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Show detailsContinuing Education Activity
Vibrio parahaemolyticus infection can cause various types of illness including gastroenteritis, wound infections, and, in more severe cases, sepsis. It is a common cause of bacterial gastroenteritis in Asia, specifically in Japan. Despite being relatively uncommon, outbreaks of Vibrio parahaemolyticus are on the rise in the United States. This activity describes the evaluation and treatment of vibrio parahaemolyticus and highlights the role of the interprofessional team in improving care for affected patients.
Objectives:
- Describe the pathophysiology of Vibrio parahaemolyticus.
- Outline the supportive management of patients affected by Vibrio parahaemolyticus.
- Review the risk factors for developing Vibrio parahaemolyticus infections.
- Outline the importance of collaboration and coordination among the interprofessional team to improve outcomes for patients with Vibrio parahaemolyticus infections.
Introduction
Vibrio parahaemolyticus infection can cause a varying degree of illness including gastroenteritis, wound infections, and in more severe cases it can cause sepsis. Although less common in the United States, it is a common cause of bacterial gastroenteritis in Asia, specifically in Japan. Despite being relatively uncommon, outbreaks of V. parahaemolyticus are on the rise in the United States.[1][2]
Etiology
First discovered in the 1950s in Japan, V. parahaemolyticus is a gram-negative bacterium found in marine and estuarine environments. It is associated with the consumption of raw seafood, especially shellfish such as mussels. V. parahaemolyticus thrive in warmer water and areas of less salinity.[3]
Epidemiology
Although a major cause of gastroenteritis in Japan, V. parahaemolyticus gastroenteritis is less common in the United States with the Center for Disease Control reporting a 2016 incidence of 0.45 cases per 100,000. The incidence in the United States has been steadily increasing. There are typically more cases during the warmer months (May through October), and cases commonly occur as part of an outbreak. Even though V. parahaemolyticus grows best in warmer waters, outbreaks have been reported in colder areas such as Alaska. Despite being found freely in saltwater, it can be found in higher concentrations in shellfish such as mussels, since they filter the water concentrating the bacteria.[4]
Pathophysiology
V. parahaemolyticus can infect the host through different routes. Infected seafood can be consumed, causing direct contact with the gastrointestinal system. The bacteria can also make their way into an open wound during exposure to saltwater. In severe cases and those with comorbidities, once inside the host the bacteria can further spread into the blood. V. parahaemolyticus has several virulence factors common to other bacteria. However, the major virulence factor of V. parahaemolyticus is thermostable direct hemolysin (TDH). TDH is present in the majority of clinical specimens (88% to 96%) but only in approximately 1% of natural populations of V. parahaemolyticus. Despite this fact, TDH has been identified as a major virulence factor, the specific mechanism by which TDH causes gastroenteritis is not completely understood. TDH is a pore-forming toxin, and researchers postulate that this could be related to its ability to cause gastrointestinal symptoms. In addition to the TDH virulence factor, V. parahaemolyticus also uses a type 3 secretion system, similar to other gram-negative bacteria. Despite its virulence factors, the majority of V. parahaemolyticus infections only result in self-limiting enteritis.
History and Physical
A detailed history is vital to a timely and successful diagnosis of a V. parahaemolyticus infection. Patients will typically present with gastroenteritis-type symptoms such as abdominal cramping, nausea, vomiting, and fever. Because these are general symptoms common to many other illnesses, the line of questioning should include any recent travel to or near the ocean or any consumption of shellfish or seafood, especially raw oysters. This condition is more common in coastal cities, but there are several cases of V. parahaemolyticus in areas distant from the sea. This is a result of patients developing symptoms after returning home from recent travel. The average time from consumption of contaminated food to the onset of symptoms is 17 hours.
In addition to asking about specific V. parahaemolyticus risk factors, information regarding relevant comorbidities should be elicited. Patients who develop an infection with concomitant liver disease, diabetes, or alcoholism have a poorer prognosis and are more likely to develop septicemia.
Physical findings are also generalized. On exam, patients may present with signs of dehydration, non-specific abdominal pain, and occasional bloody stool (approximately 7%). Be alert for signs of cellulitis, especially on body areas exposed to the water such as feet and lower legs. The examination should include a careful review of vital signs for assessment of sepsis. Due to its non-specific findings, the diagnosis is difficult to make on physical exam alone. A detailed and thorough history is essential to raising suspicion and ultimately making a diagnosis of V. parahaemolyticus.
Evaluation
For a patient with a suspected V. parahaemolyticus infection, the diagnostic method of choice is obtaining a stool culture. It is best to choose a selective medium for culture. V. parahaemolyticus grows particularly well on Thiosulfate Citrate Bile-salts Sucrose (TCBS). The bacteria can also demonstrate hemolysis as well as urease positivity. The provider should contact the laboratory and discuss suspicion for V. parahaemolyticus as this can help the lab utilize specialized techniques that can enhance the chance for successful growth. If there is suspicion of septicemia or wound infection, blood and wound cultures can also be obtained.[5]
Treatment / Management
Treatment for the majority of cases is supportive, the same as for most other causes of gastroenteritis. Appropriate initial steps include intravenous fluid rehydration and correction of electrolyte abnormalities. The typical course of infection is self-limited and in most cases does not require additional treatment. There are no recommendations for using antimotility agents to treat diarrhea. In more severe cases such as wound infections and sepsis, antibiotic treatment is indicated. There have been no large studies involving antibiotic treatment specifically for V. parahaemolyticus infection. The recommendations are based on guidelines from studies examining treatment for other Vibrio species. If the patient has a particularly severe case of gastroenteritis, doxycycline is the antibiotic of choice. For uncomplicated wound infections, treat with minocycline or doxycycline. Consider adding a third-generation cephalosporin if the wound infection is severe or if the patient is at significant risk for sepsis (has underlying liver disease, alcohol use disorder, or has diabetes mellitus). For severe cases, the patient should be admitted to the hospital for further intravenous fluid replacement and infectious disease consultation. Mild cases, with a hemodynamically stable patient, can be treated and observed in the emergency department. If the patient remains stable and does not have any signs of sepsis, they may be discharged.[6]
Prevention of V. parahaemolyticus infection is similar to other food-borne illnesses. Seafood should be stored properly and appropriately cooked before consumption. The Center for Disease Control and Prevention recommends against consuming raw oysters or other shellfish, especially in at-risk populations. Additionally, people with open wounds should avoid exposure to brackish or saltwater.
Differential Diagnosis
- Bacterial gastroenteritis
- Cholera
- Toxic shock syndrome
- Necrotizing fasciitis
Complications
- Compartment syndrome
- Reactive arthritis
- Shock
- DIC
- Multiorgan failure
Deterrence and Patient Education
Avoid consuming raw or undercooked seafood.
Pearls and Other Issues
V. parahaemolyticus infections are becoming more common. Due to the non-specific presentation, they can easily be missed. As in all patients with gastroenteritis, asking specific questions can elicit information from the patient that will prove essential to making the diagnosis.
Enhancing Healthcare Team Outcomes
Vibrio infections usually occur after the consumption of contaminated seafood. The majority of these patients present to the emergency department, hence, healthcare workers should be familiar with the signs and symptoms of the disorder. The key to preventing this infection is patient education. The public should be educated about the importance of avoiding uncooked seafood. The outcomes after a vibrio infection in healthy people are excellent, but in patients who are immunocompromised, the prognosis is guarded. Besides antibiotic therapy, some patients may need immediate fasciotomy to relieve compartment syndrome. Others may develop multiorgan failure and require intense support in the ICU. [7][8] [Level 3]
Review Questions
References
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- Klein S, Pipes S, Lovell CR. Occurrence and significance of pathogenicity and fitness islands in environmental vibrios. AMB Express. 2018 Oct 30;8(1):177. [PMC free article: PMC6207609] [PubMed: 30377851]
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- Rincé A, Balière C, Hervio-Heath D, Cozien J, Lozach S, Parnaudeau S, Le Guyader FS, Le Hello S, Giard JC, Sauvageot N, Benachour A, Strubbia S, Gourmelon M. Occurrence of Bacterial Pathogens and Human Noroviruses in Shellfish-Harvesting Areas and Their Catchments in France. Front Microbiol. 2018;9:2443. [PMC free article: PMC6193098] [PubMed: 30364306]
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- Gong XH, Wu HY, Li J, Xiao WJ, Zhang X, Chen M, Teng Z, Pan H, Yuan ZA. Epidemiology, aetiology and seasonality of infectious diarrhoea in adult outpatients through active surveillance in Shanghai, China, 2012-2016: a cross-sectional study. BMJ Open. 2018 Sep 04;8(9):e019699. [PMC free article: PMC6129037] [PubMed: 30181181]
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- Ortiz-Jiménez MA. Quantitative evaluation of the risk of Vibrio parahaemolyticus through consumption of raw oysters (Crassostrea corteziensis) in Tepic, Mexico, under the RCP2.6 and RCP8.5 climate scenarios at different time horizons. Food Res Int. 2018 Sep;111:111-119. [PubMed: 30007667]
- 6.
- Malcolm TTH, Chang WS, Loo YY, Cheah YK, Radzi CWJWM, Kantilal HK, Nishibuchi M, Son R. Simulation of improper food hygiene practices: A quantitative assessment of Vibrio parahaemolyticus distribution. Int J Food Microbiol. 2018 Nov 02;284:112-119. [PubMed: 30142576]
- 7.
- Niu B, Mu L, Xiao L, Zhang Z, Malakar PK, Liu H, Pan Y, Zhao Y. Reduction of infection risk mediated by co-culturing Vibrio parahaemolyticus and Listeria monocytogenes in refrigerated cooked shrimp. J Sci Food Agric. 2018 Sep;98(12):4454-4461. [PubMed: 29457648]
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- Pazhani GP, Bhowmik SK, Ghosh S, Guin S, Dutta S, Rajendran K, Saha DR, Nandy RK, Bhattacharya MK, Mukhopadhyay AK, Ramamurthy T. Trends in the epidemiology of pandemic and non-pandemic strains of Vibrio parahaemolyticus isolated from diarrheal patients in Kolkata, India. PLoS Negl Trop Dis. 2014 May;8(5):e2815. [PMC free article: PMC4006737] [PubMed: 24786538]
Disclosure: Benjamin Rezny declares no relevant financial relationships with ineligible companies.
Disclosure: Daniel Evans declares no relevant financial relationships with ineligible companies.
- A Novel Mouse Model of Enteric Vibrio parahaemolyticus Infection Reveals that the Type III Secretion System 2 Effector VopC Plays a Key Role in Tissue Invasion and Gastroenteritis.[mBio. 2019]A Novel Mouse Model of Enteric Vibrio parahaemolyticus Infection Reveals that the Type III Secretion System 2 Effector VopC Plays a Key Role in Tissue Invasion and Gastroenteritis.Yang H, de Souza Santos M, Lee J, Law HT, Chimalapati S, Verdu EF, Orth K, Vallance BA. mBio. 2019 Dec 17; 10(6). Epub 2019 Dec 17.
- Outbreak of Vibrio parahaemolyticus gastroenteritis associated with Alaskan oysters.[N Engl J Med. 2005]Outbreak of Vibrio parahaemolyticus gastroenteritis associated with Alaskan oysters.McLaughlin JB, DePaola A, Bopp CA, Martinek KA, Napolilli NP, Allison CG, Murray SL, Thompson EC, Bird MM, Middaugh JP. N Engl J Med. 2005 Oct 6; 353(14):1463-70.
- Growth Rates of Vibrio parahaemolyticus Sequence Type 36 Strains in Live Oysters and in Culture Medium.[Microbiol Spectr. 2022]Growth Rates of Vibrio parahaemolyticus Sequence Type 36 Strains in Live Oysters and in Culture Medium.Ellett AN, Rosales D, Jacobs JM, Paranjpye R, Parveen S. Microbiol Spectr. 2022 Dec 21; 10(6):e0211222. Epub 2022 Nov 29.
- Review Pandemic Vibrio parahaemolyticus O3:K6 on the American continent.[Front Cell Infect Microbiol. 2...]Review Pandemic Vibrio parahaemolyticus O3:K6 on the American continent.Velazquez-Roman J, León-Sicairos N, de Jesus Hernández-Díaz L, Canizalez-Roman A. Front Cell Infect Microbiol. 2014 Jan 2; 3:110. Epub 2014 Jan 2.
- Review Vibrio Parahaemolyticus: A Review on Distribution, Pathogenesis, Virulence Determinants and Epidemiology.[Saudi J Med Med Sci. 2017]Review Vibrio Parahaemolyticus: A Review on Distribution, Pathogenesis, Virulence Determinants and Epidemiology.Ghenem L, Elhadi N, Alzahrani F, Nishibuchi M. Saudi J Med Med Sci. 2017 May-Aug; 5(2):93-103. Epub 2017 Apr 20.
- Vibrio parahaemolyticus Infection - StatPearlsVibrio parahaemolyticus Infection - StatPearls
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- olfactory receptor 197 [Mus musculus]olfactory receptor 197 [Mus musculus]gi|33239156|ref|NP_666695.1|Protein
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