TY - JOUR
T1 - Predicting the public health benefit of vaccinating cattle against Escherichia coli O157
AU - Matthews, L
AU - Reeve, R
AU - Gally, DL
AU - Low, JC
AU - Woolhouse, MEJ
AU - McAteer, SP
AU - Locking, ME
AU - Chase-Topping, ME
AU - Haydon, DT
AU - Allison, LJ
AU - Hanson, MF
AU - Gunn, GJ
AU - Reid, SWJ
N1 - 1023397
PY - 2013/10
Y1 - 2013/10
N2 - Identifying the major sources of risk in disease transmission is key
to designing effective controls. However, understanding of transmission
dynamics across species boundaries is typically poor,
making the design and evaluation of controls particularly challenging
for zoonotic pathogens. One such global pathogen is
Escherichia coli O157, which causes a serious and sometimes fatal
gastrointestinal illness. Cattle are the main reservoir for E. coli
O157, and vaccines for cattle now exist. However, adoption of
vaccines is being delayed by conflicting responsibilities of veterinary
and public health agencies, economic drivers, and because
clinical trials cannot easily test interventions across species boundaries,
lack of information on the public health benefits. Here, we
examine transmission risk across the cattle–human species boundary
and show three key results. First, supershedding of the pathogen
by cattle is associated with the genetic marker stx2. Second,
by quantifying the link between shedding density in cattle and
human risk, we show that only the relatively rare supershedding
events contribute significantly to human risk. Third, we show that
this finding has profound consequences for the public health benefits
of the cattle vaccine. A naïve evaluation based on efficacy in
cattle would suggest a 50% reduction in risk; however, because
the vaccine targets the major source of human risk, we predict
a reduction in human cases of nearly 85%. By accounting for nonlinearities
in transmission across the human–animal interface, we
show that adoption of these vaccines by the livestock industry
could prevent substantial numbers of human E. coli O157 cases.
AB - Identifying the major sources of risk in disease transmission is key
to designing effective controls. However, understanding of transmission
dynamics across species boundaries is typically poor,
making the design and evaluation of controls particularly challenging
for zoonotic pathogens. One such global pathogen is
Escherichia coli O157, which causes a serious and sometimes fatal
gastrointestinal illness. Cattle are the main reservoir for E. coli
O157, and vaccines for cattle now exist. However, adoption of
vaccines is being delayed by conflicting responsibilities of veterinary
and public health agencies, economic drivers, and because
clinical trials cannot easily test interventions across species boundaries,
lack of information on the public health benefits. Here, we
examine transmission risk across the cattle–human species boundary
and show three key results. First, supershedding of the pathogen
by cattle is associated with the genetic marker stx2. Second,
by quantifying the link between shedding density in cattle and
human risk, we show that only the relatively rare supershedding
events contribute significantly to human risk. Third, we show that
this finding has profound consequences for the public health benefits
of the cattle vaccine. A naïve evaluation based on efficacy in
cattle would suggest a 50% reduction in risk; however, because
the vaccine targets the major source of human risk, we predict
a reduction in human cases of nearly 85%. By accounting for nonlinearities
in transmission across the human–animal interface, we
show that adoption of these vaccines by the livestock industry
could prevent substantial numbers of human E. coli O157 cases.
KW - 80-20 rule
KW - Cross-species transmission
KW - One health
KW - Zoonoses
U2 - 10.1073/pnas.1304978110
DO - 10.1073/pnas.1304978110
M3 - Article
SN - 1091-6490
VL - 110
SP - 16265
EP - 16270
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 40
ER -