Keywords
Microarray resequencing, Neonatal cholestasis, ATP8B1, ABCB11
Microarray resequencing, Neonatal cholestasis, ATP8B1, ABCB11
In response to the referee comments, the discussion has been edited to acknowledge that several novel sequencing technologies have become available that are likely to or have already superseded microarray resequencing for clinical sequencing. These alterations help to put the work into context of recent advances in technology.
In response to the referee comments, the discussion has been edited to acknowledge that several novel sequencing technologies have become available that are likely to or have already superseded microarray resequencing for clinical sequencing. These alterations help to put the work into context of recent advances in technology.
To read any peer review reports and author responses for this article, follow the "read" links in the Open Peer Review table.
Neonatal cholestasis is characterised by persistent hyperbilirubinaemia and has an incidence of around 1 in 2500 live births1. It can occur as a result of impaired bile acid biosynthesis, defective bile secretion by hepatocytes (due to membrane transporter defects), or extrahepatic obstruction to biliary flow. Patients present with jaundice, dark urine, pale acholic stools and hepatomegaly. Older infants may have pruritus, develop fat-soluble vitamin deficiencies and fail to thrive1. The aetiology of cholestasis is varied and includes multiple inherited causes, such as progressive familial intrahepatic cholestasis (PFIC), Niemann-Pick disease type C and arthrogryposis, renal dysfunction and cholestasis (ARC) syndrome1. Furthermore cholestasis can be subdivided into ‘low-normal’ and high gamma glutamyl transpeptidase (gGT) categories depending on the level of serum gGT activity.
Accurate diagnosis is essential in order to inform decisions on treatment and management. As an example, familial intrahepatic cholestasis 1 (FIC1) protein deficiency caused by mutations in ATP8B1 (PFIC type 1) and bile salt export protein (BSEP) deficiency caused by mutations in ABCB11 (PFIC type 2) have similar presentations, however liver transplantation is used more frequently in PFIC type 2 then type 16. Genetic testing allows accurate assessment of the genetic risk of cholestasis in families, in addition to providing definitive diagnoses. Clinical laboratories tend to use fluorescent capillary sequencing (FS; Sanger method), because it lends itself to automation and is highly sensitive. However, FS is limited by machine capacity and relatively high consumables costs.
Microarray resequencing (MR) is an alternative sequencing method previously used to detect mutations in patients with intrahepatic cholestasis2. We have performed initial testing of a 300kb custom-designed microarray (Birmingham ReseqUencing Microarray, BRUM1) in patients with known mutations4. BRUM1 includes probes to sequence two genes (ATP8B1 and ABCB11) involved in PFIC. This short research article describes further evaluation of the BRUM1 microarray using samples simultaneously tested by FS and MR in patients without previously known mutations and assesses the advantages and disadvantages of MR in clinical laboratory use.
DNA samples from 29 children (15 females) who presented with intrahepatic cholestasis in the first year of life, low-normal range gGT activity without ARC syndrome or defects in bile acid biosynthesis were used. ARC syndrome was excluded by clinical examination3 and bile acid biosynthesis disorders were excluded by determination of urinary bile acid profile by electrospray ionisation mass spectrometry. Thus there was a high likelihood of detecting mutations in ATP8B1 and ABCB11 in these samples.
Polymerase chain reaction was used to amplify the coding exons of ATP8B1 and ABCB11 plus the intron-exon boundaries prior to both FS and MR. The PCR reaction used 50ng of DNA, 0.5μM each primer (Sigma), 0.5mM dNTPs (Bioline) and 2 units of Taq DNA polymerase (Biomix Red, Bioline UK) in 1x PCR buffer.
5μl of PCR product was treated with ExoSap IT (GE Healthcare) for 30 mins at 37°C before being denatured at 85°C for 15 mins. Sequencing primers (at a final concentration of 0.5μM) was added to 1μl of BigDye 3.1 and 1x BigDye buffer (Applied Biosystems) in a final volume of 10μl. The sequencing programme was thermal cycling for 34 cycles of denaturing at 95°C for 20 seconds, annealing 50°C for 20 seconds and extension at 60°C for 4 minutes. Resulting products were precipitated using EDTA/Na acetate and ethanol and centrifuged at 4000 rpm for 30 minutes. Products were washed in 70% ethanol before being air dryed, resuspended in 10μl of HiDi formamide (Applied Biosystems) and denatured. Resuspended products were analysed using a DNA analyzer 3730xl (Applied Biosystems) and the resulting sequence traces were analysed using Sequence Analysis 5.2.2 (Applied Biosystems).
PCR product quantitation, pooling, fragmentation, labelling and hybridisation and was performed according to the GeneChip Custom Resequencing Array Protocol V2.1 (Affymetrix). Arrays were washed and stained using a FS450 fluidics station before being scanned with a GCS3000 7G scanner (Affymetrix). Intensity files were generated using AGCC (Command Console V1.0, Affymetrix) and processed in GSeq 4.1 (Affymetrix). Base calling assumed the diploid model and a quality score threshold of 2 (default settings were used for all other parameters).
ATP8B1 and ABCB11 were analysed using FS and MR. The sequence variants detected in 13 of the samples (44.5% detection rate) are listed in Table 1. Eight variants had previously been described in association with PFIC and ten variants were novel. Four of the variants were nonsense mutations (22%), two were splice site changes (11%) and the rest were missense (67%). No insertions or deletions were detected using the specifically designed probes. No mutations were detected by either technique in the remainder of the patients and therefore the cause of ‘low-normal gGT’ cholestasis remains undetermined in these cases. The negative results in these cases may be explained by whole exon deletions or duplications, intronic mutations affecting splicing, or promoter region mutations in ATP8B1 and ABCB11, as such mutations would not be detected by either strategy. In addition, it is possible that further genes are involved in the phenotype of neonatal cholestasis with low gGT.
Sample | Gene | DNA changeb | Protein changec | Zygosity | Predicted effect | Previously reported? | Microarray resequencing | Fluorescent sanger sequencing |
---|---|---|---|---|---|---|---|---|
2 | ABCB11 | c.850G>C | p.V284L | Heterozygous | Missense | Yes7 | Y | Y |
4 | ABCB11 | c.2178+1G>T | Heterozygous | Altered splicing | Yes8 | Y | Y | |
6 | ATP8B1 | c.1010T>G | p.M337R | Heterozygous | Missense | Noveld | N | Y |
ATP8B1 | c.1018A>G | p.M340V | Heterozygous | Missense | Noveld | N | Y | |
7 | ATP8B1 | c.208G>A | p.D70N | Heterozygous | Missense | Yes9 | Y | Y |
9 | ABCB11 | c.2170G>A | p.D724N | Heterozygous | Missense | Noveld | Y | Y |
12 | ABCB11 | c.2611-2A>T | Heterozygous | Altered splicing | Yes10 | Y | Y | |
17 | ATP8B1 | c.1660G>A | p.D554N | Homozygous | Missense | Yes11 | Y | Y |
ATP8B1 | c.1564G>Aa | p.D522Na | Heterozygousa | Missense | Noveld | Y | Na | |
18 | ABCB11 | c.290T>G | p.L97* | Homozygous | Truncated protein | Novel | Y | Y |
19 | ATP8B1 | c.3040C>T | p.R1014* | Heterozygous | Missense | Yes9 | Y | Y |
22 | ATP8B1 | c.1014C>G | p.N338K | Heterozygous | Missense | Noveld | N | Y |
ATP8B1 | c.1018A>G | p.M340V | Heterozygous | Missense | Noveld | N | Y | |
ABCB11 | c.1636C>A | p.Q546K | Heterozygous | Missense | Noveld | Y | Y | |
25 | ABCB11 | c.499G>A | p.A167T | Heterozygous | Missense | Yes12 | Y | Y |
ABCB11 | c.3458G>A | p.R1153H | Heterozygous | Missense | Yes10 | Y | Y | |
26 | ABCB11 | c.3484G>T | p.E1162* | Homozygous | Truncated protein | Novel | Y | Y |
29 | ABCB11 | c.483C>A | p.C161* | Homozygous | Truncated protein | Novel | Y | Y |
In sample 17, MR detected a variant not confirmed by FS, constituting a false positive result. Two samples (6 and 22) had compound heterozygous changes in ATP8B1 detected by FS but not by MR. Both samples had two variants in close proximity; therefore we speculate that these are in cis and that each sequence variant has impaired the hybridisation of surrounding probes. Our experience of testing patients for mutations in these genes suggests that false negative results arising in this manner are likely to be uncommon. However, in this cohort they occurred in 7% of samples.
MR is an attractive alternative to traditional FS for genetic testing in neonatal cholestasis. The BRUM1 microarray used in this study has a much larger capacity than was utilised in this experiment, as it contains probes for 92 genes associated with inherited disorders. Analysis of the ability of this microarray to detect known gene mutations has shown a 97% mutation detection rate for base substitutions4. The major advantage of MR is increased capacity, allowing sequencing of multiple genes in one experiment as quickly as one gene using FS. The main bottleneck is the requirement to quantify and to pool individual PCR products before hybridisation. This step is time-consuming and prone to error (due to pipetting volume variations and potential sample mix-ups). Therefore, automation to minimise such errors would be useful, if not essential, for adoption of this method into clinical laboratories. Alternatively, use of long range PCR as the preparatory step for the MR protocol could reduce the number of reactions to be pooled, although it is more sensitive to poor DNA quality than standard PCR. Finally, microfluidics-based PCR systems, such as the 48.48 Access Array (Fluidigm Corporation, San Francisco, CA), might be combined with MR to avoid the quantification and pooling step altogether. This system allows the simultaneous but separate amplification of up to 48 PCR products for up to 48 samples, in nanolitre-sized reactions, using a semi-automated process. The end product of the process is a pool of PCR products for each sample, and it is commonly used for target enrichment for next generation sequencing experiments.
Of the mutations recorded in the Human Gene Mutation Database5 in ATP8B1 and ABCB11, 24% and 16% were small insertions or deletions (indels) respectively, though their combined frequency in PFIC cases is unknown as most are private mutations. The major disadvantage of MR is it’s insensitivity for the detection of indels4. Whilst known indels can be detected with proper microarray design, novel indels will be missed. Larger insertions and deletions involving whole exons, of the type routinely detected by multiplex ligation-dependent probe amplification (MLPA; MRC-Holland, Netherlands), are not detected by either MR or FS. Another disadvantage, underscored by the results of this study, is that mis-called base substitutions (both false negative and false positive calls), are frequent and were found in approximately 10% of samples in this study.
In summary, MR allows rapid and cost-effective genetic screening in neonatal cholestasis and yields results relevant for patient management. Many clinical laboratories are experienced in oligoarray comparative genome hybridization (CGH) and thus have access to equipment required for MR, suggesting that MR could be implemented for a relatively small monetary investment. In principle, MR could be applied to many clinical scenarios involving heterogeneous conditions, especially if the mutations tend to be base substitutions. We recommend that MR methods be used for initial evaluation, with FS deployed when genetic and clinical or histopathologic findings are discordant.
In recent years, various next generation sequencing (NGS) platforms have become available which allow massively parallel resequencing experiments to be performed. In particular ‘benchtop’ sequencers like the GS Junior (Roche), Personal Genome Machine (Life technologies) and MiSeq (Illumina) are attractive to clinical laboratories because they allow fast, cheap resequencing of multiple genes, and when the capacity is used optimally the costs are lower than MR. This study has identified a significant rate of discordant results obtained by MR when compared to Sanger sequencing, and consequently we predict that NGS will be the method of choice for clinical laboratory resequencing tests.
KEM performed the experiments, analysed the data and prepared the first draft of the manuscript. CKB performed the experiments and analysed the data. SSB recruited patients and performed experiments, UB, ES, DAK, CJK and JLH recruited patients and analysed the data, ASK analysed the data, FMcD analysed the data. PG conceived the study and analysed the data. All authors were involved in the revision of the manuscript and have agreed to the final content.
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Competing Interests: No competing interests were disclosed.
Competing Interests: No competing interests were disclosed.
Competing Interests: No competing interests were disclosed.
Competing Interests: No competing interests were disclosed.
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