Matrilineage differentiation of the genus Tetragonisca using mitochondrial DNA markers and the polymerase chain reaction-restriction fragment length polymorphism technique

被引:3
|
作者
Santos, S. A. [1 ]
Bronzato, A. R. [1 ]
Moreira, B. M. T. [1 ]
Araujo, K. F. [1 ]
Ronqui, L. [2 ]
Mangolin, C. A. [1 ]
Toledo, V. A. A. [2 ]
Ruvolo-Takasusuki, M. C. C. [1 ]
机构
[1] Univ Estadual Maringa, Dept Biotecnol Genet & Biol Celular, Maringa, Parana, Brazil
[2] Univ Estadual Maringa, Dept Zootecnia, Maringa, Parana, Brazil
关键词
Stingless bee; Heterologous primer; PCR-RFLP; Bayesian analysis; ANGUSTULA HYMENOPTERA; APIDAE; MELIPONINAE; INDIVIDUALS; LATREILLE; NUMBER;
D O I
10.4238/2015.October.21.2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Meliponinae are important pollinators of plant species, and one of the most managed species is Tetragonisca angustula. Initially, two subspecies were identified in T. angustula: T. angustula angustula and T. angustula fiebrigi. Subsequently, T. a. fiebrigi was considered a species, based on the coloration of its mesepisternum. The objective of the present study was to obtain genetic markers that could differentiate the two species by amplifying regions of mitochondrial DNA and conducting polymerase chain reaction-restriction fragment length polymorphism analysis. Worker bees were collected in three Brazilian states: Parana (Maringa, Altonia, and Foz do Iguacu), Sao Paulo (Dracena, Sao Carlos, and Santa Cruz do Rio Pardo), and Rondonia (Ariquemes). Ten pairs of insect heterologous primers were tested and four were used (primer pair 1, ND2 and COI; primer pair 2, COI; primer pair 8, 16S and 12S; and primer pair 9, COII). For the restriction analysis, 13 enzymes were tested: EcoRI, EcoRV, HindIII, HinfI, RsaI, PstI, XbaI, HaeIII, ClaI, XhoI, BglII, PvuII, and ScaI. Markers were obtained (primer pair 8 cleaved with EcoRV and XbaI and primer pair 9 cleaved with HaeIII, RsaI, and XbaI) that enabled matrilineage identification in the nests studied, which confirmed that hybridization could occur between both Tetragonisca species. The beginning of speciation was probably recent, and secondary contact has resulted in crosses between T. angustula females and T. fiebrigi males. Because of this hybridization, it would be appropriate to consider them as two subspecies of T. angustula.
引用
收藏
页码:12828 / 12840
页数:13
相关论文
共 50 条
  • [41] Polymerase chain reaction-restriction fragment length polymorphisms identify mtDNA haplotypes of greenbug (Hemiptera: Aphididae)
    Shufran, KA
    JOURNAL OF THE KANSAS ENTOMOLOGICAL SOCIETY, 2003, 76 (04) : 551 - 556
  • [42] Molecular Identification of Larval Stages of Otiorhynchus (Coleoptera: Curculionidae) Species Based on Polymerase Chain Reaction-Restriction Fragment Length Polymorphism Analysis
    Hirsch, Jacqueline
    Sprick, Peter
    Reineke, Annette
    JOURNAL OF ECONOMIC ENTOMOLOGY, 2010, 103 (03) : 898 - 907
  • [43] Species identification in seven small millet species using polymerase chain reaction-restriction fragment length polymorphism of trnS-psbC gene region
    Parani, M
    Rajesh, K
    Lakshmi, M
    Parducci, L
    Szmidt, AE
    Parida, A
    GENOME, 2001, 44 (03) : 495 - 499
  • [44] Utility of MtCOI polymerase chain reaction-restriction fragment length polymorphism in differentiating between Q and B whitefly Bemisia tabaci biotypes
    Ma, Wei-Hua
    Li, Xian-Chun
    Dennehy, Timothy J.
    Lei, Chao-Liang
    Wang, Mo
    Degain, Benjamin A.
    Nichols, Robert L.
    INSECT SCIENCE, 2009, 16 (02) : 107 - 114
  • [45] Comparison of DNA Profiling between Fishes and Pork Meat using Polymerase Chain Reaction-Restriction Fragment Length Polymorphisms (PCR-RFLP) Analysis
    Shahimi, Safiyyah
    Abd Mutalib, Sahilah
    Nazri, Wan Sakeenah Wan
    Abdullah, Aminah
    Sani, Norrakiah Abdullah
    SAINS MALAYSIANA, 2018, 47 (07): : 1535 - 1540
  • [46] Molecular identification of Candida species isolated from cases of neonatal candidemia using polymerase chain reaction-restriction fragment length polymorphism in a tertiary care hospital
    Fatima, Akeela
    Bashir, Gulnaz
    Wani, Tehmeena
    Jan, Abiroo
    Kohli, Amrish
    Khan, Mosin S.
    INDIAN JOURNAL OF PATHOLOGY AND MICROBIOLOGY, 2017, 60 (01) : 61 - 65
  • [47] Identification of Zoonotic Balantioides coli in Pigs by Polymerase Chain Reaction-Restriction Fragment Length Polymorphism (PCR-RFLP) and Its Distribution in Korea
    Byun, Jae-Won
    Park, Jung-Hyun
    Moon, Bo-Youn
    Lee, Kichan
    Lee, Wan-Kyu
    Kwak, Dongmi
    Lee, Seung-Hun
    ANIMALS, 2021, 11 (09):
  • [48] Molecular Authentication of 21 Korean Artemisia Species (Compositae) by Polymerase Chain Reaction-Restriction Fragment Length Polymorphism Based on trnL-F Region of Chloroplast DNA
    Lee, Jeong Hoon
    Lee, Jei Wan
    Sung, Jung Sook
    Bang, Kyong Hwan
    Moon, Sung Gi
    BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2009, 32 (11) : 1912 - 1916
  • [49] Evaluation of different DNA extraction methods for the detection of adulteration in raw and processed meat through polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP)
    Muhammed, M. Ali
    Bindu, B. Sri Charan
    Jini, R.
    Prashanth, K. V. Harish
    Bhaskar, N.
    JOURNAL OF FOOD SCIENCE AND TECHNOLOGY-MYSORE, 2015, 52 (01): : 514 - 520
  • [50] Identification of raw and heat-processed meats from game bird species by polymerase chain reaction-restriction fragment length polymorphism of the mitochondrial D-loop region
    Rojas, M.
    Gonzalez, I.
    Fajardo, V.
    Martin, I.
    Hernandez, P. E.
    Garcia, T.
    Martin, R.
    POULTRY SCIENCE, 2009, 88 (03) : 669 - 679