Réanimation Polyvalente, CHU Dupuytren, 2 Avenue Martin-Luther King, 87042, Limoges, France.
Laboratoire de Bactériologie-Virologie-Hygiène, CHU de Limoges, Limoges, France.
BMC Infect Dis. 2022 Apr 9;22(1):355. doi: 10.1186/s12879-022-07328-z.
Capnocytophaga canimorsus infection happens frequently in immunosuppressed patients with reported domestic animal bites. Clinical presentation ranges from simple cellulitis to fulminant septic shock with disseminated intravascular coagulopathy, with an overall mortality of 30%. Conventional blood culture is often negative as this is a slow-growing pathogen. Nevertheless, the increasing use of 16S rRNA gene amplification and Sanger sequencing allows a much more rapid diagnostic confirmation. We present two case reports where 16S rRNA gene sequencing helped to diagnose Capnocytophaga canimorsus infection.
Case 1: A 53-year-old man with a history of non-cirrhotic chronic alcohol consumption was admitted to the intensive care unit (ICU) for septic shock and disseminated intravascular coagulopathy (DIC) of unknown origin. Blood cultures remained negative and a 16S rRNA PCR was performed leading to the identification of Capnocytophaga Canimorsus on day 4. Targeted antibiotic therapy with ceftriaxone for 14 days lead to overall recovery. Afterwards, the patient recalled a dog bite 2 days before hospitalization with a punctiform necrotic wound localized on a finger, which was not obvious at admission. Case 2: A 38-year-old man arrived to the emergency department for acute alcohol intoxication and history of a dog bite 2 days before. At admission, septic shock with purpura fulminans was diagnosed and required ICU hospitalization, invasive mechanical ventilation, vasopressor support and renal replacement therapy due to the rapid clinical deterioration. In the context of septic shock with purpura fulminans, DIC and recent dog bite, the diagnosis of Capnocytophaga canimorsus septic shock was suspected, and early confirmed by 16S rRNA PCR coupled to Sanger sequencing on day 2. Blood cultures became only positive for Capnocytophaga canimorsus 5 days after admission. Ceftriaxone alone was infused for 10 days in total, and the patient was discharged from the ICU on day 25.
16S rRNA gene PCR proves an important diagnostic tool when facing a sepsis of unknown origin. In these two cases of septic shock related to Capnocytophaga canimorsus, initial blood cultures remained negative at 24 h, whereas the diagnosis was achieved by 16S rRNA PCR sequencing performed from blood samples obtained at admission.
嗜二氧化碳噬纤维菌感染常发生于伴有家养动物咬伤的免疫抑制患者,临床表现从单纯蜂窝织炎到伴有弥散性血管内凝血的暴发性败血性休克不等,总死亡率为 30%。由于这是一种生长缓慢的病原体,常规血培养通常为阴性。然而,16S rRNA 基因扩增和 Sanger 测序的广泛应用使得诊断确认更为迅速。我们报告了两例 16S rRNA 基因测序有助于诊断嗜二氧化碳噬纤维菌感染的病例。
病例 1:一名 53 岁男性,有非肝硬化性慢性酒精消耗史,因不明原因的败血性休克和弥散性血管内凝血(DIC)被收入重症监护病房(ICU)。血培养仍为阴性,进行 16S rRNA PCR 检测,第 4 天鉴定出嗜二氧化碳噬纤维菌。使用头孢曲松治疗 14 天的靶向抗生素治疗导致整体康复。随后,患者回忆起住院前 2 天被狗咬伤,手指上有一个点状坏死性伤口,但在入院时并不明显。病例 2:一名 38 岁男性因急性酒精中毒和 2 天前被狗咬伤就诊于急诊部。入院时,诊断为败血性休克伴紫癜性休克,由于临床迅速恶化,需要入住 ICU、接受有创机械通气、升压药支持和肾脏替代治疗。在伴有紫癜性休克、DIC 和近期狗咬伤的败血性休克背景下,怀疑诊断为嗜二氧化碳噬纤维菌败血性休克,并在第 2 天通过 16S rRNA PCR 与 Sanger 测序早期确诊。血培养在入院后第 5 天才仅对嗜二氧化碳噬纤维菌呈阳性。总共输注头孢曲松 10 天,患者于第 25 天从 ICU 出院。
16S rRNA 基因 PCR 在面对不明原因的脓毒症时是一种重要的诊断工具。在这两例与嗜二氧化碳噬纤维菌相关的败血性休克中,初始血培养在 24 小时内仍为阴性,而通过对入院时采集的血样进行 16S rRNA PCR 测序获得诊断。