Chapter 3 Trends in Incidence of Zoonotic Foodborne Diseases in the United States in 2010–2019

In: Economics and Mathematical Modeling in Health-Related Research
Authors:
Sayansk Da Silva
Search for other papers by Sayansk Da Silva in
Current site
Google Scholar
PubMed
Close
and
Joseph E. Hibdon Jr.
Search for other papers by Joseph E. Hibdon Jr. in
Current site
Google Scholar
PubMed
Close
Open Access

Abstract

Zoonotic foodborne diseases are infections of the gastrointestinal tract that occur as a result of the ingestion of food containing pathogens that are transmitted between non-human animals and people. With the growing concern about food safety and zoonotic diseases, it is imperative to keep these illnesses under surveillance in order to develop an efficient program for control and prevention. In this work, we examine trends in the occurrence of nationally notifiable zoonotic foodborne diseases during 2010–2019 by using data retrieved from databases from the Centers for Disease Control and Prevention. We focused on some of the foodborne diseases that are particularly relevant to public health authorities: salmonellosis, Shiga toxin-producing Escherichia coli (STEC) infection, campylobacteriosis, listeriosis, and vibriosis. We analyzed the relationship between the number of cases of these diseases and the per capita consumption of animal products. Additionally, the US data on foodborne diseases were compared to the data from other countries. The results show that from 2010 to 2019 the incidence of vibriosis more than tripled and the incidence of STEC infection more than doubled. Listeriosis accounted for the lowest incident rates, ranging from 0.23 to 0.28. There is a positive association between the consumption of animal products and foodborne diseases such as STEC infection. The data shows that the incidence of these diseases is increasing and indicates that greater public health efforts are necessary to control these illnesses.

1 Introduction

Foodborne diseases (FBDs) can be described as pathological alterations that arise as a result of the ingestion of contaminated food. This contamination may be associated with a variety of causes including harmful microorganisms, toxins, and substances that can cause harm to the human body. The most common signs and symptoms of these diseases are associated with the gastrointestinal tract; including nausea, diarrhea, and vomiting as manifestations most frequently reported. Besides the gastrointestinal symptoms that are commonly seen, foodborne pathogens can also affect other parts of the body such as cardiovascular, respiratory, and musculoskeletal systems (Kuchenmüller, 2013). Although global food safety awareness has increased over the decades, FBDs constitute an economic and public health issue in many countries around the world. Their impact is particularly concerning in low- and middle-income countries where strategies for disease surveillance are not well established. International organizations such as the World Health Organization (WHO) and the Food and Agriculture Organization of the United Nations (FAO) have determined methods to analyze and keep track of specific FBDs.

The WHO (2015) estimated that about 600 million cases of illnesses caused by foodborne hazards occurred globally in 2010. Over 90% of these cases were caused by infectious agents that provoke diarrhea, and zoonotic pathogens represented the main microorganisms involved in this public health issue (WHO, 2015). The Joint WHO/FAO Expert Committee in Zoonoses (1959) described zoonoses as infections and diseases that are naturally transmitted between animals and people. The transmission of these infectious diseases is intimately related to the domestication of animals, which brings together humans and several other species of vertebrates. This close contact may have changed the dynamics of animal-human interactions in a way that facilitated the transmission of diseases from domestic animals to people. Although the domestication process had different purposes, animals farmed for food include important reservoirs for multiple foodborne microorganisms.

2 Zoonotic Foodborne Diseases

Zoonotic foodborne pathogens include a variety of infectious agents such as bacteria (e.g. Campylobacter jejuni), viruses (e.g. norovirus), and parasites (e.g. Taenia solium). However, the most common zoonotic FBDs have their etiology attributed to bacterial pathogens (European Food Safety Authority, n.d.). Moreover, these microorganisms are the leading cause when it comes to diseases transmitted through food, being responsible for more than 65% of the reported outbreaks of FBDs (Le Loir et al., 2003). Of every 10 diseases in humans, six are considered zoonotic (Phillips, 2021) with many of them being transmitted through food and water. The importance of zoonotic FBDs has been recognized at local, national, and global levels. In the United States (US), for example, salmonellosis occupies the second position in the list of top zoonotic diseases of national concern (Animal and Plant Health Inspection Service, 2020; Centers for Disease Control and Prevention [CDC], 2020).

2.1 Zoonotic Foodborne Parasites

Protozoan and helminth species of internal parasites are the organisms involved in parasitic foodborne infection in people (Murrel, 2013). Although there are divergences in terms of classifications, the Protozoa are considered to be a subkingdom of the Protista kingdom and include a variety of unicellular eukaryotic organisms (Yaeger, 1996). They are mainly microscopic organisms, and most parasitic protozoa in people have a size less than 50 micrometers (Singleton, 2018). On the other hand, helminths are multicellular organisms that are classified into two phyla: Nemathelminthes (roundworms) and Platyhelminthes (flatworms) (Mahamud et al., 2018). Nemathelminthes include approximately 500,000 species, and they can cause disease to plants, animals, and humans (John & Petri, 2020). Platyhelminths are one of the largest animal phyla and include over 20,000 species (Adell et al., 2015). The diseases caused by some parasites are classified as neglected tropical diseases, which are a group of diseases that primarily affect poor populations living in tropical and subtropical climates (WHO, 2012). This group of diseases include important zoonotic foodborne parasites such as species from the Echinococcus and Taenia genera.

2.2 Bacterial Zoonotic Foodborne Pathogens

Bacteria are prokaryotic microorganisms that have different morphologic characteristics, which are analyzed as part of their identification process. Bacteria cells have different shapes with the most common being rods, spheres, and spirals. Although their cell structure may appear simple when compared to eukaryotic cells, bacteria have a complex set of components that can determine how dangerous they are to humans. The cell wall of these microorganisms is organized in two basic forms that are defined based on the results of the Gram staining technique. Gram-positive bacteria have a cell wall with a thick layer of peptidoglycan whereas those that are Gram-negative have a thin layer of peptidoglycan and an outer membrane that is not found in Gram- positive cells.

Additionally, bacteria may carry extracellular components such as fimbriae, flagella, and capsules, which offer structural support and facilitate the agent-host interaction through bacterial colonization, mobility, and exchange of genetic materials (Bhunia, 2018a). Some surface structures are important virulence factors that give bacteria the ability to infect the host, cause disease, and bypass the immune system defenses. The pathogenicity of bacteria that cause FBDs rely on their capacity to penetrate, survive, and multiply in hosts cells along with their ability to produce toxins (Le Loir et al., 2003). Besides pathogens’ virulence factors, the host characteristics including age and immune status are also factors that need to be considered in the dynamics of FBDs.

The most common species of bacteria involved in FBDs include Salmonella enterica, Escherichia coli, and Campylobacter jejuni (Bintsis, 2017; WHO, 2020a; Zhao et al., 2014). Other pathogens with relevance to public health are species from the Vibrio genus and Listeria monocytogenes. All these microorganisms are considered important causative agents of zoonotic FBDs, and they are also responsible for economic and production losses in animal farming. Additionally, even though these pathogens can infect humans through the ingestion of contaminated food, people may become infected through different routes including direct interaction with infected animals. Moreover, food may become contaminated due to cross-contamination where bacteria on surfaces, for example, may be transferred to food during the preparation process. S. enterica serovar Enteritidis and Campylobacter jejuni have been noted to continue to be viable on dry stainless-steel surfaces at room temperature and represent a possible cross-contamination risk (Stein & Chirilã, 2017).

Table 3.1
Table 3.1

Summary of important zoonotic foodborne bacteria

Source: Authors’ elaboration

2.2.1 Salmonella spp.

Salmonellae are Gram-negative, rod-shaped bacilli that are taxonomically divided into two species: S. enterica and S. bongori (CDC, 2019a). The former is classified into six subspecies that can be distinguished from each other with the use of biochemical tests: S. enterica subsp. enterica, S. enterica subsp. salamae, S. enterica subsp. arizonae, S. enterica subsp. diarizonae, S. enterica subsp. houtenae and S. enterica subsp. Indica (Grimont & Weill, 2007). Additionally, Salmonella is a facultative intracellular microorganism that can colonize the intestinal tract of a variety of homoeothermic and poikilothermic animals (Liu, 2018). More than 2,500 serovars of Salmonella have been reported worldwide and categorized based on somatic (O) and flagellar (H) antigens (Agbaje et al., 2011). The majority of the isolates that cause disease in mammals including humans belong to S. enterica subsp. enterica, and the nontyphoidal Salmonella serovars represent the group that are zoonotic or potentially zoonotic (The Center for Food Security & Public Health, 2013).

Common sources of contaminated food include eggs, poultry, and beef, and infection occurs in the summer months with higher frequency (CDC, 2019a). Usually, an infectious dose greater than 50,000 bacterial cells is necessary to set off a disease in humans, and the onset of symptoms occur between 6 to 72 hours after the consumption of contaminated food (Coburn et al., 2007). The clinical manifestations of FBDs are generally associated with alterations in the gastrointestinal system. However, individuals in high-risk groups such as those that are immunocompromised and the elderly may develop bacteremia as a complication of an infection caused by nontyphoidal Salmonella (Acheson & Hohmann, 2001).

The diagnostic of salmonellosis can be done through laboratory tests that detect bacterial cells or genetic material in stools, body tissue, or fluids of people who have been infected (CDC, 2019b). The traditional Salmonella culture method include pre-enrichment, selective enrichment, isolation of pure culture, biochemical tests, and serological confirmation (Bhunia, 2018b). Other methods used to identify and categorize salmonellae are polymerase chain reaction (PCR) and real-time PCR assays that work by targeting a variety of Salmonella genes including 16S rRNA, agfA, and viaB (Gwida & Al-Ashmawy, 2014). Preventive and control measures include rigorous strategies throughout the food chain in order to avoid food contamination. Furthermore, basic hygiene practices and avoiding the consumption of raw animal products are examples of preventive measures that can be adopted by the general population.

2.2.2 Escherichia coli

The Escherichia genus is currently divided into five species: E. albetii, E. coli, E. fergusonii, E. hermanii, and E. vulneris (Schmidt, 2019). The species E. coli is one of the most studied in this genus, particularly in research that investigates its role in cases of FBDs. E. coli is a Gram-negative, facultative anaerobic bacillus that can be either motile or nonmotile (Desmarchelier & Fegan, 2011). This bacillus can be found in the gastrointestinal tract of a variety of species including humans, cattle, goats, and pigs. Even though most strains of E. coli are harmless, some strains are involved in cases of severe illnesses in people (WHO, 2018a). The strains of this species are serologically differentiated by O, H, and capsular (K) antigens (Nataro & Kaper, 1998). Over 700 serotypes have been identified so far, and as to serotyping strains of E. coli associated with diarrheal disease, it is necessary to determine only the O and H antigens (Doyle et al., 2020).

The term diarrheagenic E. coli is commonly used to classify the strains of this species responsible for causing gastrointestinal infections. The groups of strains of diarrheagenic E. coli can be differentiated based on their virulence factors and pathogenesis, and they include enteropathogenic E. coli (EPEC), Shiga toxin-producing E. coli (STEC), enteroinvasive E. coli (EIEC), enteroaggregative E. coli (EAEC), enterotoxigenic E. coli (ETEC), diffusely-adherent E. coli (DAEC), and adherent-invasive E. coli (AIEC) (Croxen et al., 2013; Nataro & Kaper, 1998). The STEC pathotype is also known as Verocytotoxin-producing E. coli (VTEC) or enterohemorrhagic E. coli (EHEC), and it is the group most commonly linked to foodborne outbreaks (CDC, 2014). As suggested by its name, the nomenclature of this group refers to an E. coli strain that acquired the capacity to produce Shiga toxin (Stx) through the transfer of one or both genes (i.e. stx1a and stx2a) by a Stx phage (Byrne et al., 2015; Petro et al., 2019; Travert et al., 2021). STEC is naturally found in the microbiota of ruminants, which are the most important reservoirs of this zoonotic pathogen (Ballem et al., 2020). Additionally, E. coli O157:H7 is the most important and frequently isolated serotype of STEC (Siddiqui & Yuan, 2021; Tian et al., 2018). Moreover, the low infectious dose of E. coli O157:H7 may be one of the factors why this serotype is involved in many outbreaks. As few as 10 viable bacterial cells have the potential to cause disease in humans (Ameer et al., 2021; Etcheverria & Padola, 2013).

The clinical manifestations of STEC infection comprise of severe stomach cramps, diarrhea, vomiting, and, in some cases, fever (CDC, 2014). Between 5 and 15% of the patients that have symptomatic STEC infection develop a severe condition known as hemolytic uremic syndrome (HUS), which may lead to kidney failure (Bruyand et al., 2018). In terms of diagnosis, O157 STEC can be differentiated from most natural E. coli that inhabit the intestines by their inability to ferment sorbitol within 24 hours on a selective medium such as sorbitol-MacConkey agar (Gould & STEC Clinical Laboratory Diagnostics Working Group, 2012). Additionally, PCR can be used as a molecular method for STEC identification, and it has good sensitivity and specificity for the detection in different sources of infection (Castro et al., 2017).

2.2.3 Campylobacter spp.

Over 20 species have been assigned to the Campylobacter genus, but C. jejuni and C. coli are the most commonly isolated from humans (Man, 2011). Campylobacter spp. are Gram-negative, non-spore-forming bacteria that are usually motile by means of a single polar unsheathed flagellum at one or both ends of the cell (Silva et al., 2011). Species from the Campylobacter genus have a helical shape, but they have the ability to change their structure and become rod- or coccoid-shaped (Esson et al., 2016). Campylobacter spp. are commensal microorganisms of the gastrointestinal tract of many farm, wild, and companion animals, which are reservoirs for human infection (Facciolà et al., 2017; Fitzgerald & Nachamkin, 2015). Among the zoonotic species of this genus, C. jejuni is responsible for over 81% of the cases of campylobacteriosis in people (Liu, 2018).

The incubation period (i.e. time between becoming infected and presenting symptoms) of campylobacteriosis is typically two to five days, but it can range from 1 to 10 days (WHO, 2020b). Infectious doses between 8 × 102 to 2 × 109 cells of C. jejuni have been shown to cause diarrheal diseases in humans (Black et al., 1988). As for most bacterial FBDs, the clinical manifestations of campylobacteriosis include diarrhea, intense abdominal pain, nausea, and vomiting. About 0.1% of individuals infected with campylobacteriosis develop Guillain-Barré syndrome, which is a serious autoimmune disorder that can cause muscle weakness and paralysis (Janssen et al., 2008; CDC, 2019c). Since there are no specific symptoms that can help to confirm a case of campylobacteriosis, different diagnostic methods have been used such as PCR, DNA microarray, enzyme-linked immunosorbent assay (ELISA), biochemical characterization, and serotyping (Choudhary et al., 2021).

2.2.4 Listeria monocytogenes

Listeria spp. are Gram-positive, rod-shaped, non-spore-forming, facultative aerobic bacteria that are motile by means of a few peritrichous flagella (Wang & Orsi, 2013). Listeria spp. includes 20 recognized species, and L. monocytogenes represents the most pathogenic member of the genus (Nwaiwu, 2020). Based on O and H antigens, 13 serotypes of L. monocytogenes have been identified, and the serotypes 1/2a, 1/2b, 1/2c, and 4b are the most commonly found in food and the food production environment (Jamshidi & Zeinali, 2019). Cattle and small ruminants including goats and sheep are important reservoirs of L. monocytogenes and their feces can carry this pathogen and, consequently, contaminate the soil and surrounding environment (Vivant et al., 2013). Moreover, the infective dose of L. monocytogenes has been estimated to be 10 to 100 million CFU in healthy individuals, and 0.1 to 10 million CFU in people at high risk (Government of Canada, 2012). Examples of individuals at high risk are those who are immunocompromised, pregnant, or over 65 years.

In humans, listeriosis can occurs in two forms: noninvasive listeriosis and invasive listeriosis. The former is a mild manifestation of the disease and has symptoms that include diarrhea, headache, and fever, whereas the latter is a severe form of the disease that particularly affects people at high risk and has symptoms such as fever, myalgia, septicemia, and meningitis (WHO, 2018b). It is important to mention that this disease has high mortality rates, ranging from 20 to 30% (Hernandez-Milian & Payeras-Cifre, 2014). The diagnosis of this disease is made through cultures of blood, spinal fluid, or other body cavity fluids (Mcneil et al., 2017). Furthermore, the diagnosis of listeriosis during pregnancy is difficult as about 30% of the cases are asymptomatic; however, if disease is suspected, placental cultures are considered the gold standard for diagnosis of maternal fetal listeriosis (Serventi et al., 2020).

2.2.5 Vibrio spp.

The Vibrio genus has over 70 species that are ubiquitous and abundant in aquatic environments (Kokashvili et al., 2015). The components of this genus are Gram-negative, facultative anaerobic, rod-shaped bacteria with a single polar flagellum, and, with the exception of V. cholerae and V. mimicus, all species are halophilic (Long et al., 2017). Vibrio spp. represent the cause of most human diseases associated with microorganisms of aquatic environments and seafood, and V. cholerae, V. parahaemolyticus, V. alginolyticus, and V. vulnificus the most common pathogenic species (Baker-Austin et al., 2018). In the United States, environmental factors such as temperature and salinity of water have been determined to be predictors of V. parahaemolyticus and V. vulnificus abundance (Raszl et al., 2016).

Individuals infected with Vibrio spp. may be asymptomatic or may present clinical manifestations such as diarrhea, abdominal pain, nausea, vomiting, fever, headache, and myalgia (Baker-Austin et al., 2018; Liu, 2018). In terms of microbiological diagnosis, the thiosulfate citrate bile-salts sucrose (TCBS) agar is the standard medium used for selective isolation of Vibrio species. Furthermore, culture independent methods such as PCR can be used to quantify Vibrio spp. in different sources of infection (Givens et al., 2014).

3 Food Chain and Food Contamination

Analyzing the food supply chain in terms of animal production is an essential part of understanding the dynamics of zoonotic FBDs. Several pathogens have been linked to agricultural and food preparation practices, which is one of the reasons why food safety measures are constantly being developed and put in place. Analyses have shown that agricultural drivers were associated with approximately 50% of zoonotic diseases that emerged in human since 1940 (Rohr et al., 2019). Moreover, population growth and demographic changes are expected for the next decades along with an amplification of the already intensive animal farming system (Godfray & Garnett, 2014). If no plan of effective control measures is adopted, the intensification of the food supply chain will allow the spread of pathogens in a much larger scale than the one currently seen. Because the incidence of infectious diseases typically increases proportionally with the increase of host density, the rise in human and livestock densities could also affect the spread of pathogens (Jones et al., 2013; Rohr et al., 2019). In addition, new zoonotic foodborne pathogens may appear during this process, and the development and implementation of surveillance systems is an essential step to control them.

Food contamination occurs when microorganisms or chemicals get into food products and their presence make the food unsafe. The contamination of food products may occur during different stages of the food chain such as production, processing, distribution, preparation, and the final consumption (Abebe et al., 2020). A variety of animal products are subjected to contamination, the most common being eggs, meat, poultry, and dairy products. One comprehensive approach to address issues related to food contamination is the adoption of strategies based on Hazard Analysis Critical Control Point (HACCP). This is a management system that addresses food safety through the identification, evaluation, and control of hazards (US Food and Drug Administration, 2018).

4 Global Burden of Foodborne Diseases

Foodborne diseases are a public health concern worldwide, but they affect countries at different levels. Low- and middle-income nations are the most impacted by these diseases and also the countries with the lowest performances with regards to disease surveillance. Although food safety and FBD awareness have increased globally, strategies to efficiently monitor and control the spread of foodborne pathogens still lack in those countries. Even though FBDs have been causing economic losses and public health concerns for a long time, only a few countries have assessed the burden of these infectious diseases. Moreover, not every person who becomes ill after ingestion of contaminated food seeks the healthcare system, which contributes to the gap that exists between the reported data and the real scenario. Even though this chapter does not enter into the merit of issues related to healthcare access, it is important to mention that lack of access to quality healthcare is a contributing factor for the underreport of FBDs. The lack of surveillance and data on FBDs also prevents health authorities from analyzing past trends, which could help to develop new approaches for limiting the burden.

The first estimates on global and regional burden of FBDs was presented only in 2015 and was led by the WHO. The report provides readers with estimates of incidence and mortality rates along with disease burden in terms of Disability Adjusted Life Years (DALYs) caused by 31 foodborne hazards. DALYs for a disease or condition are the total sum of the years of life lost due to premature mortality and the years lived with a disability (WHO, n.d.). Although norovirus was responsible for the most DALYs worldwide in 2010 (i.e. over 15 million DALYs), bacterial pathogens such as S. enterica and E. coli represented important causes of DALYs (WHO, 2015). Furthermore, human-to-human contact was the main route of transmission of norovirus for most regions, whereas food represented the principal route of transmission for Shiga toxin-producing E. coli, Non-typhoidal S. enterica, and Campylobacter spp. in all regions. This fact highlights the importance of research at all levels on the interplay between humans, zoonotic pathogens and their animal reservoirs, and animal food products.

5 The United States Context

Foodborne illnesses have an impact on countries’ health and economic systems worldwide. In the United States, it was estimated that foodborne pathogens caused an economic burden of $17.6 billion, which is 13% higher than the 2013 estimate (Economic Research Service, 2021). Other estimates show that the annual economic burden of FBDs in Australia and New Zealand is respectively $1.289 billion and $86 million (McLinden et al., 2014). National public health estimates on this issue show that 48 million people get sick and 3,000 die of FBDs every year (CDC, 2018). These estimates highlight the impact of FBDs in the country and the value of epidemiological analyses that keep these diseases under surveillance.

One of the tools used to monitor FBDs in the US is the National Notifiable Disease Surveillance System (NNDSS). The NNDSS is an integrated system that allows public health at all levels (i.e. local, national, and global) to share data that is used to monitor, control, and prevent the occurrence and spread of notifiable diseases and conditions (US Department of Health and Human Services, n.d.). The list of nationally notifiable infectious diseases includes zoonotic FBDs such as salmonellosis, campylobacteriosis, STEC infection, listeriosis, and vibriosis. These are diseases for which more data is necessary to develop effective control and preventive measures in order to reduce their occurrence and spread. Additionally, the Healthy People initiative set health-related national objectives on a 10-year basis for improving the health and well-being of all individuals. These objectives can be used as comparison measurements to assess the progress towards the control of infectious diseases.

6 Analysis of Trends in Zoonotic Foodborne Diseases

The trends on the incidence of many zoonotic FBDs have varied throughout the years. The US list of Nationally Notifiable Infectious Diseases and Conditions is comprised of many illnesses caused by different pathogens. Some of the zoonotic FBDs include salmonellosis, STEC infection, listeriosis, campylobacteriosis, and vibriosis. Epidemiologic data on these diseases can be retrieved from the NNDSS for the US and from the European Centre for Disease Prevention and Control for countries of the European Union. Additionally, the Public Health Agency of Canada also provides epidemiological data regarding these diseases. It has to be noted that despite the fact these diseases are commonly transmitted through contaminated food, the proportion of cases linked to food consumption is not available. Also, each disease has a case definition that includes clinical and laboratory criteria as part of its diagnosis in the United States.

Table 3.2
Table 3.2

Reported cases of zoonotic foodborne diseases in the United States, 2010–2019

Source: Authors’ elaboration

Reported cases of zoonotic foodborne diseases in the United States, 2010–2019

From 2010 to 2019, some changes were seen in the incidence rate (IR) of major zoonotic FBDs. Fluctuations were observed in the incidence of salmonellosis with rates varying from 17.59 cases per 100,000 people in 2010 to 16.63 cases per 100,000 people in 2019. Unless specified otherwise, for the remainder of this chapter, IR represents the number of cases per 100,000 people. During those 10 years, the highest rate was reported in 2018 with an incidence of 18.67. The Healthy People initiative had targeted for 2020 an incidence of salmonellosis of 11.4 (Office of Disease prevention and Health Promotion [ODPHP], 2021). This substantial decrease in new cases of salmonellosis is an ambitious aim that continues in place as an objective of the Healthy People 2030. The persistence of this disease has also been observed in other countries. The Canadian government has reported IRs of salmonellosis varying from 17.63 in 2013 to 19.24 in 2018 with a peak in 2014, when the country registered 21.56 cases of this disease per 100,000 people.

The US incidence of STEC infection has been continuously rising since 2014 when the country reported a total of 6,179 cases. An increase greater than two-fold in the number of cases was registered in 2019, accounting for an IR of 5.16. The US national objective for 2020, however, was to reduce the incidence of STEC infections to 0.6 cases per 100,000 people (ODPHP, 2021). A similar trend has been observed in European countries such as Denmark and Norway. Even though these countries have a much lower number of cases when compared to the US, the incidence of STEC infection there is increasing at a high rate. On the other hand, the Netherlands have been progressively reducing the occurrence of this disease, reporting 459 cases in 2019. Although many factors play a role in the dynamics of this infection, it was found that there is a relationship between the number of cases of STEC infection in the US and the per capita consumption of chicken in the country.

Between 2010 and 2019, the US has reported low IRs of listeriosis, ranging from 0.23 to 0.28. The highest number of cases in this period of time was observed in 2017 when the country reported a total of 887 cases, which represented an IR of 0.27. In the same year, Germany and France had the highest number of cases of listeriosis in the European Union, registering a total of 726 and 370 confirmed cases, respectively. Because of the difference in population size between these two European countries and the US, they reported a much higher IR of listeriosis for that year (i.e. Germany: 0.88 cases per 100,000 people and France: 0.55 cases per 100,000 people). An incidence higher than that of the US was also found in Canada where a rate of 0.33 was reported. The Healthy People 2020 target for this disease was a rate of 0.2 cases per 100,000 people (ODPHP, 2021). Although there is some small fluctuation in the incidence of listeriosis throughout the last decade, this disease seems to be under control. However, its high mortality rate makes it a disease that needs to be constantly under surveillance.

Campylobacteriosis became a nationally notifiable disease in the US in 2015. Annual national data on this disease has been released since then. The number of cases of this disease have been annually increasing since its first report in 2015. In 2019, the country reported 71,509 cases of campylobacteriosis, making it the nationally notifiable FBD with the highest number of cases in that year. In 2017, the US had an IR of 20.78, which was lower than that reported by most European countries in the same year. From 2015 to 2019, the IR of campylobacteriosis increased from 17.01 to 21.79. The national goal, however, was to decrease it to 8.5 cases per 100,00 by 2020 (ODPHP, 2021). Additionally, the number of cases of vibriosis has also increased over the years in the US, where the case counts more than tripled from 2010 to 2019. Yet, the highest incidence (0.91 cases per 100,000 people) was reported in 2018.

Figure 3.1
Figure 3.1

Incidence of reported cases of zoonotic foodborne diseases in the United States, 2010–2019

Source: Authors’ elaboration

7 Conclusion

It has been shown that zoonotic FBDs are on the rise in the US and other high-income countries. Although the burden of FBDs is greater in low- and middle-income countries, public health authorities of high-income nations have to be aware of epidemiological trends in order to control and prevent the increase in the IR of these diseases. Measures based on the One Health approach, which considers the human-animal-environment interface, are a way to fully understand the rise in the IR of zoonoses and to effectively develop strategies to mitigate their impact on populations. The limitations in the research of epidemiological trends include the lack of analysis of other zoonotic FBDs such as norovirus infection even though this is not considered a nationally notifiable disease. Although the diseases analyzed are commonly transmitted through the consumption of contaminated food, the proportion of cases that were related to food is not available. Additionally, the comparison of IR between countries was limited as many countries do not have a surveillance system that report data on FBDs on a regular basis. Furthermore, supplementary studies are necessary to evaluate what factors are associated with the increase in IR of zoonotic FBDs in the US and to examine the association between these diseases and food products of animal origin.

Acknowledgements

The authors acknowledge the support of Northeastern Illinois University and its Master of Public Health Program.

References

  • Abebe, E., Gugsa, G., & Ahmed, M. (2020). Review on major food-borne zoonotic bacterial pathogens. Journal of Tropical Medicine, 2020, 4674235. doi: 10.1155/2020/4674235.

    • Search Google Scholar
    • Export Citation
  • Acheson, D., & Hohmann, E. L. (2001). Nontyphoidal salmonellosis. Clinical Infectious Diseases, 32(2), 263269.

  • Adell, T., Martín-Durán, J. M., Saló, E., & Cebrià, F. (2015). Platyhelminthes. In Evolutionary Developmental Biology of Invertebrates 2 (pp. 2140). Vienna: Springer.

    • Search Google Scholar
    • Export Citation
  • Agbaje, M., Begum, R. H., Oyekunle, M. A., Ojo, O. E., & Adenubi, O. T. (2011). Evolution of Salmonella nomenclature: a critical note. Folia Microbiologica, 56(6), 497503.

    • Search Google Scholar
    • Export Citation
  • Ameer, M. A., Wasey, A., & Salen, P. (2021). Escherichia Coli (E Coli 0157 H7). StatPearls [Internet]. Treasure Island: StatPearls Publishing. Available from: https://www.ncbi.nlm.nih.gov/books/NBK507845/.

    • Search Google Scholar
    • Export Citation
  • Animal and Plant Health Inspection Service. (2020, June 8). U.S. identifies its top 8 zoonotic diseases of concern. U.S. Department of Agriculture. Retrieved August 8, 2021, from https://www.aphis.usda.gov/aphis/ourfocus/wildlifedamage/programs/nwrc/sa_spotlight/zoonotic_diseases_of_concern.

    • Search Google Scholar
    • Export Citation
  • Baker-Austin, C., Oliver, J. D., Alam, M., Ali, A., Waldor, M. K., Qadri, F., & Martinez-Urtaza, J. (2018). Vibrio spp. infections. Nature Reviews Disease Primers, 4(1), 119.

    • Search Google Scholar
    • Export Citation
  • Ballem, A., Gonçalves, S., Garcia-Meniño, I., Flament-Simon, S. C., Blanco, J. E., Fernandes, C., Saavedra, M. J., Pinto, C., Oliveira, H., Blanco, J., Almeida, G., & Almeida, C. (2020). Prevalence and serotypes of Shiga toxin-producing Escherichia coli (STEC) in dairy cattle from Northern Portugal. Plos One, 15(12), e0244713.

    • Search Google Scholar
    • Export Citation
  • Bhunia, A. K. (2018a). Foodborne microbial pathogens: mechanisms and pathogenesis. Springer.

  • Bhunia, A. K. (2018b). Salmonella enterica. In Foodborne Microbial Pathogens (pp. 271287).New York: Springer.

  • Bintsis, T. (2017). Foodborne pathogens. AIMS microbiology, 3(3), 529.

  • Black, R. E., Levine, M. M., Clements, M. L., Hughes, T. P., & Blaser, M. J. (1988). Experimental Campylobacter jejuni infection in humans. Journal of infectious diseases, 157(3), 472479.

    • Search Google Scholar
    • Export Citation
  • Bruyand, M., Mariani-Kurkdjian, P., Gouali, M., De Valk. H., King, L. A., Le Hello, S., Bonacorsi, S., & Loirat, C. (2018). Hemolytic uremic syndrome due to Shiga toxin-producing Escherichia coli infection. Medecine et Maladies Infectieuses, 48(3), 167174.

    • Search Google Scholar
    • Export Citation
  • Byrne, L., Jenkins, C., Launders, N., Elson, R., & Adak, G. K. (2015). The epidemiology, microbiology and clinical impact of Shiga toxin-producing Escherichia coli in England, 2009–2012. Epidemiology & Infection, 143(16), 34753487.

    • Search Google Scholar
    • Export Citation
  • Castro, V. S., Carvalho, R. C. T., Conte‐Junior, C. A., & Figuiredo, E. E. S. (2017). Shiga‐toxin producing Escherichia coli: pathogenicity, supershedding, diagnostic methods, occurrence, and foodborne outbreaks. Comprehensive Reviews in Food Science and Food Safety, 16(6), 12691280.

    • Search Google Scholar
    • Export Citation
  • Centers for Disease Control and Prevention. (2014, December 1). E. coli (Escherichia coli): Questions and answers. Retrieved August 5, 2021, from https://www.cdc.gov/ecoli/general/index.html.

    • Search Google Scholar
    • Export Citation
  • Centers for Disease Control and Prevention. (2018, November 5). Burden of foodborne illness: Findings. Retrieved August 8, 2021, from https://www.cdc.gov/foodborneburden/2011-foodborne-estimates.html.

    • Search Google Scholar
    • Export Citation
  • Centers for Disease Control and Prevention. (2019a, November 13). Information for healthcare professionals and laboratories. Retrieved August 9, 2021, from https://www.cdc.gov/salmonella/general/technical.html.

    • Search Google Scholar
    • Export Citation
  • Centers for Disease Control and Prevention. (2019b, December 5). Salmonella: Diagnostic and public health testing. Retrieved August 2, 2021, from https://www.cdc.gov/salmonella/general/diagnosis-treatment.html?CDC_AA_refVal=https%3A%2F%2Fwww.cdc.gov%2Fsalmonella%2Fgeneral%2Fdiagnosis.html.

    • Search Google Scholar
    • Export Citation
  • Centers for Disease Control and Prevention. (2019c, December 20). Guillain-Barré syndrome. Retrieved August 5, 2021, from https://www.cdc.gov/campylobacter/guillain-barre.html.

    • Search Google Scholar
    • Export Citation
  • Centers for Disease Control and Prevention. (2020, February 3). Zoonotic disease prioritization. Retrieved August 1, 2021, from https://www.cdc.gov/onehealth/what-we-do/zoonotic-disease-prioritization/us-workshops.html?CDC_AA_refVal=https%3A%2F%2Fwww.cdc.gov%2Fonehealth%2Fdomestic-activities%2Fus-ohzdp.html.

    • Search Google Scholar
    • Export Citation
  • Choudhary, P., Punia, A., Dahiya, S., Sharma, N., Balhara, M., Dangi, M., & Chhillar, A. K. (2021). Recent Trends in Diagnosis of Campylobacter Infection. In S. K. Gahlawat, S. Maan. Advances in Animal Disease Diagnosis, New York: CRC Press, 219228.

    • Search Google Scholar
    • Export Citation
  • Coburn, B., Grassl, G. A., & Finlay, B. B. (2007). Salmonella, the host and disease: a brief review. Immunology and Cell Biology, 85(2), 112118.

    • Search Google Scholar
    • Export Citation
  • Croxen, M. A., Law, R. J., Scholz, R., Keeney, K. M., Wlodarska, M., & Finlay, B. B. (2013). Recent advances in understanding enteric pathogenic Escherichia coli. Clinical Microbiology Reviews, 26(4), 822880.

    • Search Google Scholar
    • Export Citation
  • Desmarchelier, P., Fegan, N. (2011). Pathogens in milk Escherichia coli. In J. W. Fuquay, P. McSweeney, P. Fox. (Eds). Encyclopedia of Dairy Sciences. 2nd ed. London: Academic Press, 6066.

    • Search Google Scholar
    • Export Citation
  • Doyle, M. P., Diez-Gonzalez, F., & Hill, C. (Eds.) (2019). Food microbiology: fundamentals and frontiers. John Wiley & Sons.

  • Economic Research Service. (2021, March 10). Cost estimate of foodborne illnesses. U.S. Department of Agriculture. Retrieved July 29, 2021, from https://www.ers.usda.gov/data-products/cost-estimates-of-foodborne-illnesses/.

    • Search Google Scholar
    • Export Citation
  • Esson, D., Mather, A. E., Scanlan, E., Gupta, S., De Vries, S. P., Bailey, D., Harris, S. R., McKinley, T. J., Méric, G., Berry, S. K., Mastroeni, P., Sheppard, S. K., Christie, G., Thompson, N. R., Parkhill, J., & Grant, A. J. (2016). Genomic variations leading to alterations in cell morphology of Campylobacter spp. Scientific reports, 6(1), 113.

    • Search Google Scholar
    • Export Citation
  • Etcheverria, A. I., & Padola, N. L. (2013). Shiga toxin-producing Escherichia coli: factors involved in virulence and cattle colonization. Virulence, 4(5), 366372.

    • Search Google Scholar
    • Export Citation
  • European Food Safety Authority. (n.d.). Foodborne zoonotic disease. Retrieved July 28, 2021, from https://www.efsa.europa.eu/en/topics/topic/foodborne-zoonotic-diseases.

    • Search Google Scholar
    • Export Citation
  • Facciolà, A., Riso, R., Avventuroso, E., Visalli, G., Delia, S. A., & Laganà, P. (2017). Campylobacter: from microbiology to prevention. Journal of preventive medicine and hygiene, 58(2), E79.

    • Search Google Scholar
    • Export Citation
  • Fitzgerald, C., & Nachamkin, I. (2015). Campylobacter and arcobacter. Manual of clinical microbiology, 9981012.

  • Givens, C. E., Bowers, J. C., DePaola, A., Hollibaugh, J. T., & Jones, J. L. (2014). Occurrence and distribution of V ibrio vulnificus and V ibrio parahaemolyticus – potential roles for fish, oyster, sediment and water. Letters in applied microbiology, 58(6), 503510.

    • Search Google Scholar
    • Export Citation
  • Godfray, H. C. J., & Garnett, T. (2014). Food security and sustainable intensification. Philosophical transactions of the Royal Society B: biological sciences, 369(1639), 20120273.

    • Search Google Scholar
    • Export Citation
  • Gould, L. H., & STEC Clinical Laboratory Diagnostics Working Group. (2012). Update: recommendations for diagnosis of Shiga toxin-producing Escherichia coli infections by clinical laboratories. Clinical Microbiology Newsletter, 34(10), 7583.

    • Search Google Scholar
    • Export Citation
  • Government of Canada. (2012, April 30). Pathogen safety data sheet – infectious substances. Retrieved August 8, 2021, from https://www.canada.ca/en/public-health/services/laboratory-biosafety-biosecurity/pathogen-safety-data-sheets-risk-assessment/listeria-monocytogenes.html.

    • Search Google Scholar
    • Export Citation
  • Grimont, P. A., & Weill, F. X. (2007). Antigenic formulae of the Salmonella serovars. WHO collaborating centre for reference and research on Salmonella, 9, 1166.

    • Search Google Scholar
    • Export Citation
  • Gwida, M. M., & Al-Ashmawy, M. A. (2014). Culture versus PCR for Salmonella species identification in some dairy products and dairy handlers with special concern to its zoonotic importance. Veterinary medicine international, 2014.

    • Search Google Scholar
    • Export Citation
  • Hernandez-Milian, A., & Payeras-Cifre, A. (2014). What is new in listeriosis?. BioMed research international, 2014.

  • Jamshidi, A., & Zeinali, T. (2019). Significance and characteristics of Listeria monocytogenes in poultry products. International journal of food science, 2019.

    • Search Google Scholar
    • Export Citation
  • Janssen, R., Krogfelt, K. A., Cawthraw, S. A., Van Pelt, W., Wagenaar, J. A., & Owen, R. J. (2008). Host-pathogen interactions in Campylobacter infections: the host perspective. Clinical microbiology reviews, 21(3), 505518.

    • Search Google Scholar
    • Export Citation
  • John, D. T., & Petri, W. A. (2020). Markell & Voge’s Medical Parasitology-10th Sea Ed. Elsevier (Singapore) Pte Limited.

  • Joint, F. A. O., & World Health Organization. (1959). Joint WHO/FAOExpert Committee on Zoonoses [meeting held in Stockholm from 11 to 16 August 1958]: second report.

  • Jones, B. A., Grace, D., Kock, R., Alonso, S., Rushton, J., Said, M. Y., McKeever, D., Mutua, F., Young, J., McDermott, J., & Pfeiffer, D. U. (2013). Zoonosis emergence linked to agricultural intensification and environmental change. Proceedings of the National Academy of Sciences, 110(21), 83998404.

    • Search Google Scholar
    • Export Citation
  • Kokashvili, T., Whitehouse, C. A., Tskhvediani, A., Grim, C. J., Elbakidze, T., Mitaishvili, N., Janelidze, N., Jaiani, E., Haley, B. J., Lashkhi, N., Huq, A., Colwell, R. R., & Tediashvili, M. (2015). Occurrence and diversity of clinically important Vibrio species in the aquatic environment of Georgia. Frontiers in public health, 3, 232.

    • Search Google Scholar
    • Export Citation
  • Kuchenmüller, T., Abela-Ridder, B., Corrigan, T., & Tritscher, A. (2013). World Health Organization initiative to estimate the global burden of foodborne diseases. Rev Sci Tech, 32(2), 459467.

    • Search Google Scholar
    • Export Citation
  • Le Loir, Y., Baron, F., & Gautier, M. (2003). [i] Staphylococcus aureus [/i] and food poisoning. Genetics and molecular research: GMR, 2(1), 6376.

    • Search Google Scholar
    • Export Citation
  • Liu, D. (Ed.). (2018). Handbook of foodborne diseases. CRC Press.

  • Long, S. S., Prober, C. G., & Fischer, M. (2017). Principles and practice of pediatric infectious diseases E-Book. Elsevier Health Sciences.

    • Search Google Scholar
    • Export Citation
  • Mahmud, R., Lim, Y. A. L., & Amir, A. (2017). Protozoa and Helminths. In Medical Parasitology (pp. 34). Cham: Springer.

  • Man, S. M. (2011). The clinical importance of emerging Campylobacter species. Nature Reviews Gastroenterology & Hepatology, 8(12), 669685.

    • Search Google Scholar
    • Export Citation
  • McLinden, T., Sargeant, J. M., Thomas, M. K., Papadopoulos, A., & Fazil, A. (2014). Component costs of foodborne illness: a scoping review. BMC Public Health, 14(1), 112.

    • Search Google Scholar
    • Export Citation
  • McNeill, C., Sisson, W., & Jarrett, A. (2017). Listeriosis: A resurfacing menace. The Journal for Nurse Practitioners, 13(10), 647654.

    • Search Google Scholar
    • Export Citation
  • Murrell, K. D. (2013). Zoonotic foodborne parasites and their surveillance. Rev Sci Tech, 32(2), 559569.

  • Nataro, J. P., & Kaper, J. B. (1998). Diarrheagenic escherichia coli. Clinical Microbiology Reviews, 11(1), 142201.

  • Nwaiwu, O. (2020). What are the recognized species of the genus Listeria? Access Microbiology, 2(9), e000153.

  • Office of Disease prevention and Health Promotion. (2021, June 23). Food safety: Objectives. HealthyPeople. Culture versus PCR for Salmonella species identification in some dairy products and dairy handlers with special concern to its zoonotic importance. Retrieved August 2, 2021, from https://www.healthypeople.gov/2020/topics-objectives/topic/food-safety/objectives.

    • Search Google Scholar
    • Export Citation
  • Petro, C. D., Trojnar, E., Sinclair, J., Liu, Z. M., Smith, M., O’Brien, A. D., & Melton-Celsa, A. (2019). Shiga toxin type 1a (Stx1a) reduces the toxicity of the more potent Stx2a in vivo and in vitro. Infection and Immunity, 87(4), e0078700718.

    • Search Google Scholar
    • Export Citation
  • Phillips, J. A. (2021). The One Health Framework. Workplace Health & Safety, 69(4), 188188.

  • Raszl, S. M., Froelich, B. A., Vieira, C. R. W., Blackwood, A. D., & Noble, R. T. (2016). Vibrio parahaemolyticus and Vibrio vulnificus in South America: water, seafood and human infections. Journal of Applied Microbiology, 121(5), 12011222.

    • Search Google Scholar
    • Export Citation
  • Rohr, J. R., Barrett, C. B., Civitello, D. J., Craft, M. E., Delius, B. DeLeo, G. A., Hudson, P. J., Jouanard, N., Nguyen, K. H., Ostfeld, R. S., Remais, J. V., Riveau, G., Sokolow, S. H., & Tilman, D. (2019). Emerging human infectious diseases and the links to global food production. Nature Sustainability, 2(6), 445456.

    • Search Google Scholar
    • Export Citation
  • Schmidt, T. M. (Ed.). (2019). Encyclopedia of Microbiology. Amsterdam, Oxford, Cambridge, MA: Academic Press.

  • Serventi, L., Curi, B., Johns, R., Silva, J., Bainbridge, R., & Gaither, K. (2020). Pregnancy Complicated by Listeria Monocytogenes: A Case Report and Review of the Literature. Journal of the National Medical Association, 112(4), 428432.

    • Search Google Scholar
    • Export Citation
  • Siddiqui, S., & Yuan, J. (2021). Binding Characteristics Study of DNA based Aptamers for E. coli O157: H7. Molecules, 26(1), 204.

  • Silva, J., Leite, D., Fernandes, M., Mena, C., Gibbs, P. A., & Teixeira, P. (2011). Campylobacter spp. as a foodborne pathogen: a review. Frontiers in microbiology, 2, 200.

    • Search Google Scholar
    • Export Citation
  • Singleton, W. (2018). Invertebrate reproduction and development. Scientific e-Resources.

  • Stein, R. A., & Chirilã, M. (2017). Routes of transmission in the food chain. In Foodborne Diseases (pp. 65103). Academic Press.

  • The Center for Food Security& Public Health. (2013). Salmonellosis: Paratyphoid, nontyphoidal salmonellosis. Retrieved July 30, 2021, from https://www.cfsph.iastate.edu/Factsheets/pdfs/nontyphoidal_salmonellosis.pdf.

    • Search Google Scholar
    • Export Citation
  • Tian, K., Chen, X., Luan, B., Singh, P., Yang, Z., Gates, K. S., Lin, M., Mustapha, A., & Gu, L. Q. (2018). Single locked nucleic acid-enhanced nanopore genetic discrimination of pathogenic serotypes and cancer driver mutations. ACS nano, 12(5), 4194–4205.

    • Search Google Scholar
    • Export Citation
  • Travert, B., Rafat, C., Mariani, P., Cointe, A., Dossier, A., Coppo, P., & Joseph, A. (2021). Shiga Toxin-Associated Hemolytic Uremic Syndrome: Specificities of Adult Patients and Implications for Critical Care Management. Toxins, 13(5), 306.

    • Search Google Scholar
    • Export Citation
  • United States Department of Health and Human Services. (n.d.). National notifiable diseases surveillance system (NNDSS). HealthyPeople. Retrieved August 6, 2021, from https://health.gov/healthypeople/objectives-and-data/data-sources-and-methods/data-sources/national-notifiable-diseases-surveillance-system-nndss.

    • Search Google Scholar
    • Export Citation
  • United States Department of Health and Human Services. (2018, January 29). Hazard analysis critical control point (HACCP). Retrieved August 1, 2021, from https://www.fda.gov/food/guidance-regulation-food-and-dietary-supplements/hazard-analysis-critical-control-point-haccp.

    • Search Google Scholar
    • Export Citation
  • Vivant, A. L., Garmyn, D., & Piveteau, P. (2013). Listeria monocytogenes, a down-to-earth pathogen. Frontiers in cellular and infection microbiology, 3, 87.

    • Search Google Scholar
    • Export Citation
  • Wang, S., & Orsi, R. H. (2013). Listeria. In Foodborne infections and intoxications (pp. 199216). Academic Press.

  • World Health Organization. (n.d.). Disability-adjusted life years (DALYs). Retrieved July 29, 2021, from https://www.who.int/data/gho/indicator-metadata-registry/imr-details/158.

    • Search Google Scholar
    • Export Citation
  • World Health Organization. (2012, January 17). Neglected tropical diseases. Retrieved July 27, 2021, from https://www.who.int/news-room/q-a-detail/neglected-tropical-diseases.

    • Search Google Scholar
    • Export Citation
  • World Health Organization. (2015). WHO estimates of the global burden of foodborne diseases: foodborne disease burden epidemiology reference group 2007–2015. World Health Organization.

    • Search Google Scholar
    • Export Citation
  • World Health Organization. (2018a, February 7). E. coli. Retrieved August 3, 2021, from https://www.who.int/news-room/fact-sheets/detail/e-coli.

    • Search Google Scholar
    • Export Citation
  • World Health Organization. (2018b, February 20). Listeriosis. Retrieved August 8, 2021, from https://www.who.int/news-room/fact-sheets/detail/listeriosis.

    • Search Google Scholar
    • Export Citation
  • World Health Organization. (2020a, April 30). Food safety. Retrieved July 29, 2021, from https://www.who.int/news-room/fact-sheets/detail/food-safety.

    • Search Google Scholar
    • Export Citation
  • World Health Organization. (2020b, May 1). Campylobacter. Retrieved July 17, 2021, from https://www.who.int/news-room/fact-sheets/detail/campylobacter.

    • Search Google Scholar
    • Export Citation
  • Yaeger, R. G. (1996). Protozoa: structure, classification, growth, and development. In S. Baron (Ed.), Medical microbiology. (4th ed.). University of Texas Medical Branch at Galveston.

    • Search Google Scholar
    • Export Citation
  • Zhao, X., Lin, C. W., Wang, J., & Oh, D. H. (2014). Advances in rapid detection methods for foodborne pathogens. Journal of Microbiology and Biotechnology, 24(3), 297312.

    • Search Google Scholar
    • Export Citation
  • Collapse
  • Expand

Metrics

All Time Past 365 days Past 30 Days
Abstract Views 0 0 0
Full Text Views 227 84 2
PDF Views & Downloads 119 22 2