Fate and Transport of Zoonotic Bacterial, Viral, and - The Pork Store ...
Fate and Transport of Zoonotic Bacterial, Viral, and - The Pork Store ...
Fate and Transport of Zoonotic Bacterial, Viral, and - The Pork Store ...
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3. Common Viruses <strong>of</strong> Swine<br />
Viruses may be released from the host in<br />
an aggregated state. In general, it is assumed that<br />
aggregated viruses are more resistant to inactivation<br />
than single virus particles. In the case <strong>of</strong> NoVs, this has<br />
been demonstrated for chlorine inactivation (Thurston-<br />
Enriquez et al. 2003), because each virus particle within<br />
the aggregates must be inactivated before the whole<br />
aggregate is considered inactivated. Adsorption to<br />
sediments may decrease because <strong>of</strong> the aggregated state,<br />
which could be beneficial in terms <strong>of</strong> limiting local soil<br />
contamination, but these particles can be transported<br />
easily by the air or rainfall to other points (Tyrrel <strong>and</strong><br />
Quinton 2003; Hutchison, Avery, <strong>and</strong> Monaghan 2008).<br />
Virus-like particles as laboratory surrogates<br />
for enteric caliciviruses have been used to assay<br />
reduction <strong>of</strong> NoVs in soil columns under different<br />
conditions that resemble those in the field (different soil<br />
composition, groundwater, <strong>and</strong> rainwater) (Meschke<br />
<strong>and</strong> Sobsey 1998). <strong>The</strong> NV VLPs have been used<br />
successfully to study accumulation <strong>of</strong> NV in digestive<br />
tissues <strong>of</strong> shellfish (Loisy et al. 2004). <strong>The</strong> results were<br />
not only useful to improve shellfish safety, but also<br />
indicated that VLPs behave similarly to native virus<br />
<strong>and</strong> could be used as surrogates, at least in lab-scale<br />
experiments. Although these experiments <strong>and</strong> results<br />
can be extended to estimate <strong>and</strong> underst<strong>and</strong> what<br />
hypothetically would happen in the field, the true<br />
scenario where all the previously mentioned factors<br />
interact needs to be evaluated.<br />
At least 18 environmentally superior<br />
technologies recently have been developed for the<br />
treatment <strong>of</strong> animal manure to decrease its impact on<br />
the environment <strong>and</strong> public health (Humenik et al.<br />
2004). For animal enteric caliciviruses, the first study<br />
to investigate the effect <strong>of</strong> environmental technologies<br />
on the fate <strong>of</strong> these pathogens in animal manure under<br />
field conditions was performed recently (Costantini et<br />
al. 2007). In this study, the occurrence <strong>of</strong> PoSaV <strong>and</strong><br />
PoNoV first was assessed in fresh feces <strong>of</strong> swine; then<br />
the effects <strong>of</strong> different animal manure management <strong>and</strong><br />
treatment technologies on their survival was evaluated<br />
by RT-PCR or enzyme-linked immunosorbent<br />
assay (ELISA) (Guo et al. 2001; Wang, personal<br />
communication). Because enteric caliciviruses are not<br />
cell-culture-adapted, ELISA <strong>and</strong> RT-PCR results were<br />
Table 3.1. Detection <strong>of</strong> animal enteric viruses in<br />
pre- <strong>and</strong> post-treatment (Costantini et al. 2007)<br />
Management<br />
system <strong>and</strong><br />
treatment<br />
technology<br />
Conventional<br />
swine<br />
operation<br />
Aerobic<br />
up flow<br />
bi<strong>of</strong>iltration<br />
system<br />
Constructedwetl<strong>and</strong><br />
system<br />
Super soil<br />
system<br />
High rise hog<br />
building<br />
Enteric viruses<br />
PoNoVs a PoSaV b RV-A b RV-C b<br />
Pre-treatment<br />
Post-treatment<br />
Pre-treatment<br />
Post-treatment<br />
Pre-treatment<br />
Post-treatment<br />
Pre-treatment<br />
Post-treatment<br />
- - + + + + - -<br />
- - + - + + + +<br />
+ - + - + + - -<br />
+ - + - + + + +<br />
+ - + - + + + +<br />
Ambient<br />
temperature<br />
anaerobic<br />
digester<br />
- - + - + - + -<br />
a Determined by RT-PCR with specific primers<br />
b Determined by RT-PCR with specific primers <strong>and</strong> ELISA<br />
29<br />
combined to provide estimate prevalence <strong>and</strong> treatment<br />
effects. <strong>The</strong> presence <strong>of</strong> infectious particles could be<br />
overestimated if ELISA <strong>and</strong> RT-PCR were positive,<br />
because inactivated particles still could be detected by<br />
both techniques. ELISA-negative <strong>and</strong> RT-PCR-positive<br />
or ELISA- <strong>and</strong> RT-PCR negatives also could result in<br />
underestimation <strong>of</strong> the presence <strong>of</strong> infectious particles,<br />
because the numbers <strong>of</strong> infectious particles may be<br />
lower than the detection limit <strong>of</strong> one or both techniques,<br />
respectively. Only in case <strong>of</strong> ELISA-positive <strong>and</strong> RT-<br />
PCR-negative might it be considered that infectious<br />
particles may not be present <strong>and</strong> that the positive<br />
result on ELISA may result from detection <strong>of</strong> soluble<br />
proteins. A final definitive answer cannot be provided<br />
without an infectivity assay; therefore, for highly critical<br />
samples, it is possible to assess infectivity in vivo using<br />
calicivirus-seronegative-susceptible conventional pigs<br />
or Gn pigs. In the previously cited study (Costantini