Longistatin, a novel EF-hand protein from the ixodid tick Haemaphysalis longicornis, is required for acquisition of host blood-meals

2010 ◽  
Vol 40 (6) ◽  
pp. 721-729 ◽  
Author(s):  
Anisuzzaman ◽  
M. Khyrul Islam ◽  
Takeharu Miyoshi ◽  
M. Abdul Alim ◽  
Takeshi Hatta ◽  
...  
2007 ◽  
Vol 37 (3-4) ◽  
pp. 383-392 ◽  
Author(s):  
Xiaohong Huang ◽  
Naotoshi Tsuji ◽  
Takeharu Miyoshi ◽  
Maki Motobu ◽  
M. Khyrul Islam ◽  
...  

2021 ◽  
Author(s):  
Si-Si Li ◽  
Xiao-Yu Zhang ◽  
Xue-Jiao Zhou ◽  
Kai-Li Chen ◽  
Abolfazl Masoudi ◽  
...  

Abstract Exploring the bacterial microbiota is imperative to tick control since it has an important role in tick physiology and vector capacity. The life cycle of ticks consists of parasitic and non-parasitic stages, with a diversity of habitats and host blood meals. Whether and how these factors, such as tick developmental stages, tick organs, habitats and host blood meals affect tick bacterial microbiota is poorly elucidated. In the present study, we investigated the bacterial microbiotas of hard tick Haemaphysalis longicornis, their blood meals and habitats using 16S rRNA high-throughput sequencing. The bacterial richness and diversity in ticks varied depending on the tick developmental stage, feeding status and the tick organs. Results showed that fed ticks present a higher bacterial richness suggesting that ticks may acquire bacteria from blood meals. The significant overlap of the bacteriota of fed ticks and the host blood also support this possibility. Another possibility is that blood meals can stimulate the proliferation of certain bacteria. However, most shared bacteria cannot transmit throughout the tick life cycle, as they were not present in tick eggs. The most shared bacteria between ticks and habitats are genus of Staphylococcus, Pseudomonus, Enterobacter, Acinetobacer and Stenotrophomonas, some of them are also present in tick organ, suggesting that these environmental bacteria cannot be completely washed away and can be acquired by ticks. As tick reproductive organ, ovary showed the lowest bacterial richness and diversity compared to other organs. The predominant proportion of Coxiella in fed females and ovary further demonstrated that this genus is required for H. longicornis reproduction system. These findings further reveal that the bacterial composition of ticks is influenced by a variety of factors and will help in subsequent studies of the function of these bacteria.


2010 ◽  
Vol 59 (2) ◽  
pp. 286-289 ◽  
Author(s):  
Takeshi Hatta ◽  
Naotoshi Tsuji ◽  
Takeharu Miyoshi ◽  
M. Khyrul Islam ◽  
M. Abdul Alim ◽  
...  

2003 ◽  
Vol 115 (4) ◽  
pp. 355-363 ◽  
Author(s):  
Mie Nakajima ◽  
Michi Kodama ◽  
Haruko Yanase ◽  
Toshihiko Iwanaga ◽  
Albert Mulenga ◽  
...  

2008 ◽  
Vol 86 (4) ◽  
pp. 331-344 ◽  
Author(s):  
Damdinsuren Boldbaatar ◽  
Badgar Battsetseg ◽  
Tomohide Matsuo ◽  
Takeshi Hatta ◽  
Rika Umemiya-Shirafuji ◽  
...  

A cDNA encoding the vitellogenin receptor of the ixodid tick, Haemaphysalis longicornis Neumann (HlVgR) was cloned and characterized. The full-length cDNA is 5631 bp, including an intact ORF encoding an expected protein with 1782 amino acids. The deduced amino acid sequence of the HlVgR cDNA revealed two ligand-binding domains with four class A cysteine-rich repeats in the first domain and eight in the second domain similar to those of insect VgRs. The immunoblot analysis detected ~197 kDa protein in both tick ovary and egg. The developmental expression profile demonstrated that HlVgR mRNA exists throughout the ovarian development, and the transcriptional level is especially high in the previtellogenic period. Immuno electron microscopy analysis demonstrated that the localization of HlVgR is detected on the external surface of oocyte plasma membrane. RNAi showed that eggs of HlVgR dsRNA-injected adult ticks had not developed into fully mature oocytes and laid abnormal eggs. The Babesia parasite DNA was not detected in the eggs of HlVgR dsRNA-injected tick that fed on Babesia gibsoni infected dog, whereas it was detected in the eggs of PBS-injected ticks and noninjected ticks. Expression of HlVgR was increased by the vitellogenic hormone 20-hydroxyecdysone. These results indicate that HlVgR, which is produced by the developing oocytes, is essential for Vg uptake, egg development in the H. longicornis tick, and transovarial transmission of Babesia parasites.


2019 ◽  
Author(s):  
John B Keven ◽  
Georgia Artzberger ◽  
Mary L. Gillies ◽  
Rex B. Mbewe ◽  
Edward D. Walker

Abstract Background: Determination of bloodmeal hosts in blood-fed female Anopheles mosquitoes is important for evaluating vectorial capacity of vector populations and assessing effectiveness of vector control measures. Sensitive molecular methods are needed to detect traces of host blood in mosquito samples, to differentiate hosts, and to detect mixed host blood meals. This paper describes a molecular probe-based quantitative PCR for identifying bloodmeal hosts in Anopheles malaria vectors from Papua New Guinea.Methods: TaqMan oligonucleotide probes targeting specific regions of mitochondrial or nuclear DNA of the three primary Anopheles bloodmeal hosts – humans, pigs and dogs – were incorporated into a multiplex, quantitative PCR which was optimized for sensitivity and specificity.Results: Amplification of serially diluted DNA showed that the quantitative PCR detected as low as 10-5 ng/μl of host DNA. Application to field-collected, blood-fed Anopheles showed that the quantitative PCR identified the vertebrate hosts for 335/375 (89%) of mosquitoes whereas only 104/188 (55%) of bloodmeal samples tested in a conventional PCR were identified. Of 188 blood-fed Anopheles that were analyzed in both PCR methods, 16 (8.5%) were identified as mixed bloodmeals by the quantitative PCR whereas only 3 (1.6%) were mixed bloodmeals by the conventional PCR.Conclusions: The multiplex quantitative PCR described here is sensitive at detecting low DNA concentration and mixed host DNA in samples and useful for bloodmeal analysis of field mosquitoes, in particular mixed-host bloodmeals.


2020 ◽  
Author(s):  
John B Keven ◽  
Georgia Artzberger ◽  
Mary L. Gillies ◽  
Rex B. Mbewe ◽  
Edward D. Walker

Abstract Background: Determination of blood-meal hosts in blood-fed female Anopheles mosquitoes is important for evaluating vectorial capacity of vector populations and assessing effectiveness of vector control measures. Sensitive molecular methods are needed to detect traces of host blood in mosquito samples, to differentiate hosts, and to detect mixed host blood meals. This paper describes a molecular probe-based quantitative PCR for identifying blood-meal hosts in Anopheles malaria vectors from Papua New Guinea. Methods: TaqMan oligonucleotide probes targeting specific regions of mitochondrial or nuclear DNA of the three primary Anopheles blood-meal hosts, humans, pigs and dogs, were incorporated into a multiplex, quantitative PCR which was optimized for sensitivity and specificity. Results: Amplification of serially diluted DNA showed that the quantitative PCR detected as low as 10-5 ng/ml of host DNA. Application to field-collected, blood-fed Anopheles showed that the quantitative PCR identified the vertebrate hosts for 89% (335/375) of mosquitoes whereas only 55% (104/188) of blood-meal samples tested in a conventional PCR were identified. Of the 104 blood-fed Anopheles that were positive in both PCR methods, 16 (15.4%) were identified as mixed blood meals by the quantitative PCR whereas only 3 (2.9%) were mixed blood meals by the conventional PCR. Conclusions: The multiplex quantitative PCR described here is sensitive at detecting low DNA concentration and mixed host DNA in samples and useful for blood-meal analysis of field mosquitoes, in particular mixed-host blood meals.


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