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早发性侵袭性感染由 Corynespora cassiicola 引起,与哥伦比亚患者的 CARD9 复合杂合突变相关。

Early-Onset Invasive Infection Due to Corynespora cassiicola Associated with Compound Heterozygous CARD9 Mutations in a Colombian Patient.

机构信息

Grupo de Inmunodeficiencias Primarias, Universidad de Antioquia UdeA, Calle 70 No. 52-21, Medellín, Colombia.

Escuela de Microbiología, Universidad de Antioquia UdeA, Calle 70 No. 52-21, Medellín, Colombia.

出版信息

J Clin Immunol. 2018 Oct;38(7):794-803. doi: 10.1007/s10875-018-0549-0. Epub 2018 Sep 28.

Abstract

PURPOSE

CARD9 deficiency is an inborn error of immunity that predisposes otherwise healthy humans to mucocutaneous and invasive fungal infections, mostly caused by Candida, but also by dermatophytes, Aspergillus, and other fungi. Phaeohyphomycosis are an emerging group of fungal infections caused by dematiaceous fungi (phaeohyphomycetes) and are being increasingly identified in patients with CARD9 deficiency. The Corynespora genus belongs to phaeohyphomycetes and only one adult patient with CARD9 deficiency has been reported to suffer from invasive disease caused by C. cassiicola. We identified a Colombian child with an early-onset, deep, and destructive mucocutaneous infection due to C. cassiicola and we searched for mutations in CARD9.

METHODS

We reviewed the medical records and immunological findings in the patient. Microbiologic tests and biopsies were performed. Whole-exome sequencing (WES) was made and Sanger sequencing was used to confirm the CARD9 mutations in the patient and her family. Finally, CARD9 protein expression was evaluated in peripheral blood mononuclear cells (PBMC) by western blotting.

RESULTS

The patient was affected by a large, indurated, foul-smelling, and verrucous ulcerated lesion on the left side of the face with extensive necrosis and crusting, due to a C. cassiicola infectious disease. WES led to the identification of compound heterozygous mutations in the patient consisting of the previously reported p.Q289* nonsense (c.865C > T, exon 6) mutation, and a novel deletion (c.23_29del; p.Asp8Alafs10*) leading to a frameshift and a premature stop codon in exon 2. CARD9 protein expression was absent in peripheral blood mononuclear cells from the patient.

CONCLUSION

We describe here compound heterozygous loss-of-expression mutations in CARD9 leading to severe deep and destructive mucocutaneous phaeohyphomycosis due to C. cassiicola in a Colombian child.

摘要

目的

CARD9 缺陷是一种先天性免疫缺陷,使原本健康的人易患黏膜和侵袭性真菌感染,主要由念珠菌引起,但也由皮肤真菌、曲霉和其他真菌引起。暗色丝孢霉病是一组新兴的真菌感染,由暗色丝孢霉(暗色丝孢霉)引起,在 CARD9 缺陷患者中越来越多地被发现。棒孢属属于暗色丝孢霉,只有一名 CARD9 缺陷的成年患者报告患有由 C. cassiicola 引起的侵袭性疾病。我们鉴定了一名哥伦比亚儿童患有早期、深部和破坏性黏膜皮肤感染,由 C. cassiicola 引起,我们寻找 CARD9 突变。

方法

我们回顾了患者的病历和免疫学发现。进行了微生物学检查和活检。进行了全外显子组测序(WES),并使用 Sanger 测序在患者及其家属中证实了 CARD9 突变。最后,通过 Western blot 评估了外周血单核细胞(PBMC)中的 CARD9 蛋白表达。

结果

患者面部左侧有一个大的、硬结的、有臭味的疣状溃疡性病变,广泛坏死和结痂,由 C. cassiicola 感染性疾病引起。WES 导致患者存在复合杂合失表达突变,包括先前报道的 p.Q289无义(c.865C>T,外显子 6)突变和一个新的缺失(c.23_29del;p.Asp8Alafs10),导致外显子 2 发生移码和过早终止密码子。患者外周血单核细胞中 CARD9 蛋白表达缺失。

结论

我们在此描述了 CARD9 中的复合杂合失表达突变,导致一名哥伦比亚儿童发生严重的深部和破坏性黏膜皮肤暗色丝孢霉病,由 C. cassiicola 引起。

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