Laboratory Studies
- It is important to remember that initial laboratory findings may be unremarkable, but they may yield clues to underlying medical conditions such as chronic liver disease, chronic hemolytic anemia, hemochromatosis, diabetes, renal insufficiency, or adrenal insufficiency..
- CBC count with differential and platelet count
- Findings on blood count are initially nondiagnostic in patients with Vibrio infection.
- In patients with underlying medical conditions, such as cirrhosis, the presence of thrombocytopenia and/or schistocytes is an early indicator of disseminated intravascular coagulation (DIC).
- Serum chemistries (comprehensive metabolic panel)
- Serum electrolytes, BUN, and creatinine levels may become abnormal in patients with dehydration, hypotension, and severe sepsis.
- Monitoring serum electrolytes is essential in the treatment of severe gastroenteritis.
- Stool examination for occult blood and fecal leukocytes: The presence of either fecal occult blood or fecal leukocytes is a reliable marker for invasive infectious diarrhea.
- Stool examination for ova and parasites and stool cultures for Salmonella, Shigella, Campylobacter, Yersinia, and Vibrio species
- Stool examination for parasites and stool culture are indicated in patients who present with diarrhea and who have a history of recent travel and/or consumption of contaminated food or water.
- Perform these tests in patients with gastroenteritis, especially upon suspicion of foodborne illness.
- The physician may alert the public health department if a specific pathogen is identified in a group of people.
- Prothrombin time and activated partial thromboplastin time
- Prothrombin time (PT) and activated partial thromboplastin time (aPTT) may be prolonged in patients with DIC.
- Coagulation tests are indicated in patients who require extensive surgical debridement.
- Gram stain and culture
- Organisms may be recovered from blood (patients with sepsis), bullae or wounds (skins and soft tissue infections), and stool (gastroenteritis).
- Gram stain may reveal gram-negative rods, or studies may be used to isolate a specific pathogen for antibiotic sensitivity testing.
- Organisms may be recovered or demonstrated in other body fluids and/or exudates such as peritoneal fluid or ocular exudates.
- Blood cultures
- Blood cultures are indicated in patients with sepsis, severe skin and soft tissue infections, or unstable vital signs (eg, hypotension, multiple organ dysfunction).
- Patients with advanced liver disease, malignancies, or hemochromatosis may develop bacteremia and serious complications more often than those without these medical conditions.
- Blood cultures are frequently positive in patients with V vulnificus infections.
- Arterial blood gas
- Arterial blood gas (ABG) is indicated in patients with severe sepsis, septic shock, multiple organ dysfunction, DIC, or acute respiratory distress syndrome (ARDS).
- ABG may show severe metabolic acidosis due to tissue hypoperfusion and/or hypoxia.
Imaging Studies
- Chest radiography in patients with Vibrio infections may show fluffy bilateral pulmonary infiltrates compatible with ARDS. Radiographic examination of the injured anatomical parts, such as fingers, hand, foot, or trunk may reveal foreign objects, such as fragments of fishhooks or seashells. The presence of gas feathering in the soft tissue may help to identify other potential diagnoses, such as gas gangrene.
- CT scanning of the injured body parts may be indicated if the patient develops signs and symptoms of compartment syndrome or necrotizing fasciitis.
Other Tests
- Other tests may be unnecessary upon admission but may help identify the underlying medical conditions that predispose the patient to serious Vibrio infection and/or complications.
- Serology for HBV and HCV and serum iron studies are used to identify the etiology of advanced liver disease.
Procedures
- Aspiration of skin bullae or a wound can be performed for Gram stain and culture in patients with skin and soft tissue infections.
- Placement of central venous catheter for intravenous rehydration may be indicated in patients with profound hypovolemia or shock.
- Early wound debridement is indicated in patients with Vibrio wound infection or septicemia. A delay of wound debridement may lead to amputation. Debridement must be performed urgently if the patient develops compartment syndrome.
Histologic Findings
Findings on histologic examination of the skin and/or soft tissue in patients with noncholera Vibrio wound infection frequently demonstrate gram-negative bacilli, acute inflammatory reaction with extensive tissue necrosis, and fat infarction. In patients with rapidly progressing illness, examination of biopsy specimens of the skin may demonstrate an absence of cellular response.
2011 Estimates of foodborne illness in the united states. Available at http://www.cdc.gov/foodborneburden.
Scallan E, Hoekstra RM, Angulo FJ, Tauxe RV, Widdowson MA, Roy SL, et al. Foodborne illness acquired in the United States--major pathogens. Emerg Infect Dis. Jan 2011;17(1):7-15. [Medline].
3. Vital Signs: Incidence and Trends of Infection with Pathogens Transmitted Commonly Through Food --- Foodborne Diseases Active Surveillance Network, 10 U.S. Sites, 1996—2010. Available at http://www.cdc.gov/mmwr/preview/mmwrhtml/mm6022a5.htm?s_cid=mm6022a5_w.
Marano NN, Daniels NA, Easton AN, McShan A, Ray B, Wells JG. A survey of stool culturing practices for vibrio species at clinical laboratories in Gulf Coast states. J Clin Microbiol. Jun 2000;38(6):2267-70. [Medline].
Dechet AM, Yu PA, Koram N, Painter J. Nonfoodborne Vibrio infections: an important cause of morbidity and mortality in the United States, 1997-2006. Clin Infect Dis. Apr 1 2008;46(7):970-6. [Medline].
Centers for Disease Control and Prevention (CDC). Vibrio illnesses after Hurricane Katrina--multiple states, August-September 2005. MMWR Morb Mortal Wkly Rep. Sep 23 2005;54(37):928-31. [Medline].
Shapiro RL, Altekruse S, Hutwagner L. The role of Gulf Coast oysters harvested in warmer months in Vibrio vulnificus infections in the United States, 1988-1996. Vibrio Working Group. J Infect Dis. Sep 1998;178(3):752-9. [Medline].
Brennt CE, Wright AC, Dutta SK. Growth of Vibrio vulnificus in serum from alcoholics: association with high transferrin iron saturation. J Infect Dis. Nov 1991;164(5):1030-2. [Medline].
Hor LI, Chang TT, Wang ST. Survival of Vibrio vulnificus in whole blood from patients with chronic liver diseases: association with phagocytosis by neutrophils and serum ferritin levels. J Infect Dis. Jan 1999;179(1):275-8. [Medline].
Miyoshi S, Nakazawa H, Kawata K, Tomochika K, Tobe K, Shinoda S. Characterization of the hemorrhagic reaction caused by Vibrio vulnificus metalloprotease, a member of the thermolysin family. Infect Immun. Oct 1998;66(10):4851-5. [Medline].
Shao CP, Hor LI. Metalloprotease is not essential for Vibrio vulnificus virulence in mice. Infect Immun. Jun 2000;68(6):3569-73. [Medline].
Hilton T, Rosche T, Froelich B, Smith B, Oliver J. Capsular polysaccharide phase variation in Vibrio vulnificus. Appl Environ Microbiol. Nov 2006;72(11):6986-93. [Medline].
Lee SE, Kim SY, Kim CM, Kim MK, Kim YR, Jeong K. The pyrH gene of Vibrio vulnificus is an essential in vivo survival factor. Infect Immun. Jun 2007;75(6):2795-801. [Medline].
Wong TW, Wang YY, Sheu HM, Chuang YC. Bactericidal effects of toluidine blue-mediated photodynamic action on Vibrio vulnificus. Antimicrob Agents Chemother. Mar 2005;49(3):895-902. [Medline].
Shirai H, Ito H, Hirayama T, Nakamoto Y, Nakabayashi N, Kumagai K. Molecular epidemiologic evidence for association of thermostable direct hemolysin (TDH) and TDH-related hemolysin of Vibrio parahaemolyticus with gastroenteritis. Infect Immun. Nov 1990;58(11):3568-73. [Medline].
Nishibuchi M, Fasano A, Russell RG, Kaper JB. Enterotoxigenicity of Vibrio parahaemolyticus with and without genes encoding thermostable direct hemolysin. Infect Immun. Sep 1992;60(9):3539-45. [Medline].
Vibrio parahaemolyticus infections associated with consumption of raw shellfish--three states, 2006. MMWR Morb Mortal Wkly Rep. Aug 11 2006;55(31):854-6. [Medline].
Osaka K, Komatsuzaki M, Takahashi H, Sakano S, Okabe N. Vibrio vulnificus septicaemia in Japan: an estimated number of infections and physicians' knowledge of the syndrome. Epidemiol Infect. Oct 2004;132(5):993-6. [Medline].
Haq SM, Dayal HH. Chronic liver disease and consumption of raw oysters: a potentially lethal combination--a review of Vibrio vulnificus septicemia. Am J Gastroenterol. May 2005;100(5):1195-9. [Medline].
Liu JW, Lee IK, Tang HJ, Ko WC, Lee HC, Liu YC. Prognostic Factors and Antibiotics in Vibrio vulnificus Septicemia. Arch Intern Med. Oct 23 2006;166(19):2117-23. [Medline].
Dadisman TA Jr, Nelson R, Molenda JR. Vibrio parahaemolyticus gastroenteritis in Maryland. I. Clinical and epidemiologic aspects. Am J Epidemiol. Dec 1972;96(6):414-26. [Medline].
Howard RJ, Lieb S. Soft-tissue infections caused by halophilic marine vibrios. Arch Surg. Feb 1988;123(2):245-9. [Medline].
Klontz KC, Lieb S, Schreiber M. Syndromes of Vibrio vulnificus infections. Clinical and epidemiologic features in Florida cases, 1981-1987. Ann Intern Med. Aug 15 1988;109(4):318-23. [Medline].
Chuang YC, Ko WC, Wang ST, Liu JW, Kuo CF, Wu JJ. Minocycline and cefotaxime in the treatment of experimental murine Vibrio vulnificus infection. Antimicrob Agents Chemother. Jun 1998;42(6):1319-22. [Medline].
Anand RG, Lopez FA, deBoisblanc B. Vibrio vulnificus sepsis successfully treated with antibiotics, surgical debridement, and recombinant human activated protein C. J La State Med Soc. May-Jun 2004;156(3):130-3; quiz 133. [Medline].
Mouzin E, Mascola L, Tormey MP. Prevention of Vibrio vulnificus infections. Assessment of regulatory educational strategies. JAMA. Aug 20 1997;278(7):576-8. [Medline].
Centers for Disease Control and Prevention (CDC). Preliminary FoodNet data on the incidence of infection with pathogens transmitted commonly through food--selected sites, United States, 2003. MMWR Morb Mortal Wkly Rep. Apr 30 2004;53(16):338-43. [Medline].
Hiransuthikul N, Tantisiriwat W, Lertutsahakul K, Vibhagool A, Boonma P. Skin and soft-tissue infections among tsunami survivors in southern Thailand. Clin Infect Dis. Nov 15 2005;41(10):e93-6. [Medline].
Hlady WG, Klontz KC. The epidemiology of Vibrio infections in Florida, 1981-1993. J Infect Dis. May 1996;173(5):1176-83. [Medline].
Hollis DG, Weaver RE, Baker CN. Halophilic Vibrio species isolated from blood cultures. J Clin Microbiol. Apr 1976;3(4):425-31. [Medline].
Scallan E, Griffin PM, Angulo FJ, Tauxe RV, Hoekstra RM. Foodborne illness acquired in the United States--unspecified agents. Emerg Infect Dis. Jan 2011;17(1):16-22. [Medline].
Summary of Notifiable Diseases in United States, 2009. Available at http://www.cdc.gov/mmwr/pdf/wk/mm5853.pdf.
| Infection Type | Noncholera Vibrio Species | Cytotoxins/Enzymes |
| Gastroenteritis | V parahaemolyticus Non-01 V cholerae Vibrio fluvialis V mimicus Vibrio furnissii Vibrio hollisae Vibrio alginolyticus V vulnificus | Cytotoxin Hemolysin |
| Wound infection | V alginolyticus V vulnificus Non-01 V cholerae Vibrio damsela Vibrio carchariae V fluvialis V parahaemolyticus V mimicus | Protease Hemolysin Lipase DNAase Cytolysin |
| Septicemia | V vulnificus V fluvialis V damsela Non-01 V cholerae Vibrio cincinnatiensis | Proteases Endotoxic lipopolysaccharide |
| Vibrio Species | Gastroenteritis (%) | Wound Infection (%) | Septicemia (%) | Miscellaneous (%) |
| V parahaemolyticus | 59 | 34 | 5 | 2 |
| V vulnificus | 5 | 45 | 43 | 7 |
| Non-01 V cholerae | 67 | 9 | 15 | … |
| V alginolyticus | 5-12 | 71 | 1 | 10-15 |
| V mimicus | 85 | 3 | 3 | … |
| V fluvialis | 73 | 10 | 6 | … |
| V damsela | Rare | >95 | Rare | … |
| V furnissii | >90 | Rare | Rare | … |
| Vibrio metschnikovii | Common | Rare | Rare | … |
| V hollisae | 85 | 7 | 5 | … |
| V cincinnatiensis | Rare | Rare | Rare | Meningitis |
| Clinical Presentation | Symptoms (Frequency) |
| Gastroenteritis | Diarrhea (100%) Abdominal cramps (89%) Nausea (76%) Vomiting (55%) Fever (47%) Bloody stools (29%) Headache (24%) Myalgia (24%) |
| Wound infection | Swelling (100%) Pain (100%) Erythema (100%) Bullae (30-50%) Necrosis (30-50%) Gangrene (< 10%) |
| Septicemia | Fever (>90%) Hypothermia (< 10%) Hypotension (100%) Tachycardia (80-90%) Shock (50-70%) Bullae (80-100%) Acute respiratory distress syndrome (< 5%) Multiple organ dysfunction (30-50%) |

