Literature DB >> 26038451

Epidemiology, geographical distribution, and economic consequences of swine zoonoses: a narrative review.

Salah Uddin Khan1, Kalina R Atanasova1, Whitney S Krueger1, Alejandro Ramirez2, Gregory C Gray1.   

Abstract

We sought to review the epidemiology, international geographical distribution, and economic consequences of selected swine zoonoses. We performed literature searches in two stages. First, we identified the zoonotic pathogens associated with swine. Second, we identified specific swine-associated zoonotic pathogen reports for those pathogens from January 1980 to October 2012. Swine-associated emerging diseases were more prevalent in the countries of North America, South America, and Europe. Multiple factors were associated with the increase of swine zoonoses in humans including: the density of pigs, poor water sources and environmental conditions for swine husbandry, the transmissibility of the pathogen, occupational exposure to pigs, poor human sanitation, and personal hygiene. Swine zoonoses often lead to severe economic consequences related to the threat of novel pathogens to humans, drop in public demand for pork, forced culling of swine herds, and international trade sanctions. Due to the complexity of swine-associated pathogen ecology, designing effective interventions for early detection of disease, their prevention, and mitigation requires an interdisciplinary collaborative "One Health" approach from veterinarians, environmental and public health professionals, and the swine industry.

Entities:  

Keywords:  epidemiology; review; swine; transmission; zoonoses

Year:  2013        PMID: 26038451      PMCID: PMC3880873          DOI: 10.1038/emi.2013.87

Source DB:  PubMed          Journal:  Emerg Microbes Infect        ISSN: 2222-1751            Impact factor:   7.163


INTRODUCTION

The history of pig raising goes back as far as ∼9000 BC, likely with the domestication of wild boars in Eurasia.[1] Since then, pork has served as a major source of human nutrition. In the last 50 years, the consumption of pork and the demands of products from pigs have increased, causing the global pig population to grow from 406 million to 966 million heads.[2] Pigs are anatomically and physiologically similar to humans in terms of dentition, ocular, dermal, cardiovascular, renal, and digestive systems.[3] While these have led to great advances in human and pig health, including substituting human organs with swine organs, these shared biological characteristics sometimes have the potential to permit pathogens to cross the species barrier.[4,5] Although, pigs have been long known to serve as reservoirs for zoonotic pathogens, our understanding regarding zoonotic disease ecology in pigs is rather superficial.[6,7] As such, although many swine pathogens are well-controlled, some zoonotic pathogens have become well-established in swine populations, imparting health and economic burdens. Some of these viruses, bacteria and parasites are emerging or re-emerging in nature, while others appear sporadically or transmit to man only under certain circumstances.[8] Reducing these diseases in animals and humans often requires adopting primary or secondary prevention techniques, or a combination of both.[9] However, doing so requires extensive understanding of husbandry practices, ecological preconditions, human risk behaviors, and the modes of transmission for swine-associated zoonoses. To facilitate a better understanding of their prevention and control, this review discusses the epidemiology, geographical distribution, and economic consequences of selected swine zoonoses from a global perspective.

LITERATURE REVIEW AND DATA SUMMARIZATION

We performed literature searches in two stages: first, to identify the zoonotic pathogens associated with swine and second, to identify the literature describing specific zoonotic pathogens. For the first stage, we performed a literature review in PubMed and in Google Scholar (English only) for articles published from January 1980 to October 2012, and searched by using the following terms: (swine or pig or boar or Sus scrofa) and (zoonoses or zoonosis or zoonotic). Additional relevant articles and books published between 1970 and 2012 were identified by reviewing the references from the collection of reports and through examining the authors' collections of publications. We included other swine-associated zoonotic diseases by reviewing lists compiled by the World Organization for Animal Health (www.oie.int) and the Merck Veterinary Manual (http://www.merckmanuals.com). Once the list of zoonoses was identified, we performed disease specific literature reviews to gather epidemiology and population level disease burden data from PubMed, Google Scholar, and in authors' personal files using the following terms: (disease name or pathogen name) and (swine or pig or boar or Sus scrofa). We classified the swine-associated zoonoses in three major categories: emerging, endemic, and sporadic. An emerging zoonosis was defined when “the disease did not occur in humans before, or had occurred previously but affected only a small number of people in an isolated place, or had occurred in a population but was not recognized as a distinct disease”.[10] Diseases were defined as endemic where they appeared to cluster geographically but not in time and as sporadic when they were clustered only in time.[11] Zoonoses were sub-categorized into two groups: global occurrence and occurrence limited to a region(s) or geography. Additionally, we briefly reviewed the overall economic consequence data of swine zoonoses and swine-associated pathogens with zoonotic potential. To demonstrate global distribution of the swine-associated zoonoses, we performed “geographically weighted regression”, an exploratory spatial analysis to develop a risk map for the emerging, endemic, and sporadic swine associated zoonoses after adjusting for population and swine density (2011) for each of the countries.[12] We obtained human population density data from World Bank reports (www.worldbank.org), and pig density data from World Organization for Animal Health (www.oie.int). We did not obtain formal ethical approval because this study reviewed data from already published literatures. For this body of research, the role of the funding agencies was to provide monetary support only. They did not have any role in the project's conception, design, analysis, or manuscript preparation. A detailed list of the primary data and their references are included as supplementary materials to the manuscript.

EMERGING SWINE ZOONOSES

Emerging swine-associated zoonoses occurring worldwide

A number of emerging zoonotic swine pathogens are thought to have a worldwide distribution: hepatitis E virus (HEV), swine influenza viruses (SIV), livestock-associated methicillin-resistant Staphylococcus aureus (LA-MRSA), Streptococcus suis, Streptococcus porcinus, Clostridium difficile, Burkholderia pseudomallei, Cysticercus cellulosae (pork tapeworm), and Giardia intestinalis (Figure 1 and Supplementary Table S1).
Figure 1

Global distribution of swine-associated emerging zoonoses, 1970 to 2012. These estimates are adjusted for 2011 human and pig population density of each of the countries.

Hepatitis E virus

First isolated in 1997 in the United States (US), swine HEV infections have since been identified in numerous countries.[13] While data on human clinical infections with swine HEV is limited, experimental interspecies transmission of human and swine HEVs have been documented only between pigs and primates,[14,15,16] demonstrating their zoonotic potential. In addition, seroepidemiological studies have presented evidence of swine HEV infections among swine veterinarians,[17,18] indicating swine HEV may be causing asymptomatic infections in humans.

Influenza viruses

Since at least the 1918 influenza pandemic, public health professionals have been aware of cross-species influenza-like infections between man and pigs, but the connection was not evident until the 1920s when Dorset et. al. (1922) reported “hog flu”, later the experts began recalling similar illness in Iowa pigs five to six years before 1918 pandemic.[7,19,20] Pigs' susceptibility to both human and avian influenza viruses permit them to be infected with both mammalian and avian origin viruses. This may result in reassortment of genetic materials between multiple subtype and species adapted influenza viruses, leading to new influenza A viruses.[21] Beginning in 1958, serological studies started to report evidence of swine-origin influenza A virus in human and subsequently sporadic cases were intermittently detected.[22,23] A 2007 review of SIV infections in man documented 50 human infections, with a 14% case-fatality rate.[19] At that time such infections were generally perceived as rare and infrequent risk of human to human transmission. Since then, novel influenza virus detections have increased, and the reported numbers of swine-like influenza virus infections in man have tremendously escalated. Initial observations of high case fatality rates associated with human infection were likely biased in that novel influenza virus discovery was chiefly performed among those with serious illnesses. Later as molecular screening of influenza A strains became more widely available and surveillance increased more human SIV infections have been detected among persons with mild influenza disease. Recently, increased SIV detections among humans exposed to pigs at swine shows increased our awareness of SIV zoonoses, and it is clear that the influenza A viruses move both from pigs to man and from man to pigs.[19,24,25,26] In particular, the 2009 swine-like influenza A [A(H1N1)pdm09] pandemic heightened our awareness. First detected in North America (early 2009), these novel H1N1 swine-like viruses spread between humans within months to 214 countries[27] and by 2010, had caused an estimated 61 000 000 human infections; 274 000 hospitalizations; and 12 470 deaths.[28] Within five months of the first human infections, A(H1N1)pdm09 virus was also identified in pigs,[29,30] and now the virus is thought to be globally enzootic in many pig herds.[31,32] Novel reassortant progeny from the A(H1N1)pdm09 virus are now a major concern. For example, as of November 2013, at least 309 humans in 10 US states have now been found to be infected with influenza A H3N2 variant virus; a virus that continues to spread in the US.[33]

Methicillin-resistant staphylococcus aureus

Discovered in the early 2000's, evidence suggests that LA-MRSA evolved as methicillin-susceptible Staphylococcus aureus (MSSA) in humans, and through genetic mutation moved into livestock, and later acquired methicillin resistance.[34,35] Now identified in pigs in Asia, Europe and North America, LA-MRSA is often found colonizing noses and/or throats of pigs and may contribute to infection in persons occupationally exposed to pigs, as well as their household contacts.[36,37,38,39,40] In addition, an environmental survey illustrated airborne transmission and deposition of LA-MRSA for up to 300 meters around swine barns with LA-MRSA infected pigs,[41] further highlighting the public health risks for LA-MRSA exposure.

Emerging swine-associated zoonoses occurring in limited geographical locations

Emerging and re-emerging zoonotic swine pathogens with limited geographical distributions include Ebola Reston virus, Nipah virus, and Menangle viruses, which have the capability to cause severe diseases in humans and may have pandemic potential (Figure 2 and Supplementary Table S1).[42,43,44,45]
Figure 2

Global distribution of emerging swine-associated zoonoses occurring in limited geographical locations, 1970 to 2012. These estimates are adjusted for 2011 human and pig population density of each of the countries.

Ebola virus

Since 1976, repeated outbreaks of Ebola virus-Zaire have been reported in Africa causing 47%–100% mortality in man.[45,46] Pigs have shown the potential to transmit Ebola virus-Zaire to non-human primates.[47] Ebola-Reston viruses were first reported in an imported non-human primate in the US and later were detected in pigs in the Philippines. There have now been at least three reports documenting human infections with Ebola-Reston virus although none have been associated with pigs.[45,48,49] Experimentally, pigs are susceptible to both Ebola-Zaire and Ebola-Reston viruses,[50,51] so there are concerns that pigs could play a role in future human outbreaks.

Nipah virus

There are several emerging and re-emerging zoonotic paramyxoviruses which have involved pigs in their transmission cycle. During 1998–1999, Nipah virus was identified in Malaysia and Singapore causing widespread zoonosis. Spillover from Pteropus bats triggered an outbreak in the pig population in Malaysia in 1998. A high proportion of pigs experience morbidity to Nipah virus infection, however most cases recover after several days of clinical illness. This illness, however, decreases the economic value of the commercially farmed pigs. During the outbreak the virus rapidly spread among swine farms, when the farmers attempted to take sick pigs to market to minimize economic loss. Trading sick pigs accelerated Nipah virus spread across the country (north-to-south and to Singapore).[52] Overall human mortality due to Nipah viral infection was ∼40%. Having immediate contact with an infected pig was identified as a risk factor for Nipah virus infection,[53,54] however, a similar virus caused more than 70% case fatality among humans in Bangladesh where pig's role in the ecology of the virus remains obscure.[44,55,56]

Menangle virus

Another swine pathogen, the Menangle virus, known to cause reproductive loss and death in pigs, has recently infected at least two humans in Australia who were exposed to clinically ill pigs.[57,58] Although pig morbidity was as high as 90% in farms, the virus appears to have limited pig-to-human transmission capacity and seldom causes clinical illness in man.[58] About 33% of the fruit bats sampled from outbreak areas had neutralizing antibodies against the virus, suggesting that they potentially are a natural reservoir for the virus.[58]

ENDEMIC (NON-EMERGING SWINE ZOONOSES)

Endemic swine-associated zoonoses occurring worldwide

There exist numerous swine zoonoses that are distributed across multiple continents or at least several countries in a region (Figure 1). Human morbidity for these diseases is moderate to high with a low case fatality rate. This review for endemic swine zoonotic diseases highlights: brucellosis, Campylobacter enteritis, Escherichia coli infections, leptospiroses, listeriosis, pasteurellosis, salmonelloses, yersiniases, tuberculosis, erysipelas, West Nile virus infections, and echinococcosis (Supplementary Table S1).

Brucellosis

Each year, Brucella spp. cause more than 500 000 new cases of human brucellosis. Fortunately, the mortality remains low.[59,60,61] B. suis, the organism responsible for swine brucellosis occurs in many countries throughout the world. Abundance of wild and domestic pigs is a major driver for B. suis occurrence.[8,62] In South America, this organism has also adapted to cattle, resulting in more frequent disease outbreaks in those communities.[8] A retrospective cohort study in Argentina conducted between 2008–2011 studied human brucellosis cases from clinical samples and isolated B. suis biovar 1 in 53%, B. abortus in 27% cases and the remaining isolates were not typed.[63]

Campylobacter

Campylobacter is one of the most common human pathogens occurring globally, causing frequent gastrointestinal illness in humans.[64] It is estimated that approximately two million human cases of Campylobacter-related food-borne illness occurred in US in 1997; however, the number of cases has declined in recent years due to advances in food processing and chilling storage.[65] Foodborne outbreak investigation report from 1998–2011 suggests the majority of the human illnesses are attributed to C. jejuni, followed by C. coli. [66] A nationwide survey in Denmark demonstrated that thermophilic Campylobacter strains (C. jejuni, C. coli and C. lari) were present in 46% pigs sampled, but the serotypes commonly infecting human also came from broiler poultry and cattle.[67] However, C. coli is more commonly identified from pigs than C. jejuni.

Salmonellosis

Salmonella spp. are also a frequent cause of gastroenteritis in human.[8] During 2009, the US Center for Disease Control and Prevention (CDC) reported approximately 15 cases per 100 000 people in the US.[68] One US study identified approximately 3% of the pork products sold in supermarkets were contaminated with Salmonella.[69] A Dutch study estimated that 450 new Salmonella cases (per 100 000 persons) occur each year and 5%–25% of all the cases were associated with pork consumption.[70] However, it is estimated that only 5% of the Salmonella associated foodborne illnesses were attributed to pork.[71]

Parasitic zoonoses

Of the parasitic zoonoses, cystic echinococcosis (Echinococcus spp.) has multiple endemic foci with estimated annual human incidence rates of: 13–75 in European countries, 143 in South and Central America, 197 in East Asia, and 220 in Africa (per 100 000 population).[72] The G1, G7, and Lion strain of E. granulosus and E. multilocularis (European, and Hokkaido isolates) cause swine-associated echinococcal zoonoses.[72] Recent studies conducted in China and European countries suggested high variance in the echinococcosis prevalence [0.15%–66%] in pigs.[73,74] In Lithuania echinococcosis was more common in family owned pig farms than the industrial pig farms (13.2% versus 4.1%).[73] Other swine-associated parasitic zoonoses include cryptosporidiasis, trichinellosis, and toxoplasmosis which have a global distribution (Supplementary Table S1).

Endemic swine-associated zoonoses occurring in limited geographical locations

There are several swine-associated zoonoses endemic in specific regions of the world. This geographical isolation is due to the abundance of reservoirs and vectors, ecological factors, husbandry practices, and specific human behaviors facilitating zoonotic transmission of the diseases (Supplementary Table S1).

Yersiniosis

Food-borne bacterial enteritis caused by Yersinia enterocolitica are almost always associated with pigs or under-cooked pork products.[75,76] This psychrophilic pathogen is mostly found in Canada, the western coast of South America, Europe, Australia, New Zealand, and South Africa.[77,78,79] Yersinia pseudotuberculosis, has been frequently identified in Europe and parts of Asia, and occurs sporadically in the US. Pseudotuberculosis is commonly identified in rodents, and they are the probable source of infection among pigs. Humans often become infected via contaminated food and water.[7]

Tularemia

The zoonotic bacteria Francisella tularensis causes infections most prevalent in the US and Russia, and are sporadically reported in other Northern Hemisphere, including Scandinavia, the Czech Republics, Austria, Germany and Japan.[8] However, recent reports suggest the pathogen is enzootic in Turkey, Yugoslavia, Spain, Kosovo, and Switzerland.[80] More than 125 species of domestic and wild animals are reservoirs for this pathogen. Clinical and serological studies have identified F. tularensis infection both in wild and domestic pigs.[81,82] Transmission of this pathogen occurs via all major routes and is remarkably efficient in transmitting itself from one host to another via all major transmission routes (Table 1).[8]
Table 1

Mode of exposure/transmission of the selected pathogens from pigs to man.

The dark shade indicates an established or primary route of transmission. The lighter shade indicates a suspected route of transmission.

? denotes limited data, findings remain suspected.

Japanese encephalitis

Japanese encephalitis virus is endemic in the southern and eastern part of Asia, and the Pacific.[83] About one half of the global population are in the endemic region and about 30 000–50 000 new human cases occur annually in Asia, with 10 000 deaths, and about 15 000 cases develop permanent neurological and psychiatric sequelae.[84,85] Factors, such as presence of abundant natural reservoirs (e.g. pigs and wading ardeid water birds) and vectors mosquitoes, that prefer to breed in the irrigated rice paddy fields in close proximity to humans, have contributed to the maintenance of the pathogen's transmission cycle.[84]

Vesicular stomatitis

Vesicular stomatitis virus infects pigs, cattle, horses, and human in the countries of North and South America, Africa, and Asia.[7] Humans generally remain asymptomatic during infection, however, a small fraction of those infected may exhibit influenza-like-illness and hemorrhagic fever.[8] This virus has been identified in multiple wild and domestic mammals, arthropod vectors (particularly Phlebotomus), and shown to infect humans through direct contact, transdermal, and transcutaneous routes.[8,86] Commonly occurring swine-associated parasitic diseases are predominantly seen in focal parts of Asia (Figure 3). These include giant intestinal fluke, Asian taeniasis, gastrodiscoidiasis, Chinese liver fluke, and schistosomiasis. These diseases are frequently seen in Eastern Asia, Southeast Asia, Kazakhstan, and Russia's Volga Delta region, and in Eastern Siberia.[8,87,88,89,90,91,92,93] Multiple factors were related to elevated risk of human infection: the parasite is enzootic in animal reservoirs (including pigs) and in the environment; poor animal husbandry and particular risk behaviors like improper sanitation causing animal excreta to contaminate soil, water, aquatic plants, and other animals; ingestion of water plants, and animal products contaminated with infective states of the parasites; consuming raw or undercooked food; and occupational hazards such as agricultural workers and freshwater fishing.[8,88,90,92,93] In summary, primitive pig production practices accompanied by poor sanitation and hygiene may lead to increased regional parasitic infection.
Figure 3

Global distribution of endemic swine-associated zoonoses occurring in limited geographical locations, 1970 to 2012. These estimates are adjusted for 2011 human and pig population density of each of the countries.

Common routes of transmission for endemic swine-associated zoonoses

Globally enzootic swine-associated pathogens commonly transmit to man via direct contact, food and water contamination, fecal-oral transmission, and sometimes vector-borne routes (Table 1). Corresponding swine-associated zoonotic pathogens that are confined to specific geographic regions are more often influenced by factors affecting their ecological niches, such as vector-reservoir abundance, climatic factors, and human behaviors, particularly that of consuming undercooked food.[7,8,92]

SPORADIC SWINE ZOONOSES

Sporadic swine-associated zoonoses occurring worldwide

The majority of the swine-associated zoonoses that are sporadic in nature have a worldwide distribution. Influenza B and C viruses, clostridial infection, dermatophytosis (except Microsporum canis), sarcosporidiosis, and balantidiasis, all fall into this category (Supplementary Table S1). While the zoonosis due to influenza B virus is somewhat controversial, the influenza C virus has shown to infect both humans and pigs.[94,95,96] Nevertheless, these viruses cause low morbidity and mortality in both species.[97,98]

Tetanus

Tetanus caused by Clostridium tetani occurs globally, but most often in developing countries among rural population with poor vaccination and public health infrastructure.[99] According to World Health Organization (WHO), there were 14 132 reported cases worldwide in 2011 and 61 000 estimated deaths in children aged <5 years.[100] Domestic animals such as cattle and horses are highly susceptible to clostridial infection and contaminate the environment through fecal shedding. In the high prevalence areas like New Guinea, pigs are reported to have contributed to the zoonotic transmission of C. tetani.[99]

Ringworm

The majority of the species of zoonotic ringworm causing fungi (Microsporum nanum, M. gypseum, Trichophyton mentagrophytes, T. rubrum, and T. verrucosum) occur worldwide,[101] although M. canis seems limited to North and South America, Europe, and Africa.[102] Pigs are the reservoir for M. nanum, but are also susceptible to the other species. This fungus has a broad spectrum of hosts including mammals and rodents.[101] It is highly contagious among animal populations and often crosses the species barrier to infect humans via contaminated fomites. Although the mortality due to this ringworm is low, the cost of treatment puts this disease in the high economic burden category.[7]

Parasitic infections

Sarcosystis spp. cause zoonoses worldwide and pigs are the intermediate host for one of the causal organisms, S. suihominis. This is transmitted when humans consume undercooked pork.[7] The protozoa is generally absent among swine herds that are raised under good hygienic conditions; however, a study in Germany showed that about 30%–40% of some swine herds may carry this zoonotic pathogen.[8] Balantidium coli occurs worldwide, particularly in regions with a temperate or subtropical climate.[8] Swine are the primary host for this ciliated protozoon. Disease prevalence in humans is less than 1%, but may be markedly higher in endemic regions.[103] Most human infections are asymptomatic or limited to mild diarrhea and abdominal discomfort. However, in rare instances, the protozoa may lead to hemorrhagic lesions in the intestine, perforation, secondary bacterial infection, and generalized peritonitis.[104]

Sporadic swine-associated zoonoses occurring in limited geographical locations

The numbers of sporadically occurring zoonoses limited to particular regions are few. These zoonoses are primarily influenced by the abundance of reservoirs, and by particular human behaviors exposing them to the pathogen. One example is Pasteurella aerogenes infection, which is occasionally reported only from European countries.[105] This organism is infrequently identified in swine as a normal oral and intestinal flora.[106,107] In Europe, swine workers have acquired infection through bites from pigs.[105]

SWINE-ASSOCIATED ZOONOSES WITH LIMITED ZOONOTIC POTENTIAL

Rotavirus

Rotavirus frequently causes diarrhea in children under five years of age.[108] It is most concerning in the less developed countries within Asia and sub-Saharan Africa.[108] Rotavirus strains G3, G5, and G9, are predominantly found in pigs and other animal reservoirs. Recent evidences suggest that these viruses may exchange genetic materials with human viruses and cause increased human morbidity.[109]

West Nile virus

West Nile virus commonly occurs in Africa, Asia, Europe, and Australia, and it recently emerged and established itself in North America.[110] The virus causes clinical signs of disease in only about 20%–30% the infected humans.[111,112,113] Symptoms may range from uncomplicated fever to fatal encephalitis. Although laboratory studies suggest pigs develop enough viremia to play the role of a reservoir, the role of domestic pigs in the West Nile virus transmission remains obscure.[7,113]

Pseudorabies virus

Since 1914, there are several anecdotal reports of pseudorabies (Aujeszky's disease) in humans.[114] Between 1983 and 1986, three suspected human cases of pseudorabies were identified in Europe. Each of these patients had a history of having direct contact with cats and other domestic animals. Researchers followed up the cases and identified pseudorabies antibodies through neutralization and immunoprecipitation assays, 5–15 months after clinical onset of illness.[115] However, later serological studies were unable to detect pseudorabies antibodies in occupationally exposed populations.[114] Pigs are the only reservoir for this virus.[7]

Norovirus

Typically, swine norovirus is only detected in fecal samples of apparently healthy adult pigs; however, experimental infections have resulted in mild gastroenteritis.[116] Even though swine norovirus has not been found to cause illness in humans, antibodies against human norovirus strains have been detected in pigs.[116] Because human norovirus strains are able to replicate in pigs, there is a potential for human and swine norovirus exchanging genetic material inside a swine host resulting in novel norovirus strains with zoonotic potential.[117]

Hendra virus

Hendra virus has caused recent sporadic equine and human outbreaks in Australia with a ∼40% case fatality rate in man.[118] While Hendra virus infections have chiefly involved horses and man, laboratory studies show that pigs are susceptible to infection, which enables pigs to be a potential candidate to play a role in the disease ecology.[119]

Henipa-like virus

Recent studies identified evidence of henipa-like virus infections in pigs in Ghana and Bangladesh.[56,120] Although evidence of human infection was not yet assessed in these studies, the report of this virus in pigs concerned public health experts as other henipa-like viruses may infect humans. Hendra and Nipah viruses (Henipaviruses) have caused zoonoses in Australia, Malaysia, Singapore, India, and Bangladesh.[121] Nipah viruses caused 283 human cases and 109 deaths in Malaysia and Singapore during the 1998–1999 outbreaks.[122] Laboratory studies also confirmed that pigs are capable of being infected with Hendra viruses which naturally infect fruit bats, horses, and have caused multiple human outbreaks in Australia.[119]

Xenotransplantation-associated zoonoses

Xenotransplantation, the process of using animal tissues or organs in man, has increased during last 100 years.[5] Pig organs and tissues have become one of the most frequent transplant source in xenotransplantation. This additional pathway of transmission may enable certain pathogens to move from pigs to man. Retroviruses are a particular concern because of their history of crossing species barriers. It was hypothesized that the human immunodeficiency virus (HIV) and human T-cell leukemia virus have likely derived from simian immunodeficiency virus and simian T-cell leukemia virus, respectively.[123,124] Studies suggest that porcine endogenous retroviruses may find its way to human hosts in the same manner.[125] An in vitro study showed that human fibroblasts were susceptible to porcine lymphotropic herpesvirus and could be activated through xenotransplantation.[125,126] Genotype 3 of HEV is most commonly identified in pigs in Europe and genotype 1 is common in humans.[127,128] Recent studies suggest that HEV (particularly the genotype 3) infections are more commonly associated with organ allotransplant recipients.[129,130] Emerging pathogens such as lymphocytic choriomeningitis virus and swine torque teno viruses have shown to infect humans through swine xenotransplantation deteriorating the immune systems of the HIV/AIDS patients and leading to death.[131,132] Considering these pathogens as zoonotic should raise public health concerns and lead to defining pathogen-free swine stock for xenotransplantation.

ECONOMIC CONSEQUENCES OF SWINE ASSOCIATED ZOONOSES

Many of the emerging and re-emerging zoonoses causing diseases in humans and pigs have potential to cause severe economic consequences because of the mortality and production loss in pigs, trade sanctions on exporting animal products from an infected country or region, public health concerns leading to pig culling operations and reduced pork consumption, and public health burden of the diseases.[43,58,133] Often the decisions to control a disease using drastic measures are influenced by cultural and community context.[53,134,135] During the 1998–1999 Nipah outbreaks in Malaysia and Singapore, millions of pigs were culled to contain the outbreak that spread through the trade of sick pigs.[53] This resulted in an estimated loss of USD $97 million and a drop in local pork consumption by 80%.[136] Following the news on pandemic influenza H1N1 [A(H1N1)pdm09] outbreaks in April 2009, the reference to “swine flu” caused US pork prices to decline, reaching a low of USD $0.49 per lb in August 2009, which was about one half of the previous year's price (Figure 4). Twenty-seven countries imposed import restrictions for US pork products.[137] Although there were several other reasons for the price drop, pandemic influenza H1N1 [A(H1N1)pdm09] likely contributed to the majority of the loss. The National Pork Board estimates US pork producers lost an estimated $13.64 per head from April 24 to May 2, 2009 and the industry accumulated some USD $7.2 million in losses daily (personal communication: National Pork Board, US 2009). An excessively cautious response was observed in Egypt during the 2009 pandemic when the country culled its entire swine population over concerns that the pandemic influenza virus in pigs would pose a major public health concern.[138] In the US, swine brucellosis outbreaks caused considerable economic losses during the 1920–1950s. The country mostly eradicated the disease through changes in management and regulations; however, this disease continues to cause production losses in South America, most countries of Europe (except Britain and Scandinavia), Africa, and Southeast Asia.[7,139] Cost effectiveness analyses of the swine-associated diseases' eradication programs may encourage a country or region to allocate sufficient resources to eradicate diseases posing public health threats.
Figure 4

Emergence of pandemic influenza 2009 [A(H1N1)pdm09] in US human and pig population and the US pork price (negotiated carcass price) December 2007–2010.

In addition to the economic losses for the swine industry, swine zoonoses also cause human morbidity and mortality which have major economic consequences. However, for simplicity sake, we did not include the human economic consequences in these estimates.

DISCUSSION

In this report, we have described the epidemiology, geographical distributions, and economic consequences of major swine zoonoses. We have summarized the mechanisms of disease transmission along with the ecological and behavioral factors influencing the process. Our goal was to inform medical, veterinary, epidemiology, microbiology, and social science experts of the established and emerging threats common for humans and swine, as well as to shed light on some pathogens that may be potential future threats. The majority of emerging human pathogens are zoonotic.[140] Frequently changing husbandry practices and environmental factors (e.g. large scale domestic animal production, urbanization, interaction between wild and domestic swine populations with humans, population increases, etc.) may predispose humans and pigs to pathogens common to other species, or may allow for the adaptation of these organisms to humans or swine. Being omnivorous and having the anatomy and physiology similar to that of man, pigs are a good medium for the adaptation and increase in virulence of organisms that have so far not been identified as human pathogens.[3] Moreover, with the increase in human populations, consumption of pork and pork products has increased markedly in the last one hundred years.[2] Additionally, the scientific breakthrough that allowed xenotransplantation of porcine organs, tissues, and porcine hormones in human medicine, has opened a new pathway for future cross-species transmission of swine pathogens currently not common to humans.[5] Pathogens that first emerged in wild species and in a particular geographical region and gained the ability to infect domesticated pigs may spread to a wider territory by the trade industry of food and livestock.[52,141] Moreover, pathogens that adapt to and become established in swine have a much higher probability of spreading to humans, due to the intensity of swine farming worldwide and the close contact between pigs and humans. Swine workers are constantly exposed to bodily fluid secretions from a wide variety of swine products, and sometimes may become exposed to pathogens in ways that do not occur in natural conditions (e.g. respiratory spread of fecally-shed pathogens or aerosolization of organ fluids during slaughter house operations). Since their emergence, many of the swine-associated zoonoses have been infrequently considered as causes of human illness, especially among populations of humans that are occupationally and traditionally exposed to pigs or raw pig products. In several Asian countries, some parasitic swine zoonoses (e.g. trichinellosis, teniasis/cisticercosis) are quite common because of human food habits, particularly eating raw and undercooked food.[7,8,87] Although pigs are one of the major sources of animal protein globally, and the industry represents a large portion of the economy for many countries, steps should be taken to minimize swine-associated zoonoses of public health concern. A solution to this requires uniform understanding and consensus between the swine industry, farmers, veterinarians, clinicians, public health professionals, and other stakeholders. Addressing these complex issues requires integrative and cross-disciplinary efforts to achieve optimum health for people, pigs and their environment through the “One Health” approach.[142] Such an interdisciplinary, and inter-institutional collaborative approach provides a united platform upon which stakeholders can come together as collaborators, develop a more complete understanding regarding a complex problem, and tackle these problems with carefully designed, multiple interventions. Such a collaborative strategy has potential to gain much wider acceptability among swine farmers, the swine industry, as well as among public health professionals. Embracing the principles of “One Health” will improve swine zoonoses surveillance, raise stakeholders' awareness on swine-associated zoonoses, help reduce risky behaviors associated with swine production and pork consumption, encourage improved personal hygiene, and demonstrate the need for cost-benefit analyses of swine pathogen control efforts.
  112 in total

1.  Distribution of serotypes of Campylobacter jejuni and C. coli from Danish patients, poultry, cattle and swine.

Authors:  E M Nielsen; J Engberg; M Madsen
Journal:  FEMS Immunol Med Microbiol       Date:  1997-09

Review 2.  Brucellosis.

Authors:  Georgios Pappas; Nikolaos Akritidis; Mile Bosilkovski; Epameinondas Tsianos
Journal:  N Engl J Med       Date:  2005-06-02       Impact factor: 91.245

3.  Seroepidemiological study of filovirus related to Ebola in the Philippines.

Authors:  M E Miranda; M E White; M M Dayrit; C G Hayes; T G Ksiazek; J P Burans
Journal:  Lancet       Date:  1991-02-16       Impact factor: 79.321

4.  Transmission of lymphocytic choriomeningitis virus by organ transplantation.

Authors:  Staci A Fischer; Mary Beth Graham; Matthew J Kuehnert; Camille N Kotton; Arjun Srinivasan; Francisco M Marty; James A Comer; Jeannette Guarner; Christopher D Paddock; Dawn L DeMeo; Wun-Ju Shieh; Bobbie R Erickson; Utpala Bandy; Alfred DeMaria; Jeffrey P Davis; Francis L Delmonico; Boris Pavlin; Anna Likos; Martin J Vincent; Tara K Sealy; Cynthia S Goldsmith; Daniel B Jernigan; Pierre E Rollin; Michelle M Packard; Mitesh Patel; Courtney Rowland; Rita F Helfand; Stuart T Nichol; Jay A Fishman; Thomas Ksiazek; Sherif R Zaki
Journal:  N Engl J Med       Date:  2006-05-25       Impact factor: 91.245

Review 5.  An overview of the epidemic of highly pathogenic H5N1 avian influenza virus in Egypt: epidemiology and control challenges.

Authors:  E M Abdelwhab; H M Hafez
Journal:  Epidemiol Infect       Date:  2011-02-01       Impact factor: 2.451

6.  Reduced efficacy of ganciclovir against porcine and baboon cytomegalovirus in pig-to-baboon xenotransplantation.

Authors:  Nicolas J Mueller; Kristen Sulling; Bernd Gollackner; Shin Yamamoto; Christoph Knosalla; Robert A Wilkinson; Amitinder Kaur; David H Sachs; Kazuhiko Yamada; David K C Cooper; Clive Patience; Jay A Fishman
Journal:  Am J Transplant       Date:  2003-09       Impact factor: 8.086

7.  Echinococcosis in pigs and intestinal infection with Echinococcus spp. in dogs in southwestern Lithuania.

Authors:  R Bruzinskaite; M Sarkūnas; P R Torgerson; A Mathis; P Deplazes
Journal:  Vet Parasitol       Date:  2008-11-17       Impact factor: 2.738

Review 8.  Porcine endogenous retrovirus and other viruses in xenotransplantation.

Authors:  Linda Scobie; Yasuhiro Takeuchi
Journal:  Curr Opin Organ Transplant       Date:  2009-04       Impact factor: 2.640

9.  Recurrent zoonotic transmission of Nipah virus into humans, Bangladesh, 2001-2007.

Authors:  Stephen P Luby; M Jahangir Hossain; Emily S Gurley; Be Nazir Ahmed; Shakila Banu; Salah Uddin Khan; Nusrat Homaira; Paul A Rota; Pierre E Rollin; James A Comer; Eben Kenah; Thomas G Ksiazek; Mahmudur Rahman
Journal:  Emerg Infect Dis       Date:  2009-08       Impact factor: 6.883

10.  Past, present, and future of Japanese encephalitis.

Authors:  Tobias E Erlanger; Svenja Weiss; Jennifer Keiser; Jürg Utzinger; Karin Wiedenmayer
Journal:  Emerg Infect Dis       Date:  2009-01       Impact factor: 6.883

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  11 in total

1.  Zoonotic Diseases from Horses: A Systematic Review.

Authors:  Alexandra Sack; Fatai S Oladunni; Battsetseg Gonchigoo; Thomas M Chambers; Gregory C Gray
Journal:  Vector Borne Zoonotic Dis       Date:  2020-02-20       Impact factor: 2.133

2.  Transcription elements AREB6 and miR-34a affect apoptosis of PAMs by regulating the expression of SS2-related gene PPP1R11.

Authors:  Guisheng Liu; Junjing Wu; Mu Qiao; Jiawei Zhou; Huayu Wu; Xianwen Peng; Supamit Mekchay; Shuqi Mei
Journal:  Cell Cycle       Date:  2019-05-01       Impact factor: 4.534

3.  Nutrient loads of small-scale swine manure composting to groundwater and its prevention by covering: a case study.

Authors:  Jianbo Cheng; Junjing Qiao; Yucheng Chen; Zhimin Yang
Journal:  Environ Sci Pollut Res Int       Date:  2015-05-28       Impact factor: 4.223

Review 4.  Invited review: strategic adoption of antibiotic-free pork production: the importance of a holistic approach.

Authors:  John F Patience; Alejandro Ramirez
Journal:  Transl Anim Sci       Date:  2022-05-16

Review 5.  Zoonotic and reverse zoonotic transmission of viruses between humans and pigs.

Authors:  Helena Aagaard Glud; Sophie George; Kerstin Skovgaard; Lars Erik Larsen
Journal:  APMIS       Date:  2021-10-18       Impact factor: 3.428

6.  Molecular detection of porcine Enterocytozoon bieneusi infection in Peninsular Malaysia and epidemiological risk factors associated with potentially zoonotic genotypes.

Authors:  K Ruviniyia; D A Abdullah; S Sumita; Y A L Lim; P T Ooi; R S K Sharma
Journal:  Parasitol Res       Date:  2020-03-26       Impact factor: 2.289

7.  Dynamics of Japanese encephalitis virus transmission among pigs in Northwest Bangladesh and the potential impact of pig vaccination.

Authors:  Salah Uddin Khan; Henrik Salje; A Hannan; Md Atiqul Islam; A A Mamun Bhuyan; Md Ariful Islam; M Ziaur Rahman; Nazmun Nahar; M Jahangir Hossain; Stephen P Luby; Emily S Gurley
Journal:  PLoS Negl Trop Dis       Date:  2014-09-25

8.  Mapping the spatial distribution of the Japanese encephalitis vector, Culex tritaeniorhynchus Giles, 1901 (Diptera: Culicidae) within areas of Japanese encephalitis risk.

Authors:  Joshua Longbottom; Annie J Browne; David M Pigott; Marianne E Sinka; Nick Golding; Simon I Hay; Catherine L Moyes; Freya M Shearer
Journal:  Parasit Vectors       Date:  2017-03-16       Impact factor: 3.876

Review 9.  Global Status of Porcine circovirus Type 2 and Its Associated Diseases in Sub-Saharan Africa.

Authors:  Kayode O Afolabi; Benson C Iweriebor; Anthony I Okoh; Larry C Obi
Journal:  Adv Virol       Date:  2017-03-12

10.  A feasibility study of conducting surveillance for swine pathogens in slurry from North Carolina swine farms.

Authors:  Emily S Bailey; Laura K Borkenhagen; Jessica Y Choi; Annette E Greer; Marie R Culhane; Gregory C Gray
Journal:  Sci Rep       Date:  2020-06-22       Impact factor: 4.379

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