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Immunogenetics

, Volume 70, Issue 10, pp 619–623 | Cite as

IPD-MHC: nomenclature requirements for the non-human major histocompatibility complex in the next-generation sequencing era

  • Giuseppe Maccari
  • James Robinson
  • Ronald E. Bontrop
  • Nel Otting
  • Natasja G. de Groot
  • Chak-Sum Ho
  • Keith T. Ballingall
  • Steven G. E. Marsh
  • John A. Hammond
Open Access
Original Article

Abstract

The IPD-MHC Database is the official repository for non-human MHC sequences, overseen and supported by the Comparative MHC Nomenclature Committee, providing access to curated MHC data and associated analysis tools. To address the increasing amount and complexity of data being submitted, an entirely upgraded version of the IPD-MHC Database was recently released to maintain IPD-MHC as the central platform for the comparison of curated MHC data. As a consequence, a new level of nomenclature standardisation is required between the different species to enable data submission and to allow the unambiguous inter- and intra-species comparison of alleles. However, any changes must retain the flexibility demanded by the unique biology of different taxonomic groups. Here, we describe the rationale for a standardised nomenclature system and summarise the changes that have been driven by the requirements of implementing the IPD-MHC database. This modified nomenclature system is essential to maintain the current functionality of IPD-MHC and provide a scalable future-proof database organisation to fully exploit the bioinformatic tools used for analysis.

Keywords

MHC IPD-MHC Database Nomenclature Comparative MHC Variation 

Introduction

It was evident, from early on, that within the MHC research community, nomenclature systems were required to prevent confusion when faced with a vast array of allele sequences and to avoid potential redundancy. In 1990, guidelines were proposed to provide a set of rules for the unambiguous naming of MHC alleles (Klein et al. 1990), and shortly afterwards, the Comparative MHC Nomenclature Committee was established, with the support of the International Society for Animal Genetics (ISAG) and the Veterinary Immunology Committee (VIC) of the International Union of Immunological Societies (IUIS). In order to promote the work of the MHC committee and provide a centralised repository of manually curated and annotated sequences, the Immuno Polymorphism Database (IPD) project was established in 2003 by the HLA Informatics Group of the Anthony Nolan Research Institute (Robinson et al. 2003, 2005). The IPD project (hosted by the European Bioinformatic Institute) is a set of related databases and associated analysis tools regarding the study of polymorphic genes that function within the immune system. Above all, the IPD-MHC Database stores MHC data that has been manually curated by experts according to the official nomenclature guidelines for each species. As such, IPD-MHC section curators and the Nomenclature Committee have a symbiotic relationship, each contributing to the development and improvement of MHC nomenclature.

During the last decade, the IPD-MHC Database has faced the challenge of constant growth in size, both in sequence numbers and taxonomic groups, and the associated demand for data access and unified bioinformatic tools. As new species were added, the problems of MHC nomenclature being specific to the needs of each section became more and more prevalent. Moreover, with the advent of high-throughput sequencing methods and the increasing number of sequences deposited, the work of curators - often relying on local analysis tools - became unsustainable. The lack of a unified organisation hampered the development of unified tools for data curation and comparison; cross-group comparison tools and a generic submission tool were impossible. Ultimately, this was creating and untenable demand from each section on the database developers, severely limiting the utility of IPD-MHC.

Other problems were more historical and reflected the complexity of particular sections. Several taxonomic groups (bovins, ovins, equids, swine, and canines) conserve non-standardised names either for genes or alleles. For example, in the canine group, the DLA abbreviation (Dog Leukocyte Antigen—recalling the human naming system) is based on the common species name and is used to name alleles shared between various organisms, included domestic dog, wolf, coyote and fox. This causes the allele nomenclature to be ambiguous, as a DLA gene or allele name may refer to a specific organism, a subgroup or all the organisms within that taxonomic group. This can be avoided by providing a rigorous subdivision by species, with a one-to-one relation between species and allele. However, where available, the database retains all the information related to breeds or hybridising species. For example, all organisms previously classified as Canis lupus familiaris are now listed within the Canis lupus species, featuring in the breed field. For an exhaustive review of the current MHC nomenclature for each section, please refer to the accompanying manuscript in this issue (Ballingall et al. 2018).

To address all these issues, a complete redesign and reorganisation of the data was undertaken. In 2016, IPD-MHC Database version 2.0 was released (Maccari et al. 2017). IPD-MHC 2.0 standardised the database organisation and provided a highly scalable framework that allowed the development of bespoke analysis tools. For example, IPD-MHC 2.0 now includes genomic sequences and allows the inter- and intra-species comparison of genomic and non-genomic allele sequences for the first time. This enhanced functionality has required a new level of standardisation in the MHC nomenclature between species and groups. These are changes that have been driven by the requirements of IPD-MHC and developed in concert with the MHC Nomenclature Committee. In this manuscript, the requirements for naming new alleles will be reviewed, and an overview of required changes in the taxonomic organisation of the MHC groups is presented, together with a set of core concepts to allow a more future-proof organisation of the IPD-MHC Database. The aim is to provide a universal bioinformatic framework, that is still flexible enough to deal with the complexities of MHC diversity in all jawed vertebrate species.

MHC nomenclature requirements for IPD-MHC

The realisation of the benefits that a standardised naming scheme for MHC alleles brings is not new. The MHC Nomenclature Committee proposed a set of naming rules with the aim of unambiguously identifying MHC genes and alleles (Klein et al. 1990; Ellis et al. 2006). In particular, it was suggested to prefix a four-letter code to the gene name, coined by abbreviating the species scientific name, maintaining a register of unique names to avoid ambiguities in the nomenclature. The relevance of a centralised nomenclature repository becomes evident when the combination of possible four-letter codes is analysed. Figure 1 shows the distribution of the number of duplicated four-letter codes within the Mammalia class, where about one quarter of the generated names present at least one repetition. However, while the four-letter code was adopted by most of the current MHC taxonomic groups, primarily by the non-human primate group, some of the suggested changes were not universally accepted, and researchers have for the most part retained the original names (Ellis et al. 2006), such as the Canids, Felids and Suids groups.
Fig. 1

Four-letter codes distribution. Distribution of duplicate four-letter codes generated over all species belonging to the Mammalia class. Yellow, unique names; blue, duplicates

The MHC Nomenclature Committee is promoting the extended use of the four-letter code as an essential tool for the unambiguous comparison of data between species, together with a set of shared guidelines. These guidelines now represent the minimum requirements for the curation and naming of MHC alleles on IPD-MHC.
  • The IPD-MHC Database acts as the register of MHC species designations. When a request for the addition of an organism is received, a four-letter code is automatically generated from its scientific name by using the first two characters of the genus and species, respectively. If the name is already assigned, the next two characters of the species are used, until a unique name is generated.

  • The species four-letter code will be used to unambiguously identify genes and alleles belonging to a specific group. When that group hosts one single species, the four-letter code can be considered superfluous and can be omitted. Furthermore, as the four-letter code is unique among all groups within the IPD-MHC Database, the group prefix may be dropped. For example, swine alleles belonging to locus 1 will be named SLA-1, instead of Susc-1 or SLA-susc-1; the water buffalo (Bubalus bubalis) will use the prefix Bubu-1, as the Bovids group enumerates more than one species.

  • A hyphen divides the four-letter designation from the gene name, designated by capital letters and Arabic numerals. MHC class II genes are generally designated by the letter D, while MHC class I genes may be designated by any other letter or combination of letters. A second letter identifies families within MHC class II genes, while the third letter (A or B) identifies the chain that the sequence encodes. If an orthologous relationship to the HLA designation is obvious the same name should be used. The numbering of genes within each family (e.g., DRB1, DRB2, DRB3, etc.) should be sequential in the order of their initial discovery.

  • The gene designation is followed by an asterisk as a separator and then by an allelic string. In order to facilitate inter species comparison of genomic data, guidelines from HLA nomenclature are adopted (Marsh et al. 2010). Allele names have a unique identifier formed by four sets of digits, separated by colons which allows an unambiguous identification of each of the four sets (Fig. 2). The first two sets are mandatory and describe the allelic group and the subgroup, respectively. Alleles whose numbers differ at this level exhibit one or more differences at the amino acid level. The third set of digits describes synonymous nucleotide substitutions within the coding regions. The last set of digits was recently added to support genomic data and describes sequence polymorphism within introns or untranslated regions. The number of digits for each set might vary from group to group, as the colons allow an unambiguous identification of the four sets.

Fig. 2

Non-human MHC nomenclature. Schematics of the nomenclature system for non-human MHC alleles. Yellow, the code representing the taxonomic group/species; blue, the gene. A hyphen divides the species four letter designation from the gene name, designated by capital letters and Arabic numerals. The gene designation is followed by an asterisk, and then by an allelic string composed of up to four sets of digits, separated by colons

Changes in the taxonomic organisation

In order to align the IPD-MHC Database to the requirements listed above, a number of changes were made in the organism name assignment, some of these influencing the current nomenclature. The alleles belonging to Ovins taxonomic group are now represented with the four-letter code ‘Ovar’ to distinguish between the species belonging to that group: Ovis aries and Ovis canadensis. In the Bovins taxonomic group, Bos taurus ad Bos indicus were previously represented as separated species, each with its own unique four-letter code. In this version of the database, B. taurus and B. indicus share the name BoLA because many of the animals designated B. indicus are hybrids. This simplifies the search for alleles and also enables comparative analysis with complete datasets. Changes in the current taxonomic organisation are summarised in Table 1, together with a comparison of the previous system. It should be noted that for historical reasons, the human and Suids groups do not adopt the four-letter code designation. However, as each group includes only one species, there is no ambiguity in the allele nomenclature at the present time.
Table 1

Changes in the taxonomic organisation

Group

Scientific name

Common name

Previous designation

Current designation

Notes

OLA

Ovis aries

Domestic sheep

OLA

Ovar

 

Ovis canadensis

Bighorn sheep

OLA

Ovca

 

BoLA

Bos taurus

Cattle

Bota

 

Bos indicus

Zebu

Boin

 

Bos sp.

Cattle

BoLA

Bos sp. substitutes and represents Bos taurus, Bos indicus and their hybrids

DLA

Canis lupus

Wolf

DLA

Calu

 

Canis lupus familiaris

Domestic dog

DLA

Canis lupus familiaris is merged with the Canis lupus species.

Canis rufus

Red wolf

DLA

Caru

 

Canis simensis

Ethiopian wolf

DLA

Casi

 

Canis latrans

Coyote

DLA

Cala

 

Canis lupus baileyi

Mexican grey wolf

DLA

Caba

 
The Bovins group highlights a problem common to most of the domesticated species, where the threshold between species and breed is not always evident and finding a common rule of thumb is not a trivial task. A striking example of the subtle difference between species and breed is the Canine taxonomic group, where different species have been enumerated under the single DLA name. Hybridization between Canine species has long been recognised both in the wild and in captivity, causing problems in the taxonomy, as hybrids are not normally thought of as species. As an example, a recent study (vonHoldt et al. 2011) indicates that the red wolf (Canis rufus) may be a hybrid species between grey wolves and coyotes, as it shares genomic sequences with both. Subsequent studies found contrasting evidence, leaving the debate still open. To alleviate the taxonomic ambiguity in the Canine group, a different four-letter code will be used to distinguish different species, in contrast with the previously adopted strategy. However, all canine alleles will still retain the current nomenclature, where the DLA prefix is used for all the species belonging to the group and alleles are named in a single series for each locus. Table 2 shows the status of each taxonomic group regarding the nomenclature guidelines listed above. For an exhaustive explanation of the state of the art of each taxonomic group, please refer to the accompanying review (Ballingall et al. 2018).
Table 2

List of taxonomic groups adopting the nomenclature requirements

Alias

Full name

Nomenclature standards

Four-letter code

Gene designation

Colons

HLA

Human

-1

Yes

Yes

NHP

Non-human primates

Yes

Yes

Yes

DLA

Canids

Yes

FISH

Salmonids

Yes

Yes

OLA

Ovids

Yes

Yes

Yes

BoLA

Bovins

Yes

Yes

Yes

ELA

Equids

Yes

Yes

Yes

SLA

Suids

-1

Yes

Yes

RT1

Murids

Yes

CHICKEN

Gallus

Yes

Yes

Yes

1Groups not conforming to the nomenclature requirements for historical reasons

Summary and future development

The IPD-MHC team with the support of the Comparative MHC Nomenclature Committee have attempted to provide a common framework and set of guidelines to allow the hosting and analysis of MHC data from any species. The use of a common set of nomenclature rules across a range of species from divergent taxonomic groups, allows the storage and analysis of data in a biologically meaningful way. This allows the sharing of analysis tools and pipelines between taxonomic groups, thus improving the power and quality of data analysis. These standards on a common framework also provide future scalability of the database and readily facilitate the addition of new species and taxonomic groups as required by the research community. Furthermore, these changes represent the starting point for the development of a set of new tools for the analysis of genomic and non-genomic data, focussed on cross-species comparison. In conclusion, the suggested changes to the current nomenclature permit a much more future-proof organisation of IPD-MHC.

In 10 years, more than 10,000 sequences have been submitted to the IPD-MHC Database for curation and assignment of an official name prior to publication, providing a centralised repository for the official nomenclature and helping to drive database expansion in response to the most prominent topics in MHC research. As the amount of data increases and new species are included, inevitably, the nomenclature framework will have to adapt to meet the needs of the community. To this end, the IPD-MHC database represents the official resource for the scientific community, disseminating information and decisions made by the MHC Nomenclature Committee.

Notes

Acknowledgments

We would like to acknowledge the work of all the individuals in the MHC nomenclature committee. The authors would also like to acknowledge the work of the comparative MHC community in sequencing, identifying, and submitting the many sequences which form the core data that the IPD-MHC Database represents. In particular, we would like to acknowledge the work of Dr. Lorna J. Kennedy for curating DLA data, Prof Jim Kaufman for chicken MHC curation, Prof Shirley Ellis for BoLA data curation, Prof Lutz Walter for RT1 data curation, Dr. Unni Grimholt for fish MHC curation and Dr. Donald Miller and Prof Douglas Antczak for ELA data curation. Finally, the authors would also like to acknowledge the support provided by Paul Flicek, and the External Services Group at the European Bioinformatics Institute, which allows the IPD project to be hosted within the EBI infrastructure.

Funding

GM and JAH are supported by the funding from the Biotechnology and Biological Sciences Research Council (BBSRC) grant (BB/M011488/1). JAH is also supported by BBSRC awards BBS/E/I/00001710, BBS/E/I/00007030 and BBS/E/I/00007038. KB receives funding from the Scottish Government’s strategic research programme and the European Union’s Horizon 2020 research and innovation programme under grant agreement N°731014. The work of the IPD-MHC Databases receives support from the European Molecular Biology Laboratories and is recognised and supported by the International Society for Animal Genetics (ISAG) and the Veterinary Immunology Committee (VIC) of the International Union of Immunological societies (IUIS).

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© The Author(s) 2018

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

Authors and Affiliations

  • Giuseppe Maccari
    • 1
    • 2
  • James Robinson
    • 2
    • 3
  • Ronald E. Bontrop
    • 4
  • Nel Otting
    • 4
  • Natasja G. de Groot
    • 4
  • Chak-Sum Ho
    • 5
  • Keith T. Ballingall
    • 6
  • Steven G. E. Marsh
    • 2
    • 3
  • John A. Hammond
    • 1
  1. 1.The Pirbright InstituteWokingUK
  2. 2.Anthony Nolan Research InstituteLondonUK
  3. 3.UCL Cancer InstituteRoyal Free CampusLondonUK
  4. 4.Biomedical Primate Research CentreRijswijkThe Netherlands
  5. 5.Gift of Life MichiganAnn ArborUSA
  6. 6.Moredun Research InstituteMidlothianUK

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