How Far Can the Red Palm Weevil (Coleoptera: Curculionidae) Fly?: Computerized Flight Mill Studies With Field-Captured Weevils.

Adult Rhynchophorus ferrugineus (Olivier) captured in pheromone-baited traps in commercial date palm orchards in the Al Ahsaa Directorate, Kingdom of Saudi Arabia, were used in computerized flight mill studies to determine the flight characteristics of this highly invasive and destructive palm pest. Flight mill studies were run at three different time periods, winter (December), spring (March), and summer (May). Of the 192 weevils tethered to flight mills ∼30% failed to fly > 1 km. Of those weevils flying > 1 km (n = 139), 55% flew > 10 km, and of these flyers 5% flew > 50 km in 24 h. Flying weevils exhibited an average weight loss of 20-30% and nonflying control weevils lost ∼9-13% body weight in 24 h. Male and female weevils flying in summer (average laboratory temperature was ∼27°C) flew the longest average distances (∼25-35 km), exhibited highest weight reductions (∼30%), and greatest mortality rates (∼80%). Consequently, time of year not weevil sex or color morph had a consistent and significant effect on flight activity, weight loss, and survivorship rates. Flight activity was predominantly diurnal commencing around 5:00 a.m. and peaking between 9-11:00 a.m. before tapering off. The distribution of flight distances combined across season and sex was mesokurtic (i.e., normally distributed).

Nasal photodisinfection and chlorhexidine wipes decrease surgical site infections: a historical control study and propensity analysis.

BACKGROUND: Pre-operative decolonization therapy (DcTx) using chlorhexidine (CHG) body washes and/or intranasal mupirocin can reduce surgical site infections (SSIs), but compliance is often suboptimal. AIM: To assess the effectiveness of immediate DcTx using a novel approach of intranasal antimicrobial photodisinfection therapy (PDT) combined with CHG body wipes for the reduction of SSIs. METHODS: Between 1(st) September 2011 and 31(st) August 2012, 3068 elective cardiac, orthopaedic, spinal, vascular, thoracic and neurosurgical patients were treated with CHG in the 24h preceding surgery, and received intranasal PDT in the pre-operative area. SSI surveillance methodology remained unchanged from previous years and patients were followed for one year. Results were compared with those for a four-year historical control group of 12,387 patients as well as those for a concurrent control group of 206 untreated patients. FINDINGS: A significant reduction in the SSI rate was observed between treated patients and the historical control group [1.6% vs 2.7%, P = 0.0004, odds ratio (OR) 1.73, 95% confidence interval (CI) 1.2815-2.3453]. This significant reduction was maintained on intent-to-treat analysis (P = 0.021, OR 1.37, 95% CI 1.0476−1.7854) [corrected]. Overall compliance with DcTx was 94%. A 1:4 propensity score analysis of matched treated and untreated patients demonstrated that DcTx reduced the risk of SSIs significantly (P = 0.00026, z = 3.65). CONCLUSION: The combination of CHG wipes and PDT immediately before surgery reduced SSIs, achieved excellent compliance, and was easily integrated into the pre-operative routine.

NK T cell-induced protection against diabetes in V alpha 14-J alpha 281 transgenic nonobese diabetic mice is associated with a Th2 shift circumscribed regionally to the islets and functionally to islet autoantigen.

The onset of autoimmune diabetes is related to defective immune regulation. Recent studies have shown that NK T cells are deficient in number and function in both diabetic patients and nonobese diabetic (NOD) mice. NK T cells, which are CD1d restricted, express a TCR with an invariant V alpha 14-J alpha 281 chain and rapidly produce large amounts of cytokines. V alpha 14-J alpha 281 transgenic NOD mice have increased numbers of NK T cells and are protected against diabetes onset. In this study we analyzed where and how NK T cells interfere with the development of the anti-islet autoimmune response. NK T cells, which are usually rare in lymph nodes, are abundant in pancreatic lymph nodes and are also present in islets. IL-4 mRNA levels are increased and IFN-gamma mRNA levels decreased in islets from diabetes-free V alpha 14-J alpha 281 transgenic NOD mice; the IgG1/IgG2c ratio of autoantibodies against glutamic acid decarboxylase is also increased in these mice. Treatment with IL-12 (a pro-Th1 cytokine) or anti-IL-4 Ab abolishes the diabetes protection in V alpha 14-J alpha 281 NOD mice. The protection from diabetes conferred by NK T cells is thus associated with a Th2 shift within islets directed against autoantigen such as glutamic acid decarboxylase. Our findings also demonstrate the key role of IL-4.

Molecular mapping of idiotopes of anti-arsonate antibodies.

As part of understanding molecular function in structural terms, we have been attempting to map the idiotypic topography of specific anti-arsonate (Ars) antibodies. A panel of anti-Ars hybridomas of which the complete primary sequences are known were used. These molecules show a varied reactivity profile with a panel of monoclonal anti-idiotypic antibodies. By judicious chain recombination experiments and chemical modifications that altered this reactivity profile, we were able to identify particular amino acid residues or discreet regions of anti-Ars antibodies as having crucial roles in the expression of idiotypic determinants. Idiotopes were mapped to the heavy chain second hypervariable region and D segment, and to the light chain first and third hypervariable regions.

Complete amino acid sequence of heavy chain variable regions derived from two monoclonal anti-p-azophenylarsonate antibodies of BALB/c mice expressing the major cross-reactive idiotype of the A/J strain.

The primary structure of A/J anti-p-azophenylarsonate (anti-Ars) antibodies expressing the major A-strain cross-reactive idiotype (CRIA) has provided important insights into issues of antibody diversity and the molecular basis of idiotypy in this important model system. Until recently, this idiotype was thought to be rarely, if ever, expressed in BALB/c mice. Indeed, it has been reported that BALB/c mice lack the heavy chain variable segment (VH) gene that is utilized by the entire family of anti-Ars antibodies expressing the A/J CRI. Recently, however, it has been possible to elicit CRIA+, Ars binding antibodies in the BALB/c strain by immunizing first with anti-CRI and then with antigen. Such BALB/c, CRIA+ anti-Ars antibodies can be induced occasionally with antigen alone. VH region amino acid sequences are described for two CRIA+ hybridoma products derived from BALB/c mice. While remarkably similar to each other, their VH segments (1-98) differ from the VH segments of A/J CRIA+, anti-Ars antibodies in over 40 positions. Rather than the usual JH2 gene segment used by most A/J CRIA+ anti-Ars antibodies, one BALB/c CRIA+ hybridoma utilizes a JH1 gene segment, while the other uses a JH4. However, the D segments of both of the BALB/c antibodies are remarkably homologous to the D segments of several A/J CRIA+ antibodies sequenced previously, as are the amino terminal amino acid sequences of their light chains. These data imply that BALB/c mice express the A/J CRIA by producing antibodies with very similar, if not identical, light chain and heavy chain D segments, but in the context of different VH and JH gene segments than their A/J counterparts. The results document that molecules that share serologic specificities can have vastly different primary structures.

Junctional diversity is essential to antibody activity.

Many mechanisms of antibody diversification have been shown to exist, including combinatorial pairings of heavy and light chains, the use of multiple gene segments (combinatorial diversity), and the imprecise joining of these gene segments (junctional diversity). The contributions of each of these mechanisms to functional antibody activity has not been fully explored, especially in the case of junctional diversity. A chain recombination experiment between an anti-arsonate monoclonal antibody and an anti-oxazolone molecule in which light chains differ essentially only at the V/J junctional position show that junctional diversity may play an important role in antigen binding.

Use of JH4 joining segment gene by an anti-arsonate antibody that bears the major A-strain cross-reactive idiotype but displays diminished antigen binding.

One of the antibody families utilized by the A/J mouse in its response to p-azophenylarsonate (Ars) is characterized by the expression of the major anti-arsonate cross-reactive idiotype (CRI) of the A strain. This family has been termed the Ars-A family. A hybridoma antibody (HP 101F11 ) obtained after immunization of an A/J mouse with Ars was identified initially as displaying the CRI, but was subsequently found to bind antigen at a level much lower than most members of the Ars-A family. The results of binding studies suggested that HP 101F11 possesses reduced avidity for antigen. When isolated light and heavy chains were allowed to recombine with the heavy and light chains of a strongly antigen-binding, strongly CRI-positive antibody of the Ars-A family (HP 93G7 ), the low level of antigen binding by HP 101F11 was found to be due to a structurally variant heavy chain. Whereas antibodies of the Ars-A family with normal avidity for antigen had been shown to use the JH2 joining segment gene, amino acid sequence analysis of HP 101F11 revealed that this antibody has a JH segment with a sequence identical to that encoded by a portion of a different JH gene, JH4 . The implication that 101F11 uses the JH4 gene instead of JH2 was supported by the observation that the productively rearranged gene is associated with an Eco R1 restriction fragment 0.95 Kb smaller than the corresponding fragments of Ars-A hybridomas with normal avidity for antigen. The size difference of 0.95 Kb corresponds exactly to the known distance between the JH2 and JH4 genes in BALB/c germline DNA. In addition to the structural differences immediately attributable to the use of JH4 , HP 101F11 has shown an amino acid interchange in the DH segment, and a single amino acid deletion at the DH-JH boundary. These results show that variation among members of the Ars-A family in the DH and/or JH segments provides alternative structural forms of Ars-A antibodies upon which selective processes can operate during the course of an immune response.

Prevalence of antibodies to Haemophilus pleuropneumoniae in Iowa swine.

The prevalence of complement-fixing (CF) antibodies to Haemophilus pleuropneumoniae in Iowa swine was determined by testing samples collected randomly from each of 9 crop-reporting areas (9 to 12 counties) in Iowa in approximate proportion to the number of swine marketed annually from each area. For testing, a pooled antigen composed of serotypes 1 to 5 of H pleuropneumoniae was used in a modified direct Microtiter complement-fixation test. Of 7,348 sera tested, 2,362 or 32.1% had CF antibodies (titer greater than or equal to 1:4) to the organism. On a herd basis, 417 of 597 herds or 68.8% had at least 1 animal with CF antibodies (titer greater than or equal to 1:4) to the organism. The clinical problem with H pleuropneumoniae has become significant in recent years, but by no means is the overt disease as prevalent as animals or herds with CF antibodies to the organism.

Regulation of rates of cholesterol synthesis in vivo in the liver and carcass of the rat measured using [3H]water.

This study was undertaken to determine the mechanisms that regulate cholesterol synthesis in vivo and to quantitate the relative importance of the liver and extrahepatic tissues as sites for sterol synthesis. Rats were administered [3H]water intravenously and killed 1 hour later. The amount of [3H]water incorporated into digitonin-precipitable sterols was then measured in liver, whole blood, and the remaining tissues of the carcass. In control animals, killed at the mid-dark point of the light cycle, rates of [3H]water incorporation into sterols equaled 2290 and 103 nmol/hr per g, respectively, in the liver and carcass. Cholesterol feeding suppressed synthesis in the liver but not in the extrahepatic tissues, while fasting for 48 hr suppressed synthesis in both the liver and carcass. In fasted animals subjected to stress there was a 5-fold increase in hepatic synthesis but no change in synthesis by the extrahepatic tissues. Similarly, incorporation of [3H]water into sterols by the carcass was unaffected by light cycling while the liver showed a definite diurnal rhythm. In control rats, 34.5 mumol of [3H]water was incorporated into sterols by the whole animal per hour. Of this amount of sterol synthesis about 54% took place in the liver while the remaining amount occurred in the tissues of the carcass. With cholesterol feeding or fasting, or during the mid-light phase of the light cycle, synthesis in the extrahepatic tissues accounted for 69 to 90% of total body sterol synthesis.