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      Rapid and sensitive point-of-care detection of Orthopoxviruses by ABICAP immunofiltration

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          Abstract

          Background

          The rapid and reliable detection of infectious agents is one of the most challenging tasks in scenarios lacking well-equipped laboratory infrastructure, like diagnostics in rural areas of developing countries. Commercially available point-of-care diagnostic tests for emerging and rare diseases are particularly scarce.

          Results

          In this work we present a point-of-care test for the detection of Orthopoxviruses (OPV). The OPV ABICAP assay detects down to 1 × 10 4 plaque forming units/mL of OPV particles within 45 min. It can be applied to clinical material like skin crusts and detects all zoonotic OPV infecting humans, including Vaccinia, Cowpox, Monkeypox, and most importantly Variola virus.

          Conclusions

          Given the high sensitivity and the ease of handling, the novel assay could be highly useful for on-site diagnostics of suspected Monkeypox virus infections in areas lacking proper laboratory infrastructure as well as rapid on-site testing of suspected bioterrorism samples.

          Electronic supplementary material

          The online version of this article (doi:10.1186/s12985-016-0665-5) contains supplementary material, which is available to authorized users.

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          Most cited references17

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          Human monkeypox.

          Human monkeypox is a zoonotic Orthopoxvirus with a presentation similar to smallpox. Clinical differentiation of the disease from smallpox and varicella is difficult. Laboratory diagnostics are principal components to identification and surveillance of disease, and new tests are needed for a more precise and rapid diagnosis. The majority of human infections occur in Central Africa, where surveillance in rural areas with poor infrastructure is difficult but can be accomplished with evidence-guided tools and educational materials to inform public health workers of important principles. Contemporary epidemiological studies are needed now that populations do not receive routine smallpox vaccination. New therapeutics and vaccines offer hope for the treatment and prevention of monkeypox; however, more research must be done before they are ready to be deployed in an endemic setting. There is a need for more research in the epidemiology, ecology, and biology of the virus in endemic areas to better understand and prevent human infections.
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            Zoonotic poxviruses

            Poxviruses compromise a group of long known important pathogens including some zoonotic members affecting lifestock animals and humans. While whole genome sequence analysis started to shed light into the molecular mechanisms underlying host cell infection, viral replication as well as virulence, our understanding of poxvirus maintenance in nature and their transmission to humans is still poor. During the last two decades, reports on emerging human monkeypox outbreaks in Africa and North America, the increasing number of cowpox virus infections in cats, exotic animals and humans and cases of vaccinia virus infections in humans in South America and India reminded us that – beside the eradicated smallpox virus – there are other poxviruses that can cause harm to men. We start to learn that the host range of some poxviruses is way broader than initially thought and that mainly rodents seem to function as virus reservoir. The following review is aiming to provide an up-to-date overview on the epidemiology of zoonotic poxviruses, emphasizing orthopoxviruses. By outlining the current knowledge of poxvirus transmission, we hope to raise the awareness about modes of acquisition of infections and their proper diagnosis.
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              Rapid detection protocol for filoviruses.

              The incidence of filovirus disease outbreaks has been increasing in recent years. Although there have been advances in the developments of diagnostics, field tests are rare. Apart from family members of infected patients, health care workers are at high risk of being infected during the initial phase of an outbreak. RT-PCR has been shown to be helpful in containing outbreaks. To develop Taqman-RT-PCR for the detection of Ebola-Zaire virus (EBOV-Z), Ebola-Sudan virus (EBOV-S) and Marburg virus (MBGV). Quantitative Taqman-RT-PCRs for the detection of these viruses were developed and established on a portable Smartcycler TD. All three assays were highly sensitive and specific. The mobility of the assay system may help to contain future outbreaks.
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                Author and article information

                Contributors
                +49 30 18 754 2319 , SternD@rki.de
                vao9@cdc.gov
                sks5@cdc.gov
                Marko.Pietraszczyk@gmx.de
                lilija.miller@pei.de
                pmiethe@fzmb.de
                DornerB@rki.de
                NitscheA@rki.de
                Journal
                Virol J
                Virol. J
                Virology Journal
                BioMed Central (London )
                1743-422X
                9 December 2016
                9 December 2016
                2016
                : 13
                : 207
                Affiliations
                [1 ]Centre for Biological Threats and Special Pathogens (ZBS), Robert Koch Institute, Seestrasse 10, 13353 Berlin, Germany
                [2 ]Division of High-Consequence Pathogens and Pathology, Poxvirus and Rabies Branch, Centers for Disease Control and Prevention, Atlanta, GA USA
                [3 ]Senova GmbH, Weimar, Germany
                [4 ]FZMB GmbH, Bad Langensalza, Germany
                [5 ]Novel Vaccination Strategies and Early Immune Responses, Paul-Ehrlich-Institut, Langen, Germany
                Author information
                http://orcid.org/0000-0001-9057-4283
                Article
                665
                10.1186/s12985-016-0665-5
                5148848
                27938377
                512d816a-32c6-4f40-8b0d-e00d3f25b71d
                © The Author(s). 2016

                Open AccessThis 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. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 1 July 2016
                : 2 December 2016
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100002347, Bundesministerium für Bildung und Forschung;
                Award ID: 13N9596
                Award ID: 13N9601
                Award ID: 13N9601
                Award Recipient :
                Categories
                Methodology
                Custom metadata
                © The Author(s) 2016

                Microbiology & Virology
                orthopoxvirus,variola virus,monkeypox virus,cowpox virus,vaccinia virus,bioterrorism,zoonosis,point-of-care,rapid detection,abicap

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