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Salmonellosis

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Salmonellosis
Food poisoning
Electron micrograph showing Salmonella typhimurium (red) invading cultured human cells
SpecialtyInfectious disease
SymptomsDiarrhea, fever, abdominal cramps, vomiting[1]
ComplicationsReactive arthritis, irritable bowel syndrome[2]
Usual onset0.5–3 days post exposure[1]
Duration4–7 days[1]
TypesTyphoidal, nontyphoidal[1]
CausesSalmonella[1]
Risk factorsOld, young, weak immune system, bottle feeding, proton pump inhibitors[1]
Diagnostic methodStool test, blood tests[3][1]
Differential diagnosisOther types of gastroenteritis[2]
PreventionProper preparation and cooking of food and supervising contact between young children and pets[4]
TreatmentFluids by mouth, intravenous fluids, antibiotics[1]
Frequency1.35 million non–typhoidal cases per year (US)[1]
Deaths90,300 (2015)[5]

Salmonellosis is a symptomatic infection caused by bacteria of the Salmonella type.[1] It is the most common disease to be known as food poisoning (though the name refers to food-borne illness in general), these are defined as diseases, usually either infectious or toxic in nature, caused by agents that enter the body through the ingestion of food. In humans, the most common symptoms are diarrhea, fever, abdominal cramps, and vomiting.[1] Symptoms typically occur between 12 hours and 36 hours after exposure, and last from two to seven days.[4] Occasionally more significant disease can result in dehydration.[4] The old, young, and others with a weakened immune system are more likely to develop severe disease.[1] Specific types of Salmonella can result in typhoid fever or paratyphoid fever.[1][3] Typhoid fever and paratyphoid fever are specific types of salmonellosis, known collectively as enteric fever,[6] and are, respectively, caused by salmonella typhi and paratyphi bacteria, which are only found in humans.[7] Most commonly, salmonellosis cases arise from salmonella bacteria from animals,[8] and chicken is a major source for these infections.[9]

There are two species of Salmonella: Salmonella bongori and Salmonella enterica with many subspecies.[4] However, subgroups and serovars within a species may be substantially different in their ability to cause disease. This suggests that epidemiologic classification of organisms at the subspecies level may improve management of Salmonella and similar pathogens.[10][11][12]

Both vegetarian and non-vegetarian populations are susceptible to Salmonella infections due to the consumption of contaminated meat and milk.[13] Infection is usually spread by consuming contaminated meat, eggs, water or milk.[14] Other foods may spread the disease if they have come into contact with manure.[4] A number of pets including cats, dogs, and reptiles can also carry and spread the infection.[4] Diagnosis is by a stool test or blood tests.[1][3]

Efforts to prevent the disease include the proper washing, preparation, and cooking of food to appropriate temperature.[4] Mild disease typically does not require specific treatment.[4] More significant cases may require treatment of electrolyte problems and intravenous fluid replacement.[1][4] In those at high risk or in whom the disease has spread outside the intestines, antibiotics are recommended.[4]

Salmonellosis is one of the most common causes of diarrhea globally.[2] In 2015, 90,300 deaths occurred from nontyphoidal salmonellosis, and 178,000 deaths from typhoidal salmonellosis.[5] In the United States, about 1.35 million cases and 450 deaths occur from non-typhoidal salmonellosis a year.[1] In Europe, it is the second most common foodborne disease after campylobacteriosis.[2]

Signs and symptoms

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Enteritis

[edit]
See also: Enteritis § Infectious enteritis

After a short incubation period of a few hours to one day, the bacteria multiply in the small intestine, causing an intestinal inflammation (enteritis). Most people with salmonellosis develop diarrhea, fever, vomiting, and abdominal cramps 12 to 72 hours after infection.[15] Diarrhea is often watery and non-bloody but may be mucoid and bloody.[16] In most cases, the illness lasts four to seven days, and does not require treatment. In some cases, though, the diarrhea may be so severe that the patient becomes dangerously dehydrated and must be hospitalized. At the hospital, the patient may receive fluids intravenously to treat the dehydration, and may be given medications to provide symptomatic relief, such as fever reduction. In severe cases, the Salmonella infection may spread from the intestines to the blood stream, and then to other body sites, and can cause death, unless the person is treated promptly with antibiotics.[citation needed]

In otherwise healthy adults, the symptoms can be mild. Normally, no sepsis occurs, but it can occur exceptionally as a complication in the immunocompromised. However, in people at risk such as infants, small children, and the elderly, Salmonella infections can become very serious, leading to complications. In infants, dehydration can cause a state of severe toxicity. Extraintestinal localizations are possible, especially Salmonella meningitis in children, osteitis, etc. Children with sickle-cell anemia who are infected with Salmonella may develop osteomyelitis. Treatment of osteomyelitis, in this case, will be to use fluoroquinolones (ciprofloxacin, levofloxacin, etc., and nalidixic acid).[citation needed]

Those whose only symptom is diarrhea usually completely recover, but their bowel habits may not return to normal for several months.[17]

Typhoid fever

[edit]
See also: Typhoid fever and Paratyphoid fever

Typhoid fever occurs when Salmonella bacteria enter the lymphatic system and cause a systemic form of salmonellosis. Endotoxins first act on the vascular and nervous apparatus, resulting in increased permeability and decreased tone of the vessels, upset thermal regulation, vomiting, and diarrhea. In severe forms of the disease, enough liquid and electrolytes are lost to upset the fluid balance, cause an electrolyte imbalance, decrease the circulating blood volume and arterial pressure, and cause hypovolemic shock. Septic shock may also develop. Shock of mixed character (with signs of both hypovolemic and septic shock) are more common in severe salmonellosis. Oliguria and azotemia develop in severe cases as a result of renal involvement due to hypoxia and toxemia.[15]

Long-term

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Salmonellosis is associated with later irritable bowel syndrome[18] and inflammatory bowel disease.[19] Evidence however does not support it being a direct cause of the latter.[19]

A small number of people afflicted with salmonellosis experience reactive arthritis, which can last months or years and can lead to chronic arthritis.[20] In sickle-cell anemia, osteomyelitis due to Salmonella infection is much more common than in the general population. Though Salmonella infection is frequently the cause of osteomyelitis in people with sickle-cell, it is not the most common cause, which is Staphylococcus infection.[21]

Those infected may become asymptomatic carriers, but this is relatively uncommon, with shedding observed in only 0.2 to 0.6% of cases after a year.[22]

Causes

[edit]
An infographic illustrating how Salmonella bacteria spread from the farm
  • Contaminated food, often having no unusual look or smell[23]
  • Poor kitchen hygiene, especially problematic in institutional kitchens and restaurants because this can lead to a significant outbreak
  • Excretions from either sick or infected but apparently clinically healthy people and animals (especially dangerous are caregivers and animals)
  • Polluted surface water and standing water (such as in shower hoses or unused water dispensers)
  • Unhygienically thawed poultry (the meltwater contains many bacteria)
  • An association with reptiles (pet tortoises, snakes,[24] iguanas,[25][26] and aquatic turtles) is well described.[27]
  • Amphibians such as frogs

Salmonella bacteria can survive for some time without a host; they are frequently found in polluted water, with contamination from the excrement of carrier animals being particularly important.[citation needed]

The European Food Safety Authority highly recommends that when handling raw turkey meat, consumers and people involved in the food supply chain should pay attention to personal and food hygiene.[28]

An estimated 142,000 Americans are infected each year with Salmonella Enteritidis from chicken eggs,[29] and about 30 die.[30] The shell of the egg may be contaminated with Salmonella by feces or environment, or its interior (yolk) may be contaminated by penetration of the bacteria through the porous shell or from a hen whose infected ovaries contaminate the egg during egg formation.[31][32]

Nevertheless, such interior egg yolk contamination is theoretically unlikely.[33][34][35][36] Even under natural conditions, the rate of infection was very small (0.6% in a study of naturally contaminated eggs[37] and 3.0% among artificially and heavily infected hens[38]).

Prevention

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See also: Critical control point

The US Food and Drug Administration (FDA) has published guidelines to help reduce the chance of food-borne salmonellosis.[39] Food must be cooked to 145–165 °F (63–74 °C), and liquids such as soups or gravies should be boiled when reheating. Freezing kills some Salmonella, but it is not sufficient to reliably reduce them below infectious levels. While Salmonella is usually heat-sensitive, it acquires heat-resistance in high-fat environments such as peanut butter.[40]

Vaccine

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Antibodies against nontyphoidal Salmonella were first found in Malawi children in research published in 2008. The Malawian researchers identified an antibody that protects children against bacterial infections of the blood caused by nontyphoidal Salmonella. A study at Queen Elizabeth Hospital in Blantyre found that children up to two years old develop antibodies that aid in killing the bacteria. This could lead to a possible Salmonella vaccine for humans.[41]

A 2014 study tested a vaccine on chickens which offered efficient protection against salmonellosis.[42]

Vaccination of chickens against Salmonella essentially wiped out the disease in the United Kingdom. A similar approach was considered in the United States, but the Food and Drug Administration decided not to mandate vaccination of hens.[43]

Treatment

[edit]

Electrolytes may be replenished with oral rehydration supplements (typically containing salts sodium chloride and potassium chloride).[citation needed]

Appropriate antibiotics, such as ceftriaxone, may be given to kill the bacteria, but are not necessary in most cases.[22] Azithromycin has been suggested to be better at treating typhoid in resistant populations than both fluoroquinolone drugs and ceftriaxone. There are recommendations on choice of antibiotic to avoid promoting antibiotic resistance.[citation needed]

There is no evidence of benefit of treating healthy people with diarrhea due to non-typhoidal salmonellosis. However, the evidence for the very young, very old or people with severe diseases are uncertain.[44]

Epidemiology

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United States

[edit]
Main article: Salmonellosis in the United States

Salmonellosis annually causes, per CDC estimation, about 1.35 million illnesses, 26,500 hospitalizations, and 420 deaths in the United States every year.[45] About 142,000 people in the United States are infected each year with Salmonella Enteritidis specifically from chicken eggs, and about 30 die.[30]

In 2010, an analysis of death certificates in the United States identified a total of 1,316 Salmonella-related deaths from 1990 to 2006. These were predominantly among older adults and those who were immunocompromised.[46] The U.S. government reported as many as 20% of all chickens were contaminated with Salmonella in the late 1990s, and 16.3% were contaminated in 2005.[47]

The United States has struggled to control salmonella infections, with the rate of infection rising from 2001 to 2011. In 1998, the USDA moved to close plants if salmonella was found in excess of 20 percent, which was the industry's average at the time, for three consecutive tests.[48] Texas-based Supreme Beef Processors, Inc. sued on the argument that Salmonella is naturally occurring and ultimately prevailed when a federal appeals court affirmed a lower court.[48] These issues were highlighted in a proposed Kevin's Law (formally proposed as the Meat and Poultry Pathogen Reduction and Enforcement Act of 2003), of which components were included the Food Safety Modernization Act passed in 2011, but that law applies only to the FDA and not the USDA.[48] The USDA proposed a regulatory initiative in 2011 to Office of Management and Budget.[49]

Salmonella is found in 8% of the chicken parts tested by the USDA and 25% of ground chicken.[50]

Europe

[edit]

An outbreak of salmonellosis started in Northern Europe in July 2012, caused by Salmonella thompson. The infections were linked to smoked salmon from the manufacturer Foppen, where the contamination had occurred. Most infections were reported in the Netherlands; over 1060 infections with this subspecies and four fatalities were confirmed.[51][52]

A case of widespread infection was detected mid-2012 in seven EU countries. Over 400 people had been infected with Salmonella enterica serovar Stanley (S. Stanley) that usually appears in the regions of Southeast Asia. After several DNA analyses seemed to point to a specific Belgian strain, the "Joint ECDC/E FSA Rapid Risk Assessment" report detected turkey production as the source of infection.[53]

In Germany, food poisoning infections must be reported.[54] Between 1990 and 2005, the number of officially recorded cases decreased from about 200,000 to about 50,000.[citation needed]

Elsewhere

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In March 2007, around 150 people were diagnosed with salmonellosis after eating tainted food at a governor's reception in Krasnoyarsk, Russia. Over 1,500 people attended the ball on March 1 and fell ill as a consequence of ingesting Salmonella-tainted sandwiches.[citation needed]

In Singapore about 150 people fell sick after eating Salmonella-tainted chocolate cake produced by a major bakery chain in December 2007.[55]

South Africa reported contamination of its poultry carcasses by Salmonella. Egypt showed that Salmonella was predominant in poultry along with other non-typhoid strains. In Indonesia, the isolation of Salmonella Typhi was the main focus, while other serovars were also included from poultry. In India, Salmonella was predominant in poultry. Romania reported Salmonella serovars in poultry that affect humans.[56]

History

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Both salmonellosis and the microorganism genus Salmonella derive their names from a modern Latin coining after Daniel E. Salmon (1850–1914), an American veterinary surgeon. He had help from Theobald Smith, and together they found the bacterium in pigs.[citation needed]

Salmonella enterica was possibly the cause of the 1576 cocliztli epidemic in New Spain.[57]

Four-inch regulation

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The "Four-inch regulation" or "Four-inch law" is a colloquial name for a regulation issued by the U.S. FDA in 1975, restricting the sale of turtles with a carapace length less than four inches (10 cm).[58]

The regulation was introduced, according to the FDA, "because of the public health impact of turtle-associated salmonellosis". Cases had been reported of young children placing small turtles in their mouths, which led to the size-based restriction.[citation needed]

Regulation elsewhere

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FSSAI regulation

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The FSSAI has been established under the Food Safety and Standards Act, 2006, which is a consolidating statute related to food safety and regulation in India. FSSAI is responsible for protecting and promoting public health through the regulation and supervision of food safety. The major importance of the FSSAI License is that it ensures that the food is verified chemically and hence is safe to consume. 'Health before wealth' is a common quote as well as fact. Therefore, anything related directly to health is a matter of great sensitivity.[59]

Research

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Bacteriophage treatment

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Main article: Phage therapy

Therapy with phages or bacteriophages (viruses that infect bacteria) has been proposed as a treatment for Salmonella infections. Bacteriophages have a number of advantages over other alternatives: (i) high efficacy in killing bacteria, (ii) minimal or no side effects, (iii) no allergic effects, (iv) production is rapid and inexpensive, and (v) they are host-specific and therefore do not affect the intestinal microbiota or other saprophytic bacteria in the environmental milieu.

The use of bacteriophages is effective in the prevention and treatment of bacterial pathogens in animals. In the specific case of poultry, good results have been obtained by reducing the infection of Salmonella, E. coli and Campylobacter. Until now, the use of phage therapy to control Salmonella in poultry could reduce, but not completely eliminate bacterial colonisation.[60]

Bacteriophages are suitable to prevent or reduce the colonization of pathogenic bacteria and therefore diseases in cattle,[61] where phages are supplied either individually or in cocktail to farm animals, the routes and methods of application were examined by various authors and the application of phages through oral tube feeding or feed intake showed a reduction of pathogenic bacteria without affecting the intestinal microbiota of the host.[62] Current research is focused on improved phage delivery in a manner that avoids decreasing phage titer due to destabilization or inactivation by gastric pH extremes.

Immunological parameters of infection

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From an immunological point of view Salmonellosis is an infection caused by gram-negative bacteria infiltrating epithelial cells of the small intestine in the distal ileum whereby inducing acute inflammatory response called enteritis.[63] Salmonella can infect M-cells population overlying the Payer’s patches in the intestine, cells located in lamina propria of the intestinal mucosa and other epithelial cells.[63] After infecting cells in Peyer's patches, Salmonella can move to the mesenteric lymph nodes. This happens because lymphatic vessels are responsible for draining fluids, cells, and microbes from the intestinal tissues and carrying them to these lymph nodes. This process requires migration dependent on a factor known as CCR7. Once in the mesenteric lymph nodes, Salmonella can then enter the bloodstream, leading to a systemic infection that spreads throughout the body.[64] Virulence of the Salmonella is given by the Salmonella Pathogenicity Island 1 (SPI-1).[65] This needle-like structure, formed by a set of proteins, is known as the Type III secretion system. It enables Salmonella to effectively invade neighboring cells by injecting bacterial proteins directly into them, facilitating its spread and evasion of the host's immune defenses.[66] The first cells recruited to the Salmonella infection site are neutrophils, monocytes, and dendritic cells. Neutrophils play a key role in early defense against Salmonella, preventing its spread into the bloodstream. Studies in mice have shown that without neutrophils, there's an increase in the extracellular bacterial load during Salmonella infection. Moreover, these cells are essential for producing IFN-γ in the intestinal mucosa, which is crucial for controlling Salmonella Typhimurium through an IFN-γ-dependent mechanism.[67] Several other pro-inflammatory cytokines have been also observed after the infection of the epithelia such as IL-1α, TNFα, IL-12, IL-18 and IL-15, affecting the body-temperature by inducing fever, increase mucus production, activation of B and T leukocytes and polymorphonuclear leukocytes and macrophages recruitment to the site of infection.[68] Resident macrophages can also recognize flagellin and activate NLRC4 inflammasome complex to activate caspase-1 and IL-1β and IL-18 release.[69] Recruited monocytes are specifically adapted to regulating bacterial replication through the production of antimicrobial molecules (anti-microbial factors such as iNOS, TNF-α and IL-1β), however, they exhibit limited capability as antigen-presenting cells.[70] While monocytes help in containing the bacteria initially, the inability to effectively present antigens can delay or weaken the activation of T cells, which are necessary for a strong and specific immune response. In contrast, dendritic cells experience maturation through both direct pathways, mediated by bacteria, and indirect pathways, facilitated by cytokines in vivo, enhancing their ability to present antigens optimally. In a study focusing on the interaction between dendritic cells and intestinal epithelial cells, it was observed that when intestinal epithelial cells are stimulated by flagellin (a component of bacterial flagella, like those found in Salmonella), they trigger a specific response. This response involves the release of a molecule called CCL20. CCL20 is known to attract DCs, a type of immune cell. As a result, dendritic cells migrate towards the site of flagellin stimulation in the intestines. Recruitment of these cells to follicles plays a crucial role in initiating early T-cells mediated responses to Salmonella infection.[71] T–cell activation is limited to the draining mesenteric lymph nodes within 9–12 h since the initial infection as in any other lymph node activated T-cells specific to Salmonella were not detected.[72] Protective immunity against Salmonella appears to be primarily mediated by CD4+ T cells. This is evident in mice lacking a thymus, αβ T cells, MHC class-II, or T-bet+ Th1 cells, as they demonstrate an inability to resolve the infection.[73][74] Clearly Th1 response is crucial in response and clearance of Salmonella infection since mice depleted from T-bet or IFN-γ are unable to combat Salmonellosis. The presence of different cytokines in combination with cytokines produced from Th1 cells however suggests additional effect of Th17 response. IL-22 and IL-17 are contributing to protection against Salmonella by its mucosal production and antimicrobial peptides expression (IL-22) as well regulation of mucosal host defense and neutrophil recruitment (IL17) demonstrated by IL-17A deficient mice infected with Salmonella.[75][76] Conversely, mice lacking B-cells or γδ T cells can successfully clear the primary attenuated Salmonella infection, but a robust B-cell response is essential for resolving virulent Salmonella infections.[77] Different study revealed that B-cells are essential for protective immunity against Salmonella independent of antibody secretion because B-cells unable to secrete antibodies were still protective against Salmonella, suggesting that B-cells can serve as antigen presenting cells in this context and activate T-cells responses.[78] Further experiments focused on CD8+ cytotoxic lymphocytes revealed their crucial role in Salmonella clearance. Depletion of CD8+ T cells resulted in the failure to resolve the infection in mice.[79] These findings strongly suggest that CD4+-mediated protection is facilitated by the contribution of CD8+ cytotoxic T cells in the immune response against Salmonella. The investigation of immune memory revealed robust bacterial clearance facilitated by both CD4+ and CD8+ responses. Interestingly, this memory was not sufficient in adoptive transfer into other mice, despite possessing a potent response. However, when serum transfer was employed, the observed response indicated the crucial antibody-dependent role in secondary Salmonella infections.[80] Immunocompromised individuals (for example AIDS, malnutrition or those taking immunosuppressive treatment) are more susceptible to salmonellosis and contribute to bacteremia caused by neutropenia in immunocompromised individuals comparing immunocompetent ones.[81]

See also

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References

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  1. ^ a b c d e f g h i j k l m n o p "Salmonella". CDC. 13 November 2019. Archived from the original on 6 May 2022. Retrieved 5 May 2022.
  2. ^ a b c d Hald T (2013). Advances in microbial food safety: 2. Pathogen update: Salmonella. Elsevier Inc. Chapters. p. 2.2. ISBN 9780128089606. Archived from the original on 2017-09-10.
  3. ^ a b c "Salmonella Infections". MedlinePlus. Archived from the original on 30 April 2017. Retrieved 7 May 2017.
  4. ^ a b c d e f g h i j "Salmonella (non-typhoidal)". World Health Organization. December 2016. Archived from the original on 20 April 2017. Retrieved 7 May 2017.
  5. ^ a b Wang H, Naghavi M, Allen C, Barber RM, Bhutta ZA, Carter A, et al. (October 2016). "Global, regional, and national life expectancy, all-cause mortality, and cause-specific mortality for 249 causes of death, 1980-2015: a systematic analysis for the Global Burden of Disease Study 2015". Lancet. 388 (10053): 1459–1544. doi:10.1016/s0140-6736(16)31012-1. PMC 5388903. PMID 27733281.
  6. ^ Qamar FN, Hussain W, Qureshi S (2022). "Salmonellosis Including Enteric Fever". Pediatric Clinics of North America. 69 (1): 65–77. doi:10.1016/j.pcl.2021.09.007. PMID 34794677. S2CID 244281295.
  7. ^ "Typhoid & Paratyphoid Fever | CDC Yellow Book 2024".
  8. ^ "Salmonella and Food". 5 June 2023.
  9. ^ "Chicken and Food Poisoning". 14 November 2023.
  10. ^ Cohn AR, Cheng RA, Orsi RH, Wiedmann M (13 May 2021). "Moving Past Species Classifications for Risk-Based Approaches to Food Safety: Salmonella as a Case Study". Frontiers in Sustainable Food Systems. 5: 652132. doi:10.3389/fsufs.2021.652132.
  11. ^ O'Hagan M (10 September 2021). "Salmonella: Why it's a chicken and egg thing". Knowable Magazine. doi:10.1146/knowable-091021-1. S2CID 239248124. Retrieved 13 September 2021.
  12. ^ Ricke SC (February 2021). "Strategies to Improve Poultry Food Safety, a Landscape Review". Annual Review of Animal Biosciences. 9 (1): 379–400. doi:10.1146/annurev-animal-061220-023200. PMID 33156992. S2CID 226275729.
  13. ^ Centers for Disease Control and Prevention (CDC) (June 2002). "Outbreak of multidrug-resistant Salmonella newport--United States, January-April 2002". MMWR. Morbidity and Mortality Weekly Report. 51 (25): 545–548. PMID 12118534.
  14. ^ "Salmonella". World Health Organization. Archived from the original on 17 April 2017. Retrieved 7 May 2017.
  15. ^ a b Santos RL, Zhang S, Tsolis RM, Kingsley RA, Adams LG, Bäumler AJ (2001). "Animal models of Salmonella infections: enteritis versus typhoid fever". Microbes and Infection. 3 (14–15): 1335–1344. doi:10.1016/s1286-4579(01)01495-2. PMID 11755423.
  16. ^ "Nontyphoidal Salmonella Infections - Infectious Diseases - Merck Manuals Professional Edition". Merck Manuals Professional Edition. Retrieved 2018-09-15.
  17. ^ "What is Salmonellosis?". US Center of Disease Control and Prevention. 2019-02-08. Archived from the original on 2014-03-31.
  18. ^ Smith JL, Bayles D (July 2007). "Postinfectious irritable bowel syndrome: a long-term consequence of bacterial gastroenteritis". Journal of Food Protection. 70 (7): 1762–1769. doi:10.4315/0362-028X-70.7.1762. PMID 17685356. S2CID 42240663.
  19. ^ a b Mann EA, Saeed SA (January 2012). "Gastrointestinal infection as a trigger for inflammatory bowel disease". Current Opinion in Gastroenterology. 28 (1): 24–29. doi:10.1097/mog.0b013e32834c453e. PMID 22080823. S2CID 800248.
  20. ^ Schmitt SK (June 2017). "Reactive Arthritis". Infectious Disease Clinics of North America (Review). 31 (2): 265–277. doi:10.1016/j.idc.2017.01.002. PMID 28292540.
  21. ^ Burnett MW, Bass JW, Cook BA (February 1998). "Etiology of osteomyelitis complicating sickle cell disease". Pediatrics. 101 (2): 296–297. doi:10.1542/peds.101.2.296. PMID 9445507.
  22. ^ a b "Nontyphoidal Salmonella Infections". Merck Manual. Archived from the original on 2016-09-19. Retrieved 2016-09-19.
  23. ^ Goldberg J (24 February 2012). "Are the bacteria that make food smell and taste bad the same ones that make you sick?". Tufts.edu. Retrieved 28 May 2018.
  24. ^ Di Bella S, Capone A, Bordi E, Johnson E, Musso M, Topino S, et al. (July 2011). "Salmonella enterica ssp. arizonae infection in a 43-year-old Italian man with hypoglobulinemia: a case report and review of the literature". Journal of Medical Case Reports. 5 (1): 323. doi:10.1186/1752-1947-5-323. PMC 3156765. PMID 21781321.
  25. ^ "Reptile-Associated Salmonellosis—Selected States, 1998–2002". Centers for Disease Control and Prevention. 12 December 2003. Archived from the original on 6 October 2011. Retrieved 9 October 2011.
  26. ^ Mermin J, Hoar B, Angulo FJ (March 1997). "Iguanas and Salmonella marina infection in children: a reflection of the increasing incidence of reptile-associated salmonellosis in the United States". Pediatrics. 99 (3): 399–402. doi:10.1542/peds.99.3.399. PMID 9041295.
  27. ^ "Ongoing investigation into reptile associated salmonella infections". Health Protection Report. 3 (14). 9 April 2009. Archived from the original on 29 April 2009. Retrieved 12 April 2009.
  28. ^ "Multi-country outbreak of Salmonella Stanley infections Update". EFSA Journal. 10 (9): 2893. 21 September 2012. doi:10.2903/j.efsa.2012.2893.
  29. ^ "Playing It Safe With Eggs". FDA Food Facts. 2013-02-28. Archived from the original on 2013-03-01. Retrieved 2013-03-02. The U.S. Food and Drug Administration (FDA) estimates that 142,000 illnesses each year are caused by consuming eggs contaminated with Salmonella.
  30. ^ a b Black J, O'Keefe E (2009-07-08). "Administration Urged to Boost Food Safety Efforts". Washington Post. Archived from the original on 2011-06-04. Retrieved 2009-07-07.
  31. ^ Gantois I, Ducatelle R, Pasmans F, Haesebrouck F, Gast R, Humphrey TJ, Van Immerseel F (July 2009). "Mechanisms of egg contamination by Salmonella Enteritidis". FEMS Microbiology Reviews. 33 (4): 718–738. doi:10.1111/j.1574-6976.2008.00161.x. PMID 19207743. Eggs can be contaminated on the outer shell surface and internally. Internal contamination can be the result of penetration through the eggshell or by direct contamination of egg contents before oviposition, originating from infection of the reproductive organs. Once inside the egg, the bacteria need to cope with antimicrobial factors in the albumen and vitelline membrane before migration to the yolk can occur
  32. ^ Humphrey TJ (January 1994). "Contamination of egg shell and contents with Salmonella enteritidis: a review". International Journal of Food Microbiology. 21 (1–2): 31–40. doi:10.1016/0168-1605(94)90197-X. PMID 8155476. Salmonella enteritidis can contaminate the contents of clean, intact shell eggs as a result of infections of the reproductive tissue of laying hens. The principal site of infection appears to be the upper oviduct. In egg contents, the most important contamination sites are the outside of the vitelline membrane or the albumen surrounding it. In fresh eggs, only a few salmonellae are present. As albumen is an iron-restricted environment, growth only occurs with storage-related changes to vitelline membrane permeability, which allows salmonellae to invade yolk contents.
  33. ^ Stokes JL, Osborne WW, Bayne HG (September 1956). "Penetration and Growth of Salmonella in Shell Eggs". Journal of Food Science. 21 (5): 510–518. doi:10.1111/j.1365-2621.1956.tb16950.x. Normally, the oviduct of the hen is sterile and therefore the shell and internal contents of the egg are also free of microorganisms (10,16). In some instances, however, the ovaries and oviduct may be infected with Salmonella and these may be deposited inside the egg (12). More frequently, however, the egg becomes contaminated after it is laid.
  34. ^ Okamura M, Kamijima Y, Miyamoto T, Tani H, Sasai K, Baba E (2001). "Differences among six Salmonella serovars in abilities to colonize reproductive organs and to contaminate eggs in laying hens". Avian Diseases. 45 (1): 61–69. doi:10.2307/1593012. JSTOR 1593012. PMID 11332500. when hens were artificially infected to test for transmission rate to yolks: "Mature laying hens were inoculated intravenously with 106 colony-forming units of Salmonella enteritidis, Salmonella typhimurium, Salmonella infantis, Salmonella hadar, Salmonella heidelberg, or Salmonella montevideo to cause the systemic infection. Salmonella Enteritidis was recovered from three yolks of the laid eggs (7.0%), suggesting egg contamination from the transovarian transmission of S. enteritidis."
  35. ^ Gast RK, Jones DR, Anderson KE, Guraya R, Guard J, Holt PS (August 2010). "In vitro penetration of Salmonella Enteritidis through yolk membranes of eggs from 6 genetically distinct commercial lines of laying hens". Poultry Science. 89 (8): 1732–1736. doi:10.3382/ps.2009-00440. PMID 20634530. Archived from the original on 2011-07-24. Retrieved 2010-08-20. In this study, egg yolks were infected at the surface of the yolk (vitelline membrane) to determine the percentage of yolk contamination (a measure used to determine egg contamination resistance, with numbers lower than 95% indicating increasing resistance): Overall, the frequency of penetration of Salmonella Enteritidis into the yolk contents of eggs from individual lines of hens ranged from 30 to 58% and the mean concentration of Salmonella Enteritidis in yolk contents after incubation ranged from 0.8 to 2.0 log10 cfu/mL.
  36. ^ Jaeger G (Jul–Aug 2009). "Contamination of eggs of laying hens with S. Enteritidis". Veterinary Survey (Tierärztliche Umschau). 64 (7–8): 344–348. Retrieved 2010-08-20. The migration of the bacterium into the nutritionally rich yolk is constrained by the lysozyme loaded vitelline membrane, and would need warm enough storage conditions within days and weeks. The high concentration on of antibodies of the yolk does not inhibit the Salmonella multiplication. Only seldom does transovarian contamination of the developing eggs with S. enteritidis make this bacterium occur in laid eggs, because of the bactericidal efficacy of the antimicrobial peptides
  37. ^ Humphrey TJ, Whitehead A, Gawler AH, Henley A, Rowe B (June 1991). "Numbers of Salmonella enteritidis in the contents of naturally contaminated hens' eggs". Epidemiology and Infection. 106 (3): 489–496. doi:10.1017/S0950268800067546. PMC 2271858. PMID 2050203. Over 5700 hens eggs from 15 flocks naturally infected with Salmonella enteritidis were examined individually for the presence of the organism in either egg contents or on shells. Thirty-two eggs (0·6%) were positive in the contents. In the majority, levels of contamination were low.
  38. ^ Gast RK, Guraya R, Guard-Bouldin J, Holt PS, Moore RW (March 2007). "Colonization of specific regions of the reproductive tract and deposition at different locations inside eggs laid by hens infected with Salmonella enteritidis or Salmonella heidelberg". Avian Diseases. 51 (1): 40–44. doi:10.1637/0005-2086(2007)051[0040:cosrot]2.0.co;2. PMID 17461265. S2CID 20428394. Archived from the original on 2010-03-10. Retrieved 2010-08-20. when hens are artificially infected with unrealistically large doses (according to the author): In the present study, groups of laying hens were experimentally infected with large oral doses of Salmonella Heidelberg, Salmonella Enteritidis phage type 13a, or Salmonella Enteritidis phage type 14b. For all of these isolates, the overall frequency of ovarian colonization (34.0%) was significantly higher than the frequency of recovery from either the upper (22.9%) or lower (18.1%) regions of the oviduct. No significant differences were observed between the frequencies of Salmonella isolation from egg yolk and albumen (4.0% and 3.3%, respectively).
  39. ^ "Salmonella Questions and Answers". USDA Food Safety and Inspection Service. 2006-09-20. Archived from the original on 2009-01-15. Retrieved 2009-01-21.
  40. ^ "FDA issues peanut safety guidelines for foodmakers". Reuters. 2009-03-10. Archived from the original on 2009-03-12.
  41. ^ MacLennan CA, Gondwe EN, Msefula CL, Kingsley RA, Thomson NR, White SA, et al. (April 2008). "The neglected role of antibody in protection against bacteremia caused by nontyphoidal strains of Salmonella in African children". The Journal of Clinical Investigation. 118 (4): 1553–1562. doi:10.1172/JCI33998. PMC 2268878. PMID 18357343.
  42. ^ Nandre RM, Lee JH (January 2014). "Construction of a recombinant-attenuated Salmonella Enteritidis strain secreting Escherichia coli heat-labile enterotoxin B subunit protein and its immunogenicity and protection efficacy against salmonellosis in chickens". Vaccine. 32 (3): 425–431. doi:10.1016/j.vaccine.2013.10.054. PMID 24176491.
  43. ^ Neuman W (2010-08-24). "U.S. Forgoes Salmonella Vaccine for Egg Safety". The New York Times. ISSN 0362-4331. Archived from the original on 2016-04-17. Retrieved 2016-03-12.
  44. ^ Onwuezobe IA, Oshun PO, Odigwe CC (November 2012). "Antimicrobials for treating symptomatic non-typhoidal Salmonella infection". The Cochrane Database of Systematic Reviews. 11 (11): CD001167. doi:10.1002/14651858.CD001167.pub2. PMC 6532567. PMID 23152205.
  45. ^ "Salmonella Questions and Answers | CDC". www.cdc.gov. 2023-04-23.
  46. ^ Cummings PL, Sorvillo F, Kuo T (November 2010). "Salmonellosis-related mortality in the United States, 1990-2006". Foodborne Pathogens and Disease. 7 (11): 1393–1399. doi:10.1089/fpd.2010.0588. PMID 20617938.
  47. ^ Burros M (March 8, 2006). "More Salmonella Is Reported in Chickens". The New York Times. Archived from the original on January 9, 2016. Retrieved 2007-05-13.
  48. ^ a b c "Salmonella Lurks From Farm to Fork « News21 2011 National Project". foodsafety.news21.com. Archived from the original on 2016-06-02. Retrieved 2016-09-18.
  49. ^ "Ground Turkey Recall Shows We Still Need Kevin's Law | Food Safety News". 2011-08-12. Archived from the original on 2016-10-09. Retrieved 2016-09-18.
  50. ^ Simon B, Yeung M, Grabell I, Hwang M (29 October 2021). "America's Food Safety System Failed to Stop a Salmonella Epidemic. It's Still Making People Sick". ProPublica. Retrieved 2021-11-03.
  51. ^ Veelgestelde vragen Salmonella Thompson 15 oktober 2012, Rijksinstituut voor Volksgezondheid en Milieu [Frequently asked questions Salmonella Thompson 15 October 2012, Netherlands Institute for Public Health and the Environment].
  52. ^ "Salmonella besmetting neemt verder af, 2 november 2012, Rijksinstituut voor Volksgezondheid en Milieu" [Salmonella infections continue to decline 2 November 2012, Netherlands Institute for Public Healthand the Environment].
  53. ^ European Centre for Disease Prevention and Control, European Food Safety Authority (2012). "Multi-country outbreak of Salmonella Stanley infections Update". EFSA Journal. 10 (9): 2893. doi:10.2903/j.efsa.2012.2893. Archived from the original on 2014-04-13.
  54. ^ § 6 and § 7 of the German law on infectious disease prevention, Infektionsschutzgesetz
  55. ^ Hong L (7 December 2007). "PrimaDeli food poisoning cases increase to 153". Channel NewsAsia. Archived from the original on 8 December 2007.
  56. ^ Barbour EK, Ayyash DB, Alturkistni W, Alyahiby A, Yaghmoor S, Iyer A, et al. (January 2015). "Impact of sporadic reporting of poultry Salmonella serovars from selected developing countries". Journal of Infection in Developing Countries. 9 (1): 001–007. doi:10.3855/jidc.5065. PMID 25596565.
  57. ^ Vågene ÅJ, Herbig A, Campana MG, Robles García NM, Warinner C, Sabin S, et al. (March 2018). "Salmonella enterica genomes from victims of a major sixteenth-century epidemic in Mexico". Nature Ecology & Evolution. 2 (3): 520–528. Bibcode:2018NatEE...2..520V. doi:10.1038/s41559-017-0446-6. PMID 29335577. S2CID 3358440.
  58. ^ "Human Health Hazards Associated with Turtles". U.S. Food and Drug Administration. Archived from the original on 2007-06-09. Retrieved 2007-06-29.
  59. ^ "The Food Safety and Standards Authority of India (FSSAI)".
  60. ^ Oechslin F (June 2018). "Resistance Development to Bacteriophages Occurring during Bacteriophage Therapy". Viruses. 10 (7): 351. doi:10.3390/v10070351. PMC 6070868. PMID 29966329.
  61. ^ García P, Martínez B, Obeso JM, Rodríguez A (December 2008). "Bacteriophages and their application in food safety". Letters in Applied Microbiology. 47 (6): 479–485. doi:10.1111/j.1472-765x.2008.02458.x. PMID 19120914. S2CID 30899476.
  62. ^ Olson EG, Micciche AC, Rothrock MJ, Yang Y, Ricke SC (2022). "Application of Bacteriophages to Limit Campylobacter in Poultry Production". Frontiers in Microbiology. 12: 458721. doi:10.3389/fmicb.2021.458721. PMC 8766974. PMID 35069459.
  63. ^ a b House D, Bishop A, Parry C, Dougan G, Wain J (October 2001). "Typhoid fever: pathogenesis and disease". Current Opinion in Infectious Diseases. 14 (5): 573–578. doi:10.1097/00001432-200110000-00011. ISSN 0951-7375. PMID 11964878. S2CID 33369729.
  64. ^ Voedisch S, Koenecke C, David S, Herbrand H, Förster R, Rhen M, Pabst O (August 2009). "Mesenteric lymph nodes confine dendritic cell-mediated dissemination of Salmonella enterica serovar Typhimurium and limit systemic disease in mice". Infection and Immunity. 77 (8): 3170–3180. doi:10.1128/IAI.00272-09. ISSN 1098-5522. PMC 2715677. PMID 19506012.
  65. ^ Jones BD, Falkow S (September 1994). "Identification and characterization of a Salmonella typhimurium oxygen-regulated gene required for bacterial internalization". Infection and Immunity. 62 (9): 3745–3752. doi:10.1128/iai.62.9.3745-3752.1994. ISSN 0019-9567. PMC 303026. PMID 8063389.
  66. ^ Espina M, Olive AJ, Kenjale R, Moore DS, Ausar SF, Kaminski RW, Oaks EV, Middaugh CR, Picking WD, Picking WL (August 2006). "IpaD Localizes to the Tip of the Type III Secretion System Needle of Shigella flexneri". Infection and Immunity. 74 (8): 4391–4400. doi:10.1128/IAI.00440-06. ISSN 0019-9567. PMC 1539624. PMID 16861624.
  67. ^ Conlan JW (March 1996). "Neutrophils prevent extracellular colonization of the liver microvasculature by Salmonella typhimurium". Infection and Immunity. 64 (3): 1043–1047. doi:10.1128/iai.64.3.1043-1047.1996. ISSN 0019-9567. PMC 173878. PMID 8641757.
  68. ^ Eckmann L, Kagnoff MF (1 November 2001). "Cytokines in host defense against Salmonella". Microbes and Infection. 3 (14): 1191–1200. doi:10.1016/S1286-4579(01)01479-4. ISSN 1286-4579. PMID 11755407.
  69. ^ Miao EA, Alpuche-Aranda CM, Dors M, Clark AE, Bader MW, Miller SI, Aderem A (June 2006). "Cytoplasmic flagellin activates caspase-1 and secretion of interleukin 1beta via Ipaf". Nature Immunology. 7 (6): 569–575. doi:10.1038/ni1344. ISSN 1529-2908. PMID 16648853. S2CID 11172068.
  70. ^ Rydström A, Wick MJ (1 May 2007). "Monocyte recruitment, activation, and function in the gut-associated lymphoid tissue during oral Salmonella infection". Journal of Immunology. 178 (9): 5789–5801. doi:10.4049/jimmunol.178.9.5789. ISSN 0022-1767. PMID 17442963.
  71. ^ Pham OH, McSorley SJ (January 2015). "Protective host immune responses to Salmonella infection". Future Microbiology. 10 (1): 101–110. doi:10.2217/fmb.14.98. ISSN 1746-0913. PMC 4323267. PMID 25598340.
  72. ^ McSorley SJ, Asch S, Costalonga M, Reinhardt RL, Jenkins MK (March 2002). "Tracking salmonella-specific CD4 T cells in vivo reveals a local mucosal response to a disseminated infection". Immunity. 16 (3): 365–377. doi:10.1016/s1074-7613(02)00289-3. ISSN 1074-7613. PMID 11911822.
  73. ^ Ravindran R, Foley J, Stoklasek T, Glimcher LH, McSorley SJ (1 October 2005). "Expression of T-bet by CD4 T cells is essential for resistance to Salmonella infection". Journal of Immunology. 175 (7): 4603–4610. doi:10.4049/jimmunol.175.7.4603. ISSN 0022-1767. PMID 16177105.
  74. ^ Weintraub BC, Eckmann L, Okamoto S, Hense M, Hedrick SM, Fierer J (June 1997). "Role of alphabeta and gammadelta T cells in the host response to Salmonella infection as demonstrated in T-cell-receptor-deficient mice of defined Ity genotypes". Infection and Immunity. 65 (6): 2306–2312. doi:10.1128/iai.65.6.2306-2312.1997. ISSN 0019-9567. PMC 175320. PMID 9169768.
  75. ^ Schulz SM, Köhler G, Holscher C, Iwakura Y, Alber G (September 2008). "IL-17A is produced by Th17, gammadelta T cells and other CD4- lymphocytes during infection with Salmonella enterica serovar Enteritidis and has a mild effect in bacterial clearance". International Immunology. 20 (9): 1129–1138. doi:10.1093/intimm/dxn069. ISSN 1460-2377. PMID 18599501.
  76. ^ Lee SJ, McLachlan JB, Kurtz JR, Fan D, Winter SE, Baumler AJ, Jenkins MK, McSorley SJ (January 2012). "Temporal expression of bacterial proteins instructs host CD4 T cell expansion and Th17 development". PLOS Pathogens. 8 (1): e1002499. doi:10.1371/journal.ppat.1002499. ISSN 1553-7374. PMC 3262010. PMID 22275869.
  77. ^ Mastroeni P, Simmons C, Fowler R, Hormaeche CE, Dougan G (January 2000). "Igh-6−/− (B-Cell-Deficient) Mice Fail To Mount Solid Acquired Resistance to Oral Challenge with Virulent Salmonella enterica Serovar Typhimurium and Show Impaired Th1 T-Cell Responses to Salmonella Antigens". Infection and Immunity. 68 (1): 46–53. doi:10.1128/IAI.68.1.46-53.2000. ISSN 0019-9567. PMC 97100. PMID 10603367.
  78. ^ Nanton MR, Way SS, Shlomchik MJ, McSorley SJ (15 December 2012). "Cutting edge: B cells are essential for protective immunity against Salmonella independent of antibody secretion". Journal of Immunology. 189 (12): 5503–5507. doi:10.4049/jimmunol.1201413. ISSN 1550-6606. PMC 3518619. PMID 23150714.
  79. ^ Lee SJ, Dunmire S, McSorley SJ (17 December 2012). "MHC class-I-restricted CD8 T cells play a protective role during primary Salmonella infection". Immunology Letters. 148 (2): 138–143. doi:10.1016/j.imlet.2012.10.009. ISSN 0165-2478. PMC 3540194. PMID 23089550.
  80. ^ Mastroeni P, Villarreal-Ramos B, Hormaeche CE (September 1993). "Adoptive transfer of immunity to oral challenge with virulent salmonellae in innately susceptible BALB/c mice requires both immune serum and T cells". Infection and Immunity. 61 (9): 3981–3984. doi:10.1128/iai.61.9.3981-3984.1993. ISSN 0019-9567. PMC 281103. PMID 8359920.
  81. ^ Tumbarello M, Tacconelli E, Caponera S, Cauda R, Ortona L (September 1995). "The impact of bacteraemia on HIV infection. Nine years experience in a large Italian university hospital". The Journal of Infection. 31 (2): 123–131. doi:10.1016/s0163-4453(95)92110-9. ISSN 0163-4453. PMID 8666842.
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