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Case Report

Case Report: Whole exome sequencing identifies variation c.2308G>A p.E770K in RAG1 associated with B- T- NK+ severe combined immunodeficiency

[version 1; peer review: 2 approved with reservations, 1 not approved]
* Equal contributors
PUBLISHED 18 Oct 2016
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Abstract

Severe combined immunodeficiency is a large clinically heterogeneous group of disorders caused by a defect in the development of humoral or cellular immune responses. At least 13 genes are known to be involved in the pathophysiology of the disease and the mutation spectrum in SCID have been well documented. The widespread application of whole-exome sequencing based on next-generation sequencing has offered a new opportunity to systematically screen these genes in clinical scales. In this report, we describe the application of whole exome sequencing for arriving at a molecular diagnosis in a child suffering from B- T- NK+ severe combined immunodeficiency. Apart from making the accurate molecular diagnosis, we also add a genetic variation c.2308G>A p.E770K to the compendium of variations associated with the disease.

Keywords

Severe Combined Immunodeficiency, B- T- NK+ SCID, Whole Exome Sequencing, RAG1

Introduction

Severe combined immunodeficiency (SCID) encompasses a constellation of clinically and genetically heterogeneous diseases resulting in defects of the humoral and/or cellular immune defence mechanism1. Accurate molecular diagnosis of the disease is of prime importance, not only in offering appropriate genetic counselling, but also in understanding the exact molecular defect and would potentially enable prenatal screening2. The accurate molecular diagnosis would provide a fresh opportunity to enable cost-effective screening of family members and offer appropriate genetic counselling especially for populations where there is a high degree of consanguinity3,4. So far, arriving at a precise molecular diagnosis has been quite cumbersome, technically challenging and expensive as over a dozen genes are known to be implicated in the disease, which would require systematic targeted sequencing of each of the gene5,6. The advent of next generation sequencing, especially whole exome and sometime whole genome sequencing has significantly enabled the rapid identification of the causative genetic variations in clinical settings6.

In the present report, we describe the application of whole exome sequencing for the accurate molecular diagnosis of a case of B- T- NK+ SCID. Our report also adds a genetic variation c.2308G>A p.E770K to the compendium of variations associated with the disease.

Case report

Here we report a case of a seven-month-old boy, born out of a third degree consanguineous marriage, with a history of recurrent episodes of pneumonia, acute otitis media, diarrhea and oral thrush since two months of age. The child was pale, emaciated, febrile, and had respiratory distress with lower chest retractions. He was in compensated shock. There was no clubbing, cyanosis or lymphadenopathy. There was no facial dysmorphism and skin and hair were normal. He weighed 5.4 kg; measured 64 cm in length and head circumference was 39.5 cm. Examination of the chest showed evidence of bronchopneumonia while there was no evidence of congenital heart disease or neurological deficits. There was mild hepatomegaly with a liver span of 6.5 cm.

The baby was normal in the perinatal and postnatal period. His birth weight was normal (3.04 kg) and was asymptomatic until 2 months of age. There was a history of admission to PICU and artificial ventilation for severe pneumonia at the age of 2 months. He was admitted for 22 days during that episode. The child had gross motor developmental delay and no adverse events following immunization. He had a male sibling who expired at seven months of age due to persistent pneumonia and two unaffected female siblings, apart from a half-brother and half-sister both of whom were asymptomatic (Figure 1A).

36b97bab-ea07-4463-967f-b13b71a918db_figure1.gif

Figure 1.

(a) Pedigree of the family (b) domain mapping of the RAG1 p.E770K on RAG1 protein showing the variation lies on RAG1 domain highlighted with red triangle and (c) capillary sequencing of the locus in the proband and family members. The homozygous variation c.2308G>A in the proband is marked with an asterisk.

On investigation, the child was found to have hypochromic microcytic anemia, lymphocytopenia with absolute lymphocyte counts less than 1000/cu.mm and a normal platelet count. Liver and renal function tests were normal. The ionized calcium was 1.1 mg%. Blood culture was positive for Enterobacter species. The baby was negative for HIV infection and there was no evidence of tuberculosis. His chest X-Ray showed absence of the thymus shadow apart from evidence of bronchopneumonia.

A close workup of the immunoglobulin profile revealed hypogammaglobulinemia-IgA 23 mg%, IgG 44 mg% and IgM 26 mg%. IgE was 1 IU/L. The absolute CD3 count was 464 cells/ul (normal range 1,460–5,440 cells/ul), absolute CD19 lymphocyte count was 12 cells/ul (normal 430–3,300 cells/ul) and absolute NK cell count was 1,328 cells/ul (normal 80–340 cells/ul). Flow cytometry suggested absent B and markedly reduced T cell populations suggestive of B- T- NK+ SCID.

The child was treated with piperacillin (80mg/kg/dose Q8H), vancomycin (15 mg/kg/dose Q6H), dopamine (10 mic/kg/min), IVIG and other supportive measures and was put on cotrimoxazole (6 mg/kg/day OD) prophylaxis. He was treated with ganciclovir for CMV infection and for staphylococcal pneumonia.

The clinical diagnosis of SCID and family history of sibling death prompted us to investigate the molecular genetic correlates of the disease. Since over 13 genes are implicated in SCID and regular molecular testing was not readily available for the genes, we resorted to whole exome sequencing. After obtaining informed consent from the parents, blood was drawn after venipuncture under aseptic precautions. DNA was isolated from whole blood using salting out method7. Exome capture was performed on DNA using the Illumina Nextera rapid capture expanded exome kit using standard protocols (Illumina Inc USA). We generated 47.95 million paired end reads and an average on target coverage of over 25x on Illumina HiSeq 2500 (Illumina Inc. USA). Alignment was performed using BWA (v0.7.12-r1039)8 and Stampy (v1.0.20)9 and variants were called using Platypus (v0.8.1)10. For the prioritisation of variants, we filtered all homozygous variants, further filtered by an allele frequency of <1% in the 1000 Genome and Exac. Variants in the 13 genes were prioritised and annotated for their deleteriousness using SIFT, Polyphen and Mutation Taster annotations obtained from annovar11.

Analysis revealed a homozygous missense variation (c.2308G>A) in exon number 2 of Recombination activating gene 1 (RAG1). The variant was predicted to be highly deleterious by SIFT (score 0.000), PolyPhen2 (0.991) and Mutation Taster (1.00). The variation causes an amino acid change p.E770K, which lies on RAG1 domain of the protein (Figure 1b). The present variation was not found in the 1000 Genome (http://browser.1000genomes.org/index.html), Exac (http://exac.broadinstitute.org/) or internal control database of over 150 exomes from South East Asian ancestry. Incidentally the mutation was previously reported and analysis suggested a significantly reduced recombination activity12.

The variation was further confirmed using targeted PCR amplification around the locus and confirmed by capillary sequencing. The variant was found to be heterozygous in both the parents as well as the surviving siblings (Figure 1c). The status of the variation could not be ascertained in the sibling who died because no sample was archived and primary immune deficiency was not suspected at the time.

Discussion

Mutations in RAG1 gene cause various degrees of severe combined immunodeficiency syndrome. RAG1 is involved in the V(D)J recombination1,13. The child was suspected to have a primary immune deficiency disorder since he had unusually frequent and severe infections and in addition had lost a male sibling due to similar illness. Further, he was born to third degree consanguineous parents. The early onset of symptoms by 2 months of life with increased susceptibility to both bacterial and fungal infections was a pointer to a T cell defect or a phagocytic defect rather than to an antibody deficiency like X linked agammaglobulinemia, which usually presents by 5 to 6 months of age, when maternal antibodies are on the wane14. The immunoglobulin profile showed that there was also a B cell defect. The low absolute lymphocyte counts coupled with radiological evidence of an absent thymus shadow was proof of a T cell defect as well. Thus, a provisional diagnosis of a severe combined immunodeficiency was made even before the flow cytometry results became available and helped confirm the diagnosis.

The possibility of Omenn syndrome was not considered since there was no history of a rash and there was no lymphadenopathy or hepatosplenomegaly, nor was there eosinophilia in the peripheral smear. XR SCID is characterized by an elevated percentage of B cells and in the absence of B cells in the child ruled this out. Jak3 deficiency was also not thought of for the same reason. ADA deficient SCID is characterized by bony abnormalities including rib cage defects, which were absent.

RAG 1 or RAG 2 deficiencies are associated with a lack of both B cells and T cells and NK cells are predominant in the circulation13. With this possibility in mind, and with a view to offer genetic counselling to the family, whole exome sequencing was considered. The child was referred for a bone marrow transplant, since SCID is not compatible with life beyond infancy. The patient underwent a matched sibling donor bone marrow transplant at the age of 1 year and 3 months. Post-transplant, he developed hypertension and later developed septic shock, which were managed successfully. He is now one year three months post-transplant and off all medications including immunosuppressive therapy.

Ethics approval

The whole exome sequencing was approved by the Institutional Ethical Committee of CSIR - Institute of Genomics and Integrative Biology (IHECC proposal number 8).

Consent

Written informed consent for publication of the patients’ details and/or their images was obtained from the patients/parents of the patient.

Data availability

All the raw sequencing data are available at the NCBI Sequence Read Archive (http://www.ncbi.nlm.nih.gov/sra), accession number SRR4088561.

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Govindaraj GM, Karuthedath Vellarikkal S, Jayarajan R et al. Case Report: Whole exome sequencing identifies variation c.2308G>A p.E770K in RAG1 associated with B- T- NK+ severe combined immunodeficiency [version 1; peer review: 2 approved with reservations, 1 not approved]. F1000Research 2016, 5:2532 (https://doi.org/10.12688/f1000research.9473.1)
NOTE: If applicable, it is important to ensure the information in square brackets after the title is included in all citations of this article.
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ApprovedThe paper is scientifically sound in its current form and only minor, if any, improvements are suggested
Approved with reservations A number of small changes, sometimes more significant revisions are required to address specific details and improve the papers academic merit.
Not approvedFundamental flaws in the paper seriously undermine the findings and conclusions
Version 1
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PUBLISHED 18 Oct 2016
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Reviewer Report 20 Feb 2017
Lennart Hammarström, Department of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden 
Not Approved
VIEWS 38
Govindaraj et al. report a typical SCID patient with a known mutation in Rag1 (p.E770K) with a previously known defective recombination activity and thus, there is very little novel information in this manuscript. In fact, the manuscript is already in ... Continue reading
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HOW TO CITE THIS REPORT
Hammarström L. Reviewer Report For: Case Report: Whole exome sequencing identifies variation c.2308G>A p.E770K in RAG1 associated with B- T- NK+ severe combined immunodeficiency [version 1; peer review: 2 approved with reservations, 1 not approved]. F1000Research 2016, 5:2532 (https://doi.org/10.5256/f1000research.10202.r20355)
NOTE: it is important to ensure the information in square brackets after the title is included in all citations of this article.
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Reviewer Report 31 Jan 2017
David K. Buchbinder, Division of Hematology, Department of Pediatrics, Children's Hospital of Orange County, Orange, CA, USA 
Approved with Reservations
VIEWS 31
The authors provide a case report of a patient with severe combined immunodeficiency secondary to RAG deficiency. Whole exome sequencing was utilized to ensure a rapid and accurate diagnosis. Overall, the report is well written. Despite this there are some ... Continue reading
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Buchbinder DK. Reviewer Report For: Case Report: Whole exome sequencing identifies variation c.2308G>A p.E770K in RAG1 associated with B- T- NK+ severe combined immunodeficiency [version 1; peer review: 2 approved with reservations, 1 not approved]. F1000Research 2016, 5:2532 (https://doi.org/10.5256/f1000research.10202.r19588)
NOTE: it is important to ensure the information in square brackets after the title is included in all citations of this article.
  • Author Response 02 Oct 2017
    Vinod Scaria, GN Ramachandran Knowledge Center for Genome Informatics, CSIR Institute of Genomics and Integrative Biology, Delhi, India
    02 Oct 2017
    Author Response
    The authors provide a case report of a patient with severe combined immunodeficiency secondary to RAG deficiency. Whole exome sequencing was utilized to ensure a rapid and accurate diagnosis. Overall, ... Continue reading
COMMENTS ON THIS REPORT
  • Author Response 02 Oct 2017
    Vinod Scaria, GN Ramachandran Knowledge Center for Genome Informatics, CSIR Institute of Genomics and Integrative Biology, Delhi, India
    02 Oct 2017
    Author Response
    The authors provide a case report of a patient with severe combined immunodeficiency secondary to RAG deficiency. Whole exome sequencing was utilized to ensure a rapid and accurate diagnosis. Overall, ... Continue reading
Views
34
Cite
Reviewer Report 16 Nov 2016
Paola Itliani, Institute of Protein Biochemistry, National Research Council of Italy, Naples, Italy 
Approved with Reservations
VIEWS 34
The manuscript “Whole exome sequencing identifies variation c.2308G>A p.E770K in RAG1 associated with B- T- NK+ severe combined immunodeficiency” is the description of a case report, that is a child as a supposed case of SCID. Exactly, the authors found ... Continue reading
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CITE
HOW TO CITE THIS REPORT
Itliani P. Reviewer Report For: Case Report: Whole exome sequencing identifies variation c.2308G>A p.E770K in RAG1 associated with B- T- NK+ severe combined immunodeficiency [version 1; peer review: 2 approved with reservations, 1 not approved]. F1000Research 2016, 5:2532 (https://doi.org/10.5256/f1000research.10202.r17720)
NOTE: it is important to ensure the information in square brackets after the title is included in all citations of this article.
  • Author Response 02 Oct 2017
    Vinod Scaria, GN Ramachandran Knowledge Center for Genome Informatics, CSIR Institute of Genomics and Integrative Biology, Delhi, India
    02 Oct 2017
    Author Response
    The manuscript “Whole exome sequencing identifies variation c.2308G>A p.E770K in RAG1 associated with B- T- NK+ severe combined immunodeficiency” is the description of a case report, that is a child ... Continue reading
COMMENTS ON THIS REPORT
  • Author Response 02 Oct 2017
    Vinod Scaria, GN Ramachandran Knowledge Center for Genome Informatics, CSIR Institute of Genomics and Integrative Biology, Delhi, India
    02 Oct 2017
    Author Response
    The manuscript “Whole exome sequencing identifies variation c.2308G>A p.E770K in RAG1 associated with B- T- NK+ severe combined immunodeficiency” is the description of a case report, that is a child ... Continue reading

Comments on this article Comments (0)

Version 2
VERSION 2 PUBLISHED 18 Oct 2016
Comment
Alongside their report, reviewers assign a status to the article:
Approved - the paper is scientifically sound in its current form and only minor, if any, improvements are suggested
Approved with reservations - A number of small changes, sometimes more significant revisions are required to address specific details and improve the papers academic merit.
Not approved - fundamental flaws in the paper seriously undermine the findings and conclusions
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