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23 January 2020 First Report of Bemisia tabaci Mediterranean (Biotype Q) (Hemiptera: Aleyrodidae) in the Dominican Republic
Colmar Serra, Cindy L. McKenzie, Weiqi Luo, Lance S. Osborne
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Abstract

MED was detected for the first time in the Dominican Republic from 2 provinces (Santo Domingo and Santiago), 2 host plants (tomato and tobacco), and 2 environments (greenhouse and open field). All MED sequences were identical and determined to be of Eastern Mediterranean origin. MEAM1 was the predominant B. tabaci cryptic species present, and was detected in all but 1 sample, which was 100% MED. NW was detected twice on eggplant in different geographical regions, and once on Mexican prickly poppy in a native habitat, but always with MEAM1.

Bemisia tabaci (Gennadius) (Hemiptera: Aleyrodidae) is a large cryptic species complex of whitefly whose members are particularly invasive pests of hundreds of economically important commodities worldwide including cotton, vegetables, and ornamental crops. The first reports of B. tabaci in the Dominican Republic date back to 1975 when the New World (NW) member of the complex (biotype A) caused severe damage in beans in the southwestern provinces of San Juan and Barahona, primarily due to transmission of bean golden mosaic virus (Abreu 1978; Alvarez & Abud 1995; Serra et al. 2003). Beginning in 1988, severe attacks of B. tabaci emerged principally on tomatoes, but also on other vegetable crops including beans, cucurbits, eggplants, and okra. Extremely high whitefly populations on tomatoes covered plants with honeydew excrement, resulting in colonization of sooty-mold producing saprophytic fungi (Capnodium spp.; Capnodiaceae) leading to plant decline, reduced yields (5 and 25% in the Northwest and Southwest, respectively), and fruit with tomato irregular ripening disorder (Serra 1992; Alvarez & Abud 1995; Serra et al. 2003). Symptoms of the plant physiological disorder do not occur on tomato foliage where whitefly feed, but appear as an uneven tomato fruit color development during ripening, and are exclusively associated with B. tabaci Middle Eastern Asia Minor 1 (MEAM1 or biotype B) feeding (McKenzie & Albano 2009). Attempts to manage the whitefly with intensive chemical control caused severe pest resurgence (Serra 1992). An IPM approach centered on neem (Azadirachta indica A. Juss.; Meliaceae) extracts including oils and rotations with other selective insecticides based on population levels and action thresholds were successful due in part to preserving biological control agents that consisted primarily of mirid bugs (mainly Nesidiocoris tenuis [Reuter]; Hemiptera: Miridae), and other predators (e.g., syrphids and coccinellids), and aphelinid parasitoids (Encarsia and Eretmocerus spp.; Hymenoptera: Aphelinidae) (Serra 1992; Alvarez & Abud 1995; Evans & Serra 2002). Shortly after physiological disorders appeared in the Dominican Republic, a devastating new tomato virus was identified as tomato yellow leaf curl virus – Israel strain in 1991, and was the first report in the Western hemisphere (Nakhla et al. 1994; Polston et al. 1994). Within 3 yr, yield losses were reported as high as 50% in the northwestern Valverde and Montecristi provinces and about 90% in the southwestern Azua plain, both major tomato-growing areas (Alvarez & Abud 1995). Consequently, the management of whiteflies became very difficult due to near zero tolerance thresholds that almost paralyzed the national production of tomato concentrates. In response, host-free periods established together with the use of systemic neonicotinoid insecticides and cultural measures were part of a quite successful integrated strategy to manage the whitefly complex (Alvarez & Abud 1995; Serra 2006). In 1994, a whitefly distribution survey conducted on tomato in northwestern Dominican Republic (A. Bartlett, USDA, Phoenix, Arizona, USA, personal communication) determined NW was still omnipresent, and the dominant whitefly in all sample locations (50–75%) followed by other unknown whiteflies termed ‘X'-biotype (14–50%), and MEAM1, which was detected in only 2 locations (14–17%) (Serra et al. 1997). However, squash silverleaf disorder caused exclusively by MEAM1 feeding was found to be prevalent several yr later in cultivated or wild cucurbits in most of the monitored localities, indicating MEAM1 had spread across the country.

After several yr of management stability across B. tabaci host crops in the country, whitefly populations increased again in tomatoes, and appeared to be tolerant to insecticides. Toxicity studies conducted from 6 B. tabaci populations collected from 6 localities to 6 commercially available insecticides in 2015 at the laboratories of Centro de Tecnologías Agrícolas in Pantoja-Los Alcarrizos, Santo Domingo Province, and the Pontificia Universidad Católica Madre y Maestra, Santo Domingo, Distrito Nacional. Results confirmed some populations exhibited very high levels of resistance factors (Serra et al. 2016). Bemisia tabaci Mediterranean (MED or biotype Q) is especially capable of developing resistance (Nauen et al. 2002; Horowitz et al. 2004, 2005; Nauen & Denholm 2005), and increasing problems in controlling whitefly infestations has been associated with the appearance of MED in North America (Dennehy et al. 2005; McKenzie et al. 2009, 2012, 2014; McKenzie & Osborne 2017). The primary objective of this whitefly survey was to determine the distribution and composition of B. tabaci cryptic species populations in the Dominican Republic.

Adult whiteflies collected were immediately placed in 95% ethanol for molecular analysis. All adult whiteflies submitted from each sample were used for species determination following the protocol developed by Shatters et al. (2009). DNA was extracted from individual whiteflies by placing a single whitefly in a 1.5 mL Eppendorf tube, adding 50 µL of DNA lysis buffer, and grinding with a pestle. The pestle was rinsed with an additional 50 µL of DNA lysis buffer and collected in the same tube. Tubes were placed in a metal boiling rack, and boiled at 95 °C for 5 min, then placed directly in ice for 5 min. Tubes were then centrifuged at 8,000 g for 30 s, and the supernatant (crude DNA lysate) was transferred to another tube and stored at –80 °C for future processing.

Polymerase chain reaction (PCR) amplifications for the mtCOI gene were performed using the Btab-Uni primer set described by Shatters et al. (2009) for all whitefly samples to obtain sequences for submission to GENBANK. In the rare instances those primers were not successful, exotic whitefly primers under the conditions described by Dickey et al. (2015) were used to identify whiteflies that were not B. tabaci. Mitochondrial COI sequence analysis was performed first by PCR amplification of an approximately 600 to 800 bp mtCOI DNA fragment, then sequencing the PCR amplified DNA. The 30 µL PCR reactions were run using a BIO-RAD T100 Thermal Cycler (BIO-RAD Laboratories, Inc., Hercules, California, USA) under the conditions described by Shatters et al. (2009). Prior to