Aeromonas sp. organisms rarely cause urinary tract infection. We report for the first time a case of urinary tract infection caused by A. caviae in an adult patient with a history of increased frequency of urination, dysuria, hematuria, and weight loss.
CASE REPORTA 39-year-old Bangladeshi male presented to the emergency department of Al-Amiri Hospital, Kuwait, with a 2-month history of increased frequency of urination, dysuria, hematuria, and weight loss of 7 kg. Seven weeks earlier, he was treated with amoxicillin for 5 days by his general practitioner. But despite the therapy, his symptoms deteriorated.On examination, the patient was afebrile (37°C) with normal vital signs for his age. His suprapubic area was tender. Ultrasonography of the abdomen and pelvis revealed generalized and irregular thickening (4 to 5 mm) of the wall of the urinary bladder suggestive of cystitis. A chest X-ray was normal. Hematological examination revealed a hemoglobin level of 153 g/liter, a platelet count of 170 ϫ 10 9 /liter, a white-cell count of 7.7 ϫ 10 9 /liter, and an erythrocyte sedimentation rate of 3 mm/h (all values were within the normal range). The biochemical profile revealed an alanine aminotransferase level of 57 IU/liter, alkaline phosphatase level of 76 IU/liter, creatinine level of 80 mol/liter, and blood urea level of 2.6 mmol/liter (all were within the normal ranges). Stool culture was negative for Aeromonas spp., Salmonella spp., Shigella spp., and Campylobacter spp.The urine analysis showed an erythrocyte level of 30/hpf and a leukocyte level of 4/hpf. The urine sample was plated on cystine-lactose-electrolyte-deficient agar, MacConkey agar, and sheep blood agar (Oxoid, Basingstoke, United Kingdom) and incubated at 37°C. After 24 h, pure growth of smooth, entire colonies of about 2 mm in diameter appeared on the plates. The concentration of bacteria was calculated to be Ͼ10 5 colonies/ml of urine. The colonies were non-lactose fermenters on MacConkey agar and nonhemolytic on blood agar. One purified isolate was deposited in the BCCM/LMG Bacteria Collection, Ghent University (Belgium) (http://bccm.belspo.be /db/lmg_search_form.php) as LMG 24107. The isolate was a gram-negative, motile bacillus and was catalase and oxidase positive. The API-20E identification strip (bioMerieux, Marcy l'Etoile, France) profile obtained (3006126) identified LMG 24107 as either Vibrio fluvialis or Aeromonas caviae with differential tests of growth in KCN and growth without salt for A. caviae. Results of further biochemical characterization as described previously (1) are shown in Table 1. The extensive biochemical characterization of the isolate indicated that the isolate was not V. fluvialis (growth without salt supplementation and growth in KCN broth) and was, in fact, A. caviae. Next, we performed molecular identification of the isolate by sequencing of the 16S rRNA and gyrB genes. Bacterial DNA was extracted by the cetyltrimethylammonium bromide method (10) for 16S rRNA sequencing and by the method of Pitcher and colleagues (9...