Juan Manuel Corpa

Prof. Juan Manuel Corpa

Universidad CEU Cardenal Herrera
orcid

Research Focus & Metrics

Academic Career Length

29Years (1998-Present)

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

Representative Publications

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12 August 2010 in Molecular Microbiology
Verified
Journal Article
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DMDavid Viana Martín
David Viana Martín
JBJosé Blanco
José Blanco
María Ángeles Tormo-MasMaría Ángeles Tormo-Mas
María Ángeles Tormo-Mas
Laura Selva MartínezLaura Selva Martínez
Laura Selva Martínez
CGCaitriona M. Guinane
Caitriona M. Guinane
JPJosé R. Penadés
José R. Penadés
Summary: Staphylococci adapt specifically to various animal hosts by genetically determined mechanisms that are not well understood. One such adaptation involves the ability to coagulate host plasma, by which strains isolated from ruminants or horses can be differentiated from closely related human strains. Here, we report first that this differential coagulation activity is due to animal‐specific alleles of the von Willebrand factor‐binding protein (vWbp) gene, vwb, and second that these vwb alleles are carried by highly mobile pathogenicity islands, SaPIs. Although all Staphylococcus aureus possess chromosomal vwb as well as coagulase (coa) genes, neither confers species‐specific coagulation activity; however, the SaPI‐coded vWbps possess a unique N‐terminal region specific for the activation of ruminant and equine prothrombin. vWbp‐encoding SaPIs are widely distributed among S. aureus strains infecting ruminant or equine hosts, and we have identified and characterized four of these, SaPIbov4, SaPIbov5, SaPIeq1 and SaPIov2, which encode vWbpSbo4, vWbpSbo5, vWbpSeq1 and vWbpSov2 respectively. Moreover, the SaPI‐carried vwb genes are regulated differently from the chromosomal vwb genes of the same strains. We suggest that the SaPI‐encoded vWbps may represent an important host adaptation mechanism for S. aureus pathogenicity, and therefore that acquisition of vWbp‐encoding SaPIs may be determinative for animal specificity.

1 August 2005 in Journal of Comparative Pathology
Verified
Journal Article
Closed access
JGJ. González
J. González
MGMaria Geijo
Maria Geijo
CGC. García-Pariente
C. García-Pariente
AVA. Verna
A. Verna
Juan Manuel CorpaJuan Manuel Corpa
Juan Manuel Corpa
VPValentin Perez
Valentin Perez

27 January 2009 in Proceedings of the National Academy of Sciences
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Journal Article
Closed access
Laura Selva MartínezLaura Selva Martínez
Laura Selva Martínez
DMDavid Viana Martín
David Viana Martín
GRGili Regev-Yochay
Gili Regev-Yochay
KTKrzysztof Trzcinski
Krzysztof Trzcinski
Juan Manuel CorpaJuan Manuel Corpa
Juan Manuel Corpa
JPJosé R. Penadés
José R. Penadés
A surprising example of interspecies competition is the production by certain bacteria of hydrogen peroxide at concentrations that are lethal for others. A case in point is the displacement of Staphylococcus aureus by Streptococcus pneumoniae in the nasopharynx, which is of considerable clinical significance. How it is accomplished, however, has been a great mystery, because H 2 O 2 is a very well known disinfectant whose lethality is largely due to the production of hyperoxides through the abiological Fenton reaction. In this report, we have solved the mystery by showing that H 2 O 2 at the concentrations typically produced by pneumococci kills lysogenic but not nonlysogenic staphylococci by inducing the SOS response. The SOS response, a stress response to DNA damage, not only invokes DNA repair mechanisms but also induces resident prophages, and the resulting lysis is responsible for H 2 O 2 lethality. Because the vast majority of S. aureus strains are lysogenic, the production of H 2 O 2 is a very widely effective antistaphylococcal strategy. Pneumococci, however, which are also commonly lysogenic and undergo SOS induction in response to DNA-damaging agents such as mitomycin C, are not SOS-induced on exposure to H 2 O 2. This is apparently because they are resistant to the DNA-damaging effects of the Fenton reaction. The production of an SOS-inducing signal to activate prophages in neighboring organisms is thus a rather unique competitive strategy, which we suggest may be in widespread use for bacterial interference. However, this strategy has as a by-product the release of active phage, which can potentially spread mobile genetic elements carrying virulence genes.

1 April 2000 in Journal of Comparative Pathology
Verified
Journal Article
Closed access
Juan Manuel CorpaJuan Manuel Corpa
Juan Manuel Corpa
JGJ Garrido
J Garrido
JMJf Garcia Marin
Jf Garcia Marin
VPValentin Perez
Valentin Perez

1 April 2006 in Reproduction
Verified
Journal Article
Closed access
Juan Manuel CorpaJuan Manuel Corpa
Juan Manuel Corpa
Ectopic pregnancy denotes a pregnancy occurring elsewhere than in the cavity of the uterus. This pathology has been recognised for years and it causes numerous maternal deaths during the first trimester of pregnancy. While this condition is well-known in humans, it is rarely diagnosed in animals. However, the causes and mechanisms leading to an ectopic implantation of the ovum are not always clearly defined in humans or animals. Two types of ectopic pregnancy are mainly recognized: (1) tubal pregnancy occurs when an oocyte is fertilized and then remains in the oviduct and (2) abdominal pregnancy occurs when the gestation develops in the peritoneal cavity. The latter may be subdivided into two subtypes: the primary form, when a fertilized oocyte enters the peritoneal cavity and becomes attached to the mesentery or abdominal viscera, and the secondary form, which follows the rupture of an oviduct or the uterus after the fetus has been implanted, and the fetus is expelled into the peritoneal cavity. Cornual, ovarian and cervical ectopic locations are less frequent. Several differences exist in ectopic pregnancies between human beings and animal species. While abdominal pregnancy has been described in both human and animal species, tubal ectopic pregnancies would appear to be restricted to primates. Other than anecdotal cases, this pathological condition does not occur in laboratory, domestic or farm animals. Several factors are described as being the cause of these differences.

1 January 1999 in American Journal of Veterinary Research
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Journal Article
Closed access
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VPValentin Perez
Valentin Perez
JTJ. Tellechea
J. Tellechea
Juan Manuel CorpaJuan Manuel Corpa
Juan Manuel Corpa
MGM. Gutiérrez
M. Gutiérrez
JMJ. F. García Marín
J. F. García Marín
Objective: To investigate the relation between lesions and cellular immune response-based tests in sheep with naturally acquired paratuberculosis and to evaluate efficacy of an interferon-γ (IFN-γ) assay and the intradermal skin test. Animals: 110 and 88 adult sheep were used to evaluate the IFN-γ assay and skin test, respectively. Procedure: Before euthanasia, heparinized blood was collected and incubated with avian purified protein derivative (PPD). Interferon-γ production was assessed, using a commercial enzyme immunoassay. Skin testing in the caudal fold also was performed, using avian PPD. Sensitivity and specificity of these techniques were evaluated, using histopathologic findings as reference. Results: Of the sheep examined, 61 (55.4%) had lesions that were classified in 5 categories, according to location, extension, cellular types, and presence of acid-fast bacilli. Regarding cellular immunity test results, 55.4% of sheep with and 6.1% without pathologic changes had positive results of the IFN-γ assay. Skin test sensitivity (55.6%) and specificity (100%) were slightly greater. Conclusion: Close association between pathologic findings and cellular immune response was apparent. Most sheep with focal (tuberculoid) and some with diffuse lesions (borderline tuberculoid), all with scant or no acid-fast bacilli in the intestine, had positive results of the IFN-γ assay and skin test. Most sheep with diffuse lesions and high numbers of bacilli (borderline lepromatous) were test negative. Clinical Relevance: Cellular immune response-based and serologic tests are useful tools for seeking evidence of paratuberculosis. Each technique detects different types of immune-reacting sheep, and their simultaneous use may detect most infected animals. (Am J Vet Res 1999;60:123–127)