AMILCAR Arenal

Dr. AMILCAR Arenal


Research Focus & Metrics

Academic Career Length

3Years (2024-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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20 August 2024 in Insects
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DMDIEGO MASAQUIZA
DIEGO MASAQUIZA
LRLino Curbelo Rodríguez
Lino Curbelo Rodríguez
JZJosé Zapata
José Zapata
JMJoffre Stalin Monar
Joffre Stalin Monar
MVMaritza Lucia Vaca-Cárdenas
Maritza Lucia Vaca-Cárdenas
AAAMILCAR Arenal
AMILCAR Arenal
Seventy-five samples were collected from 15 beehives in the central highlands of Ecuador (Tungurahua–Chimborazo) to assess Africanization in managed bee populations using wing geometric morphometric and mitochondrial DNA analyses. The results indicated that when grouping the apiaries based on altitudinal floors into 2600–2800, 2801–3000, and 3001–3274 m above sea level, differences (p < 0.001) were observed. The morphotypes were similar in the first two floors, but the third indicated that altitude plays a crucial role in the differentiation of populations. When comparing with the pure subspecies, we found differences (p < 0.001); the nearest Mahalanobis distance was for Apis mellifera scutellata (D2 = 3.51), with 95.8% Africanization via father in the area. The maternal origin of all patterns belonged to lineage A (A. m. scutellata), with seven haplotypes. The most frequent haplotypes were A26 and A1; however, the A1q haplotype was not detected at the national level or in nearby countries. The identified haplotypes do not coincide with A4, which is predominant in South Africa and Brazil. The results indicate a double origin due to their presence in North Africa and the Iberian Peninsula. The formation of specific morphological groups within ecoregions is suggested.

28 February 2025 in Microbiology Research
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RGReinaldo González
Reinaldo González
HCHéctor Cabrera
Héctor Cabrera
YNYufeng Niu
Yufeng Niu
ARAlessandra Roncarati
Alessandra Roncarati
ATAdrian Toledo
Adrian Toledo
AAAMILCAR Arenal
AMILCAR Arenal
This study aimed to isolate AHL-degrading bacteria from the intestine of Penaeus vannamei and evaluate their ability to control pathogenic Vibrio harveyi in P. vannamei larvae. Twenty-seven isolates were obtained from the digestive tract of healthy Pacific white shrimp juveniles (P. vannamei) after six cycles of pasteurization at 70 °C, but only three isolates (E1LP2, E2LP1, and E2LP2) could degrade AHL. The 16S sequence results gave a high identity (>95%) with Bacillus sp. The isolates exhibited quorum-quenching abilities by degrading AHLs, thereby disrupting Vibrio quorum sensing and virulence. In Zoea and Mysis, the challenged larvae plus the administration of E1LP2 resulted in the lowest survival compared to the other groups. Isolates degrading N-acyl homoserine lactone improved the survival of shrimp Zoea and Mysis larvae when challenged with pathogenic V. harveyi. This is the first report on the use of quorum-sensing disrupter bacteria in P. vannamei larval shrimp culture. Our findings suggest that these Bacillus spp. strains have potential as biocontrol agents for sustainable shrimp aquaculture, reducing the reliance on antibiotics while mitigating vibriosis outbreaks.