Mehmet Zülfü Yildiz

Vegetative compatibility groups in Verticillium dahliae isolates from olive in western Turkey

Verticillium wilt, caused by Verticillium dahliae, is the most serious disease in olive cultivation areas in western Turkey. Two hundred and eight isolates of V. dahliae from olive (Olea europea var. sativa) trees were taken for vegetative compatibility analysis using nitrate non-utilizing (nit) mutants. One isolate did not produce a nit mutant. Nit mutants of 207 isolates were tested against tester strains of internationally known vegetative compatibility groups (VCGs) 1A, 2A, 2B, 3, 4A and 4B, and also paired in many combinations among themselves. One hundred and eighty nine of the isolates (90.9%) were strongly compatible with T9, the tester strain of VCG1A, and thus were assigned to VCG1A. Eight isolates were assigned to VCG2A and four isolates to VCG4B. One isolate was heterokaryon self-incompatible (HSI) and five isolates could not be grouped to any of the VCGs tested. Pathogenicity assays were conducted on a susceptible olive cultivar (O. europea cv. Manzanilla) and a susceptible local cotton cultivar (Gossypium hirsutum cv. Çukurova 1518). Both cotton and olive inoculated with all VCG1A isolates showed defoliating symptoms in greenhouse tests. This is the first report on VCGs in V. dahliae from olive trees in Turkey which demonstrates that VCG1A of the cotton-defoliating type is the most commonly detected form from olive plants in the western part of Turkey.

Determination of in vivo toxicity and in vitro cytotoxicity of venom from the Cypriot blunt-nosed viper Macrovipera lebetina lebetina and antivenom production

The venomous Levantine viper, Macrovipera lebetina lebetina is endemic to Cyprus. The objective of this study was to investigate in vitro cytotoxicity, in vivo lethality, and antivenom production followed by a re-immunization schedule in mice against Macrovipera lebetina lebetina venom. The LD50 value was estimated as 7.58 mg/kg within 24 hours by different venom doses administrated intraperitoneally in mice. Freunds complete and incomplete adjuvants were used for first and second immunization of mice in antivenom production. A cell-based assay was performed to determine the effects of Macrovipera lebetina lebetina venom and antivenom neutralizing potency on L929 cell viability. The snake venom toxicity and cytotoxicity were examined and comparison of results showed good correlation, the LD50 value was tenfold higher than the IC50 value. The IC50 value was 0.62 ± 0.18 mL after 48 hours treatment while the calculated value was 1.62 ± 0.25 mL for the culture media totally refreshed after two hours treatment with venom. The in vitro efficacy of antivenom against Macrovipera lebetina lebetina venom was found to be low. This is the first report that describes the in vivo and in vitro toxic effects of Macrovipera lebetina lebetina venom and antivenom production against this species.

Viper venom induced inflammation with Montivipera xanthina (Gray, 1849) and the anti-snake venom activities of Artemisia absinthium L. in rat

The present study was conducted to explore the characterization of Montivipera xanthina crude venom partially by in vitro and in vivo and the anti-snake venom activities of Artemisia absinthium L. in comparison with carrageenan-induced acute inflammation model in rats. The LD50 value was estimated as 8.78 mg/kg within 24 h by different venom doses administrated intraperitoneally in mice. The IC50 value was 0.43 ± 0.18 μg/ml after 48 h treatment while the calculated value was 0.73 ± 0.10 μg/ml for the culture media totally refreshed after 2 h treatment with venom. Wistar rats were treated intraperitoneally with A. absinthium extract, 30 min before venom or carrageenan was injected subplantarly into the left hind paw. Intraperitoneal administration of 25 and 50 mg/kg extract was inhibited venom induced paw swelling at 0.5, 1, 2 and 3 h (p < 0.05) while 12.5, 25 and 50 mg/kg extract treatment was inhibited carrageenan-induced paw swelling at 2, 3, 4 and 5 h (p < 0.05). In conclusion, the in vivo toxicity and inflammatory actions and in vitro cytotoxic actions of crude M. xanthina venom were performed as a first report and inhibition of venom-induced inflammation by methanolic extract of A. absinthium was described.

Screening for resistance of Turkish olive cultivars and clonal rootstocks to Verticillium wilt

Verticillium wilt resistance of 77 olive cultivars including 71 domestic and six foreign ones, and four clonal rootstocks available in the olive gene bank, were tested using a highly virulent isolate (D pathotype) of Verticillium dahliae. The pathogen was stem-inoculated into the own-rooted saplings. Most cultivars and rootstocks were found to be extremely susceptible to the disease. ‘Sinop No. 1’, ‘Eğriburun Nizip’, ‘Erkence’, ‘Eğriburun Tatayn’, ‘Girit Zeytini’ and ‘Marantelli’ were highly resistant, as their disease severities did not exceed 10%. Additionally, 11 domestic cultivars (‘Sarı Habeşi’, ‘Yağlık Çelebi’, ‘Zoncuk’, ‘Dilmit’, ‘Şam’, ‘Hurma Karaca’, ‘Erdek Yağlık’, ‘Melkabazı’, ‘Yün Çelebi’, ‘Kan Çelebi’ and ‘Siyah Salamuralık’), two foreign cultivars (‘Arbequina’ and ‘Frantoio’) and one wild clonal rootstock (‘D36’) were found to be resistant, with disease severities less than 30%. On the other hand, the moderately susceptible group comprised ten domestic cultivars (‘Ak Zeytin’, ‘Yağ Çelebi’, ‘Saurani’, ‘Butko’, ‘Gemlik’, ‘Otur’, ‘Yağ Zeytini’, ‘Belluti’, ‘Sinop No. 2’ and ‘Samanlı’), three foreign cultivars (‘Leccino’, ‘Chemlali’ and ‘Ascolana’) and one wild clonal rootstock (‘D9’). The number of cultivars within highly resistant and resistant groups was 17 out of the 71 domestic cultivars from all regions (four from Aegean, seven from southeastern Anatolia, two from Black Sea and three from Marmara).

Taxonomic notes on the snakes of Northern Cyprus, with observations on their morphologies and ecologies

A total of 66 specimens belonging to eleven snake species, some of which were collected during the fi eld studies of 17-31 July and 3-25 September 2003, and some others which have been previously collected and all have been deposited into the collection of ZDEU (Zoology Dept. Ege University), were evaluated taxonomically. 25 of the specimens belonged to Typhlopidae, 37 to Colubridae, three to Viperidae and one to Boidae. Th ese specimens were evaluated from the points of view of pholidosis, pattern and coloration and morphological measurements. Some biological and ecological information were also given with the brief geological history of eastern Mediterranean region.

Vegetative compatibility groups ofVerticillium dahliae from cotton in the southeastern anatolia region of Turkey

Eighty isolates ofVerticillium dahliae from the southeastern Anatolia region and 20 isolates from the east Mediterranean region from wilted cotton plants were used for vegetative compatibility analysis employing nitrate non-utilizing mutants and reference tester strains of vegetative compatibility groups (VCGs) 1A, 2A, 2B, 3, 4A and 4B. Of the 100V. dahliae isolates, 49 were assigned to VCG1A, 39 to VCG2B, nine to VCG2A and three to VCG4B. Pathogenicity assays were conducted on susceptible cotton cv. Çukurova 1518 in the greenhouse. All VCG1A isolates induced defoliation and all VCG2B isolates caused partial defoliation symptoms. Isolates of VCG2A and VCG4B caused typical symptoms of leaf chlorosis without defoliation. This is the first report on VCGs ofV. dahliae in the southeastern Anatolia region of Turkey, which demonstrates that VCG1A of the cotton-defoliating type and VCG2B of the partially defoliating type are prevalent in this region.

Combined venom profiling and cytotoxicity screening of the Radde's mountain viper (Montivipera raddei) and Mount Bulgar Viper (Montivipera bulgardaghica) with potent cytotoxicity against human A549 lung carcinoma cells

&NA; Here we report the first characterization of the endemic Mount Bulgar Viper (Montivipera bulgardaghica) and Raddes mountain viper (Montivipera raddei) venom by a combined approach using intact mass profiling and bottom‐up proteomics. The cytotoxicity screening of crude venom as well as isolated serine proteases revealed a high activity against A549 human lung carcinoma cells. By means of intact mass profiling of native and reduced venom we observed basic and acidic phospholipases type A2. Moreover, the analysis revealed snake venom metalloproteases, cysteine‐rich secretory proteins, disintegrins, snake venom serine proteases, C‐type lectins, a vascular endothelial growth factor and an L‐amino acid oxidase. Graphical abstract Figure. No caption available. HighlightsVenom characterization of Montivipera bulgardaghica and Montivipera raddei.Combined approach by using intact mass profiling and bottom‐up proteomics.Bottom‐up venomics showed the existence of several snake venom families.Intact mass profiling identified acidic and basic phospholipases A2.Cytotoxicity screening revealed a high activity against A549 lung carcinoma cells.

On the occurrence of Blanus strauchi aporus Werner, 1898 and Chalcides guentheri Boulenger, 1887 (Reptilia) in the Mediterranean ecozone of Syria

Abstract The amphisbaenian Blanus strauchi aporus has been rediscovered in Matn Abu Rayya, Tartous, with a voucher specimen, after approximately 125 years. The distribution area of Günther’s Skink Chalcides guentheri, recorded from Syria for the third time, is extended some 140 km to the north-east (Al Wardiyat, Hims) of its previous northernmost locality of Mazbud (Saida), Lebanon.

New locality records for four rare species of vipers (Reptilia: Viperidae) in Turkey

We report new localities and range extensions for four vipers from Turkey. The distribution of Montivipera wagneri is extended substantially southwards into Muş province, showing that this species is not endemic to the Aras valley as previously stated in the literature. Similarly, an unverified photograph of Montivipera albizona from Erzincan province, at its currently known eastern limit, was confirmed with new material, and its range is extended substantially southwards to the Anamos (Nur) Mountains in Hatay province. Smaller range extensions are reported for Vipera ammodytes transcaucasiana and V. darevskii.

Serological characterization and confirmation of the taxonomic status of Montivipera albizona (Serpentes, Viperidae) with an additional new locality record and some phylogenetical comments

Th is is the fi rst record of the presence of Montivipera albizona (Nilson, Andren & Flardh 1990), in Kahramanmaras province, Mediterranean Region of Turkey. Here, one young male specimen was collected and is described. Th e present record of M. albizona extends its known distribution (Kulmac Mountain Range, Sivas) some 250 km to the south-west, where the Anatolian Diagonal exhibits a bifurcation. Our data based on the electropheoretic analysis of blood-sera, indicate that the M. xanthina populations from the western Anatolia and M. albizona distributed along the Anatolian Diagonal show signifi cant diff erences, qualitatively and quantitatively. Accordingly, it is concluded that M. albizona should not be included within the polymorphic species M. xanthina which lives in western Anatolia and therefore, it should be accepted as a valid species. Moreover, the actual distributions of the related taxa in Anatolia and the geographic structure of the Anatolian Diagonal were discussed.