Guillermo J. Sanchez-Contreras

Mr. Guillermo J. Sanchez-Contreras

Mediterraneo Marine Park
orcid
Chief Veterinary Officer - Director of Research

Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 June 2015 in Developmental & Comparative Immunology
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Journal Article
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MRMaria Reichel
Maria Reichel
Tamara Munoz-CaroTamara Munoz-Caro
Tamara Munoz-Caro
Guillermo J. Sanchez-ContrerasGuillermo J. Sanchez-Contreras
Guillermo J. Sanchez-Contreras
AGAna Rubio García
Ana Rubio García
GMGerd Magdowski
Gerd Magdowski
Carlos HermosillaCarlos Hermosilla
Carlos Hermosilla

25 January 2013 in Emerging Microbes & Infections
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Journal Article
Open access
RBRogier Bodewes
Rogier Bodewes
DMDanny Morick
Danny Morick
MBMarco Wg van de Bildt
Marco Wg van de Bildt
NONynke Osinga
Nynke Osinga
AGAna Rubio García
Ana Rubio García
AOAlbert Dme Osterhaus
Albert Dme Osterhaus
In 1988 and 2002, two major phocine distemper virus (PDV) outbreaks occurred in harbour seals (Phoca vitulina) in north-western European coastal waters, causing the death of tens of thousands seals. Here we investigated whether PDV is still circulating among seals of the Dutch coastal waters and whether seals have protective serum-antibodies against PDV. Therefore seal serum samples, collected from 2002 to 2012, were tested for the presence of PDV-neutralizing antibodies. Antibodies were detected in most seals in 2002 and 2003 while after 2003 antibodies were detected only in seals less than two month-old and adult seals that probably had survived the 2002 PDV-epizootic. We estimated the current proportion of seals with antibodies against PDV at 11%. These findings suggest that at present the vast majority of seals are not immune to PDV infection. PDV re-introduction in this area may cause a major epizootic with infection of >80% and mass-mortality of >50% of the population.Emerging Microbes & Infections ...

8 June 2021 in Animals
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Journal Article
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FDFabienne Delfour
Fabienne Delfour
Ruta VaicekauskaiteRuta Vaicekauskaite
Ruta Vaicekauskaite
DGDaniel Garcia-Parraga
Daniel Garcia-Parraga
CPCristina Pilenga
Cristina Pilenga
ASAgathe Serres
Agathe Serres
TMTania Monreal-Pawlowsky
Tania Monreal-Pawlowsky
In the recent past, animal welfare studies have tried to determine the best animal welfare measures and indicators. Expression of behavioural diversity is considered a potential positive welfare indicator, and to the authors’ knowledge, it has not been validated nor studied in cetaceans. For the first time, a behavioural diversity study on bottlenose dolphins (Tursiops truncatus) groups was conducted at six European facilities. The study was carried out by the animal care staff, biologists and veterinarians and included 54 dolphins housed in several group compositions at the different participating facilities. The goal of our study was to analyse behavioural diversity in bottlenose dolphins at the group level to investigate how particular factors might impact the diversity of behaviours within the group and to discuss its implications for dolphin welfare assessments. Eight factors (i.e., “observer location”, “number of individuals”, “age class”, “sex”, “social grouping”, “presence/absence of leading male”, “presence/absence of visitors” and “enrichment provision”) impacted the behavioural diversity of the observed groups, while no significant impact of the factors “time of day” and “activity before/after observation” could be found. Our study showed the feasibility of this kind of approach for cetaceans under professional care and the relevance to considering this parameter in dolphin welfare studies, despite certain limitations that warrant further research.

5 November 2013 in PLOS ONE
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RBRogier Bodewes
Rogier Bodewes
AGAna Rubio García
Ana Rubio García
LWLidewij C. M. Wiersma
Lidewij C. M. Wiersma
SGSarah Getu
Sarah Getu
MBMartijn Beukers
Martijn Beukers
AOAlbert D. M. E. Osterhaus
Albert D. M. E. Osterhaus
Using random PCR in combination with next-generation sequencing, a novel parvovirus was detected in the brain of a young harbor seal (Phoca vitulina) with chronic non-suppurative meningo-encephalitis that was rehabilitated at the Seal Rehabilitation and Research Centre (SRRC) in the Netherlands. In addition, two novel viruses belonging to the family Anelloviridae were detected in the lungs of this animal. Phylogenetic analysis of the coding sequence of the novel parvovirus, tentatively called Seal parvovirus, indicated that this virus belonged to the genus Erythrovirus, to which human parvovirus B19 also belongs. Although no other seals with similar signs were rehabilitated in SRRC in recent years, a prevalence study of tissues of seals from the same area collected in the period 2008-2012 indicated that the Seal parvovirus has circulated in the harbor seal population at least since 2008. The presence of the Seal parvovirus in the brain was confirmed by real-time PCR and in vitro replication. Using in situ hybridization, we showed for the first time that a parvovirus of the genus Erythrovirus was present in the Virchow-Robin space and in cerebral parenchyma adjacent to the meninges. These findings showed that a parvovirus of the genus Erythrovirus can be involved in central nervous system infection and inflammation, as has also been suspected but not proven for human parvovirus B19 infection.

14 December 2015 in PLOS ONE
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RBRogier Bodewes
Rogier Bodewes
AGAna Rubio García
Ana Rubio García
SBSophie M. Brasseur
Sophie M. Brasseur
Guillermo J. Sanchez-ContrerasGuillermo J. Sanchez-Contreras
Guillermo J. Sanchez-Contreras
MBMarco W. G. van de Bildt
Marco W. G. van de Bildt
PDPadraig Duignan
Padraig Duignan
In the spring and summer 2014, an outbreak of seal influenza A(H10N7) virus infection occurred among harbor seals (Phoca vitulina) off the coasts of Sweden and Denmark. This virus subsequently spread to harbor seals off the coasts of Germany and the Netherlands. While thousands of seals were reported dead in Sweden, Denmark and Germany, only a limited number of seals were found dead in the Netherlands. To determine the extent of exposure of seals in the Netherlands to influenza A/H10N7 virus, we measured specific antibody titers in serum samples from live-captured seals and seals admitted for rehabilitation in the Netherlands by use of a hemagglutination inhibition assay and an ELISA. In harbor seals in 2015, antibodies against seal influenza A(H10N7) virus were detected in 41% (32 out of 78) pups, 10% (5 out of 52) weaners, and 58% (7 out of 12) subadults or adults. In gray seals (Halichoerus grypus) in 2015, specific antibodies were not found in the pups (n = 26), but in 26% (5 out of 19) of the older animals. These findings indicate that, despite apparent low mortality, infection with seal influenza A(H10N7) virus was geographically widespread and also occurred in grey seals.

1 May 2015 in Journal of General Virology
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Journal Article
Closed access
RBRogier Bodewes
Rogier Bodewes
Guillermo J. Sanchez-ContrerasGuillermo J. Sanchez-Contreras
Guillermo J. Sanchez-Contreras
AGAna Rubio García
Ana Rubio García
RHRebriarina Hapsari
Rebriarina Hapsari
MBMarco W. G. van de Bildt
Marco W. G. van de Bildt
AOAlbert D. M. E. Osterhaus
Albert D. M. E. Osterhaus
Various herpesviruses have been discovered in marine mammals and are associated with a wide spectrum of disease. In the present study we describe the detection and phylogenetic analysis of a novel gammaherpesvirus, tentatively called phocine herpesvirus 7 (PhHV-7), which was detected in samples collected during an outbreak of ulcerative gingivitis and glossitis from juvenile harbour seals (Phoca vitulina) at the Seal Rehabilitation and Research Centre, the Netherlands. The presence of this novel gammaherpesvirus was confirmed by viral metagenomics, while no other viruses other than four novel anelloviruses were detected. However, PhHV-7 DNA was also detected in harbour and grey seals (Halichoerus grypus) without gingivitis or glossitis. Genetic analysis of the partial polymerase gene of PhHV-7 detected in both species revealed limited sequence variation. Additional studies are needed to elucidate whether the viruses discovered played a role in the disease observed.