The whitefly Bemisia tabaci (Gennadius) (Hemiptera: Aleyrodidae) is a cryptic species complex that contains some of the most damaging pests in tropical and subtropical regions. Recent studies suggested that this complex is composed of at least 24 distinct species. We use the approach from these studies to consider the identity of B. tabaci in Argentina. Previous studies have suggested the presence of a B. tabaci presumably indigenous to the Americas and referred to as the BR biotype in Argentina. We placed the entity referred to as the BR biotype within the B. tabaci cryptic species complex using whiteflies collected in soybean and bean crops in northern and central Argentina. The whiteflies were assigned using the mitochondrial cytochrome oxidase (mtCOI) gene. Four unknown haplotypes plus two Argentina sequences from GenBank formed a cluster that was basal to the rest of the New World sequences. These sequences diverged from the consensus sequence across the range of 3.6 to 4.3%. Applying the species assignment rules of recent studies suggests that the individuals from Argentina form a separate species. A fifth unknown haplotype fell within the New World putative species and formed a distinct cluster with haplotypes from Panama. These results suggest that Argentina has two indigenous species belonging to the B. tabaci cryptic species complex. Rather than using mtCOI sequencing for all B. tabaci collected, a simple random amplified polymorphic DNA-polymerase chain reaction diagnostic was used and tested along with previously published primers designed to work specifically with the BR biotype from Brazil. These primers were either unable to distinguish between the two indigenous members of the complex in Argentina or indicated a difference when none was evident on the basis of mtCOI sequence comparison.
The whitefly, Bemisia tabaci (Gennadius), is a cryptic species complex that attacks >600 different species of plants and transmits several plant viruses causing severe economic losses. Until 2010, the B. tabaci complex comprised 24 distinct putative species. Recently, at least 15 new species have been reported. The objective of this study was to identify B. tabaci species present in bean, melon, and tomato crops in Argentina by applying phylogenetic analyses and pairwise comparison of genetic distances of mitochondrial cytochrome c oxidase subunit I (mtCOI) sequences. The 39 proposed whitefly species were identified with both analyses, and the presence in Argentina of one indigenous species, New World 2 (NW2), and two introduced species, Middle East-Asia Minor one (MEAM1) and Mediterranean, was confirmed. Common bean crop presented the three whitefly species detected, with NW2, MEAM1, and Mediterranean being present all together under field conditions. Also, Mediterranean was the only species identified in tomato, whereas MEAM1 was found in melon. To the best of our knowledge, Mediterranean is a recent invasive species in open-field agriculture in the American continent and in greenhouse tomato in Argentina. Additionally, we provide the first report of MEAM1 in common bean and melon. These findings raise several questions on the future scenario of B. tabaci and the viruses it transmits in Argentina.
Delphacodes kuscheli Fennah (Hemiptera: Delphacidae) is the main natural vector of Mal de Rio Cuarto virus (family Reoviridae, genus Fijivirus, MRCV), which infects different gramineae and causes the most important maize (Zea mays L.) disease in Argentina. MRCV—vector interactions usually are studied using different winter cereals as hosts. Under experimental conditions, <50% of D. kuscheli planthoppers fed on a MRCV-infected plant can transmit the virus to wheat (Triticum aestivum L. ). This fact is influenced by insect development stage at acquisition and the latency period. This work describes the relation between transmission efficiency and MRCV accumulation in its planthopper vector. First- and third-instar D. kuscheli nymphs were allowed to feed on MRCV-infected plants, and 9 or 17 d after the acquisition access period (AAP), viral load of transmitting and nontransmitting planthoppers was quantified by quantitative polymerase chain reaction. The transmitting planthoppers showed significantly higher viral titers than nontransmitting ones, suggesting that successful transmission is positively associated to viral accumulation in the insect. However, planthoppers of the third-instars group did not transmit the virus 9 d after AAP, even when 46% had similar titers to the transmitting insects of the other treatments. These results indicate that additional factors influence MRCV transmission efficiency when acquisition occurs in older planthoppers. This is the first precise quantitative analysis of MRCV in its main vector species and will definitely contribute to better understand planthopper—Fijivirus interactions and its epidemiological implications.
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