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CARIOS CAPENSIS (ACARI: ARGASIDAE) IN THE NESTS OF THE YELLOW-LEGGED
GULL (LARUS MICHAHELLIS) IN THE AGULI ISLAND OF RGHAIA, ALGERIA
FADHILA BAZIZNEFFAH
1,6
, TAHAR KERNIF
1,2,3,6
, ASSIA BENELJOUZI
2
, AMINA BOUTELLIS
3,4,6
,
AMIROUCHE MORSLI
5
, ZOUBIR HARRAT
2
, SALAHEDDINE DOUMANDJI
1
& IDIR BITAM
3,4,6

1
Department of Zoology, Agronomic graduate school, El Harrach, Algiers, Algeria
2
Parasite Ecology and Population Genetics, Pasteur Institute of Algiers, Algeria
3
Aix Marseille University, URMITE, UM63, CNRS 7278, IRD 198, Inserm 1095, Marseille, France
4
Faculty of Biological Sciences, University of Science and Technology Houari Boumediene, Algiers, Algeria
5
Rghaa Cynegetic centers, Algiers, Algeria
6
VALCORE laboratory. University M'hamed Bougara, Boumerdes, Algeria

ABSTRACT
During the two last years 2012 and 2013, we conducted a surveillance to identify the soft ticks species
(Acari: Argasidae) found in nests of Yellow-legged Gull (Larus michahellis), in Wetland from Rghaa (Algeria) more
specifically on the island Agueli, 1 km of the beach Rghaa. We collected 227 ticks on 31 nests. Carios capensis, soft tick
species, was identified by morphological and molecular methods using the polymerase chain reaction (PCR) targeting the
mitochondrial 16S rRNA gene. Prevalence, intensity and abundance of this ectoparasite species as well as its potential
vector role are discussed to survey the risk factors for human populations.
KEYWORDS: Carios capensis, Larus michahellis, Nests, Reghaa, Algeria
INTRODUCTION
In the Mediterranean basin, the Laridae species are numerically abundant, the Yellow-legged Gull
(Larus michahellis) experiencing strong population growth over the past forty years as well as these nests along the coasts,
particularly in the northwestern Mediterranean (Thibault et al., 1996; Oro and Martinez-Abrain, 2007). Indeed, although
non-breeding birds may travel long distances, breeding adults show more restricted movements and high breeding site
fidelity Baaloudj et al. (2012). Yellow-legged Gulls form dense colonies and reuse breeding sites year after year; they may
be exposed to a number of pathogens and arthropod vectors, such as ticks (Bosch and Figuerola, 1999; Dietrich et al.
2011). Argasid ticks are vectors of viral and bacterial agents of humans and animals. Carios capensis, a soft tick of
seabirds are known as reservoirs of pathogenic bacteria of medical importance that are found around the world Wilkinson
et al. (2014). The study by Arnal et al (2014) shows that legged Gulls in the Mediterranean basin are exposed to MEABAN
virus transmitted by soft ticks and mosquitoes, which emphasizes the need to study the spatial and temporal distribution of
the flavivirus and its potential pathogenicity for animals and humans. The objective of this study was to show the presence
of soft ticks Carios capensis in the nests of Larus michahellis in the island Aguli and evaluate the potential risk of
pathogen transmission from birds to humans.


International Journal of Botany
and Research (IJBR)
ISSN(P): 2277-4815; ISSN(E): 2319-4456
Vol. 4, Issue 3, Jun 2014, 23-30
TJPRC Pvt. Ltd.
24 Fadhila BazizNeffah, Tahar Kernif, Assia Beneljouzi, Amina Boutellis,
Amirouche Morsli, Zoubir Harrat, Salaheddine Doumandji & Idir Bitam

Impact Factor (JCC): 1.6913 Index Copernicus Value (ICV): 3.0
METHODS
Sites study
The Yellow-legged Gull frequents the swamps of Lake and Aguli Island from Rghaa. The wet zone of Rghaa
(36 47' N, 3 20' E) is a complex specific ecosystem. It is limited to the North by the Mediterranean Sea and by the
oriental part of Mitidja in the South which the first hills announced of Kabyle massive Mutin (1977). Its climate is
sub-humid to winter warm and precipitation fluctuates from year to year between 200 and 800 mm. This study was
conducted on the Aguli Island, which has an area of 29, 705 m with rare herbaceous plants growing between boulders
Ouarab et al. (2014). It is located at 1 km off Rghaa beach (Figure. 1).

Figure 1: Presentation of the Aguli Island from Rghaia Region (Algiers)

Nests Collection
This work was carried out after the bird nesting period of 2012 and 2013. The nests are recovered when the chicks
leave their nests. The Yellow-legged Gull nests are collected between the ratchets in the Aguli Island. Subsequently, the
nests are placed in individual bags to avoid loss of parasites; these bags are identified by bird species.
Conservation of Ectoparasites
The ticks were kept in 70% ethanol and sent to the WHO Collaborative Centre for Rickettsial Diseases and Other
Arthropod-borne Bacterial Diseases (Marseille, France)
Morphological Identification of Ticks
Ectoparasites were identified by their morphological characteristics using a stereomicroscope SFC-11
(MOTIC ) and an optical microscope (OPTECH ). For ticks, we used the key (Hoogstraal H (1952); Hoogstraal
H et (1956)). Pictures were made with a binocular microscope ZEISS AXIO ZOOM. V16 (URMITE, France). Finally, the
identification was confirmed by molecular biology (see next section).

Carios capensis (Acari: Argasidae) in the Nests of the Yellow-legged Gull (Larus michahellis) in the Aguli Island of Rghaia, Algeria 25

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Molecular Identification of Ticks
DNA Extraction
Ticks are rinsed with distilled water, dried on sterile filter paper, and then crushed individually in sterile
Eppendorf tubes. Thereafter, each tick was incised using a scalpel and then incubated overnight at 56C in 180 L of
Buffer G2 (30 mM Tris Cl; 30 mM EDTA; 5% Tween 20; 0.5% Triton X-100; 800 mM GuHCl) containing 20 L of
proteinase K (activity = 600 mAU/mL solution or 40 mAU/mg of protein) until lysis and then homogenized Kernif et al.,
(2012). After the pre-lysing steps, DNA extraction for 200 L of homogenization was performed using an automatic EZ1
kit (QIAGEN-BioRobot

EZ1, Tokyo, Japan), according to the manufacturers instructions
(EZ1 DNA Tissue Kit, QIAGEN

, Hilden, Germany).
Amplification by Standard Polymerase Chain Reaction (PCR) and Sequencing
DNAs were subjected to PCR by thermocycler PTC-200 Peltier model (MJ Research Inc., Watertown, Mass.)
with amplification of mitochondrial 16S rRNA gene according to Mangold et al. (1998). The PCR product was
subsequently verified by the migration of the amplicons on agarose gel 1%. The DNA sequencing reactions were
performed for all samples amplified by PCR, as described previously (Kernif et al., 2012). The Data were collected using a
capillary sequencer genetic analysis ABI Prism 3130xl (ABI PRISM, PE Applied Biosystems, USA). The sequences were
edited and assembled using Chromas Pro 1.34 (Technelysium Pty Ltd, Tewantin, Australia) software. The sequences
obtained were compared to existing sequences in the database NCBI-BLAST (basic local tool alignment mark) obtained
from the internet server (http://blast.ncbi.nlm.nih.gov/Blast.cgi).
Quantitative Real Time PCR Assay
All samples were screened by using a quantitative real-time PCR (qPCR) performed on the CFX (Applied
biosystem) incorporated primers and probes targeting a portion of the Bartonella 16S23S intergenic spacer region (ITS),
to detect DNA of Borrelia species, a real time PCR with primers and probe targeting the 16S rRNA gene was used as
previously described (Socolovschi et al. 2012), For a specific Rickettsia and Anaplasma phagocytophylum gene, we used
the previously described primer and probes (Socolovschi et al. 2012).
DATA ANALYSIS
Parasitic Indications
We calculated prevalence, abundance and the intensity of ticks found at the nests. Parasitic indications proposed
by Margolis and al. (1982).
Prevalence (P)
Prevalence is the percentage ratio of the number of infected nests (N) by parasite given by the number of nests
examined (H).
P (%) = N/H * 100
Abundance (A)
The abundance is the ratio of the total number of individuals of a species of parasite (n) on the total number of
nests examined (H).
26 Fadhila BazizNeffah, Tahar Kernif, Assia Beneljouzi, Amina Boutellis,
Amirouche Morsli, Zoubir Harrat, Salaheddine Doumandji & Idir Bitam

Impact Factor (JCC): 1.6913 Index Copernicus Value (ICV): 3.0
A = n / H
Intensity (I)
The intensity is the ratio of the total number of individuals of a species of parasite (n) on the number of infected
nests (N) I = n / N
RESULTS
During the visits to Agueli Island in June 2012, about 15 nests were recovered. At last June 2013, 16 nests were
recovered. For the both periods, we havent recovered the nests with eggs or chick and those with difficult accession.
The nests consisted mainly of plant debris recovered by Yellow-legged Gull around the marshes of the lake Rghaia and
near habitations from Rghaia beach. The birds added others debris including the feathers, bones and anything that could
be found near the nest. Among the 31 nests examined in laboratory, 18 nests were infested by the ticks including 6 of 2012
and 12 of 2013. We collected a total of 227 ticks. The abundance values of these ticks are 10.86 and 4 in 2012 and 2013
respectively. We were noted the intensity value at 27.16 and 5.33 in 2012 and 2013 respectively (table 1).
All ticks collected were morphologically identified as soft ticks Carios capensis species. Additionally, these ticks were
identified through PCR of the tick mitochondrial 16S rDNA gene. Sequence analysis showed 100% similarity to the
corresponding 16S rDNA of Carios capensis (GenBank accession no. JQ824316.1). The quantitative PCR assay showed
that all of the samples were negative for all the pathogenic tested bacteria whereas, the positive controls amplify normally.
Table 1: Prevalence, Abundance and Intensity of Carios capensis in the Nests of Larus Michahellis in the Island
Aguli
Year
Number of
Carios capensis Collected
Nests Infested by Ticks /
Total of Nests Recovered
P% Abundance Intensity
2012 163 6/15 40 10.86 27.16
2013 64 12/16 75 4 5.33
P: prevalence
DISCUSSIONS
This study has reported the first identification of Carios capensis in the nests of Larus michahellis in the island
Aguli (Reghaia, Algiers, ALGERIA). All the molecular experiments were done on the reference center for Rickettsial
Diseases and Other Arthropod-borne Bacterial Diseases (Marseille, France). The experiments were done on a place free of
soft ticks DNA and all negative controls remain negative.
As confirmed by Reeves et al (2006), our results show that Carios capensis was found in marine bird's nests of
the Gull leucophe (Larus michahellis) and it seems that it is its the only ecological nich in the marine environment.
As brought back previously, C. capensis is considered as a tick of this type of birds. On the islands of the county of
Charleston (U.S.A), C. capensis can even cause the abandonment of the nest by pelicans
(Reeves and al 2002 & Williams and al. 1999).
The role of seabirds in the ecology and epidemiology of pathogens transmitted by ticks is rarely considered, they
have a potentially important role in the maintenance and the dissemination worldwide. We know that these ticks of the
birds sea systems can harbor a variety of pathogens cited previously by Dietrich et al (2011). Such as the study of Reeves
et al (2006) where it was reported that C. capensis can convey pathogenic germs as Borrelia, Coxiella and Rickettsia.
Carios capensis (Acari: Argasidae) in the Nests of the Yellow-legged Gull (Larus michahellis) in the Aguli Island of Rghaia, Algeria 27

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Recently Duh et al (2010) have isolated a rickettsia, Rickettsia hoogstraalii from C. capensis in Georgia, in the
United States. Hutcheson et al (2005) proved experimentally that the West Nile virus can be transmitted by C. capensis.
Larvas of C. capensis can prick the man and pets during the visits of colonies (summer camps) of pelicans
Estrada-pena & Jongejan (1999). In Japan on the island of Torishima Carios capensis was collected on Albatross
Diomedea nigripes black Ushijima et al (2003), in the same country Kishimoto et al (2006) reporeted a Rickettsia detected
for the first time in seabirds transmitted by Carios capensis and C. sawaii.
Moreover, Wilkinsson et al (2014) have demonstrated that Cell lines from C. capensis will be useful on
investigating interactions between soft ticks and microorganisms Mattila et al. (2007). Then; Based on a combined
pyrosequencing approach with a conventional molecular analysis targeting the bacteria of an interest medical potential to
describe the bacterial community in two ticks of tropical seabirds, Carios capensis and Amblyomma loculosum Reeves
et al (2005) in South Carolina, United States of America have found a new agent Coxiella by PCR and sequencing the
amplicons of 64 ticks pelican Carios capensis, of Devoux Bank. Sequences of certain metabolic genes and housekeeping
genes shared 92-98 % similarity to the C. burnetii. Thus, all the visitors can be exposed to infected ticks by going on
similar islands with bird's nests.
CONCLUSIONS
During the two years of our study, we confirmed the presence of Carios capensis in the nests of Larus michahelis
with a prevalence that is higher in 2013 than in 2012. As Confirmed by the literature; C. capensis is a potential vector of
the West Nile virus and Rickettsia. Thus, further epidemiological studies with soft tiks collected from more nests and from
different countries should be performed to determine whether the invasion of pathogenic bacteria is a general phenomenon
around the Mediterranean.
REFERENCES
1. Arnal A., Gmez-Daz E., Marta Cerd-Cullar, Lecollinet S., Pearce-Duvet J., Busquets N.,
Garca-Bocanegra I., Pags N., Vittecoq M., Hammouda A., Samraoui B., Garnier R., Ramos R., Selmi S.,
Gonzlez-Sols J., Jourdain E., & Boulinier T. (2014). Circulation of a meaban-like virus in yellow-legged
gulls and seabird ticks in the Western mediterranean basin. Plos One. ; 9(3): e89601.
2. Baaloudj A, Samraoui F, Laouar A, Benoughidene M, & Hasni D.. (2012). Dispersal of yellow-legged gulls
Larus michahellis ringed in Algeria: a preliminary analysis. Ardeola 59: 137144.
3. Bosch M. & Figuerola J (1999). Detrimental effects of ticks Ornithodoros maritimuson the growth of
yellow-legged gull Larus michahellis chicks. Ardea 87: 8389.
4. Dietrich M. Gmez-Daz E.& McCoy KD (2011). Worldwide distribution and diversity of seabird ticks:
implications for the ecology and epidemiology of tick-borne pathogens. Vector-Borne Zoonotic
Dis 11: 453470.
5. Duh D, Punda-Polic V, & Avsic-Zupanc T. (2010). Rickettsia hoogstraalii sp. nov., isolated from hard- and
soft-bodied ticks. International Journal of Systematic Evolutionary Microbiology, 60, 97784.
6. Estrada-Pena A, & Jongejan F. (1999). Ticks feeding on humans: a review of records on human-biting
Ixodoidea with special reference to pathogen transmission. Experimental Applied Acarology, 23, 68571.
28 Fadhila BazizNeffah, Tahar Kernif, Assia Beneljouzi, Amina Boutellis,
Amirouche Morsli, Zoubir Harrat, Salaheddine Doumandji & Idir Bitam

Impact Factor (JCC): 1.6913 Index Copernicus Value (ICV): 3.0
7. Hoogstraal H. Notes on Egyptian ticks (Ixodoidea). I. The genus Argas (Argasidae) in the Cairo area.
Proceedings of the Egyptian Academy of Sciences. 1952;7:11427
8. Hoogstraal H. African Ixodoidea: I. Ticks of the Sudan (with special reference to Equatoria Province and
with preliminary reviews of the genera Boophilus, Margaropus, and Hyalomma). Washington (DC): US
Navy; 1956. p. 1101.
9. Hutcheson H J, Gorham C H, Machain -Williams C, Lorono-Pino M A, James A M, Marlenee NL, Winn B,
Beaty BJ& Blair CD. (2005). Experimental Transmission of West Nile Virus (Flaviviridae: Flavivirus) by
Carios capensis Ticks from North America Vector Borne and Zoonotic Diseases, 5, 293 295
10. Kernif T, Messaoudene D, Ouahioune S, Parola P, Raoult D& Bitam I. (2012). Spotted fever group
rickettsiae identified in Dermacentor marginatus and Ixodes ricinus ticks in Algeria. Ticks Tick Borne
Diseases, 3, 380-381.
11. Kishimoto T., Kurane I, Takano A., Nogami S., Fujita H., Tsurumi M., Nakamura N., Sato F., Takahashi M.,
Ushijima Y., Fukunaga M. & Watanabe H. (2006). First Detection of Rickettsia in Soft-Bodied Ticks
Associated with Seabirds, Japan. Microbiol. Immunol., 50(5), 403406.
12. Mangold A J, Bargues M D, & Mas-Coma S. (1998). Mitochondrial 16S rDNA sequences and phylogenetic
relationships of species of Rhipicephalus and other tick genera among Metastriata (Acari: Ixodidae).
Parasitology Research, 84, 478-484.
13. Margolis L, Esch GW, Holmes JC, Kuris AM, & Shad GA. (1982). The use ecological termes in parasitology
(Report of an ad hoc commitee of the American Society of Parasitologists). Journal of Parasitology, 68,
131-133.
14. Mattila J. T., Burkhardt N. Y., H. Joe Hutcheson H. J., Munderloh U. G., & Kurtti T. J. (2007). Isolation of
Cell Lines and a Rickettsial Endosymbiont from the Soft Tick Carios capensis(Acari: Argasidae:
Ornithodorinae). Journal of Medical Entomology 44(6):1091-1101.
15. Mutin L. (1977). La Mitidja, dcolonisation et espace gographique. Ed. Office Publ. Univ., Alger, 607 p.
16. Oro D & Martinez-Abrain A (2007) Deconstructing myths on large gulls and their impact on threatened
sympatric waterbirds. Anim Conserv 10: 117126.
17. Ouarab S. Talmat N. Boukhemza M. et Doumandji S. 2014. Menu trophique du goland leucophlarus
michahellis dans lot Aguli, zone humide de rghaa. European Scientific Journal. 10 (3). 96 106.
18. Reeves W, Durden L, & Wills W. (2002). New records of ticks (Acari: Argasidae, Ixodidae) from South
Carolina. Journal of Agricultural and Urban Entomology, 19, 197-204.
19. Reeves WK, Loftis AD, Priestley RA, Wills W, Sanders F, & Dasch GA.(2005). Molecular and biological
characterization of a novel Coxiella-like agent from Carios capensis. Ann N Y Acad Sci. 1063:343-5.
20. Reeves WK, Loftis AD, Sanders F, Spinks MD, Wills W, Denison A M. & Dasch GA. (2006) Borrelia,
Coxiella, and Rickettsia in Carios capensis (Acari: Argasidae) from a brown pelican (Pelecanus occidentalis)
rookery in South Carolina, USA. Experimental and Applied Acarolology, 39, 321329.
Carios capensis (Acari: Argasidae) in the Nests of the Yellow-legged Gull (Larus michahellis) in the Aguli Island of Rghaia, Algeria 29

www.tjprc.org editor@tjprc.org
21. Socolovschi C, Reynaud P, Kernif T, Raoult D, Parola P (2012) Rickettsiae of spotted fever group, Borrelia
valaisiana, and Coxiella burnetii in ticks on passerine birds and mammals from the Camargue in the south of
France. Ticks Tick Borne Dis. 2012 Dec;3 (5-6):355-60
22. Thibault J.C., Zotier R., Guyot I. & Bretagnolle V. (1996) Recent trends in breeding marine birds of the
Mediterranean region with special reference to Corsica. Colonial Water-birds, 19: 31-40.
23. Ushijima Y., Oliver Jr. J. H., Keirans J. E., Tsurumi M., Kawabata H., Watanabe H., & Fukunaga M. (2003).
Mitochondrial Sequence Variation in Carios capensis (Neumann), a Parasite of Seabirds, Collected on
Torishima Island in Japan. Journal of Parasitology: February, Vol. 89, No. 1, pp. 196-198.
24. Wilkinson DA, Dietrich M, Lebarbenchon C, Jaeger A, Le Rouzic C, Bastien M, Lagadec E, McCoy KD,
Pascalis H, Le Corre M, Dellagi K, & Tortosa P.(2007). Massive infection of seabird ticks with Coxiella
burnetii related species. Journal of Applied environmental microbiology in press.
25. Williams DC, Wills W, Durden LA, Gray EW. (1999). Ticks of South Carolina (Acari: Ixodoidea). Journal of
Vector Ecology, 24, 224 232

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