The role of wild rodents in the transmission of Trypanosoma evansi infection in an endemic area of the Canary Islands (Spain)

Trypanosoma evansi was diagnosed for the first time in camels in the Canary Islands in 1997. Several sanitary measures including treatment of infected animals were taken; however, nowadays a little area is still infected. In order to determine possible reservoirs 138 wild rodents were trapped, 64 of them in the infected farms and the remaining 74 in other areas. The captured species were Rattus rattus (24), Rattus norvegicus (69) and Mus musculus domesticus (45). Serological (CATT/T. evansi), parasitological (micro-Hematocrit Centrifugation technique and stained smears) and molecular (PCR) methods for T. evansi and T. lewisi were used as diagnostic methods. None of the examined rodents was positive for T. evansi; 18, however, showed motile trypanosomes at micro-Hematocrit Centrifugation technique and resulted positive for T. lewisi by PCR. The results would suggest that the studied rodent species would not play a relevant role in the epidemiology of T. evansi infection in Canaries.     

中新天津生态城夏季啮齿类的空间生态位

2008年夏季对中新天津生态城的啮齿动物进行调查,采用Shannon-Wiener生态位宽度指数和Pianka生态位重叠指数对啮齿动物空间生态位进行了研究。结果表明,在捕获的5种啮齿动物中,小家鼠和黑线姬鼠的空间生态位宽度指数最高,分别为0.97和0.78;褐家鼠(Bi=0.58)和黑线仓鼠(Bi=0.51)次之;大仓鼠(Bi=0.36)最低。除了黑线姬鼠与其他4种啮齿动物两两之间空间生态位重叠指数均较小(C_P<0.50)外,其他4种啮齿动物两两之间均较高(C_P>0.50)。黑线仓鼠与褐家鼠空间生态位几乎完全重叠(C_P=0.99),在10对啮齿动物中,共有7对之间的空间生态位重叠指数大于0.70。由此可见,生态城啮齿动物之间存在资源竞争,主要原因是生态城是典型的盐碱湿地,可利用资源不丰富,使得动物分布相对集中,增加种间竞争。     

Development and validation of an ELISA for the detection of leptospire-specific antibodies in rodents

An enzyme-linked immunosorbent assay (ELISA) for the detection of IgG antibodies in rodents was developed and validated with the microscopic agglutination test (MAT) and leptospiral cultures. Sonicated antigen from cultures of serovars tarassovi and pyrogenes was used. As conjugate, a combination of anti-rat and anti-hamster IgG labeled with peroxidase was used. The optimal cut-off point was determined by plotting the sensitivity and specificity for various cut-off point values by means of receiver operating characteristic (ROC) curve. Concordance between ELISA and each of the MAT titers was measured by kappa (kappa). Proportions of positive results were compared by means of McNemar's test. Total 214 rodents were trapped, but only 117 could be processed by the three techniques (culture, ELISA, MAT; 1:20, 1:40, 1:50) and used for statistical analysis. Although, MAT titers in rodents infected with the serogroup Ballum tended to be lower than those infected with the serogroup Icterohaemorrhagiae, all (20/20) were ELISA-positive and almost all (19/20) were MAT-positive.The percentage of positive results obtained by ELISA, 47.0% exceeded significantly the 40.2% obtained by MAT (1:50). Difference between ELISA and MAT (1:40) was not significant and no differences were observed between ELISA and MAT (1:20). Agreement, specificity, sensitivity and the consequent area under the ROC curve between ELISA and MAT were higher as MAT cut-off points were lowered, being optimal at 1:20. The fact that differences between ELISA and MAT were significant at 1:50, but not at 1:40 or 1:20, supports the suggestion that lower MAT titers should be considered positive in rodents. The ELISA developed to detect leptospire-specific antibodies had optimal sensitivity and specificity in relation to MAT and it is concluded that it may constitute a very useful indicator for epidemiological purposes of past or present leptospiral infection in rodents.     

The role of rodents and shrews in the transmission of Toxoplasma gondii to pigs

Inadequate rodent control is considered to play a role in Toxoplasma gondii infection of pigs. This issue was addressed in the current study by combining a 4-month rodent control campaign and a 7-month longitudinal analysis of T. gondii seroprevalence in slaughter pigs. Three organic pig farms with known rodent infestation were included in the study. On these farms, presence of T. gondii in trapped rodents was evaluated by real-time PCR. All rodent species and shrews investigated had T. gondii DNA in brain or heart tissue. Prevalence was 10.3% in Rattus norvegicus, 6.5% in Mus musculus, 14.3% in Apodemus sylvaticus and 13.6% in Crocidura russula. Initial T. gondii seroprevalence in the slaughter pigs ranged between 8% and 17% and dropped on the three farms during the rodent control campaign to 0-10%, respectively. After 4 months of rodent control, T. gondii infection was absent from pigs from two of the three farms investigated and appeared again in one of those two farms after the rodent control campaign had stopped. This study emphasizes the role of rodents and shrews in the transmission of T. gondii to pigs and the importance of rodent control towards production of T. gondii-free pig meat.     

1974～1995年三明市区家鼠组成变化及其原因分析

本文报告了１９７４～１９９５年三明市区家鼠组成的变化及其原因。１９７４～１９９５年以黄胸鼠为优势种，１９７６年至八十年代初期以黄胸鼠和褐家鼠为优势种，１９８４～１９８７年以褐家鼠为优势种，１９８７年至今以小家鼠为优势种。这种群落演变的主要原因是由于城市房屋结构的变化和大面积灭鼠等人为因素所致。     

巫溪红池坝改良草地鼠类调查报告

对重庆巫溪红池坝改良草地中鼠形动物的种类进行抽样调查、室内饲养、解剖鼠胃和洞道研究，结果显示，该改良草地中有鼠形动物2目3科4种，其对草地危害方式和为害程度均不一样。提出了改良草地中鼠害的防治措施。     

Giardia intestinalis in North Island possums, house mice and ship rats

Giardia intestinalis cysts were detected in faeces from 12.9% of 124 brushtail possums (Trichosurus vulpecula) trapped in Auckland, Hawke's Bay, the Wairarapa and Wellington; in faecal material from 61.0% of 77 ship rats (Rattus rattus) from areas of Auckland, Hawke's Bay and Wellington; and in faecal material from 25.3% of 182 house mice (Mus musculus) from the North Island. Possums and rodents in forested areas of Auckland and Wellington city water catchments were infected. The role of wild animals in maintaining and spreading Giardia in New Zealand is discussed.     

Surveys of rodent‐borne disease in Thailand with a focus on scrub typhus assessment

The epidemiology of many rodent‐borne diseases in South‐East Asia remains ill‐defined. Scrub typhus and lep‐tospirosis are common and medically significant, while other zoonotic diseases, such as spotted fever group Rickettsiae have been identified, but their overall medical significance is unknown. Rodent surveillance was conducted from June 2002 to July 2004 in 18 provinces from Thailand. Traps were set up for one to three nights. Blood and serum samples and animal tissue samples (liver, spleen, kidney and urinary bladder) were collected. Chiggermites, ticks and fleas were removed from captured rodents. A total of 4536 wild‐caught rodents from 27 species were captured over two years of animal trapping. Rattus rattus was the dominant species, followed by Rattus exulans and Bandicota indica. Almost 43 000 ectoparasites were removed from the captured animals. Approximately 98% of the ectoparasites were chigger‐mites, of which 46% belonged to the genus Leptotrombidium (scrub typhus vector). Other genera included Schoengastia and Blankaartia. Tick and flea specimens together comprised less than 1% of the sample. Among the five species of ticks collected, Haemaphysalis bandicota was the predominant species caught, followed by Ixodes granulatus other Haemaphysalis spp., Rhipicephalus spp. and Dermacentor spp. Only two species of fleas were collected and Xenopsylla cheopis (rat flea) was the predominant species. Using both commercial diagnostic kits and in‐house molecular assays, animal tissue samples were examined and screened for zoonotic diseases. Seven zoonotic diseases were detected: scrub typhus, leptospirosis, murine typhus, tick typhus, bartonella, babesiosis and trypanosomiasis. Most samples were positive for scrub typhus. Other zoonotic diseases still under investigation include borrelosis, ehrlichiosis, the plague, and other rickettsial diseases. Using geographic information systems, global positioning systems and remote sensing technology, epidemiological and environmental data were combined to assess the relative risk in different biotopes within highly endemic areas of scrub typhus in Thailand.     

Leptospira interrogans infection in domestic and wild animals in Fiji

Clinical and serological evidence has indicated that human leptospirosis in Fiji is an important disease, and the prevalence of antibody is exceptionally high. A serological survey of the rural population showed that only 12% of the people studied did not have complement fixing (CF) leptospiral antibody. As the origin of this infection could not be explained by the known distribution of leptospiral infection in domestic and wild animals, a serological survey using the complement fixation test (CFT) was undertaken as the first stage of an epidemiological investigation into human and animal leptospirosis. Sera from domestic and wild animals were tested for CF antibody to 12 leptospiral serovars, namely: pomona, copenhageni, grippotyphosa, hardjo, ballum, tarassovi, canicola, australis, bratislava, autumnalis, pyrogenes and bataviae. Antibody was detected in 27.5% of 480 cattle, 17.1% of 70 sheep, 10.3% of 252 goats, 10.0% of 480 pigs, 57.0% of 100 dogs, 55.8% of 34 rats (Rattus rattus, R. frugivorus, R. exulans and R. norvegicus), 53.1% of 32 mongooses (Herpestes auropunctatus) and 40.0% of 10 mice (species unknown.) Cross-reactivity precluded the identification of infecting serogroups with the exception of pomona in pigs and icterohaemorrhagiae, ballum and australis in dogs. Infection of dogs with a serovar of the australis serogroup may explain the predominance of serological reactions to bratislava in man. The survey revealed a significant level of leptospiral antibody in the animal populations of Fiji and indicated that cattle, dogs, rats, mongooses and mice are probably the most important maintenance hosts. Consequently, further investigation will concentrate on the attempted isolation of leptospires from these species.     

Neospora caninum detected in feral rodents

The role of rodents in the epidemiology of neosporosis was investigated by assaying brain tissue of feral mice (Mus musculus) and rats (Rattus norvegicus) for Neospora caninum. Both mouse and rat brain tissue were extracted for total DNA, and subjected to two different N. caninum-specific nested polymerase chain reaction (PCR) assays. A portion of brain tissue from the mice and rats were also assayed for N. caninum in gerbils or gamma-interferon gene knockout (KO) mice. Of the 105 feral mice tested, 10% were positive in the N. caninum-specific PCR assays. Of the 242 rats tested, 30% were positive in both assays. Although mice and rats had N. caninum by PCR testing, clinical signs of N. caninum infection were not observed nor were N. caninum parasites observed in gerbils or KO mice inoculated with the rodent brain tissue.     

Epizootiological survey of hantavirus among rodent species in Ningxia Hui Autonomous Province, China

Hantaviral antibodies were detected in the sera from Apodemus (A.) agrarius and A. peninsulae captured in Ningxia province, China by several different serological diagnostic methods. A total of 409 sera from rodent and insectivore species were collected in 1999 and examined by indirect immunofluorescent antibody assay (IFA). Among them, 19 of 191 (9.9%) sera of A. agrarius and 1 of 13 (7.7%) sera of A. peninsulae were positive for hantaviral antibodies. The other species (Rattus norvegicus, Mus musculus, Cricetulus triton, and Sorex cylindricauda) were negative. The reaction pattern of positive serum was characterized as scattered and granular virus antigens in the cytoplasm of hantavirus infected Vero E6 cells. Some of the A. agrarius sera positive for hantavirus were further examined by Western blotting (WB), enzyme-linked immunosorbent assay (ELISA), and the focus reduction neutralization test (FRNT). By WB, positive sera showed the same specific reaction pattern of baculovirus-expressed recombinant hantaviral nucleocapsid protein, as shown in hantavirus-immune serum. By ELISA, IFA-positive sera showed significantly higher optical densities (around 1.0) than the negative A. agrarius sera. Hantaan type hantavirus was neutralized with the positive sera. These results suggest that A. agrarius have hantavirus infection and may play a role as a reservoir animal for hantavirus in Ningxia Hui Autonomous Province, China.     

Factors associated with infection by Neospora caninum in dogs in Brazil

From August 2006 to 2008, 411 dogs in northeastern Brazil were evaluated for seropositivity to Neospora caninum. The dogs were clinically examined, and their owners were interviewed about the conditions in which the animals were maintained in order to assess the factors associated with infection by this parasite. A serum sample was taken from each dog for serological examination in an indirect fluorescent antibody test for N. caninum. The Yates' Chi-square test or Fisher's exact test was used to select the variables for the multivariate logistic regression model. Seropositivity was detected in 9.26% of dogs. The seropositivity rates of dogs from different environments were 2.6% (4/156) in urban areas, 13.1% (28/214) in peri-urban areas, and 14.6% (6/41) in rural areas. Factors associated with seropositivity for N. caninum were the following: contact with other dogs, access to food outside the home and residing in the peri-urban or rural environments (p<0.05). Results of this study confirm that dogs in urban, rural and peri-urban areas of northeastern Brazil are exposed to N. caninum. Control measures to prevent infection of dogs in the studied region should be focused primarily on preventing access to potential sources of infection, which include environments with other dogs, bovines, and other small intermediate hosts, such as birds and rodents.     

Bats as the main prey of wintering long‐eared owl (Asio otus) in Beijing: Integrating biodiversity protection and urban management

The loss of biodiversity from urbanized areas is a major environmental problem challenging policy‐makers throughout the world. Solutions to this problem are urgently required in China. We carried out a case study of wintering long‐eared owls (Asio otus) and their main prey to illustrate the negative effects of urbanization combined with ineffective conservation of biodiversity in Beijing. Field monitoring of owl numbers at two roosting sites from 2004 to 2012 showed that the owl population had fallen rapidly in metropolitan Beijing. Analysis of pellet contents identified only seven individuals of two species of shrew. The majority of mammalian prey comprised four bat and seven rodent species, making up 29.3% and 29.5% of the prey items, respectively. Prey composition varied significantly among years at the two sample sites. At the urban site the consumption of bats and rodents declined gradually over time, while predation on birds increased. In contrast, at the suburban site the prey composition showed an overall decrease in the number of bats, a sharp increase and a subsequent decrease in bird prey, and the number of rodent prey fell to a low point. Rapid development of real estate and inadequate greenfield management in city parks resulted in negative effects on the bird and small mammal habitat of urban areas in Beijing. We suggest that measures to conserve biodiversity should be integrated into future urban planning to maintain China's rich biodiversity while also achieving sustainable economic development.     

Epidemiology of Bartonella Infection in Rodents and Shrews in Taiwan

During the period of August 2002 and November 2004, an epidemiological investigation for Bartonella infection was conducted in small mammals in Taiwan. Using whole blood culture on chocolate agar plates, Bartonella species were successfully isolated from 41.3% of the 310 animals tested. The isolation rate of Bartonella species varied among different animal species, including 52.7% of the 169 Rattus norvegicus, 28.6% of the 126 Sucus murinus, 10% of the 10 Rattus rattus and 66.7% of the three Rattus losea. Bacteremia prevalence also varied with the origin of the animals, as 56.2% of the animals captured on farms, 38.6% of the ones captured at harbour sites and 11.8% of the animals captured from urban areas were bacteremic. Through molecular analysis of the gltA gene and 16S/23S intergenic spacer region, genetic diversity of Bartonella organisms was identified, including strains closely related to Bartonella tribocorum, Bartonella grahamii, Bartonella elizabethae, Bartonella phoceensis and Bartonella rattimassiliensis. Moreover, this is the first report of zoonotic B. elizabethae and B. grahamii identified in R. losea, the lesser rice‐field rat. Various Bartonella species were identified in R. norvegicus, compared to 97.2% of Suncus murinus with unique Bartonella species. By indirect immunofluorescence antibody test, using various rodent Bartonella species as antigens, consistently low percentage of seropositivity implied that small mammals may play a role as competent reservoirs of Bartonella species in Taiwan. Future studies need to be conducted to determine whether these Bartonella species would be responsible for human cases of unknown fever or febrile illness in Taiwan, especially zoonotic B. elizabethae and B. grahamii.     

The significance of small mammals in the epizootiology of leptospirosis in livestock]

1. Favourite species of rodents in sheds and their surroundings are rats (Rattus norvegicus, R. rattus) and house mouse (Mus musculus). From the epizootiological point of view only R. norvegicus is important as the maintenance host of L. copenhageni. 2. In surrounding of sheds vole (Microtus arvalis) and back-striped field mouse (Apodemus agrarius) are sources of infection for livestock. 3. Transmission of leptospira occurs via infected environment. The tenacity of Leptospira mozdok and L. grippotyphosa under field conditions suffices to maintain the chain of infections.     

The role of rodents and other wildlife in the epidemiology of swine toxoplasmosis

Two swine production units and their contiguous wildlife populations were used for this study. These herds were located 7 miles apart in the major swine producing area of south central Georgia. Herd A had a Toxoplasma gondii antibody prevalence of 27.6% in all ages of swine sampled, with an increased incidence of 13.6% over a 5-month period. This herd was maintained under a semi-range condition. The swine in Herd B were maintained exclusively in concrete floored, enclosed buildings. This herd had a 0.85% T. gondii prevalence. Rodents and a few other wildlife and domestic species were trapped in or around both herds. These animals were examined for Toxoplasma antibodies using the same test procedure utilized for swine sera, the indirect immunofluorescent (IIF) test. Additionally, rodent tissues were homogenized and suspensions prepared for interperitoneal (I/P) inoculation into CF₁ laboratory mice.Rodents and wildlife species examined were: Mus musculus, Peromyscus leucopus, Rattus norvegicus, Sigmodon hispidus, Procyon lotor, and Didelphis marsupalis. Feral and domestic animals other than swine that also were tested for the presence of T. gondii antibodies included two cats, two horses, and a dog. The overall prevalence of T. gondii antibodies in all non-porcine species examined was 67% for those animals in and around the premises of Herd A, and 63% for those in and around Herd B.Toxoplasma infectivity of rodents whose tissues were processed and inoculated into laboratory mice correlated well with the results of the IIF test on the serum of these wild rodents. No tachyzoites of T. gondii were found in the peritoneal exudate of laboratory mice post I/P inoculation with wild rodent tissue, with one exception.While there was no significant difference in Toxoplasma infectivity in non-porcine species on these two premises, management practices appeared to be the determining factor in swine infection with T. gondii. Excluding wildlife precluded infection.     

A serological and molecular study on Francisella tularensis in rodents from Hamadan province,Western Iran

Introduction and purposeTularemia is a zoonotic disease, the most important hosts of which are rodents. Endemic regions and reservoirs of F. tularensis are not well-researched areas in Iran. The present study aimed to study F. tularensis infection in the rodent populations of western Iran.Materials and methodsSamples were collected in different areas of Kabudar Ahang County in Hamadan province (west of Iran) from 2014 to 2017. Tularemia serological and molecular tests were conducted using the tube agglutination test and Real-time PCR method tracking the ISFtu2 gene. Positive serum samples were evaluated for cross-reactivity with brucellosis.ResultsA total of 433 rodents, collected from 33 localities, were included in the study. The most abundant species belonged to the Persian jird (Meriones persicus; 75.5%), and Libyan jird (Meriones libycus; 10.1%). Among the studied samples, three (0.74 %) were seropositive and five (1.15%) were PCR positive. Seropositive samples were two M. persicus and one M. libycus, and PCR positive rodents were four M. persicus and one M. vinogradovi. Tularemia seropositive samples showed no cross-reactivity with brucellosis.ConclusionGiven the presence of infection in rodents with tularemia agent in the studied area, it is crucial to elucidate the risks of rodent exposure to tularemia for physicians, health personnel and the general population.     

阿拉善地区不同植被生境中鼠类栖息地选择的特性

2002～2007年,在阿拉善荒漠区选择开垦区、轮牧区、过牧区和禁牧区四种植被生境,采用标志重捕法研究不同植被生境中鼠类栖息地选择的特性。结果表明:6个年度中啮齿动物群落的优势种群在四种不同植被生境中各不相同,各个群落的组成种类和主要种类的数量有较大变化;6年中不同植被生境中啮齿动物群落组成种的年平均种数为轮牧区=过牧区=禁牧区>开垦区。不同植被生境中主要组成种变化较大:开垦区为长爪沙鼠、黑线仓鼠;轮牧区为子午沙鼠、小毛足鼠;过牧区为三趾跳鼠、五趾跳鼠;禁牧区为小毛足鼠。长爪沙鼠在开垦区与其他三种干扰区间有极显著差异(P<0.01),而在其他三种干扰区间无差异;三趾跳鼠在过牧区与其他三种干扰区间有极显著差异(P<0.01)。     

3种鼢鼠线粒体DNA控制区结构及其系统发育分析

采用PCR 产物直接测序法测定了3种鼢鼠Mospalax spp.18个个体的线粒体控制区(Control region)核苷酸全序列,并进行了结构分析。通过与仓鼠亚科其他啮齿动物的控制区序列进行比较,将鼢鼠的控制区分为终止序列区、中央保守区和保守序列区3个区域。同时识别了鼢鼠中一系列保守序列,并给出了它们的一般形式。选用普通田鼠Microtus rossiaemeridionalis、褐家鼠Rattus norvegicus、小家鼠Mus musculus、鼹鼠Nannospalax ehrenbergi为外类群,采用NJ和UPGMA法构建分子系统发育树。结果显示：鼢鼠中控制区基因适于系统发育分析,根据分子系统学、形态学的结果初步认为高原鼢鼠M.baileyi和甘肃鼢鼠M.cansus达到了种级地位。     

Environmental factors associated with rodent infestations in Argentine poultry farms

1. Seasonal variations in rodent infestations were studied at poultry farms in central Argentina as well as the environmental factors associated with rodent infestations at poultry farms. 2. During the summer and winter of 1998 rodent infestation was monitored at 10 poultry farms by means of tracking stations, and 21 environmental variables were selected that a priori could be related with the extent of rodent infestation. 3. There was a higher rodent infestation in winter than in summer. 4. Species detected by rodent sightings at the poultry farms included Akodon azarae, Calomys spp. (C. laucha and possibly C. musculinus) and Mus musculus. 5. In summer, rodent infestation was positively associated with the perimeter of the farm, whereas there was an inverse relationship with the maintenance conditions of the sheds. In winter, rodent infestation was positively associated with the percentage of the borders of the farm covered with vegetation, and with the amount of plant cover, especially the amount of plant cover which was above 20 cm in height. 6. There was no significant relationship between rodent infestation and the time lag since the last application of rodenticide (first-generation anticoagulant) at the farms. 7. These results suggest that strategies for controlling rodents based solely on chemical methods may not be good enough for efficient rodent control. Farms which are properly managed, with a better control of vegetation growth at both the perimeter and within the internal area, in addition to a higher maintenance of sheds have appreciably lower rodent infestations.