Gulay Korukluoglu

Prof. Gulay Korukluoglu

Public Health Institute, University of Health Sciences, Ankara 06500, Turkey
orcid

Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

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

Representative Publications

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8 September 2011 in Eurosurveillance
Verified
Journal Article
Open access
PHPaul Heyman
Paul Heyman
CCC S Ceianu
C S Ceianu
ICI Christova
I Christova
NTN Tordo
N Tordo
MBM Beersma
M Beersma
AVA Vaheri
A Vaheri
Hantavirus infections are reported from many countries in Europe and with highly variable annual case numbers. In 2010, more than 2,000 human cases were reported in Germany, and numbers above the baseline have also been registered in other European countries. Depending on the virus type human infections are characterised by mild to severe forms of haemorrhagic fever with renal syndrome. The member laboratories of the European Network for diagnostics of Imported Viral Diseases present here an overview of the progression of human cases in the period from 2005 to 2010. Further we provide an update on the available diagnostic methods and endemic regions in their countries, with an emphasis on occurring virus types and reservoirs.

24 November 2020 in Infection
Verified
Journal Article
Closed access
PDF file
IHImran Hasanoglu
Imran Hasanoglu
Gulay KorukluogluGulay Korukluoglu
Gulay Korukluoglu
DADilek Asilturk
Dilek Asilturk
YCYasemin Coskun
Yasemin Coskun
AKAyşe Kaya Kalem
Ayşe Kaya Kalem
RGRahmet Guner
Rahmet Guner

11 August 2020 in Urologia Internationalis
Verified
Journal Article
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BKBircan Kayaaslan
Bircan Kayaaslan
Gulay KorukluogluGulay Korukluoglu
Gulay Korukluoglu
IHImran Hasanoglu
Imran Hasanoglu
AKAyse Kaya Kalem
Ayse Kaya Kalem
FEFatma Eser
Fatma Eser
RGRahmet Guner
Rahmet Guner
Introduction: The presence of new coronavirus (SARS-CoV-2) in semen and the possibility of sexual transmission have become new subjects of curiosity. There is a discrepancy regarding this issue in the literature. The presence of SARS-CoV-2 in semen has been investigated in a limited number of studies, and mostly in recovering patients. We aimed to investigate the presence of SARS-CoV-2 RNA in semen of patients with a positive nasopharyngeal swab test for SARS-CoV-2 in the acute stage. Methods: We enrolled adult male patients who were hospitalized with confirmed SARS-COV-2 infection in the study. In addition to routine laboratory and radiological tests, semen sample was obtained from volunteers and transferred to the Turkish Public Health Institution, National Virology Laboratory. The samples were processed for the detection of SARS-CoV-2 RNA on the day of collection. Results: Sixteen patients were included in the study. The median age was 33.5 years (18–54). All but one had respiratory symptoms. None of the patients had a history or symptoms of urogenital disease. All semen samples were obtained during hospitalization and in the acute stage of the infection. The median time to obtain a semen sample after positive nasopharyngeal test was 1 day (0–7). All semen samples were detected as negative for SARS-CoV-2 PCR. Discussion/Conclusion: Although all semen samples were obtained in acute stage of the infection when the nasopharyngeal swab test was positive, we did not detect SARS-CoV-2 in semen. The results of our study support the thought that sexual transmission via semen does not have an important role in the person-to-person transmission of SARS-CoV-2. We think that our study will provide new information to fill the gap in the literature.

1 December 2012 in Emerging Infectious Diseases
Verified
Journal Article
Open access
JVJessica Vanhomwegen
Jessica Vanhomwegen
MAMaria João Alves
Maria João Alves
TATatjana Avsic-Zupanc
Tatjana Avsic-Zupanc
SBSilvia Bino
Silvia Bino
SCSadegh Chinikar
Sadegh Chinikar
Philippe DuboisPhilippe Dubois
Philippe Dubois
Crimean-Congo hemorrhagic fever (CCHF) is a highly contagious viral tick-borne disease with case-fatality rates as high as 50%. We describe a collaborative evaluation of the characteristics, performance, and on-site applicability of serologic and molecular assays for diagnosis of CCHF. We evaluated ELISA, immunofluorescence, quantitative reverse transcription PCR, and low-density macroarray assays for detection of CCHF virus using precharacterized archived patient serum samples. Compared with results of local, in-house methods, test sensitivities were 87.8%–93.9% for IgM serology, 80.4%–86.1% for IgG serology, and 79.6%–83.3% for genome detection. Specificity was excellent for all assays; molecular test results were influenced by patient country of origin. Our findings demonstrate that well-characterized, reliable tools are available for CCHF diagnosis and surveillance. The on-site use of such assays by health laboratories would greatly diminish the time, costs, and risks posed by the handling, packaging, and shipping of highly infectious biologic material.

1 February 2018 in Antiviral Research
Verified
Journal Article
Closed access
JSJessica Spengler
Jessica Spengler
DBDennis A. Bente
Dennis A. Bente
MBMike Bray
Mike Bray
FBFelicity Burt
Felicity Burt
RHRoger Hewson
Roger Hewson
APAnna Papa
Anna Papa

26 June 2015 in Journal of Medical Virology
Verified
Journal Article
Open access
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APAnna Papa
Anna Papa
Katerina TsergouliKaterina Tsergouli
Katerina Tsergouli
DÇDilek Yağcı Çağlayık
Dilek Yağcı Çağlayık
SBSilvia Bino
Silvia Bino
NCNajada Como
Najada Como
Gulay KorukluogluGulay Korukluoglu
Gulay Korukluoglu
Crimean‐Congo hemorrhagic fever (CCHF) is a potentially severe disease caused by CCHF virus. As in other viral hemorrhagic fevers, it is considered that the course and outcome of the disease depend on the viral load and the balance among the immune response mediators, and that a fatal outcome is the result of a “cytokine storm.” The level of 27 cytokines was measured in serum samples taken from 29 patients during the acute phase of the disease. Two cases were fatal. Among survivors, significant differences between severe and non‐severe cases were observed in the levels of IP‐10, and MCP‐1, while the levels of IL‐1b, IL‐5, IL‐6, IL‐8, IL‐9, IL‐10, IL‐15, IP‐10, MCP‐1, TNF‐α, and RANTES differed significantly between fatal and non‐fatal cases (P < 0.05). RANTES was negatively correlated with the outcome of the disease. A striking similarity with the cytokine patterns seen in Ebola virus disease was observed. A weak Th1 immune response was seen. The viral load was positively correlated with IL‐10, IP‐10, and MCP‐1 levels, and negatively correlated with the ratio IL‐12/IL‐10. Especially IP‐10 and MCP‐1 were significantly associated with the viral load, the severity and outcome of the disease, and they could act as biomarkers and, probably, as potential targets for treatment strategies design. J. Med. Virol. 88:21–27, 2016.