell growth, proliferation, and cell migration.
There are three Rap proteins in Dictyostelium, RapA, RapB,
and RapC. RapA is a key regulator in the control of cell adhesion
and migration. Recently RapA and RapC have been
reported to have opposite functions in the regulation of cellular
processes. In this study, we demonstrate that the C-terminus
of RapC, which is not found in RapA, is essential for
the opposite functions of RapC and is able to reverse the functions
of RapA when fused to the tail of RapA. Cells lacking
RapC displayed several defective phenotypes, including spread
morphology, strong adhesion, and decreased cell migration
compared to wild-type cells. These phenotypes were rescued
by full-length RapC, but not by RapC missing the C-terminus.
Furthermore, recombinant RapA fused with the C-terminus
of RapC completely recovered the phenotypes of rapC
null cells, indicating that the functions of RapA were modified
to become similar to those of RapC by the C-terminus of
RapC with respect to cell morphology, cell adhesion and migration,
cytokinesis, and development. These results suggest
that the C-terminal residues of RapC are able to suppress and
change the functions of other Ras proteins in Ras oncogenic
signaling pathways.
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