Comparison of diagnostic performances of ten different immunoassays detecting anti-CCHFV IgM and IgG antibodies from acute to subsided phases of Crimean-Congo hemorrhagic fever

Crimean-Congo Hemorrhagic Fever Virus (CCHFV) is a geographically widespread tick-borne arbovirus that has been recognized by the WHO as an emerging pathogen needing urgent attention to ensure preparedness for potential outbreaks. Therefore, availability of accurate diagnostic tools for identification of acute cases is necessary.A panel comprising 121 sequential serum samples collected during acute, convalescent and subsided phase of PCR-proven CCHFV infection from 16 Kosovar patients was used to assess sensitivity. Serum samples from 60 healthy Kosovar blood donors were used to assess specificity. All samples were tested with two IgM/IgG immunofluorescence assays (IFA) from BNITM, the CCHFV Mosaic 2 IgG and IgM indirect immunofluorescence tests (IIFT) from EUROIMMUN, two BlackBox ELISAs for the detection of CCHFV-specific IgM and IgG antibodies (BNITM), two Anti-CCHFV ELISAs IgM and IgG from EUROIMMUN using recombinant structural proteins of CCHFV antigens, and two ELISAs from Vector-Best (IgM: μ-capture ELISA, IgG: indirect ELISA using immobilized CCHFV antigen). Diagnostic performances were compared between methods using sensitivity, specificity, concordance and degree of agreement with particular focus on the phase of the infection.In early and convalescent phases of infection, the sensitivities for detecting specific IgG antibodies differed for the ELISA test. The BlackBox IgG ELISA yielded the highest, followed by the EUROIMMUN IgG ELISA and finally the VectorBest IgG ELISA with the lowest sensitivities. In the subsided phase, the VectorBest IgM ELISA detected a high rate of samples that were positive for anti-CCHFV IgM antibodies. Both test systems based on immunofluorescence showed an identical sensitivity for detection of anti-CCHFV IgM antibodies in acute and convalescent phases of infection.Available serological test systems detect anti-CCHFV IgM and IgG antibodies accurately, but their diagnostic performances vary with respect to the phase of the infection.     

Ultrastructural study of the microsporidian chytridiopsis typographi (Chytridiopsida: Microspora) infecting the bark beetle,Ips typographus (Scolytidae: Coleoptera), with new data on spore dimorphism

Two types of sporogony of the microsporidian Chytridiopsis typographi in the midgut of adult bark beetle, Ips typographus, have been examined by means of light and electron microscopy. New data are reported on spore dimorphism and on the formation of pansporoblasts in two types of sporogony. Thin-walled spores, larger in size, are formed in a parasitophorous vacuole in the host columnar cells. Thick-walled spores are formed in a minimal vacuole in the host. The ultrastructure of the spore walls and the cyst wall are different from the organization in other microsporidia. Both spore types have identical internal structures and viable spores.     

Octosporea collembolae n. sp. (Microsporida,Microspora): A new microsporidian parasite of springtail Onychiurus quadriocellatus (Onychiuridae: Collembolae)

The life cycle of a new microsporidium, Octosporea collembolae, from the fat body of naturally infected springtails, Onychiurus quadriocellatus, is described at light and electron microscope levels. The prevalence of infection and host-parasite relationships are discussed.     

More on the life cycle of Malamoeba scolyti (Amoebidae: Sarcomastigophora) parasitizing: the bark beetle Dryocoetes autographus (Scolytidae,Coleoptera)

Some new developmental features previously unreported in, the life- cycle of an amoeba Malamoeba scolyti, which cause cysts in Malpighian tubules of the bark beetle Dryocoetes autographus, are described by means of light, phase-contrast, Nomarski interference, and electron microscopy. Two developmental phases are presumed to take place in the life cycle of M. scolyti: a phase with large multinucleate amoebae (trophozoites) developing in the gut and caecum of the host, and a phase (parasitic phase) causing cysts in the Malpighian tubules. Some data on the host-parasite relationship and rate of infection are also discussed.     

Light and electron microscope studies on Helicosporidium sp. parasitizing oribatid mites (Oribatei,Acarina) and collembola (Apterygota,Insecta) in forest soils

The life cycle of Helicosporidium sp. parasitizing natural populations of oribatid mites and collembolans in forest soils, is described by means of light, Nomarski interference, and electron microscopy. The ultrastructure of some early sporogonic stages (cysts), the young (maturing) spore, and the mature spore is discussed. Some data on the host-parasite relationships and prevalence of infection are presented.     

Gregarina hylobii and Ophryocystis hylobii n. sp. (ophryocystidae,neogregarinida) parasitizing Hylobius abietis (Curculionidae,coleoptera)

Two sporozoan parasites, Gregarina hylobii and Ophryocystis hylobii n. sp., parasitizing the adults of natural populations of Hylobius abietis are described. The gregarine G. hylobii, a parasite of the gut of H. abietis, has been reexamined and its complete life cycle, including the solitary gamonts, gametocysts, and sporoducts is described. The life cycle of the neogregarine O. hylobii infecting the Malpighian tubules of host animals examined at light and electron microscope levels is discussed. Some data on the prevalence of infections and host-parasite relationships are also discussed.