Molecular species identification, host preference and detection of myxoma virus in the Anopheles maculipennis complex (Diptera: Culicidae) in southern England, UK

被引:32
作者
Brugman, Victor A. [1 ,2 ,3 ]
Hernandez-Triana, Luis M. [3 ]
Prosser, Sean W. J. [4 ]
Weland, Chris [5 ]
Westcott, David G. [3 ]
Fooks, Anthony R. [3 ,6 ]
Johnson, Nicholas [3 ]
机构
[1] Pirbright Inst, Vector Borne Viral Dis Programme, Woking GU24 0NF, Surrey, England
[2] Univ London London Sch Hyg & Trop Med, Dept Dis Control, London WC1E 7HT, England
[3] Anim & Plant Hlth Agcy, Addlestone KT15 3NB, Surrey, England
[4] Univ Guelph, Biodivers Inst Ontario, Guelph, ON N1G 2W1, Canada
[5] Univ Guelph, Sch Environm Sci, Guelph, ON N1G 2W1, Canada
[6] Univ Liverpool, Dept Clin Infect Microbiol & Immunol, Liverpool L69 7BE, Merseyside, England
关键词
Mosquito; Anopheles; Blood-meal; Host preference; DNA barcoding; Myxoma virus; BRITISH MOSQUITOES; GREAT-BRITAIN; DNA; POPULATIONS; VECTORS; MALARIA; DISEASE; RABBITS; SPREAD;
D O I
10.1186/s13071-015-1034-8
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Background: Determining the host feeding patterns of mosquitoes by identifying the origin of their blood-meals is an important part of understanding the role of vector species in current and future disease transmission cycles. Collecting large numbers of blood-fed mosquitoes from the field is difficult, therefore it is important to maximise the information obtained from each specimen. This study aimed to use mosquito genome sequence to identify the species within Anopheles maculipennis sensu lato (An. maculipennis s.l.), identify the vertebrate hosts of field-caught blood-fed An. maculipennis s.l., and to test for the presence of myxoma virus (Poxviridae, genus Leporipoxvirus) in specimens found to have fed on the European rabbit (Oryctolagus cuniculus). Methods: Blood-fed An. maculipennis s.l. were collected from resting sites at Elmley Nature Reserve, Kent, between June and September 2013. Hosts that An. maculipennis s.l. had fed on were determined by a PCR-sequencing approach based on the partial amplification of the mitochondrial cytochrome C oxidase subunit I gene. Mosquitoes were then identified to species by sequencing a region of the internal transcribed spacer-2. DNA extracts from all mosquitoes identified as having fed on rabbits were subsequently screened using PCR for the presence of myxoma virus. Results: A total of 94 blood-fed Anopheles maculipennis s.l. were collected, of which 43 (46 %) provided positive blood-meal identification results. Thirty-six of these specimens were identified as Anopheles atroparvus, which had fed on rabbit (n = 33, 92 %) and cattle (n = 3, 8 %). Seven mosquitoes were identified as Anopheles messeae, which had fed on cattle (n = 6, 86 %) and dog (n = 1, 14 %). Of the 33 An. atroparvus that contained rabbit blood, nine (27 %) were positive for myxoma virus. Conclusions: Results demonstrate that a single DNA extract from a blood-fed mosquito can be successfully used for molecular identification of members of the An. maculipennis complex, blood-meal identification, and for the targeted detection of a myxoma virus. This study shows that An. atroparvus has a strong feeding preference for both healthy and myxoma-infected rabbits, providing evidence that this species may play a significant role in the transmission of myxomatosis among wild rabbit populations in the United Kingdom (UK).
引用
收藏
页数:8
相关论文
共 43 条
[1]  
ANDREWES C H, 1956, J Hyg (Lond), V54, P478
[2]  
Arago H. B., 1943, Memorias do Instituto Oswaldo Cruz, V38, P93
[3]   SPREAD OF MYXOMATOSIS IN THE FIRST OUTBREAK IN GREAT BRITAIN [J].
Armour, C. J. ;
Thompson, Harry V. .
ANNALS OF APPLIED BIOLOGY, 1955, 43 (03) :511-518
[4]   Detection of myxoma viruses encoding a defective M135R gene from clinical cases of myxomatosis; possible implications for the role of the M135R protein as a virulence factor [J].
Belsham, Graham J. ;
Polacek, Charlotta ;
Breum, Solvej O. ;
Larsen, Lars E. ;
Botner, Anette .
VIROLOGY JOURNAL, 2010, 7
[5]  
Benson DA, 2005, NUCLEIC ACIDS RES, V33, pD34, DOI [10.1093/nar/gki063, 10.1093/nar/gku1216]
[6]   Epidemiological perspectives on West Nile virus surveillance in wild birds in Great Britain [J].
Brugman, V. A. ;
Horton, D. L. ;
Phipps, L. P. ;
Johnson, N. ;
Cook, A. J. C. ;
Fooks, A. R. ;
Breed, A. C. .
EPIDEMIOLOGY AND INFECTION, 2013, 141 (06) :1134-1142
[7]   Barrier screens: a method to sample blood-fed and host-seeking exophilic mosquitoes [J].
Burkot, Thomas R. ;
Russell, Tanya L. ;
Reimer, Lisa J. ;
Bugoro, Hugo ;
Beebe, Nigel W. ;
Cooper, Robert D. ;
Sukawati, Supraman ;
Collins, Frank H. ;
Lobo, Neil F. .
MALARIA JOURNAL, 2013, 12
[8]  
Cambournac F. J. C., 1994, Parassitologia (Rome), V36, P215
[9]   Blood feeding patterns of mosquitoes: random or structured? [J].
Chaves, Luis F. ;
Harrington, Laura C. ;
Keogh, Carolyn L. ;
Nguyen, Andy M. ;
Kitron, Uriel D. .
FRONTIERS IN ZOOLOGY, 2010, 7
[10]   A review of the use of ribosomal DNA (rDNA) to differentiate among cryptic Anopheles species [J].
Collins, FH ;
Paskewitz, SM .
INSECT MOLECULAR BIOLOGY, 1996, 5 (01) :1-9