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1 ents an important transmission hub for viral zoonoses.
2 of concern, as well as to future coronavirus zoonoses.
3 linking urbanization to gene pool spread and zoonoses.
4 e the annualized damages from emerging viral zoonoses.
5 esis that bats harbor exceptionally virulent zoonoses.
6 g putatively undetected or so far unrealized zoonoses.
7 orm molecular surveillance to predict future zoonoses.
8 e brucellosis, one of the most common global zoonoses.
9 are responsible for the majority of emerging zoonoses.
10 identified by this review, the majority were zoonoses.
11 ntal gene transfer can help predict emerging zoonoses.
12 l switching events; 13 anthroponoses and two zoonoses.
13 st assessment of the risks posed by emerging zoonoses.
14 aintenance of livestock pathogens, including zoonoses.
15 erent members of one protein family to cause zoonoses.
16 nt illnesses with a documented potential for zoonoses.
17 rience increased vulnerability to tick-borne zoonoses.
18 oaches aimed at finding and predicting novel zoonoses.
19 enhanced biosurveillance of a vast array of zoonoses.
20 about antiviral mechanisms that suppress IAV zoonoses.
21 t on multiple fronts, especially as emerging zoonoses.
22 viral vectors for vaccines against bat-borne zoonoses.
23 well-suited to the study of livestock-origin zoonoses.
24 hip was between temperature and vector-borne zoonoses (56% of positive effects, mean Hedges' g = 0.36
27 substantial implications for a wide range of zoonoses acquired at the wildlife-human interface for wh
28 the generality of alien species facilitating zoonoses across multiple host and parasite taxa worldwid
29 ings show that variation in the frequency of zoonoses among animal orders can be explained without in
31 reveal the potential clinical importance of zoonoses and arboviruses in febrile children in Tanzania
33 Evidence from naturally occurring retroviral zoonoses and cross-species infections by animal retrovir
34 igate mechanisms of transspecies movement of zoonoses and has great potential to aid in rapid public
38 to 272 high and 41 very high-risk candidate zoonoses and showed significantly elevated predicted zoo
39 predicting the risk of outbreaks of endemic zoonoses and the need to widen the context of studies of
41 that could ultimately drive the emergence of zoonoses and the spread of antimicrobial resistance.
42 aits can help predict wildlife reservoirs of zoonoses and the vulnerability of populations to disease
43 nfectious disease processes such as emerging zoonoses and vaccine-preventable diseases, [Formula: see
44 o explain the extreme virulence of bat-borne zoonoses and, more generally, demonstrates how key diffe
45 ted number of 'missing viruses' and 'missing zoonoses' and therefore of highest value for future surv
47 h the circumstances surrounding these recent zoonoses are becoming clearer, the nature and timescale
50 -human animals, the transmission dynamics of zoonoses are necessarily influenced by the ecology of th
52 pe similar to the A(H3N2)v genotype, causing zoonoses at North American agricultural fairs, underline
53 row host tropism, reducing the occurrence of zoonoses but also impairing the development of optimal a
56 diversity of pathogens, including multihost zoonoses capable of environmental transmission (e.g., Le
57 osis is one of the most prevalent tick-borne zoonoses caused by infection with Ehrlichia chaffeensis.
58 burden of disease, with endemic and enzootic zoonoses causing about a billion cases of illness in peo
60 ronmental hazards, water and sanitation, and zoonoses control clearly show incremental benefits of On
62 to generate virulence predictions for viral zoonoses derived from diverse mammalian reservoirs, reca
65 ly test whether such "special reservoirs" of zoonoses exist, we used literature searches to construct
66 nvironmental surveillance to detect emerging zoonoses, fill gaps when clinical testing wanes, and inf
67 ion and environmental changes on the risk of zoonoses for which there are epidemiological interaction
71 riants and the threat of future Sarbecovirus zoonoses have spurred the design of vaccines that can in
72 dity and shorter lifespans tend to host more zoonoses; however, the causes of this association remain
73 and data on human outbreaks of rodent-borne zoonoses, identifying matches between empirical evidence
74 ites, pathogens and the environment, placing zoonoses in an ecological context, while identifying key
77 value of conceptualizing prophylaxis against zoonoses in terms of genetic, rather than species, diver
80 ortant infectious diseases are the result of zoonoses, in which pathogens that normally infect animal
81 scapularis is the main vector of tick-borne zoonoses including the pathogens causing Lyme disease in
82 as natural hosts for several important viral zoonoses, including Ebola, Marburg, Nipah, Hendra, and r
83 rvoir in North America for agents of several zoonoses, including Lyme disease, babesiosis, anaplasmos
84 lyses suggest that the virulence of emerging zoonoses is correlated with but not completely predictab
85 he most frequent life-threatening tick-borne zoonoses, is caused by Ehrlichia chaffeensis that lacks
87 ce that climate sensitivity is common across zoonoses, likely leading to substantial yet complex effe
88 uggesting exposure to vectors and associated zoonoses may be greater for people entering this habitat
89 nd become enzootic in swine, nascent reverse zoonoses may result in virus detections that are difficu
90 and epidemiology of the flea-borne bacterial zoonoses mentioned above with an emphasis on recent adva
92 were the result of at least two independent zoonoses of distinct viral lineages that acquired the sa
94 d diversity in the region, including reverse zoonoses of human H1N1/2009 pandemic and H3N2 viruses.
95 domestic dogs (FRD) are not only vectors of zoonoses of public health concern, but also pose direct
97 e monetary and non-monetary impacts of these zoonoses on human health, agriculture and society must b
100 mammals versus birds, the observed number of zoonoses per animal order increased as a function of the
103 Progress in understanding and combating zoonoses requires a new generation of models that addres
105 hine learning models that identify candidate zoonoses solely using signatures of host range encoded i
106 with the public-health risks posed by prion zoonoses such as bovine spongiform encephalopathy, has f
108 Prior to emergence in human populations, zoonoses such as SARS cause occasional infections in hum
112 s were unexceptional, maintaining numbers of zoonoses that closely matched expectations for mammalian
116 atural forest also increases the threat from zoonoses, where new vector-borne pathogens spill over fr
117 orthologs of arenaviral host species enable zoonoses, whereas mice and rats are not infectable becau
119 cases in Cameroon are the result of repeated zoonoses, with two distinct zoonotic lineages circulatin